Michael Verney-Elliott
16th February 1938 - 5th March 2007
The late Michael Verney-Elliott was a pioneering HIV/AIDS
dissident and one of the funniest people I ever met...
I
am extremely sorry to hear that Michael has died.
Eleni Eleopulos, on Michael Verney-Elliott's death, 6 March, 2007.
Once again I am so so sorry for your loss. Michael was really a cornerstone of the dissident movement. I am sure everybody will feel his loss. I read the article and I think that it is extremely well written and although I do not agree with everything Michael says there, it doesn't mean that I am right. It would be very good if you could publish it but most probably you will find it difficult. I think your best chance would be Medical Hypothesis, unfortunately their page charges are very high. All the best, Eleni ...The thing which most often comes to mind about Amsterdam is how much I wanted Mike to be present in my conversation with Montagnier which unfortunately did not happen. Alex, let me repeat it once again, how big a loss Mike's death is and how much we will miss him. Please send me your tribute when you finish it. Best regards, Eleni
What
stands out in my mind about
Neville Hodgkinson, 07 March, 2007.
I first met Michael in 1990,
when he and the rest of the Meditel team interviewed me in New York City, where
I was then living. For the next several years we seemed very close, and saw each
other often - Michael and Joan and the AIDS dissidents in London, Europe, North
and South America - including the Bologna conference (1994) and the
Buenos Aires conference (1995). I continued to correspond with him up
until last year, through e-mail and over the phone. Mostly I remember the
clarity of his thoughts and his enunciation, and his incisive sense of humour,
which often served to illuminate a difficult analysis. For example, he
once said: "HIV does not cause AIDS; AIDS causes HIV." - by which he
meant that the AIDS illnesses (whatever they are) cause positive readings on the
("HIV-antibody") tests, which are then used to generate bogus
"AIDS" diagnoses. As a gay man and a freethinker, Michael did not
flinch from the possibility that the deaths of hundreds of thousands of gay men
were not just an unfortunate result of an unfortunate medical blunder, but were
intended from the very beginning - intended from the very inception of the AIDS
Hoax.
John
Lauritsen, Dorchester, Massachusetts, 03 May 2007.
I
adored Michael, and I also really loved him, from the moment I first met him,
with Joan, back in 1988 I think it was. I thought he was one of the funniest,
most brilliant, outrageous and original minds I ever encountered.
Celia Farber (aka Candice), 08 March 2007.
I heard about Mike's death from Joan yesterday. I'm glad for him, I got the
impression that he wasn't enjoying life very much. On several occasions when I
found myself in your neck of the woods, I rang him and either got no answer or
he seemed too out-of-sorts to want see anybody or camp around. His Go-Back
will serve as a constant epitaph. Coincidentally, on Sunday evening as I
wended my way to Joan's for a bite to eat, I articulated for the first time
one of Mike's 90's sayings "I wish I was dead". I think I
know exactly what he meant, if people are so stupid as to persist with the
theory of infectious antibodies, then let them get on with it, but without
him. I rather feel like that now, not only about the wretched AIDS business,
but so much else in medicine...There are the ones about "From the
people who didn't bring you the virus that causes cancer, it's the virus that
doesn't cause AIDS." A propos Gallo & Montagnier, "Who
the fuck cares about who stole the fake jewels" And then there
is the one about "The virus that can do everything from splitting ends
to in-growing toenails." The one that has been bugging a lot of
late was Mike's outburst one summer evening in Joan's St. Ann's Road "How
the fuck is spunk supposed to transmit it, if there's no HIV in
semen?" At the time I just thought, what!!!
My enduring memory
of him is his constant agonising about SIV and how that fitted it with the
overall story... In those days, I was still so naive to think, it
depended on people like me (or should do), those who were trained in the
field. Little did I know how right he was actually, we who were so trained
were completely corrupted/fucked up by our wrong paradigms and
self-righteousness - people like Mike were right, someone of independence of
mind, much to my surprise.~
Hector
Volker Gildemeister, 6 &7 March, 11 April, 2007.
Calling
Mike at Meditel in the early years of the “AIDS war” –as we used to call
it- was like tuning into the Monty Python show for me.
It was just as funny, as real, as sarcastic with our opponents and as
compassionate with the AIDS victims as I perceived the Monty Python/John Cleese
shows. I could even “mention the
war” and immediately Mike would call me “Rommel” – whom he considered a
worthy match of his British rival “Monty”.
It
was a hard war to fight against that huge HIV-AIDS establishment.
But every time we won one over, not to accept the death spell associated
with that government sponsored antibody test – be it Neville Hodgkinson from
the Sunday Times or just an ordinary student – and every time we won
one over to forsake those inevitably toxic DNA chain terminators prescribed to
exterminate the long-neutralized passenger virus, HIV, we had reason to
celebrate. We felt so good about
our little celebrations, because they were based on evidence – not on
government handouts, and because our little triumphs have lived on and cheered
up – despite that global consensus that you must take toxic drugs and die
because of that undetectable but “deadly” virus.
Unlike
any other cameraman I had performed for, Mike made me feel at ease even in front
of his camera. With his sharp
questions, his knowledge and his wits, his camera was really more entertaining
than intimidating, ever since Meditel first produced “The AIDS Catch”.
Unfortunately
he, too, succumbed to the toxic side of one drug he could not let go of.
Too sad there is no more Mike Verney Elliott to turn to in the AIDS war
and no more Mike to cheer us up at meetings in Barcelona, Berlin, Berkeley and
Bologna.
Auf
Wiedersehen, Mike!
Dein Freund Peter
Peter Duesberg, A Memorial Address for Michael Verney-Elliott, 1st April, 2007.
I
miss Mike enormously. Most of all I miss his melodious voice and his innate
kindness and generosity. I think of him at intervals throughout the day. He
played a very important part in my life.
I
met him in 1986 when he was a drama producer at London Weekend Television. My
friend Carol Wiseman was working with Michael on a production there and she
called me to say that he did nothing but talk about how the science behind AIDS
was completely wrong. As a television producer making documentaries on science
and medicine, she thought he and I should get together.
We
fixed a lunch at Bertorelli’s and I ended up at the wrong one. We waited for
each other for about an hour and finally joined up at the Charlotte Street one.
Michael was fascinating. He arrived carrying a huge briefcase stuffed with
scientific papers. He felt very strongly that gay men were wrongly being blamed
for spreading AIDS through sex. It just didn’t add up and for two years he had
set about researching the views of non conformist scientists.
The
lunch lasted three hours. From that day, Michael
succeeded in leading me on an intellectual dance for the next fifteen as
we two-stepped off into five network television documentaries on the subject.
He
was a consummate performer, having studied at the London Academy of Music and
Drama and toured Europe as Hamlet. His rich voice and exquisite diction made him
the perfect narrator for the documentaries.
The
first was “AIDS - the Unheard Voices” for Channel 4 which he worked on with
producer Jad Adams. It won the Royal Television Society Award for Journalism the
first ever to be bestowed upon and independent television production company.
Mike
had an extraordinary gift with language. His wit was as acerbic as his tongue
was caustic. He could come out with a one liner that you would remember for the
rest of your life. For example when the row between Robert Gallo and Luc
Montagnier broke out as to who had “discovered” HIV first. Mike simply said
“Who care who stole the fake diamonds”.
Over
the years, he developed a strong friendship with molecular biologist Peter
Duesberg, who inspired our early work on the AIDS debate. Peter was always
amazed at Michael’s grasp of the science and his ability to glide between the
different disciplines and produce fresh and challenging perspectives.
