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Gay Vaccine Experiments And The American (Not African) Origin Of AIDS

By Alan Cantwell, MD
Copyright 2011 - All Rights Reserved

Ever since the AIDS epidemic became official in June 1981, there have been rumors that AIDS is a man-made disease. Although this theory has been discredited by "scientific consensus," there is evidence linking the outbreak of this new disease to a vaccine experiment conducted on gay men in New York City, as well as in other U.S. cities, between 1978 and 1981.


The first epidemic cases of AIDS in America were uncovered exclusively in young, previously healthy, and mostly white gay men in Manhattan in 1979. The cause was unknown until 1984 when a virus, later named HIV (human immunodeficiency virus), was accepted as the infectious agent. How a sexually transmitted disease (STD), purportedly originating in Africa, was transferred into a so-called "gay disease" in New York City was left unexplained, except for preposterous stories like the gay Canadian airline steward Gaetan Dugas, who was demonized in the media and tabloids as "the man who brought AIDS to America."



Beginning in 1974, workers in a bloodmobile provided by the New York Blood Center in Manhattan began soliciting 8, 906 gay men for a hepatitis B vaccine research study (Koblin et al, 1992). Over the next few years more that 10,000 blood samples were donated by gays willing to participate in the development of a vaccine that might prevent hepatitis B. This viral disease was an STD disproportionately affecting sexually-active homosexuals.


The AIDS epidemic in the U.S. directly traces back to this government-sponsored vaccine experiment! Eventually, 1,083 gay men were recruited to be injected with an experimental hepatitis B vaccine at the New York Blood Center. In the months before the actual experiment began, the vaccine underwent preliminary testing for safety and immune response on two hundred physicians at New York Medical Center, as well as on twenty-eight employees of Merck & Co, which made the vaccine.


The first group of men in the actual trial were inoculated in November 1978. The experiment was confidential. Each man was given an anonymous identification number, which would be the only way they could be identified by the investigators. Each man got an initial dose of vaccine, then a repeat one month after, and a final inoculation six months later. All were asked to donate blood samples for two years after the three injections. Over a period of months, all 1,083 men would be injected. Half the men were given the experimental vaccine; the other half would serve as the control group and were given useless placebo injections. In this double-blind study, neither the men nor the investigators knew who was getting the vaccine or the placebo.


This experiment ended in September 1980. The success rate in preventing hepatitis B in the group receiving the vaccine was 92.3%. Additional experimental hep B vaccine trials, all using gay men as the guinea pig, were conducted in 1979 and 1980 in Chicago, Los Angeles, San Francisco, Denver and St. Louis.


In May 1981, the men in the placebo group (who did not receive the vaccine) at the Blood Center were offered a chance to take the vaccine. As a result, 270 men were inoculated with the series of three shots and were asked to donate additional blood samples for two more years. Because men in the vaccine-recipient group and the placebo group were now both inoculated with the vaccine, it would no longer be possible to compare the two groups in terms of future HIV rates. Because the experiment was confidential and anonymous, the fate of the individual men in terms of acquiring HIV/AIDS in the future, could never be ascertained. In June 1981, after 41 cases of a new disease in homosexuals were reported to the Centers for Disease Control and Prevention in Atlanta (CDC), the AIDS epidemic became official.



The first few cases of a new disease characterized by immunodeficiency, cancer and a previously rare form of pneumonia in young gay men, were uncovered in Manhattan in 1979. By the end of 1981 there were 160 cumulative cases from New York City; a decade later, 9,000 cases had been reported in NYC. The early cases were termed "gay related immune deficiency disease," or GRID, for short. Privately, it was called "the gay plague," with homosexuals dying from "gay cancer" in the form of Kaposi's sarcoma, and/or a rapidly fatal"gay pneumonia"caused by a yeast-like fungus.


By the end of 1979, 6.6% of 378 men who had been"hepatitis B trial participants"or who had donated blood in the experiment at the Center were already HIV- positive. By 1981, it was 20%! (This was at a time when the African AIDS epidemic was unknown.) By 1984 over 40% of the trial participants were HIV-positive (Stevens et al, 1986). These infection rates were determined in 1985 when the stored gay blood samples were retested for HIV.


A different (non-vaccine) hepatitis B study, conducted from 1978 to 1980 at the San Francisco City Clinic, recruited a cohort of 6,705 homosexuals. By 1982, 41% of all reported AIDS cases in S.F. were from this cohort. By 1989, 75% of the cohort was infected with HIV-and 1,479 had developed AIDS (Rutherford et al, 1990). Activist Tom Keske has posted an essay on his website entitled: "Was AIDS in the U.S. started intentionally?" He also provides an incriminating statistical analysis linking the AIDS outbreak in San Francisco to hepatitis B vaccine experiments conducted in that city.

