The epidemic of HIV/AIDS and the epidemic
of "gay cancer"
Kaposi's sarcoma (KS) is widely known as the "gay cancer" that
often accompanied AIDS when the first cases broke out in gay men in Manhattan
in 1979. In 1994 a new "human herpes-8" virus was discovered that
is now widely accepted as the cause of all forms of KS. However, it is extremely
important to note that the new KS herpes virus (KSHV) is separate and distinct
from the human immunodeficiency virus (HIV), the virus that causes AIDS
(Acquired Immune Deficiency Syndrome). Therefore, it is now important to
recognize that two new viruses were "introduced" into gays that
produced not only the epidemic of HIV/AIDS, but also the new epidemic of
KS ("gay cancer").
Two new viral epidemics erupting exclusively in homosexuals is an unprecedented
event in medical science. Such a bizarre and unlikely scenario strongly
suggests to me that that the two epidemics of HIV and KS are more likely
to have occurred due to the deliberate or accidental "introduction"
of new viruses into gay men"-and not from two viruses suddenly appearing
"out of Africa."
The widely-held theory is that HIV originated in African primates in the
African bush. Somehow the monkey or chimpanzee virus "jumped species"
into black Africans to initiate the epidemic which has now killed 20 million
people and infected 40 million more. How this sexually-transmitted virus
came from black Africa to initially infect only young white gay men in Manhattan
has never been explained satisfactorily. Furthermore, the epidemic in America
erupted in the late 1970s, at a time when AIDS in Africa was unknown. The
AIDS epidemic in Africa appeared in the autumn of 1982, at the earliest.
The man-made origin of HIV/AIDS
The man-made theory of AIDS is generally dismissed as "conspiracy theory."
Nevertheless, AIDS researchers and writers like myself, Dr. Leonard G Horowitz,
Dr. Robert Strecker, Professor Robert Lee, and others have proposed for
two decades that HIV was seeded into gay men when they volunteered for the
experimental hepatitis B vaccine experiment which took place in Manhattan,
beginning in November 1978. Additional similar hepatitis B experiments using
gay men as guinea pigs continued in other American cities until 1981 -the
year the AIDS epidemic became official. Some of the cities included Los
Angeles and San Francisco which, along with New York City, became the three
big epicenters of the epidemic.
My two books on the man-made origin of this disease: AIDS and the Doctors
of Death  , and Queer Blood: The Secret AIDS Genocide Plot ,
provide documented evidence to support this theory. A Google internet search
using the key words -man-made origin of AIDS-has 246,000 citations to various
websites that explore this issue in detail. Despite all this, the man-made
theory remains totally ignored by the scientific establishment and the major
The origin of the new Kaposi's Sarcoma virus
Like HIV, the new KS herpes virus-8 discovered in 1994 is considered to
be yet another primate virus out of Africa with a suspected primate "viral
ancestor" hiding in the African jungle. We are expected to believe
that two primate viruses (a retrovirus and a herpes virus) jumped species
in Africa at the same time -and ended up exclusively in the blood of white
gay American men to produce a new immunodeficiency disease in 1979, now
called AIDS. This proposed scenario suggests to me that such an unlikely
African event has the markings of a scientific fairy tale, and I remain
stupefied that such nonsense can pass for "science" in the twenty-first
The origin of Kaposi's Sarcoma
KS has a long history dating back to 1872 in Vienna, Austria, when dermatologist
Moriz Kaposi described five patients with red-purple skin tumors. Before
the AIDS outbreak, KS was a very rare disease affecting mainly elderly Jewish
and Italian men. It was never considered a contagious or sexually-transmitted
In the 1960s, it was discovered that KS was a common skin cancer tumor in
blacks in Central Africa, but the disease was never associated with the
severe immunodeficiency characteristic of AIDS, nor was there any evidence
that KS in Africa was sexually transmissible. KS was rarely, if ever, seen
in African-Americans. As a dermatologist for over 30 years I never saw a
KS case in a female; and KS in young men of any race or sexual persuasion
was as rare as hen's teeth before the "introduction" of HIV.