He
was a wonderful friend and companion. He dubbed us the “Bisto Kids” one day
when we were out in the freezing with our noses glued to the window of a
restaurant waiting for Duesberg to finish a conversation with one of his
admirers.
He
was always ready to advise me on matters of dress and presentation, giving me
that final bit of confidence by saying “Strut your stuff and be a star
darling”.
I’ll
keep trying. Mike
Joan Shenton, Mike Verney-Elliott Remembered, 25 March 2007.
Being in Love

Michael Verney-Elliott in the 1990s
"Being's Name is Love.."
Alex Verney-Elliott, B & A, 2007.
"I am mortal, born to love and to suffer."
Friedrich Hölderlin (1770 - 1843).
“Love takes us where knowledge leaves off.”
Saint Thomas Aquinas (1225 - 1274).
“Love is composed of a single soul inhabiting two bodies.”
Aristotle (384-322 BCE).
“Love is all we have, the only way that each can help the other.”
Euripides (c. 480–406 BC).
“Augustine once said: I love you - I want you to be what you are.”
Martin Heidegger to Hannah Arendt, 1925.
“That which is done out of love always takes place beyond good and evil.”
Friedrich Nietzsche, Beyond Good & Evil, 1886.
"My little, wandering, charming soul, Guest of my flesh, companion, Where are you going now - Naked, rigid, pale, No longer laughing, being alone?"
Publius Aelius Hadrianus, (24.1. 76 – 10.7.138 AD).
'Homecoming'
Peaks of silver shine
silently above,
And the sparkling snow is full of roses.
Still higher above the light lives the god, pure
And holy, pleased with the divine play of light beams.
He lives there quietly and alone: his face is bright.
Down into the deep his
influence extends: it
Reveals and illumines, just as he pleases.
And now life begins again. Gracefulness
Flourishes as it did before, and the Spirit
Is present and approaches, and a joyful
Disposition fills its wings.
Friedrich Hölderlin (1770-1843).
'Another day'
Another day. I follow
another path,
Enter the leafing woodland, visit the spring
Or the rocks where the roses bloom
Or search from a look-out, but nowhere
Love are you to be seen in
the light of day
And down the wind go the words of our once so
Beneficent conversation...
Your beloved face has gone
beyond my sight,
The music of your life is dying away
Beyond my hearing and all the songs
That worked a miracle of peace once on
My heart, where are they
now? It was long ago,
So long and the youth I was has aged nor is
Even the earth that smiled at me then
The same. Farewell. Live with that word always.
For the soul goes from me to
return to you
Day after day and my eyes shed tears that they
Cannot look over to where you are
And see you clearly ever again.
Friedrich Hölderlin (1770-1843).
'Annabel Lee'
It was many and many a
year ago,
In a kingdom by the sea,
That a maiden there lived whom you may know
By the name of ANNABEL
LEE;
And this maiden she lived with no other thought
Than to love and be loved
by me.
I was a child and she was a child,
In this kingdom by the
sea;
But we loved with a love that was more than love-
I and my Annabel Lee;
With a love that the winged seraphs of heaven
Coveted her and me.
And this was the reason that, long ago,
In this kingdom by the
sea,
A wind blew out of a cloud, chilling
My beautiful Annabel Lee;
So that her highborn kinsman came
And bore her away from
me,
To shut her up in a sepulchre
In this kingdom by the
sea.
The angels, not half so happy in heaven,
Went envying her and me-
Yes!- that was the reason (as all men know,
In this kingdom by the
sea)
That the wind came out of the cloud by night,
Chilling and killing my
Annabel Lee.
But our love it was stronger by far than the love
Of those who were older
than we-
Of many far wiser than
we-
And neither the angels in heaven above,
Nor the demons down under
the sea,
Can ever dissever my soul from the soul
Of the beautiful Annabel
Lee.
For the moon never beams without bringing me dreams
Of the beautiful Annabel
Lee;
And the stars never rise but I feel the bright eyes
Of the beautiful Annabel
Lee;
And so, all the night-tide, I lie down by the side
Of my darling- my darling- my life and my bride,
In the sepulchre there by
the sea,
In her tomb by the
sounding sea.
Edgar Allan Poe (1809 - 1849)
Love Poem to Marie von Tucher
Narrow bands dividing us, fall away!
Sacrifice alone is the heart's true way!
I expand myself to you, as you to me.
May what isolates us go up in fire, cease to be.
For life is only reciprocated,
By love in love is it alone created.
To the kindred soul abandoned,
The heart opens up in strength gladdened.
Once the spirit atop free mountains has flown,
It holds back nothing of its own.
Living to see myself in you, and you to see yourself in me,
In the enjoyment of celestial bliss shall we be.
G. W. F. Hegel, April 13th, 1811.
“Love aims at the Other; it aims at him in his frailty... To love is to fear for another, to come to the assistance of his frailty. In this frailty as in the dawn rises the Loved, who is the Beloved. An epiphany of the Loved, the feminine is not added to an object and a Thou antecedently given or encountered in the neuter (the sole gender formal logic knows). The epiphany of the Beloved is but one with her regime of tenderness. The way of the tender consists in an extreme fragility, a vulnerability. It maintains itself at the limit of being and non-being, as a soft warmth where being dissipates into radiance, like the 'pale blush' of the nymphs in the Afternoon of a Faun, which 'leaps in the air drowsy with thick slumbers,' dis-individualizing and relieving itself of its own weight of being, already evanescence and swoon, flight into self in the very midst of its manifestation...The movement of the lover before this frailty of femininity, indulges in compassion, is absorbed in the complacence of the caress.”
Emmanuel Lévinas, Phenomenology of Eros; Totality & Infinity, Duquesne University Press, Pittsburgh, 1969.
“The death of the Other: a double death, for the Other is death already, and weighs upon me like an obsession with death... If death is the real, and if the real is impossible, then we are approaching the thought of the impossibility of death... Dying means: you are dead already, in an immemorial past, of a death which was not yours, which you have thus neither known nor loved, but under the threat of which you believe you are called upon to live; you await it henceforth in the future, constructing a future to make it possible at last - possible as something that will take place and will belong to the realm of experience...Loss goes with writing... Learn to think with pain... To live without a lifetime - likewise, to die forsaken by death... To write elicits such enigmatic propositions... To write is no longer to situate death in the future - the death which is always already past... To write is to know that death has taken place even though it has not been experienced.”
Maurice Blanchot, The Writing of the Disaster, University of Nebraska Press, 1995.
“He arrives - Your beauty - the beauty of the world. Your love - the beating of the universe, the loving rhythm of nature, time in harmony with the sun. In you , I behold its radiance. In you, I savour its power, I bathe in its warmth. At times, the eternal joins with the instant. We are present to each other, but between us remains eternity, while we continue to grow. How do we unite these two times?... How do I return to you?...How do I call the going beyond?... We can remain together if you do not become entirely perceptible to me, if a part of you stays in the night. Already, beauty has created a distance: a veil over us... Only love consents to a night in which I will never know you. Between those who love each other, there is a veil... I become because I recognise myself in you... With you, the world remains fluid... How do I remain in love - cultivating sun and grace?... To be silent to allow you to speak, to give birth to you. And to us, as well. To listen to the other's love.”
Luce Irigaray, Prologue - To Be Two, The Athlone Press, 2000.
