Alex Alien AIDS Archive
"The most formidable barrier to the advancement of science is the conventional wisdom of the dominant group."
Conrad Hal Waddington, Embryologist & Geneticist (1905 - 1975).
"Never doubt that a small group of committed people can change the world; indeed it is the only thing that ever has."
Margaret Mead, Cultural Anthropologist, (1901 - 1978).
"All truth goes through
three stages. First it is ridiculed. Then it is violently opposed. Finally, it
is accepted as self-evident."
Arthur Schopenhauer (1788 - 1860).
"There is no proof that HIV causes AIDS - for many reasons but most importantly, because there is no proof that HIV exists."
Eleni Papadopulos-Eleopulos, Is HIV the cause of AIDS?, Continuum, Autumn 1997.
"The HIV hypothesis ranks with the 'bad air' theory for malaria and the 'bacterial infection' theory of beriberi and pellagra [caused by nutritional deficiencies]. It is a hoax that became a scam."
Dr. Bernard Forscher, Conspiracy of Silence, The Sunday Times, 3 April 1994.
"It is a dire
example of how a distinguished scholar who has contributed much to the
advancement of science, now impedes further progress by his stubborn adherence
to a dogma of his own creation."
“An error can never become true however many times you repeat it. The truth can never be wrong, even if no one ever hears about it. Truth alone will endure; all the rest will be swept away before the tide of time.”
Mahatma Gandhi (1869 - 1948).
"Here we encounter the dogmatic stupidity proper to a signifier as such, the stupidity which assumes the shape of a tautology: a name refers to an object because this object is called that... "
Slavoj Zizek, The
Sublime Object of Ideology, Verso, 1989.
"Scientists will then have to come to terms with the awful fact that the AIDS epidemic was a mirage manufactured by scientists who believed that integrity could be maintained amidst the diverting influences of big money, prestige and politics."
Professor Hiram Caton, Conspiracy of Silence, The Sunday Times, April 1994.
"I propose there are no human retroviruses. 'HIV' is not Human, it has never been proven to be the cause of Immunodeficiency, and is not a Virus, but a misinterpreted artefact of human and simian cell cultures. Therefore the acronym 'HIV' is wrong on all counts."
Michel Verney-Elliott, 'SIV'
and Poliovaccination - A Shot In The Foot?, 1999.
"My work as a mathematical biologist has been built in large part on the paradigm that HIV causes AIDS, and I have since come to realize that there is good evidence that the entire basis for this theory is wrong. AIDS, it seems, is not a disease so much as a sociopolitical construct that few people understand and even fewer question...Why have we as a society been so quick to accept a theory for which so little solid evidence exists?...For over twenty years, the general public has been greatly misled and ill-informed."
Rebecca V. Culshaw, Ph.D., Why I Quit HIV; Lew Rockwell, March 3, 2006.
"I found that when they are speaking about HIV they are not speaking about a virus. They are speaking about cellular characteristics and activities of cells under very special conditions...I realized that the whole group of viruses to which HIV is said to belong, the retroviruses, in fact do not exist at all."
Dr. Stefan Lanka, Virologist, Zenger's, December, 1998.
"Where is the research that says HIV is the cause of AIDS? If there is evidence that HIV causes AIDS, there should be scientific documents which either singly or collectively demonstrate that fact, at least with a high probability. There is no such document."
Dr. Kary Mullis, Biochemist, 1993 Nobel Prize for Chemistry, The Sunday Times, 28 November 1993.
"A thing is what it is not because of its place in the ideal classification system but because of its place in real history. The order of concretely existing things is from now on determined not by ideal essences outside them but by the historical forces buried within them."
Gary Cutting, Michel Foucault's Archeology of Scientific Reason, Cambridge University Press, 1989.
"The HIV-causes-AIDS dogma represents the grandest and perhaps the most morally destructive fraud that has ever been perpetrated on the young men and women of the Western world."
Dr. Charles Thomas, Conspiracy of Silence, The Sunday Times, April 1994.
"Politically it stinks. Medically it stinks. Culturally it stinks. More and more people are beginning to realize this and are demanding a full-scale public investigation of what, quite literally, is turning out to be a (medical) fairy tale...Those who continue to perpetrate the myth that HIV is 'the deadly AIDS virus' have blood on their hands and will be tried as war criminals once the truth about 'AIDS' is finally brought to light."
Dr. Michael Ward, Is the 'deadly AIDS virus' Government Fraud?, New York Native, 4, February, 1991.
"The official AIDS paradigm represents the most colossal blunder in medical history. The Crimes Against Humanity committed in the AIDS War rank with any in history...If there were justice in the world, the AIDS-criminals would be brought to justice, given fair trials, and executed..."
John Lauritsen, The AIDS War, Asklepios, New York, 1993.
"All
things are subject to interpretation whichever interpretation prevails at a
given time is a function of power and not truth....Every elevation of man
brings with it the overcoming of narrower interpretations...every strengthening
and increase of power opens up new perspectives and means believing in new
horizons."
Friedrich
Nietzsche (1844-1900).
"I have attended, as a reporter, eight International AIDS Conferences. They are uniformly awful, a total waste of a journalist’s time. Mostly I go just to fortify my belief that AIDS - the entire industry and social machinery of it - is at its root a totalitarian system. By that, I mean that there is a central ideology that seeks to enforce its domination by methodically obstructing any ideas that run counter to it."
Celia Farber, Fear & Loathing in Geneva, Impressions Magazine, 24 August, 1998.
"Promoting science isn't just about providing resources, it is also about protecting free and open inquiry. It is about letting scientists like those here today do their jobs, free from manipulation or coercion, and listening to what they tell us, even when it's inconvenient especially when it's inconvenient. It is about ensuring that scientific data is never distorted or concealed to serve a political agenda and that we make scientific decisions based on facts, not ideology."
President Barack Obama, 9 March 2009.
"To an extent that undermines classical standards of science, some purported scientific results concerning 'HIV' and 'AIDS' have been handled by press releases, by disinformation, by low-quality studies, and by some suppression of information, manipulating the media and people at large. When the official scientific press does not report correctly, or obstructs views dissenting from those of the scientific establishment, it loses credibility and leaves no alternative but to find information elsewhere.."
Serge Lang, Challenges, Springer, 1998.
"On the face of it, the designation of AIDS as the most significant threat to public health is nonsense...This catastrophic vision is the AIDS mirage. I call it a mirage because health authorities embrace a contingent future as an incontrovertible truth. The passion invested in the viral epidemic dogma is transferred to the entire AIDS management program, so that the whole is seized by cataleptic rigidity (a panic symptom). Our AIDS management systems are incapable of reviewing evidence which shows that there have been mistakes about HIV causality, mistakes of diagnosis, mistakes about its transmission, mistakes about HIV antibody tests, mistakes about therapies."
Professor Hiram Caton, Why We Need AIDS; The AIDS Mirage, 1995.
"It is a mistake to believe that a science consists in nothing but conclusively proved propositions, and it is unjust to demand that it should. It is a demand only made by those who feel a craving for authority in some form and a need to replace the religious catechism by something else, even if it be a scientific one. Science in its catechism has but few apodictic precepts; it consists mainly of statements which it has developed to varying degrees of probability. The capacity to be content with these approximations to certainty and the ability to carry on constructive work despite the lack of final confirmation are actually a mark of the scientific habit of mind."
Sigmund Freud (1856-1939).
"Summary: Each type of virus particle has unique morphological characteristics. Even today no agreement exists as to what are the morphological characteristics of the particles said to be HIV. No HIV particle has all the morphological characteristics of retroviruses. Knobs are fundamental to the definition of a retrovirus - No knobs on the HIV particles. Retrovirus-like particles may appear in any culture infected or not infected. Each virus contains unique proteins. Purification absolutely necessary to prove their existence. No proof for HIV purification. The evidence is that the HIV proteins are cellular. Conclusion: No proof for the existence of unique HIV particles. No proof for HIV transmission. No proof for the existence of unique HIV proteins. No proof for the existence of a unique human retrovirus."
Eleni Papadopulos-Eleopulos, An analysis of the evidence for the existence of HIV, October 2006.
"Science is about making observations and trying to fit them into a theoretical framework. Having the theoretical framework allows us to make predictions about phenomena that we can then test. HIV 'science' long ago set off on a different path...People who ask simple, straightforward questions are labelled as loonies who are dangerous to public health...Yet HIV 'science' has declined so far that these elementary questions are addressed neither by the research groups themselves, nor the referees at Nature whose job it is to critique the papers before publication. But nobody in the HIV research community is at all bothered by this...One gets a remarkable sense of being disassociated from the real world when entering the realm of AIDS research."
Mark Craddock, HIV: Science by press conference; AIDS: VIrus- or Drug Induced?, Kluwer Academic Publishers, 1996.
"I would like to present the evidence available to me in support of the hypothesis: a) that AIDS is a typical example of epidemic hysteria, b) that the epidemic has at its core an unconscious group delusion, which can be called the group-fantasy of scapegoating, c) that the combination of these unconscious group tensions brought about a subtle and sophisticated, but nevertheless sacrificial witch hunt, in which the participants were the Moral Majority, d) that these attacks resulted in an epidemic of depression based mostly on shame; e) that the core sign of AIDS, the reduction of cell-mediated response, is one of the typical vegetative signs of severe depression; f) that the epidemic represents, in the group’s unconscious fantasies, an equivalent war, during which the group keeps careful count of the sacrifices; g) and finally that, since the epidemic is psychogenic, the prediction can be made that the group will decide when it should be over (when they have ‘had enough’), a decision which will be broadcast to the group members through the media, so that after a suitable lag period the epidemic will resolve and the incidence will descend from epidemic to endemic levels."
Caspar Schmidt, The AIDS
Cult; Asklepios Pagan Press, 1997.
Dedicated to the Memory of David Pasquarelli
December 10th 1967 - March 8th 2004
HIV does not exist

End HIV Lies
Positive Nation, December 1997/January 1998
One of the most controversial figures on the British AIDS scene is Alex Russell (pictured), editor of the magazine Death Camp and researcher for Continuum magazine. He has long argued that AIDS research and treatment are totally misdirected. Here he says that HIV simply does not exist.
In 14 years, the 'HIV' hypothesis has been unproductive and non-predictive because 'Aids' is neither an infectious epidemic nor caused by 'HIV'. To date, 'HIV' has never been isolated as a unique, exogenous 'retrovirus'. Dr Robert Gallo and Prof Luc Montagnier announced the 'discovery' of a 'retrovirus' fully aware that there was no proof for it. Gallo and Montagnier published electron micrographs of a few particles which they claimed are a 'retrovirus' and are 'HIV'. But the photographs did not prove the particles were a virus. Virologists Dr Stefan Lanka states: "The rules demonstrating the existence of HIV (and retroviruses in general) were never adhered to by those who devised them nor were they ever validated." (Continuum Vol.4, No.3) 'Retroviruses' (as a source of reverse transcription) have never been proven to exist as biological entities. All 'retroviruses' ('HIV', 'SIV', 'BIV', 'FIV', 'MIV') are hypothetical constructs. 'Retroviruses' are an over-determination of the phenomenon of reverse transcription first discovered in 1970 by Howard Temin whilst studying the Rous Sarcoma Virus. Reverse transcription is a normal process of cells associated with cellular repair mechanisms particularly of the cell membrane. Reverse transcription is not a property unique to hypothetical 'retroviruses' - it also occurs in hepatitis viruses as well as most mammalian and plant cells.
There is no Universal Gold Standard 'HIV' test to prove 'HIV' positivity. The 'HIV' antibody test does not detect a 'virus' but an assortment of proteins that are non-specific to the hypothetical 'HIV'. The proteins that are used in the 'HIV' test are merely the biological outcome of stressed white blood cells used in the lab. In 'Bio/Technology', June 1993, 'Aids' analyst, Dr Eleni Eleopulos exposed the non-specificity and unreliability of the 'HIV' 'antibody test'. Dr Eleopulos's critique supports the argument for the banning of the misleading 'HIV' tests.
There can be no Gold Standard 'HIV' test because there is no Gold Standard 'HIV' isolate. On each continent there are different criteria for 'HIV' positivity and 'Aids' definition. All evidence of 'HIV' positivity must be confirmed by pure culturing of a patient's lymphocytes and detection of whole, sell-free viral particles; so far this has never been achieved. 'HIV' is termed a 'lentivirus' ('slow virus'): lentiviruses are not known to be sexually transmitted.
The hypothetical 'HIV' is not sexually transmitted: cell-free viral particles have never been found directly in semen. In 'American Journal of Epidemiology' (Vol. 146, No.4), Nancy S. Padian et al reported: "We estimate that HIV infectivity for male-to-female transmission is low, approximately 0.0009 per contact, and that infectivity for female-to-male transmission is even lower."
Moreover, Dr David Ho admits that 99.8 per cent of putative 'HIV particles' are non-infectious; the remaining 0.2 per cent of 'viral particles' , being defective, are not capable of replication. As a transmittable entity, 'HIV' could not survive in nature. This indicates that what we are calling 'HIV' is a misinterpreted, non-transmissible, endogenous epiphenomenon that should never have been classed as a virus. 'HIV' is an artefact of cell-culture invented by Dr Robert Gallo. The phenomena collectively known as 'HIV' are non-specific: reverse transcriptase is non-specific; PCR is non-specific; Viral Load is non-specific. Each property relating to 'HIV' can be shown to pertain to the cells used in co-cultivation experiments. No particle of 'HIV' has ever been obtained pure, free of contaminants; nor has a complete piece of 'HIV' RNA (or the transcribed DNA) ever been proved to exist.
Dr John Papadimitriou states: "They have not proven that they actually have detected a unique, exogenous retrovirus. The critical data to support that idea have not been presented. You have to be absolutely certain that what you have detected is unique and exogenous, and a single molecular species....the proper controls have never been done. ('Aids: The failure of contemporary science', Neville Hodgkinson, Fourth Estate, 1996, page 375). Dr Eleopulos and her colleagues argue that the greatest ingle obstacle to understanding and solving 'Aids' is 'HIV'. 'HIV' imprinting has become unconsciously internalised on such a global scale that people will not be able to accept the brute reality that 'HIV' does not exist.
Alex Russell
|
RESPONSE TO DORA EAST: THE ARCHER ENQUIRY
On NHS Supplied Contaminated Blood and Blood Products
Wednesday, 20th May 2009
To:
Dora East, Customer
Service Centre, Department
of Health, Richmond House, 79
Whitehall, London SW1A 2NS
Dear
Dora East, Thank
you for your letter dated 6th May 2009. We were rather
perplexed and astonished that none of our questions were answered point
by point but instead we have had a ‘standard’ reply with outdated
references. Due
to the urgency and importance of these still unanswered questions we
have decided to put our letters to you and Sarah Brimson and your
replies to us in the public domain as well sending them to the editors
of The Lancet and The British Medical Journal. Furthermore:
to prove the existence of a hypothetical HIV it is absolutely imperative
and necessary that you send us an EM of purified HIV as all EMs of the
putative HIV published to date are of unpurified cell cultures. We
would be most grateful if you could answer the following to Sarah
Brimson’s unanswered claims, which are typed in italics below. “You
mention that it is your belief that HIV could not possibly survive the
manufacturing process. The Department does not believe this to be true. Before
the development of virus inactivation steps, the factor VIII manufacturing
methods of the time (prior to 1985) were typically highly conservative
processes, aimed at preserving the labile factor VIII molecule” It is not
a matter of belief, but rather, there must be evidence. Could you please
provide the relevant references? “Cyroprecipitation
is simply a controlled method of thawing plasma”. Your
statement is untrue. Cyroprecipitation is “the precipitation of a
substance in solution (e.g., antihemolytic factor in blood plasma) on exposure
to lowered temperature”. “Laboratory
studies have shown that freeze-drying, of itself, does not inactivate HIV”. What
laboratory studies? Please could you provide references which prove that
freeze drying does not inactivate HIV. Most importantly, as we stated, the
HIV experts agree that the survival of cell fee HIV outside the body is measured
in hours. But the time between collection of plasma and its processing is
several days to weeks. Freezing plasma also significantly reduces the HIV
titre. “Cell
free HIV is certainly infectious and there is a lot of data implicating this
form of the virus in transmission by several body fluids”. The fact
is that according to all the HIV experts, for HIV infectivity particles must
have knobs on their surface—this is absolutely necessary. If this is the
case then, for anybody, including yourself, to claim HIV is infectious you must
have proof for the existence of cell free particles with knobs. (Plasma is
cell free). Could you please provide some references with evidence that
proves the existence of cell free particles containing knobs? If no such
evidence is found then we all, including yourself, have no other choice to
conclude that either (a) the cell free particles are not infectious; (b)
the HIV experts are wrong—the particles are infectious even without knobs.
Please provide evidence. “A
second misconception is that HIV is present only in low concentration in plasma.
Studies using nucleic acid technology, of the early period of infection,
have shown that HIV-1 RNA is commonly present in plasma at concentrations of
250,00([350,000 copies mr1 and
that concentrations of 1,000,000 copies ml-1 are not uncommon”. (a)
Nucleic acids are not virus particles. (b)
In the CDC 2000 Revised Surveillance Case Definition for HIV Infection it is
stated: "In adults, adolescents, and children infected by other than
prenatal exposure, plasma viral RNA nucleic acid tests should NOT be used in
lieu of licensed HIV screening tests (e.g., repeatedly reactive enzyme
immunoassay)” [emphasis in original].
1
If the viral load (RNA) cannot be used to define HIV infection then
certainly it cannot be used for quantifying it. One cannot say on the one
hand “I cannot tell you if there are apples in this crate” and on the other
“This crate has a hundred apples”. (c)
According to Hans Gelderblom and other virologists, one can detect particles in
plasma at concentrations of 104 to 105 per ml and preparations can be
concentrated a thousand fold. Wei et al state “ …virtually all
HIV-1-infected individuals, regardless of clinical stage, exhibit persistent
plasma viraemia in the range of 102 to 107 virions per ml”.
2
Where are they? No one has ever seen them? No one can find
them, including the world’s leading expert in HIV electron microscopy,
Professor Hans Gelderblom from the Koch Institute in Berlin. He regards
this the Holy Grail of his research but admits it is an endeavour which he has
failed. “Moreover,
a recent study has demonstrated that a concentration of 150 copies ml-1 has been
sufficient to cause an infection in the transfusion recipient”. Please
can you kindly give us the reference? “The
nucleic acid technology is not reserved for studies with HIV, but is applied to
a wide range of specialities. It has been found to be a very robust technology.
HIV is infectious. Cell free preparations of the HIV virus have been
demonstrated to be infectious in cell free infectivity assay system. Even at low
RNA titres HIV has been shown to be infectious when transfused”. See
above. “Also,
purified cloned HIV infected three laboratory workers [Cohen J Science 1994;
226: 1641]” We could
not locate the cited reference. If you mean Science 266, page 1647,
there are no data in regard to cloning and purification. Neither such data
exist in the Abstract cited by Jon Cohen from the 1993 Berlin International AIDS
conference. “The HIV virus exists.
It has been seen [Fields Virology text book]”
The
authors of textbooks repeat what the alleged experts in the field have reported
and published. According to all the HIV experts, including Montagnier and
Gallo, the latter with other experts under oath in an Australian court case,
that to prove the existence of a new virus, the virus particles must be
purified. To date, nobody has published any such proof.
3
And see above in regard to RNA. Furthermore,
the two papers by Gluschankof et al
4
and Bess et al
5
published electron-micrographs for the first time showing what was purported to
be ‘purified HIV’ was in fact an assortment of microvesicles and cellular
debris. “HIV”
is no more than a collage of phenomena observed in cultures of tissues from AIDS
patients. The same phenomena can be found in similar, cultures subject to
the same conditions, but obtained from non-AIDS patients. The taxonomic classification
of HIV (22-23 May, 1986) was ostensibly a strategic invention to present a
nomenclature that would unify a diversely identified putative 'retrovirus':
human T-cell lymphotropic virus type III ('HTLV-III'),
immunodeficiency-associated virus ('IDAV'), aids-associated retrovirus ('ARV')
and lymphadenopathy-associated virus ('LAV'). This politically expedient
move was to enforce the 'belief' that a non-purified 'human retrovirus' caused
'immunodeficiency'. However, twenty-three years on and HIV has still not
proven to be a human immuno-deficiency virus. If HIV exists, as you claim,
then you should be able to provide us with proof. The minimum necessary
but not sufficient evidence is EM of purified virus-like particles. We ask that the Department of Health provide us with such an
electron micrograph. “You
also mention in your letter that it was the 99 per cent impurities in FVIII that
caused the immune suppression (AIDS) seen in haemophiliacs. Whilst it is true
that FVIII accounted for a very small proportion of the total protein present in
the concentrates of the time, the other proteins present were normal plasma
proteins. Haemophiliacs were exposed to all these proteins during treatment with
plasma or pooled cryoprecipitates before concentrates became available”. It is a
fact, accepted by many HIV experts, that haemophiliacs were immunosuppressed
long before the AIDS era by factor VIII infusions. That is, long before
factor VIII was contaminated by HIV. For example, UK scientist Robin Weiss
and his colleagues reported "We have thus been able to compare lymphocyte
subset data before and after infection with HTLV-III [HIV]. It is commonly
assumed that the reduction in T-helper-cell numbers is a result of the HTLV-III
virus being tropic for T-helper-cells. Our finding in this study that
T-helper-cell numbers and the helper/suppressor ratio did not change after
infection supports our previous conclusion that the abnormal T-lymphocyte
subsets are a result of the intravenous infusion of factor VIII concentrates per
se, not HTLV-III infection".
6
Which means that factors present in the preparations and not HIV are the
cause of the immune suppression. It is also accepted that prior to
the AIDS era haemophiliacs the prevalence of fatal pneumonias caused by
non-defined organisms, was much higher than in other groups. Prior to the
AIDS era the diagnosis of PCP was made by open lung biopsy, a procedure
inadvisable for haemophiliacs. Hence it is possible, as has been reported,
such deaths were PCP.
7
“The
specific step included into the manufacturing process for FVIII was shown to
eradicate HIV and there were no further transmissions of infection even though
the proteins present in the earlier products were also present in some of the
later products”. What
specific step are you referring to? If you mean heating then you must not
forget that heating does not effect only HIV but all the other proteins, the
vast majority, which are not HIV proteins. The effect of heat is not
confined to HIV but to all proteins, including factor VIII itself. Before
the AIDS era factor VIII preparations were not heated hence you cannot claim the
non-HIV proteins, that is, the majority of the proteins in factor VIII
preparations, have the same properties now as then. It is well known that
heating proteins denatures them which significantly changes their properties.
Hence, it is impossible to attribute any reduction in immunosuppression to the
destruction of HIV. “There
were more than 10,000 patients with AIDS eagerly awaiting treatment before
Retrovir was made available in 1985 [Yarchoan M 2006], suggesting Retrovir
itself is not the agent causing AIDS”. We
said “the introduction of AZT- administered in enormous doses – rapidly
killed many haemophiliacs”. You appear to have interpreted our statement as “AZT is the
cause of AIDS”. It is quite clear
that we did not say this. We merely said that the introduction of AZT
significantly increased mortality. We
would like to conclude with the words of President Barack Obama: "Promoting
science isn't just about providing resources, it is also about protecting free
and open inquiry. It is about letting scientists like those here today do their
jobs, free from manipulation or coercion, and listening to what they tell us,
even when it's inconvenient especially when it's inconvenient. It is about
ensuring that scientific data is never distorted or concealed to serve a
political agenda and that we make scientific decisions based on facts, not
ideology." President Barack
Obama, 9 March 2009. We
would be most grateful if you could answer these questions as well as provide us
with a recent EM of purified retroviral-like particles claimed to be HIV. Yours
sincerely, Alexander
Verney-Elliott Joan
Shenton, Immunity Resource Foundation Mike Hersee, HEAL London London WC1N 1PE CC: Richard
Horton, Editor, The Lancet Fiona Godlee & Tony Delamothe, Editors, The BMJ
References:
1. CDC. Guidelines for national human immunodeficiency virus case surveillance,
including monitoring for human immunodeficiency virus infection and acquired
immunodeficiency syndrome. Centers for Disease Control and Prevention. Morb
Mortal Wkly Rep 1999;48:1-27, 29-31. www.cdc.gov/epo/mmwr/preview/mmwrhtml/rr4813a2.htm 2.
Wei X, Ghosh SK, Taylor M, Johnson VA, Emini EA, Deutsch P, et al. Viral
dynamics in human immunodeficiency virus type 1 infection. Nature 1995;373:117-122. 3.
Papadopulos-Eleopulos E, Turner VF, Papadimitriou JM, Causer D, Page BA. The
Perth Group revisits the existence of HIV. http://www.theperthgroup.com/LATEST/PGRevisitHIVExistence.pdf 4.
Gluschankof P, Mondor I, Gelderblom HR, Sattentau QJ. Cell membrane vesicles are
a major contaminant of gradient-enriched human immunodeficiency virus type-1
preparations. Virol 1997;230:125-133. 5.
Bess JW, Gorelick RJ, Bosche WJ, Henderson LE, Arthur LO. Microvesicles are a
source of contaminating cellular proteins found in purified HIV-1 preparations. Virol
1997;230:134-144. http://leederville.net/links/Bess.pdf 6.
Ludlam CA, Steel CM, Cheingsong-Popov R, McClelland DBL, Tucker J, Tedder RS, et
al. Human T-Lymphotropic Virus Type-III (HTLV-III) Infection in Seronegative
Haemophiliacs after Transfusion of Factor VIII. Lancet 1985;II:233-236. 7.
Papadopulos-Eleopopulos E, Turner VF, Papadimitriou JM, Causer D. Factor VIII,
HIV and AIDS in haemophiliacs: an analysis of their relationship. Genetica
1995;95:25-50. http://www.theperthgroup.com/SCIPAPERS/ephemophilia.html
RESPONSE TO SARAH BRIMSON: THE ARCHER ENQUIRY
On NHS Supplied Contaminated Blood and Blood Products
Tuesday, 31st March 2009
To:
Sarah Brimson, Customer
Service Centre, Department
of Health, Richmond House, 79 Whitehall, London SW1A 2NS
Dear
Sarah Brimson, Thank
you for your letter dated 19th March 2009. We would be most grateful
if you could answer the following to your claims (typed in italics for
clarification). “You
mention that it is your belief that HIV could not possibly survive the
manufacturing process. The Department does not believe this to be true. Before
the development of virus inactivation steps, the factor VIII manufacturing
methods of the time (prior to 1985) were typically highly conservative
processes, aimed at preserving the labile factor VIII molecule” It is not
a matter of belief, but rather, there must be evidence. Could you please
provide the relevant references? “Cyroprecipitation
is simply a controlled method of thawing plasma”. Your
statement is untrue. Cyroprecipitation is “the precipitation of a
substance in solution (e.g., antihemolytic factor in blood plasma) on exposure
to lowered temperature”. “Laboratory
studies have shown that freeze-drying, of itself, does not inactivate HIV”. What
laboratory studies? Please could you provide references which prove that
freeze drying does not inactivate HIV. Most importantly, as we stated, the
HIV experts agree that the survival of cell fee HIV outside the body is measured
in hours. But the time between collection of plasma and its processing is
several days to weeks. Freezing plasma also significantly reduces the HIV
titre. “Cell
free HIV is certainly infectious and there is a lot of data implicating this
form of the virus in transmission by several body fluids”. The fact
is that according to all the HIV experts, for HIV infectivity particles must
have knobs on their surface—this is absolutely necessary. If this is the
case then, for anybody, including yourself, to claim HIV is infectious you must
have proof for the existence of cell free particles with knobs. (Plasma is
cell free). Could you please provide some references with evidence that
proves the existence of cell free particles containing knobs? If no such
evidence is found then we all, including yourself, have no other choice to
conclude that either (a) the cell free particles are not infectious; (b)
the HIV experts are wrong—the particles are infectious even without knobs.
Please provide evidence. “A
second misconception is that HIV is present only in low concentration in plasma.
Studies using nucleic acid technology, of the early period of infection,
have shown that HIV-1 RNA is commonly present in plasma at concentrations of
250,00([350,000 copies mr1 and
that concentrations of 1,000,000 copies ml-1 are not uncommon”. (a)
Nucleic acids are not virus particles. (b)
In the CDC 2000 Revised Surveillance Case Definition for HIV Infection it is
stated: "In adults, adolescents, and children infected by other than
prenatal exposure, plasma viral RNA nucleic acid tests should NOT be used in
lieu of licensed HIV screening tests (e.g., repeatedly reactive enzyme
immunoassay)” [emphasis in original].
1
If the viral load (RNA) cannot be used to define HIV infection then
certainly it cannot be used for quantifying it. One cannot say on the one
hand “I cannot tell you if there are apples in this crate” and on the other
“This crate has a hundred apples”. (c)
According to Hans Gelderblom and other virologists, one can detect particles in
plasma at concentrations of 104 to 105 per ml and preparations can be
concentrated a thousand fold. Wei et al state “ …virtually all
HIV-1-infected individuals, regardless of clinical stage, exhibit persistent
plasma viraemia in the range of 102 to 107 virions per ml”.
2
Where are they? No one has ever seen them? No one can find
them, including the world’s leading expert in HIV electron microscopy,
Professor Hans Gelderblom from the Koch Institute in Berlin. He regards
this the Holy Grail of his research but admits it is an endeavour which he has
failed. “Moreover,
a recent study has demonstrated that a concentration of 150 copies ml-1 has been
sufficient to cause an infection in the transfusion recipient”. Please
can you kindly give us the reference? “The
nucleic acid technology is not reserved for studies with HIV, but is applied to
a wide range of specialities. It has been found to be a very robust technology.
HIV is infectious. Cell free preparations of the HIV virus have been
demonstrated to be infectious in cell free infectivity assay system. Even at low
RNA titres HIV has been shown to be infectious when transfused”. See
above. “Also,
purified cloned HIV infected three laboratory workers [Cohen J Science 1994;
226: 1641]” We could
not locate the cited reference. If you mean Science 266, page 1647,
there are no data in regard to cloning and purification. Neither such data
exist in the Abstract cited by Jon Cohen from the 1993 Berlin International AIDS
conference. “The HIV virus exists.
It has been seen [Fields Virology text book]”
The
authors of textbooks repeat what the alleged experts in the field have reported
and published. According to all the HIV experts, including Montagnier and
Gallo, the latter with other experts under oath in an Australian court case,
that to prove the existence of a new virus, the virus particles must be
purified. To date, nobody has published any such proof.
3
And see above in regard to RNA. Furthermore,
the two papers by Gluschankof et al
4
and Bess et al
5
published electron-micrographs for the first time showing what was purported to
be ‘purified HIV’ was in fact an assortment of microvesicles and cellular
debris. “HIV”
is no more than a collage of phenomena observed in cultures of tissues from AIDS
patients. The same phenomena can be found in similar, cultures subject to
the same conditions, but obtained from non-AIDS patients. The taxonomic classification
of HIV (22-23 May, 1986) was ostensibly a strategic invention to present a
nomenclature that would unify a diversely identified putative 'retrovirus':
human T-cell lymphotropic virus type III ('HTLV-III'),
immunodeficiency-associated virus ('IDAV'), aids-associated retrovirus ('ARV')
and lymphadenopathy-associated virus ('LAV'). This politically expedient
move was to enforce the 'belief' that a non-purified 'human retrovirus' caused
'immunodeficiency'. However, twenty-three years on and HIV has still not
proven to be a human immuno-deficiency virus. If HIV exists, as you claim,
then you should be able to provide us with proof. The minimum necessary
but not sufficient evidence is EM of purified virus-like particles. We ask that the Department of Health provide us with such an
electron micrograph. “You
also mention in your letter that it was the 99 per cent impurities in FVIII that
caused the immune suppression (AIDS) seen in haemophiliacs. Whilst it is true
that FVIII accounted for a very small proportion of the total protein present in
the concentrates of the time, the other proteins present were normal plasma
proteins. Haemophiliacs were exposed to all these proteins during treatment with
plasma or pooled cryoprecipitates before concentrates became available”. It is a
fact, accepted by many HIV experts, that haemophiliacs were immunosuppressed
long before the AIDS era by factor VIII infusions. That is, long before
factor VIII was contaminated by HIV. For example, UK scientist Robin Weiss
and his colleagues reported "We have thus been able to compare lymphocyte
subset data before and after infection with HTLV-III [HIV]. It is commonly
assumed that the reduction in T-helper-cell numbers is a result of the HTLV-III
virus being tropic for T-helper-cells. Our finding in this study that
T-helper-cell numbers and the helper/suppressor ratio did not change after
infection supports our previous conclusion that the abnormal T-lymphocyte
subsets are a result of the intravenous infusion of factor VIII concentrates per
se, not HTLV-III infection".
6
Which means that factors present in the preparations and not HIV are the
cause of the immune suppression. It is also accepted that prior to
the AIDS era haemophiliacs the prevalence of fatal pneumonias caused by
non-defined organisms, was much higher than in other groups. Prior to the
AIDS era the diagnosis of PCP was made by open lung biopsy, a procedure
inadvisable for haemophiliacs. Hence it is possible, as has been reported,
such deaths were PCP.
7
“The
specific step included into the manufacturing process for FVIII was shown to
eradicate HIV and there were no further transmissions of infection even though
the proteins present in the earlier products were also present in some of the
later products”. What
specific step are you referring to? If you mean heating then you must not
forget that heating does not effect only HIV but all the other proteins, the
vast majority, which are not HIV proteins. The effect of heat is not
confined to HIV but to all proteins, including factor VIII itself. Before
the AIDS era factor VIII preparations were not heated hence you cannot claim the
non-HIV proteins, that is, the majority of the proteins in factor VIII
preparations, have the same properties now as then. It is well known that
heating proteins denatures them which significantly changes their properties.
Hence, it is impossible to attribute any reduction in immunosuppression to the
destruction of HIV. “There
were more than 10,000 patients with AIDS eagerly awaiting treatment before
Retrovir was made available in 1985 [Yarchoan M 2006], suggesting Retrovir
itself is not the agent causing AIDS”. We
said “the introduction of AZT- administered in enormous doses – rapidly
killed many haemophiliacs”. You appear to have interpreted our statement as “AZT is the
cause of AIDS”. It is quite clear
that we did not say this. We merely said that the introduction of AZT
significantly increased mortality. We
would like to conclude with the words of President Barack Obama: "Promoting
science isn't just about providing resources, it is also about protecting free
and open inquiry. It is about letting scientists like those here today do their
jobs, free from manipulation or coercion, and listening to what they tell us,
even when it's inconvenient especially when it's inconvenient. It is about
ensuring that scientific data is never distorted or concealed to serve a
political agenda and that we make scientific decisions based on facts, not
ideology." President Barack
Obama, 9 March 2009. We
would be most grateful if you could answer these questions as well as provide us
with a recent EM of purified retroviral-like particles claimed to be HIV. Yours
sincerely, Alexander
Verney-Elliott Joan
Shenton, Immunity Resource Foundation Mike Hersee, HEAL London London WC1N 1PE Tuesday, 31st March, 2009
References:
1. CDC. Guidelines for national human immunodeficiency virus case surveillance,
including monitoring for human immunodeficiency virus infection and acquired
immunodeficiency syndrome. Centers for Disease Control and Prevention. Morb
Mortal Wkly Rep 1999;48:1-27, 29-31. www.cdc.gov/epo/mmwr/preview/mmwrhtml/rr4813a2.htm 2.
Wei X, Ghosh SK, Taylor M, Johnson VA, Emini EA, Deutsch P, et al. Viral
dynamics in human immunodeficiency virus type 1 infection. Nature 1995;373:117-122. 3.
Papadopulos-Eleopulos E, Turner VF, Papadimitriou JM, Causer D, Page BA. The
Perth Group revisits the existence of HIV. http://www.theperthgroup.com/LATEST/PGRevisitHIVExistence.pdf 4.
Gluschankof P, Mondor I, Gelderblom HR, Sattentau QJ. Cell membrane vesicles are
a major contaminant of gradient-enriched human immunodeficiency virus type-1
preparations. Virol 1997;230:125-133. 5.
Bess JW, Gorelick RJ, Bosche WJ, Henderson LE, Arthur LO. Microvesicles are a
source of contaminating cellular proteins found in purified HIV-1 preparations. Virol
1997;230:134-144. http://leederville.net/links/Bess.pdf 6.
Ludlam CA, Steel CM, Cheingsong-Popov R, McClelland DBL, Tucker J, Tedder RS, et
al. Human T-Lymphotropic Virus Type-III (HTLV-III) Infection in Seronegative
Haemophiliacs after Transfusion of Factor VIII. Lancet 1985;II:233-236. 7.
Papadopulos-Eleopopulos E, Turner VF, Papadimitriou JM, Causer D. Factor VIII,
HIV and AIDS in haemophiliacs: an analysis of their relationship. Genetica
1995;95:25-50. http://www.theperthgroup.com/SCIPAPERS/ephemophilia.html
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AN URGENT RESPONSE TO: THE ARCHER ENQUIRY
On NHS Supplied Contaminated Blood and Blood Products
27th February 2009
To: The Rt.
Hon. Lord Archer of Sandwell,
QC
The House of Lords, London SW1A 0PW
| Dear Rt.
Hon. Lord Archer,
We the undersigned would like to challenge The Archer Report which omitted vital evidence regarding ‘HIV', Factor VIII and haemophilia. The case of haemophiliacs, far from proving the existence of a transmissible retrovirus ‘HIV') which is alleged to have contaminated their clotting factor, proves conclusively, in fact, quite the reverse: HIV is not - and cannot be - the cause of AIDS. ‘HIV' was never in the Factor VIII to begin with since ‘HIV' could not possibly survive the manufacturing process, including cryoprecipitation, required to produce the freeze-dried dry powder which is Factor VIII. Why did haemophiliacs start to die in appreciable numbers only after HIV was "discovered" in 1983? Surely if this alleged retrovirus was the cause of AIDS‚ we would have noticed their premature deaths before 1983: and why didn't haemophiliacs die from KS (Kaposi's sarcoma) and PCP (pneumocystis carinii pneumonia), the two original ‘AIDS' defining diseases? Gallo tried to make the case that ‘AIDS' was caused by a transmissible agent and cited cases of haemophiliacs whom it was assumed were infected via the clotting Factor VIII. This assumption was based on two premises that subsequently proved to be totally false: a) the amount of putative virus in a plasma donor/seller's blood and b) that the virus would survive the manufacture of Factor VIII from the pooled plasma. Uncritical scientists and medics accepted this supposition. It soon became apparent, however, that the supposition was wrong. First, it was assumed that plasma donors/sellers were infected with ‘HIV'‚ and carrying titres of cell-free infectious virus particles that resulted in the contamination of the pooled plasma used in the manufacturer of Factor VIII. Sometimes, these pools were as large as 30,000 donations of 600 millilitres (ml) of plasma. It was suggested that there was sufficient cell-free ‘HIV' in some of the donors to contaminate the whole batch. This supposed a massive titre of millions, if not billions, of viral particles in the infected donors. This was subsequently proved to be wrong. In the nearly 200,000 published scientific papers on HIV/AIDS, not one claims to have found a titre of more than 10 infectious particles per cubic ml of blood/plasma. There is no way that these negligible amounts of ‘HIV', even if proven to exist, could have contaminated so much Factor VIII that virtually all the haemophiliacs could be deemed infected with ‘HIV'. As Prof. Peter Duesberg rightly pointed out, the average amount of virus‚ claimed to be present in the plasma or blood of an ‘HIV-infected' individual, stands at between 1 and 1.7 infectious viral particles per cubic ml, which is absolutely negligible. Thus, paucity of virus rules out the suggestion that the putative ‘HIV' was transmitted to so many haemophiliacs in a comparatively short space of time. Studies subsequent to 1985 showed that ‘HIV' cannot survive long outside the host's body. This is confirmed by studies showing that spilled ‘HIV'‚ positive blood samples or spoiled laboratory cultures resulted in the quick death of the alleged ‘retrovirus.' It was further discovered, and admitted by the Centers for Disease Control and Prevention (CDC), that dried ‘HIV' does not survive. Therefore, Factor VIII that is subjected to cryoprecipitation (freeze drying) could not possibly contain viable, cell-free, infectious ‘HIV', even if there had been any putative ‘retrovirus' in the mix to begin with, which is extremely unlikely for reasons described above. It was the 99 percent impurities in Factor VIII that caused the immune suppression (‘AIDS') seen in haemophiliacs. Hence, the early discovery that seroconversion in haemophiliacs seems to depend on the amount and duration of consumption - it is age and dose-related. They were dependent on a product that would eventually kill them. Also, as Prof. Peter Duesberg cynically observed, "Even haemophiliacs are not immortal." The introduction of AZT - administered in enormous doses - rapidly killed many haemophiliacs. Their premature deaths exactly coincided with the fast tracking of AZT to haemophiliacs on 'compassionate' grounds in 1986-7. The Archer Enquiry stated: "We heard evidence from Mrs Sue Threakall, who told us: "We will only be able to move on and truly live our lives when we know the truth has come out and everything possible has been done to address this catastrophe". Yet The Archer Enquiry did not mention that Sue Threakall claimed that her husband Bob died from AZT (Retrovir) poisoning and not his hypothetical ‘HIV' infection. The study by Sarah Darby et al (Nature,1995) merely confirms that patients died from AZT poisoning and not from the putative ‘HIV'. Darby et al showed that the mortality of ‘HIV- positive' haemophiliac was greatly increased after the introduction of AZT in 1986. Since about half of Darby's 2,037 severe haemophiliacs were already ‘HIV-positive' by this time, surely ‘HIV-caused mortality' should have exerted a detectable influence prior to 1985 in this group. In January 1994, the CDC communicated the following experimental data and conclusion: "In order to obtain data on the survival of HIV [in Factor V111 clotting factor], laboratory studies have required the use of artificially high concentrations of laboratory grown virus ... the amount of virus studied is not found in human specimens or any place else in nature ... it does not spread or maintain infectiousness outside its host. Although these unnatural concentrations of putative ‘HIV' can be kept alive under precisely controlled and limited laboratory conditions, CDC studies have shown that the drying of even these high concentrations of ‘HIV' reduces the number of infectious viruses by 90 to 99 percent within several hours. Since the ‘HIV concentrations' used in laboratory studies are much higher than those actually found in blood or other body specimens, the drying of ‘HIV-infected' human blood or other body fluids reduces the theoretical risk of environmental transmission to that which has been observed - essentially zero." (Our emphasis.) P. H. Levine has pointed to immuno-suppression (‘AIDS') actually being caused by Factor VIII: "To understand the occurrence of AIDS in haemophilia, it is important to recognize that each vial of factor VIII concentrate will contain, depending on manufacturer and lot number, a distillate of clotting factors, alloantigenic proteins, and infectious agents obtained from between 2500 and 25,000 blood or plasma donors. Until recently, of all the protein injected in ‘factor VIII preparations', factor VIII accounted for only about 0.03-0.05% of the total. The rest included: albumin, fibrin(ogen), immunoglobulins and immune complexes (Eyster & Nau, 1978; Mannucci et al., 1992). Even the recent "high-purity" factor VIII contains "potentially harming proteins" such as isoagglutinins, fibrin(ogen), split products, immunoglobulins and, when monoclonal antibodies are used for factor VIII preparation, murine proteins in addition to albumin (Beeser, 1991)." We would like to conclude with science journalist Christine Johnson's critical observations: "No one has actually seen HIV in blood plasma. Its presence is inferred from the results of indirect and non-specific techniques applied to virus cultures." It is widely accepted that the surface of ‘HIV' must be studded with knobs containing the protein gp120, which is crucial to the virus's ability to infect cells. But experts such as Hans Gelderblom of the Koch Institute in Berlin, who has conducted most of the electron micrograph studies of HIV, say that the virus loses its knobs when it buds from the cell. This means that cell-free virus is incapable of infecting other cells. Since plasma does not contain cells, if ‘HIV' were present, it would not be inside a cell and thus it would not be capable of causing an infection. In addition, there is the dilution factor. Factor VIII concentrate is made from the blood of thousands of donors pooled together. Statistically, only one or two of these donors might be infected, so by the time their blood is merged with that of uninfected donors, only a few copies of HIV, or even none whatsoever, would be present per millilitre. (See "Bad Blood or Bad Science: Are haemophiliacs with AIDS diagnoses really infected with HIV?" by Christine Johnson in Continuum magazine, Volume 5, No. 4.) In conclusion, the hypothetical ‘HIV' is not even necessary for the development of ‘AIDS' in patients with haemophilia. We would like to end with some critical comments made by biophysicist Eleni Papadopulos-Eleopulos and colleagues: * Even the CDC accepts that a positive test in haemophiliacs is not proof of HIV infection. "It is possible that antibody to LAV [=HIV] is acquired passively from immunoglobulins found in factor VIII concentrates.... Likewise, it is possible that seropositivity is caused not by infectious virus but by immunization with non-infectious LAV or LAV proteins derived from virus disrupted during the processing of plasma into Factor VIII concentrate." (Evatt, 1985.) * Levy and his colleagues have shown that the titre of HIV in plasma of HIV-infected individuals three, six or twelve hours after phlebotomy [blood donation] "dropped from up to 500 TCID/ml to 0." [TCID = tissue culture infectious dose.] Since in most instances, if not all, the time between phlebotomy and conversion of pooled plasma to Factor VIII concentrate is considerably greater than three hours, Factor VIII is made from plasma which is cell free and, since the late 1970s, Factor VIII has been supplied as a dry powder, which may spend weeks or months awaiting use, how can one reconcile the above facts with the view that haemophiliacs are infected with HIV via contaminated Factor VIII concentrates? (Papadopulos, 1995b.) We ask for an urgent reappraisal of the HIV/Haemophilia hypothesis and a call for Haemophiliacs to be compensated for AZT induced death and not for hypothetical ‘HIV' infection. We look forward to a considered response. References: Sarah C. Darby et al, Mortality before and after HIV infection in the complete UK population of haemophiliacs., Nature 377, 79-82. 7 September 1995. Levine, P. H., The acquired immunodeficiency syndrome in persons with haemophilia., Ann. Int. Med. 103:723-726, 1985. CC: The Rt Hon Alan Johnson MP The Haemophilia Society Respect MP George Galloway
Yours sincerely, Alexander Verney-Elliott, MA Joan Shenton, The Immunity Resource Foundation (IRF) Mike Hersee, HEAL London London, 27th February 2009 |

Wednesday,
18 June 2008
Prime Minister Gordon Brown,
10
Downing Street,
London
SW1A 2AA
Dear
Prime Minister Gordon Brown,
Thank you for your letter of 16 April 2008 carefully noting my views. I replied
on the 23rd of April 2008 but still have had no reply from you.
I
want your office through the Department of Health to provide me with an electron
micrograph of purified HIV particles to prove HIV exists.
So
once again I would be grateful if you could provide me with such an electron
micrograph, as without such essential evidence all HIV testing procedures remain
invalid and illegal as such and must be withdrawn.
If
you are still unable to resolve this issue I will have to take you to the
European Court of Human Rights as HIV testing violates human rights.
Yours sincerely, Alexander Verney-Elliott
London WC1N 1PE
Wednesday,
23 April 2008
Prime
Minister Gordon Brown,
10 Downing Street,
London
SW1A 2AA
Dear
Prime Minister Gordon Brown,
Thank
you for your letter of 16 April 2006 carefully noting my views.
However
you have missed my reason for writing to you, namely, to provide me with an
electron micrograph of purified HIV particles.
So
once again I would be grateful if you could provide me with such an electron
micrograph, as without such essential evidence all HIV testing procedures remain
invalid and cannot be medically or legally justified.
London WC1N 1PE

Open House Home
|
Prime Minister Gordon Brown cannot prove that HIV exists.
Prime Minister
Gordon Brown,
Dear Prime
Minister Gordon Brown, However you have missed my reason for writing to you, namely, to provide me with an electron micrograph of purified HIV particles. So once again I would be grateful if you could provide me with such an electron micrograph, as without such essential evidence all HIV testing procedures remain invalid and cannot be medically or legally justified. Yours sincerely,
Alexander Verney-Elliott
10 Downing
Street, From the Direct Communications Unit
Dear Mr Verney-Elliott The Prime Minister has asked me to thank you for your recent letter. The views you expressed have been carefully noted. Yours sincerely M Davies
|
The Michael Verney-Elliott Memorial Prize:
£50,000 Reward for the Existence of 'HIV'
Offered by Mr. Alexander Huw Verney-Elliott.
Mahatma Gandhi (1869 - 1948)
"All truth goes through three stages. First it is ridiculed. Then it is violently opposed. Finally, it is accepted as self-evident."
Arthur Schopenhauer (1788 - 1860)
Prime Minister Gordon Brown
10 Downing Street,
London, SW 1 2A
29th March,
2008
Dear Honourable Prime Minister Mr. Gordon Brown,
I would like to bring your attention to my reward of £50,000 for
electron-micrograph (EM) evidence of the existence of HIV.
The non-isolation of HIV
was the main theme of a satellite meeting 'HIV-testing; open questions regarding
specificity' held at the 12th World AIDS Conference in Geneva in 1998. The
International Forum for Accessible Science (IFAS) hosted this session with a
panel of distinguished HIV critics including Professor Gordon Stewart, Professor
Etienne de Harven. Ten years on, the isolation of HIV has not been proven.
Contributing to this session was a panel of scientists from Perth, Western
Australia, led by biophysicist Eleni Eleopulos who argued that there had been no
isolation of HIV according to the scientifically approved standards for
retroviral isolation as discussed at the Pasteur Institute in 1973.
At the closing of press
session I asked Richard Horton, then editor of The Lancet, and the 12th
World AIDS Conference chairman, Dr. Bernard Hirschel: "The current indirect
HIV tests and PCR are not sufficient proof that HIV has been isolated.
Where is the proof that HIV exists? " None of the perplexed panel
answered.
The alleged co-discoverers of HIV Luc Montagnier and Robert Gallo agreed that to
claim the existence of a new retrovirus the minimum necessary but not sufficient
condition is to have electron microscopic (EM) evidence for the isolation
(purification) of the putative retroviral particles.
In
1997 Montagnier admitted to the French journalist Djamel Tahi that the material,
which in 1983 he claimed to represent purified HIV, did not even have particles
with the "morphology typical of retroviruses" and stated: "I
repeat we did not purify". Prof. Gallo stated: "You have
to purify." Yet when Montagnier was asked if the Gallo group purified
'HIV', he replied: "I don't know if he really purified. I don't believe
so." (1)
Dr.
Heinz Ludwig Sänger, Emeritus Professor of Molecular Biology and Virology,
Max-Planck-Institutes for Biochemy, München stated:
"Up to today there is actually no single scientifically really
convincing evidence for the existence of HIV. Not even once such a retrovirus
has been isolated and purified by the methods of classical virology."
(2)
To date there is still
no electron micrograph (EM) which shows purification of the putative
HIV particles and thus of the existence of a unique, isolated
retrovirus. What was wrongly taken to be 'purified HIV' was in fact
cellular debris as Hans Gelderblom et al demonstrated in Virology, March
1997. This brings urgently into
question the validity, efficacy and legality of all hypothetical HIV testing
procedures.
All
images of the hypothetical HIV are invariably computerized fictions of virtual
virology (often embellished with seductive psychedelic colours) and yet it has
never been possible to visualize any HIV retroviral particle by EM. In
summary, I request your office, and the Department of Health, obtain EM evidence
for the existence of purified HIV particles.
