The use of biologcial warfare, in particular when targetting civilian non-combatants is a War Crime, a Crime Against Humainity,a violation of the Geneva Conventions and the Universal Declaration of Human Rights.
The "forced" confessions of these US captured airmen, supposedly the result of North Korean Communist "brainwashing" led directly to the creation of the 20 year clandestine MK-Ultra mind-control program in 1953, initially with the stated aim of conductive "defensive" research against Manchurian Red indoctrination methods
The Year-One budget approriation for MK-Ultra was $35million in 1953 and ran continuously until it's existance was revealed publically in 1975.
Upon return to the United States, all US airmen made prisoners of war recanted their extensive confessions following extensive debriefing.
In this next Al-Jazeera documentary we hear from Professor Mauri a Japanese scienctist who has been researching this for over 20 years, made 8 visits to North Korea to speak to the survivors and the relatives and has conclused that this ABSOLUTELY happened.
He also speaks (on camera) to the last surviving captured US Airman to have made "false" confessions.
In only mildly evasive language, he admits (on camera) that his confession was genuine, his treatment was fine, he was not tortured, there was no gulag and the "re-education", "indoctrination" and "brainwashing" he recieved in order to make such convincing "flase confessions for the cameras consisted of a single book left in the prisoners' common room.
Again, this incident was the ENTIRE rationale for the whole MK-Ultra iniitiative and massive covert program in US Mind Control - Dulles and the CIA were so freaked out by how complete the "control" over the captured US serviceman was, it scared the living bejesus out of them and motivated the entire McCarthyite Reds Under the Bed paranoia of Communusit subversion.
Nuremberg Principle VI states:
"The crimes hereinafter set out are punishable as crimes under international law:
(a) Crimes against peace:
(i) Planning, preparation, initiation or waging of a war of aggression or a war in violation of international treaties, agreements or assurances;
(ii) Participation in a common plan or conspiracy for the accomplishment of any of the acts mentioned under (i).
(b) War crimes:
Violations of the laws or customs of war which include, but are not limited to, murder, ill-treatment or deportation to slave labor or for any other purpose of civilian population of or in occupied territory; murder or ill-treatment of prisoners of war or persons on the Seas, killing of hostages, plunder of public or private property, wanton destruction of cities, towns, or villages, or devastation not justified by military necessity.
(c) Crimes against humanity:
Murder, extermination, enslavement, deportation and other inhumane acts done against any civilian population, or persecutions on political, racial, or religious grounds, when such acts are done or such persecutions are carried on in execution of or in connection with any crime against peace or any war crime."
Unit 731 was a covert biological and chemical warfare research and development unit of the Imperial Japanese Army that undertook lethal human experimentation during the Second Sino-Japanese War (1937–1945) and World War II. It was responsible for some of the most notorious war crimes carried out by Japanese personnel.
Some of the numerous atrocities committed by the commander Shiro Ishii and others under his command in Unit 731 include: vivisection of living people (including pregnant women who were impregnated by the doctors), prisoners had limbs amputated and reattached to other parts of their body, some prisoners had parts of their bodies frozen and thawed to study the resulting untreated gangrene. Humans were also used as living test cases for grenades and flame throwers. Prisoners were injected with strains of diseases, disguised as vaccinations, to study their effects. To study the effects of untreated venereal diseases, male and female prisoners were deliberately infected with syphilis and gonorrhea via rape, then studied.
In other tests, subjects were deprived of food and water to determine the length of time until death; placed into high-pressure chambers until death; experimented upon to determine the relationship between temperature, burns, and human survival; placed into centrifuges and spun until death; injected with animal blood; exposed to lethal doses of x-rays; subjected to various chemical weapons inside gas chambers; injected with sea water to determine if it could be a substitute for saline; and burned or buried alive.
Japanese scientists performed tests on prisoners with plague, cholera, smallpox, botulism, and other diseases. This research led to the development of the defoliation bacilli bomb and the flea bomb used to spread the bubonic plague. Some of these bombs were designed with ceramic (porcelain) shells, an idea proposed by Ishii in 1938.
These bombs enabled Japanese soldiers to launch biological attacks, infecting agriculture, reservoirs, wells, and other areas with anthrax, plague-carrier fleas, typhoid, dysentery, cholera, and other deadly pathogens. During biological bomb experiments, scientists dressed in protective suits would examine the dying victims. Infected food supplies and clothing were dropped by airplane into areas of China not occupied by Japanese forces. In addition, poisoned food and candies were given out to unsuspecting victims and children, and the results examined.
In 2002, Changde, China, site of the flea spraying attack, held an "International Symposium on the Crimes of Bacteriological Warfare" which estimated that at least 580,000 people died as a result of the attack. The historian Sheldon Harris claims that 200,000 died. In addition to Chinese casualties, 1,700 Japanese in Chekiang were killed by their own biological weapons while attempting to unleash the biological agent, which evidences serious issues with distribution
According to Maj. Robert Peaty, of the Royal Army Ordnance Corps, who was the senior British officer at Mukden, a prisoner-of-war camp 350 miles from Pingfan, doctors from Unit 731 administered the regular injections of infectious diseases, disguised as harmless vaccinations, which eventually killed 186 Americans.