“Even before the death of the other, the inscription in me of her or his mortality constitutes me. I mourn therefore I am. I am - dead from the death of the other, my relation to myself is first of all plunged into mourning, a mourning that is moreover impossible. this is what I also call the ex-appropriation, the appropriation caught in a double bind: I must and must not take the other into myself; mourning is an unfaithful fidelity if it succeeds in interiorizing the other ideally in me, that is, in not respecting his or her infinite exteriority... If death comes to the other and comes to us through the other, then the friend no longer exists except in us, between us...being-for-death... But I can have the experience of 'my own death' by relating to myself only in the impossible experience, the experience of the impossible mourning at the death of the other. It is because I 'know' that the other is mortal that I try to keep him or her in me, in memory... being-for-death is always mediated... in the experience or in the 'non-experienceable' structure of impossible mourning. Mourning would be more originary than my being for death.”
Jacques Derrida, Interview with Maurizio Ferraris, Aut Aut 235, January-February 1990.
“At the conclusion of On Transience, Freud said that mourning should spontaneously cease one day, freeing the energy it consumed for other pursuits. The living and the dead might arrive at an uneasy truce, merely out of exhaustion or, perhaps, out of the transformation of grief, creating something new in memory of the departed... Freud was asked in his old age what should be the goals of a healthy, vital life. He is reported to have replied, "Lieben und Arbeiten" - to love and to work. Love had earned a clear place in Freud's estimation. He had come to see in its many forms the source of all emotions, behaviours, and actions. It was the inescapable essence of humanity... Through mourning and the triumph of human creativity over loss, the mourner finds again what has been lost within himself. In learning to give himself over to the symphony of life and death, he rediscovers himself, and so realizes the potential inherent in all beings to love and work.”
Matthew von Unwerth, Freud's Requiem - Mourning, Memory and the Invisible History of a Summer Walk, Continuum, 2006.
“How could one agree to speak of this friend? ... Everything we say tends to veil the one affirmation: that everything must fade and that we can remain loyal only so long as we watch over this fading movement, to which something in us that rejects all memory already belongs...What separates: what puts authentically in relation, the very abyss of relations in which lies, with simplicity, the agreement of friendly affirmation that is always maintained. We should not, by means of artifice, pretend to carry on a dialogue. What has turned away from us also turns us away from that part which was our presence, and we must learn that when speech subsides, it is not only this exigent speech that has ceased, it is the silence that it made possible and from which it returned along an insensible slope toward the anxiety of time. Undoubtedly we will still be able to follow the same paths, we can let images come, we can appeal to an absence that will imagine, by deceptive consolation, to be our own. We can, in a word, remember: without memory, without thought, it already struggles in the invisible where everything sinks back to indifference. This is thought's profound gift. It must accompany friendship into oblivion.”
Maurice Blanchot, On the Death of Georges Bataille; Friendship, Stanford University Press, 1997.
“Love remains a relation with the Other that turns to need, and this need still presupposes the total, transcendent exteriority of the other, of the beloved. But love also goes beyond the beloved. This is why through the face filters the obscure light coming from beyond the face, from what is not yet, from a future never future enough, more remote than the possible... Love aims at the Other; it aims at him in his frailty... The movement of the lover before this frailty of femininity, neither pure compassion nor impassiveness, indulges in compassion, is absorbed in the complacence of the caress... Love does not simply lead, by a more detoured or more direct way, toward the Thou. It is bent in another direction than that wherein one encounters the Thou... If to love is to love the love the Beloved bears me, to love is also to love oneself in love, and thus return to oneself... Love accordingly does not represent a particular case of friendship. Love and friendship are not only felt differently; their correlative differs: friendship goes unto the Other; love seeks what does not have the structure of an existent, the infinitely future, which is to be engendered. I love fully only if the Other loves me, not because I need the recognition of the Other, but because my voluptuosity delights in his voluptuosity... The absolutely other is the Other. He and I do not form a number.”
Emmanuel Lévinas, Totality & Infinity, Duquesne University Press, Pittsburgh, 1969.
“To have a friend: to keep him. To follow him with your eyes. Still to see him when he is no longer there and to try to know, listen to him when you know that you will see him no longer - and that is to cry. To have a friend, to look at him, to follow him with your eyes, to admire him in friendship, is to no in a more intense way, already injured, always insistent, and more and more unforgettable, that one of the two of you will inevitably see the other die. One of us, each says to himself, the day will come when one of the two of us will see himself no longer seeing the other and so will carry the other within him a while longer, his eyes following without seeing, the world suspended by some unique tear, each time unique, through which everything from then on, through which the world itself - and this day will come - will come to be reflected quivering, reflecting disappearance itself: the world, the whole world, the world itself, for death takes from us not only some particular life within the world, some moment that belongs to us, but, each time, without limit, someone through whom the world, and first of all our own world, will have opened up in a both finite and infinite - mortally infinite - way... One should not develop a taste for mourning, and yet mourn we must. We must, but we must not like it - mourning, that is, mourning itself, if such a thing exists: not to like or to love through one's own tear but only through the other, and every tear is from the other, the friend, the living, as long as we ourselves are living, reminding us, in holding life, to hold on to it.”
Jacques Derrida, Jean-Marie Benoist - The Taste of Tears; The Work of Mourning, University of Chicago Press, 2001.
It
has taken me time to Write about Michael like it had taken me time to Love about
Michale for love like being always takes time and is always a question of time
and love and being take time to come for one to become love to become being for
being is love for love is being. I love Michael and Michael was Love and Love
never dies and being in love never dies because being never dies. Michael was
pure being because Michael was pure love because pure being is pure love and
pure love is possible because pure being is possible.
Michael
was the only human being I have ever met who was pure being because he
was pure love and all love whereas all the other beings I have know have had a
fear of love as a fear of being so never came to being so never came to
love: I call these beings as abeings: as they that are not there as those that
have not come to presence - have not come to love - those that have not come to
being.
Michael had the shine: Michael shone: from the first time I met him to the time I saw him die he shined forth. Michael had the shine because he was true to his light as true to his being: something utterly and uniquely rare in to day’s dark and dead world of billions of a beings who do not shine and are not there: for to be there as a being in the world is to shine forth free from the fear of god free from the fear of abeings.
Michael
never shone so brightly as when he was dying there before me: never had Michael
looked so serene, so sweet, and so beautiful in these last few magical moments: a life
times love shone through as a burst of energy and emanation of his giving spirit
as if giving me more life as I took in all his energies and emanations. As
beings we do not die: we
become our own emanation and our sensation as a spirit that shines forever. The
Dying Beauty of His Glowing Face Shined Through His Suffering as His Spirit Left
His Body.
Being
with Michael dying was the most moving, mesmerizing and extraordinary experience
in my life: Michael erupted a euphoric elation and incredibly intensity as if
his face became on fire as a volcanic explosion of lava coming over me burning
bright with light and heat glowing radiantly and never have I seen Michael look
so serene and sublime and I was sharing his tender transition between the
biological world and the ontological world of being becoming time from being the
body.
Sensationing Michael's being leaving his body like leaking lava made me realize for the first time that there was life after death: that there is being after death: a death free from the body that wears us out of being in the world. Never had I seen Michael’s face look so radiant, so beautiful so overwhelmingly warm and glowing and caring and giving: those gift that were Michael: always giving, always caring and always loving. One of Michael’s last phrases was (when looking at old photographs of himself): “I wasn’t rubbish.” One of Michael’s major faults was to under sell his worth, his value, his talents, his genius being so self effacing and hyper-critical that he always was. And Michael being so hypercritical meant having no real friends and in that respect we were both very lucky for we had no friends only parasites.