KS is a medical enigma. How did a previously rare disease like KS in America
become a transmissible disease primarily affecting gay men? How did this
herpes KS virus escape detection during the first 15 years of the AIDS epidemic?
Why did the KS virus and HIV suddenly appear together in young gay men in
Further complicating this picture is the discovery of small bacterial forms
known as "mycoplasma", and the even more recent discovery of extremely
tiny virus-like forms of bacteria called "nanobacteria", as well
as my published reports of "cancer bacteria" as important etiologic
agents in AIDS and KS. (For details, Google: "alan cantwell" +
cancer bacteria.) All these newer bacterial agents are generally ignored
by AIDS researchers, who focus exclusively on viruses.
I believe some of the answers to questions surrounding the origin of HIV/AIDS
can be found in the annual "Progress Reports" reports of the Virus
Cancer Program and the Program's relationship to animal cancer research,
genetic engineering of viruses, cancer vaccine research, and to covert biological
warfare research. These hard-to-find annual Reports were published by the
National Institutes of Health, Public Health Service, U.S. Department of
Health, Education, and Welfare, Bethesda, Maryland.
The Virus Cancer Program (1968-1980)
The Virus Cancer Program had it roots in 1964 when Congress provided funds
to the National Institutes of Health (NIH) for intensive research into the
possible role of viruses in leukemia. In 1968 the Program, then titled the
Special Virus-Cancer Program, was enlarged to encompass all types of cancer.
On July 1, 1973 the Special Virus Cancer Program was renamed The Virus-Cancer
Program (VCP) "to integrate the Program's research activities into
the framework of the new National Cancer Plan."
The Program combined the talents of many of the nation's finest virologists,
biochemists, immunologists, molecular biologists, epidemiologists, and physicians,
in an attempt to uncover the viral cause of cancer. Two classes of cancer-causing
viruses were studied extensively: the RNA-type tumor "retroviruses"
(like HIV) and the DNA herpes-type viruses (like the KS virus).
The main goals were to collect various forms of cancer tissue and test them
in animals; to identify animal and human cancer-causing viruses; to grow
large amounts of "candidate human viruses" for testing purposes;
and to develop vaccines against these cancer viruses. In essence, the scientists
wanted to learn how to use viruses to make cancer - and to force "normal"
cells to become cancerous by subjecting to viruses.
I have studied the annual Virus Cancer Reports (VCP) covering the years
1971-1974 and 1976-1978. Each report is 300-400 pages, and the cumulative
volumes refer to thousands of animal cancer virus and genetic engineering
Biological warfare research, monkey research, and the VCP
The annual VCP Reports must be studied with an awareness that the Program
became wedded to secret military biological warfare research in the early
On October 18, 1971, as part of Richard Nixon's War on Cancer, the army's
biowarfare research laboratory at Fort Detrick, Maryland, was permanently
joined with the National Cancer Institute; and was re-titled . the Frederick
Cancer Research Center. Litton Bionetics was named as the military's prime
The primary task of the new Center was "the large scale production
of oncogenic (cancer-causing) viruses 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 new KS virus)-
and to the successful propagation of significant amounts of "human
candidate viruses." Candidate viruses were defined as animal or human
viruses that might cause human cancers. Later, the objective was to determine
if such viruses could induce (either alone or with other co-carcinogens)
human cancers (1977;58). Biowarfare scientists also had a keen interest
in the role of human and non-human primate viruses as "helper viruses"
in the production of cancer (1978;54).
A steady supply of research animals (monkeys, chimpanzees, mice, cats, etc.
) was necessary; and multiple breeding colonies were established for the
VCP. For example, a total of 2,274 primates from Africa and Asia were shipped
to Litton for military use in 1971.
Forcing cancer viruses into primates and other animals
To induce 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 were removed,
and cancer tissue and cancer viruses were injected into newborn animals
or into the womb of pregnant animals. Some animals were deliberately infected
with malaria to keep them chronically sick and immunodepressed.