The Unit 731 complex covered six square kilometers and consisted of more than 150 buildings. The design of the facilities made them hard to destroy by bombing. The complex contained various factories. It had around 4,500 containers to be used to raise fleas, six cauldrons to produce various chemicals, and around 1,800 containers to produce biological agents. Approximately 30 kg of bubonic plague bacteria could be produced in several days.
The related Unit 8604 was operated by the Japanese Southern China Area Army and stationed at Guangzhou, known historically as Canton or Kwangchow. This installation conducted human experimentation in food and water deprivation as well as water-borne typhus. According to postwar testimony, this facility served as the main rat breeding farm for the medical units to provide them with bubonic plague vectors for experiments.
After Imperial Japan surrendered to the Allies in 1945, Douglas MacArthur became the Supreme Commander of the Allied Powers, rebuilding Japan during the Allied occupation. MacArthur secretly granted immunity to the physicians of Unit 731, including their leader, in exchange for providing America, but not the other wartime allies, with their research on biological warfare.
American occupation authorities monitored the activities of former unit members, including reading and censoring their mail. The U.S. believed that the research data was valuable. The U.S. did not want other nations, particularly the Soviet Union, to acquire data on biological weapons.
The Tokyo War Crimes Tribunal heard only one reference to Japanese experiments with "poisonous serums" on Chinese civilians. This took place in August 1946 and was instigated by David Sutton, assistant to the Chinese prosecutor. The Japanese defense counselor argued that the claim was vague and uncorroborated and it was dismissed by the tribunal president, Sir William Webb, for lack of evidence. The subject was not pursued further by Sutton, who was likely aware of Unit 731's activities. His reference to it at the trial is believed to have been accidental.
Although publicly silent on the issue at the Tokyo Trials, the Soviet Union pursued the case and prosecuted twelve top military leaders and scientists from Unit 731 and its affiliated biological-war prisons Unit 1644 in Nanjing, and Unit 100 in Changchun, in the Khabarovsk War Crime Trials. Included among those prosecuted for war crimes including germ warfare was General Otozō Yamada, the commander-in-chief of the million-man Kwantung Army occupying Manchuria.
The trial of those captured Japanese perpetrators was held in Khabarovsk in December 1949. A lengthy partial transcript of the trial proceedings was published in different languages the following year by a Moscow foreign languages press, including an English language edition.
The lead prosecuting attorney at the Khabarovsk trial was Lev Smirnov, who had been one of the top Soviet prosecutors at the Nuremberg Trials. The Japanese doctors and army commanders who had perpetrated the Unit 731 experiments received sentences from the Khabarovsk court ranging from two to 25 years in a Siberian labor camp.
The Americans refused to acknowledge the trials, branding them communist propaganda.
Having been granted immunity by the American Occupation Authorities at the end of the war, Ishii never spent any time in jail for his crimes and died at the age of 67 of throat cancer.
Under the American occupation the members of Unit 731 and other experimental units were allowed to go free. One graduate of Unit 1644, Masami Kitaoka, continued to do experiments on unwilling Japanese subjects from 1947 to 1956 while working for the National Institute of Health Sciences. He infected prisoners with rickettsia and mental health patients with typhus.
“. . . As long ago as 1962, forty scientists were employed at the U.S. Army biological warfare laboratories on full-time genetics research. ‘Many others,’ it was said, ‘appreciate the implications of genetics for their own work.’ The implications were made more specific that genetic engineering could solve one of the major disadvantages of biological warfare, that it is limited to diseases which occur naturally somewhere in the world.
‘Within the next 5 to 10 years, it would probably be possible to make a new infective micro-organism which could differ in certain important respects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease.’
The possibility that such a ‘super germ’ may have been successfully produced in a laboratory somewhere in the world in the years since that assessment was made is one which should not be too readily cast aside. . .”
‘Within the next 5 to 10 years, it would probably be possible to make a new infective micro-organism which could differ in certain important respects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease.’
The possibility that such a ‘super germ’ may have been successfully produced in a laboratory somewhere in the world in the years since that assessment was made is one which should not be too readily cast aside. . .”
(A Higher Form of Killing; Robert Harris and Jeremy Paxman; Hill and Wang [SC]; ISBN 0–8090-5471-X; p. 241.)
Fort Detrick, Md., was created in the middle of World War II and became the center for America's biological warfare efforts. But that role shifted in 1969, the government says, to focus solely on defense against the threat of biological weapons.
Then called Detrick Air Field, the science and research facility housed four biological agent production plants.
Anthrax was considered the most important agent. Simulants were tested, and one bomb was readied for production in 1944. One million bombs were ordered, though the order was canceled when the war ended in 1945.
During the 1950s, the biological weapons program was among the most classified within the Pentagon. There was an emphasis on biological agents for use against enemy forces as well as plants and animals.
