Aids, Eugenics, and the Future

Nobel Laureate Montagnier: AIDS truth exposed: Un-cut exclusive footage from House of Numbers

2012-01-19T20:48:00.000+01:00

The Science of Panic: Living without any medication

2012-01-19T19:44:00.001+01:00

The science of panic (English) from la ciencia del panico on Vimeo.

Source: http://www.hivwave.gr/pages/en/

Some Good News: 96 percent of HIV transmission among Couples can be prevented by antireroviral drugs

2012-01-19T19:33:00.003+01:00

Link: http://medicalxpress.com/news/2011-12-hiv-scientific-breakthrough-year-science.html

HPTN 052 evaluated whether antiretroviral drugs can prevent
sexual transmission of HIV among couples in which one partner has HIV and the other does not. The research found that early treatment with antiretroviral therapy reduced HIV transmission in couples by at least 96 percent.

The study was funded by the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health.

The complete list of top 10 scientific breakthroughs of the year was published online today.

The editors at Science, the flagship publication of the American Academy for the Advancement of Science, said in their announcement that "In combination with other promising clinical trials, the results have galvanized efforts to end the world's AIDS epidemic in a way that would been inconceivable even a year ago.

'The goal of an AIDS-free generation is ambitious, but it is possible,' U.S. Secretary of State Hillary Clinton told scientists last month."

The first case of HIV/AIDS cure and no mention in the media. Why?

2009-11-30T17:29:00.002+01:00

FOLEY, Ala. — A Foley physician said what appears to be the first case of HIV/AIDS cure in the world is getting little mention in the media.

Dr. Awadhesh K. Gupta, medical director at Foley Walk-In Med Care, said he first heard of the medical breakthrough in April when he attended the Annual Conference of the American College of Physicians in Internal Medicine in Philadelphia.

It’s a conference Gupta tries to attend every year.

“This is the most prestigious organization of physicians in Internal Medicine and is responsible for certifying post graduate training in Internal Medicine. It is also one of the oldest,” he said.

According to Gupta, who has been practicing medicine in the South Baldwin area since 1997, the cure was first reported in early 2008 by a group of physicians from Germany at the annual conference on “Retroviruses and Opportunistic Infections” in Boston. The New England Journal of Medicine, one of the most prestigious medical journals in the world, finally published the report in its Feb. 12, 2009, issue, Gupta said.

So why has the news of the first case of HIV/AIDS cure received so little attention where the public is concerned?

“I can’t be sure as to why so little publicity,” Gupta said recently.

“My guess is that most scientific researchers are somewhat stunned that a clinician — not a research scientist — has been able to come up with the cure. Most of the big research money and big name American institutions are somewhat embarrassed to acknowledge that the very first case of HIV cure is not coming from their institutions.”

The cure, instead, is coming from Charity University Hospital in Berlin, Germany, and the doctor is Gero Huetter, who works in the Department of Hematology, Oncology and Transfusion Medicine at the same hospital.

Asked about the reaction of attendees at the medical conference in Philadelphia as regarded the news of an HIV/AIDS cure, Gupta said, “Unfortunately, because of the hectic schedule, I did not try to engage too many physicians. However, the doctor presenting this information seemed extremely excited about it.”

AN AMERICAN

WORKING IN BERLIN

As Gupta explains the case and cure in question, a 40-year-old American working in Berlin had been HIV-positive for 10 years. The patient’s HIV infection had been under control for four years with “conventional HAART treatment regimen” (Highly Active Anti-Retroviral Therapy).

When the patient developed leukemia, however, a bone marrow transplant of stem cells was done using standard protocol, which Gupta said includes radiation therapy and chemotherapy prior to the transplant.

“Remember, once you stop HIV drugs, the HIV viral count rises very rapidly, usually within a few days to a week,” Gupta said.

According to Gupta, Huetter, the German physician treating the American, deliberately chose a stem cell donor who had a gene mutation known as “CCR-5 Delta- 32,” rather than using the best matched donor.

Gupta said Huetter remembered research first observed in 1996 - research Gupta said is well known in the scientific community. That research found that certain gay men in the San Francisco area remained uninfected with HIV in spite of engaging in risky sexual activities. As it was later discovered, those men had the CCR-5 Delta-32 gene mutation.

As it turned out, the patient’s stem cell transplant was a success, Gupta said, even though the patient had to have a second stem cell transplant (from the same donor) when his leukemia relapsed.

“This patient has been off all his HIV drugs for two years now,” Gupta said. “He continues to show no detectable signs of HIV in all the known places HIV is detected — no signs of HIV in his blood, bone marrow, lymph nodes, intestines or brain.” Also, the patient’s T-cell count remains normal.

Thus, according to Gupta, within the limits of scientists’ ability to detect HIV, it appears this patient’s HIV has been “eradicated.”

CCR-5 DELTA-32

The gene mutation CCR-5 Delta-32 is found mostly in white European populations, especially northern Europeans and Scandanavians, according to Gupta, who is on the staff of South Baldwin Regional Medical Center and served as chief of medicine in 2008.

