This tells you what you are fighting against.
Judith.
>From another list:

Date: Tue, 8 Aug 2000 14:00:41 -0700
   From: "VGammill" <ygamm...@san.rr.com>
Subject: ORIGIN OF HIV --Cantwell /New Publication

Dear Friends,  AIDS researchers, publishers, and people against
genocide:

Due to the rapid  deterioration of the AIDS epidemic worldwide, and
especially in Africa, I am continuing my 20-year research into the
man-made
origin of HIV and AIDS. I  have written a new piece with  new research
and
information on this subject, which I am attaching to this posting.

The article is entitled:         The Secret Origin of AIDS and HIV
Subtitle:           How scientists produced the most horrifying plague
of
all
time -
                                    and then covered it up.

The length of the piece is about 6500 words with documenting
references.

The piece includes the following easy-to-read sections:

*The Green monkey theory
*The Special Virus Cancer Program (1962-1977)
*Biological Warfare, Primate research, and the SVCP
*The end of the SVCP and the birth of AIDS
*The pre-AIDS gay hepatitis B experiments (1978-1981)
*Kaposi's sarcoma, the KS virus, and monkey business
*Contaminated vaccines, cancer, and emerging viruses
*The African vaccine connection to the outbreak of AIDS
*Gallo and Montagnier's theories on the origin of HIV and AIDS
*"Gay and Straight" strains of HIV and sexual preference
*Solving the mystery of the origin of AIDS

Due to the seriousness of this research and writing, I am also
offering this
submission FREE OF CHARGE to websites,  conspiracy publishers, and
other
publishers, who might have interest in alerting their readership to
this
important information. All I ask is -- Please credit me as the author.
I wish to retain the copyright on this piece, but I would be delighted
and
honored to have it exhibited by you. Let me know if you decide to post
or
publish it.

Please feel free to pass this document around to interested parties.
Or as
the late "hippy" activist Abbie Hoffman might have said: STEAL THIS
POSTING!!!

The report follows:

Best regards,
Alan Cantwell, Jr., M.D.

            The Secret Origin of AIDS and HIV

 How scientists produced the most horrifying plague of all time
            - and then covered it up.

                Alan Cantwell Jr., M.D.
                        copyright 2000

The Green Monkey  Theory

Many people  have heard the  theory that AIDS is man-made. Thirty
percent
of
New York City blacks polled by The New York Times (October 29, 1990)
actually
believe AIDS is  an "ethnic weapon" designed in a laboratory  to
infect and
kill black people. Some people even think the AIDS conspiracy   theory
is
more plausible than the African  Green monkey  theory  promoted  by
the
leading AIDS scientists. Actually, the monkey theory was proven wrong
by
researchers as far back as  1988, but most AIDS educators  continued
to
promote it to the public until recently.  In  a media blitz in 1999,
the
green monkey theory was totally  replaced by the chimpanzee "out of
Africa"
theory, and the chimp origin of AIDS   was fully accepted by the
scientific
community.
    A phylogenetic "family tree" of primate viruses (which few people
could
understand) was presented to prove that HIV was descended from a
primate
virus in the African bush. Analysis of  virus  genetic data performed
by
the
"supercomputer" at Los Alamos in New Mexico indicated that HIV had
"jumped
species" from a chimp to a human around the year 1930 in Africa. (Los
Alamos
is the official home of  nuclear bomb-building, alleged Chinese spies,
and
the laboratory which directed secret human radiation experiments  on
unsuspecting civilians from the 1940s up to the beginning of the AIDS
epidemic.)
     At the  international AIDS  conference held in 2000 in South
Africa,
one
scientist claimed  the chimpanzee  virus  (SIVcpz) was "ancient" and
jumped
species as early as  1675 but didn't establish itself in the human
population
until 1930. This was  dutifully reported by science writer Laurie
Garrett,
who give all the time-honored reasons for the rapid  spread of AIDS in
Africa:  non-sterile needles, non-sterile blood products and
widespread
promiscuous sexual behavior.