また別の非ワクチン・B型肝炎の研究が1978年から1980年にかけてサンフランシスコ市クリニックで実施され、6,705人の同性愛者達を募集し、その参加者の内41%が、1982年までにAIDSに感染していたことがサンフランシスコでの報告で明らかになりました。1989年までには、このグループの75%がHIVウィルスに感染し、1,479人がAIDSを発症しました。(ラザフォード1990年) 活動家のトム・ケスケ氏は彼のウェッブサイトにこういう論文を投稿しました:「AIDSはアメリカで意図的に始められたのか?」 彼はまた、AIDSのサンフランシスコでの大発生をB型肝炎ワクチン実験に関連付ける自分に不利になるような統計分析を公開しています。

In 1984, the CDC was apparently oblivious to the extremely high rate of HIV/AIDS infection in gay men who participated in the hepatitis experiments and studies, particularly at a time when the African AIDS epidemic was still largely unknown. In its Morbidity and Mortality Weekly Report, dated Dec 14, 1984, the agency simply concluded the hepatitis B vaccine was safe-and that "epidemiologic monitoring of AIDS cases and high-risk groups confirms the lack of AIDS transmission." When later studies revealed the high incidence of HIV in these men, as noted above, there was no official comment by the CDC.


To my knowledge, the CDC never tested the vaccine given to the men at the NY Blood center; and this CDC 1984 report is often cited to refute any connection between gay experiments and the AIDS outbreak. New York City quickly became the epicenter for the American epidemic, and has remained so to this day, with morethat 100,000 New Yorkers living with HIV/AIDS.



According to Luc Montagnier in his book "Virus" (1999), the African AIDS epidemic did not begin until the Autumn of 1982 at the earliest. There is also no epidemiologic or sexual connection between gay cases and African AIDS cases.


Was HIV introduced into gay men via a contaminated vaccine? HIV is not the first simian (i.e., monkey or chimp) virus to infect mankind. Simian virus-40 (SV40) is a cancer-causing green monkey virus that contaminated the polio vaccine, and was injected into millions of people worldwide beginning in the 1950s. SV40 was also used extensively in animals to induce cancer tumors conducted as part of the largely forgotten Special Virus Cancer Program (1964-1980). For details of this Program, see my Internet article entitled 'Blaming Gays, Blacks, and Chimps for AIDS.'

HIVウィルスに汚染されたワクチンが原因で、ゲイの男性たちがHIVに感染したのでしょうか?HIVが人類に伝染するサルの最初のウィルスではありません。サル・ウィルス-40(SV40)は、ポリオワクチンを汚染した癌を発症させるミドリザル・ウィルスで、これは1950年代当初、世界中の何百万人といいう人々に注射されました。SV40は、忘れ去られてしまったスペシャル・ウィルス癌プログラム(1964-1980)の一部として実施され、癌腫瘍を発生させるために動物にも大々的に使用されました。このプログラムの詳細については、私のインターネットの記事「AIDSのことでゲイ、黒人、そして、チンパンジーを避難する」(Blaming gays, blacks, and chimps for AIDS)を参照してください。

There are strong connections between simian viruses and the experimental hep B vaccine, the gay participants, and the outbreak of AIDS. The vaccine given to gays was designed by Maurice Hilleman of Merck; and was "developed" by repeatedly injecting it into chimpanzees, as part of the safety testing of the vaccine. Could a chimp HIV-like virus have been transferred to the vaccine during the 65-week manufacturing process?


Humans and chimps have 99% of their active genetic material in common. As a result, chimps are used extensively in medical research. In 1974 veterinarians produced an AIDS-like disease in chimps by taking newborn chimps away from their mothers and feeding them virus-infected cow's milk. As a result of this interspecies transfer of virus, the chimps died of immunodeficiency, leukemia, and pneumocystis pneumonia, later known as the "gay pneumonia" of AIDS (McClure et al, 1974). Previously, leukemia had never been observed in chimps.


Also in 1974 the New York Blood Center established Vilab II, a little-publicized chimp research lab in Robertsville, Liberia, West Africa. It contained captive chimps, all of which were purposely infected with hepatitis. In 1978 Vilab began to release some chimps back into the wild and onto several islands. The Blood Center announced the closure of the lab in 2006 and the end to chimp research. Alfred Prince, a hepatitis researcher and virologist at the Blood Center, was also the Director of Vilab from 1975 to 2000.


Maurice Hilleman was well aware of simian viruses contaminating vaccines, having personally discovered SV40 in 1960 in polio vaccines. In ayoutube.com video entitled "Merck chief brings HIV/AIDS to America," posted by prolific AIDS origin researcher Leonard G Horowitz, Hilleman is recorded telling his colleagues, "I brought African greens [monkeys] in. I didn't know we were importing AIDS virus at the time" [i.e., between 1970-1974]. His colleagues are heard laughing. Someone says, "It was you who introduced AIDS virus in." This shocking interview, conducted by Edward Shorter for WGBH public television, was cut from the TV documentary, based on Shorter's book "The Health Century" (1987), due to liability issues, undoubtedly reflecting poorly on Merck where the vaccine for gays was developed. Hilleman's assertion gives credence to the "conspiratorial" view that the most likely source of an AIDS-causing simian immunodeficiency virus (SIV) virus was from a laboratory, and not from the wilds of Africa.