“Those who have this gene mutation from both parents are completely resistant to most common forms of HIV infection. You can get tested for it if you wish,” he said.

“It is believed that this genetic mutation may have happened during long periods of small pox, plague and other pandemics that devastated European populations.”

While the “American living in Berlin” case is in Gupta’s words the “first case of confirmed cure of HIV in the world,” he cites a 1989 case that is similar. Dr. John Rossi, currently at City of Hope Cancer Center in Durate, Calif., had a 41-year-old patient with AIDS and lymphoma. The patient underwent radiation and drug therapy in removing his bone marrow and receiving new cells from a donor.

Whether the donor had the CCR-5 Delta-32 gene mutation or not is not known, Gupta said, but when the patient died of his cancer at age 47 autopsy tests from eight organs and the tumor revealed no HIV.

“I have no doubts that present day high tech stem cell transplantation from CCR-5 Delta-32 donors can cure HIV,” Gupta said, noting, at the same time, that the procedure is expensive at present and has significant risks of complications and a high mortality related to the procedure itself.

Genocide in Progress with new flu virus- CDC is suspect

2009-08-10T19:28:00.001+02:00

Dr. Boyd Ed Graves International AIDS activist dies age 57

2009-08-09T11:03:00.005+02:00

(June 26, 2009; San Diego, CA) – Human Rights activist and HIV/AIDS advocate American lawyer Dr. Boyd Ed Graves died Thursday at the University of California San Diego Medical Center. Dr. Graves was 57.

Dr. Graves' two decades of human rights' work, judicial activism and research on behalf of people living with HIV/AIDS, catapulted him into the world spotlight earning him both international acclaim for his bravery and dedication as well as criticisms for his controversial conclusions about the man-made origins and purpose of the HIV/AIDS virus.

Known by “Ed” to his friends and family, Dr. Graves was a dynamic and patriotic individual who dedicated his professional and personal life to the disabled, disenfranchised and the fair daily existence of men and women worldwide.

Bloggers Comment: Sorry for the delay in posting this. But since no coverage at all on his death was on the media I was unaware.

Glutathione Accelerator - Any Good?

2009-06-09T16:45:00.000+02:00

Dallas: A possible Aids Cure?

2009-01-30T20:14:00.001+01:00

In lies we Trust. The history of American Bioterrorism

2008-08-15T16:31:00.001+02:00

Proof that AIDS was engineered to kill primarily blacks

2008-07-30T17:55:00.003+02:00

A genetic variant peculiar to Africans substantially raises their risk of infection with HIV, according to research that suggests evolved susceptibility may be helping to drive the continent’s Aids epidemic.

The 90 per cent of Africans who carry the DNA variation are 40 per cent more likely to contract HIV than those without it, after similar exposure to the virus, scientists from Britain and America have found.

As the genetic change is common among people of African ancestry but virtually unknown among other ethnic groups, it could explain in part why HIV-Aids is more prevalent in sub-Saharan Africa. The United Nations estimates that 22.5 million people there are HIV-positive, more than two thirds of the global total of approximately 33.2 million.

The variant, known as “Duffy-negative”, is so common in Africa that it could be responsible for about 11 per cent of the continent’s HIV burden, or 2.5 million cases, scientists said.

“It is an Africa-specific variant, which is why it’s so interesting in the context of Aids research,” said Robin Weiss, Professor of Infection and Immunity at University College London, a member of the study team.

“It could certainly be a contributing factor to the scale of the epidemic in sub-Saharan Africa. It’s the first time, so far as we understand, that a genetic factor that increases susceptibility to infection has come into play.”

Sexual behaviour is also involved in the epidemic in Africa, the only part of the world in which it predominantly affects heterosexuals.

The Duffy-negative gene has probably spread so widely through the African population because it provides resistance to a form of malaria called Plasmodium vivax. Professor Weiss believes it may also once have increased resistance against a precursor of the most deadly malaria parasite, Plasmodium falciparum.

These traits would have been highly advantageous in evolutionary Africa. As HIV is a new human pathogen, thought to have jumped from chimpanzees to people between 1910 and 1950, the gene’s effect on the virus would have had no negative consequences until recently. “Something that protected against malaria in the past is now leaving the host more susceptible to HIV,” Professor Weiss said.

Matthew Dolan, of the San Antonio Military Medical Centre in Texas, said: “After thousands of years of adaptation, this Duffy variant rose to high frequency because it helped protect against malaria. Now, with another global pandemic on the scene, this same variant renders people more susceptible to HIV. It shows the complex interplay between historically important diseases and susceptibility in contemporary times.”

For the study, published in the journal Cell Host & Microbe, scientists examined a group of US Air Force personnel, of whom more than 1,200 are HIV-positive, and who have been followed for nearly 22 years. The Duffy-negative genotype was seen almost exclusively in African-Americans.