The U.S. is the world's leading consumer of primates, and 55,000 are used
yearly in medical research. Primates (especially newborn and baby chimpanzees)
are the most favored lab animals because they are most similar biochemically
and immunologically to human beings. Humans share 98.4% of their DNA with
chimpanzees. Chimps were extensively used by the VCP because there would
be no official testing of cancer viruses on humans.
Robert Gallo, the discoverer of HIV in 1984, was a project officer of a
primate study contracted by Litton Bionetics that pumped cancerous human
tissue, as well as a variety of primate and other viruses, into newborn
macaques (a small species of monkey used as an animal model for human cancer).
The actual number and identity of all the primate viruses created and adapted
to human tissue during the 14 years of the SVCP is not known. In addition,
some primates were released back into the wild carrying lab viruses with
them. This fact is always ignored by molecular biologists searching for
"viral ancestors" in the African bush,
By the early 1970s, experimenters had transferred cancer-causing viruses
into several species of monkeys. Herpesvirus saimiri, a monkey virus discovered
in 1967 in the squirrel monkey, has a close genetic relationship to the
new KS herpes virus. H. saimiri virus is harmless in the squirrel monkey,
but when the virus was forced in the lab to "jump species" into
different animal species, such as the owl monkey, marmosets and rabbits,
it produces cancer in the form of fatal malignant lymphoma.
By 1971 Dharam V Ablashi of the NCI succeeded in transferring H. saimiri,
into various cell lines of human origin. (1971;35). Cancer-causing cat and
hamster viruses were also engineered into macaques and other monkey species.
By the early 1970s, it was recognized that forms of human leukemia and lymphoma
were associated with herpes-type viruses. Herpes saimiri, a DNA-type virus,
became the experimental model for the study of human leukemia and lymphoma.
"Thus far, the only DNA viruses associated with natural cancer of animals
and man are herpes viruses" (1973;15).
Luis Melendez of Harvard studied additional primate herpes viruses (H. ateles,
H. aotus, and H. saguinus) and determined their ability to induce cancer
(1973;247). Attempts were made "to find a suitable method for the large-scale
production of high-titer Herpesvirus saimiri" (1973;264). Researchers
knew: "The clinical and immunological picture of human lymphoma and
leukemia is closely approximated by the malignant disease induced in susceptible
non-human primates by H. saimiri." (1973;265).
By 1976 it was also learned that H.saimiri could spread by "contact
transmission" between squirrel and owl monkeys in the laboratory.
A monkey virus injected into humans via polio vaccines in
There are inherent dangers in vaccine production. Many vaccines are made
on living cells; and accidental contamination with bacteria, mycoplasma,
viruses, and newly-recognized "nanobacteria" are constant problems
during the manufacturing process. Laboratory additives (such as fetal bovine
[cow] serum) may also be a source of contamination. Half the flu vaccine
supply for 2004 had to be destroyed due to contamination with disease-causing
Some researchers believe that injecting living and killed viruses into the
body can result in these viruses combining with other viruses normally present
in the body, resulting in the formation of new viral disease-causing "recombinants."
The dangers of vaccines are downplayed to assure the public that vaccines
The possibility that cancer-causing primate viruses could have been "introduced"
into gays, via the experimental hepatitis B vaccine, cannot be dismissed
as paranoid fantasy. In this regard, we are told that HIV is the first primate
virus to "jump species" to produce an epidemic in millions of
humans. But, in truth, the AIDS epidemic is the second instance in which
a monkey virus has been transferred to humans.
A cancer-causing monkey virus called "simian virus 40" (SV40)
jumped species a half century ago when virus-contaminated polio vaccines
were injected into millions of people, including half the U.S. population
of that era. (For details, see: www.sv40cancer.com) Government health officials
insist there is no proof that SV40 causes human cancer. However, independent
research over the past decade indicates SV40 is clearly associated with
rapidly-fatal cancers of the lung (mesothelioma), bone marrow cancer (multiple
myeloma), brain tumors in children, and other forms of cancer.