In hospital Michael's only interest was concern and care for me all the time: even when ill and dying Michael was kind and all giving - like he has been throughout his serene and saintly life: and Michael was a saint - albeit a dissident one, an aids dissident one; an outspoken and dangerous saint: Michael was the first one in the United Kingdom to argue that 'HIV' did not exist along with his cherished colleague and friend, the 'HIV' Heretic, Eleni Eleopoulos. A doctor out of something to say asked Michael what he did and Michael replied in a droll and dull manner that he had made aids documentaries and had interviewed Montagnier who admitted that he had never isolated HIV to which the doctor looked bewildered and perplexed not knowing what to say by saying nothing.
Michael always argued that everything ever stated about 'HIV' was a set of false assumptions: it was always assumed 'HIV' was a virus, it was always assumed that HIV was sexually transmitted and it was always assumed that 'HIV' caused 'AIDS' and yet never any of these absurd assumptions has ever been proven yet such 'HIV' related-lies and propaganda are still propagated by our pusillanimous press. Michael argued rather that 'AIDS' caused 'HIV' - that 'AIDS' conditions caused endogenous 'HIV' expression waking up dormant so-called 'retrovirus'.
For Michael pusillanimous 'political correctness' produced 'HIV' propaganda which in turn epitomised the liberal lies of 'political correctness': 'everyone is at risk from an equal opportunities disease' - 'HIV effects us all' and yet everyone know that 'political correctness' is a liberal lie, an inverted-racism, an inverted sexism and inverted culturalism and no one really believes in it but they still ape and act out this slave morality: for 'political correctness' for Michael was a herd-instinct slave-morality and a fear of thinking freely for oneself: and Michael was the only one that I ever knew who really said what he thought without fear of the thought police.
Michael
always showed constant care and concern for my well being from a morning
greeting to and evening ending; always warm and radiant and loving and giving;
again it was the warmth and love in his melodious voice that caressed me so
closely with care and concern; an over whelming sense of being as belonging with
the one that one loves and being loved became so overwhelming: with Michael I
had the serene sensation of complete closeness, warmth and welcoming
all the time as if he was there solely for me alone. The moment I entered the
living room I felt Michael's intensity of being-love-there as a glowing geist,
a warming welcoming.
Michael’s love for me was always there
every single morning when he greeted me with at melodious and warm voice of true
love: “Good morning my lovely.” How I miss those tender words now no longer
having those sweet sounds: I cannot simply believe I will never hear that
serene voice ever again for it was always there and has to be there still
somewhere. I miss Mike’s warmth and love and company so much for he really
made me feel at home; the first sense of being at home I’ve ever had
because home is where love is: coming home to Michael was always the most
gleeful. Joyous and happy sensation I ever had: now I have no Michael I have no
home to come to.
Michael
was my image of being my I deal of being my Idol of being but I do not idolize
or idealize Michael as I do not have to: Michael was an ideal being an idol of
being for Michael was love and being is love: we come to be being only through
love and Michael was my first love as my first being that I ever encountered.
Looking back at looking at Michaels
glowing being shining forth love made me realize I should have died with him
there and then and gone away with him for after such an experience there is
simple and purely nothing left to live for.
The
most dreadful and devastating silence to grasp is not hearing Mike’s melodic,
soft and caressing voice that haunted me so much near the end when it was fading
and so soft yet somehow more poignant an powerful in its vulnerable child like
innocence in its radiance and purity of presence; when he said; "I’ve always
loved you – you haven’t always loved me – but you do now."
I
miss Michael’s voice so much…
Michael's
voice was not merely the sound of his being but the shine of his being beaming
forth: Michael had the most musical and melodious voice that I had even heard.
I
felt very moved by Michael’s desire to for me to retrieve his house keys and
bring them in to hospital with the aid of the wheelchair that he insisted I go
back home for. I felt I was betraying him when saying I could not possible just
take him back home and I think he knew it but the hope to return home again was
there for I promised him that he would die at home.
I
miss Michael’s smile so much…
Now
Michael is not there at home I am no longer there at home for being-home is being at
home with the being-there that you loves: home is where being is waiting. Where
two together become one being at home for at home two become one. Michael
made our home glow through his emanation, warmth and love and days after he died the
our home became homesick and homeless: cold, sad, lost and dead: Michaels being
had been so present, poignant and potent so real and radiant that when he went
the home went with him for home is being home with the one we love: being home
is being with being home where two become one being home: when one being dies
the other one becomes the other none: for one and one make one love but one
minus one love make none. I have always been homeless until Michael became my
home and now I am at home at being at home without a house to be in for the
house is always homeless always beingless for the house is where we bury the
dead and where abeings abide and abode..
I
miss Michael's being so much...
Since
Michael has disappeared my life feels empty without him there and I feel I long
to disappear with him and long for the die I die to be with him again: being
together and being in love again and forever.
I
missed Michael's time so much...
I Lived with an Abeing before I Lived with a Being - I Lived with the Hate before I Lived with the Love - I Lived with the Bad before I Lived with the Good - I Lived with the Fear before I Lived with the Care - I Lived in Dread before I Lived in Delight - I Lived with Sickness before I Lived with Shininess. Before I could not Return to Home, for Before I could not Return to Being for There was No home-there for There was No being-there: I lived in a no-place with a no-one where there was no presence of place only an absence of home where there was no presence of being only an absence of being and yet I always trembled at the thought of going back to the no-one at the no-there.
For years I lived with a mad man in fear and dread, resentment and evil, and it took me much time to set myself free from being trapped by terror to live with love and free from censorship and control. For years I lived with a mad man surrounded by books who wanted to be 100% Intellect but was mindless and beingless and loveless for this mad man was not there as being-there as presence-there for this mad man had no presence no being - that is no love: being-beingless being surrounded by books: being-mindless but being surrounded by books. The mad man feared the being of being and the sensation of sein and would rather have died than loved like most men.
Knowing
I was loved by Mike and learning to love Mike gave me a sense of belonging and
becoming a being with another being there in the world: by giving me love Mike gave me
being: gave me my being back through love through being in love: for there is
only being there where there is love there: no love there – no being
One of Mike’s most repeated questions was: “Oh Mr. Russell! What will become of us all?” If we are beings we become time as being time – if we are abeings we become nothing because there is no shining there. Only those with the shine shine-on live-on and Mike had The Shine and shone so brightly and beautifully for his re-birth for only the body dies as being lives on shining forever for time for all time. Mr. Russell Died when Mr. Verney-Elliott Died and Died together in Love.
I miss Michael's thereing so much...
Gallo was the Evil 'HIV' Lie Montagnier was the Evil 'HIV' Lie Fauci was the Evil 'HIV' Lie Ho was the Evil 'HIV' Lie Watney was the Evil 'HIV' Lie Campbell was the Evil 'HIV' Lie King was the Evil 'HIV' Lie and Michael fought the Evil 'HIV' Lie to the End. I always wanted to Kill those that blindly believed in the Evil 'HIV' Lie but Michael said it was far better that they should Live to see the Evil 'HIV' Lie unravel before they Die. But Abeings that believe in 'HIV' (like those that believe in 'GOD') are always already Dead for they Live a Dead Lie and become that Dead Lie. Michael even said that 'HIV' Fundamentalists Watney, King, Alcorn, and Campbell uncannily all had that identical: "gaunt, pasty, rat-faced, aidsy-look about them." - that is - the Kate Moss and Posh Spice wasted-away 'aids-look'.