A continent cursed

— Sub-Saharan Africa is the globe’s most Aids-affected region. In 2005, 24.5 million of its people were living with HIV and of all Aids sufferers, 64 per cent live there

— In 2005, about 2.7 million people became infected with HIV and more than two million died

— More than two million children under 15 are HIV-positive and more than 90 per cent live in Africa

— About 12 million African children under 17 have lost one or both parents to Aids

— About 72 per cent of all people needing anti-retroviral treatment live in Africa, and only one in six receives the necessary medicine

— Swaziland has the highest HIV rate, at 33.4 per cent of population. Botswana has 24.1 per cent and Zimbabwe 20.1 per cent

Source: UNAids

Have your say

Good news in furthering our understanding of this disease hence a possible approach to a cure. The link between sickle cell disease among African-Americans and Afro-Caribbeans is established. Genes suitable for one environment and not so in another and so the consequences. Ignore conspiracy theories

Cheryl , Kingston, Jamaica

What Whites largely do not know is that they all have black blood. We were the first created, and from our "MIX" all the rest were created. Therefore not only Blacks are susceptible to AIDS to that degree. If it targets the Black Gene it will find it in the white man hidden away. Same goes for all .

HELEN K MAYERS, Maxwell, B'dos, W.I.

the saying that a continent that is cursed is in my terms of opinion very absurd to say ,who are you to claim that the continent of africa is cursed,this cursed continent shall one day raise from the ashes and shall claim her place in the world but i ask who you are to call the people of god cursed

source: http://www.timesonline.co.uk/tol/life_and_style/health/article4345263.ece

Ugandians not dying fast enough. International Eugenists (Aids experts) want them to engage in casual sex

2008-07-01T08:24:00.002+02:00

The Rev. Sam L. Ruteikara, co-chair of Uganda’s National AIDS-Prevention Committee, writes in today’s Washington Post:

But will the money allocated for AIDS stop the spread of the virus in sub-Saharan Africa, where 76 percent of the world’s HIV-AIDS deaths occurred last year?

Not if the dark dealings I’ve witnessed in Africa continue unchecked. In the fight against AIDS, profiteering has trumped prevention. AIDS is no longer simply a disease; it has become a multibillion-dollar industry.

In the late 1980s, before international experts arrived to tell us we had it all “wrong,” we in Uganda devised a practical campaign to prevent the spread of HIV. We recognized that population-wide AIDS epidemics in Africa were driven by people having sex with more than one regular partner. Therefore, we urged people to be faithful. Our campaign was called ABC (Abstain, or Be Faithful, or use Condoms), but our main message was: Stick to one partner. We promoted condoms only as a last resort.

Because we knew what to do in our country, we succeeded. The proportion of Ugandans infected with HIV plunged from 21 percent in 1991 to 6 percent in 2002. But international AIDS experts who came to Uganda said we were wrong to try to limit people’s sexual freedom. Worse, they had the financial power to force their casual-sex agendas upon us.

PEPFAR calls for Western experts to work as equal partners with African leaders on AIDS prevention. But as co-chair of Uganda’s National AIDS-Prevention Committee, I have seen this process sabotaged. Repeatedly, our 25-member prevention committee put faithfulness and abstinence into the National Strategic Plan that guides how PEPFAR money for our country will be spent. Repeatedly, foreign advisers erased our recommendations. When the document draft was published, fidelity and abstinence were missing.

He continues:
International suppliers make broad, oversimplified statements such as “You can’t change Africans’ sexual behavior.” While it’s true that you can’t change everybody, you don’t have to. If the share of men having three or more sexual partners in a year drops from 15 percent to 3 percent, as happened in Uganda between 1989 and 1995, HIV infection rates will plunge. It is that simple.

We, the poor of Africa, remain silenced in the global dialogue. Our wisdom about our own culture is ignored.

Telling men and women to keep sex sacred — to save sex for marriage and then remain faithful — is telling them to love one another deeply with their whole hearts. Most HIV infections in Africa are spread by sex outside of marriage: casual sex and infidelity. The solution is faithful love.

So hear my plea, HIV-AIDS profiteers. Let my people go. We understand that casual sex is dear to you, but staying alive is dear to us. Listen to African wisdom, and we will show you how to prevent AIDS.

AIDS HIV BAYER CORPORATION HEMOPHELIA TAINTED BLOOD SUPPLY

2008-03-12T16:26:00.002+01:00

This has been long forgotten and no one is America was prosecuted. Eugenics in action!

Dr. David James preview - conscious media network

2008-02-04T13:51:00.000+01:00

British doctor David James talks about Esmog and the ETAScan. For the full interview go to http://www.consciousmedianetwork.com/

Why we should not trust the health market.

2008-01-22T08:22:00.000+01:00

By Giorgio Vitali, MD, Rome

In order to get an idea of what happens in the “research” it is necessary to briefly describe the organization of one of the crucial aspects of “science”, especially “medicine”: the publication of articles, through which the discoveries and outcomes of experiments are made known. Thanks to qualified magazines such as: The lancet, The British Medical Journal, New England Journal of medicine, JAMA, to quote just a few of the most authoritative, the doctors of the whole world are informed on the most innovative results of medicine and pharmacology.

The publication however has also another vital role for science: “it represents the most critical test for a scientific theory or a datum, which are submitted to the judgement of the final court: the scientific community and public, as explained by prof. P.Duesberg, professor of Molecular Biology at the University of California, AIDS expert of world wide fame.