The Special Virus Cancer Program (1962-1977)

    Conveniently forgotten by  scientists and  medical journalists was
the
fact that surgeons  had been  transplanting  chimpanzee  parts into
human
beings for decades. When  Keith Reemtsma died in June 2000, at age 74,
he
was
hailed as a pioneer in cross-species organ transplants (now known as
xenotransplantation).  By 1964 he had already placed six chimpanzee
kidneys
into six patients.  All his  patients died, but eventually Reemtsma
succeeded
in many successful  human-to-human organ transplants.
    Much more likely to have spread animal viruses to human beings is
the
largely forgotten  Special Virus Cancer Program (SVCP). This  research
program  was responsible  for  the development, the seeding, and the
deployment of various animal viruses,  which were  capable of
producing
cancer and immune system damage when  transferred between animal
species and
into human cells and tissue.
    The SVCP began in 1964 as a government-funded program of the
National
Cancer Institute (NCI)  in Bethesda, Maryland. Originally designed
to
study
leukemia and lymphoma forms of cancer,  the program was soon enlarged
to
study all forms of cancer.
    The SVCP  marshalled many of the nation's finest virologists,
biochemists, immunologists, molecular biologists, and epidemiologists,
at
the most prestigious institutions  in a coordinated attempt to assess
the
role of viruses in causing  human cancer.  Many of  the top  AIDS
scientists,
including Dr. Robert Gallo (the co-discoverer of  HIV), Myron (Max)
Essex
(of "cat AIDS"  fame), and Peter Duesberg (who claims HIV is not the
cause
of
AIDS), were connected with the Program.
    The scope of the program was international and included scientists

from
Japan, Sweden, Italy, the Netherlands, Israel, and even Uganda,
Africa.  A
main mission of the SVCP was to collect various  human and animal
cancers
from around the world and to  grow large amounts of cancer-causing
viruses.
In the process, many animal  viruses were adapted to human cells.
These
cultured viruses would  then  be shipped to researchers throughout the
world.
    An annual report of the accomplishments of the SVCP was published
by
the
NCI.  The 1971 SVCR report indicates  a mouse leukemia virus had been
adapted
to grow in human cells. A "hybrid virus" - a mixture of a mouse
sarcoma and
a
cat (feline) leukemia virus - was engineered and grown in cat cells.
Chicken
and feline retroviruses produced cancer  in monkeys. Mouse-cat virus
hybrids
and feline leukemia virus were adapted to human cells in tissue
culture.
Thus, "species jumping" was a common occurrence in these experiments.