I
would like to conclude with a couple of quotes that aptly apply to Gallo and
Montagnier:
"The most formidable barrier to the advancement of science is the
conventional wisdom of the dominant group."
C. H. Waddington, Geneticist.
"It is a dire
example of how a distinguished scholar who has contributed much to the
advancement of science, now impedes further progress by his stubborn adherence
to a dogma of his own creation."
Johann Wolfgang von
Goethe, Maximen und Reflexionen, Texstelle 586.
References:
(1)
Luc
Montagnier, Did Montagnier Discover HIV? Interview with Luc Montagnier,
by Djamel Tahi; Continuum, Winter 1997.
(2)
Dr. Heinz Ludwig Sänger: Letter to Süddeutsche Zeitung 2000.
Yours sincerely,
Mr. Alexander Verney-Elliott,
London WC1N 1PE
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The Michael Verney-Elliott Memorial Prize: £50,000 Reward for the Existence of 'HIV' Offered by Mr. Alexander Huw Verney-Elliott.
Mahatma Gandhi (1869 - 1948)
Arthur Schopenhauer (1788 - 1860)
|
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SEE RED & BOYCOTT Project (RED) Auction Sotheby’s New York 14th February 2008
|
World AIDS Day 2007
- Deconstructing 'HIV'
Amun: 12/01/07 05:38 AM
Ten years
ago electronmicrographs (EMs) were published in Virology, March 1997 (Gluschankof
et al and Bess et al) clearly depicting what was assumed to be
'HIV' was in fact cellular debris and mircrovesicles proving that no one is
'HIV' positive but rather 'positive' for an arbitrary assortment of
microvesicles and cellular debris. What has wrongly been named as 'HIV is merely
an endogenous epiphenomenon of microvesicles and nebulous cellular matter. These
historic EMs deconstruct 'HIV' showing that there was no 'purified HIV' there to
begin with but rather cellular contamination instead.
It is the papers by the proponents of the 'HIV' hypothesis who actually take it
apart and expose its flaws, absurdities, anomalies, errors and contradictions,
along with history (time) which is always the greatest deconstructive critique
for it is time itself that unravels and exposes the 'HIV' hypothesis as failed,
unfounded and ungrounded. Deconstruction - as Derrida stated - is always already
at work within texts - and all papers that purport to propagate 'HIV' are
actually arguing that 'HIV' does not exist.
Hans Gelderblom of Berlin's Robert Koch Institute co-authored the first paper in
Virology showing 'purified HIV' to be 'purified microvesicles'. What was assumed
to be 'purified HIV' was in fact "an excess of vesicles" - particles
of cellular proteins. The hypothetical 'HIV' is in fact a collection of
endogenous microvesicles and cellular proteins (which also never seem to form
particles - so how can they be infectious)?
The key fact to remember is that cell-free infectious 'HIV' viral particles have
never, repeat never, been visualised, isolated and recovered from fresh donor
blood and semen. To date: 'HIV' has never been visualised under electron
microscopy so there is no empirical evidence that anyone is 'HIV' positive and
all the images you have been shown are coloured-in computerized fantasies with
dishs-aerials.
The rules demonstrating the existence of 'HIV' (and retroviruses in general)
were never adhered to by those who devised them nor were they ever validated. No
particle of 'HIV' has ever been obtained pure, free of contaminants; nor has a
complete piece of 'HIV RNA' (or the transcribed DNA) ever been proved to exist.
So confident am I that no such electron-micrograph evidence for the existence of
'HIV' can be produced by adhering strictly to the Etienne de Harven methodology,
I am prepared to offer the sum of $100,000 to the first person to submit just
such a micrograph, prepared under stringent laboratory conditions. I do not want
'markers' for 'viral activity' which are at very best, inaccurate. I want visual
evidence of myriad active, infectious viral particles, clearly morphologically
defined recovered from a fresh sample of bodily fluid, unadulterated with any
other kinds of cells: i.e: CEM,H9 cancer cells. As Peter Duesberg and Harvey
Bialy stated in Nature: "...infectious units, after all, are the
only clinically relevant criteria for a viral pathogen." (Nature,
375, 1995, p. 197) Once again, to paraphrase Peter Duesberg, an alleged 'virus'
which is not doing anything cannot be 'causing' anything.
As Virologist Dr. Stefan Lanka observed: The rules demonstrating the existence
of HIV (and retroviruses in general) were never adhered to by those who devised
them nor were they ever validated. No particle of HIV has ever been obtained
pure, free of contaminants; nor has a complete piece of 'HIV RNA' (or the
transcribed DNA) ever been proved to exist.
Dr. Stefan Lanka stated: "I found that when they are speaking about HIV
they are not speaking about a virus. They are speaking about cellular
characteristics and activities of cells under very special conditions...I
realized that the whole group of viruses to which HIV is said to belong, the
retroviruses, in fact do not exist at all." (Zenger's Magazine,
December, 1998).
We need to 'raise awareness' that:
'HIV' is not a retrovirus.
'HIV' is not an STI/STD.
'HIV' does not cause 'AIDS'.
No one is 'living with HIV.'
'HIV' DOES NOT EXIST
World AIDS Day 2007
Alex Verney-Elliott, London
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In the United Kingdom from January 18, 2007 crystal meth is to be reclassified in the UK as a “Class A” drug. Crystal meth is now classed among the most harmful drugs. Poppers (Amyl-, Butyl-, and Isobutyl-Nitrite) should also now be upgraded and reclassified as a “Class A” drug because the illegal drugs long-term effects can be lethal to gay men’s health. In the early 1980s poppers were documented to cause the development of KS (Kaposi's sarcoma) which was one of the original ‘AIDS’ defining conditions. Crystal meth and poppers are contributing to ‘AIDS’ amongst gay men and not the hypothetical ‘HIV’. Chemical agents in drugs like crystal meth and cocaine can stimulate cells to express hitherto dormant passenger viruses which are then misidentified as being the hypothetical ‘HIV’. Crystal meth was recently found to manufacture a synthetic (artificial) ‘new strain of HIV’ in a New York patient. It has been argued and demonstrated that crystal meth is making gay men test ‘HIV’ positive (and – ironically – not the non-isolated ‘HIV’). The Body readers may be too young to remember that up to 1983 ‘AIDS’ was originally called GRID (Gay Related Immune Deficiency) and was acknowledged to be caused by recreational drug addiction on the commercial gay scene. Remember: all the original ‘AID’S cases in the United States were young gay men who were recreational drug users with PCP and KS; and all the heavy crystal meth and poppers-uses had KS. To repeat: crystal meth, along with ecstasy, special K, MDA, quaaludes, LSD, cocaine, and poppers were seen as the original causes of ‘AIDS’ amongst gay men in the late 1970s and the early 1980s before ‘HIV’ was ‘invented’ as the ‘politically correct’ cause of ‘AIDS’. But today we (conveniently) forget that in the early 1980s the medical literature considered ‘AIDS’ to be GRID (Gay Related Immune Deficiency) caused by the drug-induced gay life and history now shows this hypothesis to be correct (even if ‘politically incorrect’ and ‘unfashionable’). As Prof. Peter Duesberg has observed: in the West, ‘AIDS’ is caused by long-term recreational drug use and in the developing world ‘AIDS’ is caused by TB, malaria and disease conditions relating to poverty and malnutrition. We are now seeing the spread of drug-induced ‘AIDS’ in Russia where there are growing drug epidemics; globally, wherever we see drug epidemics we also see the spread of 'false-HIV-positivity' because recreational drugs are well know now to make the non-specific ‘HIV’ tests to run ‘positive’. No one is ‘HIV positive’ – they are 'drug-positive’. Recreational drugs are making many gay men test ‘HIV’ positive. We must call on the Terrence Higgins Trust and Gay Men Fighting AIDS to warn gay men that crystal meth and poppers can cause ‘AIDS’ amongst gay men and crystal meth and cocaine are well documented (in the medical literature) to make the non-specific ‘HIV’ tests to run ‘positive’. The THT and GMFA have been irresponsibly and unethically been misinforming gay men for over 20 years now of the Drug/AIDS hypothesis whilst uncritically endorsing the profitable but still unproven HIV/AIDS hypothesis. Gay men are not testing ‘HIV’ positive because of ‘HIV’ but because of ‘life-style choices’ like recreational drug use – but the THT & GMFA – and the gay community (whatever that is) are still in ‘denial’ about the true situation and still need blind ‘HIV’ belief to mask this reality (also because gay men never want to grow up and love living in a fantasy world like the ‘HIV’ fantasy world). Whilst the THT has called the reclassification of crystal meth as a “pragmatic move” that brings it in line with other drugs of this nature, it does not go far enough in warning gay men that it can cause 'AIDS' through long term use. The THT and GMFA should also demand the upgrading of poppers to a “Class A” drug but they will never do this because poppers make millions of pounds profit for the commercial gay scene where pink profit is always seen as far more important than gay men’s health. Will Nutland, the THTs head of health promotion stated: “Experiences from other parts of the world show us that crystal meth can have a detrimental effect on communities as well as the lives of individuals,” said “This decision increases the powers and resources available to the police and enables them to do more to tackle crystal meth use in the UK. However, reclassification needs to come hand in hand with funding for education and effective treatment services.” Recreational drugs like crystal meth are actually causing ‘AIDS’ (GRID) amongst gay men as well as making them test ‘HIV’ positive and it is high time that the Terrence Higgins Trust and Gay Men Fighting AIDS began to ‘inform’ them of these brute facts - and stop living in the cosy careerist and concealed ‘HIV’ mass-hypnosis group-fantasy trance. When will the THT and GMFA wake up from their politics of denial and warn gay men of the real causes of ‘AIDS’ (GRID) and ‘inform’ gay men that ‘HIV’ does not exist? |
An Open Letter to the THT & GMFA: Making Crystal meth & Poppers Class A Drugs
| Author: Alex Russell | Today at 9:09am |
From January 18, 2007 crystal meth is to be reclassified in the UK as a “Class A” drug. Crystal meth is now classed among the most harmful drugs. Poppers (Amyl-, Butyl-, and Isobutyl-Nitrite) should also now be upgraded and reclassified as a “Class A” drug because the illegal drugs long-term effects can be lethal to gay men’s health. In the early 1980s poppers were documented to cause the development of KS (Kaposi's sarcoma) which was one of the original ‘AIDS’ defining conditions. Crystal meth and poppers are contributing to ‘AIDS’ amongst gay men and not the hypothetical ‘HIV’. Chemical agents in drugs like crystal meth and cocaine can stimulate cells to express hitherto dormant passenger viruses which are then misidentified as being the hypothetical ‘HIV’. Crystal meth was recently found to manufacture a synthetic (artificial) ‘new strain of HIV’ in a New York patient. It has been argued and demonstrated that crystal meth is making gay men test ‘HIV’ positive (and – ironically – not the non-isolated ‘HIV’). Gay.com readers may be too young to remember that up to 1983 ‘AIDS’ was originally called GRID (Gay Related Immune Deficiency) and was acknowledged to be caused by recreational drug addiction on the commercial gay scene. Remember: all the original ‘AID’S cases in the United States were young gay men who were recreational drug users with PCP and KS; and all the heavy crystal meth and poppers-uses had KS. To repeat: crystal meth, along with ecstasy, special K, MDA, quaaludes, LSD, cocaine, and poppers were seen as the original causes of ‘AIDS’ amongst gay men in the late 1970s and the early 1980s before ‘HIV’ was ‘invented’ as the ‘politically correct’ cause of ‘AIDS’. But today we (conveniently) forget that in the early 1980s the medical literature considered ‘AIDS’ to be GRID (Gay Related Immune Deficiency) caused by the drug-induced gay life and history now shows this hypothesis to be correct (even if ‘politically incorrect’ and ‘unfashionable’). As Prof. Peter Duesberg has observed: in the West, ‘AIDS’ is caused by long-term recreational drug use and in the developing world ‘AIDS’ is caused by TB, malaria and disease conditions relating to poverty and malnutrition. We are now seeing the spread of drug-induced ‘AIDS’ in Russia where there are growing drug epidemics; globally, wherever we see drug epidemics we also see the spread of 'false-HIV-positivity' because recreational drugs are well know now to make the non-specific ‘HIV’ tests to run ‘positive’. No one is ‘HIV positive’ – they are 'drug-positive’. Recreational drugs are making many gay men test ‘HIV’ positive. We must call on the Terrence Higgins Trust and Gay Men Fighting AIDS to warn gay men that crystal meth and poppers can cause ‘AIDS’ amongst gay men and crystal meth and cocaine are well documented (in the medical literature) to make the non-specific ‘HIV’ tests to run ‘positive’. The THT and GMFA have been irresponsibly and unethically been misinforming gay men for over 20 years now of the Drug/AIDS hypothesis whilst uncritically endorsing the profitable but still unproven HIV/AIDS hypothesis. Gay men are not testing ‘HIV’ positive because of ‘HIV’ but because of ‘life-style choices’ like recreational drug use – but the THT & GMFA – and the gay community (whatever that is) are still in ‘denial’ about the true situation and still need blind ‘HIV’ belief to mask this reality (also because gay men never want to grow up and love living in a fantasy world like the ‘HIV’ fantasy world). Whilst the THT has called the reclassification of crystal meth as a “pragmatic move” that brings it in line with other drugs of this nature, it does not go far enough in warning gay men that it can cause 'AIDS' through long term use. The THT and GMFA should also demand the upgrading of poppers to a “Class A” drug but they will never do this because poppers make millions of pounds profit for the commercial gay scene where pink profit is always seen as far more important than gay men’s health. Will Nutland, the THTs head of health promotion stated: “Experiences from other parts of the world show us that crystal meth can have a detrimental effect on communities as well as the lives of individuals,” said “This decision increases the powers and resources available to the police and enables them to do more to tackle crystal meth use in the UK. However, reclassification needs to come hand in hand with funding for education and effective treatment services.” Recreational drugs like crystal meth are actually causing ‘AIDS’ (GRID) amongst gay men as well as making them test ‘HIV’ positive and it is high time that the Terrence Higgins Trust and Gay Men Fighting AIDS began to ‘inform’ them of these brute facts - and stop living in the cosy careerist and concealed ‘HIV’ mass-hypnosis group-fantasy trance. When will the THT and GMFA wake up from their politics of denial and warn gay men of the real causes of ‘AIDS’ (GRID) and ‘inform’ gay men that ‘HIV’ does not exist? |
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A criminal complaint against South African Treatment Action Campaign leader Zackie Achmat has been served on the Prosecutor of the International Criminal Court (ICC) at The Hague. Particularized in a 59-page draft bill of indictment, the complaint seeks Achmat’s prosecution on a charge of genocide, arising from his direct criminal role in the deaths of thousands of South Africans, mostly black, mostly poor, from poisoning with so-called antiretroviral drugs. The complaint and the ICC’s service receipt can be downloaded and printed at www.tig.org.za. Adv Anthony Brink Chairman, Treatment Information Group Cape Town
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AZT on Trial at The Hague
AIDS Myth Exposed MSN Groups
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World AIDS Day 2006: Raising 'HIV/AIDS' Awareness We urgently need to raise 'HIV/AIDS' Awareness to stop the epidemic spread of AIDS-related Myths, HIV-related Lies and Pharmogenocide: Iatrogenic 'AIDS' ('AIDS' caused by 'anti-retroviral' drugs). World AIDS Day should be renamed as World LIES Day - for World AIDS Day is a day of Lies, Lies, and Lies to keep the 'HIV' Lie Machine and 'HIV' Careerists continue with their profitable pharmogenocide lies. We need to 'raise awareness' that: 'HIV' is not a retrovirus. 'HIV' is not an STI/STD. 'HIV' does not cause 'AIDS'. No one is 'living with HIV.' No one is 'HIV' positive. Cell-free 'HIV' has never been found or recovered in fresh samples of semen or blood. The fact to remember is that cell-free infectious 'HIV' viral particles have never, repeat never, been recovered from fresh donor semen and blood. 'HIV' have never been visualised under electron microscopy. Whilst 'HIV' is not an infection, 'HIV' Ideology is highly 'infectious' and 'contagious' and 'spread' through the 'HIV' Interpellation techniques such as the highly hypnotic 'HIV' Testing ritual rites of 'HIV' Indoctrination and 'HIV' Propaganda - with pernicious lies like: 'Everyone is at Risk!' There is no such thing as 'HIV' Science only 'HIV' Politics, 'HIV' Propaganda, 'HIV' Theology - for 'HIV' has become the new 'GOD': blind 'GOD' Belief has been displaced by blind 'HIV' Belief. But the weak ones of the world want to believe in 'God' - the weak ones of the world want to believe in 'HIV': they need something to worship and fear all at once: yet 'GOD' - like 'HIV' - does not exist. The weak ones of the world - 'the they' - want to believe in nothing rather than themselves: they need the 'nothing-GOD' - they need the 'nothing-HIV'. If you tell 'the they' - the weak ones of the world - that 'GOD' and 'HIV' do not exist they will become hysterical, irrational, panic, and scream a stream of invective expletives and emotive abuse at you pulling chimpanzee grimaces and spitting at you and then drooling like a rabid dog growling with madness and sadness: for they desperately need a big daddy father figure to fuck them into submissive passivity of slave morality: 'HIV' is the new 'GOD' they need to control them, order them, to rule them, to enslave them: 'HIV' Belief like 'GOD' Belief is Slave Morality! Both 'GOS' and 'HIV' have never been isolated as unique identities in themselves but are an epiphenmomenon of a thing yet unidentified and thus misidentified: there is not GOD' like there is no 'HIV'. The (political) taxonomic classification of 'HIV' was a tragic case of mistaken identity: the thing had no properties of the name baptised: 'it' was never proven to cause 'immunodeficiency' or even to be a 'virus' at all. The taxonomic classification of 'HIV' (22-23 May, 1986) was ostensibly a strategic invention to present a nomenclature that would unify a diversely identified putative 'retrovirus': human T-cell lymphotropic virus type III ('HTLV-III'), immunodeficiency-associated virus ('IDAV'), aids-associated retrovirus ('ARV') and lymphadenopathy-associated virus ('LAV'). The not so hidden agenda behind this politically expedient move was to enforce the 'belief' that an alleged 'human retrovirus' caused 'immunodeficiency'. Like 'GOD' does not exist 'HIV' does not exist so we must de-programme and 'raise awareness' amongst 'diagnosed' (hypnotised) homosexuals and blacks that they are not 'HIV' positive: they must be 'informed' of the following facts: 'HI'V is not sexually transmitted. It is only ever been an assumption that 'HIV' is an STI based on the apparent existence of clusters of cases. 'HIV' is merely an endogenous marker for oxidative stress, antigenic overload and recreational drug use in the West. Testing 'HIV positive' merely indicates a cluster of people who had indulged in identical behaviour: it is important to remember that originally clusters of cases of beriberi, pellagra and scurvy were also assumed to be caused by a transmissible infection: all this was subsequently shown to be totally wrong. Beriberi, pellagra and scurvy were not caused by a transmissible agent but were all caused by a shared vitamin deficiency. Similarly: 'AIDS' is not caused by a transmissible agent ('HIV') but by exposure to multiple pathogenic insults caused by life style in the West and by well known endemic conditions relating to Third World countries. No one 's 'HIV' positive at all. Hans Gelderblom of Berlin's Robert Koch Institute co-authored the first paper in Virology, March 1997, showing 'purified HIV' to be 'purified microvesicles'. What was assumed to be 'purified HIV' was in fact "an excess of vesicles" - particles of cellular proteins. The hypothetical 'HIV' is in fact a collection of endogenous microvesicles and cellular proteins (which also never seem to form particles - so how can they be infectious)? Cell-free viral 'HIV' particles have never ever been visualised in any freshly donated bodily fluid including semen, blood, etc. 'HIV' has never ever proven to be a sexually transmitted retrovirus. As Virologist Dr. Stefan Lanka observed: The rules demonstrating the existence of HIV (and retroviruses in general) were never adhered to by those who devised them nor were they ever validated. No particle of HIV has ever been obtained pure, free of contaminants; nor has a complete piece of 'HIV RNA' (or the transcribed DNA) ever been proved to exist. Dr. Stefan Lanka stated: "I found that when they are speaking about HIV they are not speaking about a virus. They are speaking about cellular characteristics and activities of cells under very special conditions...I realized that the whole group of viruses to which HIV is said to belong, the retroviruses, in fact do not exist at all." (Zenger's Magazine, December, 1998).
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December 1st 2006
| Author: Alex Russell | Today at 11:31am |
| World
AIDS Day 2006: Raising 'HIV/AIDS' Awareness
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The Editor, Gay Times: For publication
5th September, 2006
Dear
Gay Times,
Regarding
the letter ‘party drugs’ (Gay Times, September, 2006) your
anonymous correspondent unwittingly recollects what many of us knew in the
early 1980s that recreational drugs cause AIDS amongst gay men:
“We
all agree it was the drugs that got us where w are today…If crystal meth
isn’t a major problem in the UK now, it will be.”
Yet really the correspondent sees the only danger of drugs as helping to facilitate ‘unsafe sex’ and thus still assuming that HIV is a sexually transmitted retrovirus that causes AIDS.
The
fact is that HIV has never been isolated or recovered directly from semen or
been proven to be an STI/STD or to cause AIDS. There are over 70 conditions -
including drug-use - that are known to make the non-specific HIV tests run
‘positive’. It is the chemical agents in drugs like Special K, cocaine,
ecstasy and crystal meth that are really making gay men test HIV positive –
and, ironically, not HIV.
Chemical
agents in drugs like cocaine and crystal meth can stimulate cells to express
hitherto dormant passenger viruses which are then misidentified as being the
hypothetical HIV. Crystal meth was recently found to manufacture a new strain
of HIV in a New York patient.
Gay
Times
readers
may be too young to remember that up to 1983 AIDS was originally called GRID
(Gay Related Immune Deficiency) and was acknowledged to be caused by
recreational drug addiction on the gay scene. Remember: all the original AIDS
cases in the United States were young gay men who were recreational drug users
with PCP and KS; and all the heavy poppers-uses had KS.
In
1984 HIV was then invented as the ‘politically correct’
equal-opportunities cause of AIDS to take the heat off of the gays and promote
the lie that ‘everyone was at risk’.
Your
correspondent also stated: “You’re doing everything to get this
thing…” This ‘thing’ is not HIV but an internal expression (as
an endogenous epiphenomenon) of recreational drug use (amongst many other
things).
The
bottom line is that recreational drugs are actually making many gay men test
‘HIV’ positive and causing AIDS (GRID) and it is high time that
the Terrence Higgins Trust and Gay Men Fighting AIDS began to inform
them of these facts.
Yours
sincerely,
Alexander Russell
London
References:
http://www.virusmyth.net/aids/data/cjtestfp.htm
http://www.healtoronto.com/hivtest.html
The Editor, Gay Times
Dear Editor,
Yours sincerely Alex Russell
'AIDS'
is accelerated ageing and not caused by 'HIV'
08/22/06 04:23 AM
A recent
development in America shows people over the age of 60 testing so-called 'HIV'
positive' - so what we call 'AID$' in young people is really a form of
accelerated aging and old people testing 'HIV' positive is a natural phenomenon
- as the 'HIV' test is a test for the aging process and a life time's collection
of anti-body complexes - so the 'test' is an endogenous marker for the history
of the patient's cumulative pathologies and the aging process (and nothing to do
with 'HIV').
Thus the vast majority of people over the age of 65 would test 'HIV' positive!
When young people succumb to full-blown 'AID$' it is as if they are fighting a
life-times diseases concentrated into a short space of time and the
immune-system just cannot cope. Young homosexuals with 'AID$' always look
prematurely aged: gay men of 30 look like 75 plus - just like long-term
recreational drug users who also looked aged. What we call 'AID$' in the West is
accelerated aging amongst gay men and recreational drug addicts brought about by
massive recreational drug use, repeated STDs resulting in massive dependency on
broad spectrum antibioltics which lose there efficacy.
The arbitrary and non-specific 'viral load' test has nothing to do with the
alleged amount of 'HIV' in the blood stream or the accelerated aging process of
'AID$' yet it has become the surrogate marker for the hard selling of AVRs
(anti-retroviral drugs) to diminish an alleged high 'viral load' - but they do
not improve health or show a decrease in mortality.
Whilst highly expensive 'AVRs' (anti retroviral drugs) do not cure 'AID$' but
merely target a chaemeric 'virus', bowel cancer drugs like Avastin and Erbitux
have been turned down in the UK deemed as not being 'cost effective'. We are
told that bowel cancer is the third most common cancer in the UK, with around 50
people dying each day from the disease. Yet how many die each day from 'AIDS' in
the UK? One? Two? And usually die by iatrogenic-'AIDS' as well.
It affects one in 18 people and represents roughly 13 per cent of all new cancer
cases in men and women. As far as we know bowel cancer - unlike 'AID$' - is not
a self-inflicted condition - so why should people with bowel cancer be penalised
whilst homosexuals and drug users with 'AID$' be exempt and given preferential
treatment in the UK? Why is 'AID$' always given priority over other
disease-conditions?
There are no such drug-formulae as 'AVRs' or 'HAART' (Highly Active
Antiretroviral Therapy) and they are certainly not 'cost effective' anyway so
why were they licensed? Highly expensive 'AVRs' are a total waste of scarce NHS
resources because they do not cure 'AID$' but target a phantom 'retrovirus' of
virtual virology.
So which should be the priority disease for treatment in the UK: - unfashionable
and boring bowel cancer or the politically-correct self-inflicted
high-life-style condition of choice called 'AID$'?
Bowel cancer affects us all - 'AID$' does not. 'HIV' does not cause 'AID$'.
Alex Russell
References:
In the USA, 10-15% of all reported new HIV infections occur among people over
the age of 50, with a quarter of these among the over 60’s. This amounted to
around 78,000 people in April 2005, and the percentage of new infections
occurring in this age group are rising.1 This is an increase of 18,000 people or
30%.2 In the UK, current data suggest that 8% of adults living with HIV or AIDS
fall into the over 50 age category. (Older People, HIV & AIDS; AVERT.ORG).
HIV/AIDS is accelerated ageing of the immune system with spill over to the whole
organism.
Conf Retroviruses Opportunistic Infect 1997 Jan 22-26; 4th:81 (abstract no. 91)
Hotschkiss G, Britton S; Center for Biotechnology, Novum, Sweden.
Telomers
from HIV/AIDS patients are reduced in length compared to age matched controls
and the reduction correlates to stage of infection. At least 1 kilobase
difference in length compared with uninfected age matched controls is noticeable
in patients before AIDS. Once AIDS is established the difference is greater. Our
study material is PBL from 50 HIV infected patients in different stages of the
disease compared with agematched controls without HIV infection or with other
infections. Since this difference in telomer length is observed in a mixed cell
population where the HIV susceptible cells are in minority we assume that CD4
lymphocyte cell death and replacement during HIV infection results in an ageing
of a stem cell pool common to cells other than the lymphocytes. This results in
a general ageing process which is compatible with the clinical presentation. We
hope to present telomer studies from other cellular compartments distinct from
the blood lymphoid system
An
Open Letter to John Moore: New York Times
08/22/06 04:13 AM
To: New
York Times
The Editor, Opinion,
The Op-Ed Page,
229 West 43rd Street,
New York, NY 10036
An Article for the Op-Ed Page: Opinion
Reply to John Moore and Nicoli Nattrass
London: 23rd June, 2006
Dear John Moore and Nicoli Nattrass,
In your article 'Deadly Quackery' (Opinion, The New York Times, 4th June, 2006),
you stated:
"H.I.V. causes AIDS. This is not a controversial claim but an established
fact, based on more than 20 years of solid science."
Contrary to your unfounded claim, this is not an "established fact"
but a proposition, a hypothesis, an assumption based entirely upon an arbitrary
correlation between 'HIV' (whatever that is) and 'AIDS' (whatever that is).
Correlation is not proof of causation. The case of the haemophiliacs proves that
HIV cannot be the cause of AIDS.
Soon after HIV tests were introduced in 1985, it was noticed that many
haemophiliacs were shown to be 'HIV positive'. Robert Gallo seized upon this as
evidence that AIDS was caused by an infectious, transmissible organism, presumed
to have been conveyed to the haemophiliacs as a contaminant in their clotting
factor preparations.
However, in the light of subsequent research, we can now see that the case of
haemophiliacs, far from proving the existence of a transmissible retrovirus(HIV)
alleged to have contaminated their clotting factor, proves conclusively, in
fact, quite the reverse: HIV is not - and cannot be - the cause of AIDS.
Why did haemophiliacs start to die in appreciable numbers only after HIV was
"discovered" in 1983? Surely if this alleged retrovirus was the cause
of AIDS’ we would have noticed their premature deaths before 1983: and why
didn't haemophiliacs die from KS (Kaposi's sarcoma) and PCP (pneumocystis
carinii pneumonia), the two original "AIDS" defining diseases?
Gallo tried to make the case that AIDS was caused by a transmissible agent and
cited cases of haemophiliacs whom it was assumed were infected via the clotting
factor VIII. This assumption was based on two premises that subsequently proved
to be totally false: a) the amount of putative virus in a plasma donor/seller's
blood and b) that the virus would survive the manufacture of factor VIII from
the pooled plasma.
Uncritical scientists and medics accepted Gallo's assumption. It soon became
apparent, however, that the supposition was wrong. First, it was assumed that
plasma donors/sellers were infected with HIV’ and carrying huge titres of
cell-free infectious virus particles that resulted in the contamination of the
pooled plasma used in the manufacturer of factor VIII. Sometimes, these pools
were as large as 30,000 donations of 600 millilitres (ml) of plasma. It was
suggested that there was sufficient cell-free "HIV" in some of the
donors to contaminate the whole batch. This supposed a massive titre of
millions, if not billions, of viral particles in the infected donors. This was
subsequently proved to be wrong. In the nearly 200,000 published scientific
papers on HIV/AIDS, not one claims to have found a titre of more than 10
infectious particles per cubic ml of blood/plasma ( and even this negligible
titre was based on surrogate markers!). There is no way that these negligible
amounts of HIV, even if proven to exist, could have contaminated so much factor
VIII that virtually all the haemophiliacs could be deemed infected with HIV. As
Peter Duesberg rightly pointed out, the average amount of virus’ claimed to be
present in the plasma or blood of an HIV-infected individual, stands at between
1 and 1.7 infectious viral particles per cubic ml, which is absolutely
negligible.
Thus, paucity of virus rules out the suggestion that HIV was transmitted to so
many haemophiliacs in a comparatively short space of time.
Studies subsequent to 1985 showed that HIV cannot survive long outside the
host's body. This is confirmed by studies showing that spilled HIV’ positive
blood samples or spoiled laboratory cultures resulted in the quick death of the
alleged "virus." It was further discovered, and admitted by the
Centers for Disease Control and Prevention (CDC), that dried HIV does not
survive. Therefore, factor VIII that is subjected to cryoprecipitation (freeze
drying) could not possibly contain viable, cell-free, infectious HIV, even if
there had been any putative "virus" in the mix to begin with, which is
extremely unlikely for reasons described above.
It was the 99 percent impurities in factor VIII that caused the immune
suppression (AIDS) seen in haemophiliacs. Hence, the early discovery that
seroconversion in haemophiliacs seems to depend on the amount and duration of
consumption - it is age and dose-related.. They were dependent on a product that
would eventually kill them. Also, as Duesberg cynically observed, "Even
haemophiliacs are not immortal."
The introduction of AZT - administered in enormous doses - rapidly killed many
haemophiliacs. Their premature deaths exactly coincided with the fast tracking
of AZT to haemophiliacs on 'compassionate' grounds in 1986-7
Haemophiliac mortality increased only after the introduction of AZT in 1986.
Since about half of Darby's 2,037 severe haemophiliacs were already HIV-positive
by this time, surely HIV-caused mortality should have exerted a detectable
influence prior to 1985 in this group. Only Duesberg's theory can explain why
the explosion of haemophiliac mortality should occur only on the heels of HIV
testing: The cytotoxic pharmaceutical drugs and psychological terror that
invariably accompany a positive HIV test also contributed to the increased
mortality.
In January 1994, the CDC communicated the following experimental data and
conclusion: "In order to obtain data on the survival of HIV [in factor V111
clotting factor], laboratory studies have required the use of artificially high
concentrations of laboratory grown virus ... the amount of virus studied is not
found in human specimens or any place else in nature ... it does not spread or
maintain infectiousness outside its host. Although these unnatural
concentrations of HIV can be kept alive under precisely controlled and limited
laboratory conditions, CDC studies have shown that drying of even these high
concentrations of HIV reduces the number of infectious viruses by 90 to 99
percent within several hours. Since the HIV concentrations used in laboratory
studies are much higher than those actually found in blood or other body
specimens, drying of HIV-infected human blood or other body fluids reduces the
theoretical risk of environmental transmission to that which has been observed -
essentially zero." (My emphasis.)
Ironically, the very original suggestion that haemophiliacs were proof of the
HIV/AIDS hypothesis can now be used to deconstruct this redundant and failed
paradigm. There is absolutely no way that HIV could have been transmitted via
commercial clotting factors.
I would like to conclude with science journalist Christine Johnson's critical
observations: "No one has actually seen HIV in blood plasma. Its presence
is inferred from the results of indirect and non-specific techniques applied to
virus cultures. AIDS expert Jay Levy of the University of California was able to
find what he believed were HIV particles in the plasma of only 30 percent of the
AIDS patients he studied, and then, it was at a low concentration - 10
infectious particles per millilitre. Levy concedes that this isn't enough to
establish an infection."
It is widely accepted that the surface of HIV must be studded with knobs
containing the protein gp120, which is crucial to the virus's ability to infect
cells. But experts such as Hans Gelderblom of the Koch Institute in Berlin, who
has conducted most of the electron micrography studies of HIV, say that the
virus loses its knobs when it buds from the cell. This means that cell-free
virus is incapable of infecting other cells. Since plasma does not contain
cells, if HIV were present, it would not be inside a cell and thus it would not
be capable of causing an infection.
In addition, there is the dilution factor. Factor VIII concentrate is made from
the blood of thousands of donors pooled together. Statistically, only one or two
of these donors might be infected, so by the time their blood is merged with
that of uninfected donors, only a few copies of HIV, or even none whatsoever,
would be present per millilitre. (See "Bad Blood or Bad Science: Are
haemophiliacs with AIDS diagnoses really infected with HIV?" by Christine
Johnson in Continuum magazine, Volume 5, No. 4.)
The CDC accepts that a positive test in haemophiliacs is not proof of HIV
infection: "It is possible that antibody to LAV [=HIV] is acquired
passively from immunoglobulins found in factor VIII concentrates.... Likewise,
it is possible that seropositivity is caused not by infectious virus but by
immunization with non-infectious LAV or LAV proteins derived from virus
disrupted during the processing of plasma into factor VIII concentrate." (Evatt,
1985.)
Since in most cases the time between phlebotomy and conversion of pooled plasma
to factor VIII concentrate is considerably greater than three hours, factor VIII
is made from plasma which is cell free and, since the late 1970s, factor VIII
has been supplied as a dry powder, which may spend months awaiting use, how can
one reconcile the above facts with the view that haemophiliacs are infected with
HIV via contaminated factor VIII concentrates?
Yours sincerely,
Alexander Russell, MA
London,
England, UK.
AIDS is accelerated ageing and not a viral condition
AIDS Myth Exposed MSN Group Sent: 21/08/2006
Alex Russell
Conf Retroviruses
Opportunistic Infect 1997 Jan 22-26; 4th:81 (abstract no. 91)
Hotschkiss G, Britton S; Center for Biotechnology, Novum, Sweden.
To: New York Times
The Editor, Opinion,
The Op-Ed Page,
229 West 43rd Street,
New York, NY 10036
An Article for the Op-Ed Page: Opinion
Reply to John Moore and Nicoli Nattrass
London: 23rd June, 2006
Dear John Moore and Nicoli Nattrass,
In your article 'Deadly Quackery' (Opinion, The New York Times, 4th June, 2006), you stated:
"H.I.V. causes AIDS. This is not a controversial claim but an established fact, based on more than 20 years of solid science."Contrary to your unfounded claim, this is not an "established fact" but a proposition, a hypothesis, an assumption based entirely upon an arbitrary correlation between 'HIV' (whatever that is) and 'AIDS' (whatever that is). Correlation is not proof of causation. The case of the haemophiliacs proves that HIV cannot be the cause of AIDS.Soon after HIV tests were introduced in 1985, it was noticed that many haemophiliacs were shown to be 'HIV positive'. Robert Gallo seized upon this as evidence that AIDS was caused by an infectious, transmissible organism, presumed to have been conveyed to the haemophiliacs as a contaminant in their clotting factor preparations.However, in the light of subsequent research, we can now see that the case of haemophiliacs, far from proving the existence of a transmissible retrovirus(HIV) alleged to have contaminated their clotting factor, proves conclusively, in fact, quite the reverse: HIV is not - and cannot be - the cause of AIDS.Why did haemophiliacs start to die in appreciable numbers only after HIV was "discovered" in 1983? Surely if this alleged retrovirus was the cause of AIDS’ we would have noticed their premature deaths before 1983: and why didn't haemophiliacs die from KS (Kaposi's sarcoma) and PCP (pneumocystis carinii pneumonia), the two original "AIDS" defining diseases?Gallo tried to make the case that AIDS was caused by a transmissible agent and cited cases of haemophiliacs whom it was assumed were infected via the clotting factor VIII. This assumption was based on two premises that subsequently proved to be totally false: a) the amount of putative virus in a plasma donor/seller's blood and b) that the virus would survive the manufacture of factor VIII from the pooled plasma.Uncritical scientists and medics accepted Gallo's assumption. It soon became apparent, however, that the supposition was wrong. First, it was assumed that plasma donors/sellers were infected with HIV’ and carrying huge titres of cell-free infectious virus particles that resulted in the contamination of the pooled plasma used in the manufacturer of factor VIII. Sometimes, these pools were as large as 30,000 donations of 600 millilitres (ml) of plasma. It was suggested that there was sufficient cell-free "HIV" in some of the donors to contaminate the whole batch. This supposed a massive titre of millions, if not billions, of viral particles in the infected donors. This was subsequently proved to be wrong. In the nearly 200,000 published scientific papers on HIV/AIDS, not one claims to have found a titre of more than 10 infectious particles per cubic ml of blood/plasma ( and even this negligible titre was based on surrogate markers!). There is no way that these negligible amounts of HIV, even if proven to exist, could have contaminated so much factor VIII that virtually all the haemophiliacs could be deemed infected with HIV. As Peter Duesberg rightly pointed out, the average amount of virus’ claimed to be present in the plasma or blood of an HIV-infected individual, stands at between 1 and 1.7 infectious viral particles per cubic ml, which is absolutely negligible.Thus, paucity of virus rules out the suggestion that HIV was transmitted to so many haemophiliacs in a comparatively short space of time.Studies subsequent to 1985 showed that HIV cannot survive long outside the host's body. This is confirmed by studies showing that spilled HIV’ positive blood samples or spoiled laboratory cultures resulted in the quick death of the alleged "virus." It was further discovered, and admitted by the Centers for Disease Control and Prevention (CDC), that dried HIV does not survive. Therefore, factor VIII that is subjected to cryoprecipitation (freeze drying) could not possibly contain viable, cell-free, infectious HIV, even if there had been any putative "virus" in the mix to begin with, which is extremely unlikely for reasons described above.It was the 99 percent impurities in factor VIII that caused the immune suppression (AIDS) seen in haemophiliacs. Hence, the early discovery that seroconversion in haemophiliacs seems to depend on the amount and duration of consumption - it is age and dose-related.. They were dependent on a product that would eventually kill them. Also, as Duesberg cynically observed, "Even haemophiliacs are not immortal."The introduction of AZT - administered in enormous doses - rapidly killed many haemophiliacs. Their premature deaths exactly coincided with the fast tracking of AZT to haemophiliacs on 'compassionate' grounds in 1986-7Haemophiliac mortality increased only after the introduction of AZT in 1986. Since about half of Darby's 2,037 severe haemophiliacs were already HIV-positive by this time, surely HIV-caused mortality should have exerted a detectable influence prior to 1985 in this group. Only Duesberg's theory can explain why the explosion of haemophiliac mortality should occur only on the heels of HIV testing: The cytotoxic pharmaceutical drugs and psychological terror that invariably accompany a positive HIV test also contributed to the increased mortality.In January 1994, the CDC communicated the following experimental data and conclusion: "In order to obtain data on the survival of HIV [in factor V111 clotting factor], laboratory studies have required the use of artificially high concentrations of laboratory grown virus ... the amount of virus studied is not found in human specimens or any place else in nature ... it does not spread or maintain infectiousness outside its host. Although these unnatural concentrations of HIV can be kept alive under precisely controlled and limited laboratory conditions, CDC studies have shown that drying of even these high concentrations of HIV reduces the number of infectious viruses by 90 to 99 percent within several hours. Since the HIV concentrations used in laboratory studies are much higher than those actually found in blood or other body specimens, drying of HIV-infected human blood or other body fluids reduces the theoretical risk of environmental transmission to that which has been observed - essentially zero." (My emphasis.)Ironically, the very original suggestion that haemophiliacs were proof of the HIV/AIDS hypothesis can now be used to deconstruct this redundant and failed paradigm. There is absolutely no way that HIV could have been transmitted via commercial clotting factors.I would like to conclude with science journalist Christine Johnson's critical observations: "No one has actually seen HIV in blood plasma. Its presence is inferred from the results of indirect and non-specific techniques applied to virus cultures. AIDS expert Jay Levy of the University of California was able to find what he believed were HIV particles in the plasma of only 30 percent of the AIDS patients he studied, and then, it was at a low concentration - 10 infectious particles per millilitre. Levy concedes that this isn't enough to establish an infection."It is widely accepted that the surface of HIV must be studded with knobs containing the protein gp120, which is crucial to the virus's ability to infect cells. But experts such as Hans Gelderblom of the Koch Institute in Berlin, who has conducted most of the electron micrography studies of HIV, say that the virus loses its knobs when it buds from the cell. This means that cell-free virus is incapable of infecting other cells. Since plasma does not contain cells, if HIV were present, it would not be inside a cell and thus it would not be capable of causing an infection.In addition, there is the dilution factor. Factor VIII concentrate is made from the blood of thousands of donors pooled together. Statistically, only one or two of these donors might be infected, so by the time their blood is merged with that of uninfected donors, only a few copies of HIV, or even none whatsoever, would be present per millilitre. (See "Bad Blood or Bad Science: Are haemophiliacs with AIDS diagnoses really infected with HIV?" by Christine Johnson in Continuum magazine, Volume 5, No. 4.)The CDC accepts that a positive test in haemophiliacs is not proof of HIV infection: "It is possible that antibody to LAV [=HIV] is acquired passively from immunoglobulins found in factor VIII concentrates.... Likewise, it is possible that seropositivity is caused not by infectious virus but by immunization with non-infectious LAV or LAV proteins derived from virus disrupted during the processing of plasma into factor VIII concentrate." (Evatt, 1985.)
Since in most cases the time between phlebotomy and conversion of pooled plasma to factor VIII concentrate is considerably greater than three hours, factor VIII is made from plasma which is cell free and, since the late 1970s, factor VIII has been supplied as a dry powder, which may spend months awaiting use, how can one reconcile the above facts with the view that haemophiliacs are infected with HIV via contaminated factor VIII concentrates?
Yours sincerely,Alexander Russell, MA
London, WC1N 1PE,
England, UK.
28.06.06:Dear John Moore,
Please could you reply to my response regarding your Op-Ed in The New York Times. You have not proven that 'HIV' exists or causes 'AIDS'.Yours sincerely, Alex Russell MA29.06.06:Dear Mr Russell,
No.Yours sincerely,John Moore PhD
30.06.06:
Dear John Moore PhD,
Why 'No'? What does 'No' mean? No - you cannot answer my questions? No - I have no answers? You said: 'No' because you know you have no answers.A critical reading of S.C. Darby et al., 'Mortality before and after HIV infection in the complete UK population of haemophiliacs' Nature 7 Sept. 1995, vol.377 pp.79-82, showed that the mortality of seropositive haemophiliacs in the UK was stable until 1986 and suddenly shot up to coincide exactly with the introduction of AZT - you cannot face the fact that it was AZT (iatrogenic 'AIDS') that indiscriminately slaughtered the haemophiliacs - not 'HIV'.Yours sincerely, Alex Russell MA.
Sent: Sunday, July 02, 2006 5:16 PMSubject: Re: Alex Russell's reply to John Moore's 'reply'
You asked: "Please could you reply to my response below regarding your Op-Ed in the New York Times."
I answered: "No". (i.e., I declined to reply to your question).John Moore
Sent: Sunday, July 02, 2006 9:02 PM
Subject: Re: Alex Russell's reply to John Moore's 'reply'
Dear John Moore,Why did you decline to answer my question? Surely, if you are in the right - it should be easy to refute my comments. However, if I am right, and 'HIV' is non-transmittable sexually and could not possibly have contaminated clotting factor VIII (8), then how do you explain the so-called 'HIV' positivity in haemophiliacs world wide? Please bear in mind that the CDC themselves have admitted that 'HIV' could not possibly have survived the freeze-drying used in its manufacturing process used in commercially produced clotting factor (VIII) 8. So how were the haemophiliacs 'infected' with 'HIV'? They were not 'infected' by their clotting factor! What is your explanation? You have to answer this one!PS: In the ringing words of Oliver Cromwell - "I beseech you, in the bowels of Christ, think it possible that you may be mistaken."Yours sincerely, Alex Russell MA.
Message Received: Sep 28 2006, 02:29 PM
Dear Mr Russell,
No. Again.
Yours sincerely,
John Moore PhD
Message Sent: Sep 28 2006, 11:29 AM
Subject: Re: Lethal effects of AZT reported in The Lancet
Dear Dr. Moore,Despite your curt response 'No' (29, June, 2006) to my invitation to comment on the lethal effects of AZT on haemophiliacs, would you care to comment on the enclosed report?
Barnesworld Blogs, September 12, 2006
Lancet To Publish Long Overdue Erratum: AZT Lethal for Hemophiliacs
Hemophilia is a serious disease -- blood won't clot, huge risk of internal bleeding, big need for blood transfusions. And these transfusions placed those with this rare, single gene disorder in the original AIDS 4-H club (Haitians, Homosexuals, Heroin users and Hemophiliacs).
A well-cited paper by Goedert et al., Risks of immuodeficiency, AIDS and death related to purity of factor viii concentrate, published in the Lancet in 1994, describes a large multi-center trial to compare the benefits of highly purified clotting factor versus a less purified product for those unfortunate enough to suffer both hemophilia and the AIDS stigmata. The abstract reads:
In HIV-infected subjects with haemophilia, CD4 counts seem to fall more slowly in those on high-purity factor VIII (FVIII) than on intermediate-purity product. We evaluated whether risks for AIDS or death were associated with either product among 411 HIV-infected individuals. The relative hazard of AIDS was slightly elevated for both current (1.34) [corrected] and cumulative (1.01 per month) use of high-purity products (neither significant). The corresponding hazards for death were 1.49 and 1.03 (neither significant). Thus we found no evidence that high-purity FVIII concentrates retard the development of AIDS.
All well and good. But take a close look at the key table from this paper. It seems that some of these hemophiliacs were also being "medicated" with the chain-terminating nucleoside analog and failed cancer drug, AZT. And wouldn't you know, the risk of hemophiliacs on AZT developing AIDS was 4.5-fold elevated, and they were more than twice as likely to die. How ya like them poisoned apples!
This is, by far, the most important variable in the multi-authored "parametric model".
How did the many, senior scientist authors let this damning line into an otherwise bland table? The "quick and dirty" answer is that the junior level preparation of the graphics to go with the manuscript was not too swift, and the senior scientist crew was inattentive and no one noticed that the computer-generated, "total" data-package required editing. More to the point, and more significantly, why did the referees not question this? (They did not since it is never discussed, or even mentioned anywhere in the text.)But science is self-correcting, even if the wheels of the mill of truth grind exceedingly slow but fine (or something like that).
Shortly after the discordant entry was called to my attention by our good friend doc Bialy (whose slide is linked above), we alerted the highly esteemed, very British editors of the Lancet to this minor anomaly, and the clear demonstration of the extreme toxicity of AZT. Perhaps in line with a trend started by the honest publication in August of some very provocative (to put it mildly) results of newer "antiretroviral therapy", they agreed to print an erratum in the very first issue with the beautiful, redesigned cover we sent them (and which is reproduced below), and to elevate the important, but previously overlooked, major conclusion of the Godert study to its proper place in a suitably retitled article: Risks of Immunodeficiency, AIDS and Death Related to AZT Intoxication.
Although this may come a little late for the thousands of hemophiliacs who had their lives shortened by AZT, we think the editors still deserve a "Bravo" on the strength of what all our grandmother's told us about better late than never being almost, always true.So, Bravo, guys and gals, but in the future try and get it right the first time OK?
13 September / Update:It has come to our attention through various means that Dean Esmay was not alone in "almost falling for it". In fact, many actually fell, head first and with no safety net! We know it would have avoided all this misunderstanding (sic) if the title of the piece had been "Lancet Needs to Publish a Long Overdue Erratum", but honestly would it have packed even a fraction of the "punch" ?14 September / Update1. Richard Berkowitz writes:
"In 1989 or 1990 the New England Journal of Medicine published findings that compared AIDS patients given 1200mg of AZT compared with those given 600mg AZT. Their findings? People with the higher dose had twice the mortality."Do some of you knuckleheads understand that the more AZT one takes, the sicker one gets? Since AZT is garden variety cancer chemo, why would anyone but a propagandist for Big Pharma be surprised by this? Y'all should listen to Mr. Berkowitz. He was there in the thick of it in NY, when AZT was unleashed on a frightened populace. Very tragic.
2. Library trip aborted! One kind fellow (thank you very much, Sir) sent me the pdf. Pharma Ditz and George, y'all have the quote right:
"Subjects who had started [AZT] had an increased risk of AIDS, probably because [AZT] was administered first to those whom clinicians considered to be at highest risk. "
My bad for missing this, but so what? It's pure speculation. Whenever medicine kills, the underlying disease is blamed. (See Pluda paper, where excess lymphoma rates were attributed to the virus, not the AZT)
Hank B
p.s. AZT is dangerous stuff. It screws with your DNA. Best to be avoided. Should not have been given to hemophiliacs.Posted by HankBarnes on September 12, 2006 at 04:14 PM | Permalink
http://barnesworld.blogs.com/barnes_world/2006/09/the_mathematics.htmlYours sincerely,
Alexander Russell, MA
London, WC1N 1PE,
England, UK
Re:
An Open Letter to Robert Gallo
04/22/06 01:23 PM
The Case of the
Haemophiliacs proves that HIV cannot be the cause of AIDS
FICTION:
“acquired immunodeficiency syndrome (AIDS) was first recognized in 1981 and
has since become a major worldwide pandemic. AIDS is caused by the human
immunodeficiency virus (HIV). By leading to the destruction and/or functional
impairment of cells of the immune system, notably CD4+ T cells, HIV
progressively destroys the body's ability to fight infections and certain
cancers.”