The Army says no biological weapons were used during the Korean War, though such allegations were made by the Chinese and the Koreans.
Growing Protests
One plan at Fort Detrick in the late 1950s was to use the yellow fever virus against an enemy by releasing infected mosquitoes by airplane or helicopter. Detrick's labs were capable of producing a half-million mosquitoes per month, with plans for up to 130 million per month.
The military also tested bombs in Utah with brucella suis, a bacterium that can lead to fever and influenzalike sickness. And scientists at Fort Detrick also worked on a number of possible pathogens that could destroy crops or trees.
By the 1960s, the U.S. biological warfare program had begun to decline, with funding gradually decreasing. There were growing protests in the United States over the use of defoliants in Vietnam and anger about a sheep-kill incident in Utah. That incident occurred in 1968, when 3,000 sheep were found dead in the Skull Valley area, adjacent to the Army's Dugway Proving Ground. Although the findings were not conclusive, it was believed that nerve agents had somehow drifted out of Dugway during a test of aerial spraying.
In 1969, the Army announced that 23 U.S. soldiers and one U.S. civilian had been exposed to a sarin nerve agent on the Japanese island of Okinawa, while cleaning sarin-filled bombs. The incident created international concerns and revealed that the Army had secretly positioned chemical munitions in Southeast Asia.
That same year, President Nixon took action against biological and chemical weapons. He reaffirmed a no-first-use policy for chemical weapons, renounced the use of biological weapons and limited research to defensive measures only.
Leading Researcher
The Army fort that had its beginnings during World War II is now a sprawling campus of brick government buildings outside Frederick, Md., located an hour's drive north of Washington, D.C.
Government scientist Bruce E. Ivins worked at the heart of Fort Detrick, inside the main building of the U.S. Army Medical Research Institute for Infectious Diseases. It was there that he was one of the leading researchers on anthrax vaccines. The building houses a number of highly secure labs where anthrax spores would be used.
Ivins, who died on July 29, helped investigate the deadly anthrax attacks in 2001. He apparently had been notified that he was to be prosecuted for the five deaths connected to the anthrax attacks.
Blaming Gays, Blacks, and Chimps for AIDS
Are species-jumping animal virus experiments responsible for the HIV Holocaust?
Paranoia magazine
by Alan Cantwell, M.D.
In the fall of 1986 the Soviets shocked the world by claiming that HIV was secretly developed at Fort Detrick, the U.S. Army's biological warfare unit. Although the claim was dismissed as "infectious propaganda", Russian scientists had worked hand in hand with biological warfare scientists in the transfer of viruses and virus-infected tissue into various non-human primates (monkeys, apes, chimps) during the 1970s before AIDS appeared. With improved international relationships, the Russian accusation vanished.
Although evidence supporting the man-made theory has never been mentioned in the major U.S. media, the theory continues to be ridiculed. For example, in the San Francisco Chronicle,( "Quest for the Origin of AIDS", January 14, 2001), William Carlsen writes: "In the early years of the AIDS epidemic, theories attempting to explain the origin of the disease ranged from the comic to the bizarre: a deadly germ escaped from a secret CIA laboratory; God sent the plague down to punish homosexuals and drug addicts; it came from outer space, riding on the tail of a comet."
AIDS certainly did not come from the hand of God or outer space. However, there is ample evidence to suspect the hand of man in the outbreak of AIDS that first began in the late 1970s in New York City.
Creating AIDS in animals before the epidemic
In 1974 veterinarians actually created an AIDS-like disease when newborn chimps were removed from their mothers and weaned exclusively on virus-infected milk from cows infected with "bovine C-type virus." Within a year the chimps died of leukemia and pneumocystis pneumonia (the "gay pneumonia" of AIDS). Both diseases had never been observed in chimps before this virus-transfer experiment.
Also downplayed is the laboratory creation of feline leukemia and "cat AIDS" by the transfer of HIV-like cat retroviruses in the mid-1970s. These experiments were conducted at Harvard by Myron (Max) Essex, later to become a famous AIDS researcher. All this man-made creation of AIDS in laboratory animals directly preceded the "mysterious" 1979 introduction of HIV into gay men, the most hated minority in America.
Nowadays, scientists hunt for "ancestor" viruses of HIV in chimps in the African wild and ignore all the immunosuppressive viruses that were created in virus laboratories shortly before AIDS. No consideration is given to any of these lab viruses as possible man-made ancestors of the many "strains" of HIV (and HIV-2) that jumped species to produce AIDS in humans.
The gay experiments that preceded AIDS (1978-1981)
Scientists also discount any connection between the official outbreak of AIDS in 1981 and the experimental hepatitis B vaccine program (1978-1981) at the New York Blood Center in Manhattan that used gays as guinea pigs shortly before the epidemic. Curiously, the exact origin of AIDS in the United States remains unstudied. Health authorities simply blame promiscuous gay men, but never adequately explain how a black heterosexual African disease could have transformed itself exclusively into a white young gay male disease in Manhattan.