Biological Warfare,  Primate Research and the SVCP

    Also joining forces with the SVCP at the NCI were  the miltary's
biological warfare researchers. On October 18, 1971, President Richard
Nixon
announced that the army's  biowarfare laboratories at nearby Fort
Detrick,
Maryland, would be converted to research on the cause, prevention,
and
treatment of cancer. As part of  Nixon's so-called  War on Cancer, the
military biowarfare unit was retitled the new Frederick Cancer
Research
Center. Litton Bionetics was named as the military's  prime contractor
for
this project.
    The 1971 annual report noted that one  of the primary tasks  of
the now
jointly connected  National Cancer Institute-Frederick Cancer Research
Center
was "the large scale production of oncogenic (cancer-causing) and
suspected
oncogenic viruses to meet research needs on a continuing basis."
Special
attention was given to primate viruses (the alleged African source of
HIV)
and  "the successful propagation of significant amounts of human
candidate
viruses."
    Candidate viruses were animal or human viruses that might be
capable of
intiating human cancers.   And  primate cancer-causing  viruses were
adapted
to 'normal' human cells.
    A steady supply of research animals (monkeys, chimpanzees, mice,
and
cats) was necessary, which resulted in the establishment of  breeding
colonies for the SVCP.   Healthy animals were shipped in from various
parts
of the world  for breeding purposes and experimentation; and
virus-infected
animals were shipped out again to various labs.
    By 1971, a total of 2,274 primates had been inoculated at
Bionetics
Research Laboratories, under contract to Fort Detrick. Over 1000 of
these
monkeys  had already died or had been transferred to other primate
centers.
(Some animals were eventually released back into the wild). By this
time,
experimenters  had spread lymphoma-producing viruses into several
species
of
monkeys, and had also isolated a monkey virus (Herpesvirus saimiri)
that
would have a  close genetic relationship to a new Kaposi's sarcoma
virus
that
produced the "gay cancer" of AIDS a  few years later.
    In order  to prime primates and other research animals to acquire
cancer,
their  immune system was deliberately suppressed by drugs, radiation,
or
cancer-causing chemicals or substances. The thymus gland and/or the
spleen
was removed, and viruses were injected into newborn animals or into
the
womb
of pregnant animals. Some  animals were also  injected with malaria to
keep
them chronically sick  and immunodepressed.
    Primates (especially newborn and baby chimpanzees)  were the most
favored
lab  animals because they were most similar biochemically and
immunologically
to human beings,  and because there would  be no official testing of
these
lab  viruses on humans.   An irradiated rhesus monkey colony supplied
animals
for transplantation experiments.
    Robert Gallo was a project officer of a primate study contracted
by
Bionetics that pumped cancerous human tissue, as well as a variety of
chicken
and monkeys viruses  into newborn macaques (a small species of
monkey).
This
1971 SVCP report (NIH-71-2025) declared: "Inasmuch as tests for the
biological activity of candidate human viruses will not be tested in
the
human species, it is imperative that  another system be developed for
these
determinations and, subsequently for the evaluation of vaccines or
other
measure of control. The close phylogenetic relationship of the lower
primates
of man justifies utilization of these animals for these purposes."
    Researchers at Bionetics  evaluated  the long-term cancer effects
of
injecting human and animal cancer material into various species of
monkeys.
Newborn monkeys,   irradiated monkeys,  and monkeys primed with
cancer-causing chemicals,  were injected with blood ("using multiple
sites
and volumes as large as possible") taken from  various forms of human
leukemia. In other studies, tissue cultures infected with various
animal
viruses were inoculated into primates. Many kinds  of human cancer
tissue
were injected into the animals. How many "new" and "emerging" viruses
were
created and adapted by the SVCP is not known. And it  is unlikely that
complete records of this animal cancer virus experimentation will ever
be
examined.
    Cats were also bred  for leukemia and sarcoma cancer studies. An
inbred
germfree colony of mice was established.  Mouse cancer viruses were
manipulated to produce resistant and non-resistant strains. These
adapted
viruses  would be employed in the  1980s in human gene replacement
experiments. Such experiments utilized a weakened strain of the mouse
leukemia virus to  infect and "taxi-in" the missing genes to
genetically-defective human cells.

The End of the SVCP and the Birth of  AIDS

    By 1977 the SVCP came to a inglorious end. According to Gallo,
"Scientifically, the problem was that no one could supply clear
evidence of
any kind of human tumor virus, not even a DNA virus, and most
researchers
refused to concede that viruses played any role in human cancers.
Politically, the Virus Cancer Program was vulnerable because it
attracted  a
great deal of money and attention and had failed to produce dramatic,
visible
results."
    Despite all this, the  SCVP was the birthplace of genetic
engineering,
molecular biology, and the human genome project.  More than any other
program
it built up the field of animal retrovirology, which led to the vital
understanding of cancer and immunosuppressive retroviruses in humans.
Like
manna from heaven,  AIDS in gays   put the virologists back in
business. And
HIV, a cancer-causing and immunosuppressive retrovirus,   would make
Robert
Gallo the most famous  scientist in the world.
    Few people understand clearly  that AIDS is a new form of cancer,
and
this aspect of AIDS has not been publicized for obvious reasons.
Physicians
have always told their patients that cancer is not contagious or
sexually
transmitted. Virologists  wanted AIDS  and "gay cancer" to be a new
disease
because HIV  was supposedly brand new. It was easier to blame gays for
initiating this  new disease with their sexual lifestyle than it was
to
point
the finger at scientists. And if  AIDS was connected to animal cancer
research, some people might wonder if the new disease had anything to
do
with
all those species jumping experiments in the 1970s. Making people
understand
that AIDS is cancer would only confuse them.
     And so, instead of looking for the source of HIV in the thousands
of
animal cancer experiments performed througout the world, the
virologists
insisted on looking for the source of the virus in primates in the
African
rainforest.