Michael was the Good and the Good is that which Gives and Michael gave his Love all His Life to Others and Gave Love to Others as ahead of Himself.
Michael was truly there to love - Michael loved me: I was Loved - I was there. Michael is still there. Love like being never dies. Love there. Being there.
No one is there in the world now for Michael was the last being on earth that is the last love on earth that is the last there on earth for no one is there.
After
Michael went away nothing has happened - nothing new - all the same old
Labour Lies, the same old 'HIV' Lies; the same old 'dumbing down' of science and culture - I realised
then that Michael was missing nothing at all now as if the world ended when Michael
ended as if we were really all the dead and not Michael: for we are all dead now
but don't know it: we live a death-culture and live death-lies whilst the being-dead
are free from lies free from fear.
I always knew that Michael would die one day but I never knew Michael would die one day.
Where is Michael being being now? Where is the being of being-dead? Where is being Dead?
I was Loved for Michael loved me - therefore I am love - I am being.
With
Michael being away a way of being as loving has come to close.
I cannot say: Good Bye to You for I cannot say: God Be with You as God cannot be with You but Time will be with You so I say: Time Bye as Time Be with You.
I can say: Love Bye to You as Love Be with You for Now You are All Love as all Time for Now You are all Being Love for Being Time as a Time Being Being Love.
I do not Accept that Michael is Dead for that would be a form of Madness for to Accept Death is to Forget Being as Accepting Death is the Denial of Being Dead.
I Know Now that I should have Died with Michael and Now wish I had Died with Michael for I Have Nothing to Live for Now but Death and Being with Michael.
I did Die with Michael where My death Died for Michael giving Him Life to Live on ahead of My Death to Come back again to be with Him both being Dead Alive.
Michael James Guy Verney-Elliott (1938-2007), State Scholarship to Magdalen College, Oxford; student actor, Hamlet; tour of Germany; diverse career included: vision mixer, Sir Winston Churchill State Funeral, 1965 (ITV); senior vision mixer: Upstairs, Down Stairs, Helen - A Woman of Today; television producer and writer, The Gentle Touch, writer and producer Channel 4/Meditel AIDS The Unheard Voices, AZT: Cause for Concern; also thinker, theorist, carpenter, dress maker, and the founder of the AIDS dissident movement in the UK being the first person to prove that 'HIV' does not exist.
Alex
Verney-Elliott July 1st 2007
Michael Verney-Elliott (far left) acting in the late 1950s
'SIV' AND POLIOVACCINATION - A SHOT IN THE FOOT?
By Michael Verney-Elliott
Introduction.
I
propose there are no human retroviruses. What are being called 'human'
retroviruses are more likely to be simian (monkey) viruses which infected humans
as contaminants in poliovaccines since 1961 when live poliovirus vaccines began
to be made utilising the kidney cells of African green monkeys. What are
being called 'HIV'-1 and 'HTLV'-1 are in fact both simian viruses known as
SIVAGM and STLVAGM when they are found in wild-caught African green monkeys.
As a result, millions of men, women and particularly children have been exposed
to these simian viruses wherever the polio vaccines have been tested and used
for some 40 years. Where infection has occurred, the viruses are harmless,
usually dormant, classic passenger viruses. 'HIV' is in fact merely SIVAGM
partially speciated to a human host.
SIVAGM
infected humans in exactly the same way as Simian Virus 40 (SV40), a
previous poliovaccine contaminant, is known to have done from the mid 1950's
until c.1962. SV40 has been a largely latent virus for some 40 years until
its recent reactivation in certain human cancers in the late 1990's. SIVAGM also remains dormant until reactivated years later and is probably
no more capable of disease causation, or perhaps even horizontal transmission,
than SV40. The contaminant SIVAGM infected male and female infants alike,
and will only be detectable by an antibody response when subsequently
reactivated in adulthood, usually in people with an already compromised immune
system, principally caused by mainly avoidable risk behaviours in the West, and
mainly unavoidable risks imposed by poverty and environmental conditions
prevailing in the 3rd World. SIVAGM/'HIV' is not the cause of AIDS but an
epiphenomenal surrogate marker for immune suppression and AIDS risk.
On April 23rd 1984, the world was told that the 'probable' cause of AIDS had been found - a novel 'human' retrovirus called variously LAV, ARV, and HTLV-111. Subsequently, despite a complete lack of convincing scientific evidence, which persists to this day, that this virus actually causes immunosuppression by direct or indirect killing of T4 cells, in a pre-emptive move the novel retrovirus was named 'HIV' (Human Immunodeficiency Virus) by an international committee (1986). From the outset, no-one seems to have realised, or will not admit, that 'HIV' is not 'human'; that like all other retroviruses, it is difficult to transmit horizontally, especially sexually; and perhaps most importantly, that the two human diseases alleged to be caused by 'human retroviruses' are as novel as those viruses. The most fearful acronym of our time is wrong at all points: 'HIV' is not Human; it has never been proven to be the cause of Immunodeficiency; and may not even be a Virus at all, but a misinterpreted artefact of human and simian cell cultures.
Why vaccines?
The
probability that a virus, 'HIV', has recently infected the human population (see
below) inevitably raises the question of where it came from.
All sorts of theories abound, from spontaneous zoonosis (accidental
cross-over from another animal species - monkey bites man etc.) to risibly
sinister conspiracy theories about a
doom-bug created at the behest of Pentagon red-necks for use in germ warfare. A
strong possibility was the accidental introduction of an animal retrovirus into
the human bloodstream as a contaminant in a widely used vaccine.
This is still the most logical and scientifically plausible explanation
of how an animal retrovirus could infect humans on such a world-wide scale in
such a short space of time, approximately 40 years.
Disasters
resulting from the use of vaccines are legion.
Viera Scheibner 1
and Leon Chaitow
2 in their books on the dangers of
vaccination give extensive, fully referenced details of such tragedies.
Having learnt of these and many other vaccine disasters by the
mid-1980's, when I still believed 'HIV' was the cause of AIDS, I wondered if an
animal virus, a precursor of 'HIV', had got into the human bloodstream by
mistake, and if AIDS was a man-made disaster.
Prof. Cedric Mims in his standard work The Pathogenesis of Infectious Disease 3 states: "Many vaccines contain large numbers of irrelevant antigens, derived either from the micro-organism itself or from the culture system used to produce it. It would be better to replace these crude soups with cocktails of defined polypeptides." Intrigued by the phrase 'crude soups', I went to see Prof. Mims at Guys Hospital in 1988. He explained that it was difficult, if not impossible, at that time to make a vaccine which does not contain contaminants, despite the most stringent precautions taken in the manufacturing process. These contaminants might be other viruses, infectious stretches of DNA/RNA, bacteria (unlikely), alloantigenic cell debris etc.
The SV40 precedent.
By
1960, the '50's US polio epidemic had begun to abate, and the polio vaccine
devisers - Salk, Sabin and Koprowski - were being congratulated, when two
virologists called Sweet and Hilleman dropped a bombshell.
They had recently isolated a new monkey virus from the kidney cells of
rhesus monkeys, until then the species most commonly used in the manufacture of
polio vaccines. The fortieth simian virus to be isolated, it was named Simian
Virus 40 (SV40). Subsequent
experiments with human cell cultures soon showed that infection with this virus
caused cell transformation, and tumours in laboratory animals: SV40 was
therefore deemed carcinogenic. By
the time the virus was first isolated, millions of contaminated doses of both
live and killed poliovirus vaccine had been administered world-wide, especially
in Central Africa. The formaldehyde
treatment used to kill the polio virus did not kill all the SV40 particles, so
Salk's killed poliovirus vaccine contained live, ostensibly cancer-causing SV40.