This statement is pure assumption based upon an unproven hypothesis and there is
no published paper in the scientific literature that supports this claim that
HIV exists and causes AIDS. In the Gallo and Montagnier papers published in
Science by two research groups, there is no proof of the isolation of a
retrovirus from AIDS patients. In 1981 AIDS was not first recognised: what was
first recognised was KS and PCP in gay men who had a long history of repeated
STDs, massive dependence on broad spectrum antibiotics, and recreational drug
and popper consumption (amyl nitrites). What was later invented as ‘HIV’ was
merely an endogenous marker for certain risk behaviour.
FICTION:
“Most AIDS symptoms result from the development of opportunistic infections
and cancers associated with severe immunosuppression secondary to HIV.”
The alleged association is meaningless when you consider that one in three
people will develop cancer independent of HIV. 38% of AIDS related
diseases/conditions are not dependent on immune suppression: i.e: KS, dementia,
diarrhea, etc.
FICTION:
“The diseases associated with AIDS, such as PCP and Mycobacterium avium
complex (MAC), are not caused by HIV but rather result from the
immunosuppression caused by HIV disease.”
What is this hypothetical 'HIV disease'? How does HIV destroy cells? What is the
mechanism? If you cannot say exactly how HIV destroys immune cells then you are
not entitled to say it does. Association is not proof of causation. There is no
such thing as 'HIV disease'.
FICTION:
“AIDS and HIV infection are invariably linked in time, place and population
group.”
So why the embarrassingly elastic ‘incubation’ period between hypothetical
‘infection’ and the on set of so-called ‘symptoms’ – in some case
estimated to be as long as 25 years?
FICTION::
“HIV can be detected in virtually everyone with AIDS.”
Contrary to this claim, HIV has never been detected or found in anyone - with or
without AIDS.
Cell-free HIV has never been found or recovered in fresh samples of semen or
blood. The key fact to remember is that cell-free infectious HIV viral particles
have never been recovered from fresh donor semen and blood. It is still an
unproven hypothesis that HIV is an STD/STI.
The case of the haemophiliacs proves conclusively that HIV cannot be the cause
of AIDS. Soon after HIV tests were introduced in 1985, it was noticed that many
haemophiliacs were shown to be HIV positive. Robert Gallo seized upon this as
evidence that AIDS was caused by an infectious, transmissible organism, presumed
to be conveyed to the haemophiliacs as a contaminant in their clotting factor
preparations.
However, in the light of subsequent research, we can now see that the case of
haemophiliacs, far from proving the existence of a transmissible retrovirus
(HIV) alleged to have contaminated their clotting factor, proves conclusively,
in fact, quite the reverse: HIV is not — and cannot be — the cause of AIDS.
Why did haemophiliacs start to die in appreciable numbers only after HIV was
“discovered” in 1983? Surely if this alleged retrovirus was the cause of
AIDS‚ we would have noticed their premature deaths before 1983: and why didn't
haemophiliacs die from KS (Kaposi’s sarcoma) and PCP (pneumocystis carinii
pneumonia), the two original “AIDS” defining diseases?
Gallo tried to make the case that AIDS was caused by a transmissible agent and
cited cases of haemophiliacs whom it was assumed were infected via the clotting
factor VIII. This assumption was based on two premises that subsequently proved
to be totally false: a) the amount of putative virus in a plasma
donor/seller’s blood and b) that the virus would survive the manufacture of
factor VIII from the pooled plasma.
Uncritical scientists and medics accepted this supposition. It soon became
apparent, however, that the supposition was wrong. First, it was assumed that
plasma donors/sellers were infected with HIV‚ and carrying titres of cell-free
infectious virus particles that resulted in the contamination of the pooled
plasma used in the manufacturer of factor VIII. Sometimes, these pools were as
large as 30,000 donations of 600 millilitres (ml) of plasma. It was suggested
that there was sufficient cell-free “HIV” in some of the donors to
contaminate the whole batch. This supposed a massive titre of millions, if not
billions, of viral particles in the infected donors. This was subsequently
proved to be wrong. In the nearly 200,000 published scientific papers on
HIV/AIDS, not one claims to have found a titre of more than 10 infectious
particles per cubic ml of blood/plasma. There is no way that these negligible
amounts of HIV, even if proven to exist, could have contaminated so much factor
VIII that virtually all the haemophiliacs could be deemed infected with HIV. As
Peter Duesberg rightly pointed out, the average amount of virus‚ claimed to be
present in the plasma or blood of an HIV-infected individual, stands at between
1 and 1.7 infectious viral particles per cubic ml, which is absolutely
negligible.
Thus, paucity of virus rules out the suggestion that HIV was transmitted to so
many haemophiliacs in a comparatively short space of time.
Studies subsequent to 1985 showed that HIV cannot survive long outside the
host’s body. This is confirmed by studies showing that spilled HIV‚ positive
blood samples or spoiled laboratory cultures resulted in the quick death of the
alleged “virus.” It was further discovered, and admitted by the Centers for
Disease Control and Prevention (CDC), that dried HIV does not survive.
Therefore, factor VIII that is subjected to cryoprecipitation (freeze drying)
could not possibly contain viable, cell-free, infectious HIV, even if there had
been any putative “virus” in the mix to begin with, which is extremely
unlikely for reasons described above.
It was the 99 percent impurities in factor VIII that caused the immune
suppression (AIDS) seen in haemophiliacs. Hence, the early discovery that
seroconversion in haemophiliacs seems to depend on the amount and duration of
consumption - it is age and dose-related.. They were dependent on a product that
would eventually kill them. Also, as Duesberg observed, “Even haemophiliacs
are not immortal.”
The introduction of AZT — administered in enormous doses — rapidly killed
many haemophiliacs. Their premature deaths exactly coincided with the fast
tracking of AZT to haemophiliacs on 'compassionate' grounds in 1986-7.
Haemophiliac mortality increased only after the introduction of AZT in 1986.
Since about half of Darby's 2,037 severe haemophiliacs were already HIV-positive
by this time, surely HIV-caused mortality should have exerted a detectable
influence prior to 1985 in this group. Only Duesberg's theory can explain why
the explosion of haemophiliac mortality should occur only on the heels of HIV
testing: The cytotoxic pharmaceutical drugs and psychological terror that
invariably accompany a positive HIV test also contributed to the increased
mortality. AZT - not HIV - killed the haemophiliacs.
In January 1994, the CDC communicated the following experimental data and
conclusion: "In order to obtain data on the survival of HIV [in factor V111
clotting factor], laboratory studies have required the use of artificially high
concentrations of laboratory grown virus ... the amount of virus studied is not
found in human specimens or any place else in nature ... it does not spread or
maintain infectiousness outside its host. Although these unnatural
concentrations of HIV can be kept alive under precisely controlled and limited
laboratory conditions, CDC studies have shown that drying of even these high
concentrations of HIV reduces the number of infectious viruses by 90 to 99
percent within several hours. Since the HIV concentrations used in laboratory
studies are much higher than those actually found in blood or other body
specimens, drying of HIV-infected human blood or other body fluids reduces the
theoretical risk of environmental transmission to that which has been observed
— essentially zero."
Ironically, the very original suggestion that haemophiliacs were proof of the
HIV/AIDS hypothesis can now be used to deconstruct this redundant and failed
paradigm. There is absolutely no way that HIV could have been transmitted via
commercial clotting factors.
I would like to conclude with science journalist Christine Johnson’s critical
observations: “No one has actually seen HIV in blood plasma. Its presence is
inferred from the results of indirect and non-specific techniques applied to
virus cultures. AIDS expert Jay Levy of the University of California was able to
find what he believed were HIV particles in the plasma of only 30 percent of the
AIDS patients he studied, and then, it was at a low concentration — 10
infectious particles per millilitre. Levy concedes that this isn't enough to
establish an infection."
It is widely accepted that the surface of HIV must be studded with knobs
containing the protein gp120, which is crucial to the virus's ability to infect
cells. But experts such as Hans Gelderblom of the Koch Institute in Berlin, who
has conducted most of the electron micrography studies of HIV, say that the
virus loses its knobs when it buds from the cell. This means that cell-free
virus is incapable of infecting other cells. Since plasma does not contain
cells, if HIV were present, it would not be inside a cell and thus it would not
be capable of causing an infection.
In addition, there is the dilution factor. Factor VIII concentrate is made from
the blood of thousands of donors pooled together. Statistically, only one or two
of these donors might be infected, so by the time their blood is merged with
that of uninfected donors, only a few copies of HIV, or even none whatsoever,
would be present per millilitre. (See “Bad Blood or Bad Science: Are
haemophiliacs with AIDS diagnoses really infected with HIV?” by Christine
Johnson in Continuum magazine, Volume 5, No. 4.)
I would like to conclude with some critical comments made by biophysicist Eleni
Papadopulos-Eleopulos and colleagues:
* Even the CDC accepts that a positive test in haemophiliacs is not proof of HIV
infection. "It is possible that antibody to LAV [=HIV] is acquired
passively from immunoglobulins found in factor VIII concentrates.... Likewise,
it is possible that seropositivity is caused not by infectious virus but by
immunization with non-infectious LAV or LAV proteins derived from virus
disrupted during the processing of plasma into factor VIII concentrate." (Evatt,
1985.)
* Levy and his colleagues have shown that the titre of HIV in plasma of
HIV-infected individuals three, six or twelve hours after phlebotomy [blood
donation] "dropped from up to 500 TCID/ml to 0." [TCID = tissue
culture infectious dose.]
Since in most instances, if not all, the time between phlebotomy and conversion
of pooled plasma to factor VIII concentrate is considerably greater than three
hours, factor VIII is made from plasma which is cell free and, since the late
1970s, factor VIII has been supplied as a dry powder, which may spend weeks or
months awaiting use, how can one reconcile the above facts with the view that
haemophiliacs are infected with HIV via contaminated factor VIII concentrates? (Papadopulos,
1995b).
I would like to end with the conclusion from an interview with Eleni
Papadopulos-Eleopulos:
“The proteins said to belong to HL23V were defined in the same manner as the
HIV proteins. By antibody reactions. So, when the antibodies were shown to be
non-specific, HL23V disappeared. In the case of HL23V it was relatively easy
because the antibodies occurred in so many people who were never going to get
leukaemia they were bound to be something unrelated and that's what was
eventually proven at Sloan Kettering and the National Cancer Institute. My group
thinks that scientists will eventually accept that the same is true of HIV
antibodies. You see AIDS patients are inundated with antibodies to so many
different things a few of these could easily react with two or three of the ten
proteins present in the ‘HIV’ test. That's all that’s required to be HIV
positive. In fact, there's now ample evidence that antibodies produced as a
result of infection with the two germs that infect ninety percent of AIDS
patients react with all the HIV proteins. I mean the germs known as mycobacteria
and yeasts that between them cause two of the commonest AIDS defining diseases.
We have a paper on this in press in the British journal Current Medical
Research and Opinion. If that's the case how can anyone say these antibodies
prove infection with HIV or that these diseases are caused by HIV?”
Alex Russell, April 22,
2006
Re: An Open Letter
to Robert Gallo
04/22/06 04:08 PM
"All things are subject
to interpretation whichever interpretation prevails at a given time is a
function of power and not truth....Every elevation of man brings with it the
overcoming of narrower interpretations...every strengthening and increase of
power opens up new perspectives and means believing in new horizons."
Friedrich Nietzsche (1844-1900).
You stated: “It is so sad that a person cannot understand the science they are
posting and reading. The age of the information you post is actually very old,
it has been proven wrong many times over, but if you feel you want to deny the
validity of HIV/Aids please do so. But you have to understand that the truth is
above in the information I posted earlier, you may think that your views are the
only right views, but so do the people who believe in Mormonism, Hinduism,
Christianity, Buddhism, Jehovah.
Maybe you notice that people who have different opinions to the few denialist
groups are not allowed to post on there sites, there posts are immediately
removed because they do not want anything to be shown on there but there posts
and outdated information that they keep changing the dates on to make them look
like they are new. Most of us that are affected by this disease for so many
years have seen this same information posted repeatedly. I guess you would not
know about this though, but you seem intelligent enough to understand (I hope)
that the information is not current, and is not wanted at this site just as the
information refuting everything your group says is not wanted on their sites.”
Correct and objective information is never ‘old’ or ‘out dated’. Our
counter-critique (information) is not wanted here because it deconstructs the
HIV Ideological Belief System which is uncannily similar to Scientology as a
frightening form of mind-body control. You need to ask yourself why you need
this HIV Mind Control? Why do you need to believe HIV Science Fiction? Many gay
men want to believe in HIV becuase they cannot take responsibility for their own
actions and admit that thier lifestyle is killing them not HIV - they are in
'denial' that 'AIDS' is a self-inflicted lifestyle. Like 'AIDS' in Africa is due
to poverty, malnutrition, TB and malaria - and nothing to do with HIV.
The information or rather disinformation at this HIV Ideology website is not
current at all but built upon an error based upon the misconception that HIV
exists and has been isolated. All the information presented here at this website
is an error built and based upon a lie – HIV. HIV is an error we need to
examine and subject to fresh open minded scrutiny – and not censorship – as
is the case here. Censorship will not end the HIV Lie. HIV is an error that can
never become true as Mahatma Gandhi observed: “An error can never become true
however many times you repeat it. The truth can never be wrong, even if no one
ever hears about it. Truth alone will endure; all the rest will be swept away
before the tide of time.”
HIV Belief is a postmodern theology based upon superstition, denial, ignorance,
fear and control like all regressive and reactionary religions. The weak need
‘HIV’ Belief like the weak need organised religion to control them just like
those who believe in Mormonism, Hinduism, Christianity, Jehovah.
All information based upon the HIV/AIDS hypothesis is out of date because HIV
has past its sell by date. The hallmark of a sound hypothesis is that
predictions based upon it will be fulfilled. This has never been the case with
the HIV/AIDS hypothesis despite the fact that they have continually finagled the
figures and moved the goal posts in expanding the definition of ‘AIDS’ to
make it into an equal opportunities disease. They remove any of the critical
posts here at this site that deconstruct the absurdities, anomalies and the
contradictions of the HIV/AIDS Ideological Belief System which threatens the
obscene and vast profits of the HIV Pharmaceutical Industry.
Robert Gallo still has not been able to answer Roberto Giraldo and Etienne de
Harven’s rebuttal to him: I wonder why not?
I would like to leave you all with the following quotes:
"The most formidable barrier to the advancement of science is the
conventional wisdom of the dominant group."
Conrad Hal Waddington, Embryologist & Geneticist (1905-1975).
"There is no proof that HIV causes AIDS - for many reasons but most
importantly, because there is no proof that HIV exists."
Eleni Papadopulos-Eleopulos, Is HIV the cause of AIDS?, Continuum, Autumn 1997.
"The HIV hypothesis ranks with the 'bad air' theory for malaria and the
'bacterial infection' theory of beriberi and pellagra [caused by nutritional
deficiencies]. It is a hoax that became a scam."
Dr. Bernard Forscher, Conspiracy of Silence, The Sunday Times, 3 April 1994.
"Scientists will then have to come to terms with the awful fact that the
AIDS epidemic was a mirage manufactured by scientists who believed that
integrity could be maintained amidst the diverting influences of big money,
prestige and politics."
Professor Hiram Caton, Conspiracy of Silence, The Sunday Times, April 1994.
"I propose there are no human retroviruses. 'HIV' is not Human, it has
never been proven to be the cause of Immunodeficiency, and is not a Virus, but a
misinterpreted artefact of human and simian cell cultures. Therefore the acronym
'HIV' is wrong on all counts."
Michel Verney-Elliott, 'SIV' and Poliovaccination - A Shot In The Foot?, 1999.
"I found that when they are speaking about HIV they are not speaking about
a virus. They are speaking about cellular characteristics and activities of
cells under very special conditions...I realized that the whole group of viruses
to which HIV is said to belong, the retroviruses, in fact do not exist at
all."
Dr. Stefan Lanka, Virologist, Zenger's, December, 1998.
"Where is the research that says HIV is the cause of AIDS? If there is
evidence that HIV causes AIDS, there should be scientific documents which either
singly or collectively demonstrate that fact, at least with a high probability.
There is no such document."
Dr. Kary Mullis, Biochemist, 1993 Nobel Prize for Chemistry, The Sunday
Times,
28 November 1993.
"The HIV-causes-AIDS dogma represents the grandest and perhaps the most
morally destructive fraud that has ever been perpetrated on the young men and
women of the Western world."
Dr. Charles Thomas, Conspiracy of Silence, The Sunday Times, April 1994.
Alex Russell
Open Letter to Amanda Elliot, managing editor, Positive Nation:
Exposing the NHS 'HIV' Fraud
AIDS Myth Exposed MSN Groups Sent: 06/03/2006 14:15
Alex Russell
An Open Letter to Andrew Sullivan, Time Magazine.
AIDS Myth Exposed MSN Groups Sent: 23/01/2006 21:59
Dear Andrew Sullivan:
Is TIME Magazine’s Blog ‘Drugs & Negs’ (Sunday, January 22, 2006) a sick, cynical joke, being pushed by pernicious profiteering ‘HIV’ pharmaceuticals? :
"In the current HIV prevention discussion, this idea [Jon Cohen, Protect or Disinhibit, New York Times, 22 January, 2006] is well worth airing and perhaps pursuing: Why not put all HIV-negative men on a simple anti-retroviral regimen as a prophylaxis, rather than as a treatment? In any single case, the likelihood of possible transmission drops (because the drugs kill off the virus before it can take hold of a new immune system). The big studies being done will help confirm whether there are collective behavioural adjustments that undermine the effort to reduce transmission. My own view is that gay men, if the studies pan out, could and perhaps should embark on a proactive campaign to get as many sexually active men as possible on meds. It's a way for HIV-negative men to do something which is not simply defensive in nature, and make decisions about their health in a moment outside the inevitable irrationality of a sexual encounter. We're used to taking pills after we've become sick. Why not take them before - as a prevention technique? Even a mild decline in transmission could drastically alter the dynamic of the epidemic - for the better. Next up: involve vulnerable African-American women in the same discussion."
This idea is insane! This is pure ‘HIV’ pseudo science: insanity – madness – irrationality: the wicked world of ‘HIV’ virtual virology. Preventing what? ‘HIV’ is not a ‘virus’. ‘HIV’ is not an ‘infection’. HIV is not an STD. No one on earth is ‘HIV’ positive.
To date: Cell-free HIV has never been found or recovered in fresh samples of semen or blood. The key fact to remember is that cell-free infectious HIV viral particles have never, repeat never, been recovered from fresh donor semen and blood. ‘HIV’ have never been visualised under electronmicroscopy.
Whilst ‘HIV’ is not an infection, ‘HIV’ Ideology is highly 'infectious' and 'contagious' and 'spread' through the ‘HIV’ Interpellation techniques such as HIV Testing ritual rites of ‘HIV’ Indoctrination and ‘HIV’ Incarceration. We must de-programme and raise awareness amongst ‘diagnosed’ gay men that they are not ‘HIV’ positive: they must be ‘informed’ of the following facts:
HIV is not a
retrovirus.
HIV is not an infectious agent.
HIV does not cause AIDS.
No one is ‘living with HIV’
HIV is not sexually transmitted. It is only ever been an assumption that HIV is
an STI based on the apparent existence of clusters of cases. HIV is merely an
endogenous marker for oxidative stress, antigenic overload and recreational drug
use in the West.
Testing HIV positive merely indicates a cluster of people who had indulged in
identical behaviour: it is important to remember that originally clusters of
cases of beriberi, pellagra and scurvy were also assumed to be caused by a
transmissible infection: all this was subsequently shown to be totally wrong.
Beriberi, pellagra and scurvy were not caused by a transmissible agent but were
all caused by a shared vitamin deficiency. Similarly: ‘AIDS’ is not caused
by a transmissible agent (‘HIV’) but by exposure to multiple pathogenic
insults caused by life style in the West and by well known endemic conditions
relating to Third World countries.
Hans Gelderblom of
Berlin's Robert Koch Institute co-authored the first paper in Virology, March
1997, showing 'purified HIV' to be 'purified microvesicles'. What was assumed to
be 'purified HIV' was in fact "an excess of vesicles" - particles of
cellular proteins. The hypothetical 'HIV' is in fact a collection of endogenous
microvesicles and cellular proteins (which also never seem to form particles -
so how can they be infectious)? Cell-free viral 'HIV' particles have never ever
been visualised in any freshly donated bodily fluid including semen, blood, etc.
'HIV' has never ever proven to be a sexually transmitted retrovirus.
As Virologist Dr. Stefan Lanka observed: The rules demonstrating the existence
of HIV (and retroviruses in general) were never adhered to by those who devised
them nor were they ever validated. No particle of HIV has ever been obtained
pure, free of contaminants; nor has a complete piece of 'HIV RNA' (or the
transcribed DNA) ever been proved to exist.
Dr. Stefan Lanka stated:
“I found that when they are speaking about HIV they are not speaking about a
virus. They are speaking about cellular characteristics and activities of cells
under very special conditions...I realized that the whole group of viruses to
which HIV is said to belong, the retroviruses, in fact do not exist at all.”
(Zenger's, December, 1998).
In the words of John Lauritsen:
“I still regard
‘AIDS’ as the greatest blunder and the greatest hoax in medical history…
an epidemic of incompetence and an epidemic of
lies…It's time for gay men to wake up, look at ‘AIDS’ rationally, and put
an end to the sacrificial ritual. We didn't deserve this, and we should no
longer go along with it.” (AIDS: A Death Cult, John Lauritsen, 4
January 2004).
The HIV Lie is both hypnotic and seductive because people prefer to believe in
lies than in truth and in our society lies are lucrative. In 2006 we must all
put an end to the terrorism of the HIV Lie.
This open Letter to Andrew Sullivan is dedicated to the memory of genius Yale
mathematician Serge Lang (1927-2005).
"To an extent
that undermines classical standards of science, some purported scientific
results concerning 'HIV' and 'AIDS' have been handled by press releases, by
disinformation, by low-quality studies, and by some suppression of information,
manipulating the media and people at large. When the official scientific press
does not report correctly, or obstructs views dissenting from those of the
scientific establishment, it loses credibility and leaves no alternative but to
find information elsewhere." Serge Lang, Challenges, Springer Verlag
1998.
References and Further
reading:
15 YEARS OF AIDS By A. Hässig, H. Kremer, S. Lanka, W-X Liang, K. Stampfli: http://www.virusmyth.net/aids/data/ah15years.htm
HIV: Reality or Artefact?, By Stefan Lanka, Continuum, April/May 1995: http://www.virusmyth.net/aids/data/slartefact.htm
Fear of Losing HIV: http://aids-info.net/micha/hiv/aids/fearaids.html
John Lauritsen & Ian Young, The AIDS Cult: Essays on the gay health
crisis, Asklepios USA 1997, 224 pages, ISBN 0-943742-10-2.
Joan Shenton, Positively False; Exposing the myths around HIV and AIDS,
IB Tauris, London 1998, ISBN 1-86064-333-7.
Peter H. Duesberg, Inventing the AIDS Virus, Regnery USA 1996, ISBN
0-89526-470-6.
Roberto A. Giraldo, AIDS and Stressors, Impresos Begon, 1997:205p, USA.
ISBN 958 9458 03 3.
Serge Lang, Challenges, Springer Verlag 1998, 816 pages, ISBN
0-387-94861-9.
Yours sincerely, Alex Russell, MA
Gay.com
UK & Ireland
11th January 2006
| Re: 'HIV' tests are non-specific and non-standardised | ||||
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Gay.com
UK & Ireland
10th January 2006
| Re: 'HIV' tests are non-specific and non-standardised | ||||
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Gay.com
UK & Ireland
10th January 2006
| Re: 'HIV' tests are non-specific and non-standardised | ||||
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Gay.com
UK & Ireland
8th January 2006
| The Fear of Losing 'HIV' | ||||
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Gay.com
UK & Ireland
6th January 2006
| 'HIV' tests are non-specific and non-standardised | ||||
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Gay.com
UK & Ireland
5th January 2006
| Censorship of AIDS Critique at Gay.com | ||
|
| “An
error can never become true however many times you repeat it. The truth
can never be wrong, even if no one ever hears about it.” Mahatma
Gandhi Gay.com are censoring surfers and sufferers from having and sharing important medico-scientific information (‘informed choices’) on their HIV Message Board. Why? Why are they keeping you all ignorant from having information and attaining knowledge? Gay.com do not want gay men to be told the truth about AIDS and GRID (Gay Related Immune Deficiency) and propagate profitable HIV propaganda to vulnerable and often ignorant or unaware surfers and sufferers who may be seeking unbiased ‘information’. Our Government, The BBC, The Guardian, The Observer, and our AIDS Organisations have been blatantly lying to the gay community for over twenty years now in promoting HIV propaganda. They will go on and lie and lie and lie on behalf of the obscenely wealthy pharmaceutical multinationals who ‘own’ and ‘control’ the BMA, and the medico-science journals such as the BMJ, The Lancet, New Scientist, Nature and Science who propagate HIV propaganda. The BMJ Online has also stopped the AIDS debate and is now censoring dissenting critique. Why? Gay.com seems to be following suit and silencing democratic debate. Why? What do they fear? It is high time that the gay community stopped being so servile and supine and started questioning and demand an end to the HIV lies. Those tested ‘positive’ should demand proof that you are ‘HIV positive’. They should demand to see electronmicrograph images of HIV. Perversely and disturbingly many gay men actually want to believe in HIV and cannot live without HIV Belief and cannot live without HIV lies: they need the HIV lie: they live a lie. Such is the power of HIV Ideology. HIV Ideology is all about careerism, making money, monitoring men and telling lucrative lies. Remember: the HIV Industry is a multibillion dollar business and there are simply too many people making too much money out of it to put an end to the lucrative lie machine. But those who are diagnosed as ‘HIV positive’ - who keep the parasitic HIV Industry profitable - should stand up and say: no: I am not HIV positive! Gay.com makes the following statement regarding their HIV message board: “The HIV message boards are designed for people seeking support from their peers on issues related to HIV. Many newly diagnosed people benefit greatly by listening to the experiences of those that have been positive for some time, and people living with HIV have a great deal of advice, information and support to offer other GAY.COM visitors…GAY.COM will continue to provide the ‘Ask the Doctor’ service for medically related HIV questions answered by a HIV specialist Doctor”
What is an ‘HIV specialist Doctor’ Such so-called HIV specialist
doctors and the ‘Ask the Doctor’ service should be ‘informing’
GAY.COM surfers and ‘AIDS’ sufferers the following in 2006:
Fear of Losing HIV: http://aids-info.net/micha/hiv/aids/fearaids.html |
Gay.com
UK & Ireland
4th January 2006
| Re: Raising HIV Awareness in 2006 | ||||
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Gay.com
UK & Ireland
3rd January 2006
| Re: Raising HIV Awareness in 2006 | ||||
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||||
Gay.com
UK & Ireland
1st January 2006
| Raising HIV Awareness in 2006 | ||
|
Gay.com
makes the following statement regarding their HIV message board:
“The HIV message boards are designed for people seeking support from their
peers on issues related to HIV. Many newly diagnosed people benefit greatly by
listening to the experiences of those that have been positive for some time, and
people living with HIV have a great deal of advice, information and support to
offer other GAY.COM visitors…GAY.COM will continue to provide the ‘Ask the
Doctor’ service for medically related HIV questions answered by a HIV
specialist Doctor”
Such so-called HIV specialist doctors and the ‘Ask the Doctor’ service
should be ‘informing’ GAY.COM surfers and ‘AIDS’ sufferers the following
in ‘raising HIV awareness’ in 2006:
HIV is not a retrovirus.
HIV is not an infectious agent.
HIV does not cause AIDS.
No one is ‘living with HIV’
HIV is not sexually transmitted. It is only ever been an assumption that HIV is
an STI based on the apparent existence of clusters of cases. HIV is merely an
endogenous marker for oxidative stress, antigenic overload and recreational drug
use in the West.
Testing HIV positive merely indicates a cluster of people who had indulged in
identical behaviour: it is important to remember that originally clusters of
cases of beriberi, pellagra and scurvy were also assumed to be caused by a
transmissible infection: all this was subsequently shown to be totally wrong.
Beriberi, pellagra and scurvy were not caused by a transmissible agent but were
all caused by a shared vitamin deficiency. Similarly: ‘AIDS’ is not caused
by a transmissible agent (‘HIV’) but by exposure to multiple pathogenic
insults caused by life style in the West and by well known endemic conditions
relating to Third World countries.
To date: Cell-free HIV has never been found or recovered in fresh samples of
semen or blood. The key fact to remember is that cell-free infectious HIV viral
particles have never, repeat never, been recovered from fresh donor semen and
blood. It is homophobic nonsense to say 'HIV' is sexually transmitted via anal
sex as well as scientifically totally unproven. HIV is not an STD.
Hans Gelderblom of Berlin's Robert Koch Institute co-authored the first paper in
Virology, March 1997, showing 'purified HIV' to be 'purified microvesicles'.
What was assumed to be 'purified HIV' was in fact "an excess of
vesicles" - particles of cellular proteins. The hypothetical 'HIV' is in
fact a collection of endogenous microvesicles and cellular proteins (which also
never seem to form particles - so how can they be infectious)? Cell-free viral
'HIV' particles have never ever been visualised in any freshly donated bodily
fluid including semen, blood, etc. 'HIV' has never ever proven to be a sexually
transmitted retrovirus.
As Virologist Dr. Stefan Lanka observed: The rules demonstrating the existence
of HIV (and retroviruses in general) were never adhered to by those who devised
them nor were they ever validated. No particle of HIV has ever been obtained
pure, free of contaminants; nor has a complete piece of 'HIV RNA' (or the
transcribed DNA) ever been proved to exist.
Dr. Stefan Lanka stated:
“I found that when they are speaking about HIV they are not speaking about a
virus. They are speaking about cellular characteristics and activities of cells
under very special conditions...I realized that the whole group of viruses to
which HIV is said to belong, the retroviruses, in fact do not exist at all.” (Zenger's,
December, 1998).
It must be remembered that in 1981, all the original GRID (Gay Related Immune
Deficiency) cases had KS and PCP and were all heavy users of recreational drugs
and the AIDS establishment at the time saw the drug/AIDS hypothesis as a viable
and logical explanation of these early cases. All those with KS were all heavy
abusers of poppers.
In reality in the West GRID is much more of an accurate description of what’s
going on in the West than the vague acronym AIDS. But because gay community
leaders found the term GRID offensive and politically incorrect, it was changed
– largely to take the heat of the gays. Also AIDS was much more of an ‘equal
opportunities disease’ where “everyone was at risk” of acquiring (even if
we know this not to be true today).
The immunological-stressors of the 'gay life style' : oxidative stress,
antigenic overload, recreational drug use, indiscriminate prescribing of broad
spectrum antibiotics, flu jabs, untreated STDs, toxic semen from antiretroviral
and heavy recreational drug abuse are a constellation of conditions we now
nominate as ‘AIDS’ – but in reality is what rightly used to be called
GRID. Today it would appear that the evidence points to something predominantly
toxic rather than infectious being transmitted: an active/top gay man practicing
‘bare back’ sex and taking both recreational and antiviral drugs is
transmitting all this toxic waste: so condoms may help to stop this spread and
other real STDs. We need studies investigating the possibility and probability
of toxic semen causing GRID.
Yet gay men would far rather believe that is HIV that is doing all the damage
and not the toxicity of recreational and antiretroviral drugs: such are the
politics of ‘denial’. HIV Belief is merely a ‘denial’ that ‘AIDS’
(GRID) is caused by the consumer gay life style. It must also be remembered that
all the first ‘AIDS’ cases in the West were gay men with KS and PCP and all
abused poppers.
The over use of antibiotics has played a major contribution to the development
of ‘AIDS’ (GRID) in the West. This indiscriminate prescribing of broad
spectrum antibiotics led to all sorts of problems that could not have been
foreseen. The recent stories of fatalities from clostridium difficile are
explained as resulting from an over use of antibiotics destroying beneficial
bacteria which would normally have kept the clostrdium under control. In the
early days of AIDS (GRID) there were wide spread reports of intractable ‘gay
bowel syndrome’ caused by shigella, giardia lamblia, and amebiasis among many
gut parasites – this was probably due entirely to the same mechanism. Gay
men’s habitual dependence on antibiotics led to GRID and AIDS.
Toxoplasma gondii is a commonly occurring parasite found in cats and therefore
presumably amongst people who keep cats: so why does toxoplasma gondii cause
dementia and death principally in gay men? Over prescription of antibiotics
would seem to be the reason.
All these common gut parasites - shigella, giardia lamblia, toxoplasma gondii,
and amebiasis – would normally have been kept in check by friendly ‘good’
bacteria which were unfortunately killed off by the inappropriate use of the
antibiotics that man gay men prophylactically like sweeties. This is why
GRID/AIDS is largely – if unwittingly – a self inflicted condition amongst
gay men and now can cost hundreds of thousands of pound per patient per year to
treat but they are not treating GRID or AIDS – but HIV – which is merely a
marker – and not a cause of GRID and AIDS.
Remember: HIV has never been truly isolated and HIV has never been proven to
exist yet the BBC News (November 2005) reported that it costs: “hundreds of
thousands of pounds per patient during their life time to treat HIV”. So it is
costing the British tax payer hundreds of thousands of pounds per patient during
their life time to treat a virtual virus that does not exist when the true
complex causes of GRID amongst gay men are being ignored by denial: largely
because it is perceived as ‘judgemental’ to ‘criticise’ the consumer gay
life style as the cause of ‘AIDS’ (GRID): on the contrary: there are even
leaflets offering gay men ‘advise’ on how to take recreational drugs safely
with antiretroviral drugs and ‘AIDS’ chariot’s and HIV specialists still
fail to warn gay men that poppers (amyl nitrite) can contribute to KS and
‘AIDS’ (GRID) because poppers are perceived ‘politically correct’ and
make massive profits for the gay consumer industry.
Whilst HIV is not an infection, HIV Ideology is highly infectious and contagious
and spread through the HIV Testing ritual rites of HIV Indoctrination and HIV
Incarceration.
HIV Belief is psychologically contagious being spread through mass-hypnosis via
the mass-media and also via HIV Education - that is: HIV Indoctrination and HIV
Interpellation. And HIV Interpellation is very seductive and hypnotic acting
like an ‘ideological cement’ (Louis Althusser) and security blanket giving
the diagnosed subject an identity to believe in by be baptised: ‘HIV
positive’ – and ‘coming out as ‘HIV’ positive (that is ‘being
controlled’ and ‘contained’ as an ideological identity): Althusser’s
theory of ‘ideological interpellation’ is aptly activated by the HIV Belief
System which acts as a ‘social cement’ in ‘hailing the subject’ as
‘imagining’ itself to be ‘HIV positive’. Such is the power of Ideology
and ideological belief though HIV belief is really much more to do with
theological belief than ideological belief.
Such ‘social cementing’ and ‘ideological interpellation’ is initiated by
proclaiming: ‘I am HIV’. Thus to tell that person that they are not
‘HIV’ is to shatter that ideology: that illusion, interpellation, and
indoctrination.
The epidemic of group hysteria is specific to certain groups, therefore HIV
cannot be an epidemic of pathogenic origin. The HIV Cult – like Scientology -
is an example of ‘epidemic hysteria’. AIDS (GRID) are also psychologically
contagious.
Caspar Schmidt, in The Group-Fantasy Origins of AIDS, nominates ‘AIDS’ as a
"bio-psycho-social disorder" and proposes that chronic and inescapable
fear can elicit a biochemical reaction in the body, which in time causes "psychogenically-reduced
cell-mediated immunity."
For Schmidt, ‘AIDS’ can be explained through the concept of group fantasy
– people are collectively in a trance: "I would like to present the
evidence available to me in support of the hypothesis: a) that AIDS is a typical
example of epidemic hysteria, b) that the epidemic has at its core an
unconscious group delusion, which can be called the group-fantasy of
scapegoating, c) that the combination of these unconscious group tensions
brought about a subtle and sophisticated, but nevertheless sacrificial witch
hunt, in which the participants were the Moral Majority, d) that these attacks
resulted in an epidemic of depression based mostly on shame; e) that the core
sign of AIDS, the reduction of cell-mediated response, is one of the typical
vegetative signs of severe depression; f) that the epidemic represents, in the
group’s unconscious fantasies, an equivalent war, during which the group keeps
careful count of the sacrifices; g) and finally that, since the epidemic is
psychogenic, the prediction can be made that the group will decide when it
should be over (when they have ‘had enough’), a decision which will be
broadcast to the group members through the media, so that after a suitable lag
period the epidemic will resolve and the incidence will descend from epidemic to
endemic levels."
Author John Lauritsen expands the argument that psychosis and psychosomatic
conditions are induced by the psychological terrorism of ‘HIV/AIDS’
propagandists: "Highly sophisticated psychological techniques are being
used to make gay men perceive themselves as sick, and become sick, in order to
qualify as consumers of AZT. The ‘Living With HIV’ campaign is, quite
literally, a form of voodoo" – or government approved euthanasia. Thus
the group fantasy of ‘HIV/AIDS’ unified a fragmented gay community with the
solidarity of pseudo-disease-identity: ‘I’m HIV’.
How many people have committed suicide from being tested HIV positive and from
HIV Terrorism: HIV bone-pointing death- sentencing? How many HIV Kubler-Ross
Counsellors have sentenced those tested HIV positive to a premature death?
Psycho-social factors have arguably contributed to the unnecessary deaths of
thousands of gay men from testing HIV terrorism.
In 1980 Robert Gallo's HL23V was 'decommissioned', 'declassified', 'unnamed' and
was agreed to be 'non-existent' - it is now time for the terrorising and
sacrificial-signifier HIV to be 'decommissioned', 'declassified', 'unnamed'
because the stigmatised signified thing is non-existent. What will be the
devastating consequences of unnaming HIV?
We can only end HIV Stigmatism and HIV Terrorism by ending this HIV Occultism:
that is HIV Belief and HIV Ideology and wake gay men up from the deep sleep of
HIV Hypnosis and HIV Hysteria.
I realise how difficult it may be for many gay men diagnosed as HIV positive to
give up their HIV Belief and HIV Benefits: indeed: giving up what many now
perceive as the 'luxurious and lucrative' HIV Life Style and not forgetting all
those thousands of HIV Careerists having to give up such prestigious and
profitable posts. But sooner or later the HIV Edifice will crack ands crumble in
ruins. In 2006 it is time to go back to the beginning again when GRID was the
cause. We can only solve GRID by removing HIV from the equation: we need more
GRID research and no more HIV research, which is at a dead end.
In the words of John Lauritsen:
“I still regard ‘AIDS’ as the greatest blunder and the greatest hoax in
medical history… an epidemic of incompetence and an epidemic of lies…It's
time for gay men to wake up, look at ‘AIDS’ rationally, and put an end to
the sacrificial ritual. We didn't deserve this, and we should no longer go along
with it.” (AIDS: A Death Cult, John Lauritsen, 4 January 2004).
The
HIV Lie is both hypnotic and seductive because people prefer to believe in lies
than in truth and in our society lies are lucrative. In 2006 we must all put an
end to the terrorism of the HIV Lie.
This article is dedicated to the memory of genius Yale mathematician Serge Lang
(1927-2005).
"To an extent that undermines classical standards of science, some
purported scientific results concerning 'HIV' and 'AIDS' have been handled by
press releases, by disinformation, by low-quality studies, and by some
suppression of information, manipulating the media and people at large. When the
official scientific press does not report correctly, or obstructs views
dissenting from those of the scientific establishment, it loses credibility and
leaves no alternative but to find information elsewhere."
Serge Lang, Challenges, Springer Verlag 1998.
References and Further reading:
John Lauritsen & Ian Young, The AIDS Cult: Essays on the gay health
crisis,
Asklepios USA 1997, 224 pages, ISBN 0-943742-10-2.
Joan Shenton, Positively False; Exposing the myths around HIV and AIDS', IB
Tauris, London 1998, ISBN 1-86064-333-7.
Peter H. Duesberg, Inventing the AIDS Virus, Regnery USA 1996, ISBN
0-89526-470-6.
Roberto A. Giraldo, AIDS and Stressors, Impresos Begon, 1997:205p, USA. ISBN 958
9458 03 3.
Serge Lang, Challenges, Springer Verlag 1998, 816 pages, ISBN 0-387-94861-9.

December 1st 2005
The
United Kingdom HIV Epidemic That Never Was:
How
The AIDS Establishment Will Extricate Itself From The HIV Scam
By
Alex Russell
"To
an extent that undermines classical standards of science, some purported
scientific results concerning 'HIV' and 'AIDS' have been handled by press
releases, by disinformation, by low-quality studies, and by some suppression of
information, manipulating the media and people at large. When the official
scientific press does not report correctly, or obstructs views dissenting from
those of the scientific establishment, it loses credibility and leaves no
alternative but to find information elsewhere."
Serge
Lang, Challenges, Springer Verlag 1998, 816 pages, ISBN 0-387-94861-9.
Alex Russell is an artist and writer who lives and works in London, England. This article is dedicated to the memory of Serge Lang (1927-2005).
As the HIV hypothesis has failed in all its predictions, the AIDS establishment is now devising strategies to unwind the epidemic that never was. I want to look at two of its tactics: 1) To say HIV is becoming less and less pathogenic; 2) To say diagnosed people are starting to lose their HIV positivity either spontaneously or through changes in lifestyle.
Keith Alcorn, senior editor of the National AIDS Manual (U.K.), for example, recently made a rather revealing, albeit contradictory, statement:
So HIV is becoming “less fit each time” but ”is still a life-threatening infection” — work that one out. Evidently, researchers at Case Western Reserve University in Cleveland, Ohio, and the Institute of Tropical Medicine in Antwerp, Belgium, compared a dozen HIV-1 samples from 1986-89 with a dozen from 2002-03. They found that 75 percent of the newer samples appeared “less fit” than those of 15 years ago, both in terms of spread within individuals and transmission to others. Their results were reported in October in the online journal AIDS.
HIV researcher Miguel E. Quinones-Mateu, PhD, has stated: “The idea that HIV-1 is already evolving to a less virulent virus, after its estimated original introduction into susceptible human populations some 80 years ago, may be easy to understand, but perhaps more difficult to demonstrate.” [3]
One reason it would be “more difficult to demonstrate” is because there was never any evidence that HIV is virulent (pathogenic).
To keep the charade going, the AIDS establishment is moving the goalposts (yet again), now by claiming that HIV is mutating beyond pathogenicity — that HIV is less pathogenic today than when it was “discovered” (invented). Is HIV really losing its pathogenicity? Or has the establishment — having come to the realization that HIV was never pathogenic to start with — beginning to backpedal and dig its escape tunnels?
In the future, to save face, it will attempt to bail out by claiming that ‘HIV’ has become non-pathogenic — just as Eric Artz, lead author of the study comparing HIV-1 samples, predicts [1]:
"This was a very preliminary study, but we did find a pretty striking observation in that the viruses from the 2000s are much weaker than the viruses from the ‘80s…. Maybe in another 50 to 60 years, we might see this virus not causing death."
There was never any evidence that HIV did cause death. It was only for political reasons that Robert Gallo and Luc Montagnier insisted that HIV was causing immune suppression, but without presenting any hard evidence to support their claim other than association. And association does not prove causation.
Artz also raises the question: Is the “decrease” in the AIDS cases after 1996 due to antiretroviral drugs or to a “much weaker” HIV?
University of Portsmouth researcher Ford Hickson has stated, "The majority of people with HIV in Britain are gay or African or both. The majority of people who will have sex with them will be gay or African or both. Unless we focus our efforts on the needs of gay men and Africans in Britain, we have little hope of reducing this national crisis."
Hickson fails to see why it is that gays or Africans have group-specific reasons for testing “HIV-positive:” The gay “lifestyle” and African poverty. They test “HIV positive” — not because of‘ HIV (which has never been truly isolated), but because of gay behavioural and African environmental risk factors.
In the British Medical Journal, [4] Gordon Dougan of Imperial College’s Centre for Molecular Microbiology and Infection, wrote:
"The trends underlying the rapid and substantial increases in HIV diagnoses among heterosexual people in the United Kingdom are complex and sometime misunderstood. Although the number of people becoming infected with HIV through heterosexual intercourse in the United Kingdom is rising steadily, most of the overall rise in HIV diagnoses among heterosexuals is among people who originate from and were infected abroad, mainly in Africa."
On critical examination of Dougan et al you will see — yet again — that the vast majority of supposed heterosexual cases of HIV in the U.K. originate mainly from Africa, where conditions such as TB and malaria are well documented to give an HIV-positive test result. Thus Dougan et al's findings inadvertently support the thesis that HIV cannot possibly be "acquired through heterosexual intercourse" in the U.K., because we have had huge rises in STI/STD rates but no equivalent HIV rises.
HIV figures (data source: SOPHID:2003) in the U.K. point to some unexplained anomalies concerning the disproportionate spread of “HIV.” Again, if HIV is a STD, why is it still restricted rigorously to the original “high-risk” groups like homosexuals?
The vast majority of homosexual HIV cases in the U.K. are white (13,440 out of a total of 15,454), whereas the vast majority of heterosexual HIV cases in the U.K. are black (11,068 out of a total of 15,998). The media have recently presented the misleading claim that the U.K. is in the grip of an heterosexual HIV epidemic, but what they did not mention is that more than 75 percent of the heterosexual HIV cases were imported from abroad, particularly from sub-Saharan Africa, the Caribbean, India, Asia, etc.
HIV has never been proven to spread from person to person — that has only ever been an assumption; an unproven supposition purely based on non-specific and non-standardized HIV tests. Andy Davies, a reporter on BBC-TV’s current affairs show Panorama, [5] has related that the number of sexually active people under 25 infected with chlamydia is now thought to number just under half a million. The BBC reported that between 1995 and 2004, chlamydia rates more than trebled from 32,288 annual diagnoses to 103,932; gonorrhoea rates rose from 10,580 to 22,320; and syphilis from 141 diagnoses to 2,252 (an increase of 1,497 percent).
So if HIV is an STI, where are the rises in endemic HIV heterosexual cases in the U.K.? If it really were an STI, there would be hundreds of thousands of heterosexual HIV cases in the U.K. Remember the U.K. has had a huge explosion in teenage heterosexuals STD rates, but no HIV epidemic amongst this group. Why not?
Davies has further reported that around 500 people in Britain each year die of an “HIV-related condition.” But what are these “conditions” other than markers for endogenous HIV expression — or, rather, HIV is a marker for certain conditions — and not a cause of or contributor to them. How many white teenage and adult heterosexuals have Kaposi’s Sarcoma (KS) and Pneumocystis Carinii Pneumonia (PCP), the two original AIDS-defining conditions? KS and PCP are still solely restricted to homosexuals in the West. Why? If HIV is an STI and causes AIDS, there should be hundreds of thousands of white heterosexuals in the West with KS and PCP.
What Davies omits to tell us is how many people die of those same so-called “HIV-related conditions,” who are not “HIV-positive.” What we are not told is how many people have those alleged HIV-related conditions because these diseases are non-notifiable. These so-called “HIV-related conditions” have always existed, despite HIV, not because of it.
On Oct. 25, the BBC News’ U.K. edition, in a report titled “Are Aids orphans overlooked?” repeated the United Nations charity UNICEF’s claim that in Africa, “Every minute, a child is infected with HIV.” What are they actually saying? Is an “infected” baby being born every minute? Or are they claiming that a child is being newly “infected” every minute by some unknown mechanism? Are they all being HIV tested? Do they have active-productive “infections”? If so, what titre of HIV do they carry?
As a Sept. 10 story in The Guardian noted [2], “Incredibly, there are probably only 184 white, British, heterosexual men and women who have contracted HIV in the U.K. through having sex with someone from the same demographic group in the last 20 years.”
The hallmark of a sound scientific hypothesis is that predictions based on it will be fulfilled. None of the alarmist and apocalyptic predictions based on the HIV/AIDS hypothesis has ever been fulfilled and never can be because the hypothesis is wrong.
In April 1993, The Lancet published a letter from Gordon Stewart, professor emeritus of public health at Glasgow University and a former World Health Organization adviser on AIDS, which pointed out that previous AIDS projections for 1992 were up to 10 times higher than the actual figure, largely because of false assumptions about heterosexual spread:
"I have been trying to put this across for nearly four years. I have tried numerous journals. The response has either been rejection, or silence…. Nobody wants to look at the facts.… I've sent countless letters to medical journals ... they simply ignore them. The fact is, this whole heterosexual AIDS thing is a hoax."
Stewart [6] went on: "... since 1990, Nature, Science, the New England Journal of Medicine, the British Medical Journal and other mainline, peer-reviewed journals have preferred to reject papers by others, besides my colleagues and myself, containing verifiable data that throws doubt on the claim that AIDS is capable of causing epidemics in general populations of developed countries.… The Lancet has published some short letters, but has consistently refused to publish fuller reasons for dissent.…"
Stewart realized, based on his many years of experience in tracking real infectious diseases, that predictions of future AIDS case numbers in the U.K. should be based on behavioor patterns observed in the key high-risk groups — homosexuals, recreational drug users, etc. — rather than the sole criterion of an alleged “infectious agent,” i.e., HIV, the assumed cause of AIDS. History has proven that Stewart’s insightful predictions and observations basing AIDS on behavior patterns and not on a sole infectious agent have come true. Investigative journalist Neville Hodgkinson [7] confirms this:
“The belief in HIV as a sexually transmitted virus that would in time put heterosexuals at risk as much as gay men was never correct. AIDS has stayed confined to groups of people who have non-HIV risks in their lives, including recreational drugs, severe poverty, multiple infections, and the relatively easy access into the bloodstream of foreign body fluids received through anal sex.”
Scanning a worldwide map of HIV prevalence rates, you will see that high rates directly coincide with areas with growing recreational drug use and/or areas affected by TB, malaria and conditions relating to poverty and malnutrition. The growing drug epidemics of Kazakhstan and Thailand and other Eastern European and Central and East Asian countries directly coincide with their alleged increase in HIV infection rates. It is becoming increasingly clear that HIV in these countries is merely a marker for recreational drug addiction: it has nothing to do with needles — it is the drugs themselves that cause false HIV positivity. Rising drug addiction epidemics are cynically being reclassified as “AIDS” epidemics. Thus, the putative HIV test can just as equally indicate localized drug addiction. Cocaine in vivo has the same mitogenic effect as do laboratory mitogens in awakening previously dormant retroviruses in cell cultures: cocaine use can give a false HIV-positive test result [8]. That both intravenous and oral drug users develop positive HIV-antibody tests was shown as far back as 1988, when Claire Sterk, PhD, reported in The Lancet that a higher percentage of prostitutes who use oral drugs (84 percent), than intravenous (46 percent), test positive.
An earlier study carried out amongst prostitute women in London, Paris and Hamburg showed that only those prostitute women who used recreational drugs tested positive on the putative HIV test. The London prostitutes that were not drug users all tested negative. A similar pattern was observed amongst prostitute women in a study in New York of female crack cocaine addicts.