A Washington Times report (September 21, 2003) states, "Some of the
polio vaccine given to millions of American children from 1962 until 2000
could have been contaminated with a monkey virus that shows up in some cancers,
according to documents and testimony to be delivered to a House committee
Wednesday." The SV40 story is detailed in the recently published, The
Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus,
Contaminated Polio Vaccine, and the Millions of Americans Exposed.
The VCP and links to bio-warfare and secret human experimentation
Every annual report of the VCP makes clear that human experimentation with
these newly created and genetically-engineered viruses would not be undertaken.
However, the 1972 Report (p 262) also states: "Since man will not be
used as an experimental recipient, it is necessary to gain proof of oncogenicity
by other means."
It is well-known in science that medical doctors will not totally accept
laboratory findings in animals as absolute proof. An experimental finding
in animals must also be proven in humans. It cannot be assumed that covert
human testing of suspected cancer-causing viruses did not take place in
the thousands of experiments conducted under the auspices of the VCP, particularly
with its strong ties to covert biowarfare research. The U.S. military has
a long history of secret human experimentation. For proof, Google: secret
human medical experimentation.
Merck and Co, Inc. made most of the experimental hepatitis B vaccine that
was immediately followed by AIDS cases. Some of the experimental vaccine
was manufactured at the NIH. George Merck, who founded the drug company,
was the leading biowarfare advisor to President Roosevelt during WW2. He
was a central figure in creating the army's biowarfare laboratory at Ft.
Detrick, Maryland, which later became an integral part of the NCI.
Merck's role in the VCP was "to conduct investigations designed to
develop vaccines or other agents effective for the prophylaxis and therapy
for human neoplasia (cancer) of suspected viral etiology" (1972;139).
Great interest was taken in developing anti-herpes virus vaccines. Research
involved a new type of herpes vaccine using "purified viral protein
vaccines" and a "subunit vaccine" utilizing only a piece
of the herpes virus (1977;135).
The Merck company declared: "Since live attenuated or killed virus
vaccines for potentially oncogenic viruses would not be acceptable for human
use due to the danger of transfer of functional genetic material, this project
was initiated to determine whether vaccines to purified viral antigens acceptable
for use in humans were of practical value." (1977;160) (This proposed
"purified" herpes vaccine was similar in type to the experimental
"purified" hepatitis B vaccine injected into gays the following
It is my contention that the introduction of HIV and the KS virus into gay
people, the most hated minority in America, was not an accident of nature
due to monkeys in the jungle.
Would scientists deliberately infect gay men with AIDS to finally prove
that animal cancer viruses cause cancer? In the January 1987 issue of MD
magazine, an Oklahoma internist wrote: "Homosexuality is a sin, deserving
the death penalty." With that kind of mentality not rare in the medical
and scientific world, the answer to the question is, undoubtedly, yes.
The VCP and biohazards
The VCP was a biological disaster waiting to happen. What would happen if
one or more of these dangerous cancer and immunosuppressive viruses escaped
from the laboratory and produced a worldwide biologic holocaust?
The 1978 report from the Office of Biohazard Safety of the VCP states: "The
inadequate care and handling of animals during the past several years have
created a potential for the occurrence of infection of humans with simian
(primate) microorganisms and cross infection between species. Such interspecies
disease transmission may seriously compromise the integrity of the experiment
as well as the health of the experimenter. Due to the magnitude of biomedical
research employing tissue cultures. Frequent evaluation of tissue culture
cross-contamination is very important."
The yearly large-scale production of lethal cancer viruses
By the late 1970s the mixing of animal cancer viruses with human cells to
produce new "xenotropic" viruses was commonplace. The human cells
in question were placenta ("afterbirth") cells from patients with
immune disease, and cells from leukemia (1978, p 192). Xenotropic viruses
are viruses taken from one species and transplanted into another different
species. All these experiments represent "species jumping" performed
in a laboratory.