Worse still, Salk's poliovirus seed stock, later used by Sabin in an
attenuated form in his live poliovaccine, was contaminated with SV40.
Crucially, although not a retrovirus, the SV40 genome, which consists of
circular, double-stranded DNA, is known to integrate into the human genome,
making the infection permanent.
The
principal species of monkey used to make polio vaccines were originally rhesus
macaques, cynomolgus and African greens, the last species being almost
universally adopted from 1961 onwards (Research in Virology, Vol 144,
p177). Ironically, in seeking to
replace the Asian rhesus monkey, a natural reservoir of SV40, with a 'safer'
species, the major world poliovaccine manufacturers adopted African greens, a
species which would be found in the 1980's to be natural carriers of several
retroviruses, potential contaminants of their vaccines.
At the suggestion of Maurice Hilleman, co-discoverer of SV40, who in turn
was acting on the advice of William Mann, Director of the Washington DC
Zoological Park, (Nature Medicine, Vaccine Supplement, May 1998,
pp 509-510) and starting in the early '60's, more
than 10,000 wild-caught African greens were eventually being exported annually
from sub-Saharan Africa to meet the needs of poliovaccine manufacturers
worldwide.4
By 1988, it was found that up to 70% of wild-caught African greens
were infected with SIV (Simian Immunodeficiency Virus), >50% homologous with
'HIV', designated SIVAGM;
and up to 40% with an STLV (Simian T-cell Leukaemia Virus) 95-100%
homologous with HTLV1, the alleged cause of adult T-cell leukaemia in humans.
(Essex and Kanki, Scientific American, October 1988 pp.44-51).
For
several anxious years post 1960, the polio vaccine developers waited to see if
there would be an increase in the incidence of human infantile cancers, based on
the grim in vitro evidence against SV40, but by November 1967 they were
confident enough to announce to an international conference that SV40 infections
had not caused a significant increase in cancer.
Their findings were published in Monograph No.29, issued by the US
National Institutes of Health (NIH) in December 1968.
However, everyone concerned had received a salutary shock.
In 1967 no-one mentioned a 'long incubation period', 'slow' viruses or
any of the specious mechanisms used later to explain the 'delayed' pathogenicity
of 'HTLV1' and 'HIV', the first two 'human' retroviruses later considered to
cause disease. By the same token, in April 1984 no-one was prepared to admit
that the 'probable cause of AIDS' they were so keen to promote was also most
probably a vaccine contaminant, and that, as I hope to show, we were merely
seeing a re-run of the SV40 fiasco, with infinitely wider implications.
By
1998, SV40, the carcinogenic monkey virus known to have infected millions of
humans via dirty vaccines, had come back to haunt us nearly forty years later.
Phyllida Brown reported in New Scientist (24.8.96, p.16) that a
mechanism had recently been demonstrated whereby reactivated SV40 might be
responsible for a lung cancer, mesothelioma, more frequently associated with
asbestosis. Other researchers
linked rare bone cancers and brain tumours with SV40.
However, Ms. Brown's report wisely cautions that SV40 may merely be an
"innocent bystander". In
a later update (New Scientist, 1.2.97) Prof. Robin Weiss, a leading
British AIDS expert, predicted that further tests will confirm the presence of
SV40 in samples from mesothelioma patients: "...But whether it causes
cancer we just don't know." What
is beyond doubt is that simian viruses could and did contaminate poliovaccines,
and could and did infect human cells - permanently.
Much
debate now centres on whether SV40 is causing or contributing to the cancers
after many years of latency, or is merely a reactivated harmless passenger
virus. I take the latter view, and
that SIVAGM contaminated subsequent batches of poliovaccine in exactly the
same way, only to emerge years later as a harmless passenger active in people
who are immune suppressed for other reasons.
Indeed, SV40 can be exonerated from causing human cancers for some of the
same reasons given by Peter Duesberg for HTLV 1 not being the cause of leukaemia
in his ground-breaking paper in Cancer Research (1.3.87).
In
1994, I attended a lecture by Prof. Weiss in Oxford in which he responded to a
question by admitting that the 'HIV'-contaminated vaccine theory was
scientifically feasible. On January
16th 1997, the British Government withheld permission for xenotransplants, the
use of animal organs in human replacement surgery, until further research is
carried out into the dangers of animal viruses infecting the patient.
Interviewed on TV that evening, Prof. Weiss explained that hitherto
unknown animal viruses could be transmitted in animal organ transplants, as they
could not be 'screened out'. In
writing on the dangers inherent in xenotransplants, Frederick Murphy, Dean and
Professor of Virology at UC Davis, acknowledges that despite heat and
irradiation treatments of animal sera , "...viruses occasionally survive
such treatments." 5
Nature (13.3.97 p.126) gave a more specific warning of the dangers of transmitting "Type C retroviruses" in animal transplants. The article by Jonathan Stoye explains that animal viruses may be ecotropic, meaning they can only infect animals of the same species; or xenotropic, meaning they can infect the cells of other species. SV40 was obviously one of the latter category and there is mounting evidence that SIV (Simian Immunodeficiency Virus), another xenotropic monkey virus, infected humans, on a world-wide scale, in poliovaccines from 1961 for some 25 years until at least 1985, and perhaps later.
Why 'retroviruses'?
Historically,
by 1984 virology had moved on several notches since the discovery of SV40 in
1960. A previously studied but
incompletely understood group of viruses shot to the forefront with the
discovery in 1970 by Howard Temin and his colleagues of the phenomenon of
reverse transcription and the enzyme reverse transcriptase, and the name
'retroviruses' was coined to describe RNA viruses which encoded this enzyme and
uses it to effect infection, integration and replication.
Throughout the 70's, most 'retrovirologists' were convinced that their
pet viruses would prove to be the cause of everything from human cancers to
multiple sclerosis, but all to no avail. 'AIDS'
was to be the saviour of the
retrovirologists, however many virological, microbiological and epidemiological
rules they had to bend or ignore to shoehorn 'HIV' in as the qualifying
causative agent.
From
the outset, 'HIV' was claimed to have genetic similarities to previously studied
animal retroviruses classified as 'lentiviruses', because they are alleged to
cause disease slowly - maedi visna virus in sheep,
encephalitis-arthritis virus in goats and equine infectious anaemia virus
in horses. The whole concept of
'slow' viruses is highly suspect, and as Peter Duesberg has said, "There
are no slow viruses, only slow virologists."
However, 'HIV'1 and a virus subsequently found in West Africa, 'HIV'2,
were classified as lentiviruses. This
ruse was adopted to explain the variable time lag between infection with 'HIV'
and the appearance of AIDS symptoms, currently thought to average some 11 years.