Who has the task of establishing whether or not a work is worth publishing? The evaluation is made within the so-called "peer-review process". This process provides that the articles submitted to a magazine are examined by some "referees", that is experts of a particular medical division, to whom the magazine director asks to evaluate the quality, scientifical accuracy and originality of the works. Basically they give their technical opinion based on which the director decides to publish the article or not.

In order to ensure transparency and objectivity of the judgements, the authors of the articles should not know the names of the referees and viceversa. This is how it should be. As a matter of fact, says DUESBERG, the peer-review is a form of CENSORSHIP with some ambiguous aspects. Positive, when scientists who do not have a conflict of interests (very few, admittedly) may eliminate publications based on non scientific evidences or suppositions already refuted. Negative because the scientific ideology uses the peer-review mainly to eliminate those innovations which threaten the orthodoxy’s suppositions and investments.

Duesberg speaks from experience: considered a luminary in point of AIDS and Cancer, having isolated the first gene considered responsible for inducing cancers and having mapped the retroviruses’ genetic structure, (which brought him in 1986 to be elected in the most important American scientific association, the National Academy of Science) Duesberg has jeopardized a very promising profession by opposing what he calls the " Hiv dogma", that is the most credited theory on the causes of AIDS, according to which it is the Hiv retrovirus that induces immunodeficiency.

According to Duesberg there is no scientifically ascertained link between the virus and the desease and anti-retrovirus drugs not only are useless, but in some cases they accelerate the DEATH of patients, as it is the case of AZT by GLAXO.

And this is not everything. Writes Flavia Bruno, from “Centro Studi comunicazione sul farmaco, Facoltà di farmacia, Università di Milano, " In a society living out of deep complexities such as ours, the lack of scientific knowledge leads (or should lead) to a principle of caution, based on which one should not delay effective measures to prevent serious damages and the possible consequences on collective health”. But this is an illusion. Not only the falsity of almost all scientific publications has been proven, but if this is valid for the habitual readers of scientific magazines, what should we say of the large majority of the Italians graduated in medicine who DO NOT READ ANYTHING AT ALL?

To what, to whom do they believe? The answer is obvious: to the shabbiest publications provided by the Industry. And it is absolutely useless to talk about the PRINCIPLE OF CAUTION formulated by the European Community two years ago, since in Italy, not only it is unkown, but it is not applicable either, inasmuch our country has not yet acknowledged the relevant Directive in question. And in case it was acknowledged, it would be a huge worry to succeed in obliging the relevant public entities to apply it within the medical context.

Source: http://www.curenaturalicancro.com/why-not-trust-health-market.html

The Merchants of aids

2008-01-19T08:38:00.000+01:00

Read the entire article: http://aidseugenics.blogspot.com/2008/01/merchants-of-aids-full-article.html

July 27, 1990: Aids is man-made - By William Cooper [Killed by Law enforcement in 2001]

2008-01-18T13:20:00.000+01:00

Did irrational fear cause a bunch of powerful politicians to order the creation of the HIV virus and consequently the deaths of millions of people? The year 2000 has passed and civilization did not collapse, so how about releasing the cure now and paying damages to the families of the millions of people that died with your virus. And why aren't we arresting those people listed below in this article and charging them with genocide.

Bill cooper:

During my talks in Las Vegas last weekend I revealed a few things about aids that I have been keeping close to my chest. I have already revealed that I saw that AIDS was man made to eliminate the undesirable elements of society while I was attached to Naval Security and Intelligence. I stated this fact in my paper "The Secret Government." Now for the rest of the story.

The first study was made in 1957 by scientists meeting in Huntsville Alabama. That study resulted in "Alternative 3." Another study was made by the Club of Rome in 1968 to determine the limits to growth. The result of the study was that civilization as we know it would collapse shortly after the year 2000 unless the population was seriously curtailed. Several Top Secret recommendations were made to the ruling elite by Dr. Aurelio Peccei of the Club of Rome. The chief recommendation was to develop a microbe which would attack the auto immune system and thus render the development of a vaccine impossible.

-
The orders were given to develop the microbe and to also develop a cure and a prophylactic. The microbe would be used against the general population and would be introduced by vaccine administered by the World Health Organization. The prophylactic was to be used by the ruling elite.

The cure will be administered to the survivors when they decide that enough people have died. It will be announced as newly developed. This plan was called Global 2000. The cure and the prophylactic are suppressed. Funding was obtained from the U.S. Congress under H.B. 15090 where $10 million was given to the Department of Defense to produce "a synthetic biological agent, an agent that does not naturally exist and for which no natural immunity could have been acquired." "Within the next 5 to 10 years it would probably be possible to make a new infective microorganism which could differ in certain important aspects 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 project was carried out at Fort Detrick Maryland. Since large populations were to be decimated the ruling elite decided to target the "undesirable elements of society" for extermination. Specifically targeted were the black, hispanic, and homosexual populations.