Researchers claim HIV incubated in Africa for more that a half century until AIDS broke out there in 1982. However, in the U.S. there was no incubation period for gay men. As soon as homosexuals signed up as guinea pigs for government-sponsored hepatitis B vaccine experiments, they began to die with a strange virus of unknown origin. The hepatitis B experiments began in Manhattan in the fall of 1978; the first few cases of AIDS (all young gays from Manhattan) were reported to the CDC in 1979.
Scientists have also failed to explain how a brand new herpes virus was also introduced exclusively into gays, along with HIV, in the late 1970s. This herpes virus is now believed to be the cause of Kaposi's sarcoma, the so-called "gay cancer" of AIDS. Before AIDS, Kaposi's sarcoma was never seen in healthy young men. Identified a decade after HIV, in 1994, this KS virus is closely related to a primate cancer-causing herpes virus extensively studied and transferred in animal laboratories in the decade before AIDS.
Also downplayed to the public is a new microbe (Mycoplasma penetrans), also of unknown origin, that was introduced into homosexuals, along with HIV and the new herpes virus. Thus, not one but three new infectious agents were inexplicably transferred into the gay population at the start of the epidemic (HIV, the herpes KS virus, and M.penetrans).
In his book, Virus [2000], Luc Montagnier (the French virologist who co-discovered HIV) blames promiscuous American gay tourists for bringing this new mycoplasma to Africa, and for bringing back HIV. He provides no evidence for this homophobic theory. Nor does he mention the various mycoplasmas that were passed around in the 1970s in scientific labs, and the fact that these microbes were frequent contaminants in virus cultures and vaccines.
Why are all these simultaneous introductions of new infectious agents into gay men ignored by scientists? Surely a credible explanation would be important in determining the origin of HIV and AIDS.
Why are scientists so opposed to the man-made theory? And why do they believe so passionately in the chimp theory? One explanation might be that scientists don't want the public to know what happened to the tens of thousands of imported primates who were held captive in laboratories throughout the world in the decade before AIDS.
The forgotten Special Virus Cancer Program (1964-1977)
Rarely mentioned by AIDS scientists and media reporters is the fact that surgeons have been transplanting chimpanzee parts (and chimp viruses) into people 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 primate (chimp and monkey) viruses to human beings is the largely forgotten Special Virus Cancer Program (SVCP). This research program was responsible for the development, the production, the seeding, and the deployment of various animal cancer and immunosuppressive AIDS-like viruses and retroviruses. These laboratory created viruses were capable of inducing disease when transferred between animal species and also when transplanted 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, the program was soon enlarged to study all forms of cancer. The scope of the program was international and included scientists from Japan, Sweden, Italy, the Netherlands, Israel, and Africa. The 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. As a result, thousands of liters of dangerous man-made viruses were adapted to human cells and shipped around the world to various laboratories. The annual reports of the SVCP contain proof that species jumping of animal viruses was a common occurrence in labs a decade before AIDS.
The SVCP gathered together the nation's top virologists, biochemists, immunologists, molecular biologists, and epidemiologists, to determine the role of viruses and retroviruses in the production of human cancer. Many of the most prestigious medical institutions were involved in this program.
Connected with the SVCP were the most famous future American AIDS scientists, such as Robert Gallo (the co-discoverer of HIV), Max Essex of "cat AIDS" fame, and Peter Duesberg, who claims HIV does not cause AIDS. Gallo and Essex were also the first to promote the widely accepted African green monkey theory of AIDS. This theory was proven erroneous as far back as 1988, but was heavily circulated among AIDS educators and the media until the theory was superceded by the chimp theory in the late 1990s.
Biowarfare research, primate research and the SVCP
Also joining forces with the SVCP at the NCI were the military'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 cancer research. As part of Nixon's so-called War on Cancer, the military biowarfare unit was retitled the new Frederick Cancer Research Center, and Litton Bionetics was named as the military's prime contractor for this project.
According to the 1971 SVPC annual report, the primary task 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 cause human cancers.
For these experiments a steady supply of research animals (monkeys, chimpanzees, mice, and cats) was necessary; and multiple breeding colonies were established for the SVCP. Primates were shipped in from West Africa and Asia for experimentation; and virus-infected animals were shipped out to various labs worldwide.
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 the early 1970s, experimenters had transferred cancer-causing viruses into several species of monkeys, and had also isolated a monkey virus (Herpesvirus saimiri) that would have a close genetic relationship to the new Kaposi's sarcoma herpes virus that produced the "gay cancer" of AIDS in 1979.
In order 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 viruses were injected into newborn animals or into the womb of pregnant animals. Some animals were injected 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 similar biochemically and immunologically to human beings. Humans share 98.4% of their DNA with chimpanzees. Chimps were extensively used by SVCP because there would be no official testing of "candidate" lab viruses on humans.
In the decade before AIDS, 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 monkey viruses, into newborn macaques (a small species of monkey that carries a close relative of the KS virus).
Recorded in the 1971 SVCP report (NIH-71-2025), Gallo's project notes state:
"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 measures of control. The close phylogenetic relationship of the lower primates to man justifies utilization of these animals for these purposes."