By 1977 the Program was producing "approximately 60,000 liters (15,840
gallons) of tissue culture-grown viruses, propagated in over 40 different
cell lines, and distributed in over 1250 shipments to over 250 participating
laboratories throughout the world."
Also in 1977 Electro-Nucleonics Laboratories processed 8,044 liters (2,024
gallons) of virus-containing fluids harvested from several tissue culture
systems. About half this volume was concentrated xenotropic viruses. That
same year Pfizer drug company produced 28,000 liters
(7,392 gallons) of virus harvest fluids. The vast majority included primate
viruses, such as the Mason-Pfizer monkey virus, woolly monkey sarcoma virus
and baboon endogenous virus. (This baboon virus contaminated Gallo's lab
at the NCI). Litton produced 37,438 liters (9,984 gallons) of retrovirus
material consisting essentially of four agents: mouse mammary tumor virus,
Raucher murine (rat) leukemia virus, Gross murine leukemia virus and baboon
The VCP made clear that: "Attempts are being made to chronically infect
cell cultures of human epithelial and fibroblast cells and similar cell
cultures from non-human primates (marmosets) with simian sarcoma virus,
gibbon ape leukemia virus and baboon endogenous virus" (1977;183).
A few years later primates in the African bush would be blamed for starting
AIDS and the KS epidemics.
The VCP and the creation of an AIDS-like disease in chimps
In 1969 the military biowarfare experts predicted that a biological agent
would be developed within a decade that would have a devastating effect
on the immune system and for which there would be no treatment. (For details
of this congressional testimony, Google: Donald M MacArthur + biowarfare.)
The VCP had a keen interest in acquiring "information and materials
from carefully selected patients suffering from immunodeficiency diseases"
(1972;318). This is made clear in a 1973 Progress Report (p249) from the
University of Minnesota entitled, "The search for tumor virus related
information in human immunodeficiency patients with cancer" The researchers
proposed "continuation of studies linking immunodeficency, cancer,
and oncogenic viruses."
As biowarfare expert MacArthur predicted, new cancer-causing monster viruses
(like HIV) were created by the VCP which had a deadly effect on the immune
system. In one experiment recorded in the 1973 Report (p169), later published
in Cancer Research in 1974, newborn chimps were taken away from their mothers
at birth and weaned on milk from cancer virus-infected cows. Some of the
chimps sickened and died with two diseases that had never been observed
in chimpanzees. The first was Pneumocystis carinii pneumonia (later known
as the "gay pneumonia" of AIDS); the second was leukemia, a cancer
of the blood.
Cancer-Causing viruses and "helper" viruses
As the 1970s began it was clear that some cancer-causing viruses could not
produce cancer unless a "helper" virus was present. Certain chicken,
cat and mouse sarcoma viruses were found to be "defective" and
unable to induce cancerous changes. However, when a "helper" leukemia
virus was added to the mix, the sarcoma virus was able to induce cancer.
Mixing of a mouse sarcoma virus with a cat leukemia virus produced a "hybrid
virus" which could grow continuously in cat cells. Such a "hybrid
virus" was adapted to human embryonic (fetal) cells (1971, p22). Thus,
it is obvious that "species jumping" experiments were commonplace
during the years of the VCP.
By the late 1970s it was known that "type C RNA viruses" (the
retroviruses connected with sarcomas and lymphomas and leukemias) existed
normally in cells as "endogenous viruses" within the cellular
genomes of many mammalian species. By 1977, the year the experimental hepatitis
B vaccine was being made, scientists in the VCP aimed "to determine
the oncogenic potential of putative human viruses" and "to begin
viral vaccine (conventional or other) testing and immunization programs"
(1977;32). The exact methods by which this was to be accomplished was not
Primate virus contamination of human cells
The possibility that animal cancer viruses could cause contamination of
viral laboratories and viral research was an accepted risk for the VCP.
Primate virus contamination problems have plagued the laboratories of the
world's most famous AIDS researchers, much to their embarrassment.
A decade before Gallo discovered HIV, he reported a "new" and
"human" and cancer-associated "HL-23 virus" that was
eventually determined to be not one but three contaminating primate viruses
(gibbon-ape virus, simian sarcoma virus, and baboon endogenous virus).