However, again as mentioned by Duesberg in Continuum, an unknown
time lag between infection and disease is one of the classic hallmarks of a
harmless passenger virus
'HIV'2, the second 'human immunodeficiency virus' found soon after 'HIV'1 and thought to have originated in West Africa, differs genomically sufficiently from 'HIV'1 for it to be considered a separate virus. 'HIV'2 is considered less pathogenic than 'HIV'1, and is mostly found in healthy people, of both sexes. An SIV found in sooty mangabey monkeys (SIVSM), also common to West Africa, has a very close genetic similarity to 'HIV'2, but I have no evidence of that species having been used to make vaccines. However, sooty mangabey monkeys exported from West Africa for animal experiments were known to have caused fatal infections in other species in primate research centres in the US since the early '60's.5 It is quite possible that their strain of SIV found its way into vaccines via this accidental spread to other species of primates, including rhesus macaques. In addition, Charles Gilks mentions in Nature (28.11.91, p.262) that sooty mangabey blood was directly injected into human volunteers during research into primate malarial parasites and may thus have spread SIVSM to humans. Moreover, as I hope to show, all sorts of simian viruses contaminated laboratory cultures in the US and elsewhere with monotonous regularity, as Robert Gallo found to his embarrassment in 1975.
Why 'SIV's?
Since
their isolation in the mid-'80's, Simian Immunodeficiency Viruses (SIV's) have
been very closely studied for clues about how 'HIV' causes AIDS.
At least five monkey species carry SIV in the wild (claims of natural
infection of chimpanzees are suspect, see below), but none of these naturally
SIV-infected lower primates except the African green seems to have been used in
the regular production of human poliovaccines.
Intensive study of the various SIV's shows that despite the considerable
genetic differences between 'HIV'1 and SIVAGM,
all the global subtypes of 'HIV'1 (currently at least ten) have more in common
with the SIVAGM than any other SIV.
Research into the SIV's further shows them all to remain harmless,
classic passenger viruses in their natural hosts.
We
are assured that although related, SIVAGM
differs sufficiently - >50% - in its genetic makeup from 'HIV' to rule it out
as the precursor of the 'human' virus. Many
papers have been published minutely detailing the genetic differences in the two
viruses, replete with all sorts of arcane jargon, philogenetic trees etc.
However, this comparison is illogical, as 'HIV' is believed to be
mutating rapidly, often an indication of a recent change of host species.
Current research shows that 'HIV subtypes' already vary world-wide in
their genomic structure by 30% (WHO figures) and 40% (Eleopulos et al, Continuum).
As it is widely supposed that 'HIV' is hypermutant and can readily
hybridise and genetically recombine with other viruses as well as with its own
quasispecies, this may explain why individuals can have so many different
strains of 'HIV' simultaneously, dependent on any other vaccines or infections
they have received, as well as their own specific genetic susceptibilities.
So quickly does 'HIV' mutate that it was acknowledged ten years ago that
there is no such thing as a typical 'HIV' viral isolate . (Science,
26.8.88, p.1039) Thus, logically
there can be no universal Gold Standard 'HIV' test because there is no universal
Gold Standard 'HIV' isolate.
Instability
may be the hallmark of a virus in the process of speciation - adapting to
survive in a new host species - but research (Johnson et al, J.Virol.
1990;
64: pp 1086-1092) has shown that SIVAGM
also has a high degree of heterogeneity in the various different isolates
found in the four different varieties of African green monkeys from different
parts of Africa, plus a high degree of mutability, comparable to 'HIV' in
humans. This leads researchers studying why SIVAGM
does not cause disease in African greens to conclude that SIVAGM's mutability per se cannot be the cause of disease in its
natural host, although 'HIV''s mutability has been proposed as a cause of AIDS
in humans. Thus, to measure the two
'moving target' genomes of 'HIV' and SIVAGM
against each other is as misleading and meaningless in percentage terms as
comparing two whisps of smoke.
To
complicate matters further, it is now common laboratory practise to co-infect
human cell cultures with 'HIV'1 and SIVAGM
or SIVSM,
forcing a shotgun wedding between the two allegedly different viruses. The
artefact offspring of this union, known as 'chimeric viruses', are named
'Simian-Human Immunodeficiency Viruses', (SHIV's).
Whether there is a 'typical' genome of a SHIV is a moot point, but Jon
Cohen's description is worth noting: "SHIV is the monkey virus SIV
dressed in the outer, or envelope, proteins of the human AIDS virus." 6, (my italics.)
This is also a pretty accurate description of 'HIV' if my hypothesis is
correct, and is consistent with an animal virus adapting to a new human host,
because the envelope proteins are most immediately subject to change as the
virus mutates to survive in its new host environment.
I propose SHIV is merely the result of adding 'HIV', i.e. partially human
speciated SIVAGM, to the original SIVAGM
taken directly from the monkey, and recombining them genetically in human
cells. Thus a 'SHIV' is merely SIVAGM doubly passaged through human cells.
Research
by Ronald Desrosiers et al, published in Science (1.6.90) found
that as well as the essential Gag, Pol and Env genes found in all conventional
retroviruses, 'HIV' and SIVAGM have very
similar non-essential, or supernumerary genes, including Tat, Rev, Vip, Vpr and
Nef. It seems unlikely that two
highly mutable viruses, independently evolving over thousands of years, in
different species, would have picked up or deleted the same supernumerary genes
by chance, as Essex and Kanki acknowledged in their Scientific American
article two years earlier in October 1988.
It has been argued that SIVAGM cannot be the precursor of 'HIV' because the monkey virus has a specific gene, VPX, which is absent from 'HIV', which has instead a gene called VPU, which is genetically quite similar. On the other hand, 'HIV' 2 and SIV from sootey mangabeys both have a VPX gene. These genes are supposed to have something to do with aiding the viruses to infect simian and human macrophages. However, retroviruses are very adept at dropping genes not necessary for their survival, so perhaps 'HIV' 1 can survive better in humans by shedding its VPX gene, or mutating it to VPU.
Linkage of AIDS to vaccines.
Once
the WHO decided on the extermination of smallpox, saturation vaccination
campaigns were mounted world-wide, and the disease was declared globally
eradicated by 1979. Starting on 11 May 1987, the Times ran a short series
of articles raising the possibility that AIDS was a man-made disaster
"triggered" by the WHO anti-smallpox campaign.
That story was in part based on a recent report of a US army conscript,
from no known 'risk group', who had rapidly developed an AIDS-like illness and
died, shortly after being given, among others, a smallpox vaccination on
induction. Even after civilians
were no longer considered at risk of smallpox, troops were still routinely
vaccinated against it as a precaution against possible use of smallpox as a germ
warfare weapon by an enemy. When a
global map of the world's AIDS hotspots, particularly in the Third World, was
superimposed over another map of the most intense anti-smallpox vaccination
areas, the two tallied very closely. (The
same theory fits the global concentrations of anti-polio vaccination even more
closely.) Significantly, when
Robert Gallo, who originally claimed to have discovered the 'AIDS virus', was asked to comment by the Times on the
suggestion that smallpox vaccinations may have triggered AIDS, he gave an
enigmatic reply: "...I have been saying for some years that the use of live
vaccines such as that used for smallpox can activate a dormant infection
such as HIV." (The Times, 11.5.87, my italics) He makes no mention of live poliovaccines, but they had been
widespread since the late '50's. However,
he does acknowledge that 'HIV' infection can remain dormant until activated by
other factors. The key words are
'activate' and 'dormant'.