モーリス・ヒルマンは1960年にSV40ウィルスをいくつかのポリオワクチンの中に個人的に発見した経験があり、サル型ウィルスを含んでいる数種類のワクチンの事は良くわかっていました。多数の作品を残すAIDS起源の研究者であるレオナルド・G・ホロウィッツにより投稿されたYoutube.comのビデオ「マークの所長がHIV/AIDSをアメリカに持ってきた」(Merck chief brings HIV/AIDS to America)の中では、ヒルマンが彼の同僚たちにこう話しているのが記録されています…「私がアフリカのミドリザルを持ち込んだんだ。その当時、AIDSを輸入していたとは知らなかったんだ。(言い換えれば、1970~1974年の間)そして、彼らの同僚達が大声で笑っているのが聞こえます。誰かがそして言います、「AIDSウィルスを持ち込んだのは君だったんだよ」。ボストンのWGBHテレビ局主催のエドワード・ショーターがホスト役を務めたこの驚くべきインタビューは、ショーターの書いた本、「ザ・ヘルス・センチュリー(世紀)」(1987年)によると、ゲイに投与したワクチンを開発したマーク社の評判を落とすという理由で、責任諸問題のためにドキュメンタリーのテレビ番組からカットされてしまいました。ヒルマンの主張は、「十中八九、AIDSの原因となるサル免疫不全ウィルス(SIV)のウイルスの出処は研究室からであり、アフリカの荒野からではない」という「共謀の」見解に証拠を提示することになりました。

The close timeline between the hepatitis B vaccine trials, as well as the high incidence of HIV/AIDS in the participants, and the outbreak of the "gay plague" can hardly be denied. There are few sources, outside of medical journal reports, that reveal details of the experiment. The best source is June Goodfield's "Quest for the Killers" (1985), in a chapter entitled 'Vaccine on trial.' She emphasizes the dangerous aspects of the vaccine experiment, due to the pooling of the blood, as well as the concern regarding possible contamination of the vaccine. Hers is the only source revealing that some of the vaccine was made by the National Institutes of Health (NIH). "Was something wrong with the vaccine, possibly contamination? This was no theoretical fear, contamination having been suspected in one vaccine batch made by the National Institutes of Health, though never in Merck's."



Determining the simian ancestry of HIV is not the same as determining the origin of the AIDS epidemic in America. HIV is emphatically a "new virus" in humans, although its origin in simians may be ancient. The American AIDS epidemic clearly began in the late 1970s. The purported African origin of American AIDS is largely based on the genealogy of the AIDS virus in Africa. I could never understand why scientists never looked for a simian ancestor of HIV in the various primate virus labs and primate colonies in the U.S.


The simian "roots" of HIV depend on who is doing the genetic analysis. Some researchers claim that HIV has been circulating in humans since the 1930s, others date it back a century or more. A new "phylo-geographic" study suggests monkey SIVs are ancient and date back 32,000 to 75,000 years (Worobey et al, 2010).


The public was first told that HIV originated in Africa in green monkeys. This changed in 1999 when a SIV found in chimpanzees was widely accepted as the closest ancestor virus of HIV (Gao et al, 1999). Four years later, geneticists reversed themselves again, claiming HIV "didn't start its life in chimps" but arose through hybridization of two monkey strains of SIV that recombined in the chimpanzee host (Bailes et al, 2003). In other words, the ancestors of HIV were a mix of monkey immunodeficiency viruses transferred into chimps, which subsequently recombined to form a new hybrid virus with mixed genetic material. By the way, chimps are considered apes, have bigger bodies than monkeys, and are most closely related to humans. Monkeys have tails and are structurally closer to four-legged animals like cats and dogs.


Lost in all this conflicting genetic mumbo-jumbo, that few people can comprehend (including myself), was the fact that extensive mixing of simian viruses and the creation of hybrid viruses was going on for years in labs around the world in the years immediately preceding AIDS. This, in fact, is the basis of the AIDS "conspiracy theory," which proposes that the ancestor of HIV most likely originated in animal species transfer experiments in a virus laboratory. Yet this explanation is never considered by scientists. These genetic studies of HIV origin, widely reported in the major media, continue to reinforce the public perception that HIV/AIDS started in Africa.


There is no attempt made here to fully explain the origin of the horrible outbreak of AIDS in Africa beginning around 1983. This will up to future medical historians to unravel. Suffice it to say that sub-Saharan Africa has been the testing ground for pharmaceuticals and vaccines for many decades, and for massive vaccine programs with reuse of needles which could also spread HIV from person to person.


In "AIDS and the Doctors of Death" (1988), I mentioned a London Times explosive front page article connecting AIDS to extensive vaccine programs in Africa, and entitled "Smallpox vaccine triggered AIDS virus" (May 11, 1987). Robert Gallo, the co-discoverer of HIV, was quoted as saying, "The link between the WHO program and the epidemic is an interesting and important hypothesis. I cannot say it actually happened, but I have been saying for some years that the use of live vaccines such as that used for smallpox can activate a dormant infection such as HIV. "The full Times story never appeared in the major media in the U.S., but is available online.


Researchers have known for a long time that the particular strain of HIV that infected American gays is "subtype B." The prevalent strains in Africa are different, again suggesting that American AIDS cases did not come from Africa cases. Unlike some strains in Africa, which date back to the 1930s, a recent study by Perez-Losada at al (2010), indicates "subtype B" is quite new, dating back to around 1968, a decade before the hep B experiment. Max Essex claims the American B strain has an affinity for anal tissue and is more easily transmitted by homosexual contact and intravenous drug use, whereas the HIV subtypes in Africa tend to fuel heterosexual epidemics via a vaginal mucosal route.