The name of the project that developed AIDS is MKNAOMI. The African continent was infected via smallpox vaccine in 1977. The U.S. population was infected in 1978 with he hepatitis B vaccine through the Centers for Disease Control and the New York Blood Center. You now have the entire story. The order was given by the POLICY COMMITTEE of THE BILDERBERG GROUP based in Switzerland. Other measures were also ordered. The one you will be able to check the easiest is the Haig - Kissinger Depopulation Policy which is administered by the State Department.

When you put this information out do not edit it and please give me and this board full credit as the source of the information. Please post the board phone number with this file. That is how I stay alive. This board is THE CITIZENS AGENCY FOR JOINT INTELLIGENCE, SYSOP - WILLIAM COOPER, (602) 567-6725

To aid you in your research of this CRIME the name of the report was "THE LIMITS TO GROWTH" A REPORT FOR THE CLUB OF ROME'S PROJECT ON THE PREDICAMENT OF MANKIND. In April 1968 the study began in the Accademia dei Lincei in Rome Italy. They met at the instigation of Dr. Aurelio Peccei.

The Top Secret recommendations of the results of the study were made by Dr. Aurelio Peccei who pledged not to use the prophylactic and not to take the cure should the microbe be developed and should he contract the disease. Dr. Peccei was hailed as a great hero for deciding to take the same risk as the general population. The public results of the study were published in 1972. The MIT project team that participated in the study are listed below:

Dr. Dennis L. Meadows, director, United States

Dr. Alison A. Anderson, United States (pollution)

Dr. Jay M. Anderson, United States (pollution)

Ilyas Bayar, Turkey (agriculture)

William W. Behrens III, United States (resources)

Farhad Hakimzadeh, Iran (population)

Dr. Steffen Harbordt, Germany (socio-political trends)

Judith A Machen, United States (administration)

Dr. Donella H. Meadows, United States (population)

Peter Milling, Germany (capital)

Nirmala S. Murthy, India (population)

Roger F. Naill, United States (resources)

Jorgen Randers, Norway (population)

Stephen Shantzis, United States (agriculture)

John A. Seeger, United States (administration)

Marilyn Williams, United States (documentation)

Dr. Erich K. O. Zahn, Germany (agriculture)

When the study was completed in 1969 U.N. Secretary General U Thant
made this statement:

"I do not wish to seem overdramatic, but I can only conclude from the information that is available to me as Secretary-General, that the Members of the United Nations have perhaps ten years left in which to subordinate their ancient quarrels and launch a global partnership to curb the arms race, to defuse the population explosion, and to supply the required momentum to development efforts. If such a global partnership is not forged within the next decade, then I very much fear hat the problems I have mentioned will have reached such staggering proportions that they will be beyond our capacity to control." U Thant, 1969

MKNAOMI was developed by the Special Operations Division (SOD) scientists at Ft. Detrick, Maryland under the supervision of the CIA and for the CIA. A reference to the project MKNAOMI can be found in "The Intelligence Community" By Fain et al, Bowker, 1977.

I swear that all of the above information is true and correct to the best of my memory and knowledge. I give this information to the people of the world in hopes that someone will have the courage and resources to help me end this madness. The illuminati (the order) are in complete control of most of the world and they have declared war against the general populations of all nations. We must stop them at all costs. Please help me for I cannot do it alone. Please send this file without editing to everyone that you know and ask them to do the same. God bless you all.
-

Bill was killed by the Apache County Sherrifs Department during a raid on his home in November of 2001. He is now buried on a hill in Eagar, Arizona. Perhaps he knew too much.

William Cooper

All information and opinions contained in this article are those of the author and not necessarily those of the owner of this blog. I encourage everyone to do their own research and make their own decisions as to its validity

Kissinger, Eugenics and Nazis

2008-01-15T13:54:00.000+01:00

Excerpts from Article SUPERVIRUSES, CONTAMINATED VACCINES AND THE CURRENT AND COMING PLAGUES by Leonard Horowitz, DMD, MPH, Ph.D.
http://www.consumerhealth.org/articles/display.cfm?ID=19990303202939

HENRY KISSINGER

No epidemic in earth's history has ever evolved without major social and political upheaval, so you have to examine the decade prior to 1978 when the first AIDS cases emerged. Going back to 1968, Henry Kissinger was appointed National Security Advisor, which made him the most powerful man in American intelligence, overseeing the FBI, CIA and foreign policy.

Almost immediately, Kissinger selected the option to develop immune system ravaging microorganisms for germ warfare as an alternative to nuclear weapons. You must create the organisms, and then test them where the hand of America will not show. Where is that? Central Africa, Zaire and Angola, the heart of the African AIDS belt and close to ground zero for the first Ebola virus outbreak.

"AIDS is a lousy biological weapon, but it is a fabulous population reducing agent. "

"Ebola is an ideal weapon. It kills nine out of ten people within three weeks. It has proteolytic enzymes that turn your internal organs and blood vessels to mush. That is why it is far better than nuclear weapons. You still have all the infrastructure. "

Why destroy the property when you can own it? What is Kissinger's relationship to all this?

You have to go back to 1955.