A proponent of the drug/AIDS hypothesis, Peter Duesberg, the world’s leading retrovirologist, argues [9] “that the long-term consumption of recreational drugs (such as cocaine, heroin, nitrite inhalants, and amphetamines) and prescriptions of DNA chain-terminating and other anti-HIV drugs, cause all AIDS diseases in America and Europe that exceed their long-established, national backgrounds, i.e. >95 percent. Chemically distinct drugs cause distinct AIDS-defining diseases: for example, nitrite inhalants cause Kaposi's sarcoma, cocaine causes weight loss, and AZT causes immunodeficiency, lymphoma, muscle atrophy and dementia. The drug hypothesis predicts that AIDS: (1) is non-contagious; (2) is non-random, because 85 percent of AIDS causing drugs are used by males, particularly sexually active homosexuals between 25 and 49 years of age; and (3) would follow the drug epidemics chronologically.”
It must be remembered that in 1981, all the original GRID (Gay Related Immune Deficiency) cases were heavy users of recreational drugs and the AIDS establishment at the time saw the drug/AIDS hypothesis as a viable and logical explanation of these early cases. GRID is much more of an accurate description than the vague acronym AIDS. But because gay community leaders found the term GRID offensive, it was changed. Also AIDS was much more of an equal opportunities syndrome where “everyone was at risk” of acquiring (even if we know this not to be true today).
Recreational drugs are known to cause endogenous HIV expression. A recent scare story from New York alleging a new “super strain” of HIV was (mis) “diagnosed” from a man in his mid-40s who took crystal methamphetamine. Crystal methamphetamine is oxidative; it depletes glutathione and induces apoptosis/cell death, and depletes CD4s and cultures and activates endogenous HIV expression.
Crystal methamphetamine, an addictive stimulant, itself depletes the immune system (not HIV). Regarding this spurious “super strain” of HIV, a cynical Robert Gallo noted, "The odds are enormous that it is not going to go anywhere."
The final twist in the HIV tale is the disappearing virus act [10]: The News Of The World recently reported that Andrew Stimpson of Largs, Ayrshire, who allegedly “caught the virus” from his HIV-positive boyfriend Juan is now HIV-free. Stimpson recalled, "The doctor had said I could live for 10 years, 20 years, maybe 40 years. I had just turned 22 but after the diagnosis, my energy for life was completely lost.… I remember after the repeat tests, my doctor came into the room saying, ‘You've cured yourself! This is unbelievable, You're fantastic!'… I was baffled; I couldn't understand how anyone could cure themselves of HIV… I didn't understand how I could be negative after one year, especially because I had been having unprotected sex with my partner after the diagnosis, believing we had nothing to lose."
The News of the World went on: “Doctors were astonished at his continuing excellent health, unusual for an HIV sufferer. So in October 2003, he was offered a repeat HIV test — and the result came back negative … He was tested again twice and again the results were negative.”
Lisa Power, head of policy at the Terence Higgins Trust, the leading HIV and AIDS charity in the U.K., says, "If Andrew has been cleared of the virus, that needs to be investigated thoroughly to see if it can be reproduced in any way. This could be of major interest to HIV researchers. We need to find out precisely what's happened with this person."
There was no “virus” there in the first place. How do we really know that Andrew Stimpson was HIV positive to begin with? Were viable, active, infectious HIV particles isolated and recovered directly from his blood or semen? Cell-free HIV has never been found or recovered in fresh samples of semen or blood. HIV has never been truly isolated or proven to exist. Yet the BBC News (November 2005) reported that it costs: “hundreds of thousands of pounds per patient during their life time to treat HIV”. So it is costing the British tax payer hundreds of thousands of pounds per patient during their life time to treat a virtual virus that does not exist: when will this madness end?
So there was no isolated evidence that Stimpson was HIV positive to begin with. No one has ever proven to be HIV positive. All “positives” are false positives. It would be fascinating to find out how many hemophiliacs, diagnosed “HIV” positive in the 1980s, would still test positive today. If they were retested now, how many would prove to be “HIV” negative? I would strongly advise hemophiliacs, who tested HIV positive in the mid-1980s, to be retested now to see if they seroreverted in the meantime. This would also mean that they were false positives to begin with. Another tactic the AIDS establishment will use to end the HIV scam is to say that more and more people are seroreverting and losing their HIV either naturally or by taking vitamins. [11].
Following on from the Stimpson case, the AIDS establishment will soon be announcing that many more are “curing” and “clearing” themselves of HIV: a cynical strategy to end the HIV scam. Yet false HIV-positive rates will continue to rise rapidly in proportion to the huge rise in global recreational drug epidemics, where HIV is an endogenous marker of drug use. Maybe the HIV test will be reclassified as a test for recreational drug use, TB, malaria and malnutrition.
To try and end the epidemic that never was, the AIDS establishment may very well announce to the mass media that HIV has become non-pathogenic and that people will then start losing their HIV positivity. The cruel irony being that no one was ever HIV positive to begin with.
References:
1. Aids virus 'could be weakening.’ BBC News. Sept. 29, 2005.
2. Where it's really hurting. Cathy Scott-Clark and Adrian Levy. The Guardian, Sept. 10, 2005.
3. Miguel E. Quinones-Mateu. Is HIV-1 evolving to a less virulent (pathogenic) virus? AIDS 2005, 19 1689–1690.
4. Dougan et al. HIV infections acquired through heterosexual intercourse in the United Kingdom: findings from national surveillance. BMJ, March 11, 2005)
5. Andy Davies, reporter. Love Hurts. BBC 2 Panorama, London, Oct. 16, 2005.
6. Gordon Stewart. A paradigm under pressure. Index on Censorship, Vol.28, No.3, May/June 1999
7. Neville Hodgkinson. Molecular Miscarriage: Is the HIV Theory a Tragic Mistake? Mothering Magazine, Issue 108, September/October 2001.
8. Sterk C. (1988) Cocaine and HIV seropositivity. The Lancet i:1052-1053.
9. Peter Duesberg and David Rasnick. The AIDS Dilemma: drug diseases blamed on a passenger virus. Genetica 104: 85-132. 1998.
10. I'm First In World To Be Cured Of HIV. Gemma Calvert. The News of the World. Nov. 13, 2005.
11. Hugh Muir, James Meikle. Mysterious case of the man who claims to have beaten HIV by taking vitamins. The Guardian, Monday, Nov. 14, 2005.
Gay.com
UK & Ireland
1st December 2005
| World AIDS Day: Letter to The Guardian | ||||
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| An Open Letter to Clint Walters | ||||
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Gay.com
UK & Ireland
20 November 2005
| Re: HIV+ man becomes HIV- with no drugs |
| Author: Alex Russell | Today at 12:44pm |
| How
do we really know that Andrew Stimpson was 'HIV' positive to begin with?
Were viable, active, infectious 'HIV' particles isolated and recovered
directly from his blood or semen? Cell-free 'HIV' has never been found in
fresh samples of semen or blood. So Stimpson was never 'HIV' positive to begin with: no one has ever proven to be HIV positive: all 'positives' are false positives. It would be fascinating to think how many haemophiliacs diagnosed 'HIV' positive in the 1980s were retested now: how many would prove to be 'HIV' negative? I would strongly advise haemophiliacs who tested 'HIV' positive in the mid 1980s to be retested now to see if they seroreverted in the meantime. This would also mean that they were false positives to begin with. A tactic that they will use to end the 'HIV' Scam is to say that more and more people are seroreverting and 'losing their HIV' either naturally or by taking vitamins. Will the THT, NAM and the UK Coalition of People Living with HIV and AIDS or Positive Nation now start promoting cheap unprofitable vitamins instead of expensive and profitable 'anti-retrovirals'? What will happen to the 'HIV' Pharmaceuiticals profits if vitamins prove to be the answer? Yet Stimpson is not an isolated case as all the media misinforms us: there are documented cases of many infants and adults seroreverting to 'HIV' negative in both the West and in Africa. Yet there was no ‘HIV’ there in the first place. Soon the mass media will be announcing that many more are 'curing themselves' of ‘their HIV’ - yet another strategy to end the ‘HIV’ Scam. The other strategy that they are now playing out to end the 'HIV' Scam is to say that 'HIV' is becoming less and less pathogenic and is evolving into a state of non-pathogenicity. Miguel E. Quinones-Mateu stated: “The idea that HIV-1 is already evolving to a less virulent virus after its estimated original introduction into susceptible human populations some 80 years ago may be easy to understand but perhaps more difficult to demonstrate.” (Is HIV-1 evolving to a less virulent (pathogenic) virus? Miguel E. Quinones-Mateu, Editorial Comment, AIDS 2005, 19 1689–1690). The reason it would be “more difficult to demonstrate” is because there was never any evidence that 'HIV' was ever virulent (pathogenic) to begin with: 'HIV' was always non-pathogenic. To keep the charade going they are moving the goal posts (yet again) by now claiming that 'HIV' is mutating beyond pathogenicity, that 'HIV' is now less pathogenic today than when 'HIV' was ‘discovered’ (invented). Is 'HIV' really losing its pathogenicity – or have they come to the realisation that HIV was never pathogenic to start with and are now beginning to back peddle and dig their escape tunnels? The THT, NAM, UK Coalition and the BBC will eventually announce that 'HIV' is non-pathogenic and that the diagnosed will all start losing ‘their HIV’ with the help of vitamins. PS: They are claiming the PIs may have an immunomodulatory effect and act in the absence of an antiviral effect. This raises the questions: (a) “These effects [T4 increase] may be seen before significant changes in the plasma RNA levels or in the absence of antiviral effect” . The entire purpose of giving PIs is to decrease the viral load. So why give them? (b) Why give PIs which are very toxic and not give other less toxic, immunomodulatory agents such as antioxidants? PIs are apparently relieving oxidative stress: if the patients are surviving by taking PIs it is because it is the oxidative stress which is the true cause of ‘AIDS’ which is being alleviated. But PIs have also been implicated to cause cardiovascular complications. Previous studies demonstrated that the PI ritonavir (RTV) caused endothelial dysfunction in porcine arteries. |
|

THE AIDS DEBATE
Letters to Red Flags
On: “Occam’s razor, Tolstoy’s blender” by Stephen Strauss
Friday, September 09, 2005
REPLY TO STEPHEN STRAUSS
In his polemical piece, “Occam's razor, Tolstoy's blender and the Tragedy of Hemophiliac AIDS,” Stephen Strauss writes, “Something that is almost never mentioned, that absolutely convinces me personally HIV is the cause of AIDS … hemophiliacs.” The statement is rather revealing.
Strauss does not ask himself why it is that the HIV/hemophiliac hypothesis is “almost never mentioned.” The reason is that Robert Gallo, Luc Montagnier, Anthony Fauci and David Ho are too embarrassed today to discuss it because they got the facts wrong. Subsequent research has shown that all the original assumptions about HIV contaminating the clotting factor were totally mistaken.
The case of hemophiliacs, far from proving the existence of a transmissible retrovirus (HIV) alleged to have contaminated their clotting factor, proves conclusively, in fact, quite the reverse: HIV is not — and cannot be — the cause of AIDS.
Why did hemophiliacs start to die in appreciable numbers only after HIV was “discovered” in 1983? Surely if this alleged retrovirus was the cause of AIDS‚ we would have noticed their premature deaths before 1983. And why didn't hemophiliacs die from KS (Kaposi’s sarcoma) and PCP (pneumocystis carinii pneumonia), the two original “AIDS” defining diseases?
Gallo tried to make the case that AIDS was caused by a transmissible agent and cited cases of hemophiliacs whom it was assumed were infected via the clotting factor VIII. This assumption was based on two premises that subsequently proved to be totally false: a) the amount of putative virus in a plasma donor/seller’s blood and b) that the virus would survive the manufacture of factor VIII from the pooled plasma.
Uncritical scientists and medics accepted this supposition. It soon became apparent, however, that the supposition was wrong. First, it was assumed that plasma donors/sellers were infected with HIV‚ and carrying titres of cell-free infectious virus particles that resulted in the contamination of the pooled plasma used in the manufacturer of factor VIII. Sometimes, these pools were as large as 30,000 donations of 600 millilitres (ml) of plasma. It was suggested that there was sufficient cell-free “HIV” in some of the donors to contaminate the whole batch. This supposed massive titres of millions, if not billions, of viral particles in the infected donors. This was subsequently proved to be wrong. In the nearly 200,000 published scientific papers on HIV/AIDS, not one claims to have found a titre of more than 10 infectious particles per cubic ml of blood/plasma. There is no way that these negligible amounts of HIV, even if proven to exist, could have contaminated so much factor VIII that virtually all the hemophiliacs could be deemed infected with HIV. As Peter Duesberg rightly pointed out, the average amount of virus‚ claimed to be present in the plasma or blood of an HIV-infected individual, stands at between 1 and 1.7 infectious viral particles per cubic ml, which is absolutely negligible.
Thus, paucity of virus rules out the suggestions that HIV was transmitted to so many hemophiliacs in a comparatively short space of time.
Studies subsequent to 1985 showed that HIV cannot survive long outside the host’s body. This is confirmed by studies showing that spilled HIV‚ positive blood samples or spoiled laboratory cultures resulted in the quick death of the alleged “virus.” It was further discovered, and admitted by the Centers for Disease Control and Prevention (CDC), that dried HIV does not survive. Therefore, factor VIII that is subjected to cryoprecipitation (freeze drying) could not possibly contain viable, cell-free, infectious HIV, even if there had been any putative “virus” in the mix to begin with, which is extremely unlikely for reasons described above.
It was the 99 percent impurities in factor VIII that caused the immune suppression (AIDS). Hence, the early discovery that seroconvertion in hemophiliacs seems to depend on the amount and duration of consumption. They were dependent on a product that will eventually kill them. It is age- and dose-related. Also, as Duesberg wittingly observed, “Even hemophiliacs are not immortal.”
The introduction of AZT — administered in enormous doses — rapidly killed many hemophiliacs. Their premature deaths exactly coincided with the fast tracking of AZT.
Hemophiliac mortality increased only after the introduction of AZT in 1985. Since about half of Darby's 2,037 severe hemophiliacs were already HIV-positive by this time, surely HIV-caused mortality should have exerted a detectable influence prior to 1985 in this group. Only Duesberg's theory can explain why the explosion of hemophiliac mortality should occur only on the heels of HIV testing: The cytotoxic pharmaceutical drugs and psychological terror that invariably accompany a positive HIV test caused the increased mortality.
In January 1994, the CDC communicated the following experimental data and conclusion: "In order to obtain data on the survival of HIV [in factor V111 clotting factor], laboratory studies have required the use of artificially high concentrations of laboratory grown virus ... the amount of virus studied is not found in human specimens or any place else in nature ... it does not spread or maintain infectiousness outside its host. Although these unnatural concentrations of HIV can be kept alive under precisely controlled and limited laboratory conditions, CDC studies have shown that drying of even these high concentrations of HIV reduces the number of infectious viruses by 90 to 99 percent within several hours. Since the HIV concentrations used in laboratory studies are much higher than those actually found in blood or other body specimens, drying of HIV-infected human blood or other body fluids reduces the theoretical risk of environmental transmission to that which has been observed — essentially zero." (My emphasis.)
Ironically, the very original suggestion that hemophiliacs were proof of the HIV/AIDS hypothesis can now be used to deconstruct this redundant and failed paradigm. There is absolutely no way that HIV could have been transmitted via commercial clotting factors.
I would like to draw Stephen Strauss’ attention to science journalist Christine Johnson’s critical observations: “No one has actually seen HIV in blood plasma. Its presence is inferred from the results of indirect and nonspecific techniques applied to virus cultures. AIDS expert Jay Levy of the University of California was able to find what he believed were HIV particles in the plasma of only 30 percent of the AIDS patients he studied, and then, it was at a low concentration — 10 infectious particles per millilitre. Levy concedes that this isn't enough to establish an infection.
It is widely accepted that the surface of HIV must be studded with knobs containing the protein gp120, which is crucial to the virus's ability to infect cells. But experts such as Hans Gelderblom of the Koch Institute in Berlin, who has conducted most of the electron micrography studies of HIV, say that the virus loses its knobs when it buds from the cell. This means that cell-free virus is incapable of infecting other cells. Since plasma does not contain cells, if HIV were present, it would not be inside a cell and thus it would not be capable of causing an infection.
In addition, there is the dilution factor. Factor concentrate is made from the blood of thousands of donors pooled together. Statistically, only one or two of these donors might be infected, so by the time their blood is merged with that of uninfected donors, only a few copies of HIV, or even none whatsoever, would be present per millilitre. (See “Bad Blood or Bad Science: Are hemophiliacs with AIDS diagnoses really infected with HIV?” by Christine Johnson in Continuum magazine, Volume 5, No. 4.)
It is no wonder the HIV/hemophiliac myth-making machine is never mentioned and, to quote Stephen Strauss, “So forgotten indeed.”
I would like to conclude with some critical comments made by biophysicist Eleni Papadopulos-Eleopulos and colleagues:
* Even the CDC accepts that a positive test in hemophiliacs is not proof of HIV infection. "It is possible that antibody to LAV [=HIV] is acquired passively from immunoglobulins found in factor VIII concentrates.... Likewise, it is possible that seropositivity is caused not by infectious virus but by immunization with non-infectious LAV or LAV proteins derived from virus disrupted during the processing of plasma into factor VIII concentrate." (Evatt, 1985.)
* Levy and his colleagues have shown that the titre of HIV in plasma of HIV-infected individuals three, six or twelve hours after phlebotomy [blood donation] "dropped from up to 500 TCID/ml to 0." [TCID = tissue culture infectious dose.]
Since in most instances, if not all, the time between phlebotomy and conversion of pooled plasma to factor VIII concentrate is considerably greater than three hours, factor VIII is made from plasma which is cell free and, since the late 1970s, factor VIII has been supplied as a dry powder, which may spend weeks or months awaiting use, how can one reconcile the above facts with the view that hemophiliacs are infected with HIV via contaminated factor VIII concentrates? (Papadopulos, 1995b.)
Alexander Russell,
MA
London, England
Positive Voices UKC
Alternative viewpoints on HIV/AIDS
Saint Bob Geldof is a naive HIV Pharmaceutical Pimp for G8
| Posted on Monday, 27 June, 2005 - 10:54 am: |
Positive Voices UKC
Alternative viewpoints on HIV/AIDS
Saint Bob Geldof is a naive HIV Pharmaceutical Pimp for G8
Reply to John Walker
| Posted on Sunday, 3 July, 2005 - 1:18 am: |
No: the original 'Flat Earthers' were
the vast majority - not the dissenting minority - who actually argued that the
world was round. It is the naive and gullible 'HIV' believers who are today's
Flat Earthers.
Why does an allegedly horizontally transmitted virus, 'HIV', remain almost
exclusively in one group of people - homosexual men - for 20 years in the West?
Why is it more difficult for heterosexuals to be 'infected' with 'HIV' than
homosexuals? This is completely illogical. In the West, homosexual men have been
terrorised into wearing condoms and yet they still get 'AIDS' because they're
doing all the recreational drugs.
Conversely, heterosexuals in the West clearly are not using condoms – as is
proved by the massive rise in STDs and unwanted pregnancies – and yet they do
not get 'AIDS'. Young straight teenagers in the UK are practicing 'unsafe' sex
yet are not becoming 'HIV' positive - why not? (Sky News: 24th March. 2005).
Teenage STD rates are rising in the UK and USA but there is no endemic 'HIV'
epidemic in this group. Why not? There is no evidence that 'HIV' is an STD.
Homosexuals are testing 'HIV' positive because of a multiplicity of other
conditions including recreational drug use. What we have wrongly been nominating
as 'HIV' is merely an endogenous marker for cellular disturbance/irregularities.
Why has there never been an endemic heterosexual 'HIV' (or 'AIDS') epidemic in
the UK? It is obviously not because they are all using condoms. Hundreds of
thousands of straights don't practice 'safe sex' in the UK so why don't they get
'HIV' or 'AIDS'? How would Saint Bob Geldof, Sir Elton John, Nick Partridge or
Bernard Forbes answer that one? (They import 'AIDS' from Africa and pretend that
we have an endemic heterosexual 'HIV/AIDS' epidemic in the UK!)
It could be argued that homosexuals use condoms far more than heterosexuals –
yet homosexuals still get 'AIDS' in the West whilst heterosexuals in the West
are not getting 'AIDS'. Therefore the 'AIDS/Gay-Drug Lifestyle' hypothesis makes
more sense logically even though politically incorrect. Homosexuals need to
practice 'safe drug' use: condoms alone will not stop 'AIDS' even if they may
help to prevent the spread of real STDs. (Remember: in 1981 around 24 young
homosexuals in the USA were diagnosed as having GRID (aka: 'AIDS') with Kaposi's
sarcoma (KS) and all of them were heavy poppers users. Today homosexuals are not
warned about the lethal dangers of poppers because of political correctness and
the damage that may be done to healthy poppers profits. Meanwhile we are gassing
gay men.
Some of you may be older enough to remember when 'AIDS' was originally known as
GRID: Gay-Related Immuno-Deficiency in the early 1980s before they invented
'HIV' and turned 'AIDS' into an 'equal opportunities disease' that 'affects us
all': but today we know that was yet another Government Big Lie: clearly not
'everyone is at risk' from 'AIDS' today - contrary to John Hurt's 'AIDS'
tombstone dooms day prophecy advert transmitted in 1986.
Saint Bob Geldof is not 'raising awareness' but promoting ignorance, further
deaths and playing right into the hands of Bush, Blair and the Multinational
Pharmaceuticals. Saint Bob Geldof is a actually propagating Capitalist
Colonialism and suffering from Acquired Intellectual Deficiency Syndrome. None
of the predictions based on the 'HIV/AIDS' hypothesis has ever been fulfilled
and never can be because the hypothesis is wrong.
I advise you all to read the following by Dr. Roberto Giraldo:
AIDS is Neither an Infectious Disease nor is Sexually Transmitted, by Roberto
Giraldo, MD, Continuum Spring 1998:
The error over the etiology of AIDS was committed in part due to microbiologic
prejudice in the mind of researchers, health professionals, journalists, and the
public at large. This prejudice comes from the exaggeration of the germ theory
of disease promulgated by Pasteur and Koch, which brought many benefits to the
medical field at the time. Unfortunately, today they continue to think as at the
end of the last century - that all is infectious, that all is contagious, and
that it should be a microbe that causes every-thing. The world was prepared by a
century of panic over microbes to mistake the etiology of AIDS. It was not
possible to avoid it.
Another contribution to the error about the cause of AIDS is the failure in
research methodology to fulfil epidemiological requirements. None of the
postulates on which the infectious hypothesis of AIDS is based fulfil the
requirements of the research method. None of the bases of the HIV-AIDS
hypothesis has been demonstrated at an objective level. They are theoretical
assumptions, created by the minds of those who generate and defend that
hypothesis. Practically the entire world has become accustomed to believe all
that we are told by the so-called men of science. Currently, the critical and
questioning capabilities of 'the people' are null. They do not ask for the
necessary proofs for the affirmations that can look objective. The worst
epidemic that the contemporary world suffers is an epidemic of crises in the
scientific method. It is more extensive than the AIDS epidemic. There will be
more consequences unless we take a pathway paved with an authentic objective
research methodology.
The scientific community has been wrong many times in this century, by
considering as infectious diseases that are not - pellagra, scurvy and beriberi.
The error currently made with AIDS has a larger magnitude due to the
catastrophic repercussions on thousands of people that suffer from this toxic
syndrome. Guilt for the error made with AIDS falls on a few researchers and
health institutions of the United States government. The majority of people in
the world simply believed the so-called men of science. Analysis, understanding
and solution of the error will force inter-national medical authorities to
rethink their tactics and strategies in the health care of people. This will
lead to questions, investigations and solutions to the unfair forms by which men
socially relate amongst themselves in modern society, which in the end are the
reason for the existence of AIDS. Let us go back to Hippocratic medicine. Let us
divulge and stimulate the discussion about the cause of AIDS.
Letter to Tony Delamothe, BMJ Web Editor
20th June 2005
Dear
Tony,
Thank
you for your frankness: your manic and hysterical response unwittingly reveals
that you yourself know that what you are propounding regarding 'HIV/AIDS' is
utter rubbish and that you will eventually be exposed. Like the Editors of Nature,
Science, The Lancet et al you must fear and dread being debunked and
castigated over your uncritical and slavish endorsement and propagation of the
'HIV' fraud.
I
find your attitude cowardice, immature, irrational, totally unprofessional and
anti-scientific. You obviously cannot think critically or autonomously for
yourself on the 'HIV/AIDS' debate but merely mimic the idiotic 'HIV'
inanities. You obviously never properly peer review papers relating to
'HIV/AIDS' at BMJ.
My
rapid response to Nyasha Chin'ombe was justified and warranted and attempted
to answer some of the anomalies surrounding his questions regarding 'HIV'
vaccines: what is the point of you publishing his rapid response if you do not
want it contested, challenged, answered? How can you have a one sided debate?
All you will end up doing is publishing ‘HIV’ related-monologues preaching
to the converted and protecting the ‘HIV’ industry. How does pernicious
censorship advance medical science?
You
are still accountable to the scientific community for presenting balanced and
unbiased opinions, papers and letters regarding ‘HIV/AIDS’. I accuse you
Tony Delamothe of scientific and editorial irresponsibility.
Consensus
science is bad science: it is only those who have thought beyond, around or
above the prevailing paradigm who have ever truly advanced the course of
science and medicine. Those who believe that something is true because
‘everybody says so’ would do well to remember the wrong opinions
concerning scurvy, pelllagra, beriberi, and smon – and blush for shame.
“A
theory is a good theory if it satisfies two requirements: It must accurately
describe a large class of observations on the basis of a model that contains
only a few arbitrary elements, and it must make definite predictions about the
results of future observations.”
Stephen Hawking
None of the predictions based on the ‘HIV/AIDS’ hypothesis has ever been fulfilled and never can be because the hypothesis is wrong. It has come to something when people who wish to pursue reasoned scientific debate must be relegated to your Trash bin.
I
take it as a great complement to be terminated in your Trash bin. I leave you
to your conscience which must be as shabby and shaky as your grasp of 'HIV'
science. You can only stifle the truth for so long and then God help. You come
across as a very frightened man.
bmj.com
| |||
| Alexander
H Russell, Writer/artist/philosophera WC1N 1PE Send response
to journal: | PhD student Nyasha
Chin'ombe (South Africa) inadvertently reveals why there will never be
an 'AIDS' (aka: 'HIV') vaccine: deconstruction is at work within his
text and he actually argues against the possibility of an 'HIV' vaccine:
"HIV vaccinology is still one of those areas of medical research where even angels fear to tread and we enter at own perils. More than two decades down the line, we are all still groping in the dark. Our early dark ages emphasized on the development of vaccines that could produce neutralizing antibodies." If you are identified as 'HIV antibody positive' you have nothing to worry about because you are already vaccinated. How would an artificially produced vaccine be any improvement on naturally generated antibodies? If you are already producing 'HIV' antibodies, as 'AIDS' analyst Peter Duesberg explains, you are already vaccinated: "the show is over for the virus." It is precisely because these antibodies are neutralising that little or no virus has ever been found in a fresh sample of any human bodily fluid from an 'HIV' positive person. That antibodies in effect restrict the 'HIV' to complete latency - which is what they are meant to do. No two identical genomes of 'HIV' have ever been found - not even in the same patient - so how can one have a universally relevant 'HIV' vaccine? There will never be a vaccination against 'HIV': your own body will provide that (because it is an endogenous epiphenomenon). There will never be a vaccination against 'AIDS': How do you vaccinate against poverty, malnutrition, collapse of the medical infrastructure, diarrhoea, poor sanitation and dirty drinking water: all contributory factors to immune-suppression and 'AIDS' in Africa. I would like to ask Nyasha Chin'ombe how would such a putative 'HIV' vaccine be tested ethically? A vaccine can only be tested, and its efficacy judged, by directly challenging its ability to counteract the pathogen concerned. The only way to do this would be to advise the volunteer vaccinees to indulge in what is considered to be 'high risk' behaviour: unprotected sex with multiple partners and massive consumption of recreational drugs (including poppers). Or alternatively, let the vaccine volunteers live in dire poverty in areas where TB and malaria are endemic. To date: no one has ever answered these issues at BMJ rapid responses. In the more than unlikely event of a successful 'HIV' vaccine being devised, the implications are alarming for a country's blood supply. If there is nothing to distinguish vaccine-generated antibodies from an acquired infection, and antibody-positive blood is screened out of the blood supply, this suggests that countries with wide scale vaccination, i.e. in the Third World, will have large shortfalls in blood supplies for transfusion. Will vaccinees be told not to donate blood, setting up a form of 'positive' discrimination? How long would the observation period need to be to verify that the vaccine does in fact protect? Would the vaccine trial need run the alleged 10 to 15 year 'incubation period' to verify the non-appearance of symptoms? How would one know that the vaccine is protecting the individual until this period has elapsed and the volunteer remains symptom free? Would people from 'low risk' groups (drug-free middleclass white heterosexuals) be encouraged to volunteer for the vaccine? What would the point be? Please could Nyasha Chin'ombe address and answer these urgent and unanswered questions? Censorship of Critical 'AIDS' Analysis at BMJ rapid responses will not banish the problem. As the 'AIDS' Act Up activist slogan states: 'Silence equals Death'. Competing interests: None declared |
||
bmj.com
censored: unpublished
Right of Replay to Bennett: Censorship of Critical 'AIDS' Analysis at BMJ rapid responses? 16 June 2005 Alexander H Russell,
Writer/artist/philosopher
WC1N 1PESend response to journal:
Re: Right of Replay to Bennett: Censorship of Critical 'AIDS' Analysis at BMJ rapid responses?
"Truth always rests with the minority, and the minority is always stronger than the majority, because the minority is generally formed by those who really have an opinion, while the strength of the majority is illusory, formed by the gangs who have no opinion." Soren Kierkegaard, The Diary of Soren K. pt.5 sect.3, no 128 (1850).
Nicholas Bennett stated in his customary patronising and condescending manner:
"My point is that the use of the BMJ forums as an outlet for alterative views is simply unnecessary, except to add a fake veneer of respectability to peoples' opinions. If the Perth Group and others want to debate in public they are welcome to post to misc.health.aids where no post is edited, moderated or censored, and in fact many of the contributors to the BMJ forum have done exactly that."
The so called 'alternative' views on 'HIV/AIDS' being voiced by myself and The Perth Group at BMJ rapid responses are in fact 'contesting views' and equally valid. As 'AIDS' analysts we do not use 'alternative' views but contesting critical scientific argument. Thus Bennett sets up a false polarity/opposition between so-called 'alternative' ('dissident') views and the so-called 'establishment' views of 'consensus science'. It can be argued that 'consensus science' is bad science. Science can only develop and grow by contesting and critiquing 'commonsense' assumptions and suppositions. The only true advancements in science and medicine have been made by men and women who thought beyond the prevailing paradigm and general wisdom.
As C.H. Waddington; geneticist so succinctly put it: "The most formidable barrier to the advancement of science is the conventional wisdom of the dominant group."
The BMJ weak argument for halting the 'HIV/AIDS debate at rapid responses is that we repeat the same points 'again and again and again'. There is a very logical reason for why we have had to make the same points 'again and again and again': it is simply because Bennett, Flegg and Floyd et al have consistently refused to answer any of our 'points' and repeatedly obfuscate ad infinitum. Bennett, Flegg and Floyd et al have also made that 'same' points before 'again and again and again' in their rapid responses - but BMJ never ever seem to tire of them repeating - 'again and again and again' - the same old unproven and tired 'HIV' Mantras.
I strongly suspect the real reason - the (not so) hidden agenda for the halting of the 'HIV/AIDS' debate at rapid responses is that pressure had been put upon the Editors of the BMJ by the medical establishment because the 'debate' may 'confuse' and 'upset' the public, to say nothing of damaging the reputations of those who have so uncritically, subserviently and shamefully perpetuated and propagated the 'HIV' charade for so long now.
Most importantly Bennett, Flegg and Floyd et al have never been able to answer the 'haemophilia' and 'HIV' question. The key to the whole 'HIV' thing is the case of the haemophiliacs. We were told originally that they were 'infected' with 'HIV' by their contaminated clotting factor, Factor VIII. However, it is now well known - although not admitted - that 'HIV' could not possibly have survived the freeze drying process used in the manufacture of Factor VIII - but no one has ever admitted this. Meanwhile thousands of haemophiliacs have been paid many thousands of pounds in compensation for something which never happened, and they are still living now - longer than they have ever done before despite the fact that they are allegedly 'infected' with 'HIV'. The case of the haemophiliacs represents the madness and illogicality of the whole 'HIV/AIDS' paradigm. I would like to remind Bennett that he hallmark of a sound hypothesis is that all predictions based upon it will be fulfilled: to date no prediction based upon the 'HIV/AIDS' hypothesis has ever been fulfilled.
Bennett goes on: "The apparent restriction of views on the BMJ forums is actually no such thing - it is simply defining the remit and barriers of the forum…"
In the context of Noam Chomsky's 'propaganda model' analysis Bennett sets the agenda and frames the debate within the closed confines of the 'HIV/AIDS' paradigm: anyone that critiques and deconstructs this 'belief system' is then 'marginalised' and nominated (incorrectly) as 'dissident' or 'alternative' when in fact they are nothing of the kind: they merely offer critical deconstructive analysis of the 'HIV/AIDS' paradigm. Thus we must stop using the misleading and marginalising terms such as 'alternative' and 'dissident' and start using the terms 'analysis' and 'deconstruction'.
Bennett uses what Chomsky terms as 'filters' (an essential ingredient of Chomsky's propaganda model) by simplifying and editing out the anomalies, contradictions and flaws inherent in the 'HIV/AIDS' hypothesis and using popular media sound bites such as 'HIV causes AIDS' or 'HIV infection' – but never being able to cite critical scientific proof regarding these simple minded statements which are merely media manufactured mythical folklore.
At BMJ rapid responses Bennett serves as a subservient propagandist of 'HIV' Ideology for 'manufacturing consent' of the 'HIV' Hegemonic Order. The scientific journals and global media serve the interests of the 'HIV' Industry as Noam Chomsky put it: "They set the general framework. They determine, they select, they shape, they control, they restrict in order to serve the interests of dominant, elite groups in the society." The dominant groups (Nature, Science, BMJ and The Lancet) perpetuate and propagate the 'HIV/AIDS' paradigm and set the agenda and frame the debate within the closed confines of the 'HIV/AIDS' hypothesis and it is Bennett, Flegg and Floyd et that reproduce and sell this dominant 'HIV' Ideology.
In concluding I would like to point Bennett, BMJ and rapid responses readers to the following quotes regarding the pernicious censorship of the 'HIV/AIDS' debate and the perversion of the peer review system:
"The general public accepts what the media tells them. And the media has blown up the virus as being the cause of AIDS, and the scientific community - parts of it - have blown up the virus as the cause of AIDS because it is more convenient to have a neat explanation than to be in that situation in which we often are in science at which the problems, the questions, still face us, and our knowledge proceeds gradually to overcome those difficulties." Dr Walter Gilbert, Nobel Laureate, Chemistry, 1980.
"To an extent which undermines classical standards of science, the scientific establishment has handled purported scientific results concerning AIDS by press releases rather than by scientific exchanges, thereby manipulating the media at large." Serge Lang, Letter to the Council, National Academy of Sciences, USA.
"The peer review system at present is being abused to obstruct or prevent scientific discussion, by Scientific American-Pour la Science, in addition to the major international magazines such as Nature and Science, and the funding agencies in the United States." Serge Lang: To the cc list for the HIV-Pour la Science file.
"...since 1990, Nature, Science, the New England Journal of Medicine, the British Medical Journal and other mainline, peer-reviewed journals have preferred to reject papers by others besides my colleagues and myself containing verifiable data that throws doubt on the claim that AIDS is capable of causing epidemics in general populations of developed countries...The Lancet has published some short letters but has consistently refused to publish fuller reasons for dissent..." Prof. Gordon Stewart, A paradigm under pressure, Index on Censorship, Vol.28, No.3, May/June 1999.
Finally I would like to draw your attention to the following news article: 'A virus like none other before it' by Roger Bate in Business Day, Opinion & Analysis; Thursday 16th June, 2005 at the following url:
http://www.businessday.co.za/articles/opinion.aspx?ID=BD4A54595
Competing interests: None declared

LETTERS TO RED FLAGS
15th June, 2005
On HIV
The unproven medical hypothesis that 'HIV causes 'AIDS has resulted in the unsafe convictions of Feston Konzani, Mohammed Dica and Paolo Matias for allegedly 'infecting' with 'HIV'.
Feston Konzani, an African asylum seeker, has been jailed for 10 years in 2004 at Teesside Crown Court for allegedly 'infecting' three women with 'HIV'. Konzani was accused of inflicting "grievous bodily harm" on the two women aged 25 and 26 and a young girl of 15.
The Court of Appeal stated that the women never consented to the specific risk of contracting "a potentially fatal disease" alleged to be HIV. Yet the Court of Appeal presented no evidence that 'HIV' is a fatal condition; merely assumed it to be so. The three women claimed that they became "infected" with HIV after having sex between February 2000 and May 2003 with Konzani. How do they know they were "infected" by Konzani? Did these women come from areas in Africa or the Third World where TB, malaria and leprosy are endemic and are well known to cause false positive readings on HIV tests?
In 2003 Mohammed Dica was convicted at Inner London Crown Court of two counts of 'biological' grievous bodily harm allegedly 'infecting' women with 'HIV' and sentenced to 8 years in prison.
How do we really know that Konzani and Dica are 'HIV' positive and really 'infected' these women? Were viable, active, infectious 'HIV' particles isolated and recovered directly from their blood or semen? Cell- free HIV has never been found in fresh samples of semen.
The research of Padian et al (1) shows that it is extremely difficult for a man to 'infect' a woman. Did the prosecution prove unequivocally that the three women were HIV negative prior to meeting the accused? Were these females all virgins prior to intercourse with Konzani?
The defence lawyers for Konzani and Dica obviously did not know that there are arguments in the scientific literature that 'HIV' has never been truly isolated or proven to be sexually transmitted. The Crown Prosecution Service (CPS) make the false assumption that the HIV tests are reliable and proof of putative 'HIV infection' and/or that 'HIV' is an 'infectious disease' and that HIV is an STD. These are all unproven suppositions.
The CPS needs to be informed that the 'HIV' tests are non-specific and non-standardised. All current 'HIV' tests lack a 'gold standard' against which they could be evaluated to ensure that 'HIV' is being detected. There is no gold standard HIV test because there is no gold standard 'HIV' isolate.
In addition to being inaccurate, 'HIV' tests are not standardised. This means that there is no nationally or internationally accepted criterion for what constitutes a 'positive' result. Different countries have different criteria as to what constitutes a 'positive' test result. Standards also vary from lab to lab within the same country and can even differ from day to day at the same lab.
Paolo Matias is the fifth man in the UK to be jailed for alleged "reckless transmission of HIV" and for causing (hypothetical and unproven) "grievous bodily harm" to his girl friend despite the fact that to 'HIV' has never been scientifically proven to be a sexually transmitted retrovirus or to be the cause of 'AIDS'. Again: were viable, active, infectious 'HIV' particles isolated and recovered directly from Paolo Matias's blood or semen?
We need to drop the term "grievous bodily harm" simply because 'HIV' has never been scientifically proven to be a sexually transmitted 'infectious' agent that causes 'AIDS'. What has been wrongly nominated as 'HIV' is merely an endogenous marker for cellular irregularity found in specific groups.
Judge Michael Stokes QC makes the false assumption that 'HIV' is an STD and causes 'AIDS' when he told Matias: "Having sexual intercourse when you knew you were HIV positive, therefore likely to pass it on to her, is unforgivable."
Judge Michael Stokes QC needs to be informed that the 'HIV' is not an STD and that tests are non-specific and non-standardised. All current 'HIV' tests lack a 'gold standard' against which they could be evaluated to ensure that 'HIV' is being detected. There is no gold standard 'HIV' test because there is no gold standard 'HIV' isolate. There is simply no hard scientific evidence that anyone is 'HIV' positive.
Therefore these current cases made against people for 'HIV transmission' are all unsafe, absolutely absurd and have no scientific basis or credibility: power is knowledge. Knowledge is freedom from false prosecutions. Yet there is evidently another trial, the first involving a homosexual, due to take place this summer.
I would argue on scientific grounds that their convictions are unsafe because they depend upon the unproven assumption that 'HIV' is transmitted horizontally via sexual intercourse and that 'HIV' tests are reliable and proof of 'HIV infection'. Emeritus Prof. Gordon Stuart, Public Health, Glasgow UK stated: "At present there is no scientific basis for using these tests to prove HIV infection." Whilst Chief UK virologist Philip Mortimer stated: "It may be impossible to relate an antibody response specifically to HIV infection."
The horizontal (sexual) transmission of 'HIV' has never been scientifically proven: it is mere supposition that 'HIV' is sexually transmitted. If 'HIV' were a genuine STD it would spread equally through the general population and be equally bi-transitive between the sexes. We have seen huge rises in STD rates and unwanted pregnancies in the UK without a concurrent spread of 'HIV'. There is no endemic heterosexual 'HIV' epidemic in the UK.
We need to drop the term "reckless transmission" simply because 'HIV' has never been proven to be a sexually transmitted 'infectious' agent. What we are (wrongly) calling 'HIV' is merely an endogenous marker for cellular irregularity.
Why does an allegedly horizontally transmitted virus, 'HIV', remain almost exclusively in one group of people - homosexual men - for 20 years in the West? Why is it more difficult for heterosexuals to be 'infected' with 'HIV' than homosexuals? This is completely illogical.
Feston's QC, Timothy Roberts, submitted that the convictions were "unsafe" because of "two legal errors", at the Court of Appeal in London. The real grounds for appeal should have been that 'HIV' has not been proven to be transmitted sexually. To stop this potential medical McCarthyism we need a public inquiry into the validity of HIV testing as well as scientific proof that 'HIV' is an STD.
To date: in a Court of Law there has never ever been any scientific proof presented that 'HIV' exists as an isolated, sexually transmiited retrovirus or that 'HIV' has been truly isolated from a fresh blood or semen sample.
Should Konzani, Dica and Matias be granted another appeal their defence councils might care to consider calling the following as expert witnesses* to verify that a) HIV is not the cause of AIDS; and b) and HIV is not transmitted sexually; and c) that the HIV tests are notoriously unreliable and non-specific. Christine Johnson (2) recorded over 70 conditions drawn from the medical literature known to give a false- positive 'HIV' test result:
*Advocate Barrister Anthony
Brink
Dr. Stefan Lanka
Dr. Karl Krafeld
Dr. Roberto Giraldo
Dr. David Rasnik
Prof. Sam Mhlongo
Prof. Peter Duesberg
Prof. Etienne de Harven
Yours sincerely;
Alex Russell
The Association for the Critical Analysis of AIDS
London, WC1N
References:
(1) Padian NS, et al (1997). Heterosexual transmission of human immunodeficiency virus (HIV) in northern California: results from a ten- year study. American Journal of Epidemiology. 146:350-357.
(2) Christine Johnson, Whose antibodies are they anyway?, Continuum Magazine, Vol.4 No.3. *
* Conditions that cause ‘false positives’ on the non-specific HIV tests can include: past or present infection with a variety of bacteria, parasites, viruses, and fungi including tuberculosis, malaria, leishmaniasis, influenza, leprosy and a history of sexually transmitted diseases; the presence of polyspecific antibodies, anti-carbohydrate antibodies, naturally-occurring antibodies; hypergammaglobulinemias, the presence of auto-antibodies against a variety of cells and tissues, vaccinations, and the administration of gamma globulins or immunoglobulins; the presence of auto-immune diseases like erythematous systemic lupus, sclerodermia, dermatomyositis and rheumatoid arthritis; the existence of pregnancy and multiparity; a history of rectal insemination; addiction to recreational drugs; several kidney diseases, renal failure and hemodialysis; a history of organ transplantation; presence of a variety of tumours and cancer chemotherapy; many liver diseases including alcoholic liver disease; haemophilia, blood transfusions.
To: Tony Delamothe, BMJ Web Editor
10th June 2005
Dear Tony,
Dear Alexander,
The message was meant for you in the plural. The editorial reads (see my italics):| "We
will no longer offer the AIDS deniers and their opponents
space to continue their shouting match of the deaf, with
online content equivalent to some 20 print BMJs devoted to
their row.7
" So expect to see no more of Bennett, Flegg and Floyd either. Since this issue is obviously of overwhelming importance to you, and you don't feel you've reached closure, couldn't you set up something like a rapid response function yourself, elsewhere. There, both sides can carry on until one side finally admits defeat. * I'm reassured on your use of aliases. Thanks for that. Tony Delamothe |
Dear Alexander
Putting it bluntly, we don't want to hear from you -
ever again - on HIV/AIDS.
Regardless of whether you believe your views fall within or
against the conventional paradigm, your responses over the years have really
been drumming a single message. Can you read what's featured below and say
you've never made that same point before (again and again and again)?
You may have missed the following editorial: http://bmj.bmjjournals.com/cgi/content/full/330/7503/1284
so can I direct your attention to the section on AIDS deniers
**
We'd welcome responses from you that contribute to the discussion
of other topics, but please be aware that the next phase of our campaign to
revitalise rapid responses is to ban the use of aliases (and if that fails, to
ban the people who use them).
Tony Delamothe
web editor
Dear BMJ Editors,
My rapid response works within the 'HIV' Paradigm and is not
'alternative' or 'dissenting' and aims to answer Steven Stern's polemic.
Yours sincerely, Alex
Russell
bmj.com
| |||
| Alexander
H Russell, artist/writer/philosopher WC1N 1PE Send response
to journal: | GP Steven Stern
stated:
"It would, as a General Practitioner, have been useful to see a list of the illnesses which were designated as pointers to earlier diagnosis in those patients with a late HIV diagnosis." Yes: it would be very interesting indeed: "to see a list of the illnesses which were designated as pointers to earlier diagnosis in those patients with a late HIV diagnosis." It would be interesting because these illnesses ('pointers') in themselves maybe responsible for causing endogenous 'HIV' expression. Rather than the unproven hypothesis that 'HIV' causes 'AIDS' – it could be argued that 'AIDS' (illnesses) cause 'HIV'. I would argue that certain illnesses are 'pointers' (markers) for endogenous 'HIV' expression. The list of the illnesses and conditions could include classic 'AIDS' conditions: TB, KS, malaria, and disease conditions relating to malnutrition and poverty. Immigrants test so-called 'HIV positive' because they come from areas where TB and malaria are highly present and both diseases are very well known to make the non-specific 'HIV' test run 'positive'. Has any one found actual 'HIV' in their blood stream - and I do not just mean surrogate markers? 'HIV' is invariably found in people with many other different kinds of antibodies due to concurrent infections with other pathogens: how do we know that one these is not responsible for the killing of T 4 cells? For instance: reactivated herpes viruses are highly cytotoxic. Has Steven Stern ever found evidence of 'HIV infection' in an individual with no other pathogens present? I very much doubt it. What we are calling 'HIV' is in fact merely an endogenous marker for other pathogens. It is acknowledged by supporters of the 'HIV' hypothesis that many of the so-called 'HIV positive' people in Africa, India and oththe developing world - where malaria and TB are endemic - will test 'positive': these are 'false positives'. I would argue that all 'HIV positives' are 'false positives'. Returning to Stern's original question: it would be interesting to see what other illnesses are 'pointers' and markers for causing endogenous 'HIV' expression. Stern inadvertently implies that what we have been nominating as 'HIV' is in fact an endogenous marker ('pointer') for specific illnesses and disease conditions which 'HIV' is an effect of – and not a cause. Competing interests: None declared | ||
Positive Voices UKC Alternative viewpoints on HIV and AIDS
The Case of Paolo Matias & The Criminalisation of supposed 'HIV' Transmission
Posted on Saturday, 4 June, 2005 - 4:29 pm:
Paolo Matias is the fifth man in the
UK to be jailed for alleged "reckless transmission of HIV" and for
causing "grievous bodily harm" to his girl friend despite the fact
that to date 'HIV' has never been scientifically proven to be a sexually
transmitted retrovirus or to be the cause of 'AIDS'.
We need to drop the term "grievous bodily harm" simply because 'HIV'
has never been scientifically proven to be a sexually transmitted 'infectious'
agent that causes 'AIDS'. What has been wrongly nominated as 'HIV' is merely an
endogenous marker for cellular irregularity found in specific groups.
Judge Michael Stokes QC makes the false assumption that 'HIV' is an STD and
causes 'AIDS' when he told Matias: "Having sexual intercourse when you knew
you were HIV positive, therefore likely to pass it on to her, is
unforgivable."
Judge Michael Stokes QC needs to be informed that the 'HIV' is not an STD and
that tests are non-specific and non-standardised. All current HIV tests lack a
'gold standard' against which they could be evaluated to ensure that 'HIV' is
being detected. There is no gold standard HIV test because there is no gold
standard HIV isolate. There is simply no hard scientific evidence that anyone is
'HIV' positive.
Therefore these current cases made against people for 'HIV transmission' are all
unsafe, absolutely absurd and have no scientific basis or credibility: power is
knowledge. Knowledge is freedom from false prosecutions. Yet there is evidently
another trial, the first involving a homosexual, is due to take place this
summer.
Will the so-called homosexual community go on making a rod for its own back (pun
not intended) by supporting the unproven belief that 'HIV' is an STD - and
therefore likely to instigate further stigma, fear, irrationality, witch hunts,
unsafe convictions, criminalisation, incarceration? Probably: people fear
thinking autonomously and empowering themselves: they feel safer in numbers
following heard belief systems and never question what they are told.
Unfortunately, the so-called 'HIV' community is absolutely initiated and
interpellated into the unproven supposition that 'HIV' is an STD and causes
'AIDS' so they are hoist by their own petard: they cannot think out of this
simplistic nonsensical ideology and anyone who dares to have the temerity to
criticise 'HIV' Ideology is automatically branded as an 'HIV' denisalist.
The retard and quasi-religious term 'HIV denialist' is the slave-morality
herd-instinct of the blind 'HIV' believer: anyone who critiques and questions
this Scientology-like 'HIV' Belief system is violently attacked with emotive
abuse and irrational fear fuelled by bitter hated and bitter resentment. The
so-called 'HIV' community do not want 'informed choices' or 'informed debate'
but idiotic dogma and blind belief like all reactionary and regressive retard
religions.
I would argue on legal and scientific grounds that these recent convictions
against people for 'HIV transmission' are all unsafe because they depend upon
the unproven assumption that 'HIV' is transmitted horizontally via sexual
intercourse and that 'HIV' tests are reliable and proof of 'HIV infection' and
that 'HIV' causes 'AIDS'.
The horizontal (sexual) transmission of 'HIV' has never been scientifically
proven: it is mere supposition that 'HIV' is sexually transmitted. If ‘HIV’
were a genuine STD it would spread equally through the general population and be
equally bi-transitive between the sexes. We have seen huge rises in STD rates
and unwanted pregnancies in the UK without a concurrent spread of 'HIV'. There
is no endemic heterosexual 'HIV' epidemic in the UK.
Alex Russell, The Association for the Critical Analysis of AIDS
Feston Konzani & Mohammed Dica are Not Guilty of transmitting 'HIV'
Positive Voices UKC Alternative viewpoints on HIV and AIDS
Criminalisation of HIV Transmission
Posted on Sunday, 29 May, 2005 - 11:29 pm:
Regarding the recent
convictions for so-called “reckless transmission” of HIV, Dr. Catherine
Dodds, research fellow, Sigma Research, stated: “In the last 100 years no one
has ever been convicted for transmitting any other disease. Why HIV? Why now? We
need answers – we need action.” (Positive Nation, Issue 112, May 2005).