The Pre-AIDS Gay Hepatitis B Experiments (1978-1981)

    As the SVCP was winding down, thousands of gay men were signing up
as
guinea pigs for government-sponsored hepatitis B vaccine experiments
in
New
York, Los Angeles, and  San Francisco. In a few years these cities
would
become the epicenters for "gay-related immune deficiency syndrome, "
later
known as AIDS.
    Could virus-contaminated vaccines lie at the root of AIDS?  In
the
early
1970s the hepatitis B vaccine  was developed in chimpanzees, now
widely
accepted as the animal from which HIV supposedly evolved.  To this
day,
some
people are fearful about taking the  hepatitis B vaccine because of
its
original connection to gay men and AIDS; and older physicians remember
the
original experimental hepatitis vaccine was made from the pooled blood
serum
of  hepatitis-infected homosexuals.
    Was HIV  "introduced" into gays during these vaccine trials when
thousands of homosexuals were injected in New York beginning in 1978,
and
in
the West Coast cities in 1980-1981?
    AIDS  first erupted in gays living in New York City in 1979 a few
months
after the experiment began in Manhattan.  The astounding and
statistically
significant  fact is that 20% of the gay men who volunteered for the
hepatitis  B experiment in New York  were discovered to be
HIV-positive in
1980 (a year before AIDS became "official" in 1981).  This would mean
that
Manhattan men had the highest incidence of HIV anywhere in the world,
including Africa, the supposed birthplace of HIV and AIDS. The fact is
that
definite, proven cases of AIDS in Africa would not appear until 1982.
    Some researchers are convinced that these vaccine experiments
served as
the vehicle through which HIV was "introduced" into the gay population
in
America.  Nevertheless, AIDS scientists have downplayed any connection
of
AIDS with the vaccine.
     My own extensive research into the hepatitis B experiments   is
presented in  AIDS and the Doctors of Death: An Inquiry into the
Origin of
the AIDS Epidemic, published in 1988. Also included in this book is
evidence
suggestingpatient
Zero" story of 1987, which claimed a  promiscuous gay Canadian airline
steward brought AIDS  to America.   Montagnier "is doubtful that the
American
epidemic could have developed from a single patient."
    Montagnier admits that he stands apart from Robert Gallo on many
matters.
In a mind-blowing statement he declares  "Gallo was not a medical
doctor,
but
rather a biochemist by training. His limited experience with viruses
at the
time perhaps explains his misinterpretations and the contaminations
that
occurred in his laboratory." ( Gallo has always declared himself as a
physician. If he is not, then we certainly do have a conspiracy
problem on
our hands.)
    What is obvious from their authored books is that while the
continent of
Africa dies, these two top scientists in AIDS research continue their
vendetta in print, and continue to promote their own pet  theories on
the
origin of HIV and AIDS to an adoring scientific community.

"Gay and Straight" Strains of HIV and Sexual Preference

    It is common knowledge that  AIDS is  a heterosexual disease in
Africa,
and that AIDS  started exclusively as a gay disease  in the United
States.
Although the public was told early on that  "no one is immune from
AIDS",
the
fact remains that even now (20 years after the first AIDS cases) 80%
of the
new AIDS cases in America are gay men, IV drug addicts, and their
sexual
partners. Why is this? Certainly HIV does not discriminate between
sexual
preference and race! Or does it?
    In the mid-1990s molecular biologists identified  at least 8
different
subtypes (or "clades" or "strains") of HIV that were infecting various
people
around  the world. Remarkably, it turns out that the "B" strain is the
predominant strain infecting gays in the U.S. Even more remarkable is
that
this strain of HIV   has an "affinity" to infect rectal tissue, thus
explaining why gays are more  likely to get AIDS than straights.  In
contrast, the HIV strains common  in Africa have an affinity for
vaginal and
cervical cells, as well as for cells of the foreskin of the penis.
Thus, HIV
is more likely to infect heterosexuals in Africa.
    How do we know this? Max Essex (a Harvard veterinarian who
performed
pre-AIDS  experiments transferring feline leukemia virus between cat
populations)  tested subtype E strains of HIV from Thailand. He
discovered
that this Asian strain readily infected women's  genital cells of  the