THE INTERNATIONAL BANKSTERS WHO RUN THE WORLD

In 1955 Kissinger was made the nuclear weapons study group director for the Council of Foreign Relations by Nelson Rockefeller. This is not a government agency.

It is approximately 3,000 of the wealthiest most powerful military medical industrialists who dictate policy for all of the heads of state who are all puppets. The international banksters run the world.

They are the international bankers, international industrialists, and medical and military industrialists.

THE NEW WORLD ORDER

That same year (1955), Kissinger finished his Ph.D. thesis at Harvard entitled The Meaning of History in which he describes the contemporary evolution of the New World Order. You can pull his thesis off the shelf in the stacks in the library at Harvard. The phrase, New World Order, was made famous by George Bush who frequently talked about it. You have to be blind if you don't see that this one world government agenda is rapidly unfolding.

Also in 1955, Bertrand Russell, who is from an aristocratic English family with ties to high level British intelligence and the shadow governors (banksters), wrote in his book The Impact of Science on Society:

"I do not pretend that birth control is the only way in which population can be kept from increasing. War has hitherto been disappointing in this respect, but perhaps bacteriological war may prove more effective. There are three ways of securing a society whose population is stable: birth control, infanticide or really destructive wars which creates general misery except for the powerful minority. These considerations prove that a scientific world society cannot be stable unless there is a world government with a monopoly of armed force."

NAZI MASS DEPARTURE FROM GERMANY

Just before the end of WWII, Kissinger was godfather to Project Paperclip which was the exfiltration of approximately 2,000 Nazis out of Germany before the war's end, along with all the vast fortunes. Most people think all the Nazis went to the Nuremburg trials. Not true. Most were fined about $5,000 and jailed for a few years, then released to join their colleagues in America working for the CIA and intelligence for American industry. We have declassified documents to prove that 2000 came to the U.S. and 11,000 went to France. Seven books have already been written about it.

Among the Nazis who got out were some of the most hideous names in contemporary history. In 1938, the Dulles brothers, the law firm which represented John D. Rockefeller's Standard Oil, engineered the partnership between John D. Rockefeller's Standard Oil and I.G. Farben, Germany's leading industrial organization which held the patent on the gas that killed millions of people. I.G. Farben and the Third Reich were inseparable partners, and the Rockefellers were partners with I.G. Farben.

The American Red Cross, largely controlled by Rockefeller, supplied the Nazis with false identification. Laurance Rockefeller created the New York City Blood Council which became the international "blood banksters". These are the people who allowed countless people around the world to get HIV contaminated blood.

They knew for years it was contaminated with HIV but they let it be used anyway.

THE CANCER INDUSTRY AND THE SUPPRESSION OF ALTERNATIVE MEDICINE

In the 1920's Rockefeller and Sloan created the cancer industry.

Also in the 20's, they had another agenda, the monopolization of American medicine, and it was determined that holistic therapies and alternative medicine were quackery and fraud.

EUGENICS

In the same decade, an interesting union was forming between the Rockefeller family, Prescott Bush (George Bush's father), William Draper III, the Royal family in England, and a few other financiers who inspired the eugenics agenda. Eugenics simply means the study of the genetic differences between the races.

It led to the racial hygiene laws, and the study of the genetic predisposition for diseases among the races.

The racial hygiene laws that you think Hitler came up with were in fact originated in 1928 by the Rockefellers, Prescott Bush and the Royal family and others, aiming for population reduction and supremacy of the master race.

NAZI MONEY BURIED IN NEW CORPORATIONS

At the end of the war Hitler ordered Martin Bormann, financial director of the Third Reich, to bury the treasure not only for Germany's economic recovery, but for the rise of the Fourth Reich.

So Bormann buried it into 750 corporations as determined by their partners I.G. Farben and the Rockefellers, to establish a monopoly over the world's pharmaceutical and chemical industries because this would be essential for the "New Ordnung" or "New Order".

Among the 750 corporations that received the money, one of the principle recipients was Merck and Co., the people who produced along with Dr. Hilleman the vaccine that plausibly delivered AIDS to the world.

Merck has remained a major biological weapons contractor for CIA's top secret project NKNaomi, and Kissinger has remained all these years a major consultant to Merck.

2002: Eleven microbiologists mysteriously dead over the span of just five months

2008-01-15T10:58:00.000+01:00

Scientists' deaths are under the microscope
By ALANNA MITCHELL, SIMON COOPER AND CAROLYN ABRAHAM
COMPILED BY ALANNA MITCHELL

Saturday, May 4, 2002 – Print Edition, Page A1

Eleven microbiologists mysteriously dead over the span of just five months. Some of them world leaders in developing weapons-grade biological plagues. Others the best in figuring out how to stop millions from dying because of biological weapons.

Suspicious deaths
The sudden and suspicious deaths of 11 of the world's leading microbiologists.
Who they were:

1. Nov. 12, 2001-Benito Que was said to have been beaten in a Miami parking lot and died later.

2. Nov. 16, 2001-Don C. Wiley went missing. Was found Dec. 20. Investigators said he got dizzy on a Memphis bridge and fell to his death in a river.