Whilst Lisa Power, Head of Policy and Public Affairs, Terrence Higgins Trust,
stated we need to “…encourage a national debate about using criminal law to
regulate public health.” (Positive Nation, Issue 112, May 2005).
To stop this potential medical McCarthyism we need a public inquiry into the
validity of HIV testing. To date the debate has been largely framed and the
agenda set by the proponents of the HIV paradigm: the hypothesis that HIV is a
sexually transmitted infection and causes AIDS. To date this assumption is an
unproven supposition unsupported by hard science.
The Crown Prosecution Service (CPS) make the false assumption that the HIV tests
are reliable and proof of putative 'HIV infection' and/or that HIV is an
'infectious disease' and that HIV is an STD. These are all unproven
suppositions.
Feston Konzani, an African asylum seeker, has been jailed for 10 years in 2004
at Teesside Crown Court for allegedly 'infecting' three women with HIV. Konzani
was accused of inflicting "grievous bodily harm" on the two women aged
25 and 26 and a young girl of 15.
The Court of Appeal stated that the women never consented to the specific risk
of contracting “a potentially fatal disease” alleged to be HIV. Yet the
Court of Appeal presented no evidence that ‘HIV’ is a fatal condition;
merely assumed it to be so. The three women claimed that they became
"infected" with HIV after having sex between February 2000 and May
2003 with Konzani. How do they know they were "infected" by Konzani?
Did these women come from areas in Africa or the Third World where TB, malaria
and leprosy are endemic and are well known to cause false positive readings on
HIV tests?
In 2003 Mohammed Dica was convicted at Inner London Crown Court of two counts of
'biological' grievous bodily harm allegedly 'infecting' women with HIV and
sentenced to 8 years in prison.
How do we really know that Konzani and Dica are 'HIV' positive and really
'infected' these women? Were viable, active, infectious HIV particles isolated
and recovered directly from their blood or semen? Cell-free HIV has never been
found in fresh samples of semen.
The research of Padian et al (1) shows that it is extremely difficult for a man
to ‘infect’ a woman. Did the prosecution prove unequivocally that the three
women were HIV negative prior to meeting the accused? Were these females all
virgins prior to intercourse with Konzani?
The defence lawyers for Konzani and Dica obviously did not know that there are
arguments in the scientific literature that HIV has never been truly isolated or
proven to be sexually transmitted.
The CPS needs to be informed that the HIV tests are non-specific and
non-standardised. All current HIV tests lack a 'gold standard' against which
they could be evaluated to ensure that 'HIV' is being detected. There is no gold
standard HIV test because there is no gold standard HIV isolate.
In addition to being inaccurate, HIV tests are not standardised. This means that
there is no nationally or internationally accepted criterion for what
constitutes a 'positive' result. Different countries have different criteria as
to what constitutes a 'positive' test result. Standards also vary from lab to
lab within the same country and can even differ from day to day at the same lab.
We would argue on scientific grounds that their convictions are unsafe because
they depend upon the unproven assumption that HIV is transmitted horizontally
via sexual intercourse and that HIV tests are reliable and proof of ‘HIV
infection’. Emeritus Prof. Gordon Stuart, Public Health, Glasgow UK stated:
"At present there is no scientific basis for using these tests to prove HIV
infection." Whilst Chief UK virologist Philip Mortimer stated: "It may
be impossible to relate an antibody response specifically to HIV
infection."
The horizontal (sexual) transmission of HIV has never been scientifically
proven: it is mere supposition that 'HIV' is sexually transmitted. If HIV were a
genuine STD it would spread equally through the general population and be
equally bi-transitive between the sexes. We have seen huge rises in STD rates
and unwanted pregnancies in the UK without a concurrent spread of HIV. There is
no endemic heterosexual 'HIV' epidemic in the UK.
We need to drop the term “reckless transmission” simply because HIV has
never been proven to be a sexually transmitted ‘infectious’ agent. What we
are calling HIV is merely an endogenous marker for cellular irregularity.
Why does an allegedly horizontally transmitted virus, HIV, remain almost
exclusively in one group of people - homosexual men? Why is it more difficult
for heterosexuals to be 'infected' with HIV than homosexuals? This is completely
illogical.
Feston's QC, Timothy Roberts, submitted that the convictions were
"unsafe" because of "two legal errors", at the Court of
Appeal in London. The real grounds for appeal should have been that HIV has not
been proven to be transmitted sexually.
Should Konzani and Dica be granted another appeal their defence councils might
care to consider calling the following as expert witnesses* to verify that a)
HIV is not the cause of AIDS; and b) and HIV is not transmitted sexually; and c)
that the HIV tests are notoriously unreliable and non-specific. Christine
Johnson (2) recorded over 70 conditions drawn from the medical literature known
to give a false-positive 'HIV' test result:
*Advocate Barrister Anthony Brink
Dr. Stefan Lanka
Dr. Karl Krafeld
Dr. Roberto Giraldo
Dr. David Rasnik
Prof. Sam Mhlongo
Prof. Peter Duesberg
Prof. Etienne de Harven
Yours sincerely;
Alex Russell
Mike Hersee
Nigel Edwards
Michael Verney-Elliott
The Association for the Critical Analysis of AIDS
WC1N 1PE
Joan Shenton
Immunity Resource Foundation
London W11 3QS
References:
(1) Padian NS, et al (1997). Heterosexual transmission of human immunodeficiency
virus (HIV) in northern California: results from a ten-year study. American
Journal of Epidemiology. 146:350-357.
(2) Christine Johnson, Whose antibodies are they anyway?, Continuum Magazine,
Vol.4 No.3. *
* Conditions that cause ‘false positives’ on the non-specific HIV tests can
include: past or present infection with a variety of bacteria, parasites,
viruses, and fungi including tuberculosis, malaria, leishmaniasis, influenza,
leprosy and a history of sexually transmitted diseases; the presence of polyspecific
antibodies, anti-carbohydrate antibodies, naturally-occurring antibodies;
hypergammaglobulinemias, the presence of auto-antibodies against a variety of
cells and tissues, vaccinations, and the administration of gamma globulins or
immunoglobulins; the presence of auto-immune diseases like erythematous systemic
lupus, sclerodermia, dermatomyositis and rheumatoid arthritis; the existence of
pregnancy and multiparity; a history of rectal insemination; addiction to
recreational drugs; several kidney diseases, renal failure and hemodialysis; a
history of organ transplantation; presence of a variety of tumors and cancer
chemotherapy; many liver diseases including alcoholic liver disease;
haemophilia, blood transfusions.
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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"Since Plato, it is the old philosophical injunction: to learn to live is to learn to die. Less and less, I have not learned to accept death. I remain uneducable about the wisdom of learning to die." (Jacques Derrida, Le Monde interview, August, 2004). Derrida delivered before Derrida died - or did Derrida die? How did Derrida do 'Death'? Or did Derrida undo 'Death'? Deconstruct 'Death'? Science has a limited, reductionist, 'commonsense' understanding of 'Death' - whereas Philosophy rethinks 'Death'. How do we know Derrida 'Died'? Because others 'Die' before us? Only others assume and suppose we 'Die' because we go all stiff and are stripped of the Psyche and the Sensations of our Being – the Psyche and Sensation of our Being alive. But where do our Psyche and Sensation of Being drift? Where does Dasein drift? What oozes out of the 'Dead'? Sensation! We do not 'Die' but become Other (Sensations) as otherwise to Being, otherwise to Dasein. In 'Life' we are always already 'Dying' all the Time so 'Death' does not exist in-itself only out-itself - as out of oneself: from 'Borning' we are always already 'Dying': we 'Die' many more times psychically and physically in the sense that we are always already shape-shifting and meandering-mutating: we are never the same subject for a split second so hence we 'Die' and are 'Born' every single second as an attuned afresh sensation. 'Death' is the exiting and the expelling of sensationing from the Body. Physical 'Death' is thus the oozing out of the Psyche and the Sensations from the Body (Corpse). We do not (usually) experience 'Death' – others experience the moment, movement, music of our 'Death' - in our place - on our behalf. Yet we all introject and incorporate - the 'Dead': we wear the 'Dead'- that is - we all become Crypts of the 'Dead' (keeping them alive and wearing their Psyche and Sensation) - but most of us do not know this and carry the dead like one carries a coal sack or as Jacques Derrida deals the: "dead object remains like a living dead abscessed in a specific spot in the ego" (Derrida, The Ear of The Other). "Death" is the dematerialisation and desemenisation of the Body and the dissemination of the Psyche and Sensation: the deaded-body disperses, jettisons, our psyche – thinking – sensationing to outer regions sensation-scapes: therefore 'Absolute Death' is always already an 'Absolute Impossibility' – just as 'Absolute Life' is also an 'Absolute Impossibility'. The 'Living' incorporate The 'Deading'. Some of us have actually experienced Being-Death as being-dead (being beheaded and decapitated from the mind-body dualism) and floating free – from the heaviness of being (embodied emheaded): as an out of body experience and near death experience. 'I' experience being dead: 'Death' is not a possibility. 'Death' is not a question or an issue for Being: 'Dying' as Living is. Dasein is for 'Dying' as Being is for Deathing as a Life Sentence is for Doing Time. One could argue that what is important is not 'Death' itself - but Dying (Living), the manner, music, metre and the style in which the being Lives and 'Dies' as it aims toward 'Death' ('Life'). For Heidegger 'Death' is our metre, movement, music of our being toward 'Death' – the way we walk the way we wonder the way we wander towards 'it': in 'Death' we become 'Death' in-itself as 'being-dead' is an essential state of 'being- alive' on different levels of our musical psychic sensation: our measure and measuredness: our 'Death' or 'Deathness' could be said to be the metre of our Music and Time: our being is constituted and incorporated by our Time of 'Death' as the 'Death' of our Time: the metre of our Music of Being (psychic-sensation). Our oozed out Ontological relationship with Being and Time is the Time of our 'Life' as the Time of our 'Death': that is: the way we all do Time is the way we all do 'Death' and we all do 'Life': everyone in a sense in a sensation - is 'doing time' (not just those in prison): the Style - the way we do Time is the sign and sensation of the way we do 'Death' – both in sickness and in health. We all daily do 'Death' (like 'Life') differently - because we all do 'Death' ('Life') differently because we all do Time differently. A Good Death is not 'Dying' on Time but 'Dying' in Time with Style. A Good Birth can set the moment, movement, music for 'A Good Death': some beings are never (truly) born so some beings never (truly) 'Die' – they are disembodied and beheaded from the Psyche and Sensation scapes so sloth and drift derailed from Dasein as the living-dead: they do not have The Shine. 'Doing Life' is an orchestral overture for 'Doing Death' via the Way we all Do Time and it is the Style in which we do 'Death' as Dasein. 'Death' is the only Uncertainty in Life. As an Absolute Impossibility 'Death' is all the time not in Time. Being and Time negate the Possibility of 'Death'. Heidegger on dreary Dasein and 'Death': "...Dasein constantly is its not-yet as long as it is, it also already is its end. The ending we have in view when we speak of death does not signify a being-at-an-end of Dasein, but rather a being toward the end of this being. Death is a way to be that Dasein takes over as soon as it is." (Being & Time). "...death is the inmost, not-relational, certain, and as such, indefinite possibility not to be bypassed of Dasein. ...As the end of Dasein death is in the being of this being toward its end." (Being & Time). Derrida on the (im)possibility of 'Death': "Is the most distressing, or even the most deadly infidelity, that of a possible mourning which would interiorise within us the image, idol, or ideal of the other who is dead and lives only in us? Or is it that of impossible mourning which…refuses to take the other within oneself, as in the tomb of some narcissism?" (Jacques Derrida, Memories of Paul de Man; The Work of Mourning). "Ours To Derrida Or Die". References: Heidegger, Martin; Being & Time, 1927. Abraham, Nicolas and Maria Torok; The Wolf Man¹s Magic Word: A Cryptonymy. 1976. Trans. Nicholas Rand. Minneapolis: U of Minnesota P, 1986. Derrida, Jacques; The Ear of the Other, Trans. Peggy Kamuf. Ed. Christie, MacDonald. Lincoln: U of Nebraska P, 1985. Derrida, Jacques; Memories of Paul de Man; The Work of Mourning, University of Chicago Press. http://www.humanities.uci.edu/remembering_jd/butler_judith.htm Competing interests: None declared |
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H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett stated regarding critical 'AIDS' Analysts: "There is no consistent view or aim, reflected in the regular confused posts from newcomers to the dissident discussion boards. Practically the only thing uniting them is a refusal to accept the conventional thought." On the contrary, critical 'AIDS' Analysts absolutely accept the 'conventional thought' (rules of virus isolation, etc), which is precisely why we are questioning the proponents of the ‘HIV’ Hypothesis who constantly ignore conventional thought about the practice of isolation, etc. It is precisely the total lack of "conventional thought" (and conventional scientific practice) that mars the thinking of the proponents of the 'HIV/AIDS' Hypothesis. For instance: when Koch’s Postulates, the tried, trusted and 'conventional' method of proving the existence of a pathogen were completely unfulfilled by 'HIV', the supporters of the 'HIV' Hypothesis declared the Postulates to be rubbish. Moreover, the 'conventional' rules for retrovirus isolation laid down at a conference at the Pasteur Institute in 1974 were flagrantly ignored by the scientific team working at the very same institute in 1983, who claimed to have found a retrovirus in the tissues a homosexual man suffering from lymphadonopathy merely by finding what they claimed to be reversetranscriptase activity and other dubious surrogate markers. However, when subsequently challenged, Luc Montagnier, the leader of the team, admitted that they did not find or isolate any viral particles, and despite heroic laboratory efforts - described by Montagnier, as "Roman efforts" – no 'HIV' was found. If 'HIV' does not fit the conventional rules, they rubbish those rules, move the goal posts and rewrite the rules of the game – then shoehorn 'HIV' in as a 'killer pathogen' when in fact it is nothing of the kind. From the outset it was claimed, in order to explain the embarrassingly elastic incubation period of 'HIV/AIDS' – said to be anything from 10 to 30 years between putative 'infection' and onset of disease - that 'HIV' was a lentivirus, a slow acting retrovirus. Yet now we are told that 'HIV' causes 'AIDS' in a matter of months in Africa and the Third World. Is 'HIV' a 'lentivirus' or not? As Peter Duesberg stated: "There are no slow viruses – only slow virologists." Why is it that there is still no heterosexual 'HIV' epidemic in the West whilst there is allegedly a heterosexual 'HIV' epidemic in South Africa? We are not 'dissidents' or 'denialists' but deconstructionists – critical and autonomous 'AIDS' Analysts teasing out the absurdities, anomalies, inconsistencies and contradictions of the redundant 'HIV' Hypothesis. It is the propagators of 'HIV' dogma who persistently refuse to accept 'conventional thought' (and practice) and merely make up the rules as they go along – changing the rules of 'virtual virology' virtually daily – to patch up the tottering 'HIV' Hypothesis. Competing interests: None declared |
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H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nassim C. Kamdar refreshingly stated regarding dumping the term 'AIDS' Dissidents: "I think it is high time to review the term 'aids dissidents' which puts one in the inadvertently similar position as the "insurgents" in Iraq; A negative concept that automatically creates in the mind of those with a herd mentality an emotional detachment from anything associated with the "dissidents"; and artificially compartmentalises researchers in this field. Since AIDS 'dissidents' are neither 'anti-government' nor 'anti-anything' can we, at least, avoid using the term in our own discussions. To get the ball rolling, 'AIDS-theory analysts' which recognises a common effort towards a common goal." Kamdar is shrewd in adopting this strategy/tactic and we should follow Nassim's stance and start using the term 'AIDS' Analysts or 'AIDS' Critical Theorists or even 'AIDS' Deconstructionists since such analytical -critical-intellectual terms lifts so-called 'dissenters' out of the arbitrary binary opposition between 'them' and 'us': 'insiders' versus 'outsiders', 'establishment' versus 'dissident'. We are not 'AIDS' dissidents but 'AIDS' Reappraisers and The Group for the Scientific Reappraisal of the HIV-AIDS Hypothesis came into being as a group of signatories of an open letter to the scientific community. The letter (June 6, 1991) had been submitted to the editors of Nature, Science, The Lancet and The New England Journal of Medicine. The unpublished letter stated: "It is widely believed by the general public that a retrovirus called HIV causes the group diseases called AIDS. Many biochemical scientists now question this hypothesis. We propose that a thorough reappraisal of the existing evidence for and against this hypothesis be conducted by a suitable independent group. We further propose that critical epidemiological studies be devised and undertaken." Many so-called 'AIDS' dissidents are well respected and 'established' scientists, doctors, philosophers, cultural theorists, lawyers, journalists, as well as Noble Laureates Kary B. Mullis (Nobel Prize in Chemistry, 1993) and Walter Gilbert (Nobel Prize in Chemistry, 1980); and Serge Lang, arguably one of the most brilliant mathematicians in the United States; and not forgetting retrovirologist, Peter H. Duesberg, Ph.D., professor of Molecular and Cell Biology at the University of California, Berkeley. Duesberg isolated the first cancer gene through his work on retroviruses in 1970, and mapped the genetic structure of these viruses. This, and his subsequent work in the same field, resulted in his election to the National Academy of Sciences in 1986. Duesberg was also the recipient of a seven-year Outstanding Investigator Grant from the National Institute of Health. Here are a few quotes from established 'AIDS' Analysts on the flawed and failed 'HIV/AIDS' Hypothesis: Prof. Serge Lang: "For a decade, there has been increasing concern about 'AIDS,' and a virus called 'HIV' which is said to cause 'AIDS'. Having named this virus 'HIV - Human Immunodeficiency Virus - contributes to making people accept that 'HIV is the cause of AIDS'. However, to an extent that undermines classical standards of science, some purported scientific results concerning 'HIV' and 'AIDS' have been handled by press releases, by misinformation, by low-quality studies, and by some suppression of information, manipulating the media and people at large…A number of scientists have questioned the established view that 'HIV is the cause of AIDS,' and they have given evidence that this view - I call it dogma - may be invalid." - Serge Lang, HIV and AIDS: Have We Been Misled? Questions of Scientific and Journalistic Responsibility, Yale Scientific, Fall 1994. Kary Mullis, Ph.D: "Where is the research that says HIV is the cause of AIDS? There are 10,000 people in the world now who specialize in HIV. None has any interest in the possibility HIV doesn't cause AIDS because if it doesn't, their expertise is useless...I can't find a single virologist who will give me references which show that HIV is the probable cause of AIDS. If you ask a virologist for that information, you don't get an answer, you get fury." - Kary Mullis, Ph.D. Nobel Prize in Chemistry, 1993, for inventing the polymerase chain reaction [PCR]. Walter Gilbert, Ph.D: "Duesberg is absolutely correct in saying that no one has proven that AIDS is caused by the AIDS virus. And he is absolutely correct that the virus may...not be the cause of AIDS." - Gilbert, Ph.D., Nobel Prize in Chemistry, 1980. Peter H. Duesberg, Ph.D: "If you think a virus is the cause of AIDS, do a control without it. To do a control is the first thing you teach undergraduates. But it hasn't been done. The epidemiology of AIDS is a pile of anecdotal stories, selected to fit the virus-AIDS hypothesis. People don't bother to check the details of popular dogma or consensus views." - Peter H. Duesberg, Ph.D., Professor of Cell & Molecular Biology Member, National Academy of Sciences. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Bennett sated: "Clearly women and heterosexual men do get AIDS -KS. It is biased towards homosexual men, but not restricted!" Can Bennett cite one example of a white male or female heterosexual AIDS-KS in the West? If AIDS-KS is caused by HHV-8 - as Bennett would like us all to believe - then there would have been hundreds or thousands heterosexual AIDS-KS cases in the West by now. How many BMJ rapid response readers have seen hundreds or thousands of heterosexuals with AIDS-KS in the UK? Or even just one case of heterosexual AIDS-KS in the UK? Where are all the heterosexual AIDS-KS cases in the West? Bennett continues: "In addition, his comment that 'all STDs have their origin in the heterosexual community and find their way into the homosexual community horizontally through sexual transmission by bisexual men' clearly shows he is forgetting that the introduction of HIV into the west was through homosexuals. They were the first risk group to be identified and several contact tracings show that 'patient zero' for a slew of early cases was a gay flight attendant, and similar cases were seen in the 'patient zeros' of other chains/networks of infected people in Europe (homosexual, travel to the US or Africa)." What utter rubbish: Bennett is basing his entire argument on the purely anecdotal case of Gaetan Dugas, the flight attendant known sensationally as 'the angel of death'. This media manufactured apocalyptic anecdote proves absolutely nothing. Scientific fact does not depend on mere media anecdotes and unproven suppositions. If the course of the supposed 'spread' of 'HIV' in the West is down to one person you have no case - apart from it being totally unbelievable. So where did homosexuals acquire 'HIV' from? Anecdotal cases mean nothing: how and why did 'HIV' remain rigidly locked within a specific group of people: male homosexuals in the West? Bennett simply cannot explain why there has never been a heterosexual 'HIV' epidemic in the West. And the crass 'condom campaign' argument does not wash since there have been huge rises in STD rates in the West. There's no way a real infectious pathogen could remain confined to homosexuals in the West for more than 20 years. History has proved to us that 'HIV' is not an STD - no matter how much Bennett likes to keep on pretending otherwise. Bennett stated in a recent rapid response (1 April, 2005): "It should not be forgotten that HIV is itself an infection." I can only assume that Bennett's unfounded statement is an April Fool. Bennett has not provided proof that 'HIV' is an 'infection' so "it should be forgotten". If 'HIV' were a truly infectious agent there would be hundreds of thousands of 'HIV' positive male and female heterosexuals in the West by now – 20 years on - since the socio-political invention of 'HIV'. Thus: 'HIV' cannot be an infection or a pathogen. Can Bennett explain in precise detail the mechanism of sexual transmission of 'HIV', considering that a sufficient quantity of cell-free infectious 'HIV' particles to be deemed an infectious dose – has never been found in any semen sample taken from homosexual men – or indeed – any 'HIV' positive man. Bennett goes on: "As regards HIV viability in syringes, this very work has, once again, been performed. Viable HIV has been cultured from syringes after up to 6 weeks at room temperature, albeit at low levels at the later time-points." I am not talking about 'culturing' but the recovery of fresh, infectious cell-free 'HIV' from syringes: this has never been achieved. Bennett concludes: "Duesberg's 'HIV-free AIDS cases' are an empty set of clearly non-AIDS patients. Harris points out (as I have been trying to do) that since AIDS is a decline in a specific subset of immune system cells, proper analysis of these "HIV free AIDS cases" shows that they do not have AIDS. By expecting only AIDS patients to have AIDS-indicator diseases both Duesberg and followers like Russell are demonstrating a lack of clinical experience, or simple literature analysis. This over- simplistic black-and-white thinking is characteristic of AIDS denialists, but unfortunately a side effect of media portrayal of science in precisely this manner. By cutting it up into bitesize chunks, one necessarily removes the underlying logic and explanations behind the conclusions. One form of 'non-HIV AIDS', idiopathic CD4 lymphopenia, (ICL) is very different from AIDS - to quote from Harris." Harris is wrong and has moved the goal posts in re-defining 'AIDS' to dodge the embarrassing ICL issue. Contrary to Harris and Bennett's claims: 'ICL' is not different (from the CDC's) definition of 'AIDS' – rather: ICL is 'AIDS' without 'HIV' – a concept that Harris and Bennett cannot seem to grasp - so fixated are they with the 'HIV' cause. For Harris and Bennett's "over-simplistic black-and-white thinking" anyone deemed to be 'HIV' positive with a disease-condition will automatically have 'AIDS'. Does Bennett really know what 'AIDS' is? We are not "AIDS denialists" - as Bennett so patronisingly states - but we are 'AIDS' deconstructionists: teasing-out the absurdities, anomalies, contradictions inherent in the simplistic black-and-white 'AIDS' construct characteristic of the sound-bite 'AIDS' believers. As Peter Duesberg has argued: not all 'AIDS' diseases/conditions can be explained by immunodeficiency:(1) "Some of the AIDS diseases could possibly be autoimmune diseases. Certainly not all. 38 percent of American AIDS cases have nothing to do with immune deficiency. 38 percent. 10 percent are Kaposi sarcomas, 19 percent are this so-called wasting disease...They name it AIDS, that's all. None of these 38 percent have anything whatsoever to do with immunodeficiency, but they're called AIDS…There's not one AIDS disease that's new. What is new is only the incidence of these diseases in 20-to 45-year-old men, mostly, and a few women, has gone up." (1): Peter Duesberg, interviewed by Bob Guccione, Jr., Spin Magazine, September, 1993. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett stated regarding the spurious HHV-8 - KS connection: "Regardless of the laboratory findings of popper exposure, it fails to explain why all KS lesions from all four types of KS, including AIDS- KS, contain HHV8." Then how does Bennett explain that a ubiquitous HHV-8 can be the cause of AIDS-KS exclusively in homosexual men in the West? There is no such thing as a pathogen that can be solely restricted to a single group of people. Has it never occurred to Bennett that evidence of an active virus may be the result of a disease condition rather than a cause of a disease condition? It has long been know that herpes simplex 1 and 2 are persistent infections which most of the time remain dormant. However, once reactivated by other factors they cause cold sores and genital lesions. It has never been shown that either of these common herpes viruses is restricted to or originated in homosexual men. Why therefore does Bennett presume that a further herpes virus, HHV-8, only occurs in homosexual men in the West? Bennett totally fails to see that HHV-8 is a by-product - rather than a causative agent - of KS: you cannot have a pathogen (HHV-8) restricted to homosexual men. Can Bennett quote a single example of a blood transfusion transmitting HHV8-KS? More importantly, is there a single example of a medical worker contracting KS whilst working with KS patients? Why is AIDS-KS restricted virtually exclusively to homosexual men in the West who use poppers (amyl-nitrites)? Why don't haemophiliacs get KS from Factor VIII? For the same reason that they didn’t get 'HIV' from Factor VIII; it is a physical impossibility due to the manufacture involving cryoprecipitation. Bennett stated regarding the poppers (amyl nitrite) - KS connection: "The issue of poppers in KS has been addressed several times. Ascher et al found no correlation between popper use and risk of AIDS, independant of HIV infection. Others have found that they may have an effect IN ADDITION TO HIV infection and of course the use of poppers during a sexual act that could transmit HHV8, found in all forms of KS, is a reasonable hypothesis!" So why do not heterosexuals get AIDS-KS in the West? You cannot have a pathogen restricted to one group of people: where are the female and male heterosexual cases of Western AIDS-KS? Is Bennett suggesting that HHV-8 causes 'AIDS' type KS in homosexuals but not in anybody else it infects? I challenge Bennett to find me one single case, anecdotal or otherwise, of a hospital worker infected with 'AIDS' or KS as a result of nursing patients? In the case of truly infectious diseases there are invariably examples where nursing staff have been infected and succumbed to the said disease: where are the examples of this happening with AIDS-KS? Bennett inadvertently supports my argument that poppers cause KS: "one study showed a 7-fold higher risk of HHV8 infection in those who used poppers compared to those who didn't." Exactly: poppers (amyl nirtites) are re-activating a ubiquitous latent herpes virus – HHV-8 – and thus it could be argued that if HHV-8 is the cause KS – and is reactivated by the use of poppers then poppers are the cause of KS in homosexuals. Yet Bennett makes the unfounded claim that it is: "…the underlying HHV8 infection that is responsible for KS." Does Bennett suppose that HHV-8 is restricted exclusively to homosexual men in the West? HHV-8 is ubiquitous but usually dormant. Bennett goes on with more unfounded assertions and assumptions about KS: "In contrast to Mr Russell's claim that KS has nothing to do with sexual transmission, this data shows just the opposite". The data show nothing of the kind: KS has never been known or shown to be sexually transmitted: if it were there would be hundreds of thousands of heterosexual AIDS-KS cases in the West by now. Bennett goes on regarding the myth of 'HIV' transmission via discarded syringes: "It is true that bisexuals and homosexual IV drug users who shared needles were thought to lead to a heterosexual explosion in HIV infection. This has in fact been shown to happen, but on a much smaller scale than expected." Precisely: it didn't happen at all. In other words: it just does not happen. Has active, infectious 'HIV' ever been recovered from a discarded syringe? If so, where is this recorded? It is thought to be a possibility that 'HIV' may be transmitted this way but there has never been any scientific evidence to prove it. No doubt also Bennett will remember in detail the anecdotal case of Dr. Veronica Prego, an Argentine-born physician, who received wide spread publicity during the 1980s after she was alleged to have been 'infected' with 'HIV' as a result of a needle stick injury sustained whilst working in a US hospital. However, Dr. Prego could not be specific of the month or even the year the incident is supposed to have happened (if it happened at all) but she nevertheless sued the hospital for negligence and was awarded some six million dollars; she retired to South America and nothing more has been heard of her. It is a pretty safe bet had she died of 'AIDS' we would have heard it by now as a justification for the needle stick theory of 'HIV' transmission. However, there is no evidence that anyone has ever recovered cell-free infectious 'HIV' from a discarded or even shared syringe: this is pure assumption based on a desire to fit the 'HIV' hypothesis. No doubt Nicholas Bennett will recall in the early days of AIDS research it was presumed that a transmissible agent, 'HIV', at that time largely restricted to homosexuals would find its way to heterosexual community via a 'bridging group', bi-sexual men. Nobody considered at that time the patent absurdity of this premise: all STDs have their origin in the heterosexual community and find their way into the homosexual community horizontally through sexual transmission by bisexual men. To argue that a disease originates in a minority group and finds its way into the majority is to argue that water flows up hill. To date: there is not one single recorded example of a health worker nursing 'AIDS' patients contracting either 'AIDS' or 'HIV' or KS despite allegedly being exposed to the infectious agents supposed to cause these conditions. Bennett makes an unfounded assumption: *HIV infection is the only independent predictive factor for the classic AIDS-defining conditions." This is not the case as by 1993 Peter Duesberg cited some 4,600 'HlV' -free AIDS cases (1). An embarrassed Centers for Disease Control rapidly invented a new name for these 'HIV'-free AIDS cases - ICL - Idiopathic CD-4 Lymphocytopenia. In other words, 'AIDS' without 'HIV'. (1) By 1993, at least 4621 HIV-free AIDS cases had been documented in the US, Europe, and Africa with the clinical AIDS definition. Even Jaffe, again upon request, reported 89 HIV-free AIDS cases (per. com., 1993). The cases recorded in Table 1 suffered from one or more of the over 25 heterogeneous AIDS-defining diseases and from AIDS-defining immunodeficiencies without diseases. Some of these proved to be HIV-free even by PCR amplification of viral RNA and DNA. (The HIV Gap In National AIDS Statistics, Peter H. Duesberg, Bio/Technology 11 Aug. 1993). Competing interests: None declared |
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H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett misrepresented what I stated regarding my argument that 'HIV' is a misinterpreted 'HERV': "Mr Russell has missed the point. I shall re-phrase: can he supply the Genbank Accession number and reference the sequence(s) of the HERV(s) which he is proposing activates to create the HIV genome deposited under accession 1906382? If such sequences are not intact (i.e. exist as scattered fragments) can he propose a mechanism by which they would be expressed and recombine to form the full-length sequence? If not, then I politely suggest he has no evidence whatsoever to support his view that HIV is a HERV!" The 'HIV' genome model is science fiction and absurd nonsense. There is no such thing as a definitive 'HIV' isolate to begin with – so how can there be an 'HIV' genome? There is no 'HIV' genome. When it is alleged that 'HIV's recovered from different parts of the same body have differing genomes - which is the true 'HIV' genome? No two identical genomes have ever been recovered - not even from the same individual - so what are they talking about? Typically: viruses which cause disease have identical genomes. There is no gold standard 'HIV' genome because there is no gold standard 'HIV' isolate and no gold standard 'HIV' test. Bennett concluded: "I have pointed out previously that animal retroviruses are sexually transmitted, and in a preferentially male to female pattern [1]. I have also shown that barrier contraception can prevent HIV transmission, which suggests it's an endogenous sexually transmitted retrovirus [2]. 1. Portis et al J Virol. 1987 Apr;61(4):1037-44. 'Horizontal transmission of murine retroviruses.' 2. de Vincenzi N Engl J Med. 1994 Aug 11;331(6):341-6. "A longitudinal study of human immunodeficiency virus transmission by heterosexual partners. European Study Group on Heterosexual Transmission of HIV." These references are pure supposition and speculation and do not prove that retroviruses are sexually transmitted – they are merely assumed to be so: hardly what constitutes concrete evidence. How does Bennett suppose the maedi-visna virus is transmitted? If the paper by de Vincenzi were really true we would have had millions of heterosexual cases of 'HIV' infections in the West by now – 20 years on - but we have nothing of the kind. This alone proved that 'HIV' has to be an endogenous epiphenomenon ('HERV') and is (re)activated in the original 'high-risk' groups whose specific disease conditions cause 'HERV' (aka:'HIV') expression. Padian et. al. seemingly contradicts de Vincenzi emphasising the insignificance of heterosexual intercourse in transmitting 'HIV'. In this 10 year study, the authors state: male-to-female transmission was approximately eight times more efficient, than female-to-male transmission and male-to-female per contact infectivity was estimated to be 0.00090.(1) Inadvertantly, Padian et. al. support my thesis that 'HIV' is a 'HERV' and not an exogenously acquired (sexually transmitted) retrovirus. Reference:(1) Padian NS, Shiboski SC, Glass SO, Vittinghoff E. Heterosexual transmission of human immunodeficiency virus (HIV) in Northern California: Results from a ten-year study. Am J Epidemiol 1997;146:350-357. Of interest Bennett may care to read The Perth Groups challenge to Peter Duesberg on the putative 'HIV' genome: Papadopulos-Eleopulos et. al. Reply to Duesberg (II); Eleni Papadopulos-Eleopulos, Valendar F. Turner, John M. Papadimitriou & David Causer, Continuum, February-March 1997: We gratefully acknowledge Peter Duesberg's criticisms of our paper 'HIV Isolation: Has it really been achieved?'. (1) Before responding it will be useful to define some terms and objectives. 1. 19 'HIV' genomes Duesberg: "...the weakest point of the HIV-non-existentialists is their failure to explain the origin of '19 sequences encompassing the full -length" 10-kb-HIV-1 genome" and "19 full-length HIV genomes"…". (a) Let us repeat that the claim of the existence of "19 sequences encompassing the full length, 10-kb-HIV-1 genome", "19 full-length HIV genomes" is not one of our making but that of the HIV experts we quote. The same experts accept that of the "19 full-length HIV genomes", no two are the same either in sequence or even in length; (b) The question we set out to answer in our critique was not what is the origin of the 19 full-length HIV-1 sequences but does the presently available data prove that these sequences represent the genome of a unique, exogenous retrovirus, HIV? The answer, we repeat, is NO. Nonetheless, although it was not our task to determine the origin of these sequences, we did present a number of alternative mechanisms that science offers as a "rational origin for such sequences" in addition to "viruses or other infectious agents". 2. Odds of assembly "Remember the odds of coming up with even one nucleotide sequence of 9150 bp by chance are astronomically low namely, 1 in 49150 which is very close to 0." It is apparent that we and Peter Duesberg are referring to two entirely different systems, one completely random and the other heavily biased by cell and culture conditions. True, the probability of assembling a particular sequence of RNA (DNA) of 9150 bases randomly selecting each of the four nucleotides is one in 49150 However, this statistical reasoning bears no resemblance to how nucleic acid polymers are assembled either in vivo or in vitro and thus on the probability of finding a particular unique sequence. That this is the case is best illustrated by Spiegelman’s minivariant, a 220-nucleotide stretch of RNA of unique length and sequence which was discussed in our Continuum paper. The probability of assembling such a unique RNA stretch by chance is 1 in 4220, also "very close to 0"" yet, under certain conditions in the laboratory, the Spiegelman minivariant is frequently produced indicating that the assembly of nucleotides is anything but a random process. Furthermore, the 19 unique sequences do not have to be assembled from the four, individual nucleotides. They may result, for example, by recombination of: (a) stretches of pre-existing cellular DNA sequences; (b) stretches of DNA sequences of endogenous retroviruses which form 1% of the cellular DNA, a phenomenon accepted to take place quite frequently and to result in the assembly of novel genomes. It is also accepted that the conditions affect the recombination both qualitatively and qantitatively. It is significant that as far back as 1985 both Gallo and Montagnier accepted that it is not possible to generate "HIV" and the effects attributed to it unless the cells are activated (stimulated) and that this year Chermann and his colleagues showed that the infected cultures contain fragments of the "HIV genome" but after PHA stimulation there is an increase in the "full-length genome" and a concomitant decrease in the fragments. (2) Whatever the odds may be of obtaining by chance the conditions necessary to generate "even one nucleotide sequence of 9150 bp", it is certain not 1 in 49150. 3. Viral genome Duesberg: "The non-HIV-existentialists also fail to realize that available isolation efforts have already adequately identified the 9150 bases as the genome of a virus". ln our extensive search of the HIV literature we could not find even one reference, (although it is possible we may have missed some), in which the HIV genome was reported to of 9150 nucleotides. The closest length was reported Montagnier’s group who, in 1984, reported it to be 9.1 to 9.2 kbases and, in 1985, as 9193 bases. (3,4) lf the 9150 base DNA is the genome of a virus then an absolutely necessary but not sufficient condition is that the virus in all infected individuals will have a length of 9150 bases. Yet, two HIV genomes of the same length have yet to be reported. More importantly, the length of an RNA (DNA) fragment, no matter how often such a fragment is detected, provides no information regarding its origin. The only way to prove it belongs to a unique virus is to isolate a viral particle and demonstrate it has a genome of 9150 bases. This has not been done and the"available isolation efforts" do not contain even suggestive evidence let alone proof that a 9150 base long RNA is a constituent of a particle, any particle much less a viral particle. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett strangely stated: "The KS association with gays in the early part of the epidemic is to me easily explained by the co- epidemic of HHV8 infection in that sexually-distinct group." The fact that it is in a "distinct group" means that it cannot be caused by an infectious agent. An infectious agent cannot be restricted to a specific group of people. Perhaps Bennett may recall in the early days of 'AIDS' it was predicted that bi-sexual males would transmit the supposed causative agent of 'AIDS' to the heterosexual community acting as a bridging group. Had Bennett's theories concerning HHV-8 been true then they would have also conveyed HHV-8 (and KS) into the heterosexual community – if this has been the case then where are the heterosexual examples of KS in the West or even Thailand? It may be of interest to Bennett that the only recorded example of an haemophiliac developing KS occurred in a haemophiliac who was homosexual and addicted to amyl nitrites (poppers). Would Bennett care to explain this? You cannot have a herpes virus restricted to a specific group of people. Homosexuals use amyl nitrites (poppers) far more often than heterosexuals and I would like to remind Bennett that all the original 'AIDS' cases in the United States were homosexuals with KS and all were addicted to amyl and butyl nitrites. Bennett seems to have a blind spot regarding amyl nitrites being a major contributory factor in causing KS. All the homosexuals I knew with KS invariably admitted that they were heavy users of amyl and butyl nitrite inhalents. A mere coincidence? It is not politically correct to state that amyl nitrite causes KS. Poppers make huge profits. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to journal:
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Nicholas Bennett stated: "If HIV is a harmless endogenous phenomenon…Mr Russell has not presented any evidence whatsoever that such a phenomenon is (a) possible and (b) where it comes from." Regarding 'HIV' (or rather 'HERV'): It doesn't come from anywhere: it is already there (in us) but something has reactivated it. I would argue that all 'retroviruses' are endogenous and harmless. If it is 'endogenous' it obviously means that it doesn't come from the outside but rather has been in the human genome for generations but it is only recently that we have developed the scientific ability to detect it. Bennett must learn to distinguish between the finding of novel phenomena and genuinely new phenomena: what we have wrongly classified as 'HIV' has always been there (endogenous) – so why is 'HIV' only now suddenly causing disease? Isn't it rather remarkable that 'HTLV-1' and 'HIV' only started causing disease after we had started to study them: wasn't it kind of them to wait to cause disease - until all those desperate, failed cancer researchers - who had staked everything on retroviruses causing cancer - found themselves a new gravy train to keep their labs funded and going. By the same token, why was smoking only comparatively recently associated with lung cancer when people smoked just as heavily at the end of the 19th century, through World War 1, the roaring 20's, World War 2, the 50's; was there a noticeable increase in lung cancer in these decades? No. Were pushy epidemiologists sleeping during these years? Retrovirologists should have classified 'HIV' as 'HERV' (Human Endogenous Retrovirus) in the first place. Originally Robert Gallo was against the name 'HIV' and wanted the new name to be 'human retrovirus' ('HRV'). It must be remembered that the nomenclature 'HIV' never had unanimous support from Harold Varmus's Human Retrovirus Subcommittee. Nearly half of the members preferred the compound name, HTLV-III/LAV. Others, including Gallo, Essex and Temin preferred 'human retrovirus' (HRV). I advise Bennett, BMJ Editors and the scientific community to stop using the nomenclature 'HIV' and start using the nomenclature 'HERV' (1). Because 'HIV' is merely a 'HERV'. Here is a simple explanation why 'HIV' cannot be a highly infectious exogenous entity as Bennett assumes and supposes. Please will Bennett pay us all the curtsey of reading and mastering Peter Duesberg’s seminal paper quoted below then we can be sure we are all singing from the same hymn sheet. Unless Bennett can understand just what the world's leading authority on retroviruses is saying he should refrain from any further comment. As Duesberg explained in Cancer Research (March 1st 1987), the human genome is littered with innumerable retroviral genomes which lie dormant like so many burnt-out micro-chips; occasionally they maybe stirred into some form of reactivation. What Duesberg does not comment on is if they are reactivated are they then transmissible? I would argue that they are not for several reasons: 1) The number of viral particles expressed is so minute as to be hardly measurable (like 'HIV') so this would not constitute an infectious dose. 2) Duesberg acknowledges that a high percentage of these few viral particles are defective and either a) are incapable of infecting another cell or b) should they infect the cell they are incapable of replication. 3) The Perth Group have shown that mature cell-free retroviral particles shed the outer env gp 120 spikes which in theory are supposed to hook on to the CD4 receptors - thus they are not able to infect another cell. Regarding the alleged 'infection' by 'retroviruses', as far back as 1983, Robert Gallo pointed out that "the viral envelope which is required for infectivity is very fragile. It tends to come off when the virus buds from infected cells, thus rendering the particles incapable of infecting new cells". From this it follows that if 'HIV' is transmitted at all it is transmitted vertically from female to offspring genetically. Many researchers principally Padian et al have shown the difficulty and virtual impossibility of direct horizontal transmission by sexual means of 'retroviruses' – and indeed no one has ever described in precise detail the supposed method of sexual transmission of 'HIV' – it has only ever been a pure supposition to support a mere hypothesis. Bennett, Noble, Flegg and Floyd have still not provided evidence that 'HIV' is an endogenous sexually transmitted retrovirus. It has been repeatedly shown that no animal lentivirus is sexually transmitted – and 'HIV' is allegedly a lentivirus - so why should it be an exception? (1)Reference: 1. Johnson, W.E. & Coffin, J.M. 1999. Constructing primate phylogenies from ancient retrovirus sequences. Proceedings of the National Academy of Sciences, 96: 10254-10260. Abstract: The genomes of modern humans are riddled with thousands of endogenous retroviruses (HERVs), the proviral remnants of ancient viral infections of the primate lineage. Most HERVs are non-functional, selectively neutral loci. This fact, coupled with their sheer abundance in primate genomes, makes HERVs ideal for exploitation as phylogenetic markers. Endogenous retroviruses (ERVs) provide phylogenetic information in two ways: (i) by comparison of integration site polymorphism and (ii) by orthologous comparison of evolving, proviral, nucleotide sequence. In this study, trees are constructed with the noncoding long terminal repeats (LTRs) of several ERV loci. Because the two LTRs of an ERV are identical at the time of integration but evolve independently, each ERV locus can provide two estimates of species phylogeny based on molecular evolution of the same ancestral sequence. Moreover, tree topology is highly sensitive to conversion events, allowing for easy detection of sequences involved in recombination as well as correction for such events. Although other animal species are rich in ERV sequences, the specific use of HERVs in this study allows comparison of trees to a well established phylogenetic standard, that of the Old World primates. HERVs, and by extension the ERVs of other species, constitute a unique and plentiful resource for studying the evolutionary history of the Retroviridae and their animal hosts. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett stated: "The fact that HIV infection precedes a CD4 T cell decline that is not seen in any other human condition is proof enough. It isn't even required that HIV directly kills the T cells, even though it does." Until Bennett can clearly describe the precise mechanism by which 'HIV' destroys cells he is in no position to state that it does so - this is pure speculation. Moreover, 'HIV' is invariably found in people with many other different kinds of antibodies due to concurrent infections with other pathogens: how do we know that one these is not responsible for the killing of T 4 cells? For instance: reactivated herpes viruses are highly cytotoxic. Has Bennett ever found evidence of 'HIV infection' in an individual with no other pathogens present? I very much doubt it. What we are calling 'HIV' is in fact merely an endogenous marker for other pathogens. It is not a "fact that HIV infection precedes a CD4 T cell decline" but mere supposition because there is no such activity as 'HIV infection' to begin with so Bennett's statement is simply an absurd assumption and has no scientific foundation whatsoever. How can an endogenous epiphenomenon ('HIV') be an 'infections' agent in the first place? What evidence does Bennett have that 'HIV' is destroying T cells by 'infection'? There is no empirical evidence cited in a reference paper for this hypothetical assumption: it is no more than speculation, supposition and wishful-thinking on Bennett's part. Harvey Bialy, former Editor-at-Large for Nature Biotechnology and Research Editor of Bio/Technology, asked Dr. Jerold Lowenstein, of the University of California Medical Center, San Francisco, at the symposium, 'The Role of HIV in AIDS: Why There is Still a Controversy' (The Pacific Division of the American Association for the Advancement of Science) on the 21st of June,1994: "You made the statement that HIV replicates in and destroys t-cells. This is the crux of the entire debate. What is your evidence?…What is your evidence that HIV is destroying t-cells by infection? I would love to see it. I've been waiting ten years for it." As entirely expected, there was no response from Dr. Lowenstein. In the late 1980s Luc Montagnier admitted that there was no evidence for 'HIV' directly killing T cells. By April 10th, 1990, Montagnier explained to a researcher colleague that the cell deaths in cell cultures containing 'HIV' were caused by a contaminating mycoplasma. When that was eradicated, using doxycyline, the cell killing stopped despite the fact that the cultures contained 'HIV'. This was clear evidence that this 'strain' of 'HIV' - which had previously been considered cytotoxic - was, indeed, harmless. It is interesting to consider how many other examples in laboratories throughout the world have observed similar 'cell killing' strains of 'HIV' which were in fact due to mycoplasma contamination. When Dr. Shyh-Ching Lo infected four silver leaf monkeys with this same mycoplasma they all developed 'AIDS' like symptoms in short period of time and died. They were not 'infected' with 'SIV'. In conclusion, I advise Bennett to read the following by The Perth Group: A CRITICAL ANALYSIS OF THE HIV-T4-CELL-AIDS HYPOTHESIS by Eleni Papadopulos-Eleopulos,1 Valendar F.Turner,2 John M. Papadimitriou,3 David Causer,1 Bruce Hedland-Thomas,1 & Barry Page1 1: Department of Medical Physics, 2: Department of Emergency Medicine, Royal Perth Hospital, Perth, Western Australia; 3: Department of Pathology, University of Western Australia. Abstract: The data generally accepted as proving the HIV theory of AIDS, HIV cytopathy, destruction of T4 lymphocytes, and the relationship between T4 cells, HIV and the acquired immune deficiency clinical syndrome are critically evaluated. It is concluded these data do not prove that HIV preferentially destroys T4 cells or has any cytopathic effects, neither do they demonstrate that T4 cells are preferentially destroyed in AIDS patients, or that T4 cell destruction and HIV are either necessary or sufficient prerequisites for the development of the clinical syndrome. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Theo HM Fenton stated: "…the views repeated ad nauseam by the HIV- denialists (and the anti-vaccine propagandists) are so outlandish that nobody could possibly take them seriously." On the contrary: the views expressed by the 'HIV' Monotheists are so outlandish that nobody could possibly take them seriously as you will notice when reading the following questions concerning the anomalies, contradictions and paradoxa regarding the redundant 'HIV/AIDS' hypothesis: a) Why is 'HIV' supposed to spread like wildfire in Africa horizontally (heterosexually) but not this way in the West? Why is 'HIV' prejudiced against 'infecting' white heterosexuals in the West? Why is 'HIV' so racist? b) Young girls in the UK are practicing 'unsafe' sex yet are not becoming 'HIV' positive - why not? (Sky News: 24th March. 2005). Teenage STD rates are rising in the UK and USA but there is no endemic 'HIV' epidemic in this group. Why not? c) Why is 'HIV' alleged to have an elastic incubation period of 10 to 30 years? If 'HIV' is meant to be a 'lenti-virus' why is 'HIV' suddenly supposed to be a 'quick-virus' in Africa? How would a 'lenti-virus' survive in nature? Can they explain the eternally long, and unpredictable, incubation period of 'HIV' between so-called 'infection' and 'disease'? d) Why does 'HIV', unlike any other pathogenic virus, only causes disease in the presence of neutralizing antibodies? e) What is their evidence that 'HIV' is destroying t-cells by 'infection'? There is still no empirical evidence or scientific reference paper for this hypothetical assumption - it is no more than pure speculation and wishful (non) thinking. Supporters of the 'HIV/AIDS' Hypothesis - like Fenton, Bennett, Flegg, Floyd (just like politicians and theologians) - can never directly answer questions put to them by the dissenting 'HIV' critics and: 1. say blatantly untrue things 2. say irrelevant things and make unfounded assertions 3. engage in emotive ad hominem attacks 4. speculate and make assumptions 5. ignore and distort points made by the opposition 6. invent outlandish science fictions 7. shift the goal posts and make up the rules of the game Fenton unwittingly demonstrates that 'HIV' Monotheism is more about blind faith than hard science. Today the 'HIV' Industry has much more to do with religion and politics than science, as Phillip Johnson stated: "For essentially political reasons, HIV science has been ruled by unexamined assumptions. It is time at long last to have the scientific debate that wasn't allowed to occur ten years ago. Let the politics be put aside, and let the science begin." I would like to point Fenton to a typical example of what happens when one directly questions the simple-minded 'commonsense' folk-law of 'HIV' Belief as Kary Mullis, the 1993 Nobel Laureate in Chemistry, did. Mullis was writing a report on the use of his PCR invention for 'HIV', when he came across the phrase, 'HIV is the probably cause of AIDS'. In his own words: "I asked the guy sitting beside me, "What is the support for that, what's the reference?" And he said, "You don't need a reference, everybody knows that." "I assumed there must be such a reference, and that there might be a controversy over who got credit for it, because I was under the impression that Gallo and Montagnier might have been fighting over who had first shown that HIV was the cause of AIDS.... I went back over their early papers, and found that neither of them had shown that HIV was the probable cause of AIDS." "And then finally, Luc Montagnier came to San Diego, and gave a talk, and I thought, this guy will know. [laughter] After the meeting I asked him, and he first mentioned the CDC report, and I said I had already looked at it, that it wasn't what I was looking for - that I wanted a scientific paper that would support the notion that HIV is the probable cause of AIDS, not the consensus of a bunch of people who'd already begun looking at it. He said, "Well, let's see ..." (and there was a little knot of people around us at that point, thinking, the man must have an answer to that question), and he said, "Why don't you quote the SIV work?" And I said to myself, "Oh my god! There really isn't such a paper, there can't be, or he wouldn't have to refer ... to a virus that might kill a monkey ... to illustrate the probability that HIV is the cause of AIDS!" (Reference: The Presentations at the HIV Symposium at AAAS Conference; Charles A. Thomas Jr., Kary B. Mullis, and Phillip E. Johnson. "What Causes AIDS: It's an Open Question". Reason, June 1994). Competing interests: None declared |
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| Alexander
H Russell, artist/writer/philosopher WC1N 1PE Send response to