vagina
and cervix.  But the "gay"  B strain of HIV  did not infect them as
easily.
    AIDS experts tell us American AIDS came from Africa, but the
strain of
HIV prevalent in gay men is almost never seen in Africa! How is this
possible?
Were strains of  HIV  engineered to adapt easily to cells likely to be
infected in gay sex? Or adapted to genital cells  involved in vaginal
sex?
     We know scientists in the SVCP were able to adapt certain
retroviruses
to infect specific  kinds of  cells. As early as 1970 biowarfare
scientists
were learning to design certain infectious agents (particularly
viruses)
that
would attack the cells of  certain racial groups.
    More recently, in 1997, Stephen O'Brien and Michael Dean of the
Laboratory of Genomic Diversity at the National Cancer Institute have
shown
that one out of ten white people have AIDS-resistant  genes, whereas
blacks
in Africa have none. Is this simply another  peculiarity of a virus
that
jumped species in the African bush?  Or is HIV a designer virus,
specifically
adapted in its subtypes to infect certain racial groups and gay
people?
    When AIDS appeared in 1981, health officials assured the "general
public"
 that there was nothing to fear. "AIDS is a gay disease" was the
phrase
repeated over and over again in a media blitz. As late as 1987, Robert
Gallo
told Playboy reporter David Black, "I personally don't know of a
single case
(in America) of a man getting the (AIDS) virus from a woman through
heterosexual intercourse."
    In Africa, where AIDS affects men and women in equal numbers,
Gallo's
explanation to Black was: "It happens, but that may be due to
differences in
sexual practices, more promiscuity or to a greater incidence of
venereal
disease." Gallo give Playboy his reassurance of the future of
heterosexual
AIDS in America: "AIDS will never become an overwhelming danger to the
general public."

Solving the Mystery of the Origin of AIDS

    The pre-AIDS species jumping experiments of  the  Special Virus
Cancer
Program   (SVCP) have been largely expunged from the  history of HIV
and
AIDS. The viral contamination problems inherent in viral research have
also
been downplayed. As a result,  the origin of HIV and AIDS has been
distorted
and obscured.
    A serious  examination of  the SVCP provides  "missing links" to
the
possible laboratory origin of HIV.  The ability of  SVCP scientists
to
produce "new" diseases with cancer-causing animal viruses is a matter
of
record. The ability of animal viruses  to easily contaminate
laboratory
experiments and vaccine manufacture is also well known. All these
factors
make  the man-made theory of AIDS  rational and compelling.

    Some areas of HIV/AIDS history that require further analysis are:
The connection between AIDS  and  cancer
The connection of HIV to known (pre-AIDS) animal cancer lab viruses
The connection of the SVCP to the outbreak of AIDS
The connection of vaccine programs to the outbreak of AIDS
The connection of biological warfare research to the outbreak of AIDS
The disinformation surrounding the origin of AIDS
The disinformation blaming the "victims" of AIDS for the disease
The total secrecy of biological warfare and its implications for
science
The wedding of cancer and AIDS scientists to biological warfare
scientists
The "sworn to secrecy" problem  of  the government/military
scientists
The wedding of government to medical science for military b/w purposes
The long history of secret medical experiments on unsuspecting
citizens

    All these factors need to be explored more fully and  impartially
in
order to more fully elucidate the man-made, laboratory origin of HIV
and
AIDS.
    To continue to ignore these issues is to ignore the fate of
countless
millions who will die from AIDS and other "emerging viruses" in the
future.
    The  Special Virus Cancer Program (and biowarfare experimentation
worldwide) has forever changed the course of history of medical
science,
resulting in the current dangers of biological terrorism and the fear
of
newly emerging man-made viruses and other infectious agents.
    To study the theories of  origin of HIV/AIDS and to ignore the
SVCP with
its biowarfare implications is like studying the Holocaust and failing
to
mention  the Nazis. Some readers may find this analogy offensive, but
in
light of the close connection of the SVCP with the outbreak of HIV and
AIDS,
it is suggested that final judgement be reserved until all the
pertinent
facts are ascertained.
    The SVCP and "the hand of man" lie  at the root of HIV. The
flowering of
the worldwide epidemic of AIDS is proof that the seeds were well
planted.