Researchers at Bionetics injected human and animal cancer material into various species of monkeys to determine the cancer effect. Newborn and irradiated monkeys 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. How many "new" and "emerging" viruses were created and adapted to human tissue and to various primates is not known. Some primates were released back into the wild carrying lab viruses with them. The possible spread of these lab viruses to other animals in the wild has been ignored by scientists searching for the origin of HIV and its close relatives in African animals.
Cats were also bred for leukemia and sarcoma cancer studies. Germ free colonies of inbred mice were 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 beings.
The end of the SVCP and the birth of AIDS
By 1977 the SVCP came to an 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 SVCP 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. As the SVCP was winding down, thousands of gay men were signing up as guinea pigs in government-sponsored hepatitis B vaccine experiments in New York, Los Angeles, and San Francisco. These same cities would soon become the three primary epicenters for the new "gay-related immune deficiency syndrome," later known as AIDS.
Two years after the termination of the SCVP, the introduction of HIV into gay men (along with a herpes virus and a mycoplasma) miraculously revived retroviral research and made Gallo the most famous scientist in the world. Could virus-contaminated hepatitis vaccines lie at the root of AIDS? In the early 1970s the hepatitis B vaccine was developed in chimpanzees. To this day, some people are fearful about taking the hepatitis B vaccine because of its original connection to gay men and AIDS.
Was HIV (and the KS herpes virus and a new mycoplasma) introduced into gays during these vaccine trials when thousands of homosexuals were injected in Manhattan beginning in 1978, and in the West Coast cities in 1980-1981?
As mentioned, the first gay AIDS cases erupted in Manhattan a few months after the gay experiment began at the NY Blood Center. When a blood test for HIV became available in the mid-1980s, the Center's stored gay blood specimens were reexamined. Most astonishing is the statistically significant fact 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 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. And epidemic cases in Africa did not appear until 1982.
Although denied by the AIDS establishment, a few researchers are convinced that these vaccine experiments served as the vehicle through which HIV was introduced into the gay population. 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 [1988], and in Queer Blood: The Secret AIDS Genocide Plot [1993].
These books also debunk the preposterous "Patient Zero" story of 1987, which claimed a promiscuous gay Canadian airline steward brought AIDS to America. The highly implausible story was sensationalized in the media and served to further obscure the origin of AIDS in America and blame gay promiscuity. Even Montagnier is doubtful that the U.S. epidemic could have developed from a single patient.
Never mentioned by proponents of the chimp theory is the fact that the New York Blood Center established a chimp virus laboratory in West Africa in 1974. One of the purposes of VILAB II, at the Liberian Institute for Biomedical Research in Robertsfield, Liberia, was to develop the hepatitis B vaccine in chimps. A few years later this vaccine was inoculated into gays at the Center.
Chimps were captured from various parts of West Africa and brought to VILAB. Alfred Prince, Head of virology at the NY Blood Center, has been the director of Vilab for the past 25 years. The lab prides itself by releasing "reha bilitated" chimps back into the wild.
Also closely allied with "pre-AIDS" development of a hepatitis B vaccine is the little publicized primate colony outside New York City called LEMSIP (the Laboratory for Experimental Medicine and Surgery). Until disbanded in 1997, LEMSIP supplied New York area scientists with primates and primate parts for transplantation and virus research.
Founded in 1965, LEMSIP was affiliated with the New York University Medical Center, where the first cases of AIDS-associated Kaposi's sarcoma were discovered in 1979. Researchers at NYU Medical Center were also heavily involved in the development of the experimental hepatitis B vaccine used in gays; and the Medical Center received government grants and contracts connected with biological warfare research beginning in 1969, according to Leonard Horowitz, author of Emerging Viruses: AIDS and Ebola [1996].
Scientific disinformation and the 1959 HIV-positive blood test from Africa
By predating HIV back to the 1930s, the chimp theory effectively discredits the man-made theory of AIDS, which dates the introduction of HIV to the late 1970s. Only time will tell whether the chimp theory will hold up to further scientific scrutiny.
Conspiracy theorists believe some wildly popular AIDS origin stories in the press reek of scientific disinformation. One example is the Patient Zero story. Another is the media blitz surrounding the English sailor who supposedly contracted AIDS in 1959. This now-disproven story made worldwide headlines in 1990 and obviously served to contradict the underground conspiracy theory (particularly among African-Americans) that AIDS was man-made.
The New York Times (July 24, 1990) declared:
"The case also refutes the widely publicized charges made by Soviet officials several years ago that AIDS arose from a virus that had escaped from a laboratory experiment that went awry or was a biological warfare agent. The human retrovirus group to which the AIDS virus belongs was unknown at the time. Nor did scientists then have the genetic engineering techniques needed to create a virus."
Several years later, the case was discovered to be not a case of AIDS because the sailor's tissue remains were accidentally (or deliberately) contaminated with HIV.