Hilleman's hepatitis B vaccine was intentionally made from the pooled blood of 300 highly sexually-active gay and intravenous drug abusers in Manhattan. These men were the carriers of the hepatitis virus Hilleman required to manufacture his vaccine. As mentioned, the vaccine was developed in chimps,and took 65 weeks to make. His vaccine brew was collected in 1977. The specific year is important because there are no reports of AIDS cases at that time; and no stored American blood testing positive for HIV before that year.


In "Vaccinated" (2007) Paul Offit, a pediatrician and vaccine developer who works for Merck, theorizes that although "HIV was likely present in the blood from which he made early preparations of his vaccine, Hilleman's choice of pepsin, urea, and formaldehyde had completely destroyed it."


In "Vaccinated, " Offit is critical of my AIDS origin research. He writes, "The publisher of Alan Cantwell's book, Aries Rising Press, was founded by Cantwell himself to promote his uninformed views on the origin of the AIDS epidemic." Offit claims the American blood supply was "heavily contaminated" with HIV in the mid-1970s. He offers no documentation for this statement, nor are there any studies (or epidemic AIDS cases) which document this.


The earliest HIV-positive blood specimens in the American epidemic were uncovered in 1978-they are those deposited into the Blood Center by gay participants of the hep B experiment. There is no record of any other stored blood in the U.S testing positive for HIV, with one exception. According to "Virus Hunters of the CDC" (1996), author Joseph McCormick states six hundred blood specimens from Zaire, Africa, were sent to the CDC in 1976 during the Ebola virus outbreak. When re-tested in the mid-1980s for HIV, five of the specimens were positive. One has to wonder if other labs in the U.S were also harboring HIV-infected African blood used in animal (or human) research.


Unlike Offit, I have never promoted the idea that HIV was contained in Hilleman's blood brew in 1977. Yet Offit insists HIV first entered the U.S. a few years before Hilleman began working on his vaccine. He notes Hilleman would be "the first (and last) to use human blood to make a vaccine. He didn't know until years later that the blood was heavily contaminated with HIV."


Offit makes no mention of Hilleman importing HIV/AIDS via his monkeys and chimps, nor does he cite the 20% HIV infection rate of the men who participated in the trial at the Blood Center in 1981. He simply assures us the vaccine given to gay men was safe and free of HIV.



The development of a hepatitis B vaccine has a dark history. Less than a decade before the gay experiment, sixty mentally retarded children at Willowbrook State School, on Staten Island, NY, were fed live hepatitis B virus. In another experiment, the serum from a patient with hepatitis B was injected intravenously into 25 retarded children with dire results. They sickened, some severely, and turned yellow with jaundice. According to Hilleman, "They were the most unethical medical experiments ever performed in children in the Unites States."


It is indeed shameful to read the history of covert human experimentation over the past decades, which likely continues up to the present. Most appalling were "the human radiation experiments" of the Cold War era affecting millions of unsuspecting Americans, and extending into the mid-1970s. For all the morbid details, google: human medical experimentation.

過去数十年の間にかけて行われた隠密の人間への実験の歴史、それは現在まで続けられていそうでありますが、そのような歴史を読むのは実に恥ずべきことであります。最も恐ろしいのは、冷戦時代に行われていた「人間を使った放射能実験」であり、これは何百万人もの疑う事を知らないアメリカ人達に影響を及ぼし、1970年代の半ばまで続けられました。その恐ろしい出来事の詳細の全てについては、「human medical experimentaion」(人間の医療的実験)でぐぐってください。(google

I will mention only one recent revelation (2010) uncovered by Susan Reverby, quite by accident, while researching the notorious Tuskegee Syphilis study. According to the Wikipedia entry, "In a 1946 to 1948 study in Guatemala, U.S. researchers used prostitutes to infect prison inmates, insane asylum patients, and Guatemalan soldiers with syphilis and other sexually transmitted diseases, in order to test the effectiveness of penicillin in treating sexually transmitted diseases. They later tried infecting people with" direct inoculations made from syphilis bacteria poured into the men's penises and on forearms and faces that were slightly abraded . . . or in a few cases through spinal punctures. The study was sponsored by the U.S. Public Health Service, the National Institutes of Health and the Pan American Health Sanitary Bureau (now the World Health Organization's Pan American Health Organization) and the Guatemalan government.

ここで1つだけ最近(2010年)暴露された事実について話してみたいとおもいます。これはスーザン・レヴァビーにより、悪評高いタスキギー梅毒の研究について調査をしていた時に、全く偶然に明らかにされたことです。ウィキペディアの登録によると、「1946年から1948年の間にグアテマラで行われた研究で、アメリカの研究家達は、性的感染症の治療へのペニシリンの有効性を試験するために、売春婦を使って、囚人たち、精神病院の患者たち、そして、グアテマラの兵士たちに梅毒やその他の性的感染症に感染させたのです。 彼等はのちに、梅毒のバクテリアから作られた直接接種を男性達のペニスや前腕、そして、顔などに若干皮膚をすり減らした部分に垂らして、または、数例では脊椎穿刺により梅毒に感染させようと試みました。この研究は、アメリカの公衆衛生局(PHS)、国立衛生研究所(NIH/http://www.nih.gov/)、パン・アメリカン・ヘルス衛生局(今でいう世界保健機関(WHO)の全米保健機構(【略】PAHO))、そして、グアテマラ政府がスポンサーとして後押ししました。

Further details of the experiment that recruited 5,500 people and infected 1,300 people (including orphaned children) with sexually transmitted diseases were released on August 30, 2011. In one instance, a dying woman was deliberately infected with gonorrhea bacteria in her eyes and elsewhere. Seven women with epilepsy were injected with syphilis germs into the back of the spine, resulting in bacterial meningitis in all cases. Eighty-three people died. The U.S. Public Health Service is the former name of the CDC. The fact that this government study was initiated by both the CDC and the NIH, the two leading and most prestigious health organizations in America, is chilling.