3. Nov. 21, 2001-Vladimir Pasechnik, former high-level Russian microbiologist who defected in 1989 to the U.K. apparently died from a stroke.

4. Dec. 10, 2001-Robert M. Schwartz was stabbed to death in Leesberg, Va. Three Satanists have been arrested.

5. Dec. 14, 2001-Nguyen Van Set died in an airlock filled with nitrogen in his lab in Geelong, Australia.

6. Feb. 9, 2002-Victor Korshunov had his head bashed in near his home in Moscow.

7. Feb. 14, 2002-Ian Langford was found partially naked and wedged under a chair in Norwich, England.

8. 9. Feb. 28, 2002-San Francisco resident Tanya Holzmayer was killed by a microbiologist colleague, Guyang Huang, who shot her as she took delivery of a pizza and then apparently shot himself.

10. March 24, 2002-David Wynn-Williams died in a road accident near his home in Cambridge, England.

11. March 25, 2002-Steven Mostow of the Colorado Health Sciences Centre, killed in a plane he was flying near Denver

The first three died in the space of just over a week in November. Benito Que, 52, was an expert in infectious diseases and cellular biology at the Miami Medical School. Police originally suspected that he had been beaten on Nov. 12 in a carjacking in the medical school's parking lot. Strangely enough, though, his body showed no signs of a beating. Doctors then began to suspect a stroke.

Just four days after Dr. Que fell unconscious came the mysterious disappearance of Don Wiley, 57, one of the foremost microbiologists in the United States. Dr. Wiley, of the Howard Hughes Medical Institute at Harvard University, was an expert on how the immune system responds to viral attacks such as the classic doomsday plagues of HIV, ebola and influenza. He had just bought tickets to take his son to Graceland the following day. Police found his rental car on a bridge outside Memphis, Tenn. His body was later found in the Mississippi River. Forensic experts said he may have had a dizzy spell and have fallen off the bridge.

Just five days after that, the world-class microbiologist and high-profile Russian defector Valdimir Pasechnik, 64, fell dead. The pathologist who did the autopsy, and who also happened to be associated with Britain's spy agency, concluded he died of a stroke.Dr. Pasechnik, who defected to the United Kingdom in 1989, played a huge role in Russian biowarfare and helped to figure out how to modify cruise missiles to deliver the agents of mass biological destruction.

The next two deaths came four days apart in December. Robert Schwartz, 57, was stabbed and slashed with what police believe was a sword in his farmhouse in Leesberg, Va. His daughter, who identifies herself as a pagan high priestess, and several of her fellow pagans have been charged. Dr. Schwartz was an expert in DNA sequencing and pathogenic micro-organisms, who worked at the Center for Innovative Technology in Herndon, Va. Four days later, Nguyen Van Set, 44, died at work in Geelong, Australia, in a laboratory accident. He entered an airlocked storage lab and died from exposure to nitrogen.

Other scientists at the animal diseases facility of the Commonwealth Scientific and Industrial Research Organization had just come to fame for discovering a virulent strain of mousepox, which could be modified to affect smallpox. Then in February, the Russian microbiologist Victor Korshunov, 56, an expert in intestinal bacteria of children around the world, was bashed over the head near his home in Moscow.

Five days later the British microbiologist Ian Langford, 40, was found dead in his home near Norwich, England, naked from the waist down and wedged under a chair. He was an expert in environmental risks and disease. Two weeks later, two prominent microbiologists died in San Francisco. Tanya Holzmayer, 46, a Russian who moved to the U.S. in 1989, focused on the part of the human molecular structure that could be affected best by medicine. She was killed by fellow microbiologist Guyang (Matthew) Huang, 38, who shot her seven times when she opened the door to a pizza delivery. Then he shot himself.

The final two deaths came one day after the other in March. David Wynn-Williams, 55, a respected astrobiologist with the British Antarctic Survey, who studied the habits of microbes that might survive in outer space, died in a freak road accident near his home in Cambridge, England. He was hit by a car while he was jogging.The following day, Steven Mostow, 63, known as Dr. Flu for his expertise in treating influenza, and a noted expert in bioterrorism, died when the airplane he was piloting crashed near Denver.

So what does any of it mean?" Statistically, what are the chances?" wondered a prominent North American microbiologist reached last night at an international meeting of infectious-disease specialists in Chicago. Janet Shoemaker, director of public and scientific affairs of the American Society for Microbiology in Washington, D.C., pointed out yesterday that there are about 20,000 academic researchers in microbiology in the U.S.

Still, not all of these are of the elevated calibre of those recently deceased. She had a chilling, final thought. When microbiologists die in a lab, there's a way of taking note of the deaths and adding them up. When they die in freakish accidents outside the lab, nobody keeps track.

This site is being developed

2008-01-12T18:09:00.000+01:00

Please bare with us while we are developing this site. It is not complete at the moment.

We will be posting our information during January.

Any comments are welcome.