The baboon virus was discovered in the early 1970s at the Southwest Foundation
for Research and Education in San Antonio, Texas, which hosted a chimpanzee
breeding colony and produced simian viruses for research. The baboon virus
somehow made its way into the blood cells of a Texas women with leukemia.
When the infected cells reached Gallo's lab they were apparently joined
with an additional monkey virus and an ape virus. How these three viruses
contaminated Gallo's lab is unknown. However, George Todaro, an equally
famous virologist, was quoted as saying, "You can get three viruses
into a virus preparation easily just by being sloppy, and Gallo had plenty
of sloppy people." (See John Crewdson's Science Fictions: A Scientific
Mystery, A Massive Cover-Up, and the Dark Legacy of Robert Gallo, p20).
As late as 1986 Max Essex of Harvard "discovered" a new human
AIDS retrovirus that he found in the blood of healthy Africans. Eventually
this virus also proved to be a monkey virus that originated in a nearby
primate colony. Somehow the animal virus had worked its way into Essex's
lab and blood samples.
Interestingly, both Gallo and Essex, the two foremost American AIDS researchers,
were the leading proponents of the African green monkey theory of AIDS.
Now the more widely accepted theory, proposed by Beatrice Hahn (who worked
in Gallo's lab when he proposed the green monkey theory), claims the virus
traces back to chimpanzees in the African wild. Hahn has never commented
on the primate contamination problems in Gallo's lab.
Could the primate "ancestors" of the RNA-type HIV retrovirus and
the DNA-type herpes saimiri-like KS herpes virus have accidentally -or deliberately-worked
their way into the experimental hepatitis B vaccine? The extremely high
incidence of both these "new" viruses in the gay men who volunteered
for the hepatitis experiments certainly provide enough additional circumstantial
evidence to make the man-made theory of AIDS as plausible as the monkey
out of Africa theory.
The gay hepatitis B experiments (1978-1981)
The experimental hepatitis B vaccine injected into gays was unlike any other
vaccine previously made. It was developed in chimpanzees and manufactured
in a year-long process of sterilization and purification of the pooled blood
of 30 gay men who were hepatitis B virus carriers. During the first gay
experiment (November 1978-October 1979) at the New York Blood Center, there
was great concern that the vaccine might be contaminated. According to June
Goodfield's Quest for the Killers, p 86, "This was no theoretical fear,
contamination having been suspected in one batch made by the National Institutes
of Health, though never in Merck's." The men were given three inoculations
of the vaccine over a period of time. The vaccine was successful with 96%
of the men developing protective antibodies against the hepatitis B virus.
It has been assumed by some that these men were immunosuppressed due to
their promiscuity and history of venereal disease. Although the young men
in the study were indeed "promiscuous" (this was a requirement
for entrance into the study), they were in excellent health. Despite many
previous sexual partners, these volunteers had never contracted evidence
of hepatitis B infection. Furthermore, immunosuppressed people often do
not respond to the vaccine.
The men in the Manhattan experiment had the highest rate of HIV ever recorded
for that time period (over 20% of the men were HIV-positive in 1981, and
over 40% in 1984). Therefore, it must be assumed that many, if not most,
of these men eventually died of AIDS. The actual number of AIDS deaths among
the men in the experiment has never been revealed, nor have their medical
records been studied. Attempts to secure this information have been rebuffed
due to the "confidential" nature of the experiment.
The end of the VCP and the birth of AIDS
By 1980 the VCP came to an inglorious end with the inability to prove that
viruses were involved in human cancer. More than any other program it built
up the field of animal retrovirology, which led to a more complete understanding
of how cancer and immunosuppressive retroviruses caused disease in humans.
The VCP was the birthplace of genetic engineering, molecular biology, and
the human genome project. I am convinced the VCP (and not Africa) is the
birthplace of HIV/AIDS as well.