In 1998 the media alerted the public to further evidence that AIDS started in Africa. The proof consisted of an old 1959 stored frozen blood specimen discovered to be HIV-positive. Researchers claimed the tiny amount of serum contained fragments of HIV "closely related" to a virus found in 3 chimpanzees in the African wild and in the frozen remains of a chimp named Marilyn, discovered in a freezer at Fort Detrick.
The 1959 specimen was obtained from a Bantu man living in Kinshasa, the Congo. His name and health status were not recorded. Details of the history and testing of this specimen (later heralded as the "world's oldest HIV-positive blood sample") are recorded in The River: A Journey to the Source of HIV and AIDS [1999], by journalist Edward Hooper who theorizes that HIV was introduced into Africans via the polio vaccine programs in the late 1950s. Hooper claims the polio vaccine was prepared using chimp kidney cells contaminated with the ancestor virus of HIV.
When tested for HIV in the mid-1980s, the 1959 blood sample was the only specimen out of 700 stored frozen Congo bloods that tested positive for HIV. Originally collected by Arno Motulsky on a Rockefeller grant, the African sample was one of many sent to the University of Washington in Seattle and used for genetic testing and included in a report, "Population Genetic Studies," published in 1966. Around 1970, the remaining 672 frozen bloods were flown to Emory University in Atlanta for further genetic tests.
In 1985 the specimens again changed hands, this time for HIV testing by Andre Nahmias, a virologist and animal researcher associated with the Yerkes Primate Center at Emory. The Congo specimens were tested along with 500 other blood specimens taken from blacks living in sub-Saharan Africa between the years 1959 and 1982. Initially over 90% of specimens taken in 1959 tested positive for HIV by the ELISA test. However, these HIV-positive tests were later determined to be false-positive. After the examinations at Emory, the specimens were shipped to Harvard University in Cambridge, Massachusetts, for HIV testing in Max Essex' lab.
Three specimens initially tested HIV-positive, but finally only the 1959 specimen from the unidentified Bantu man was confirmed HIV- positive. Around the time of these examinations, Essex's lab was unknowingly contaminated with primate viruses.
In 1986, Essex discovered a new "human" AIDS virus that later proved to be a contaminating monkey virus. The source of the primate virus traced back to a captive monkey at a primate center in nearby Southborough, Massachusetts. This primate contamination at his lab resulted in the erroneous green monkey theory, heavily popularized by Gallo and the media.
Also unpublicized is the little known fact that Gallo's lab at the National Cancer Institute was plagued with contamination by primate viruses. In 1975 he reported a new human "HL-23" virus that eventually proved to be three contaminating ape primate viruses (gibbon-ape virus, simian sarcoma virus, and baboon endogenous virus). Gallo claims he has no idea how these viruses contaminated his research.
In 1996 Hooper convinced Nahmias to turn over the remaining 1959 specimen to David Ho of Rockefeller University in Manhattan for PCR testing. In 1996 Ho was named Time magazine's "Man of the Year", at a time when few people had ever heard of him. Ho is also the director of the Aaron Diamond AIDS Research Center, affiliated with Rockefeller University since 1996. The Diamond Center is also now connected with the New York Blood Center, home of the gay vaccine experiments that gave birth to AIDS.
Ho determined the tiny amount of the remaining specimen did not contain live virus, nor was the complete virion of the virus present. Instead, some fragments of the virus (about 15% of the total genome) were tested and presented to the scientific world as the oldest specimen of HIV in the world. Ho's PCR results cannot be confirmed by independent investigators because the 1959 specimen is now totally used up.
When published in the journal Nature on February 5, 1998 ("An African HIV-1 sequence from 1959 and implications for the origin of the epidemic"), Hooper's name appeared on the report, along with Ho, Bette Korber, Nahmias, and others, The report was heavily publicized as proof that HIV existed in the African population in 1959.
Although there are no HIV-positive tissue specimens from Africa from the 1960s and 1970s, and no proven cases of AIDS either, Hooper relies heavily on this 1959 test to support his theory that HIV entered the African population via the polio vaccines programs in the late 1950s.
In The River Hooper quickly dismisses the claims of physician Robert Strecker, the first whistle-blower of man-made AIDS, as well as the research in Horowitz's Emerging Viruses, and in my own books, AIDS & The Doctors of Death, and Queer Blood.
In condemning AIDS biowarfare research, Hooper declares, "Sadly, supporters of the Streckers have continued to peddle their ill-informed and outdated versions of the myth, blaming variously the Soviets, the CIA, the Germans, and the World Health Organization (WHO) well into the nineties." He dismisses the hepatitis B vaccine connection to AIDS by noting that only two of the 826 gay vaccinees had developed AIDS by 1983.
Hooper ignores the fact that by 1981 over 20% of the men in the trials were HIV-positive and that by 1982, over 30% of the men were HIV-positive. He dismisses the World Health Organization's African smallpox vaccine connection by saying, "there is no reason for either HIV or SIV [simian immunodeficiency virus] to be accidentally present in the vaccine." Hooper fails to consider the possibility that the vaccines could have been deliberately contaminated with HIV. Hooper has been a United Nations official, but no details of this are included in his book .