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Tony Floyd stated: "I don't doubt that for a second Dr Fenton - after years of denying the rest of the world's progress in HIV they are unlikely to stop and say 'oh, dammit, there is a virus and it does kill people, how could we have missed that!?'." Tony Floyd is absolutely correct in stating that 'HIV' heretics: "are unlikely to stop and say 'oh, dammit, there is a virus and it does kill people, how could we have missed that!?" – simply because his statement is untrue: there is no "virus" there in the first place and therefore "it" does not "kill people". Tony Floyd then goes on to make a blatantly false statement: "The fact that Peter Duesberg has himself cultured the virus will remain a conundrum for them." This will not "remain a conundrum" for us because Duesberg has not "cultured the virus" and has not been directly involved in 'HIV' research. Duesberg has had to rely on the unproven suppositions, assertions and assumptions of other researchers in the 'HIV' field who have got it all entirely wrong. I suggest Floyd contact Duesberg directly to find out for himself first hand: duesberg@uclink4.berkeley.edu Actually 'HIV' is beneath Duesberg's contempt! Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Theo HM Fenton, Consultant Paediatrician, stated: "A plea to Nicholas Bennett, Tony Floyd, and Peter Flegg: don't waste your time with the denialists - you won't change their views." Yet again we have that tired, quasi-religious nomination, "denialists" used by those theologians who follow the monotheist 'HIV' Belief system. Ironically, Fenton's question is actually directed to Nicholas Bennett, Tony Floyd, and Peter Flegg: "you won't change their views!" Indeed, Bennett, Floyd, and Flegg are today's 'flat-earthers' propagating the majority-establishment belief in 'HIV'. Mr. Fenton concludes: "Perhaps these dissenters are desperately trying to convince themselves that everything's okay. Why not leave them be?" On the contrary: "these dissenters are" not "desperately trying to convince themselves that everything's okay" - nothing could be further from the truth - and the situation is quite the reverse: we are trying to convince the scientific community "that everything is not ok" because 'AIDS' is a multifactorial condition and not caused by a single pathogen - alleged to be 'HIV'. Once it became blatantly clear that the predicted 'AIDS' epidemic in the West was not going to materialise, the 'AIDS' establishment decided to take the show on the road and are today playing it for all its worth in Africa and Asia. TB and malaria have been cynically reclassified as 'AIDS' in Africa – so what was 'AIDS' in Africa before it was TB and malaria? Could Bennett, Floyd, Flegg and Fenton please tell us? There can never be a vaccine against 'AIDS' because you cannot have a vaccine against asbestosis in South African townships, - you simply cannot have a vaccine against Third World living conditions: - poverty, malnutrition, lack of sanitation, etc, which are today being reclassified as 'AIDS'. Whilst in the West, homosexual men have been terrorised into wearing condoms and yet they still get 'AIDS' because they're doing all the recreational drugs. Conversely, heterosexuals in the West clearly are not using condoms – as is proved by the massive rise in STDs and unwanted pregnancies – and yet they do not get 'AIDS'. How do Bennett, Floyd, Flegg and Fenton explain that one – or, rather, get out of that one? In BMJ rapid responses Bennett, Floyd, and Flegg have never been able to explain why there has never been an endemic heterosexual 'HIV' (or 'AIDS') epidemic in the UK. It is obviously not because they are all using condoms. Indeed: it could be well argued that homosexuals use condoms far more than heterosexuals – yet homosexuals still get 'AIDS'. I suggest to Mr. Fenton: everything’s not ok and that we need a multifactorial model for 'AIDS' causation(s). I advise him to read the following by Dr. Roberto Giraldo: AIDS is Neither an Infectious Disease nor is Sexually Transmitted, by Roberto Giraldo, MD, Continuum Spring 1998: The error over the etiology of AIDS was committed in part due to microbiologic prejudice in the mind of researchers, health professionals, journalists, and the public at large. This prejudice comes from the exaggeration of the germ theory of disease promulgated by Pasteur and Koch, which brought many benefits to the medical field at the time. Unfortunately, today they continue to think as at the end of the last century - that all is infectious, that all is contagious, and that it should be a microbe that causes every-thing. The world was prepared by a century of panic over microbes to mistake the etiology of AIDS. It was not possible to avoid it. Another contribution to the error about the cause of AIDS is the failure in research methodology to fulfil epidemiological requirements. None of the postulates on which the infectious hypothesis of AIDS is based fulfil the requirements of the research method. None of the bases of the HIV-AIDS hypothesis has been demonstrated at an objective level. They are theoretical assumptions, created by the minds of those who generate and defend that hypothesis. Practically the entire world has become accustomed to believe all that we are told by the so-called men of science. Currently, the critical and questioning capabilities of 'the people' are null. They do not ask for the necessary proofs for the affirmations that can look objective. The worst epidemic that the contemporary world suffers is an epidemic of crises in the scientific method. It is more extensive than the AIDS epidemic. There will be more consequences unless we take a pathway paved with an authentic objective research methodology. The scientific community has been wrong many times in this century, by considering as infectious diseases that are not - pellagra, scurvy and beriberi. The error currently made with AIDS has a larger magnitude due to the catastrophic repercussions on thousands of people that suffer from this toxic syndrome. Guilt for the error made with AIDS falls on a few researchers and health institutions of the United States government. The majority of people in the world simply believed the so-called men of science. Analysis, understanding and solution of the error will force inter-national medical authorities to rethink their tactics and strategies in the health care of people. This will lead to questions, investigations and solutions to the unfair forms by which men socially relate amongst themselves in modern society, which in the end are the reason for the existence of AIDS. Let us go back to Hippocratic medicine. Let us divulge and stimulate the discussion about the cause of AIDS. Competing interests: None declared |
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infections acquired through heterosexual intercourse in the United
Kingdom: findings from national surveillance
Dougan et al. (11 March 2005) |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Segundo R. Leon stated regarding the Dougan et al. paper: 'HIV infections acquired through heterosexual intercourse in the United Kingdom: findings from national surveillance' (BMJ, 11 March 2005): "When the AIDS epidemic started all the world focus their eyes in the homosexual and gay population as the reason to become infected by the HIV. Now things are changing, heterosexual relationships are increasing the number of people infected with HIV…So, the HIV epidemic is increasing not only in the undeveloped world as in the developed world, the main effort should be focus in the prevention, using condom, promoting abstinence or through promoting fidelity." This is a typical example of misreading the evidence and actually contradicts Dougan et al's findings: which are that there is no endemic heterosexual 'HIV' epidemic in the UK: the vast majority of heterosexual 'HIV' cases are imported from abroad. The UK's alleged and assumed 'endemic HIV epidemic' is "overall" imported from abroad, as Dougan et al. clearly state: "The trends underlying the rapid and substantial increases in HIV diagnoses among heterosexual people in the United Kingdom are complex and sometime misunderstood. Although the number of people becoming infected with HIV through heterosexual intercourse in the United Kingdom is rising steadily, most of the overall rise in HIV diagnoses among heterosexuals is among people who originate from and were infected abroad, mainly in Africa." On critical examination of 'HIV infections acquired through heterosexual intercourse in the United Kingdom: findings from national surveillance' by Dougan et al. (BMJ, 11 March 2005) you will see – yet again – that the vast majority of supposed heterosexual cases of 'HIV' in the UK originate mainly from Africa, where conditions such as TB and malaria are well documented to give an 'HIV' positive test result. The anomaly and paradox that Dougan et al. cannot seem to confront is that why should 'HIV' be so much more infectious in Africa than in the UK? We know it cannot be about condom use since we have huge rises in STD rates in the UK. Dougan et al's findings merely confirm my long-standing argument that 'HIV' simply cannot possibly "acquired through heterosexual intercourse" (as the title of Dougan et al's suggests). If 'HIV' really were an STD it would have 'infected' thousands, if not hundreds of thousands, of people by now – also: if we also take into account that we have recently seen a huge rise in teenage STD rates in the UK. Recent UK 'HIV' figures (Data Source: SOPHID:2003) point to some unexplained anomalies concerning the disproportionate spread of 'HIV'. If 'HIV' is an STD why is it still restricted rigorously to the original 'high-risk' groups like homosexuals? The vast majority of homosexual 'HIV' cases in the UK are white (13,440 out of a total of 15,454); whereas the vast majority of heterosexual 'HIV' cases in the UK are black (11,068 out of a total of 15,998). The media have recently presented the misleading claim that the UK is in the grip of an heterosexual 'HIV' epidemic but what they did not mention is that over 75% of the heterosexual 'HIV' cases were imported from abroad particularly from sub-Saharan Africa, the Caribbean, India, Asia, etc. Why is there such a difference in the distribution of 'HIV/AIDS' in the developed West (including Australia) and the developing world (Africa, India, Asia, etc)? It has nothing to do with so-called 'education' (the 'safe-sex' mantra and “using condoms’ as Segundo R. Leon suggests). Whilst there is obviously no endemic heterosexual 'HIV' epidemic in the UK, inadvertently, what Dougan et al. seem to be suggesting is that 'HIV' is merely a marker for 'risk-behaviour' still rigorously confined to the original 'high-risk' groups: promiscuous homosexuals in the West and people from Africa and the developing world. Thus regarding the supposed 'sexual transmission' of 'HIV', I suggest Segundo R. Leon and Dougan et al. read Nancy Padian, et. al., 'Heterosexual Transmission of Human Immunodeficiency Virus (HIV) in Northern California: Results from a Ten-Year Study,' American Journal of Epidemiology, Vol. 146, #4 (August 15, 1997), pp. 350- 57. This paper makes it abundantly clear that 'HIV' is extremely unlikely to be transmitted horizontally (sexually) in the USA - so why should the UK and Africa be any different? Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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All the recent rapid responses to BMJ's Editorial: 'HIV testing' by Manavi and Welsby (5 March 2005) make the false assumption that the 'HIV' tests are proof of putative 'HIV infection' and/or that 'HIV' is an 'infectious disease' and that 'HIV' is an STD. These are all unproven suppositions. All 'HIV' tests are non-specific and non-standardised. All current 'HIV' tests lack a 'gold standard' against which they could be evaluated to ensure that 'HIV' is being detected. There is no gold standard 'HIV' test because there is no gold standard 'HIV' isolate. In addition to being inaccurate, 'HIV' tests are not standardised. This means that there is no nationally or internationally accepted criteria for what constitutes a 'positive' result. Different countries have different criteria as to what constitutes a 'positive' test result. Standards also vary from lab to lab within the same country and can even differ from day to day at the same lab. Feston Konzani, a 28-year-old African asylum seeker, has has been jailed for 10 years at Teesside Crown Court for allegedly 'infecting' three women with 'HIV'. Feston Konzani was accused of inflicting "grievous bodily harm" on the two women aged 25 and 26 and a young girl of 15. The three women claimed that they became "infected" with 'HIV' after having sex between February 2000 and May 2003 with Konzani. How do they know they were "infected" by Konzani? The horizontal (sexual) transmission of 'HIV' has never been scientifically proven only ever assumed: it is only ever a mere supposition that 'HIV' is sexually transmitted. Also in 2003 Mohammed Dica was convicted at Inner London Crown Court of two counts of 'biological' grievous bodily harm allegedly 'infecting' women with 'HIV' and sentenced to 8 years in prison. How do we know that Feston Konzani and Mohammed Dica are 'HIV' positive and really 'infected' these women? Were viable, active, infectious 'HIV' particles isolated and recovered directly from their blood? If not we are making a false assumption that these incarcerated men have an active 'HIV' infection. Feston's QC, Timothy Roberts, submitted that the convictions were "unsafe" because of "two legal errors", at the Court of Appeal in London. The real grounds for appeal should have been that 'HIV' has not been proven to be transmitted horizontally. Why should 'HIV' be more readily transmitted male to female but not female to male? In which case where do heterosexual males get 'HIV' from? Where does the active (insertive) homosexual get 'HIV' from? How does a passive (receptive) homosexual transmit 'HIV' to an active (insertive) homosexual? What is the precise mechanism of hypothetical 'HIV infection'?. We have seen huge rises in STD rates and unwanted pregnancies in the UK and USA without a concurrent spread of 'HIV'. These anomalies convince me that 'HIV' is not an STD. There is no endemic heterosexual 'HIV' epidemic in the UK. Feston Konzani and Mohammed Dica are innocent of the charges laid against should not be banged up in prison for an alleged crime they did not commit. It is the 'HIV' test that should go on trial for misdiagnosing thousands of people world-wide. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Fiona R Middleton stated: "Many consent forms for HIV testing do not discuss the medical benefits of diagnosing HIV early in the course of the disease." Consent forms for 'HIV' testing also do not discuss the fact that these spurious tests are non-specific and non-standardised. In reply to Fiona R Middleton, Peter Flegg stated unwittingly: "People who know what they are doing, who know what the tests mean and who know what the implications of HIV are must be involved in the feed back of any 'positive' HIV results." In the "feed back" regarding Feston Konzani, a 28-year-old African asylum seeker, who has been jailed for 10 years at Teesside Crown Court for allegedly 'infecting' three women with 'HIV' - what do these "tests mean"? Also in 2003 Mohammed Dica was convicted at Inner London Crown Court of two counts of 'biological' grievous bodily harm allegedly 'infecting' women with 'HIV' and sentenced to 8 years in prison. How do we know that Feston Konzani and Mohammed Dica are 'HIV' positive and really 'infected' these women? Were viable, active, infectious 'HIV' particles isolated and recovered directly from their blood? If not we are making a false assumption that these incarcerated men have an active 'HIV' infection. Feston's QC, Timothy Roberts, submitted that the convictions were "unsafe" because of "two legal errors", at the Court of Appeal in London. The real grounds for appeal should have been that 'HIV' has not been proven to be transmitted horizontally. Why should 'HIV' be more readily transmitted male to female but not female to male? In which case where do heterosexual males get 'HIV' from? Where does the active (insertive) homosexual get 'HIV' from? How does a passive (receptive) homosexual transmit 'HIV' to an active (insertive) homosexual? What is the precise mechanism of hypothetical 'HIV infection'?. We have seen huge rises in STD rates and unwanted pregnancies in the UK and USA without a concurrent spread of 'HIV'. These anomalies convince me that 'HIV' is not an STD. There is no endemic heterosexual 'HIV' epidemic in the UK. Fiona R Middleton should inform her patients that all 'HIV' tests are non-specific and non-standardised. All current 'HIV' tests lack a 'gold standard' against which they could be evaluated to ensure that 'HIV' is being detected. There is no gold standard 'HIV' test because there is no gold standard 'HIV' isolate. In addition to being inaccurate, 'HIV' tests are not standardised. This means that there is no nationally or internationally accepted criteria for what constitutes a 'positive' result. Different countries have different criteria as to what constitutes a 'positive' test result. Standards also vary from lab to lab within the same country and can even differ from day to day at the same lab. Feston Konzani and Mohammed Dica are innocent of the charges laid against should not be banged up in prison for an alleged crime they did not commit. It is the 'HIV' test that should go on trial for misdiagnosing thousands of people world-wide. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Neil D. Macdonald headline for his BMJ rapid response is misleading. "Misconceptions about HIV transmission in the UK: men who have sex with men, not heterosexuals, remain at greatest risk of acquiring HIV in the UK." Why should this be, after a quarter of a century? Why does an allegedly horizontally transmitted virus, 'HIV', remain almost exclusively in one group of people -homosexual men? Why is it more difficult for heterosexuals to be 'infected' with 'HIV' than homosexuals? This is completely illogical. Ruth Ruprecht and her colleagues (1) have shown that 'SIV', and by analogy 'HIV', is infinitely more infectious via oral sex than anal sex. Ruprecht et al stated: "To study oral virus transmission in primate models, we exposed rhesus macaques of various ages to cell-free simian immunodeficiency virus (SIV), including uncloned and molecularly cloned viruses. In neonates, viremia and AIDS developed after nontraumatic oral exposure to several SIV strains. Furthermore, chimeric simian human immunodeficiency viruses containing the HIV-1 envelope can also cross intact upper gastrointestinal mucosal surfaces in neonates. In adult macaques, infection and AIDS have resulted from well-controlled, nontraumatic, experimental oral exposure to different strains of SIV. These findings have implications for the risks of HIV-1 transmission during oral-genital contact." Heterosexuals are having oral sex and yet there is no heterosexual 'HIV' epidemic in the UK. Some 80% of reported heterosexual cases of 'HIV/AIDS' are imported from Africa, the Caribbean, S.America etc. If 'HIV' were a genuine STD it would spread equally through the general population. Why is it assumed that ‘HIV’ is principally spread through semen deposited in the rectum when 'HIV' has never been found in infectious quantities in semen taken from a person deemed to be 'HIV' positive? Why should 'HIV' be more readily transmitted male to female but not female to male? In which case where do heterosexual males get 'HIV' from? Where does the active (insertive) homosexual get 'HIV' from? How does a passive (receptive) homosexual transmit 'HIV' to an active (insertive) homosexual? What is the precise mechanism of hypothetical 'HIV infection'?. We have seen huge rises in STD rates and unwanted pregnancies in the UK and USA without a concurrent spread of 'HIV'. These anomalies convince me that 'HIV' is not an STD. There is no endemic heterosexual 'HIV' epidemic in the UK. Reference: (1) Ruth M. Ruprecht et al, Oral Transmission of Primate Lentiviruses, The Journal of Infectious Diseases, volume 179 (1999), page S408. Competing interests: None declared |
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| Alexander
H Russell, Writer/artist/philosopherw WC1N 1PE Send response to
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I was alarmed and appalled by Trevor G. Stammers' blasé statement: "For many years now, I have been doing HIV tests and Hep B status without making a great song and dance about it with the patient. It is high time this became standard practice." I strongly suggest that Trevor G. Stammers should make a "song and dance about it" and inform his patients that all 'HIV' tests are non- specific and non-standardised. All current 'HIV' tests lack a 'gold standard' against which they could be evaluated to ensure that 'HIV' is being detected. There is no gold standard 'HIV' test because there is no gold standard 'HIV' isolate. In addition to being inaccurate, 'HIV' tests are not standardised. This means that there is no nationally or internationally accepted criteria for what constitutes a 'positive' result. Different countries have different criteria as to what constitutes a 'positive' test result. Standards also vary from lab to lab within the same country and can even differ from day to day at the same lab. Does Trevor G. Stammers know that none of the proteins used in 'HIV' antibody tests are particular to 'HIV' and none of the antigens said to be specific to 'HIV' are found only in persons who test 'HIV' positive. Many people diagnosed as 'HIV' positive do not have these 'HIV antigens' in their blood. I advise Trevor G. Stammers to read what Dr. Valender Turner stated in an interview with Huw Christie: "You just can't put the words 'HIV' and 'antibodies' next to each other and claim you've proved they exist. Or a virus exists. All the test indicates is that some antibodies in patients react with some proteins present in cultures of tissues from the same patients. But given that information what a scientist is obliged to do next is make the comparison with the virus gold standard. Before pronouncing the test highly specific for diagnosing HIV infection. In fact, do you see that the origin of the proteins used in the tests doesn't matter? They don't have to come from HIV. I mean we diagnose Epstein-Barr virus infection without using proteins from the Epstein-Barr virus. Horse red blood cells are not constituents of that virus. What counts is the correlation between certain reactions and the presence or absence of the virus." (Do Antibody Tests Prove HIV Infection? Interview with Dr. Valendar F. Turner by Huw Christie, Continuum winter 1997). The medical literature records over seventy conditions known to give a 'false positive' result on 'HIV' tests. Factors known to cause false-positive 'HIV' antibody test results include: alcoholism, Anti-carbohydrate antibodies, Naturally-occurring antibodies, Leprosy, Tuberculosis, Renal (kidney) failure, Flu vaccination, Herpes simplex I, Malaria, Systemic lupus erythematosus, Organ transplantation, Hepatitis, Haemophilia, Haematologic malignant disorders/lymphoma, Primary biliary cirrhosis, Stevens-Johnson syndrome, T-cell leukocyte antigen antibodies, Proteins on the filter paper, Epstein-Barr virus, Visceral leishmaniasis. The manufacturers of these non-specific and non-standardised 'HIV' tests cautiously state in the literature enclosed with the test kit: "At present there is no recognized standard for establishing the presence and absence of HIV-1 antibody in human blood. Therefore sensitivity was computed based on the clinical diagnosis of AIDS and specificity based on random donors"1 "Do not use this kit as the sole basis of diagnosing HIV-1 infection"2 "The Amplicor HIV-1 Monitor test is not intended to be used as a screening test for HIV or as a diagnostic test to confirm the presence of HIV infection"3 1. Abbott Laboratories, Diagnostic Division, 66-8805/R5; January, 1997 2. HIV-1 Western Blot Kit, Epitope, Inc., Organon Teknika Corporation PN201-3039 Revision #8 3. Roche Diagnostic Systems, Inc., Amplicor HIV-1 Monitor Test Kit. US:83088. June 1996). In conclusion Trevor G. Stammers may like to inform his patients of the following: 'Everyone Reacts Positive on the ELISA Tests for HIV', by Dr. Roberto A. Giraldo Continuum, Winter 1998/9 5(5): 8-10: The following are three possible explanations for why undiluted specimens of blood always react positive at the ELISA test: Since all undiluted blood specimens react positive on the ELISA test, a test that supposedly tests for antibodies to HIV, the results presented here suggest that every single human being has HIV antibodies. And this suggests that everybody has been exposed to HIV antigens. This would mean that all of us have been exposed to the virus that is believed to be the cause of AIDS. The people that react positive even at a dilution of 1:400, would be the ones that have had the highest level of exposure to HIV antigens. The rest of the people - the ones that only react positive with undiluted serum [1:1] - would have had a lower level of exposure to HIV. Everybody has different levels of HIV infection. It is also believed worldwide that a person that reacts positive for antibodies against HIV has not only been exposed to but is infected with a deadly virus that causes immunodeficiency. Therefore, the positive reactions of all undiluted serums would mean that everybody, or at least all the blood samples that I have tested, including my own, are infected with this "deadly" virus. The ones that react positive at a ratio of 1:400 would simply have a higher level of 'deadly' infection than the "deadly" infection had by the ones that only react positive with undiluted serum. The test is not specific for HIV. The results presented here could also mean that the tests used for detecting antibodies to HIV are not specific for HIV, as has been explained previously. In this case, there would be reasons other than HIV infection, past or present, to explain why a person reacts positive to it. The test also reacts positive in the absence of HIV. The scientific literature has documented more than 70 different reasons for getting a positive reaction other than past or present infection with HIV. All these conditions have in common a history of polyantigenic stimulations. Since there is no scientific evidence that the ELISA test is specific for HIV antibodies, a reactive ELISA test at any concentration of the serum would mean presence of non-specific or polyspecific antibodies. These antibodies could be present in all blood samples. They are most likely a result of the stress response, having no relation to any retrovirus, let alone HIV. In this case, a reactive test could be a measure of the degree of one’s exposure to stressor or oxidizing agents. The inevitable conclusion is that all positive reactions for antibodies to HIV are simply false positives. If nobody is positive for HIV, then people who react positive on the ELISA test do so due to something other than HIV. Competing interests: None declared |
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bmj.com
5th March 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Peter Flegg stated regarding Ms. Butler's criticisms of him: "Ms Butler accuses me of 'professional ignorance', claiming I have little idea about..immunity’, or 'how vaccines actually work’ and 'little understanding about host responses and immune mechanisms.'…Competing interests: 8 years undergraduate and postgraduate training and experience in Infectious Diseases in Africa, 9 years subspecialty training and experience in the UK in Infectious Diseases and Tropical Medicine, 3 years postgraduate research leading to an MD thesis on immune dysfunction in drug users, and 8 years experience as a consultant specialising in Infection, Immunodeficiency and HIV Medicine." And yet still after "8 years experience as a consultant specialising in Infection, Immunodeficiency and HIV Medicine" Flegg has not been able to prove to BMJ rapid response readers that 'HIV' is an STD, or even that 'HIV' causes 'AIDS'. Flegg has not been able to explain to BMJ rapid response readers why there is still no white heterosexual 'HIV' epidemic in the UK despite recent huge rises in STD rates. Flegg has never been able to answer any of my questions at BMJ rapid responses regarding my radical 'HIV' critiques here despite his "8 years experience" in the field. Ms. Butler's critical judgements of Flegg are wholly justified in this context. Clearly "8 years experience" has taught him nothing regarding the flaws, paradoxa and anomalies of the redundant 'HIV' hypothesis and Flegg also fails to register that there will never be an 'HIV' vaccine and also that there is no such thing as what he calls "HIV Medicine": there are simply no such entities as 'anti-retroviral' drugs in reality. Does Flegg still support 'HIV' testing? Vaccination makes the immune system lazy. After vaccination the immune system never has to deal with a full-scale antigenic assault. Since the introduction of vaccines medicine has been about the survival of the weakest/sickest. Competing interests: None declared |
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bmj.com
1st March 2005
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| Alexander
H Russell, Writer/artist/philosophera WC1N 1PE Send response to
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David Rasnick is correct in stating that the headline proclaiming the: "Sharp rise in deaths in South Africa is largely due to AIDS" is factually wrong. Surely the headline should have read: "Sharp rise in deaths in South Africa is largely due to TB and Asbestos." Nancy Jacobs, assistant professor of history and Africana studies stated regarding Asbestos in South Africa: "It is arguably South Africa's single largest environmental health catastrophe. In areas where asbestos was mined for decades, the disease burden is staggering. In some areas, it is estimated that over 20 percent of the population is sick." Cynthia Ferguson reported: "A fine — often invisible — dust covers their villages. It finds its way into their schools and houses, blows across their playgrounds, and settles into the earth they till. The dust is asbestos, the lingering vestige of a once thriving industry in South Africa. Although the mines were shut down in the 1990s, they have left a legacy of disease that will continue to sicken and kill South Africans for years to come." (George Street Journal, January 25, 2002). Whilst spending obscene amounts of money on cyto-toxic 'anti- retroviral' drugs for an 'AIDS' epidemic that simply just does not exist in South Africa, the Asbestos tragedy is largely being ignored probably because it is not a profitable enterprise for pharmaceuticals. Recently the South African lawyer and journalist Anthony Brink has initiated the 'anti-AZT' movement in South Africa as reported in the following Sunday Times SA interview (30th January, 2005): THEY said there was no Aids epidemic in Africa. They said that Aids was caused by everything from diesel fumes to exposure to electromagnetic fields, not HIV. And President Thabo Mbeki invited them to help form health policy in South Africa. However, dissidents — claiming that experts had failed to prove a link between HIV and Aids in those four years — vowed to carry their message to the streets. Leaders of the health profession warned that 'crackpot theories' were becoming 'fashionable' among an increasing number of ordinary citizens. This week, the man who first got Mbeki interested in dissident thinking, Advocate Anthony Brink, teamed up with Dr Matthias Rath, a fringe natural-medicine figure, and took to the streets of Cape Town. Forming the newest face of the movement, the pair organised protests with traditional healers against the Treatment Action Campaign, accusing it of being a front for drug companies by ignoring the role of traditional remedies in fighting the disease. Brink also organised a mass meeting in Athlone, Cape Town, on Thursday, putting a new slant — African solutions — on his anti-AZT line. He declared: "I'm completely obsessed with doing all in my power to bring to the attention of the South African public the fact that AZT is deadly poisonous and completely useless." In a series of letters this year, Brink has been trying to convince the Medicines Control Council not to provide AZT and nevirapine to HIV- positive pregnant women. The MCC has never responded. Brink said he still had close links with Tshabalala-Msimang and Mbeki. He said: "It is all a load of rubbish. Aids is not a disease, it’s a syndrome. It is a basketful of primordial diseases including common diseases like TB." (Sunday Times SA By Rowan Philp and Edwin Lombard: abridged). Competing interests: None declared |
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bmj.com
28th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Peter Flegg stated: "Russell has merely confirmed this is exactly what Lanka stated - and further he goes on to detail how Lanka considers that viruses such as Influenza, Herpes, Vaccinia, Polio, Adenovirus and Ebola virus do not exist (specifically 'an attempt of fraud committed by the researchers and medical scientists involved'). Perhaps these viruses also are considered by Russell to be "endogenous epiphenomena"? I look forward to his explanation as to how lifestyle factors alone are responsible for the diseases they cause." Peter Flegg repeatedly fails to understand what Stefan Lanka and I are arguing: how do we really know what we are nominating as 'viruses' really are 'viruses' that is all. How does Flegg know that: Influenza, Herpes, Vaccinia, Polio, Adenovirus and Ebola are true 'viruses': or are they really some other mutations that have not been truly identified and classified correctly? Contrary to Flegg's claim, I am not nominating these unidentifiable entities as "endogenous epiphenomena." Also I have not said that "lifestyle factors alone are responsible for the diseases they cause." My question to Flegg is: do diseases cause viruses? Does 'AIDS' cause (endogenous) 'HIV' expression? We know now that 'HIV' is not a 'virus' because it does not cause a disease: however 'anti-retroviral' drugs are able to do what 'HIV' never could do: cause 'AIDS'. Flegg will go on at BMJ rapid responses pretending that 'HIV' causes 'AIDS' because it is his job to do so and he cannot confess to his patients that he may have made a tragic error. Flegg is trapped within the 'HIV' Belief System without an emergency escape exit. Competing interests: None declared |
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bmj.com
25th February 2005
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| Alexander
H Russell, artist/writer/philosopher WC1N 1PE Send response to
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Peter Morrrell asks Alexander Russell regarding the nature of 'viruses': "Why does he think it is obvious or blatantly obvious that all other viruses are not also 'epiphenomena,' 'disease markers' or 'endogenous entities?' Just as he states about retroviruses, these entities are *assumed* to be pathogenic, they are assumed to be causes of disease states, NOT the products of disease states. How is the causation of their pathogenicity so solidly proven? How is it proven that they are not also products or mere 'associative factors' rather than causes of disease processes? Why cannot what Alex Russell says about retroviruses also apply to many other or indeed all viruses? Why are all viruses not 'endogenous epiphenomena' or 'disease markers' and therefore merely associative factors and *products* rather than causes of disease processes? What is the big objection, seeing that he agrees with my previous contention that deranged cells perhaps produce viruses?" Peter Morrell's interesting and thought provoking questions are principally answered in my recent rapid response replies to Peter Flegg. See: 'Peter Flegg grossly misrepresented Stefan Lanka out of context' (BMJ rapid response: 24th February 2005) and: 'Reply to Flegg regarding 'retroviruses'…' (BMJ rapid responses: 23rd February 2005). We have to keep on asking: is the proliferation of an alleged 'virus' the symptom of a disease or a cause of a disease? We are told that the rhinovirus causes the common cold but how do people who have been completely isolated catch the common cold? Where do 'viruses' start? All 'viruses' have to start somewhere: we have to think in terms of how 'viruses' are vectored. But how do we nominate what a 'virus' really is to begin with? Most of us know now that 'HIV' is not a 'virus' and we also know now that 'retroviruses' are not 'viruses'. Is the so-called 'Ebola virus' a true 'virus'? We have to deconstruct the taxonomic classification system that designates and nominates what a 'virus' really is. Also: we need to de-subjectivise’ and de-ontologise 'viruses' and relocate the negativity of 'viruses' in a positive light: the 'negative-dialectic' of a 'virus' as Theodor Adorno might have said. A 'virus' has a job to do and has its own logic for doing so: a 'virus' needs to erase, eradicate, deconstruct something for its own ends. As human beings we subjectivise and ontologise 'viruses' (like 'cancers') as 'bad' things or as 'enemies' to be eradicated. Obviously 'viruses' and 'cancers' are seen in a 'negative light' by most human beings. Yet 'cancers' and 'viruses' are merely doing their own thing as transformers of being in the world. There is a school of thought that 'viruses' are a cleansing device expelling waste matter from cells. We need to rethink what a 'virus' is and learn to relate to 'viruses' as a part of our evolving being in the world. As constantly mutating human beings we could be said to be 'viruses' in ourselves: maybe 'Virus' is the very core of our being just like 'Geist' or 'Spirit'? What are 'viruses' (and 'cancers') trying to tell our embodied being anyway? What we should be asking is: Why does the human body need 'viruses' and 'cancers'? That is the question. Peter Morrell may find Virologist, Stefan Lanka’s succinct summary on the nature of viruses and virology of interest: A little virology Viruses are essentially just packages of genetic information enclosed in a coat which consists of proteins. They can reproduce themselves only by infecting a suitable host cell and appropriating the chemical machinery they find there. The proteins making up the viruses are characteristic for each species of virus. Apart from enveloping and transporting the genetic information intact, the composition of proteins for a given virus results in a specific shape for the virus particle. This much is generally known. Less well-known is the existence of other particles which look like viruses but aren't, and are nonchalantly referred to as "virus-like" particles. Such particles are far from rare, found, for example, always in placentas, and very frequently in the artificial environment of laboratory cell cultures. They have served to muddy the waters considerably as far as AIDS research is concerned, because particles just like these have been called HIV. To date, none of these has been characterised and shown to exist as an entity which one may justifiably call a virus. No evidence for the existence of HIV Such evidence has up till now never been produced for HIV. No photograph of an isolated HIV particle has ever been published nor of any of its proteins or nucleic acids. No control experiments as mentioned above have been published to date. What has been shown are photographs of virus-like particles in cell cultures, but none of isolated viruses, let alone of a structure within the human body having the shape ascribed to HIV. What the whole world has seen are models representing HIV with dish aerials, said to be receptors with which the virus attaches itself to cells. (HIV; REALITY OR ARTEFACT?, Stefan Lanka, Continuum, April/May 1995). Competing interests: None declared |
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bmj.com
24th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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For the second time at BMJ rapid responses Peter Flegg has grossly misrepresented Stefan Lanka by citing him out of context: "Forgive me if I find it quite ironic that a writer/artist/philosopher (Russell) suggests to a postdoctoral PhD fellow in Infectious Diseases (Bennett) that he should sadly obtain "some form, any form, of education in the field" in order to appreciate that HIV does not exist, while quoting a "virologist" (Lanka) who believes that "viruses which are claimed to be very dangerous in fact do not exist at all" as the source for his evidence." I do not "find it quite ironic" but merely a public display of Flegg's ignorance here: one has to study virology in the first place to realise where virology has gone wrong. Lanka does not lazily accept our dominant fashionable virological paradigms where as Bennett and Flegg do: they believe what they are told in text books. Flegg, as a physician, and Bennett, as a postdoctoral PhD fellow in Infectious Diseases, have a curiously naïve and layman's 'commonsense' world view of what constitutes 'virology' and 'viruses': they still believe what they are told in text books without doing their own deconstructive critiques. Yet again (see BMJ rapid responses: 1st November, 2004) Flegg lifts quotes out of context and thus distorts the meaning of what Lanka and I are actually saying. My original quote was from Dr, Stefan Lanka was: "I already had a somewhat critical attitude when I started studying molecular genetics, so I went to the library to look up the literature on HIV. To my big surprise, I found that when they are speaking about HIV they are not speaking about a virus. They are speaking about cellular characteristics and activities of cells under very special conditions. I was so deeply shocked…So for a long time I studied virology, from the end to the beginning, from the beginning to the end, to be absolutely sure that there was no such thing as HIV. And it was easy for me to be sure about this because I realized that the whole group of viruses to which HIV is said to belong, the retroviruses - as well as other viruses which are claimed to be very dangerous - in fact do not exist at all." (Stefan Lanka interviewed by Mark Gabrish Conlan, Zenger's Magazine, San Diego -October 1998). Lanka raises legitimate questions here that need to be addressed: what exactly is a 'virus'? What evidence is there that 'Ebola' is a real isolated 'virus'? It could even be argued that Ebola was a man made laboratory artefact, as Dr. Leonard G. Horowitz has claimed? (See: Dr. Leonard G. Horowitz, Emerging Viruses: AIDS and Ebola - Nature, Accident or Genocide?, Tetrahedron Publishing Group, 1996). I ask Flegg: what constitutes a 'virus'? Who authorises the peer- reviewing and policing of the taxonomic classification of 'viruses'? Who in authority authorises the authors of 'viruses'? What is a 'virus'? What are the 'politics' of 'virus' inventing? After all: today science is totally corrupted by politics. Who says so? To clarify the complex situation to Flegg I conclude with what Stefan Lanka wrote in December 2001: "In the case of the influenza- herpes-, vaccinia-, polio-, adeno- and ebola-viruses each photo shows only a single particle; nobody claims that they´re isolated particles, let alone particles that have been isolated from humans. In summary, it must be said that these photos are an attempt of fraud committed by the researchers and medical scientists involved, as far as they assert that these structures are viruses or even isolated viruses. To what extent the involved journalists and authors of textbooks have contributed to this fraud knowingly or only out of gross negligence, I don´t know. Everyone who starts a researcher in the medical literature, will quickly encounter statements and references that Koch´s first postulate can´t be fulfilled (i.e. Großgebauer: Eine kurze Geschichte der Mikroben, 1997 ["a little story of the microbes"]; editor: Verlag für angewandte Wissenschaft). How these authors who claim the existence of viruses could overlook that, remains a riddle. Could it be that the term 'Contagium' = 'Gift' (poison/toxin) = 'Virus' from the 18th and 19th century was applied in the 20th century to the cell components which were named 'viruses' since the electron microscope was introduced in 1931? And in order to hide this, the 'disease causing viruses' have often been described but never been isolated? And then they were used as seemingly logical explanation for poisonings and adverse affects of vaccination, as Luhmann (1995) (i.e.) writes about the symptomatic of Hepatitis B, which was observed for the first time in 1985 following smallpox vaccinations, and 1938 following measles vaccinations? The copies in the textbooks show only structures within cells and nothing that looks like isolation and thus homogenous. The biochemical characterization, which is crucial, lacks completely." (Dr. Stefan Lanka Exposes The 'Viral Fraud': Pictures of 'Isolated Viruses' Debunked, December, 2001). Flegg, as a physician, and Bennett, as a postdoctoral PhD fellow in Infectious Diseases, are obviously not going to admit that they made a tragic mistake and inform patients and the public alike that 'HIV' is not an 'infectious virus' but endogenous epiphenomenon: they are interpellated and seemingly trapped within the 'HIV' paradigm and refuse to re-educate themselves but continuously repeat the mythical 'HIV' mantra. The taxonomic classification of 'HIV' (22-23 May, 1986) was ostensibly a political move and a strategic invention to present a nomenclature that would unify a diversely identified putative 'retrovirus': human T-cell lymphotropic virus type III ('HTLV-III'), immunodeficiency-associated virus ('IDAV'), aids-associated retrovirus ('ARV') and lymphadenopathy-associated virus ('LAV'). The not so hidden agenda behind this politically expedient move was to enforce the 'belief' that an alleged 'human retrovirus' caused 'immunodeficiency'. Thus the manufacturing of 'HIV' hegemonic (misinformed) consent reinforced a 'retroviral' episteme for 'AIDS' causation. However, to date, 'HIV' has still not proved to be a human immuno-deficiency virus. If the function of a name is to designate its individuality, then clearly 'HIV' was a baptism by mistaken identity. The moment of fictional baptism was reported in Science (Harold Varmus et al., 9 May, 1986), in which eleven of the thirteen members of a subcommittee - ("empowered by the International Committee on the taxonomy of Viruses") - nominated 'HIV'. I would like to remind Flegg and Bennett that there was no isolated evidence then (as now) that this material was a putative 'retrovirus' that caused 'immunodeficiency'. The acronym 'HIV' is misleading and meaningless and should no longer be used by scientific journals and the scientific community and the mass media alike. Competing interests: None declared |
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bmj.com
23rd February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Flegg stated: "Alexander Russell writes: What isolated evidence does Nicholas Bennett have that 'retroviruses' really exist? and Sadly if Bennett had some form, any form, of education in the field he would know better and realise that 'retroviruses' do not exist. The Friend murine leukemia virus is a retrovirus or should I write a 'retrovirus'. Make up your mind! Did de Harven record electron micrographs of Friend leukemia complex or not?" Yes: whatever kind of particles they were, de Harven recovered them form mice but they were wrongly nominated as 'retroviruses'. I advise Flegg that he should write 'retrovirus' in single inverted comas as this nomenclature is a misclassification. Why were alleged 'animal retroviruses' only found in specific groups of deliberately bred laboratory animals? Why did alleged 'retroviruses' only start causing human disease once the intensive study of 'retroviruses' begun? Doesn’t it strike anyone how fortuitous it was that just as we began to study 'human retroviruses' so carefully we should discover two new disease – both as 'novel' as the 'retrvoriuses' alleged to cause them? For one to have been found would have been amazing – but two? I don't buy it. Or could it be that they had to invent two new diseases – 'Adult T-cell Leukaemai' and 'AIDS' in order to justify wasting tax payers money on a hitherto fruitless scientific endeavour: 'retrovirology'? I suggest that the 'scientific community' stop using the nomenclature 'retrovirus' and the acronym 'HIV' as they are misclassified objects of taxonomy. Neither of the two alleged 'human retroviruses' encodes an oncogene. Again I must refer Flegg to Peter Duesberg's paper of Cancer Research, March 1st, 1987: he points most emphatically that 'HTLV-1' originally alleged to cause 'Adult T-cell Leukaemia' (a disease unknown to medicine before the mid 1970’s) cannot possibly be the cause of cancer for three main reasons: 1) There is no evidence that cancer is transmissible – infectious disease 2) The 'HTLV-1' is alleged to infect cells, randomly inserting its genome so that no two cells are infected in the same place. This should predict that if 'HTLV-1' were to cause cancer the resulting cancers would be polyclonal. However, all naturally occurring cancers are monoclonal. 3) 'HTLV-1' is profoundly conventional 'retrovirus' which does not encode an oncogene. It is worth remembering that Peter Duesberg and his colleague Peter Vogt were the discoverers of oncongenes and therefore should know what they are talking about. Competing interests: None declared |
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bmj.com
21st February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Regarding 'endogenous entities' and 'epiphenomena' Peter Morrell stated: "I thank Alex Russell for explaining what 'epiphenomenon' and 'endogenous entity' mean in regard to HIV…However, he has not said if this theory proposes that ALL viruses should be regarded as 'epiphenomena,' 'disease markers' and 'endogenous entities,' or whether this idea should be confined solely to the so-called retroviruses?" I thought it was blatantly obvious that not all 'viruses' are an 'epiphenomena,' 'disease markers' and 'endogenous entities'. I was writing specifically about 'HIV' and 'retroviruses' which are these 'epiphenomena', 'disease markers' and 'endogenous entities' - and which were wrongly classified as 'viruses'. Peter Morrell concludes: "Can Alex Russell please therefore also explain what makes this theory of AIDS superior to the standard HIV theory? In particular, can he state what specific facts of the disease this theory explains better, more clearly and neatly than the standard HIV hypothesis? Or, to put it another way, what facts of the disease are not satisfactorily explained by the HIV hypothesis that the epiphenomenon idea explains better? I thank him in advance for these further clarifications." All Peter Morrell's questions are best answered by Peter Duesberg's superior drug/AIDS hypothesis which better explains 'AIDS' than does the redundant 'HIV/AIDS' hypothesis. All the predictions based upon the 'HIV/AIDS' have been proven wrong. We have also had thousands of 'HIV' - free 'AIDS' cases therefore 'HIV' fails to meet Koch's first postulate. Duesberg's first three parts to his theory rely on Koch's 1st, 2nd, 3rd postulates: (1) free virus is not detectable in most cases of AIDS; (2) virus can only be isolated by reactivating virus in vitro from a few latently infected lymphocytes among millions of uninfected ones; (3) pure HIV does not cause AIDS upon experimental infection of chimpanzees or accidental infection of healthy humans. The standard and simplistic 'HIV' theory also does not explain why 'AIDS' is solely restricted to specific 'high-risk groups' proving also that 'HIV' is not an STD: there is no white heterosexual 'HIV' epidemic in the West. We must go back just before 'AIDS' was invented to1981 when five young homosexuals, who were previously healthy, were diagnosed as having Pneumocystis carinii pneumonia (PCP). Soon after these cases another twenty-four young homosexuals were diagnosed as having Kaposi's sarcoma (KS) and these cases initiated the term 'Gay Related Immune Deficiency', or 'GRID'. In all these cases all the young homosexuals were heavy recreational drug users, particularly 'poppers' (amyl nitrites) and the correlation between KS and popper-use is 100%. Why is it that only homosexuals who use poppers get KS? It is as absurd as saying that they all drank cyanide but only died because they had 'HIV'. To try and blame KS on a novel herpes virus is ludicrous because you cannot have a herpes virus restricted to one group of people. By the early 1980s it was not seen as 'politically correct' to state that recreational drugs cause immune damage and premature death so 'HIV' was soon invented to take the blame (and the heat off the homosexuals) and the dangers of recreational drug-use were tragically ignored and soon forgotten. Hence: 'HIV' was purely an invention of 'political correctness' and the social construction of an 'equal opportunities disease'. It must be remembered that all the first 'GRID' and 'AIDS' cases were heavy consumers of recreational drugs and the 'AIDS' establishment at the time saw the 'drug/AIDS' hypothesis as a viable contributory explanation of these early cases. Recreational drugs are known to cause endogenous 'HIV' expression. A recent 'scare story' from New York alleging a new 'super strain' of 'HIV' was (mis) 'diagnosed' from a man in his mid forties who took crystal methamphetamine. Crystal methamphetamine is oxidative, it depletes glutathione and induces apoptosis/cell death and depletes CD4's and cultures and activates endogenous 'HIV' expression. Crystal methamphetamine, an addictive stimulant, itself depletes the immune system (not 'HIV'). Regarding this spurious 'super strain' of 'HIV', a cynical Dr. Robert Gallo stated: "The odds are enormous that it is not going to go anywhere." Here is a summary of Peter Duesberg's drug/AIDS hypothesis which should answer Peter Morrell's questions neatly and eloquently. The AIDS Dilemma: drug diseases blamed on a passenger virus, by Peter Duesberg & David Rasnick, Genetica 104: 85-132. 1998: Almost two decades of unprecedented efforts in research costing US taxpayers over $50 billion have failed to defeat Acquired Immune Deficiency Syndrome (AIDS) and have failed to explain the chronology and epidemiology of AIDS in America and Europe. The failure to cure AIDS is so complete that the largest American AIDS foundation is even exploiting it for fundraising: 'Latest AIDS statistics 0,000,000 cured. Support a cure, support AMFAR.' The scientific basis of all these unsuccessful efforts has been the hypothesis that AIDS is caused by a sexually transmitted virus, termed Human immunodeficiency virus (HIV), and that this viral immunodeficiency manifests in 30 previously known microbial and non- microbial AIDS diseases. In order to develop a hypothesis that explains AIDS we have considered ten relevant facts that American and European AIDS patients have, and do not have, in common: (1) AIDS is not contagious. For example, not even one health care worker has contracted AIDS from over 800,000 AIDS patients in America and Europe. (2) AIDS is highly non-random with regard to sex (86% male); sexual persuasion (over 60% homosexual); and age (85% are 25-49 years old). (3) From its beginning in 1980, the AIDS epidemic progressed non- exponentially, just like lifestyle diseases. (4) The epidemic is fragmented into distinct subepidemics with exclusive AIDS-defining diseases. For example, only homosexual males have Kaposi's sarcoma. (5) Patients do not have any one of 30 AIDS-defining diseases, nor even immunodeficiency, in common. For example, Kaposi's sarcoma, dementia, and weight loss may occur without immunodeficiency. Thus, there is no AIDS -specific disease. (6) AIDS patients have antibody against HIV in common only by definition-not by natural coincidence. AIDS-defining diseases of HIV-free patients are called by their old names. (7) Recreational drug use is a common denominator for over 95% of all American and European AIDS patients, including male homosexuals. (8) Lifetime prescriptions of inevitably toxic anti-HIV drugs, such as the DNA chain-terminator AZT, are another common denominator of AIDS patients. (9) HIV proves to be an ideal surrogate marker for recreational and anti-HIV drug use. Since the virus is very rare (< 0.3%) in the US/European population and very hard to transmit sexually, only those who inject street drugs or, have over 1,000 typically drug-mediated sexual contacts are likely to become positive. (10) The huge AIDS literature cannot offer even one statistically significant group of drug-free AIDS patients from America and Europe. In view of this, we propose that the long-term consumption of recreational drugs (such as cocaine, heroin, nitrite inhalants, and amphetamines) and prescriptions of DNA chain-terminating and other anti- HIV drugs, cause all AIDS diseases in America and Europe that exceed their long-established, national backgrounds, i.e. >95%. Chemically distinct drugs cause distinct AIDS-defining diseases; for example, nitrite inhalants cause Kaposi's sarcoma, cocaine causes weight loss, and AZT causes immunodeficiency, lymphoma, muscle atrophy, and dementia. The drug hypothesis predicts that AIDS: (1) is non-contagious; (2) is non-random, because 85% of AIDS causing drugs are used by males, particularly sexually active homosexuals between 25 and 49 years of age, and (3) would follow the drug epidemics chronologically Competing interests: None declared |
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bmj.com