5,500人の人達を募集し、1,300人の人達(中には孤児の子供たちも含まれていました)に性的感染症に感染させた実験のさらなる詳細が2011年8月30日に公開されました。1つの事例では、死にかけている女性に意図的に彼女の目などに淋病のバクテリアに感染させました。てんかんになっている七人の女性たちは脊椎の後ろ側に梅毒の細菌を注射され、全てのケースで細菌性髄膜炎が発症しました。83人の人達が死にました。アメリカの公衆衛生局(PublicHealth Service[パブリック・ヘルス・サービス])は疾病対策予防センター(CDC)の旧名になります。この政府の研究が疾病対策予防センター(CDC)と国立衛生研究所(NIH)…それらはアメリカの優れた最も一流の二つの保健機関なのですが…により行われたという事実は、身も凍る思いです。

When asked about the Guatemala experiment, Harold Jaffe of the CDC was quoted as saying: "Are there other stories that haven't come to light? We don't want to feed on the paranoia in the media, for example, of biological warfare, or AIDS as a cooked-up infection in a foreign country, but stories like this have to remind people of these stories" ('Presidential panel slams 1940s Guatemalan STD study,' by Louisa Kasdon, posted on the BU.edu website, Aug 31, 2011). Jaffe has been the top officer at the CDC covering AIDS since the very beginning. However, this is the first time I ever heard a CDC official blaming AIDS on a "cooked-up infection in a foreign country."



Vaccines are big business with worldwide sales of 25 billion; and AIDS has spawned a huge industry as well. A CBS news report (Jan 8, 2010) declared: "Got AIDS? Lifetime cost: $618,900."


I am not anti-vaccine, although I would like to know exactly how a vaccine is produced-from start to finish-before it is injected into me. And such knowledge is impossible to obtain, due to proprietary concerns of the manufacturers. Ordinarily, I decline vaccines unless absolutely necessary. I stopped taking yearly flu shots in 1991 when I read in The New York Times that some people were testing HIV-positive after injection with the "Beijing flu" shot that year. This was deemed to be a false-positive reaction, but the CDC was not sure what was causing the peculiar result.


Childhood vaccinations are necessary, of course, to prevent certain diseases. And more and more pediatricians are refusing to treat children whose parents refuse to vaccinate them according to the prescribed schedule, which includes 11 vaccines, and as many as 20 shots by 2 years of age (Offit et al, 2002). For some of my personal negative views on vaccines, see 'Vexing over vaccines' on the net.

ワクチンに関しての私の幾つかの個人的な悲観的な見解をおしりになりたい場合には、ネットで「Vexing over vaccines」(ワクチンのことでイライラさせる)で検索してみてください。

For anyone who thinks that vaccine makers are always your friend, I would recommend "The Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus, Contaminated Polio Vaccine, and the Millions of Americans Exposed" by Debbie Bookchin and Jim Schumacher (2004). They explore the history of the polio vaccine, the contamination problems with SV40 , the ensuing vaccine-related cancer problems, and the government's cover-up of the problem over the past three decades. I discovered that federal regulations require only that vaccine manufacturers screen for viruses by observing the effects of viruses on tissue cell cultures, as viewed with an ordinary light microscope. This was surprising to me because viruses are too small to be seen microscopically. Thus, vaccines are not directly tested for virus contamination, but are tested indirectly with a light microscope. Apparently virus contamination of vaccine lots is suspected only if cells (viewed in the light microscope) undergo evidence of viral infection. If a contaminating virus in a vaccine has no effect on cells, this testing procedure would obviously be ineffective. I discovered that federal regulations require only that vaccine manufacturers screen for viruses by observing the effects of viruses on tissue cell cultures, as viewed with an ordinary light microscope. This was surprising to me because viruses are too small to be seen microscopically. Thus, vaccines are not directly tested for virus contamination, but are tested indirectly with a light microscope. Apparently virus contamination of vaccine lots is suspected only if cells (viewed in the light microscope) undergo evidence of viral infection. If a contaminating virus in a vaccine has no effect on cells, this testing procedure would obviously be ineffective.

もし、貴方がワクチン製造会社はいつも貴方の友人であると思われるのならば、次の本を購入し読まれるのをお勧めます:「ウィルスとワクチン:ガンを発症させるサル型ウィルス、汚染されたポリオワクチン、そして、無防備な何百万人ものアメリカ人達」《著者:Debbie Bookchin と Jim Schumacher (2004年)》

When the gay experiments ended in 1981, HIV was already in the nation's blood supply. And there was no way to test for it. Within a year, the disease was no longer confined to male homosexuals. It was clearly an STD that could also be transmitted by body fluids and by blood transfusion. In 1982 the first AIDS cases in blood transfusion recipients and hemophiliacs were recorded.