As the VCP was winding down in the late 1970s, the gay experiments began
in New York City, and continued in other cities, such as San Francisco and
Los Angeles. These cities would rapidly become the three primary epicenters
of the new and unprecedented "gay-related immune deficiency syndrome,"
later known as AIDS.
The introduction of HIV and the KS herpes virus into gay men (along with
some "novel" and now-patented mycoplasmas discovered at the Armed
Forces Institute of Pathology) miraculously revived the career of Robert
Gallo and made him the most famous virologist in the world. And, of course,
turned the "failure" of the VCP into a triumph.
When Gallo's blood test for HIV became available in the mid-1980s, the New
York Blood Center's stored gay blood specimens were reexamined. Most astonishing
is the fact that 20% of the gay men who volunteered for the hepatitis B
experiment in Manhattan were discovered to be HIV-positive in 1980 (one
year before the AIDS epidemic became "official" in 1981). This
signifies that Manhattan gays in 1980 had the highest incidence of HIV anywhere
in the world, including Africa, the supposed birthplace of HIV and AIDS.
In addition, in 1982, in an AIDS trial in New York City one out of five
gay men (20%) tested positive for the new KS herpes-8 virus when stored
blood samples were re-examined by epidemiologists at the NCI in 1999.
Rarely mentioned by AIDS historians is the fact that the New York Blood
Center established a chimp virus laboratory for viral vaccine research in
West Africa in 1974. One of the purposes of VILAB II, in Robertsfield, Liberia,
was to develop the hepatitis B vaccine in chimps. The lab also prides itself
by releasing "rehabilitated" (but virus-infected) chimps back
into the wild.
Also conveniently forgotten in the history of AIDS is LEMSIP (The Laboratory
for Experimental Medicine and Surgery), the primate colony located outside
New York City. For many years, until disbanded in 1997, LEMSIP supplied
scientists with primates and primate parts (and unknown primate viruses)
for transplantation and virus research. Primate parts (and primate viruses)
were experimentally transplanted in human beings as early as the 1960s.
LEMSIP was also affiliated with New York University Medical Center, where
the first cases of AIDS-associated Kaposi's sarcoma were discovered in 1979.
Researchers at NYU were also heavily involved in the development of the
experimental hepatitis B vaccine used in gays. According to Leonard Horowitz,
author of Emerging Viruses: AIDS and Ebola, NYU Medical Center received
government grants and contracts connected with biological warfare research
beginning in 1969.
The evidence gathered here is a tiny fraction of the circumstantial evidence
supporting the man-made theory of AIDS. Scientists have a
long and proven history of covertly experimenting on people "in the
name of science." Anyone who takes the time to study the reports of
the VCP will recognize that human experimentation with cancer viruses was
undoubtedly considered and ultimately desired. Is the fact that HIV/AIDS
appeared within a decade of this dangerous cancer virus experimentation
a coincidence? Should AIDS be blamed on human sexuality, gays, blacks, and
monkeys? I think not.
There is nothing wrong or unpatriotic or "conspiratorial" in presenting
the vast amount of evidence that connects out-of-control animal cancer experimentation
and biowarfare research with the birth of AIDS. What is wrong, however,
is the unwillingness of the scientific establishment and the media and the
public to look at it.
Dr. Cantwell is a retired dermatologist and has written two books on the
man-made origin of AIDS; and two books on the infectious origin of cancer,
all published by Aries Rising Press, PO Box 29532, Los Angeles, CA 90029
(www.ariesrisingpress.com). Email: firstname.lastname@example.org. Many of his
writings can be found on www.google.com by typing in "alan cantwell"
+ articles. His latest book is Four Women Against Cancer: Bacteria, Cancer
and the Origin of Life. His books are also available on www.amazon.com and
also through Book Clearing House @ 1-800-431-1579
Alan Cantwell M.D.
FOUR WOMEN AGAINST CANCER
All information posted on this web site is
the opinion of the author and is provided for educational purposes only.
It is not to be construed as medical advice. Only a licensed medical doctor
can legally offer medical advice in the United States. Consult the healer
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