20th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Regarding David Ho's debunked 'virological mayhem model' Nicholas Bennett stated: "Ho et al found 3,500 tissue-culture infectious doses of HIV per milliliter of peripheral blood. How much HIV would Mr Russell like?" The 'gung-Ho' theory purporting to show 'high viral titres' was completely demolished within a very short time, not least by a letter from Peter Duesberg and Harvey Bialy grudgingly published in Nature (375, 1995, p. 197). It is worth quoting at length: "The senior researcher [George Shaw] of the Wei et al paper has previously claimed that the method they used overestimates by at least 60,000 times the real titre of infectious HIV [Piatak et al, Science, 259, pp 1749-1754, 1993]. 100,000/60,000 is 1.7 infectious HIV's per ml ... Further, Ho and a different group of collaborators have just shown [Cao, et al New Eng. J. Med 332, pp 201-208, 1995] that more than 10,000 'plasma virions', detected by the branched-DNA amplification assay used in their Nature paper, correspond to less than one (!) infectious virus per ml. And infectious units, after all, are the only clinically relevant criteria for a viral pathogen.” [my emphasis] Moreover, David Ho's mathematical calculations have been challenged by Prof. Serge Lang, the greatest mathematical mind in America, as being rubbish, a typical example of a gigo – 'garbage in, garbage out' - Lang stated: "Ho and Shaw (among other authors) engage in the practice of throwing math and statistics at people, pretending to give a mathematical model for HIV infection and its purported effects, namely the destruction of CD4 T- cells. There is developing a substantial history of criticisms of these papers. We have already mentioned some criticisms in the preceding section, concerning control groups. We now list other criticisms which have developed over the last five years." (The Case of HIV: We Have Been Misled, Serge Lang, Yale Scientific, Spring 1999, Volume 72, Nos. 2 & 3, pp. 9-19). According to Mark Craddock, (School of Mathematics, University of New South Wales, Sydney), the Nature papers (12 January, 1995) by Wei et al (Viral dynamics in human immunodeficiency virus type 1 infection ) and Ho et al (Rapid turnover of plasma virions and CD4 lymphocytes in HIV-1 infection) should have failed peer review for the following reasons alone: 1) Obvious mathematical errors, 2) Unjustified assumptions unrelated to the empirical data, 3) Lack of control groups: (a) "Neither group compared the rate of T4 cells generated in the HIV positive patients with HIV negative controls", (b) "It must surely be admitted that the system they are trying to study, namely the interaction of HIV with T4 cells, might behave substantially differently in people who are not being pumped full of new drugs, in addition to 'antiretrovirals' like Zidovudine?" Yet these flawed papers got past the peer reviewers and instigated the fatal consequences of 'early intervention' ('hit early, hit fast') which translated is a cynical marketing strategy for the 'anti-retroviral' drug pharmaceuticals. It could be argued that David Ho's 'virological mayhem model' was only ever devised to hard-sell 'anti-retroviral' drugs in asymptomatic patients. Here is Mark Craddock's critique of the Ho and Shaw Nature papers: "The logic [of Ho and Shaw] here is remarkable. It is claimed that HIV sends the immune system into overdrive as measured by a supposedly accelerated production of T4 cells...But where are the healthy controls? How can this production of T cells be ascribed to HIV if there is no comparison made with healthy people? And even if there were a comparison, how can the production be unambiguously attributed to the ‘battle’ with HIV?...Does what Shaw and Ho say actually make sense?... Is their mathematical analysis sound?...As a mathematician, I was intrigued by the claim of John Maddox, editor of Nature, that the new results provide a new mathematical understanding of the immune system. Unfortunately, my confidence in this claim was badly shaken when it turned out that on the very first page of the Shaw paper (Wei et al., p 117) they make an appalling mathematical error. And in the same paragraph make an assumption which turns out, by their own admission to have no basis in observation, and which they give no justification for...They are trying to estimate viral production rates by measuring viral loads at different times and trying to fit the numbers to their formula for free virus. But if their formula is wrong, then their estimates for viral production will be wrong too..." ('HIV: Science by Press Conference', AIDS - Virus or Drug Induced?', Kluwer Academy, 1996). Craddock concludes in his analysis of the flawed Ho and Shaw papers: "Ho uses the analogy of a sink with water pouring into it but the drain is open. He argues that the virus is killing slightly more cells than the body can replace and so you get a slow decline in T cells. In terms of his analogy, the water flows out of the sink slightly faster than it flows in. A better analogy would be that as the water level drops, the drain gets bigger. So the process speeds up. Ho and Shaw’s data if you read it correctly predicts that AIDS should develop in a matter of days after infection or at most a few months. This is what exponential growth is all about. The virus grows exponentially, doubling in number every 2 days in the absence of an immune response they say. So when the immune response is weakest, before antibody production, it should kill every T cell in the body quickly. This does not happen. I wonder how they explain this?" (Analysis of the Ho and Shaw Papers, Mark Craddock PhD, School of Mathematics, University of New South Wales, Australia). If Ho and Wei were correct, it would be possible to pellet down virions from fresh plasma taken from a person who has had a recent 'high viral load' test result, and to see tightly packed identical viral particles using EM, but so far this has never been achieved with HIV'. And again: if Ho's 'viral mayhem model' was correct, why, in the previous decade of 'HIV' research, did no one ever see these alleged 'high viral titres'? More importantly, why, in the presence of these teeming quantities of putative 'virus' did they need to amplify it using PCR to find it at all – especially if 'HIV' is deemed to be at such high titres? Bennett concludes: "HIV has certainly been isolated to extraordinary levels of purity from lab cultures of peripheral blood and lymph nodes." Precisely - but never in pure culture, always in co-culture, utilising cell lines which are themselves suspected of harbouring virus. It is also worth remembering that cultures exclude anything resembling an immune response or any form of viral inhibitor. Cultures produce artefacts which are very easily misinterpreted – "To culture is to disturb"! Contrary to Bennett's unfounded claim, 'HIV' has never been recovered and purified from a fresh blood or semen sample. 'HIV' has certainly not been truly isolated. As Peter Duesberg stated in 1987, 'HIV' is restricted to virtually complete latency by antibodies and a latent 'virus' cannot cause a disease. Competing interests: None declared |
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bmj.com
20th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Bennett stated: "RNA viruses (with the exception of the retroviruses which must integrate) do largely replicate in the cytoplasm, since this is far easier than trying to enter the nuclear membrane and there are reasonable numbers of free ribonucleotides in the cytoplasm." What isolated evidence does Nicholas Bennett have that 'retroviruses' really exist? Dr. Stefan Lanka, virologist and molecular biologist, stated: "I already had a somewhat critical attitude when I started studying molecular genetics, so I went to the library to look up the literature on HIV. To my big surprise, I found that when they are speaking about HIV they are not speaking about a virus. They are speaking about cellular characteristics and activities of cells under very special conditions. I was so deeply shocked…So for a long time I studied virology, from the end to the beginning, from the beginning to the end, to be absolutely sure that there was no such thing as HIV. And it was easy for me to be sure about this because I realized that the whole group of viruses to which HIV is said to belong, the retroviruses - as well as other viruses which are claimed to be very dangerous - in fact do not exist at all." (Stefan Lanka interviewed by Mark Gabrish Conlan, Zenger's Magazine, San Diego -October 1998). What we are wrongly calling 'retroviruses' are in fact the body's own creation: what I nominate as 'endogenous entities' or an 'epiphenomenon'. Sadly if Bennett had some form, any form, of education in the field he would know better and realise that 'retroviruses' do not exist. No photograph of an isolated 'HIV' particle has ever been published and yet Bennett 'believes' it has but without offering us the evidence. Competing interests: None declared |
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bmj.com
18th February 2005
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| Alexander
H Russell, artist/writer/philosopher WC1N 1PE Send response to
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Peter Morrell stated: "Several times in his recent posts Alex Russell has referred to HIV as "an epiphenomenon" and the viruses purportedly involved as 'endogenous entities.' Can he please explain in greater detail what he means by these terms?" An epiphenomenon is an associative factor found in a disease which cannot be shown to be either causative or contributory to said disease – association is not proof of causation. Morrell continues: "For example, as I provisionally grasp this idea, does he mean to say that viruses are simply random products of deranged cells?" In some cases, yes, they are - where viral proteins can be shown to originate in the nucleus of the cell. Most viruses replicate in the cytoplasm. Morrell continues: "Does he then further mean to say that such 'endogenous entities' cannot realistically be regarded as the *causes* of a disease process, but that they might be better understood as mere 'associative factors' or even products of a disease? It would be very helpful if Alex Russell could clarify these points." It would seem that endogenous viruses are activated or released in response to a prior disease condition. This may be the case with hepatic viruses which are released by the liver and subsequently interpreted to be the cause of the liver disease: i.e: hepatitis. In other words the liver becomes diseased for other reasons - pathogenic assault, alcoholism, etc. and then may release endogenous virus particles in response to the disease rather than instigating the disease. However, hepatitis viruses when generated replicate at a huge rate and massive titres are recorded; this has never been the case with 'HIV'. It is high time that many of the cherished assumptions about virology be re-examined – not least assumptions concerning so-called 'retroviruses'. For instance is 'HIV' a lentivirus or not? If 'HIV' is never found at a sufficient titre in vivo to be considered an infectious dose – some 200 particles or more per ml of blood etc. - then it is unlikely to be transmitted horizontally or only with the greatest difficulty, as shown by the studies of Padian and others. Traditionally, as Peter Duesberg reminds us, retroviuses are transmitted vertically from female to offspring. The idea that highly infectious 'HIV' is teeming in the blood and semen of infectees, and therefore very easily spread, has never been demonstrated and is completely false. It is my hypothesis that what we are calling 'HIV', assuming it to be an exogenous, infectious virus, is merely an over-interpretation of the antibodies raised against a constellation of hitherto unobserved endogenous proteins expressed by perturbed cells. The Perth Group have dealt with each of the 'HIV' proteins in turn showing them all to be standard cellular proteins; indeed they argue that all data presented so far are consistent with the 'HIV' proteins being cellular. Using 'HIV' antibodies as probes, 'HIV' proteins have been identified in the tissues of persistently HIV-negative, healthy individuals, including in blood platelet and skin cells, thymus, tonsil and brain. (1). Reference: 1) Papadopulos-Eleopulos, E., Turner, V.F., Papadimitriou, J.M. (1993), "Is a positive Western blot proof of HIV infection?", Bio/Technology, 11:696-707. Competing interests: None declared |
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bmj.com
16th February 2005
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| Alexander
H Russell, artist/writer/philosopher WC1N 1PE Send response to
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Regarding my quest for Bennett to isolate 'HIV' he obfuscated yet again: "Additionally, one wonders if Mr Russell is aware that the De Harven methodology, as I questioned previously is not actually capable of isolating pure virus? Perhaps some other form of isolation should be performed, like genetic cloning?" Regarding "genetic cloning": I ask Bennett what is the use of cloning something unless you are absolutely sure of what it is you are cloning? It is imperative that isolation and purification has to precede genetic cloning. Contrary to Bennett’s claim, Etienne de Harven's methodology is far more rigorous at isolation/purification of virus than other methods and all other indirect surrogate markers which are non-specific. I would ask Bennett to take a look at the elctronmicrogrgraph published in the paper by Etienne de Harven (1) and he will notice that de Harven uses three arrows to indicate impurities. Now look at the elctronmicrograph by Gelderblom et al (2) where three arrows arbitrarily point to questionable particles identified as ‘HIV’. In all honesty Bennett, which of these two electronmicrographs represents the more purified virus? The putative 'HIV' is in fact a collection of endogenous microvesicles and cellular proteins (which also never seem to form particles - so how can they be infectious)? The very title of their paper gives the game away: Cell membrane vesicles are a major contaminant of gradient-enriched human immunodeficiency virus type-1 preparations; Gluschankof P, Mondor I, Gelderblom HR, Sattentau QJ. (Virology, 230:125- 133, 1997). Hence Gelderblom's images are mistakenly labelled as 'purified HIV' but are in fact a compost heap of microvesicles and cellular debris. Three arrows point to barely discernible dots alleged to be 'HIV'. Gelderblom’s image shows three ambiguous particles in a swamp of microvesicles and cellular debris– hardly isolated 'virus'! So how does Bennett explain all the other gunge in the image? Isolation means – need I remind Mr. Bennett – separation from everything else. As The Perth Group have rigorously argued: the isolation of ‘HIV’ has never been achieved. Therefore we must stop using the acronym ‘HIV’. In another paper in the same issue of Virology by Bess et al., the authors admitted that all sorts of debris and extraneous matter banded at the same level as retroviruses in the sucrose medium, principally cellular microvescicles, something that Etienne de Harven had observed even in the 1960's. Material that bands at 1.16 does not represent purified retrovirus ('HIV'); therefore in examining the proteins that make up this soup, which belong to 'HIV' and which are merely cell debris etc? How can one derive a vaccine from all this stuff? Bennett goes on: "Culture and PCR on the other hand provide a standard scientific approach to amplifying what is already there to more manageable levels. Does Mr Russell have issue with using telescopes to amplify the sight of a distant star or planet? Why with PCR for HIV?" If you have to amplify the putative 'HIV' in the first place by using PCR to show that it is there at all then there was obviously not enough 'virus' present to have any pathogenic relevance or even an infectious relevance. Bennett concludes: "However, as Hans Gelderblom has said, virus titres are likely to be too low unless a modified protocol is used, but since isolation has been achieved for cultured HIV perhaps the methods employed there might be transferable (rapid harvest, anion exchange chromatography, Optiprep centrifugation etc)." If virus titres are too low then obviously ‘HIV’ is not an infectious agent and cannot be doing anything. Again I ask Bennett: if the alleged virus titres are that low how can they have any pathogenic or even infectious relevance? A virus that is not doing anything cannot be causing anything. Or as Peter Duesberg and Harvey Bialy wrote in Nature: "...infectious units, after all, are the only clinically relevant criteria for a viral pathogen." Peter Duesberg and Harvey Bialy (Nature, 375, 1995, p. 197). References: 1) PROBLEMS WITH ISOLATING HIV, Etienne de Harven, MD. Brussels – European Parliament – December 08, 2003. 2) Cell membrane vesicles are a major contaminant of gradient- enriched human immunodeficiency virus type-1 preparations; Gluschankof P, Mondor I, Gelderblom HR, Sattentau QJ. (Virology, 230:125- 133, 1997). PROBLEMS WITH ISOLATING HIV, Etienne de Harven, MD. Brussels – European Parliament – December 08, 2003: "To demonstrate the problem’s magnitude it appears necessary to compare current results on HIV with those obtained, previously, in experimental pathology, on another retrovirus known to be significantly associated with a particular leukaemia of laboratory mice, the Friend leukaemia. Both retroviruses, i.e. the Friend leukaemia virus, and the HIV hypothetically related to AIDS, share extremely similar morphology under the electron microscope, have identical diameters, and sediment at the same density in sucrose gradients. A direct comparison between isolating and purifying these two different retroviruses is, therefore, entirely appropriate. Mice suffering from the Friend leukaemia have considerable numbers of retroviral particles in their blood stream. This phenomenon, described as 'Viraemia' in the past, would be called 'Viral load', in today ’s terminology. From only a few ml of the blood plasma of leukaemic mice, the viral particles could be readily separated by a simple technique of ultrafiltration, then sedimented by high-speed centrifugation and finally prepared for electron microscopy. On this electron microscope image, a uniform population of virus particles is clearly recognized. They all have the same diameter and morphology, and one has to look very carefully to identify rare, non-viral structures, attesting to the high degree of purification of these retroviral particles. Such samples of purified retrovirus were successfully used to identify viral proteins and to extract viral RNA. The method applied to achieve this purification of a typical retrovirus is rapid, inexpensive and highly reproducible. Most surprisingly, nobody has ever succeeded in demonstrating HIV particles in the blood of any AIDS patient by this simple method, even though patients were selected for presenting a so-called high 'Viral load' as determined by PCR methods. This embarrassing lack of electron microscope evidence for substantiating the nature of the so-called viral load in AIDS patients was first reported during an important AIDS conference that took place in Pretoria, S.A., in May 2000. None of the AIDS experts present at that conference could demonstrate the presence of retroviral particles in the blood of AIDS patients." Competing interests: None declared |
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bmj.com
9th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Tony Floyd stated: "These days you cannot just dismiss thousands of scientific papers without being challenged and asked for references when you've quoted someone. With so many precedents provided by the 'perth group' you surely can't blame me for being suspicious as to whether or not arguments presented here have a factual basis?" You can "dismiss thousands of scientific papers" if they are all based upon a mistaken premise that 'HIV' has been isolated. I wish Floyd would be far more "suspicious" of the 'HIV/AIDS' hypothesis than being its passive propagator. I would like to remind Tony Floyd that the peer review system has completely broken down when it comes to publishing so-called 'HIV' research papers because there is no contesting counter-critique. As the legendary mathematician Serge Lang observed: "The peer review system at present is being abused to obstruct or prevent scientific discussion, by Scientific American-Pour la Science, in addition to the major international magazines such as Nature and Science, and the funding agencies in the United States." Serge Lang: To the cc list for the HIV-Pour la Science file. Serge Lang goes on: "To an extent that undermines classical standards of science, some purported scientific results concerning 'HIV' and 'AIDS' have been handled by press releases, by disinformation, by low-quality studies, and by some suppression of information, manipulating the media and people at large. When the official scientific press does not report correctly, or obstructs views dissenting from those of the scientific establishment, it loses credibility and leaves no alternative but to find information elsewhere.." Serge Lang, Challenges, Springer, 1998. And Professor Gordon Stewart stated: "...since 1990, Nature, Science, the New England Journal of Medicine, the British Medical Journal and other mainline, peer-reviewed journals have preferred to reject papers by others besides my colleagues and myself containing verifiable data that throws doubt on the claim that AIDS is capable of causing epidemics in general populations of developed countries..." Prof. Gordon Stewart, A paradigm under pressure, Index on Censorship, Vol.28, No.3, May/June 1999. As a student Tony Floyd should always be questioning current scientific paradigms because consensus science is bad science and also challenge his teacher's assumptions and propositions. Or as C.H. Waddington; geneticist, stated: "The most formidable barrier to the advancement of science is the conventional wisdom of the dominant group". Nicholas Bennett stated: "I prefer to see it that we are supplying evidence that directly counters the (worthless) logic behind Mr Russell's arguments. Many, myself included, would reject an argument if it weren't supported by some evidence. Such evidence includes a reasonably sound knowledge base of the field (so that, for example, arguments that HIV virions MUST be isolated from peripheral blood, prior to claiming causation, can be rejected out of hand." The logic behind my arguments are based upon deconstructing the illogical 'HIV/AIDS' hypothesis. There is no "reasonably sound knowledge" that 'HIV' has been isolated from peripheral blood and Nicholas Bennett is not "supplying evidence" to prove that 'HIV' exists but merely quoting reference papers which are all based upon the mistaken premise that 'HIV' has been isolated. Nicholas Bennett's so-called "supplying evidence" merely means reiterating (and taking on trust) what Gallo, Montagnier or Ho happen to publish – and not deconstructing their flawed logic. Nicholas Bennett and Tony Floyd should be more critical and open minded to the counter-evidence rather be mere protectors and propagators of the flawed and failed 'HIV' hypothesis. Competing interests: None declared |
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bmj.com
8th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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As predicted, Nicholas Bennett sidetracked my challenge for him to isolate 'HIV' via Etienne de Harven’s methodology with the following obfuscation: "Can he please give citations where the De Harven method of peripheral blood isolation of simple retroviruses was used to prove infection with the following viruses: Influenza, Rabies, Epstein Barr Virus, Human papilloma virus and Adenovirus. Since these are such important and/or common human pathogens one would naturally expect such a procedure to have been performed." Because the listed viruses above are not 'retroviruses'. I am quoting de Harven's methodology specifically in the case of the Friend murine oncovirus. Etienne de Harven's methodology of virus isolation detected tightly packed identical viral particles. Therefore this methodology should be used to detect the hypothetical 'HIV' if it is present in bodily fluids of a person deemed to be 'HIV' positive. If that methodology does not succeed in detecting tightly packed identical viral particles then there is no viral titre and the virus cannot be causing a disease. Will Nicholas Bennett please stop prevaricating and admit pathogenically significant quantities of cell free infectious 'HIV' have never been found in any fresh sample of any bodily fluid. If you have to use PCR to augment the amount of virus before you actually find it or see it then there was obviously not much there to start with as Kary Mullis, the Nobel Prize winner for inventing PCR, observed: "quantitative PCR is an oxymoron" and I think he is in a better position to know this than Nicholas Bennett who has not won the Nobel Prize for isolating 'HIV' – indeed nor have Gallo or Montagnier. Neither Gallo or Montagnier published electronmicrographs of tightly packed identical viral ('HIV') particles. Isolation of 'HIV' has never been achieved because it does not exist. Back to my still unanswered question: if Nicholas Bennett is so sure that 'HIV' exists he should be able to isolate it via Etienne de Harven's methodology and it would take about two to three days of his time. If Nicholas Bennett is convinced that 'HIV' is in the peripheral blood in sufficient quantities to cause disease then it should be possible to pellet it down using the methodology describe by de Harven. Reference: NO RETROVIRUSES CAN CAUSE AIDS, VIRUS ISOLATION EXPERT ETIENNE DE HARVEN CONCLUDES; Retrovirus Pioneer Rejects HIV-AIDS Model, Rappraising AIDS VOLUME 6, No. 11 & 12, by Paul Philpott. Isolation standards De Harven says that the collective lessons of retrovirology by 1970 led to an important fundamental conclusions: a 1.16 gm/ml band qualified as a retroviral isolate only after electron microscopy showed that it looked like one, and unstimulated cultures showed that it behaved like one. This is because on many occasions virologists obtained 1.16 gm/ml bands that flunked the electron microscopy test, including bands that contained nothing at all that even vaguely resembled viruses. And some 1.16 gm/ml bands that did resemble retroviral isolates failed to demonstrate any replicative capacity at all, and therefore qualified as isolates of non-viral objects that resembled retroviruses. De Harven says this conclusion holds even for 1.16 gm/ml bands that contain reverse transcriptase, which virologists have "found not to be unique for retroviruses, but instead a normal constituent of many cells." Gallo lowers the standards Nonetheless, prior to HIV's official birth in 1984, Gallo published the only three claims for isolation from human subjects of retroviruses, each one of which he said caused a different form of human leukemia. His claims flunked the strict criteria established previously by scientists demonstrating the existence of retroviruses in lab animals, and causally linking those retroviruses to cancer. Gallo's "evidence" resembled what he'd later use to demonstrate HIV's existence and causal role in AIDS: the presumption that all 1.16 gm/ml bands that contain reverse transcriptase are "retroviral isolates"; the presumption that anything that vaguely resembles a retrovirus is a retrovirus; the use of stimulated cultures; micrographs of those cultures, but not of the density-purified bands; the failure to obtain them from uncultured plasma; the failure to use unstimulated cultures; the failure to obtain these bands from most of the patients examined; the failure to demonstrate that these bands affect virgin cultures in a way that explains the disease (rather than transforming the culture cells, Gallo's 1.16 gm/ml bands required that the culture cells already be cancerous); the failure to demonstrate that his bands contained a single RNA species and that it coded for the proteins in the band; the failure to demonstrate that the RNA contained a gene — in this case, an onc-gene — that could explain the disease. "Why no micrographs of the 1.16 gm/ml bands themselves?" de Harven asks. "Most probably, Gallo's electron microscopy results from his 'isolates' were negative and swiftly ignored. The faith in retroviruses as pathogens assumed quasi-religious proportions," de Harven laments. "Since electron microscopy could not demonstrate viruses in the 1.16 bands from human subjects, we forgot about microscopy and started relying on 'markers.' Microscopy is time-consuming and skill-demanding. Who has time for that? Not when research funding was getting difficult and when major pharmaceutical corporations were starting to finance 'crash programs' for speedy answers. "When retroviruses are legion, molecular markers provide a useful approach to quantification probably better than direct particle counting under the electron microscope (which I always found difficult). But without isolates, the use of markers is methodological nonsense. 'Markers' of what? We know that all of the so-called 'HIV markers' are totally non- specific." Competing interests: None declared |
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bmj.com
7th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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In replying to my rapid response Floyd sarcastically stated: "I think Google is a great search engine, however search with "is the earth flat?" and you get several assurances that it is indeed. If I put up my own web site stating that Philip Mortimer (or any other credentialed virologist) decided that HIV didn't exist you might find it with Dr Google, but that doesn't mean it is true." Floyd's absurd allusion to "is the earth flat?" with those who argue that "HIV didn’t exist” is entirely inept since the original 'flat earthers’ were the vast majority – the established view point – and not the dissenters – the minority view point. Indeed: it is 'HIV' Believers who are today's 'flat earthers'. Floyd concludes: "Asking for a reference was not meant to get under your skin Mr Russell. Us mere students are taught to always check the evidence and the credibility of the source if available." If you "mere students are taught to always check the evidence and the credibility of the source if available" you will find out that Luc Montagnier and Robert Gallo did not isolate 'HIV' in the first place. There is absolutely no point in Floyd endlessly citing references at BMJ rapid responses if he himself does not rigorously critique and deconstruct them. Floyd (like Bennett, Noble and Flegg) likes to give the impression of intellectual rigour by quoting us an endless list of (worthless) references to authorise, sanction and legitimate his (lack of) argument(s). Competing interests: None declared |
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bmj.com
6th February 2005
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| Alexander
H Russell, artist/writer/philosopher WC1N 1PE Send response to
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Nicholas Bennett concluded in his condescending reply to Bruno Spagnoli: "Vast amounts of money have been spent on HIV research, arguably at the expensive of other areas of important healthcare, but most of this money seems to me to be involved in the blue-skies molecular research of unravelling the virus. There is no need to re-invent the wheel by performing proof of causation experiments over and over again, at least not by the arguments put forward by people such as the Perth Group." Indeed: vast amounts of money – billions of US research dollars - have been spent - and wasted - on 'inventing the virus' – not "unravelling the virus". Indeed: there is no "need to re-invent the wheel" as Nicholas Bennett rightly states but to use well tried and tested methods in virus isolation: something that has never been done with the hypothetical and non-isolated 'HIV'. Regarding my earlier questions concerning the lack of visual evidence of 'HIV' isolation, Bennett replied with his usual obfuscation: "There is no reason why an EM need be performed if other tests with appropriate controls will provide the same evidence. The EM picture will only show images of, hopefully, similarly shaped particles. There is only a superficial reason to assume that De Harven’s technique will work on HIV, when it was developed for a different virus." If Nicholas Bennett is so convinced that 'HIV' is a real 'virus' then Etienne de Harven’s well tried and tested methodology for viral isolation should work. De Harven’s standardised isolation methodology works for all viruses if they are present at a titre high enough to cause disease. The fact that this method has never been used for 'HIV' is because no virus would be seen: there just simply is no virus ('HIV') there – even in patients deemed to have a so-called 'high viral load'. I agree with Nicholas Bennett that there is no need to "re-invent the wheel" and therefore ask him to use de Harven's well known, tried and tested isolation methodology and prove to us that 'HIV' exists and that those billions of dollars spent on so-called 'HIV Research' ('HIV' Careerism') were not entirely wasted. Bruno Spagnoli and The Perth Group maybe interested in replying to Nicholas Bennett's alarming admission: "I accept that it means that EM of peripherally isolated HIV will likely never be done - because it doesn't need to be done." To prove that 'HIV' exists it most certainly does need to be done - but Nicholas Bennett is right in stating it never will be done: they know that there is no real 'HIV' there in the first place so have to invent all sorts of indirect 'surrogate markers' and conjuring tricks of the virtual virology trade. If Nicholas Bennett is so sure that 'HIV' exists he should be able to isolate 'HIV' via de Harven's methodology - and not sidetrack us with all the usual indirect surrogate metaphysical markers: it would take about two weeks of his time: a very short time in the twenty years of 'HIV' Research. Competing interests: None declared |
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bmj.com
5th February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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In answer to Tony Floyd’s request, here is the required Philip Mortimer 1992 reference for his following statement: "It may be impossible to relate an antibody response specifically to HIV-1 infection."(1) 1). Mortimer P et al. Towards error free HIV diagnosis. Public Health Laboratory Service, UK. 1992. I suggest Floyd cut his customary condescending, patronising tone and read it. In future I suggest Floyd opens up Google and types in 'Mortimer', 'HIV' and 'test' and trawl through the resulting urls. I found the reference in ten seconds so why can't he? Competing interests: None declared |
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bmj.com
2nd February 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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The following references from 'HIV' test literature supplied by Bennett are misleading and untrue: "The COBAS AmpliScreen™ HIV-1 Test, version 1.5 (v1.5) is a qualitative in vitro test for the direct detection of Human Immunodeficiency Virus Type 1 (HIV -1) RNA in human plasma." "This product is intended for use as a donor screening test to detect HIV-1 RNA in plasma samples from individual human donors, including donors of Whole Blood and blood components, Source Plasma and other living donors." "Human Immunodeficiency Virus (HIV-1) is the etiologic agent of Acquired Immunodeficiency Syndrome (AIDS). HIV-1 infection can be transmitted by sexual contact, exposure to infected blood or blood products, or by an infected mother to the fetus." The Vironostika package insert (an ELISA-based test) states: "The Vironostika HIV-1 Plus O Microelisa System is intended for use as an aid in diagnosis of infection with HIV-1." and "Published data indicate a strong correlation between the acquired immunodeficiency syndrome (AIDS) and a retrovirus referred to as Human Immunodeficiency Virus (HIV). Both HIV serotypes have been isolated from patients with AIDS and AIDS- related complex (ARC), as well as from apparently healthy individuals at high risk for AIDS." The Reveal Rapid Antibody test states: "Human Immunodeficiency Virus (HIV) causes Acquired Immune Deficiency Syndrome (AIDS)." "The Reveal™ Rapid HIV -1 Antibody Test is intended for use as a point-of-care test to aid in the diagnosis of infection with HIV-1." The Cambridge Biotech Western Blot kit states: "The Enzyme-Linked lmmunosorbent Blot Technique (“Western Blot”), has been used to detect antibodies to Human lmmunodeficiency Virus Type 1 (HIV -l), which has been recognized as the etiological agent of the Acquired lmmunodeficiencv Syndrome (AIDS)."
What does 'recognised' here mean? 'HIV' has been chosen arbitrarily as the "etiological agent of the Acquired lmmunodeficiencv Syndrome (AIDS)". Bennett concludes with a totally unjustified assumption: "Faced with the knowledge that a person has anti-HIV-1 antibodies, and knowing that HIV is a life-long infection, the obvious conclusion (and diagnosis) is of HIV infection." Bennett should be made aware of the following regarding the spurious, pseudoscience surrounding 'HIV' testing:
Emeritus Prof. Gordon Stuart, Public Health, Glasgow UK stated: "At present there is no scientific basis for using these tests to prove HIV infection." Chief UK virologist Philip Mortimer stated: "It may be impossible to relate an antibody response specifically to HIV infection." The manufacturers cautiously state in their literature enclosed with the 'HIV' test kit: "At present there is no recognized standard for establishing the presence and absence of HIV-1 antibody in human blood. Therefore sensitivity was computed based on the clinical diagnosis of AIDS and specificity based on random donors"1 "Do not use this kit as the sole basis of diagnosing HIV-1 infection"2 "The Amplicor HIV-1 Monitor test is not intended to be used as a screening test for HIV or as a diagnostic test to confirm the presence of HIV infection"3 1. Abbott Laboratories, Diagnostic Division, 66-8805/R5; January, 1997 2. HIV-1 Western Blot Kit, Epitope, Inc., Organon Teknika Corporation PN201-3039 Revision #8 3. Roche Diagnostic Systems, Inc., Amplicor HIV-1 Monitor Test Kit. US:83088. June 1996)(13-06-83088-001 (Also see: Abbott Test Halted After Inaccurate HIV Results, Chicago Tribune (CT) - FRIDAY, April 5, 1996 Edition: BUSINESS Page: 1 Word Count: 402). In 'Tests for HIV are Highly Inaccurate', Dr. Roberto Giraldo wrote: "Some of the conditions that cause false positives on the so-called 'AIDS test' are: past or present infection with a variety of bacteria, parasites, viruses, and fungi including tuberculosis, malaria, leishmaniasis, influenza, the common cold, leprosy and a history of sexually transmitted diseases; the presence of polyspecific antibodies, hypergammaglobulinemias, the presence of auto-antibodies against a variety of cells and tissues, vaccinations, and the administration of gamma globulins or immunoglobulins; the presence of auto-immune diseases like erythematous systemic lupus, sclerodermia, dermatomyositis and rheumatoid arthritis; the existence of pregnancy and multiparity; a history of rectal insemination; addiction to recreational drugs; several kidney diseases, renal failure and hemodialysis; a history of organ transplantation; presence of a variety of tumors and cancer chemotherapy; many liver diseases including alcoholic liver disease; hemophilia, blood transfusions and the administration of coagulation factor; and even the simple condition of aging, to mention a few of them. It is interesting to note that all of these conditions that cause the 'HIV tests' to react positive in the absence of HIV, are conditions which are present with varied distribution and concentration in all of the conventionally recognized AIDS risk groups in the developed countries, as well as in the vast majority of inhabitants of the underdeveloped world. This means that in all probability many drug users [including mothers], certain gay males, and some haemophiliacs in the developed countries, as well as the vast majority of inhabitants in most countries of Africa, Asia, South America and the Caribbean, who have positive reactions to the tests for HIV, may very well do so due to conditions other than being infected with HIV…There is no justification for the fact that both patients and the general public have had all of the preceding facts withheld from them. Without the merits and demerits of the tests for HIV, people cannot make informed decisions." (Being 'HIV-positive' does not mean that a person is infected with 'HIV'; Tests for HIV are Highly Inaccurate, Dr. Roberto Giraldo). Competing interests: None declared |
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| Chris Smith is not 'HIV' positive... |
| Positive
Voices: Alternative viewpoints on HIV and AIDS
UKC Posted on Sunday, 30 January, 2005 - 12:45 pm: |
bmj.com
28th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett stated: "I would argue that the lack of a 'white heterosexual epidemic' of HIV in the developed world is largely due to an effective public education campaign in the 1980's." History has shown this to be blatantly untrue. Can Bennett explain why, if everyone has been using condoms to prevent the supposed spread of 'HIV', there has been such a massive increase in STI/STD's and unwanted pregnancies in the West? Today thousands of white heterosexuals practice condom-free 'unsafe sex' yet there is no heterosexual 'HIV' epidemic in the West. Bennett further stated: "Two large questions arise from Mr Russell's continual ascertation that HIV is endogenous: If that were so, wouldn't we expect a 'white heterosexual epidemic' regardless of public health campaigns?" No: for several simple reasons: 1. 'HIV' does not cause 'AIDS'. 2. 'HIV' is a harmless, endogenous epiphenomenon. 3. 'HIV' is an ubiquitous, usually dormant entity; it will only be detectable in those who are susceptible to certain diseases due to a) lifestyle in the developed world – homosexuals, drug-users, and b) prevailing endemic diseases such as malaria and TB and other diseases related to poverty and malnutrition in the developing world. The vast majority of white heterosexuals are not 'diseased' and therefore will not test 'HIV' positive. However, despite practicing 'safe sex' using condoms since the mid nineteen eighties homosexuals still form the largest group at people at risk for 'AIDS' in Europe and the USA. It can be argued that homosexuals use condoms far more responsibly than heterosexuals so why should they still form the largest group at the risk for 'AIDS' - how can this be? If stopping this supposed spread of 'HIV' by condom use does not prevent 'AIDS' – then what is causing it? It has become obvious to anyone who observes that 'AIDS' is not an 'equal opportunities disease' since it is clear now that not 'everyone is at risk' - as we were all originally promised. After 20 years, still only certain specific groups in Western society develop 'AIDS' - therefore 'HIV' cannot be the cause of disease. When the predicted epidemic of 'AIDS' in the general population in the West proved to be a flop and people stayed away in their millions the cynical powers that be took their dog and pony show on tour to Africa and all points East to the developing world where it is yet again a resounding flop. Now even Bill Gates and Tony Blair realise that the true causes of deaths in Africa are the old enemies malaria, TB and poverty in general as they stated at the World Economic Forum (BBC News: January 27, 2005). Bennett goes on: "If that were so, wouldn't HIV DNA be found in all cells of all human beings, rather than only some cells in HIV+ human beings?" Fragments of DNA identical to that of 'HIV' are found in all human beings. For instance, the gene that encodes reverse transcription is found in all mammalian and plant cells, but the process of reverse transcription was only recognised by Temin and his colleagues in 1970. Bennett concludes: "As regards sexual transmission, I refer Mr Russell to the work of McMichael and others with the HIV-resistant prostitutes in Nairobi." How many female prostitutes in Europe and USA have 'HIV'? Early studies preceding condomania showed that only those European prostitutes using recreational drugs tested 'HIV' positive. No female prostitutes have been known to 'infect' their clients with 'HIV'. As for supposed 'sexual transmission', I suggest Bennett reads Nancy Padian, et. al., "Heterosexual Transmission of Human Immunodeficiency Virus (HIV) in Northern California: Results from a Ten-Year Study," American Journal of Epidemiology, Vol. 146, #4 (August 15, 1997), pp. 350- 57. This paper makes it abundantly clear that 'HIV' is extremely unlikely to be transmitted sexually in the USA. Why should Africa be different? Remember: people living in the consumer capitalist West are far more sexually promiscuous (practicing unsafe sex) than those living in poverty and disease stricken Africa and the developing world. Bennett, Noble and Flegg have not proven to BMJ rapid response readers that 'HIV' is an STI/STD. Why not? Mr. Bennett goes on: "Mr Russell can say that the predictions haven't been fulfilled, but that is just his opinion, rather than the facts. I repeat: HIV serology precedes AIDS." It has nothing to do with my 'opinion'. What are these so called 'facts' Bennett speaks of? Saying that "HIV serology precedes AIDS" is an absurd circular (non) argument where the one ('HIV') is built into the definition of the other ('AIDS'); you simply cannot have one without the other. Bennett cannot see the idiotic circularity of the 'HIV/AIDS' construct where one defines the other. Thus this 100% constructed 'perfect correlation' ('HIV' = 'AIDS' and 'AIDS' = 'HIV') is not a natural coincidence but a 'perfect artefact' of the artificial definition of 'AIDS' by its hypothetical cause, 'HIV'. It is one of the purest examples of circular logic. By using such chicanery there will always be a 100% correlation between 'HIV' and 'AIDS' and Bennett is tragically trapped and interpellated into this idiocy. Correlation is not proof of causation. Dr Kary Mullis, Nobel Prize winner for Chemistry and inventor of PCR (Polymerase Chain Reaction) stated regarding the uselessness of the 'HIV/AIDS' hypothesis: "Years from now, people will find our acceptance of the HIV theory of AIDS as silly as we find those who excommunicated Galileo...As applied, the HIV theory is unfalsifiable, and useless as a medical hypothesis… I can't find a single virologist who will give me references which show HIV is the probable cause of AIDS. If you ask...you don't get an answer, you get fury." Dr Kary Mullis thinks that the 'HIV/AIDS' hypothesis is "one hell of a mistake." As Professor Peter Duesberg observed: TB + 'HIV' = 'AIDS'. TB – 'HIV' = TB. Dementia + 'HIV' = 'AIDS' Dementia – 'HIV' = Stupidity As Duesberg argued: 'AIDS' is defined as any of 30 existing diseases in the presence of the putative 'HIV'. Therefore the correlation between 'HIV' and 'AIDS' is 100% by definition. Duesberg said: "It was a great triumph for the AIDS establishment to take these different diseases and put them all in the same uniform labelled AIDS" . The 'HIV/AIDS' hypothesis has failed all its predictions. Competing interests: None declared |
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bmj.com
25th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett stated regarding the redundant 'HIV/AIDS' hypothesis: "The main predictions of the HIV/AIDS theory are that: HIV serology should precede AIDS. HIV serology should predict HIV detection via other means (e.g. culture, PCR, antigen testing). Pharmacological intervention against the virus should inhibit the viral replication in vitro and in vivo, and result in restoration of the immune dysfunction seen in AIDS and pre-AIDS complex patients. HIV serology should, obviously, appear to be transmissible and associate with the individuals and risk groups associated with AIDS. All of these are true and have been discussed here before". Contrary to Mr. Bennett's claim, none of the above is true. The hallmark of a sound hypothesis is that predictions based upon it will be fulfilled. This has never been the case with the 'HIV/AIDS' hypothesis. None of the predictions based upon the 'HIV/AIDS' hypothesis has been fulfilled. The predicted white heterosexual 'HIV/AIDS' epidemic in the West has never materialised proving conclusively that 'HIV' is not an STI or STD but an endogenous epiphenomenon. 'HIV' is merely an indicator/marker – an 'effect' of cellular irregularities which may result in a disease state but not invariably so. So called 'HIV antibodies' are an 'effect' (and not a proven 'cause') in at least seventy medical conditions known long before 'AIDS' was invented to explain them. Some 30 old diseases have been cynically remarketed as 'AIDS' in order to justify the extortionate sums demanded by pharmaceutical companies for so-called 'antiretroviral' drugs which they themselves admit to not eradicate 'HIV': one cannot eradicate an endogenous entity wrongly classified as 'HIV'. Mr. Bennett has still not proven 'HIV' to be a sexually transmissible exogenous retrovirus. In an experiment Dr. Roberto Giraldo has proven 'HIV' to be an endogenous entity: if you apply the 'HIV' test to undiluted blood then everyone tests 'HIV positive' proving 'HIV' to be an endogenous epiphenomenon - a marker - and not a cause - of certain disease conditions. As Medical researcher Dr. Roberto Giraldo stated from: 'Everyone Reacts Positive on the ELISA Test for HIV': Everybody has different levels of HIV infection. It is also believed worldwide that a person that react positive for antibodies against HIV has not only been exposed to but is infected with a deadly virus that cause immunodeficiency. Therefore, the positive reactions of all undiluted sera would mean that everybody, or at least all the blood samples that I have tested, including my own infected with this "deadly" virus. The ones that react positive at a ratio of 1:400 would simply have a higher level of "deadly" infection than the "deadly" infection had by the ones that react positive only with undiluted serum. Competing interests: None declared |
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bmj.com
25th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Regarding the death of Makgatho Mandela, Mr. Peter Flegg naively stated: "How presumptuous of Alexander Russell to claim he knows better than Nelson Mandela what factors contributed to the death of his son, Makgatho. The fact that various sources initially stated different possible causes (gall bladder complications, pancreatic cancer) is not unusual in a society where many euphemisms have arisen to disguise the diagnosis of HIV and avoid the stigmatisation associated with it." Mr. Flegg fails to see here that Nelson Mandela is a true 'HIV Believer' (blinded by faith) - whereas I am an 'HIV' atheist – so I can be far more objective and disinterested and see through the 'disguise' (mask) of 'HIV' fundamentalism and see what is really going on. Nelson Mandela cannot see what really killed his son because he is blinded by his 'HIV' belief. In fact 'HIV positivity' was the 'disguise' (metaphor, euphemism) for the late Makgatho Mandela’s alcoholism. Alcoholism and liver damage are known to give false 'HIV positive' test results – and Nelson Mandela and Peter Flegg – as 'informed' people – should know this. It is more than likely that Makgatho Mandela's alcoholism gave him a false 'HIV positive' diagnosis. Indeed: 'HIV' is a 'disguise' and a 'euphemism' that stands in as a 'marker' for over seventy medical illnesses/conditions. Factors known to cause false-positive 'HIV' antibody test results include: Anti- carbohydrate antibodies, alcoholism, Naturally-occurring antibodies, Leprosy, Tuberculosis, Renal (kidney) failure, Flu vaccination, Herpes simplex I, Malaria, Systemic lupus erythematosus, Organ transplantation, Hepatitis, Haemophilia, Haematologic malignant disorders/lymphoma, Primary biliary cirrhosis, Stevens-Johnson syndrome, T-cell leukocyte antigen antibodies, Proteins on the filter paper, Epstein-Barr virus, Visceral leishmaniasis. Mr. Flegg reveals his blind spot here: "Why does Mr Russell think that antiretroviral drug 'poisoning' is implicated in his death?" Simply because 'HIV' has never been shown to cause illness, disease or death whilst 'antiretroviral' drugs are known to cause 'AIDS’ related – disease/conditions and death. The severe toxicity of Nevirapine can cause inflamed pancreas glands and liver-related problems and these were presenting symptoms in Makgatho Mandela's final illness. The biggest killer in the USA for those diagnosed spuriously as 'HIV positive' (whatever that may mean) at present is from liver failure due entirely to the 'anti-retroviral' drugs taken. Yet of course Mr. Flegg would like us all to 'believe' that 'HIV' was the killer – when in fact it is the 'anti-retroviral' drugs themselves that are the killers - and ironically cause 'AIDS'. Mr. Flegg simply cannot confront this brute fact: he has to 'believe' in 'HIV' to save his skin. Finally Mr. Flegg absurdly asserted: "HIV infection itself is well documented as contributing to problems within the biliary tree which may require surgery." This is absolute nonsense and pure science fiction. There is no evidence of active 'HIV' infection in anybody deemed to be 'HIV positive' for the hypothetical 'HIV antibodies'. This means that said 'antibodies' are restricting 'HIV' to latency. Ergo: 'HIV' cannot be 'doing' anything and therefore cannot be 'causing' anything. The only thing standing between the people of South Africa and 'HIV' Pharmogenocide is their poverty: they simply cannot afford the 'antiretroviral' drugs - a blessing in disguise. Fortunately they cannot afford the lethal toxic drugs that contributed in killing Makgatho Mandela. The irony is that the death of Makgatho Mandela can be directly ascribed to the 'antiretroviral' drugs that Nelson Mandela – for political reasons – is seeking to force President Mbeki to procure and sanction for the people of South Africa. However, President Mbeki is quite rightly sceptical, cynical and critical about the efficiency and legality of these 'AIDS' inducing drugs. Nelson Mandela is inadvertently initiating Iatrogenic 'AIDS' Competing interests: None declared |
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bmj.com
18th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Regarding the death of Makgatho Mandela, Mr. James Whitehead stated: "I agree with Nicholas Bennett on this. And I think we should not speculate and should show are deepest sympathy to his family and his father. I hold Mr Nelson Mandela in high regard even if I always don't agree with everything he believes, I spent some time myself campaigning for him and his people to be freed. I always find commentary like this distasteful and unscientific." On the contrary: we should speculate and ask questions. How can my commentary be "distasteful and unscientific" when it merely asked legitimate 'scientific' questions regarding the mystery surrounding Makgatho Mandela’s death? According to The Observer (David Beresford, Johannesburg, Sunday January 16, 2005): "Ironically, hospital sources have told The Observer Makgatho did not die of an Aids-related illness, but of a pancreatic cancer. He had been on anti-retrovirals for some time and his Aids was described as being 'well under control'. It would, however, have affected his body's capacity to fight the problem with his pancreas." Why? Are ARVs (anti-retrovirals) suitable for treating pancreatic cancer? Yet hours after Makgatho died in a Johannesburg hospital last week, Nelson Mandela announced that his son had died of "Aids-related complications" - and not of pancreatic cancer. Why? Did the ARVs accelerate Makgatho Mandela's death? Also The Sunday Times (16, January, 2005) printed as a lead letter one from David Rasnick headlined "Drugs, not AIDS, probably killed Mandela's son", as follows: Makgatho Mandela's death is more consistent with drug toxicity than Aids - HIV had nothing to do with his pancreas and gall-bladder problems ("Lawyer with his father's humity", January 9). An article by Craif Timberg in the January 7 issue of the Washington Post "Mandela says Aids led to death of son" is revealing about what actually killed the former President Nelson Mandela's son. Timberg says: "A spokesman for the Mandela family, Isaac Amuah, said in a phone interview that the immediate cause of Makgatho's death was complications from a gall-bladder operation. But he said that Aids was a contributing factor and that Mandela was determined to portray the death as resulting from Aids to demystify the disease." A gall-bladder operation implies liver problems. The leading cause of death among HIV-positive people in the US is now liver failure. Liver failure is not (yet) an Aids-defining disease. All anti HIV drugs cause liver toxicity. We learn from Timberg that "Makgatho...had been receiving antiretroviral treatment for more than a year". Information about what really killed Mandela's son must be made public because Mandela's own actions have turned his death into a political and international issue. - Dave Rasnick, via email. Like Mr. Whitehead, I also "hold Mr Nelson Mandela in high regard" which is precisely why I wanted to know what his son really died of. Sadly, Makgatho Mandela's death was used as a shoddy political manoeuvre by Nelson Mandela to challenge President Thabo Mbeki who quite rightly doubts the very existence of 'HIV' and 'AIDS' in Africa. Regarding Makgatho Mandela: were viable, active, infectious 'HIV' particles isolated and recovered from his blood or any other tissue? If not we are making a false assumption and a 'pure speculation' that he had an active 'HIV' infection. The obituaries of Rudollf Nureyev John Curry, Oscar Moore, Denholm Elliott, Arthur Ashe, Kimberley Bergalis, Ryan White, Kenny Everett, Freddie Mercury and Derek Jarman reported that they had died of 'HIV' related or 'AIDS' related causes/conditions: I would argue that this is indeed 'pure speculation'. I would 'speculate' and argue that they really died as a result of AZT and ARV poisoning and yet their deaths were misleadingly put down to those nebulous nominations of 'HIV related' or 'AIDS related'. Competing interests: None declared |
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bmj.com
13th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Recently a grief-stricken 86 year old Nelson Mandela told a news conference that his only surviving son, Makgatho Mandela, had "died of Aids" and had been "HIV positive" (whatever that means). Makgatho, an attorney, was said to have died in Johannesburg at the age of 54 from 'Aids-related causes'. What are these nebulous 'causes'? What HAART regimes or ARVs (so-called 'antiretroviral' drugs) was Makgatho Mandela taking? When asked if Makgatho was on ARVs, Dr Isaac Amuah said: "he had received the best treatment in the country". Is that what really killed him? Why did a relatively well-off and middleclass man like Makgatho die from so-called 'AIDS' related causes? Apparently a spokesman for the Mandela family, Isaac Amuah, said that the immediate cause of Makgatho's death was "complications from a gall bladder operation". Is this 'HIV' or 'AIDS' related? Have people ever died from 'complications' arising from 'gall bladder surgery' with out the hypothetical 'HIV infection'? But Amuah also said that 'AIDS' was "a contributing factor" and Mandela seemed determined to portray the death as resulting from 'AIDS' in order to "demystify the disease". But Mandella is in actual fact 'mystifying the disease' even more: 'AIDS' is not a 'disease' but a syndrome of some 30 well known diseases/conditions which have always existed in Africa. No one dies of 'AIDS' per se: they die of a particular illness/condition. Today it seems that anyone who is diagnosed as 'HIV positive' and becomes ill their condition will automatically be nominated as 'HIV' related. – even if one is shot dead or dies in a car accident! This is as ludicrous as suggesting that prior to 'HIV' that no one ever died of anything! What were South African blacks dying of before 'HIV' and 'AIDS' were invented? Boredom? The question is: what did Makgatho Mandela really die from? What were the final presenting illnesses that Makgatho had? What is the fatality rate in men of 54 and above from gall bladder complications and pancreatitis who are 'HIV' negative? How could 'HIV' have adversely effected the outcome? Could it not be possible that the recently administered 'treatment' (ARVs?) could have caused the 'complications' with the 'gall bladder surgery'? Makgatho’s health seems to have got far worse after he started taking the 'treatment'. Did Makgatho die from the cytotoxic lethal effects of ARVs (HAART regimes)? Are ARVs now the biggest cause of 'AIDS'? Did ARVs kill Makgatho Mandela? Competing interests: None declared |
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bmj.com
11th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Dr. Joe Thomas stated: "The Tsunami disaster could contribute to inadequate safe blood, shortage of clean injecting equipments for injecting drug users, an insufficient supply of condoms and health care; and the vulnerability of displaced people, especially women and children to sexual abuse and violence. In addition, during the periods of population displacement, HIV/AIDS prevention and care is often disrupted. The HIV epidemic presents key challenges to both humanitarian and development assistance, and to the interface between them. The challenges raised by the HIV pandemic in the Asia Pacific are only beginning to be fully realised now, and HIV is clearly a massive crisis in all the Tsunami affected areas and can be described as an emergency." This is pure 'HIV' propaganda cynically exploiting the Tsunami tragedy. To date: 'HIV' has never been isolated from blood or blood products, injecting equipment or semen. As 'HIV' is an endogenous entity how can condoms eradicate it? The aftermath of the Tsunami tragedy could lead to disease conditions which will make people test ‘HIV positive’. Remember: 'HIV' does not cause 'AIDS': rather certain disease conditions cause endogenous 'HIV' expression. There is no "HIV pandemic in the Asia Pacific": there are specific disease conditions that make people test 'HIV positive': hence: 'HIV' is merely an endogenous marker for prevailing disease conditions in this region. We know poor sanitation, malaria and TB make people test ‘HIV’ positive. Dr. Joe Thomas concludes: "Though natural calamities do not transmit HIV, however, some of the post disaster situations may provide a fertile environment which would enhance vulnerability of individuals to HIV." Of course, natural calamities do not transmit 'HIV' and neither do human beings: to repeat: 'HIV' is not a transmissible agent. Yet the 'post disaster situation' may indeed provide 'a fertile environment' which 'would enhance vulnerability of individuals' to endogenous 'HIV expression'. History has shown us that 'HIV' has remained rigorously locked into the original 'high-risk groups': 'death-styles' relating to poverty in the Third World and 'lifestyles' relating to excess and wealth in the West. Diseases relating to poor sanitation, malnutrition and poverty following the Tsunami tragedy will no doubt make many more people test 'HIV positive': the Tsunami Syndrome is indeed 'marker' for endogenous 'HIV' expression. The aftermath of 'Tsunami' will cause endogenous 'HIV' expression: this cannot be prevented: it is already there. Competing interests: None declared |