Despite his massive research, Hooper seems naïve about the continuing transfer of viruses between various primate species at primate centers. For example, in 1995 he interviewed Preston Marx at LEMSIP. At that time Marx was a representative of David Ho's organization, the Aaron Diamond Research Center.
Hooper writes:
"I was shocked by the cavalier way in which tissues and sera from one species had been introduced into other species, long after the risks of cross-species transfer had been highlighted by the SV40 [polio vaccine] debacle, and I was astonished that survivors from troops that had been stricken by mystery illnesses could have been casually sold to other centers, for use in experiments there. Furthermore, this apparent lack of monitoring and central control seemed to be echoed in other fields, like xenotransplantation (the transplanting of organ or cells from one species to another) - and here, of course, the implications were even more frightening."
By predating his polio vaccine theory back to the late 1950s, Hooper greatly simplified his theory of AIDS origin. He ignored all those animal viruses that were placed into human tissue in the 60s and 70s, and all those dangerous viral creations that were genetically altered for cancer research, vaccine research, and secret biological warfare.
The chimp in the freezer at Fort Detrick
On February 1, 1999 Lawrence K Altman, longtime physician-writer for The New York Times, dutifully reported "the riddle of the origin of the AIDS virus has apparently been solved." A team of researchers, headed by Beatrice Hahn at the University of Alabama, performed viral studies on three chimps in the African wild and had also studied the frozen remains of a chimp, discovered by accident in a freezer at Fort Detrick. The chimp had tested positive for HIV in 1985. On the basis of all this research, Hahn declared that a common subspecies of chimp (Pan troglodytes troglodytes) was the animal source of the virus "most closely " related to HIV.
In a media blitz U.S. government scientists presented a phylogenetic ancestral "family tree" of primate viruses (which few people could understand) to prove that HIV was genetically descended from a chimp virus in the African bush. Molecular analysis of virus genetic data, performed by Bette Korber and the supercomputer Nirvana at the Los Alamos National Labor atory in New Mexico, indicated that HIV had jumped species from a chimp to a human in Africa around the year 1930. (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.)
Beatrice Hahn theorized that the epidemic started when a hunter cut himself while butchering chimp meat and subsequently became infected. Scientists readily accepted Hahn's notion that the AIDS virus and its closest relatives jumped species from chimps to humans on multiple occasions, thereby explaining the origin of the three separate subtypes of HIV-1 (M, N, and O), as well as HIV-2.
Chimps in West Africa are hunted for food, as well as for medical experimentation. Young chimps are especially prized for scientific research and are usually caught by shooting their mothers. Many die from stress and inhumane conditions during capture and transport to laboratories and zoos in Western nations.
Due to all this killing, chimps are now an endangered species. During the past century the African chimp population has dropped from two million to less than 150,000. Despite the mass killing of chimps, they are still blamed for causing the worldwide epidemic of AIDS.
Beatrice Hahn is no stranger to primate theories, having worked in Gallo's lab when he was heavily promoting the green monkey theory in the mid-1980s and the "close relationship" of the monkey virus to HIV. Now Hahn's virus was claimed to be a closer relative than the contaminating monkey virus in Essex' lab that formed the basis of the false green monkey theory.
Media journalists paid no attention to these discrepancies. Hahn's new chimp findings, along with the old 1959 blood specimen, fully convinced the AIDS establishment, and an adoring media, that Africa was indeed the source of HIV and the AIDS epidemic.
The 2000 London Origin of AIDS Conference
When Hooper's book appeared in the fall of 1998, molecular scientists quickly used the new chimp virus data to completely discredit Hooper's polio vaccine theory. AIDS in Africa could not be caused by a virus jumping species in the 50s if it had already jumped species back in the 1930s. Researchers refused to believe scientists could have played any role in the origin of HIV and AIDS.
Hooper bypassed the biowarfare theory by predating HIV back to the 50s. Now scientists bypassed Hooper by dating HIV back several decades earlier. The fact that there was no African epidemic until the early 1980s did not seem pertinent. To make their view official, a small group of scientists proposed an "invitation only" meeting to settle the origin matter once and for all.
In October 2000 the Royal Society of London held a two-day conference on the origins of HIV. Obviously, the biowarfare theory of AIDS was not discussed. On the contrary, one professor emphatically declared "all human infectious diseases have an animal origin." Although there never was a disease like AIDS (until scientists started to flagrantly pass viruses around to repeatedly break the species barrier ), the same professor declared that "natural transfer of these infections is a common event in animal populations."
Using the viral fragments from the 1959 specimen and comparing them with the select viruses contained in the data bank at Los Alamos , Betty Korber refined her computer calculations to establish a likely date of 1940, "with confidence levels extending from 1871 to 1955." The Rega Institute in Antwerp estimated the transfer could have occurred between 1590 and 1760, with 1675 the most likely date.