So why were gay men the only sexually-active Americans originally infected with HIV? In my view, the most likely explanation is the vaccine was contaminated with an SIV that escaped detection during the long and dangerous manufacturing process, which included repeated safety test in chimpanzees. An alternate explanation is that a laboratory-derived SIV was introduced deliberately as a genocidal agent against gay people that would eventually spread to the "general population." In other words, a covert Guatemala-type STD experiment using gays as guinea pigs.


Sometimes, despite great care in the manufacturing process, a virus will slip through and wreak havoc. Such was the case with Cutter Laboratories in Berkeley, California, in 1957 with their polio vaccine that was accidentally contaminated with a live, virulent polio virus. The result was 200,000 infected people. Seventy thousand people became ill; 200 were permanently paralyzed; and 10 died, according to Offit's "The Cutter Incident"(2005).


Once HIV was seeded into gays, it could easily spread sexually and through body fluids. A decade before the epidemic, in a lab accident involving green monkeys in 1967, a highly dangerous simian hemorrhagic virus infected 31 workers in a vaccine facility in Marburg, Germany, resulting in 7 deaths. In several instances, the virus was transferred to sexual partners. Four cases were acquired by hospital personnel caring for victims. Infection in these instances most probably was incurred through contactwith the patients'blood (Luby and Sanders, 1969).


Since 1984, gay men have been excluded from donating blood. This policy includes any man who has had sex with another man since 1977. This was the year Hilleman began work on his vaccine made from pooled blood. This also is the "accepted" year when HIV first entered the nation's blood supply, although the source of this SIV has never been determined. However, the most likely source was close by- in primates held in laboratories and primate centers. Or in African blood samples, like those stored at the CDC.



There is a great deal of evidence pointing to AIDS as a man-made disease on the Internet, but the theory is routinely pooh-poohed as paranoia and conspiracy theory. See the Wikipedia page entitled 'Discredited AIDS origin theories.' However, it is fact that there was fear concerning the safety of the hepatitis B vaccine. When the commercial vaccine made by Abbott Laboratories became available to the public, it was unpopular. Many health professionals refused the vaccine because it was made from pooled gay blood; and they were afraid thevaccine could transmit AIDS. As a result, a new vaccine was eventually engineered using yeast cells instead of human blood.

インターネットには人為的に作られた病気としてのAIDSに注意を向ける証拠はかなり沢山ありますが、その理論はいつも決まって妄想症とか陰謀論などとして嘲り笑われています。ウィキペディアのページで「信用を失ったAIDSの起源説」(Discredited AIDS origin theories)を見てください。しかし、B型肝炎のワクチンの安全性について不安があったのは事実です。アボット研究所により作成されたその市販のワクチンが一般の人達に提供されるようになった時、そのワクチンは人気がありませんでした。多くの医療従事者たちがそれを拒否しました。何故なら、それはゲイの血液から作られたからです。そして、彼等はそのワクチンはAIDSを人々に感染させてしまうのではないかと恐れていました。結果的に、新しいワクチンが人間の血液ではなくて酵母細胞を使って操作され作られました。

Every African-American has heard the rumor that AIDS was engineered to kill off the black race. Thirty percent of blacks in New York City polled by The New York Times (October 29, 1990) actually believed that AIDS might be an ethno-specific bio-weapon designed in a laboratory to wipe them out.


George W Merck, president of Merck during World War 2, was America's biological weapons industry director. According to Leonard Horowitz's, New York University Medical Center was listed among the top biological weapons contracting labs by 1969. The NY Blood Center is affiliated with NYUMC. In 1971 a large part of the Army's biological warfare unit at Fort Detrick was transferred over to the National Cancer Institute (NCI) by president Richard Nixon. As a result, bio-warfare experimentation went under cover at the NCI, which is part of the National Institutes of Health (NIH).


As noted, Goodfield mentions that the NIH made part of the hep B vaccine used on gays, and contamination was suspected. In his later years, Hilleman himself wrote extensive articles on biological warfare, convinced that vaccines could be developed to protect people against bioterrorism.


In the Spring of 1986, Robert Strecker, was promoting his view of AIDS as a "bio-attack" against humanity. He briefly received negative media attention in TIME magazine ('Infectious propaganda', November 17, 1986). When I asked how it was possible for AIDS to start as a purely gay disease, when such an event was biologically improbable, he told me:"Because they put it there. Do you recall the hepatitis B vaccine trials in gay men? That's where the virus was introduced."


After a quarter century of study, Strecker's explanation still makes more sense to me that any other theory of AIDS origin. Ridiculous stories like "Patient Zero" and a handful of suspected "old cases" of so-called AIDS from the 1950s and 60s were sensationalized by the media in an attempt to show that AIDS existed long before the actual epidemic. Indeed, very rare cases of Kaposi's sarcoma ("gay cancer") and pneumocystis pneumonia have always existed, but never in epidemic form, nor as an STD. In my view, these reports reeked of misinformation and disinformation; and they served to obfuscate the real origin connected to government experiments conducted on gay men.