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bmj.com
5th January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Mr. Bennett stated: "I would have an open mind to HIV being endogenous, were it not for the fact that it clearly isn't." The case of haemophiliacs proves that Mr. Bennett is completely wrong here. It was initially supposed by Dr. Robert Gallo and others that haemophiliacs were infected with 'HIV' which had contaminated their clotting factor; indeed, this was one of the chief arguments used by Gallo to propound the theory that 'AIDS' was caused by a transmissible agent. However, by 1994 it was admitted by no less an authority than the CDC that the chances of 'HIV' having got into the clotting factor and survived cryoprecipitation were "essentially zero"*. It is stated that the source plasma obtained by plasmapheresis and fresh frozen plasma from whole blood donation are best suited for the preparation of Factor VIII. The interval between collection and freezing of plasma is about six hours. The plasma is kept frozen for long periods of time, days to weeks, and is then thawed for processing. How could the hypothetical 'HIV' survive this? The clotting factor itself did the damage as it consisted of 99% impurities – fibrinogen, alien proteins, cell debris, etc. all of which had to be assimilated by the recipients' liver. Thus how did the haemophiliacs become infected with 'HIV'? Add to this the fact that no one has been able to explain how so much clotting factor should have been contaminated so rapidly as to infect some 80% of haemophiliacs taking commercially produced Factor VIII worldwide. Who were the mysterious paid 'donors' who were regularly selling plasma in commercially run plasmapheresis bucket shops? No one has ever found any explanation for this phenomenon. Does Mr. Bennett suppose that homosexuals with 'HIV' were in the habit of selling their plasma in the USA? Where did all the 'HIV' come from? The fact is that both 'HIV' and in all probability, Hepatitis B virus are both endogenous and are expressed under certain disease conditions. After all, neither 'HIV' nor Hepatitis B have ever been recovered from stored commercial clotting factors. Another coincidence: both 'HIV' and Hepatitis B replicate via reverse transcription – a common cellular phenomenon. What we are calling an 'exogenous retrovirus' ('HIV') is in fact an endogenous epiphenomenon which may be interpreted as a marker for a tendency towards certain disease conditions, most of which are 'risk- group' specific. Any true exogenous virus would not have remained locked- up in specific risk groups in the West for 30 years. History has shown us clearly that what we have wrongly nominated as a sexually transmitted exogenous retrovirus ('HIV') is in fact an endogenous epiphenomenon. It is ironical that the haemophiliacs who were first cited to prove the existence of 'HIV' as an exogenous transmissible agent a decade later should prove conclusively that 'HIV' is an endogenous entity. *Reference: "Since the HIV concentrations used in laboratory studies are much higher than those actually found in blood or other body specimens, drying of HIV-infected human blood or other body fluids reduces the theoretical risk of environmental transmission to that which has been observed-essentially zero." - CDC Fact sheet on HIV transmission, January, 1994. Competing interests: None declared |
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bmj.com
3rd January 2005
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Can the 'sixth sense' of animals warn - and save us - from future Tsunami ? Recent news reports state that Sri Lankan wildlife conservationists have said the huge waves that killed over 25,000 people along the Indian Ocean island's coast seemingly missed wildlife, with apparently no dead animals found: "No elephants are dead, not even a dead hare or rabbit. I think animals can sense disaster. They have a sixth sense. They know when things are happening," H.D. Ratnayake, deputy director of Sri Lanka's Wildlife Department, said Wednesday. The waves washed floodwaters up to 2 miles inland at Yala National Park in the ravaged southeast, Sri Lanka's biggest wildlife reserve and home to hundreds of wild elephants and several leopards. "There has been a lot of anecdotal evidence about dogs barking or birds migrating before volcanic eruptions or earthquakes. But it has not been proven," said Matthew van Lierop, an animal behaviour specialist at Johannesburg Zoo: "There have been no specific studies because you can't really test it in a lab or field setting," he told Reuters. Other authorities concurred with this assessment: "Wildlife seem to be able to pick up certain phenomenon, especially birds ... there are many reports of birds detecting impending disasters," said Clive Walker, who has written several books on African wildlife..." So-called 'sixth sense' – akin to 'near death experience' (NDE) and 'out of body experience' (OBE) - cannot be explained by commonsense, biology, psychology or theology but maybe by ontology – the study of our being in the world – and in the case of NDE/OBE – being out the world. The 'sixth sense' could be nominated as 'Invasive Body Experience' (IBE): the experience of attuning to distant sensations coming towards one. We know animals experience this sixth-sense 'IBE' – as well as some more 'developed' human-animals: (human beings living closer to their primordial instinct rather than their post-modern intellect). Yet so many 'senseless' human beings are cut-off from their primordial 'sixth sense' through 'intellectualising' (analysing) and 'rationalizing' and forgetting their primordial instinctive being and subconscious sensationing powers. Martin Heidegger gets close to the primordial ontology of 'sixth sense' with his imagings of 'attunement' (Stimmung): that 'mooding scape' which is 'tuned-in' to a coming 'event' (Ereignis). The Ereignis on the Horizon here being the Tsunami. Whilst it is very difficult to 'prove' psychologically and scientifically that 'sixth sense' exists it has been empirically observed in the actions of animals moving to higher grounds just before a Tsunami approaches. Therefore animal observation studies are urgently needed. Instincting and Sensationing 'tunes' one's 'attunement' toward listening to the approaching Tsunami which automatically attunes others who switch on their 'sixth sense' antennae towards the seascape that is sending in the Tsunami. For a very few human animals - but for many other animals - 'attunement' is a collective 'mooding' initiated directly from 'instinct' which is a primordial knowledge of nature. The 'intellect' has no 'sixth sense' and cannot sense danger – whilst instinct – the antenna of the 'sixth sense' is a primordial form of radar. The Tsunami which instigates and initiates the menacing mood of the animals is not 'in them', as it were, but in an approaching aura that comes over the region or scape that sets the scene of the threatening 'mooding-sensation': here the Tsunami: an awesome atmosphere of an approaching threat that many animals seem to attune to – whilst most humans are out-of-tune with. Regarding the Tsunami: the 'intellect' will give you the 'how' and the 'why' – but only the 'sense' (instinct) can tell you the 'when'. Dr. Phil Cummins, seismologist at GeoScience Australia in Canberra, had warned the world that this Asian Tsunami was on the cards over a year ago and had asked for a Tsunami warning system in the Indian Ocean. In September 2004, Dr. Cummins published a paper summarising his case for a Tsunami warning system in the Indian Ocean. Dr Cummins told The Sunday Times he did not resent anyone for not heeding his call earlier: "No one thought that this could happen so soon," he said. "They were listening and waiting for me to make a stronger case. The problem was there were no historical accounts of a tsunami affecting the entire Indian Ocean Basin . . . or I hadn't found them yet." The International Co-ordinating Group for the Tsunami Warning System in the Pacific (ITSU) seems too slow and out of tune. Is there some study that could be set up to see whether animals' sensitivities could be harnessed to monitor the approach of a Tsunami, earths quakes, etc? Similarly could dolphins be trained to relay information concerning under sea seismic activity? With the threat of any further Tsunami we urgently need to start sensationing (sensing) again – and this may one day save us from further natural disasters. As we are largely under-developed in the area of 'sensationing' maybe more 'developed' animals like elephants and dolphins could teach us how to 'sense' and thus help us in this urgent area of research? References: Tsunami Adds to belief in Animals' "Sixth Sense": Reuters Report by Ed Stoddard, 30th December 2004. How did it all go so wrong? The Sunday Times, Australia - 1st Jan 2005. Competing interests: None declared |
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bmj.com
31st December 2004
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| Alexander
Hr Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Dr. Peter J. Flegg has still not answered my questions regarding his defence of the 'HIV' hypothesis, 'anti-retroviral' drug regimes and 'HIV' testing. Yet Dr. Flegg has a responsibility to his patients to answer these legitimate questions regarding the making of 'informed choices'. Regarding so-called 'informed choices' and 'informed consent' would Flegg mention to his patients that 'HIV' has never been proven to exist as an isolated entity? Flegg also has direct responsibility for the 'toxic waste' ('anti-retroviral drugs') he may have to prescribe his patients - such as AZT (Retrovir) and other lethal cytotoxic HAART regimes. 1) What convinces Flegg that 'HIV' is more lethal or toxic than 'AZT'? 2) If a patient on AZT or any HAART regime dies, what 'cause of death' is put down on the death certificate? Is it ever AZT poisoning or HAART poisoning – or is it always nominated as 'HIV' related: - "due to complications arising from HIV infection" - as the mythic 'AIDS speak' mantra usually goes? 3) Does Flegg 'inform' his patients that all the 'HIV' tests are non- specific and non-standardised? The medical literature records over seventy conditions known to cause 'false positive' results. Factors known to cause false-positive 'HIV' antibody test results include: Anti-carbohydrate antibodies, Naturally-occurring antibodies, Leprosy, Tuberculosis, Renal (kidney) failure, Flu vaccination, Herpes simplex I, Malaria, Systemic lupus erythematosus, Organ transplantation, Hepatitis, Haemophilia, Haematologic malignant disorders/lymphoma, Primary biliary cirrhosis, Stevens-Johnson syndrome, T-cell leukocyte antigen antibodies, Proteins on the filter paper, Epstein-Barr virus, Visceral leishmaniasis. The manufacturers of these non-specific and non-standardised 'HIV' tests cautiously state in the literature enclosed with the test kit: "At present there is no recognized standard for establishing the presence and absence of HIV-1 antibody in human blood. Therefore sensitivity was computed based on the clinical diagnosis of AIDS and specificity based on random donors"1 "Do not use this kit as the sole basis of diagnosing HIV-1 infection"2 "The Amplicor HIV-1 Monitor test is not intended to be used as a screening test for HIV or as a diagnostic test to confirm the presence of HIV infection"3 1. Abbott Laboratories, Diagnostic Division, 66-8805/R5; January, 1997 2. HIV-1 Western Blot Kit, Epitope, Inc., Organon Teknika Corporation PN201-3039 Revision #8 3. Roche Diagnostic Systems, Inc., Amplicor HIV-1 Monitor Test Kit. US:83088. June 1996)(13-06-83088-001 (Also see: Abbott Test Halted After Inaccurate HIV Results, Chicago Tribune (CT) - FRIDAY, April 5, 1996 Edition: BUSINESS Page: 1 Word Count: 402). Flegg recently stated in a BMJ rapid response: "…no-one would propose giving potentially toxic drugs to HIV 'uninfected persons' in some form of comparative study." I would argue that every person on this planet is "HIV uninfected" and ask Flegg if it is really legal, rational, logical or ethical to prescribe a cytotoic drug like AZT or any HAART regime to anyone? It could be argued in a court of law that John Curry, Oscar Moore, Denholm Elliott, Arthur Ashe, Kimberley Bergalis, Ryan White, Kenny Everett, Freddie Mercury and Derek Jarman died as a result of AZT poisoning and yet their deaths were misleadingly put down to those nebulous nominations of 'HIV related' or 'AIDS related'. Yet for many dissenting critics AZT became known as 'AIDS by prescription'. Bob Guccione, Jr. asked Peter Duesberg why AZT became known as 'AIDS by prescription': B.G: "Explain why you have called AZT "AIDS by prescription?" P.D: "It's AIDS by design. It was designed over 20 years ago as a chemotherapy. And chemotherapy is a rational but desperate treatment for cancer. The rationale is, 'Let's kill all the growing cells for several weeks'. The hope is the cancer is going to be totally dead, and you are only half dead and recover. Chemotherapy is a rough treatment. You lose your hair, you lose weight, you get pneumonia, you get immune deficiency, you literally get AIDS, you have nausea, all the AIDS symptoms, because it's severe cellular intoxication. You kill a lot of good cells, too. Often the treatment works, the cancer is indeed dead and you survive and recover. Now you give that drug to somebody indefinitely. Not just for two or three weeks. Every six hours, your HIV-positive person takes 250 mg of AZT. So they lose weight, they become anemic, they lose their white cells, they have nausea, they lose their muscles. Like Rudolf Nureyev, they cannot even stand on their own legs. And then they die. Like Kimberly Bergalis, Nureyev, Arthur Ashe, Ryan White, and many others. That's what you call AIDS by prescription." (Duesberg Spin Interview, from Spin Magazine, September, 1993). Can Flegg prove that any of his patients are "HIV infected" that is - really prove that they are 'HIV' positive? Does Flegg really offer his patients 'informed choices' or merely 'HIV' propaganda? Does Flegg still defend and endorse HAART drug regimes and 'HIV' testing given the facts cited above? Competing interests: None declared |
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bmj.com
31st December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Regarding my questions concerning the lack of visual evidence of 'HIV' isolation, Mr. Bennett replied with yet more glaring obfuscation: "There is no reason why an EM need be performed if other tests with appropriate controls will provide the same evidence. The EM picture will only show images of, hopefully, similarly shaped particles. There is only a superficial reason to assume that De Harven’s technique will work on HIV, when it was developed for a different virus." If 'HIV' is a genuine, real 'virus' then de Harven’s well tried and tested methodology for viral isolation should work very well. De Harven’s standardised isolation methodology works for all viruses if they are present at a titre high enough to cause disease. The fact that this method has never been used for 'HIV' is because no virus would be seen: there just simply is no virus ('HIV') there – even in patients deemed to have a so-called 'high viral load'. Mr. Bennett concludes: "I'm also waiting for Mr Russell to acknowledge that he was wrong when he said that no animal retrovirus was transmitted horizontally, and that he accepts that preferential male to female transmission is entirely normal for such a virus." Like 'HIV', 'SIV', 'BIV', 'FIV', 'MIV' are hypothetical constructs and have not been isolated or proven to be exogenous entities: it has only ever been assumed that they are exogenous, sexually transmitted retroviruses but no study to date has proven this. Until Mr. Bennett can show that these 'HIV' associated genetic sequences are actually derived from viral particles by obtaining pure retroviral particles he will never be able to prove that 'HIV' is exogenous and a sexually transmitted retrovirus. Mr. Bennett must know that such pictures of densely packed, pure retroviral 'HIV' particles must be obtained from the fresh plasma of 'HIV' positive subjects rather than derived from cell culture. It is unscientific to call a genetic sequence an 'exogenous retrovirus' when the possibility that it could instead result from still unknown endogenous genetic processes. What Mr. Bennett is still naively calling 'HIV' is an endogenous epiphenomenon and not an exogenous entity. Hence: 'HIV' is not an STD. I ask Mr. Bennett to give up his closed 'HIV' Belief system and open his mind and read: 'The Isolation of HIV: Has it been achieved? The Case Against', by Eleni Papadopulos-Eleopulos, Valendar F.Turner, John M. Papadimitriou, and David Causer. CONCLUSION to claim that "The existence of the retrovirus HIV predicts that HIV DNA can be isolated from the chromosomal DNA of infected cells", one must first have proof of the existence of a unique molecule of DNA which is the genome of a unique retrovirus particle, HIV-1, which can only be obtained by isolating the retroviral particle. At present there is no such proof. Fisher et al and Levy et al selected a portion of the RNA which from the supernatant of "infected" HUT78 cells banded at 1.16gm/ml or had a certain length, reverse transcribed it and called it "HIV-1 DNA" . However, since neither they nor anybody else before or after them has shown that this RNA (cDNA) was even the constituent part of a particle, any particle retroviral or otherwise, the claim that the DNA is "Full length HIV-1" or "HIV- specific" cannot be substantiated. In the cell extracts of "transfected" cells Fisher et al and Levy et al found some proteins with molecular weights similar to the "HIV proteins" which reacted with AIDS patient sera. They also found reverse transcription of A(n).dT15 in the cell supernatant but presented no evidence that the proteins or the RT were constituents of a particle, viral or otherwise, and thus cannot claim that they have proven that the "transfected" cells "produce particles that contain reverse transcriptase, HIV specific antigens". Although Fisher and colleagues had an electron micrograph showing virus-like particles in the culture supernatant, they did not prove that the particles were indeed retroviral particles, or even that they had some of the most basic morphological and physical features of retroviral particles and thus they "could reflect non-viral material altogether". Competing interests: None declared |
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bmj.com
19h December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Mr. Bennett did not answer my points regarding his extraordinary admission in a recent rapid response: "I accept that it means that EM of peripherally isolated HIV will likely never be done - because it doesn't need to be done." Why doesn't it need to be done? It most certainly does need to be done - but Mr. Bennett is right in stating it never will be done, but not for the reason he states. The fact is that the current crop of virtual virologists dare not use the earlier, tried and trusted methods of viral isolation to find HIV in peripheral blood - because they know they would not find any particles at all. By affecting to disdain to use ultra centrifugation, pelletting down etc. they can perpetuate the myth of HIV proliferation and pathogenicity by using indirect 'surrogate markers', as introduced by Dr. Robert Gallo, Dr. David Ho and others. Electronmicroscopist Prof. Etienne de Harven, in criticising the loss of precision due to the abandonment of EM in identifying and quantifying viruses, pointed out that the pretext they used for their abandonment (like Mr. Bennett) was that EMs were unnecessary, time consuming and too costly: de Harven stated: "Dangerously enough, EM was progressively dismissed in retrovirus research after 1970. Molecular biologists started to rely exclusively on various 'markers', and what was sedimenting in sucrose gradient at density 1.16 gm/ml was regarded as 'pure virus'. It is only in 1997, after fifteen years of intensive HIV research, that elementary EM controls were performed, with the disastrous results." These "disastrous results" published in Virology 1997 (Gluschankof et al. and Bess et al.) did not show purified/isolated 'HIV' but a mass of cellular debris and microvesicles with three ambiguous dots which were arbitrarily identified as 'HIV'. Yet the authors of these papers give us no rational or logical explanation why these dots are 'HIV'. If the methods of viral detection using indirect surrogate 'markers' Mr. Bennett trusts really work, then it is axiomatic that using the earlier methodology will only confirm their findings. It is time to clear up this point before 'HIV' research becomes even more irrational and ludicrous. Surely it would be worthwhile to spend a mere a few days with basic EM equipment to confirm visually the results obtained by using Mr. Bennett's "superior techniques"? Can Mr. Bennett isolate 'HIV' via Prof. Etienne de Harven's well tried and tested methodology and give us real direct visual evidence that 'HIV' exists? Virtual virology - indirect 'surrogate markers' - will not suffice. Competing interests: None declared |
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bmj.com
17h December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Dr. Peter J. Flegg has still not answered my following questions and has not provided BMJ rapid response readers with visual references proving that 'HIV' exists but merely points to the NIAID 'HIV' propaganda document which has no credible scientific proof (that 'HIV' exists and causes 'AIDS') but assumptions, suppositions and unproven hypotheses signifying nothing. Please could Dr.Flegg possibily answer the following questions: 1) What convinces Dr. Flegg that 'HIV' is more lethal or toxic than 'AZT' or any 'anti-retroviral' HAART regime? 2) If a patient on AZT or any HAART regime dies, what "cause of death" is put down on the death certificate? Is it ever: "AZT poisoning" or "HAART poisoning" – or is it always "HIV related" - "due to complications arising from HIV infection"? 3) Where is the visual reference for a published electronmicrograph of isolated/purified 'HIV'? To date none have been published. The images published in Virology 1997 (Gluschankof et al. and Bess et al.) did not provide visual confirmation that 'HIV' had been isolated/purified (proven to exist). Dr. Flegg recently stated in a BMJ rapid response: "…no-one would propose giving potentially toxic drugs to HIV 'uninfected persons' in some form of comparative study." I would strongly argue that we are all "HIV uninfected persons". As Dr. Roberto A. Giraldo stated: unless the blood sample in grossly diluted, everyone will test positive for 'HIV' – which in fact means that no one is 'infected' with 'HIV'. Would Dr. Flegg still prescribe AZT or any HAART regime after reading the following text by Dr. Roberto A. Giraldo? 'Everyone Reacts Positive on the ELISA Tests for HIV', by Dr. Roberto A. Giraldo Continuum, Winter 1998/9 5(5): 8-10: The following are three possible explanations for why undiluted specimens of blood always react positive at the ELISA test: Since all undiluted blood specimens react positive on the ELISA test, a test that supposedly tests for antibodies to HIV, the results presented here suggest that every single human being has HIV antibodies. And this suggests that everybody has been exposed to HIV antigens. This would mean that all of us have been exposed to the virus that is believed to be the cause of AIDS. The people that react positive even at a dilution of 1:400, would be the ones that have had the highest level of exposure to HIV antigens. The rest of the people - the ones that only react positive with undiluted serum [1:1] - would have had a lower level of exposure to HIV. Everybody has different levels of HIV infection. It is also believed worldwide that a person that reacts positive for antibodies against HIV has not only been exposed to but is infected with a deadly virus that causes immunedeficiency. Therefore, the positive reactions of all undiluted serums would mean that everybody, or at least all the blood samples that I have tested, including my own, are infected with this "deadly" virus. The ones that react positive at a ratio of 1:400 would simply have a higher level of 'deadly' infection than the "deadly" infection had by the ones that only react positive with undiluted serum. The test is not specific for HIV. The results presented here could also mean that the tests used for detecting antibodies to HIV are not specific for HIV, as has been explained previously. In this case, there would be reasons other than HIV infection, past or present, to explain why a person reacts positive to it. The test also reacts positive in the absence of HIV. The scientific literature has documented more than 70 different reasons for getting a positive reaction other than past or present infection with HIV. All these conditions have in common a history of polyantigenic stimulations. Since there is no scientific evidence that the ELISA test is specific for HIV antibodies, a reactive ELISA test at any concentration of the serum would mean presence of non-specific or polyspecific antibodies. These antibodies could be present in all blood samples. They are most likely a result of the stress response, having no relation to any retrovirus, let alone HIV. In this case, a reactive test could be a measure of the degree of one’s exposure to stressor or oxidizing agents. The inevitable conclusion is that all positive reactions for antibodies to HIV are simply false positives. If nobody is positive for HIV, then people who react positive on the ELISA test do so due to something other than HIV. Competing interests: None declared |
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bmj.com
11h December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Mr. Peter Flegg revealingly stated: "I see no point of tackling broad queries such as "What is the evidence that 'HIV' exists?", which has been debated to exhaustion with the Perth Group over the years- if they do not believe any of the evidence put to them from hundreds of experts in the field, thousands of publications, and several papers specifically addressing this issue from centres like the NIAID, I doubt anything I could say here will change their mind." I would like to remind Mr. Flegg that all the above mentioned 'evidence' that 'HIV' exists from "thousands of publications" and from "hundreds of experts in the field" is all based upon a mistaken premise that 'HIV' has been isolated (i.e. exists) and has shown to be a causative agent of a disease. The Perth Group "do not believe in any of the evidence" purely and simply because there is no evidence – which is why the Perth Group rightly persist in their rigorous scientific questioning and debating and thinking – what scientists are supposed to do: science is no about belief or believing. Centres like NIAID are merely a propaganda institution disseminating, perpetuating and propagating 'HIV' propaganda. Mr. Flegg will always point BMJ Rapid Response readers to NIAID as a 'reference' point of 'authority' without having the intellectual autonomy (or scientific rigour) to question the NIAID Bible belt of 'HIV' belief. The hallmark of a viable hypothesis is that predictions based upon it will be fulfilled: this has never been the case of the 'HIV/AIDS' hypothesis: all the figures have had to be finagled; definitions (of 'AIDS') expanded; new diseases added in to keep the figures up; and most recently, in Africa, the diseases malaria and TB (which have always killed millions) are now bracketed with 'HIV/AIDS'. Hence: thousands of papers based upon a mistaken premise are completely worthless: Mr. Flegg can quote as many thousands of these metaphysical 'HIV' related papers but they are all based upon science fiction – not science fact. Here is a quick and easy 'do-it-yourself' AZT and 'HIV' Test for Mr.Peter J. Flegg: 1) What convinces Mr.Flegg that 'HIV' is more lethal or toxic than 'AZT'? 2) If a patient on AZT or any HAART treatment regime dies, what 'cause of death' is put on the death certificate? Is it ever AZT poisoning or HAART poisoning – or is it always 'HIV' related - "due to complications arising from HIV infection" (as the usual 'AIDS speak' mantra goes)? There is no evidence that 'HIV' is the cause of anything – apart from rising profits for ‘HIV’ multinational pharmaceuticals. 3) Where is the reference for a published electronmicrograph of isolated/purified 'HIV'? To date none have been published. The papers published in Virology 1997 by Gluschankof et al. and Bess et al. did not give us visual confirmation that 'HIV' had been isolated/purified (i.e. proven to exist). 4) If Mr. Flegg had the 'knowledge' (insight) that 'HIV' had not been isolated/purified (had not been proven to exist) – would he still prescribe his hypothetical patients cytotoxic AZT and HAART regimes? Mr. Flegg recently stated in a BMJ rapid response: "…no-one would propose giving potentially toxic drugs to HIV 'uninfected persons' in some form of comparative study." I would argue that every person is 'HIV' uninfected and ask Mr. Flegg if it is really legal, rational, logical or ethical to prescribe a cytotoic drug like AZT to anyone? Or as Dr. Roberto A. Giraldo stated: unless the blood sample in grossly diluted, everyone will test positive for 'HIV' – which in fact means that no one is 'infected' with 'HIV'. Would Mr. Flegg still prescribe AZT or any HAART cocktail after reading the following text by Dr. Roberto A. Giraldo?
'Everyone Reacts Positive on the ELISA Tests for HIV', by Dr. Roberto A. Giraldo Continuum (London) Winter 1998/9 5(5): 8-10: Discussion: The following are three possible explanations for why undiluted specimens of blood always react positive at the ELISA test: 3.1. Everybody has HIV antibodies. It is accepted worldwide that the ELISA test for HIV detects antibodies against what is known as the Human Immunodeficiency Virus (3-6). And the pharmaceutical company that commercializes the ELISA kits states that "Abbott HIVAB HIV-1 EIA is an in vitro qualitative Enzyme Immunoassay for the Detection of Antibody to Human Immunodeficiency Virus Type 1 (HIV-1) in Human Serum and Plasma". Since all undiluted blood specimens react positive on the ELISA test, a test that supposedly tests for antibodies to HIV, the results presented here suggest that every single human being has HIV antibodies. And this suggests that everybody has been exposed to HIV antigens. This would mean that all of us have been exposed to the virus that is believed to be the cause of AIDS. The people that react positive even at a dilution of 1:400, would be the ones that have had the highest level of exposure to HIV antigens. The rest of the people - the ones that only react positive with undiluted serum [1:1] - would have had a lower level of exposure to HIV. 3.2. Everybody has different levels of HIV infection. It is also believed worldwide that a person that reacts positive for antibodies against HIV has not only been exposed to but is infected with a deadly virus that causes immunedeficiency. Therefore, the positive reactions of all undiluted serums would mean that everybody, or at least all the blood samples that I have tested, including my own, are infected with this "deadly" virus. The ones that react positive at a ratio of 1:400 would simply have a higher level of 'deadly' infection than the "deadly" infection had by the ones that only react positive with undiluted serum. 3.3. The test is not specific for HIV. The results presented here could also mean that the tests used for detecting antibodies to HIV are not specific for HIV, as has been explained previously. In this case, there would be reasons other than HIV infection, past or present, to explain why a person reacts positive to it. The test also reacts positive in the absence of HIV. The scientific literature has documented more than 70 different reasons for getting a positive reaction other than past or present infection with HIV All these conditions have in common a history of polyantigenic stimulations. Since there is no scientific evidence that the ELISA test is specific for HIV antibodies, a reactive ELISA test at any concentration of the serum would mean presence of non-specific or polyspecific antibodies. These antibodies could be present in all blood samples. They are most likely a result of the stress response, having no relation to any retrovirus, let alone HIV. In this case, a reactive test could be a measure of the degree of one’s exposure to stressor or oxidizing agents. The inevitable conclusion is that all positive reactions for antibodies to HIV are simply false positives. If nobody is positive for HIV, then people who react positive on the ELISA test do so due to something other than HIV. Competing interests: None declared |
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bmj.com
7th December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Regarding the impossibility of isolating 'HIV', Mr. Bennett unwittingly has completely given the game away: "It is not so much laziness as using superior techniques (faster, cheaper, more accurate) which render others redundant: but I accept that it means that EM of peripherally isolated HIV will likely never be done - because it doesn't need to be done." It most certainly does need to be done - but Mr. Bennett is right in stating it never will be done, but not for the reason he states. The fact is that the current crop of virtual virologists DARE not use the earlier, tried and trusted methods of viral isolation to find HIV in peripheral blood - because they know they would not find any particles at all. By affecting to disdain to use ultra centrifugation, pelletting down etc. they can perpetuate the myth of HIV proliferation and pathogenicity by using indirect markers, as introduced by Robert Gallo, David Ho and others. In his book 'Virus Hunting - AIDS, Cancer & the Human Retrovirus: A Story of Scientific Discovery', Gallo readily admits that when he was working on HTLV1, a novel human retrovirus he suspected was the cause of adult T cell leukaemia, he was puzzled when he could never find any virus in the infected tissues of the elderly patients. It was he who suggested the use of surrogate markers as an acceptable alternative to actually finding and recovering virus using the traditional methods. Thus virtual virology was born -virologists were no longer required to demonstrate, with visual confirmation, the presence of virus in a patient's blood. They could just assume it was there by using antibody evidence, reverse transcription assays etc. Goodbye empirical observation, hello viral theology! 'HIV' research is not based upon hard science but is a matter of belief akin to religious faith: you cannot see the Holy Ghost but you are required to believe in it in order to belong to the club. However, as Peter Duesberg observed in his seminal paper published in Cancer Research (March 1st, 1987) viruses and other pathogens, typically when they cause a disease can be found at high titre, sufficient to cause cell destruction or intoxication at a faster rate than the body can replace them. The result is a disease condition. This just did not seem to be the case with HIV, which a) appeared to infect very few cells, and b) appeared to be restricted to latency by the antibody response. The apparent inactivity of 'HIV' worried those who sought to blame a retrovirus for 'AIDS', and that is what led David Ho and others to the theory behind 'viral load' testing. This purported to show that far from being an indolent virus restricted to latency by the immune system, HIV was hyperactive, creating billions of new particles daily, whilst the body simultaneously created billions of new cells to counter the viral proliferation. Ho was not bothered that such huge HIV titres had never been observed, nor the fact that the hallmark of HIV infection, if the experts were correct, should be the disappearance of cells, not a massive increase. Once again, it was left to Peter Duesberg to debunk a ridiculous, but still widely believed hypothesis, in a fully referenced letter he wrote with his colleague Harvey Bialy to Nature, which was grudgingly published in a much edited form. ("HIV an illusion" Nature 375: 197, 18 May 1995.) In their letter they point out that the methodology used by Ho et al and Wei et al, in two papers published in the same edition of Nature, grossly overestimated the numbers of viral particles claimed to be in a ml of plasma. "Here we would point out only that the central claim of the Ho et al and Wei et al papers-that 105 HIV virions per ml plasma can be detected in AIDS patients with various nucleic-acid amplification assays is misleading. The senior author of the Wei et al. paper has previously claimed that the PCR method they used overestimates by at least 60,000 times the real titer of infectious HIV: 100,000/60,000 is 1.7 infectious HIVs per ml, hardly the "virological mayhem" alluded to by Wain-Hobson. Further, Ho and a different group of collaborators have just shown that more than 10,000 "plasma virions," detected by the branched-DNA amplification assay used in their Nature paper, correspond to less than one (!) infectious virus per ml. And infectious units, after all, are the only clinically relevant criteria for a viral pathogen." (My emphasis) Eminent electronmicroscopist Prof. Etienne de Harven*, in criticising the loss of precision due to the abandonment of EM in identifying and quantifying viruses, pointed out that the pretext they used for their abandonment (like Mr. Bennett) was that EMs were unnecessary, time consuming and too costly: de Harven stated: "Dangerously enough, EM was progressively dismissed in retrovirus research after 1970. Molecular biologists started to rely exclusively on various 'markers', and what was sedimenting in sucrose gradient at density 1.16 gm/ml was regarded as 'pure virus'. It is only in 1997, after fifteen years of intensive HIV research, that elementary EM controls were performed, with disastrous results." These "disastrous results" published in Virology (Gluschankof et al. and Bess et al.) did not show purified/isolated 'HIV' but a mass of cellular debris and microvesicles with three ambiguous dots which were arbitrarily identified as 'HIV'. De Harven concludes: "In conclusion, and after extensive reviewing of the current AIDS research literature, the following statement appears inescapable: neither electron microscopy nor molecular markers have so far permitted a scientifically sound demonstration of retrovirus isolation directly from AIDS patients." (REMARKS ON METHODS FOR RETROVIRAL ISOLATION by Etienne de Harven, Continuum, Spring 1998.) If the methods of viral detection using indirect 'markers' Mr. Bennett trusts really work, then it is axiomatic that using the earlier methodology will only confirm their findings. It is time to clear up this point before 'HIV' research becomes even more irrational and ludicrous. Surely it would be worth while to spend a mere three or four days with basic EM equipment to confirm visually the results obtained by using Mr. Bennett's "superior techniques"? Hence, Mr. Bennett's statement is absurd and pure madness: "I accept that it means that EM of peripherally isolated HIV will likely never be done - because it doesn't need to be done." It does need to be done and urgently: can Mr. Bennett do it - and prove that 'HIV' exists? *Etienne de Harven worked in electron microscopy (EM) primarily on the ultra-structure of retroviruses throughout his professional career of 25 years at the Sloan Kettering Institute in New York and 13 years at the University of Toronto. In 1959 he was the first to report on the EM of the Friend virus in murine (mouse) leukaemia, and in 1960 to coin the word "budding" to describe steps of virus assembly on cell surfaces. Competing interests: None declared |
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bmj.com
3rd December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Mr. Nicholas Bennett stated: "The problem with Mr Russell's argument, is that you do not have to isolate something to know what it looks like." Mr. Bennett’s statement is ludicrous and an oxymoron and merely typifies the kind of sloppy science surrounding 'HIV' research. His statement is absolute nonsense: if the hypothetical 'HIV' has not been isolated how do we know what it looks like? I must remind Mr. Bennett that isolation means separating the target virus from all other contaminants. You have to establish which are viral proteins and which are contaminant proteins. No one has ever published EM images of isolated/purified 'HIV' recovered from a fresh blood sample or any other bodily fluid. Sloppy thinking and sheer laziness allowed scientists to get way with stating that material banding 1.16 in a sucrose density gradient represented 'pure retrovirus'. However, when this banded material was finally photographed under electronmicroscopy in 1997 it was revealed that practically all the banded material consisted of contaminants – microvescicles, cellular debris, etc., with just a few ambiguous dots which may or may not have represented the sought after hypothetical 'retrovirus'. It would be impossible from that mix when broken down into its constituent proteins to distinguish actual viral proteins from debris proteins. As for the point of knowing what something looks like, morphologically identical particles to those purporting to be 'HIV' can be found in the majority of placentas examined as well as in lymph node tissues biopsied from people with swollen lymph glands but with no indication of so-called 'HIV infection'. Luc Montagnier himself described the tissue cultures used in 'HIV' research as a "retroviral soup". When certain cell-lines are used it is possible using stimulants to activate previously latent endogenous retroviruses - yet another danger when making judgements based purely upon results obtained from cell culture. Mr. Bennett continues: "One early paper (from 1988) shows several EM micrographs of HIV showing the characteristic "truncated cone" core that is not seen in normal retroviruses." Please note: Mr. Bennett forgets to add that these particles are only ever observed in cell culture (in vitro)and have never been seen in this degree of clarity in any fresh blood or in any other bodily fluid. Laboratory conjuring tricks produce laboratory artefacts which should not be used for purposes of extrapolation. In a typical viral disease sufficient virus to cause the disease should be observable in the relevant tissues: this has never been the case for 'HIV'. Merely to say that the 'virus' is doing its lethal work from the comparative safety of the lymph nodes is a total cop out. Competing interests: None declared |
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bmj.com
1st December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Udaya S Mishra stated: "It is concerting to note that women are sharing four times the burden of HIV as compared with men, but this is a definite reflection of women's lack of power of negotiation in relation to sex. Consensual sex need not only account for mutual agreement but also mutual responsibility of its consequence. Reproduction related consequence rested entirely with women for which women bore the contraceptive responsibility on them to protect themselves from the evils of excess reproduction. Unlike contraception, prevention of HIV needs a greater realization by men as they become the transmitting agent of infection in the absence of power of sexual negotiation in women." This statement makes the assumption that ‘HIV’ is an 'infectious' STD but this is still an unproven supposition. 'HIV' has not been detected in cervico-vaginal secretions using visual confirmation by electronmicroscopy. And even if this were so, how would the insertive partner be 'infected' either cervically or anally? How does 'HIV' get into the blood stream of the insertive partner? There is no evidence to suggest and support a sexual mode of transmission of 'HIV' at all. Why is it more difficult for women to 'infect' men with 'HIV'? Where are all these Western white women with hypothetical 'HIV infection'? Why should 'HIV' be more readily transmitted male to female but not female to male? In which case where do heterosexual males get 'HIV' from? Also, where does the active (insertive) homosexual get 'HIV' from? How does a passive (receptive) homosexual transmit 'HIV' to an active (insertive) homosexual? What is the precise mechanism of hypothetical 'HIV infection'?. Recent UK 'HIV' figures (Data Source: SOPHID:2003) point to some unexplained anomalies concerning the disproportionate spread of 'HIV'. If 'HIV' is an STD why is it still restricted rigorously to the original 'high-risk' groups? The vast majority of homosexual 'HIV' cases in the UK are white (13,440 out of a total of 15,454); whereas the vast majority of heterosexual 'HIV' cases in the UK are black (11,068 out of a total of 15,998). The media have recently presented the misleading claim that the UK is in the grip of an heterosexual 'HIV' epidemic but what they did not mention is that over 75% of the heterosexual 'HIV' cases were imported from abroad particularly from sub-Saharan Africa, the Caribbean, India, Asia, etc. Why is there such a difference in the distribution of 'HIV/AIDS' in the developed West (including Australia) and the developing world (Africa, India, Asia, etc)? It has nothing to do with so-called 'education' (the 'safe-sex' mantra and condom use). We have seen huge rises in STD rates and unwanted pregnancies in the UK and USA without a concurrent spread of 'HIV'. These anomalies convince me that 'HIV' is not an STD. There is no endemic heterosexual 'HIV' epidemic in the UK. What these recent figures suggest is that 'HIV' is merely a marker for 'risk-behaviour' still rigorously confined to the original 'high-risk' groups: promiscuous homosexuals in the West and people from the developing world. With the advent of World AIDS Day the British media are perpetuating and propagating politically correct 'HIV' propaganda that "everyone is at risk" from an "equal opportunities disease". When will these lies stop? Competing interests: None declared |
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bmj.com
1st December 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Mr. Peter J Flegg stated: "The facts are that dissidents simply refuse to accept that what they see is HIV, and quibble about the degree of contamination, or insist that they will only accept images obtained from blood but not other bodily fluids or tissue samples or culture specimens." We "refuse to accept" because these arbitrary images have not proven to be indisputably isolated 'HIV'. They have never found 'HIV' in blood, semen or any bodily fluids: the only images ever shown purporting to be 'HIV' were derived from laboratory cultures and as such should be highly suspect as mere laboratory artefacts. Mr. Peter J Flegg disturbingly and unthinkingly concludes: "Until the Perth Group and others like Alexander Russell move past their mental block of isolation the dissidents will continue to think of HIV as pixie dust. I just wish the 40 million people currently living with HIV could be afforded the same luxury." The unanswered question of "isolation" is not a "mental block" but an extremely important fact in which the whole of the 'HIV' hypothesis is based. How can a global pandemic be attributed to a pathogen which has never been isolated? How can any treatment devised against this pixie dust phantom be anything other than misguided and therefore totally dangerous? Thus true "isolation" of 'HIV' is the only proof we have that 'HIV' exists. So far this has not been achieved. So why are we still using the acronym 'HIV'? There is every probability that far from being antibodies against exogenous retroviral proteins, the gp41 antibody is an auto-immune antibody against the endogenous cellular protein actin (which forms the cytoskeleton of cells); and similarly, the p24 antibody is an auto-immune antibody against the endogenous protein myosin. These two auto-immune antibodies would thus be extremely damaging to cells and set up an illness very similar to Lupus Erythematosus. This is a far more plausible explanation for cell destruction rather than the myriad, unconvincing hypotheses concerning 'HIV' cyto-toxicity. 'AIDS' is largely an auto-immune disease. Therefore, an 'HIV' vaccine could actually make matters far worse. These alleged 40 million people can be "afforded the same luxury" if they also think of 'HIV' as "pixie dust". No one is "living with HIV". Rather: 40 million people are living with the fairy tale illusion of "pixie dust". But has "pixie dust" been truly isolated? Competing interests: None declared |
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bmj.com
27th November 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Mr. Bennett stated that: "We know the particles are HIV because, by the standards of distinguishing any other pathogen, they appear to be HIV." This is a ridiculous, circular argument – we don’t even know what ‘HIV’ looks like because it has never been isolated. How does Mr. Bennett know what 'HIV' looks like? We have not yet established what 'HIV’ looks like. No one has ever seen 'HIV' – not even Mr. Bennett. Why has Mr. Bennett still not provided an EM (electronmicrograph) reference of isolated/purified 'HIV'? How does Mr. Bennett know the 'particle' he is looking at is a virus? Mr. Bennett cannot escape the fact that Robert Gallo and Luc Montagnier did not isolate a virus. There is still no evidence that 'HIV' is a virus. Mr. Bennett stated: "I would say that there is plenty of evidence that HIV is an infectious agent." Where is this evidence? 'HIV' is presumed to be an infectious agent based purely upon rather shaky epidemiological evidence. However, no one has described in scrupulous detail how 'HIV' is transmitted from one individual to another. For instance what is the precise mechanism by which the receptive partner (heterosexual female or homosexual male) infects the insertive partner? Why is it that 'HIV' appears to be unidirectional? For a pathogen to survive in nature and spread in an epidemic form it has to be bi-directional in its transmission. This does not appear to be the case with 'HIV'. It is seldom or never found in peripheral blood of infectees so therefore how is 'HIV' transmitted from one individual to another. Certainly there is no evidence that animal retroviruses are transmitted sexually so why do we make the assumption that 'HIV' is transmitted this way? Traditionally retroviruses are alleged to be transmitted from female to offspring either in the womb or during breast-feeding but there is no suggestion that animal retroviruses are transmitted in semen. Nobody knows what 'HIV' looks like. Can Mr. Bennett provide an EM of isolated 'HIV'? Competing interests: None declared |
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bmj.com
25th November 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Nicholas Bennett stated: If HIV is a harmless endogenous phenomenon and the drugs are toxic, can Mr Russell explain the fact that HIV seropositivity (i.e. infection) produces disruption of lymph node architecture." How do we know that the particles are 'HIV and how do we know it is 'HIV' that is disrupting the lymph nodes? What else is in there? If 'HIV' is sequestered in the lymph nodes, as claimed, how can it be actively damaging the immune system? There are cases recorded in the literature of people who have never tested 'HIV' positive who nevertheless have swollen lymph nodes. On examination, the nodes are shown to contain particles morphologically identical to 'HIV'. However there is no evidence that these particles are destroying the lymph nodes, merely that they are being sequestered there. On examination the tissues were shown to contain morphologically identical particles to 'HIV'. Hoe does Mr. Bennett explain that morphologically identical particles to 'HIV' can be found in virtually all placental tissue examined under electronmicroscopy? What is "HIV seropositivity (i.e. infection")? There is still no evidence that 'HIV' is an 'infectious' agent; it is only assumed to be. Competing interests: None declared |
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bmj.com
24th November 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Robert A. Da Prato asked: "I assume that the 99+% accuracy of ELISA tests at detection of HIV indicates both very high specificity and very high sensitivity for this test. I also assume that there is published evidence supporting this claim, which has been touted for at least 10 years. Can anyone reference the original paper(s)?" In science never "assume" anything. The ELISA tests are non-specific to 'HIV' because the antibodies detected cross-react with over 70 conditions. Emeritus Prof. Gordon Stuart, Public Health, Glasgow UK stated: "At present there is no scientific basis for using these tests to prove HIV infection." Chief UK virologist Philip Mortimer stated: "It may be impossible to relate an antibody response specifically to HIV infection." Even the manufacturers cautiously state in the literature enclosed with the test kit: "At present there is no recognized standard for establishing the presence and absence of HIV-1 antibody in human blood. Therefore sensitivity was computed based on the clinical diagnosis of AIDS and specificity based on random donors"1 "Do not use this kit as the sole basis of diagnosing HIV-1 infection"2 "The Amplicor HIV-1 Monitor test is not intended to be used as a screening test for HIV or as a diagnostic test to confirm the presence of HIV infection"3 1. Abbott Laboratories, Diagnostic Division, 66-8805/R5; January, 1997 2. HIV-1 Western Blot Kit, Epitope, Inc., Organon Teknika Corporation PN201-3039 Revision #8 3. Roche Diagnostic Systems, Inc., Amplicor HIV-1 Monitor Test Kit. US:83088. June 1996)(13-06-83088-001 (Also see: Abbott Test Halted After Inaccurate HIV Results, Chicago Tribune (CT) - FRIDAY, April 5, 1996 Edition: BUSINESS Page: 1 Word Count: 402). In 'Tests for HIV are Highly Inaccurate', Dr. Roberto Giraldo wrote: "Some of the conditions that cause false positives on the so-called 'AIDS test' are: past or present infection with a variety of bacteria, parasites, viruses, and fungi including tuberculosis, malaria, leishmaniasis, influenza, the common cold, leprosy and a history of sexually transmitted diseases; the presence of polyspecific antibodies, hypergammaglobulinemias, the presence of auto-antibodies against a variety of cells and tissues, vaccinations, and the administration of gamma globulins or immunoglobulins; the presence of auto-immune diseases like erythematous systemic lupus, sclerodermia, dermatomyositis and rheumatoid arthritis; the existence of pregnancy and multiparity; a history of rectal insemination; addiction to recreational drugs; several kidney diseases, renal failure and hemodialysis; a history of organ transplantation; presence of a variety of tumors and cancer chemotherapy; many liver diseases including alcoholic liver disease; hemophilia, blood transfusions and the administration of coagulation factor; and even the simple condition of aging, to mention a few of them. It is interesting to note that all of these conditions that cause the 'HIV tests' to react positive in the absence of HIV, are conditions which are present with varied distribution and concentration in all of the conventionally recognized AIDS risk groups in the developed countries, as well as in the vast majority of inhabitants of the underdeveloped world. This means that in all probability many drug users [including mothers], certain gay males, and some haemophiliacs in the developed countries, as well as the vast majority of inhabitants in most countries of Africa, Asia, South America and the Caribbean, who have positive reactions to the tests for HIV, may very well do so due to conditions other than being infected with HIV…There is no justification for the fact that both patients and the general public have had all of the preceding facts withheld from them. Without the merits and demerits of the tests for HIV, people cannot make informed decisions." (Being 'HIV-positive' does not mean that a person is infected with 'HIV'; Tests for HIV are Highly Inaccurate, Dr. Roberto Giraldo). Competing interests: None declared |
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bmj.com
23rd November 2004
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| Alexander
H Russell, Writer/artist/philosopher WC1N 1PE Send response to
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Dr Musa A. Garbati alarmingly stated: "For a pandemic that is spreading around the world, infecting more than 14,000 individuals per day,3 this move by WHO if not followed by the provision of alternative ARVs is likely to be the disaster of the year. Alternatives should not just be made available but affordable to those that need it most." What evidence does Dr. Garbati have for these fictitious figures of "14,000 individuals per day" being 'infected' with 'HIV'? Even the 'AIDS' establishment admit - and are agreed - that 'HIV' is very difficult to 'transmit'. These wildly inflated figures are abstract and arbitrary and are all based on 'guesstimates' which in the past have invariably been wrong. How many of these alleged "14,000" individuals have had a 'positive' ELISA 'HIV' test, confirmed by Western Blotting, and further confirmed by the recovery of a significant quantity of viable infectious 'HIV' particles from said patient? The answer may surprise Dr. Garbati: zero. What studies have ever been carried out to recover 'HIV' particles from the blood of these individuals? The answer is none. If "14,000 individuals" are being 'infected' by 'HIV' daily then where is the 'HIV' epidemic in the West? Where are all the 100,000s of Western heterosexuals with 'HIV' or 'AIDS'? There is no heterosexual 'HIV' epidemic in the West (or anywhere else in the world for that matter). Does Dr Garbati realise that TB, malaria and disease conditions relating to poverty in the developing world make these non-standardised and non- specific arbitrary 'HIV' tests run 'positive'? What we are wrongly calling 'HIV' is merely an endogenous marker for 'risk-behaviour' in the West and disease-conditions relating to poverty and malnutrition in the developing world. So-called 'anti-retroviral' drugs cannot cure 'AIDS' related conditions such as TB and malaria. All 'anti-retroviral' drugs can do is interfere with the bodies natural metabolism and make matters worse. There is no such thing as an 'anti- retroviral' drug anyway because 'HIV' is really an endogenous epiphenomenon. What poor Africans really need is clean water, sanitation, nourishing food and not over priced and highly toxic 'antiretrovirals'. All endemic diseases of Africa are made infinitely worse by malnutrition: their bodies do not have the basis resources to fight disease. The last things poor Africans need is expensive and lethal 'anti-retroviral' drugs. We now see Septrin is being touted as the great, low-cost saviour antibiotic for 'AIDS' related illnesses in African children, halving the death rates previously attributed to the hypothetical 'HIV' infection. We are told that co-trimoxazole has the advantage of being cheap and readily available, whereas 'anti-retroviral' drugs are much more expensive. Co- trimoxazole costs less than ten cents per person a day. It is well known that antibiotics are powerless against viruses – including 'retroviruses' - so if the patients are recovering when put on Septrin this must be because Septrin is active against bacterial infections. However, if it is claimed that 'X' million children a year die of malaria with or without 'HIV' then the malaria is obviously the main problem and 'HIV' is irrelevant. If Septrin is halving 'AIDS' deaths t | |||
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Posted by: Alexander Huw Verney-Elliott | Saturday, 21 June 2008 at 05:03 AM