In
1988, I met Mme. Simone Delarue, an anti-vaccinationist seeking to repeal French
compulsory vaccination laws, citing evidence of damage caused to children by
vaccines. When she raised the
possibility with the French Health Ministry that 'HIV' had been a contaminant in
poliovaccines made using African green monkey cells, a spokeswoman wrote back,
reassuring her that the French vaccine producers stopped using African greens
in 1982, and switched to the 'patas rouges' species. (Mme. Delarue, personal
communication.) Why the sudden
switch from greens to reds? I
suggest that when what was claimed to be the first 'human' retrovirus, HTLV-1,
thought at that time to cause leukaemia, proved to be
>90% homologous to a simian retrovirus, STLV,
found in 1982 in Japan, the French decided to be cautious and change
species. Negligence suits can be expensive! The French must have congratulated themselves on their
prescience when it was subsequently claimed by Myron Essex et al (Scientific
American, October 1988), that whereas both STLV and SIV infect a high
percentage of wild caught African greens, neither retrovirus is carried
by wild-caught patas rouges.
As a further result of meeting Mme. Delarue, I was contacted by two desperately worried Native American women, Bernadine Aitcheson and Mary Ann Wells, who belong to the Dena Ina tribe in Alaska. They were seeking international help, because the children in the tribe had been forcibly co-opted into a US Government Hepatitis B (HBV) vaccine trial at school, and many of the previously healthy children had been infected with Respiratory Syncytial Virus (RSV), with many falling ill with acute lung disease, and there were several deaths. There was a strong probability that the HBV vaccine had been contaminated with RSV. I remembered that many of the original San Francisco and New York PWA's had earlier volunteered for HBV vaccine trials in the late 1970's. Could it be that what was being diagnosed as PCP was due not to the PC fungus but RSV contamination of their HBV vaccine? RSV and PCP pneumonia are so similar that careful differential diagnosis is strongly advised 7. There is also evidence to suggest that RSV infection can reactivate dormant 'HIV' 8, as can subsequent infections with herpes viruses etc.9, and even SV40 may have a role to play in 'HIV' expression due to a degree of homology between 'HIV''s LTR and SV40's "core transcriptional enhancer elements." 10
The Kyle article.
By
1992, I was no longer interested where 'HIV' came from - Peter Duesberg's
arguments had totally convinced me that 'HIV' was harmless.
Moreover, no animal retrovirus is known to be characteristically sexually
transmitted.11
My interest in the vaccine origin of 'HIV' was reawakened when that most
orthodox journal The Lancet (7.3.1992, pp 600-601) published an article
by Walter S. Kyle, in their Viewpoint feature, called "Simian Retroviruses,
poliovaccine, and the origin of AIDS." 12.
Kyle
describes how an analysis of three samples of Sabin live virus poliovaccine,
manufactured by Lederle, and carried out by the US Bureau of Biologics (BOB) in
1976, had revealed viral contaminants visible under electronmicroscopy,
subsequently confirmed as ''Type C RNA viruses'' - virologyspeak for
retroviruses. Action was taken at the highest level. After an "unprecedented" deliberation of twenty
months, a specially appointed US Government committee, with the full
co-operation of the National Institutes of Health,
the Food and Drugs Administration, and BOB, gave the go-ahead to use the
vaccine, providing the manufacturers guaranteed to limit the number of
contaminant retroviral particles to no more than 100/ml in future lots from a
previously estimated level of 1000-100,000/ml.
Everyone concerned, up to governmental level, had seemingly acted in the
interests of public safety.
As
for the millions potentially already exposed to such contaminants for some
fifteen years...? At least the US
government had made an attempt to lock the stable door, however belatedly. Those retroviral particles must have been deemed neither
carcinogenic nor cytopathic, and harmless to humans in such a small dose, or the
vaccine would not have been cleared for take-off. Lederle, a company of the highest possible reputation, both
then and now, openly used African Green monkey cells in the production of their
vaccine in 1976. If any companies
manufacturing live poliovaccines subsequent to that enquiry still allowed
contaminant retroviruses in their product, it would only have been on the advice
of the highest scientific authorities, and subject to very stringent government
restrictions, so obviously no blame can be attached to the manufacturers.
Similarly, the late Albert Sabin cannot be 'blamed' for the contamination
of the vaccines referred to by Kyle as "Sabin virus vaccines." Sabin, and Hilary Koprovsky, merely worked on the development
of the three live, attenuated poliovirus strains used in the vaccines, and were
not responsible for the manufacturers' methods of production.
Kyle
mentions that the 'Type C RNA viruses' were not specified in 1976, so it could
be argued that SIVAGM, an alleged 'lentivirus',
has not been proved to be in the vaccine. However,
the test used to confirm 'Type C' RNA viral infection, a recently (1975) devised
'reverse-transcriptase activity' assay, would not distinguish between Type C, or
lentiviruses, or spumaviruses (nor, incidentally, from the hepatitis B virus
which also replicates using reverse transcriptase, which was not realised in
1976, when RT activity was wrongly considered the sine qua non of retroviral
infection). Moreover, no-one
isolated or characterised African green SIV until 1985.
By
1994 Robin Weiss stated quite clearly that all the known SIV's
infect human lymphocytes, utilising the same CD4 cell receptor as 'HIV' 13, and there is evidence that at least two
SIV researchers have been infected by accidental needlestick injuries. (New
England Journal of Medicine, 20.1.94, pp209-210)
It is also a certainty that those 'unspecified' viruses would have been
subjected to intensive and continuous study long after 1977, if the SV40
precedent was anything to go by. Kyle
states that such contaminant retroviral particles were subsequently found, using
PCR, in poliovaccines manufactured as late as 1985, and perhaps later.
The
1976 US government committee must also have been made fully aware of the
outbreaks of disease since the early '60's in primate research centres
throughout the country in California, Oregon, New England, Washington etc.
Monkey species imported for research purposes from Africa and Asia which
would never have encountered each other in the wild, were being housed together
in these centres, and in transit facilities.
Inevitably, they transmitted disease causing agents one to another. 4,5
These diseases had been observed since the '60's, so with the revelation
that simian retroviruses may have contaminated poliovaccines in 1976, and by
implication for many years before that, memories of the SV40 débacle rang
warning bells loud enough for the US government to take action.
By
1984 and the awareness of AIDS, these simian diseases had been studied in some
detail, and were classified as Simian AIDS (SAIDS), and the hunt was on to find
a causative agent. A paper on SAIDS
14 written
in 1984 is well worth re-reading in 1999. The
sick animals, rhesus macaques, developed 'AIDS-like' symptoms within months and
died - but, unlike human AIDS, with
no long incubation period, and no neutralising antibodies.
Most importantly, there was no evidence of sexual activity between
animals of different species sharing the same pens.
Many of the sick macaques were less than one year old and not sexually
active, and inter-species sexual activity was not observed.
Moreover, some of the disease symptoms in the macaques correlated with
reactivation of SV40, including brain diseases.
In late 1984, the first SIV was found in the blood of the diseased
macaques, and later shown not to be natural to the species in the wild.
The macaques were thus infected since their captivity. At the same time, these macaque SIV's were shown readily to
infect human lymphocytes. By 1985
it was found that the macaques had been infected in captivity with SIVAGM
from naturally infected African greens.
Kyle's paper is based on the orthodox assumption that 'HIV' is the ipso facto cause of AIDS. However, Kyle believes that the preponderance of gay cases resulted from repeated monthly doses of potentially SIVAGM contaminated live Sabin poliovaccine, from 1974 onwards, as a treatment for genital herpes lesions, particularly widespread in gay men in the United States 12. The late Rock Hudson appears to have used the poliovaccine for this purpose (Root-Bernstein, Rethinking AIDS, page 185). I never heard of such an unorthodox use of the vaccine being practised in Europe, but the gay preponderance of AIDS was and is just as marked in Europe and Australasia. Incidentally, in the mid '80's, a US patent was