Despite my intense interest in this, I have discovered over the past three decades that most people are not interested in AIDS and where it came from. The idea of man-made AIDS, I suspect, is simply too painful for people to consider. In essence, the subject is taboo. However, it seems to me that after 25 million AIDS deaths worldwide, and over 500,000 dead Americans, that some better explanation is required than merely blaming a"species jumping"monkey virus in the African jungle-or gay sex.


This was most evident in April, 2008, when the outspoken Reverend Jeremiah Wright accused the government of inventing the AIDS virus as a genocide program against people of color. As the spiritual advisor to Barack Obama, Wright almost derailed Obama's run for the presidency. The future president quickly disassociated himself from his former pastor, and the accusation was quickly squelched by the major media without discussion. Wright had read Horowitz's book on man-made AIDS,"Emerging Viruses: AIDS and Ebola"(1996). He had carefully studied the infamous Tuskegee syphilis study, and he bluntly told the media."I believe our government is capable of doing anything."


The rumor that AIDS is a man-made disease will never go away. The reason is simple: It is the most logical explanation of how and why the AIDS epidemic first erupted as the "gay plague" among the most hated minority in America.



Alan Cantwell, MD, writes frequently about the origin of AIDS. He is the author of "AIDS & the Doctors of Death" and "Queer Blood" ; both published by Aries Rising Press, PO Box 29532, Los Angeles, CA 90029. His books are available from Amazon.com and through ariesrisingpress.com

アラン・キャントゥウェル、メリーランド州、はしばしばAIDSの起源について書いています。彼は、「AIDSと死の医者達」「同性愛者の血液」の著者であります。両方の書籍とも、Aries Rising Press, PO Box 29532,Lost Angels,CA 90029により出版されています。彼の書籍はAmazon.COM、そして、ariesrisingpress.comより購入ができます。











  • MMS
  • MMS2
  • グリーンクレー
  • ゼオライト
  • ビタミンD3
  • カルシウム
  • マグネシウム
  • 亜鉛
  • ビタミンK2(納豆)
  • B-50




一日にビタミンD3、5000IU x 20錠 x 10日間。
その後、一週間毎に、5000IU x 10錠、7錠、そして、5錠、4錠と減らしています。


比率は、カルシウム : マグネシウム = 1 : 1 または カルシウム : マグネシウム = 0.5 : 1。
放射能が食品にまぎれている可能性がある地域なら、1 : 1の割合でカルシウムを多めに接種したほうがいいですが、そうでなければ、カルシウムはマグネシウムの半分くらいで結構です。






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Mechai Viravaidya
From Wikipedia, the free encyclopedia

Mechai Viravaidya (born January 17, 1941, Thai: มีชัย วีระไวทยะ) is a former politician and activist in Thailand who has popularized condoms in that country.[1]

Since the 1970s, Mechai has been affectionately known as "Mr. Condom", and in that time condoms are referred to as "mechais" in Thailand[2] From the time that he began his work, the average number of children in Thai families has reduced from 7 to 1.5.[3]

Mechai was born in Thailand to a Scottish mother and a Thai father, both of whom were doctors. They met whilst studying in Edinburgh[4] He is one of four children. His younger brother, Sunya, is the founder of the Pattaya International Hospital. One of his two sisters, Sumalee, was formerly a journalist in Bangkok. Mechai was educated at Geelong Grammar School and (The) University of Melbourne in Australia. In the mid-1960s he returned to Thailand and started to work in family planning, emphasizing condoms. In 1973, he left government and founded a non-profit service organization, the Population and Community Development Association (PDA), to continue the work to improve the lives of the rural poor. Among other things, he held condom blowing contests for school children, encouraged taxi cab drivers to hand out condoms to their customers, and founded a restaurant chain called Cabbages and Condoms where condoms, rather than mints or fortune cookies, are given to customers together with the bill.
メチャイ氏は、タイでスコット人の母とタイ人の父の間に生まれ、両方とも医師でした。メチャイ氏はオーストラリアの大学に行き、1960年代半ばに彼はタイに戻り、家族計画の分野で、コンドームを推奨して仕事をするようになりました。1973年に政府を離れ、非営利サービス組織「人口と共同体発展協会(the Population and Community Development Association=PDA)」を設立し、農村貧困者達の生活を向上する仕事を続けました。数ある中で強いてあげるなら、学校の子供達の為にコンドーム膨らましコンテストを開催したり、また、タクシー運転手にコンドームを配るよう奨励したり、キャベツとコンドームというレストラン・チェーン店を開き、そこでお客さんに領収書を渡す時に、ミントや幸運のクッキーなどを渡す代わりにコンドームを渡すようなサービスを始めました。

Mechai served as deputy minister of industry from 1985 to 1986 under prime minister Prem Tinsulanonda. He served as senator from 1987 until 1991. During this time AIDS appeared in Thailand, and he increased his efforts to promote sexual-safety awareness.
A military coup in 1991 installed prime minister Anand Panyarachun; Panyarachun then appointed Viravaidya minister for tourism, information and AIDS. He was able to start a large and quite successful education campaign and served until 1992. In 2004, Mechai again became a senator.