REFERENCES:
Butel JS: Simian virus 40, poliovirus vaccines, and human cancer:
research
progress versus media and public interests. Bulletin World Health
Organization 78:195-198, 2000.
Cantwell Jr, A: AIDS & The Doctors of Death: An Inquiry into the
Origin of
the         AIDS    Epidemic. Los Angeles: Aries Rising Press, 1988.
Cantwell Jr, A: Queer Blood: The Secret AIDS Genocide Plot.  Los
Angeles:
Aries       Rising Press, 1993.
Cantwell AR Jr: Bacteriologic investigation  and histologic
observations of
        variably acid-fast bacteria in three cases of Kaposi's
sarcoma.
     Growth  45: 79-89, 1981.
Cantwell AR Jr: Kaposi's sarcoma and variably acid-fast bacteria in
vivo  in
two         homosexual men. Cutis  32: 58-64,68, 1983.
Cantwell AR Jr: The Cancer Microbe.  Los Angeles: Aries Rising Press,
1990.
Cantwell AR Jr: "Gay cancer, emerging viruses, and AIDS." New Dawn
(Melbourne), Sept 1998.
Connor S: "AIDS science on trial." New Scientist,  February 12, 1987,
pp
49-58.
Faden RR (Chair): The Human Radiation Experiments: Final Report of the
President's Advisory Committee. New York: Oxford University Press,
1996.
Gallo R: Virus Hunting: AIDS, Cancer and the Human Retrovirus. New
York:
Basic       Books, 1991.
Garrett L: "AIDS virus traced to 1675."  Newsday, July 11,2000.
Gold M: A Conspiracy of Cells. Albany, NY: State University of New
York
Press,      1986
Hatch R: Cancer Warfare. Covert Action Bulletin 39, Winter, 1991.
"HIV sub-types showing signs of spreading differently," All Things
Considered
        (NPR), 10-02-1995.
Hooper E: The River: A Journey to the Source of HIV and AIDS.  Boston,
MA:
Little,         Brown and Company, 1999
Horowitz LG: Emerging Viruses: AIDS & Ebola.  Rockport, MA:
Tetrahedron
    Publishing Group, 1996.
Larson CA: Ethnic weapons. Military Review, Nov 1970, pp 3-11.
Ljungqvist KI: AIDS Tabu.  Stockholm: Carlssons Bokforlag, 1992.
Mathew A, Ennis FA, Rothman AL: Transient decreases in human T cell
proliferative responses following vaccinia immunization. Clin Immunol
96: 100-107, 2000.
Montagnier L: Virus.   New York: WW Norton Co, Inc,  2000.
O'Brien SJ, Dean M: In search of AIDS-resistence genes. Scientific
American,
    September  1997,  pp 28-35.
O'Brien TR, Kedes D, Gamem D, et al: Evidence for concurrent epidemics
of
human herpesvirus 8, and human immunodeficiency virus type I in US
homosexual men: rates, risk factors, and relationship to Kaposi's
sarcoma.
J Infectious Disease 180: 1010-1017, 1999.
 Special Virus Cancer Program (Progress Report #8). Bethesda, MD:
National
Institutes of Health, July 1971.
Special Virus Cancer Program (Progress Report #9). Bethesda, MD:
National
Institutes of Health, July 1972.
Stevens CE, Taylor PE, Zang EA, et al: Human T-cell  lymphotropic
virus
type
III     infection in a cohort of homosexual men in New York City. JAMA
255;
    2167-2172, 1986.
Quinnan GV Jr (Ed): Vaccinia Viruses as Vectors for Vaccine Antigens.
New
York:       Elsevier, 1985.

Related Websites:
http://www.bhc.edu/EastCampus/leeb/aids/index.html
http://aidsbiowar.com

Acknowledgement: I am grateful to Robert E Lee, Vincent  Gammill,
Billi
Goldberg,  and Boyd "Ed" Graves,  for their contributions of research
material for this study.

[Dr. Cantwell is a medical researcher and author of  AIDS & The
Doctors of
Death, and Queer Blood, both published by Aries Rising Press, PO Box
29532,
Los Angeles, CA 90029, USA. These books are available on the Internet
at
Amazon.com, Barnes & Noble,  or through mail order at Book Clearing
House @
1-800-431-1579. ]





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