Hooper spoke but his views were largely ignored by the molecular biologists. Preston Marx warned about more human diseases caused by viruses emerging from primates, None of the speakers mentioned what happened to the thousands of liters of animal viruses that were passed around the world by the Special Virus Cancer Program in the decade before AIDS.
Instead, the London conferees alerted the public to a new view of medical science, championed by the virologists. The "Last Word" at the conference was that "all human viral infections were initially zoonotic (animal) in origin. Animals will always provide a reservoir for viruses that could threaten human populations in the future." And the scientists predicted: "There is still a myriad of current unknown viruses in animal populations on land, sea, and air with the potential to cause human disease." Apparently, none of these viruses were in animal laboratories.
AIDS, cancer, genetic science and covert human medical experimentation
Although rejected completely by most scientists, the man-made theory of AIDS is a rational explanation for the origin of HIV. This theory is partly based on an awareness of the gene-polluting activities and species jumping virus experiments of irresponsible scientists during the two decades before the epidemic.
In addition, the record clearly shows that scientists and biowarfare scientists experiment secretly on unsuspecting people. Horrific aspects of the Cold War Human Radiation Experiments attest to the fact that covert medical experimentation is not an "X-Files" fantasy or a totally paranoid belief.
It is easy to understand why researchers might want to obscure the man-made origin for AIDS and blame primates. It is now apparent that most of the major researchers promoting the African primate origin of AIDS were connected with the largely secret Special Virus Cancer Program, or are scientists involved in the transfer of viruses in animal research, particularly primate research.
From the very beginning of the epidemic, researchers disclaimed any connection between AIDS and cancer, as well as any connection between HIV and animal retrovirus cancer research. In 1984, Gallo originally named HIV a cancer-causing "leukemia/lymphoma" virus. To obscure the cancer connection, the name was immediately changed to "lymphotropic" virus.
My own Kaposi's sarcoma research, first published in medical journals in 1981, showed "cancer-associated bacteria" as possible infectious agents in "classic" KS tumors. Before HIV was discovered in 1984, additional papers in 1982 and 1983 showed similar cancer bacteria in the enlarged lymph nodes and KS tumors of gay men with "gay cancer" and AIDS. Since the 1950s, cancer-associated bacteria have been linked to viruses, as well as to mycoplasmas. This aspect of cancer research has been suppressed for decades by the cancer establishment. A history of this research and its relevancy to AIDS is the subject of my books, AIDS: The Mystery and the Solution [1984] and The Cancer Microbe: The Hidden Killer in Cancer, AIDS and Other Immune Diseases [1990].
Gallo, in his 1991 book, falsely claims that no infectious agent had ever been found in KS. The refusal of AIDS scientists to recognize cancer microbe research, published in peer reviewed scientific journals, is a further indication that the AIDS establishment seeks to control all aspects of HIV research in such a way as to never connect the origin of AIDS with previous cancer research and covert biological warfare research. This cover-up conceals the possibility that AIDS, in reality, is a new man-made form of infectious and contagious cancer.
Could a small coterie of government scientists concoct a bogus (but scientifically plausible) primate theory of AIDS origin and bamboozle the public to believe it in order to cover-up the truth?
In the 1930s the highly respected German scientific community was entirely transformed by fascist beliefs proclaiming the genetic inferiority of the Jews and the genetic superiority of the German Master Race. This Nazi takeover of science and the media eventually led to the murder of millions in the Holocaust. Could the genetic science surrounding the origin of AIDS obscure a genocidal and world depopulation program of man-made origin? It is time for the man-made theory of HIV to be examined fairly.
Proponents of this theory should not be dismissed as paranoid conspiracy theorists; and AIDS educators should educate themselves about this hidden history of AIDS and its implications for the origin of HIV.
How many more species jumping viruses will we have to endure before we question the integrity and the agenda of scientists who still blissfully jump viruses between species in animal laboratories?
Lawrence K. Altman, the Times reporter who in 1999 wrote that the origin of the AIDS virus was solved, recently asked "Where did AIDS come from?" Now seemingly undecided, Altman answers, "We can only guess. Determining the answer would be important because discovering how AIDS came to be an epidemic might prevent a similar catastrophe in the future." ("The AIDS questions that linger," January 30, 2001).
It doesn't take a rocket scientist to figure out how researchers could have created HIV and how they could have transferred the virus to gay and blacks in a covert medical experimentation for genocidal or population control purposes.
The secrecy and scientific disinformation surrounding the Human Radiation Experiments of the Cold War era has taught us how easily government scientists can fool the public on scientific matters. And when it comes to scientific monkey business, researchers know that most people are chumps.
Dr. Alan Cantwell is a retired dermatologist and AIDS and cancer researcher, who has written extensively on the man-made origin of AIDS. E-mail address: alanrcan@aol.com Dr, Cantwell's books are available toll-free in the USA from Book Clearing House @ 1-800-431-1579, and on the internet at Amazon.com
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Cantwell AR Jr: Variably acid-fast bacteria in vivo in a case of reactive lymph node hyperplasia occurring in a young male homosexual. Growth 46: 331-336, 1982.
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