In 1995 he was appointed an Honorary Officer of the Order of Australia, for "service to Australian-Thai relations and contributions to the world AIDS debate".[5]
As of 2007, he continues to oversee rural development and health initiatives as the Chairman of PDA, now the largest NGO in Thailand, with 600 employees and 12,000 volunteers. On May 29, 2007, PDA was awarded the 2007 Bill & Melinda Gates Foundation's Gates Award in recognition of its pioneering work in family planning and HIV/AIDS prevention.[6] This award came with funds of $1,000,000.[7]

An interesting side note is the family planning clinic which openly operates next to the Cabbages and Condoms restaurant. This is one of several places in Bangkok where poor women can receive pregnancy termination, a practice which is legal in the country per Section 305 of the Thailand penal code, but often perceived as illegal.[8][9] The clinic is permitted by the authorities due to the dangers of unsafe abortion by Thai women because of "economic difficulties".[10]
In 2006 he won praise from the toilet industry (but criticism from the retail industry) for proposing that retailers be obliged to build a public toilet for every 10 square metres of retail space.[11]


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( ´ ▽ ` )ノ

HIV ウィルスのワクチン
OHSU research helps explain why an AIDS vaccine has been so difficult to develop
URL : http://www.ohsu.edu/xd/about/news_events/news/2012/09-09-ohsu-research-aids-vacci.cfm


For decades, a successful HIV vaccine has been the Holy Grail for researchers around the globe. Yet despite years of research and millions of dollars of investment, that goal has still yet to be achieved. Research by Oregon Health & Science Univ. scientists explains a decades-old mystery as to why slightly weakened versions of the monkey AIDS virus were able to prevent subsequent infection with the fully virulent strain, but were too risky for human use, and why severely compromised or completely inactivated versions of the virus were not effective at all.
何十年にもわたり、HIVのワクチンの作成は世界中の研究家たちが渇望して望んでいるワクチンでした。しかし、何年もの研究や何百万ドルもの投資にも関わらず、そのゴールはまだ達成されませんでした。オレゴン健康科学大学(Oregon Health & Science Univ.=以後、OHSUと省略)の研究家たちによる研究で、何故猿のAIDSウィルスの少し弱化したバージョンが、完全に猛毒なウィルス株に感染するのを防ぐことができて、しかしながら、人間への使用は危険すぎたのか、そして、何故、極度に機能を劣化させた、または、不活性化されたバージョンのウィルスが全く効果がなかったのかについて、何十年もの間疑問とされて来たこの謎を明らかにする説明がされました。
The research was conducted at OHSU’s Vaccine and Gene Therapy Institute and is published online in the journal Nature Medicine.
その研究はOHSUの「ワクチンと遺伝子セラピー研究所」(Vaccine and Gene Therapy Institute)で実施されました。そして、ネイチャー・メディスン(Nature Medicine)のジャーナル紙にオンラインでその結果が投稿さました。
Traditionally, there have been two methods for creating vaccines to combat infectious disease. The first approach utilizes a live, yet weakened strain of the disease in question. This weakened strain is not strong enough to cause illness yet potent enough to activate the immune system so that it can detect and fight a disease if it enters the body in the future. The second approach makes use of a dead form of the disease. As with the other approach, the introduction of the disease in a safe form educates and prepares the body for a possible future invasion.
In the early 1990s, a slightly weakened version of SIV, the monkey counterpart to HIV, was shown to protect monkeys for infection with the fully virulent version, but this weakened version was still able to cause AIDS in some monkeys and the protection was lost if the vaccine virus was further weakened.
“Efforts to develop a live attenuated virus are analogous to the tale of ‘Goldilocks and the Three Bears,’” explained Louis Picker, associate director of the OHSU Vaccine and Gene Therapy Institute.“The field was looking for a vaccine that was ‘not too hot,’ or ‘not too cold,’ but ‘just right.’ The problem was that it appears that weakening a virus to the level that is ‘just right’ is impossible. However, we thought that understanding the mechanism responsible for the protection afforded by the too-dangerous-for-clinical-use attenuated vaccine would allow us to design a vaccine that would be both effective and safe”.
The research shows that the protection is due to anti-viral T cells maintained in lymphoid tissue by persistent live attenuated virus; weakening the virus prevents this persistence and curtails protection. Thus, unlike most vaccines, an effective HIV vaccine might have to persist in the body to be effective.
Picker’s group has developed another persistent virus named cytomegalovirus (CMV) engineered to express SIV or HIV proteins and serve as the transport system (vector) used to raise protective immune responses against these AIDS-causing viruses. In May 2011, the Picker lab published findings that demonstrated how immune responses elicited by their vaccine candidate were able to completely control SIV in a significant number of exposed animals.
CMV is a persistent virus that most people carry, causes few or no symptoms, and elicits very strong cellular responses that are maintained for life. These immune responses are characterized by a type of T cell called an effector memory T cell that has potent anti-viral function and localizes in the same tissues targeted by the AIDS-causing viruses. Picker and his team hypothesize that CMV vector-generated anti-HIV responses would be constantly on the alert for HIV and would be able to intercept and stop HIV infection immediately after exposure.


( ´ ▽ ` )ノ















『男性同型、超リアル形状』とありますが、いろんな形があると思いますので 、メーカーに問い合わせするほうがいいかも・・・


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