Thank You

Gallo and Litton Bionetics: Creators of Aids

2008-01-12T17:57:00.000+01:00

Where did AIDS come from? Some say it doesn't matter, as long as we find a cure. But what if the man and money that created it, are still spreading it along with lies and half-truths? Watch this clip from In Lies We Trust: The CIA, Hollywood & Bio terrorism, to learn where AIDS really originated. A video from Dr. Leonard Horowitz.

Note: Dr. Jonathan Mann, UN aids czar was killed in a plane crash in 1988. Coincidence or murder?

Boyd Graves: Letter to Ninth Circuit Court

2008-01-12T17:39:00.001+01:00

January 9, 2008

Cathy Catterson, Clerk of the Court
United States Court of Appeals
for the Ninth Circuit
P.O. Box 193939
San Francisco, Ca 94119-3939

Re: The U.S. Attorney letter of January 7, 2008;
Case No. 07-056782 (Graves v. U.S.A.)

Dear Ms. Catterson:

I write in response to the U.S. Attorney’s letter of January 7, 2008, to you regarding the government’s desire to not adhere to the Briefing Schedule issued by the Court on December 14, 2007.

We find it strange the U.S. Attorney is now seeking to say the government had no prior knowledge of the federal litigation that has been persisting in the U.S. courts since September 1998. The origin of HIV/AIDS is not a “frivolous” issue as the Courts have held. There is a significant evidence base in U.S. law and fact for the allegation and the conclusion our government made AIDS.

Here, reading the 1/7/8 letter form the U.S. Attorney, one would be led to believe the U.S. Attorney has been left out of the picture by design or accident. This is simply untrue. The U.S. Attorney has been sent each and every court document that has been filed.

A review of the U.S. Attorney’s email will also show notification to the U.S. Attorney from the lower court as well.

A review of the docket reveals the U.S. Attorney was listed and served in this case in March 2007. The record clearly shows the U.S. Attorney General was served via certified mail return receipt requested on May 17, 2007.

The U.S. Attorney should be further compelled to respond to this individual lawsuit and the more important Constitutional questions of ‘state liability’ for the breach of the basic right to life. We find it peculiar the U.S. Attorney has not begun an inquiry of its own in support of my “right to life”.

The U.S. Attorney simply tried to ride the wave of the errant dismissal and is now crying foul on appeal. In any event, the U.S. Attorney owes a responsibility and duty to the American people to begin the review and investigation of the U.S. Special Virus (Cancer) Program (1962 – 1978). The American people and the people of the world are entitled to know the truth about the synthetic origin of HIV/AIDS and its ten year old CURE, U.S. patent#5676977. See, www.uspto.gov.

The U.S. Attorney should be working for the American people, not trying to slither away from the greatest human holocaust in the history of the world with silence and denial.

Please alert me if I need to file a formal motion to enjoin the U.S. Attorney to this so necessary appeal.

Sincerely,

Boyd Ed Graves, J.D.

Boyd Graves: Interview with Alex Jones

2008-01-12T17:36:00.001+01:00

Dr. Boyd Graves discusses how HIV was made by the United States Government

1988: Dr. Jonathan Mann : Killed in Plane Crash

2008-01-12T17:33:00.000+01:00

World leader in AIDS fight dies in Swissair crash

Dr. Mann
September 3, 1998
Web posted at: 3:12 p.m. EDT (1512 GMT)
In this story:

Warned world about spread of AIDS
Urged testing of AIDS vaccine
Wife contributed to development of vaccines

From CNN Medical Correspondent Dan Rutz

(CNN) -- World leaders in the war against AIDS are in shock over the loss of two of their most trusted and admired colleagues. Dr. Jonathan Mann and his wife, Dr. Mary Lou Clements-Mann, were aboard the Swissair jetliner that crashed off the coast of Canada on Wednesday night.

In the 1980s, Mann launched the Joint United Nations Program on HIV/AIDS, becoming one of the first to recognize the global threat. He was head of the program from 1986 to 1990.

"In the '80s, he was truly a visionary at a time when it was absolutely not clear how devastating and epidemic AIDS would become," said Peter Piot, executive director of UNAIDS. "He pulled off what he called a global response both in developing and developed countries."

Warned world about spread of AIDS
As director of the International AIDS Conference six years ago in Amsterdam, Mann warned of a complacency among world leaders in the fight against AIDS.

"The gap between the intensifying pace of the pandemic and the lagging national and global response is widening rapidly and dangerously, and global vulnerability to AIDS is increasing," he said.

Mann started his career at the Centers for Disease Control and Prevention after graduation. He resigned from the Harvard School of Public Health in December to be dean of Allegheny University of the Health Sciences' School of Public Health in Philadelphia.

Urged testing of AIDS vaccine
Two months ago, Mann voiced impatience over what he considered unconscionable delays in widespread testing of a vaccine to prevent AIDS -- what many in public health consider the only way to control the worldwide explosion of new cases.

"We must now work to develop the vaccine that will prevent disease and we must do this in a way that respects the urgency of the problem," he said.

To some, he became the conscience for the AIDS research effort, with his eloquent defense of those most vulnerable to the disease. AIDS, he noted, disproportionately affected the poor or disenfranchised members of society including gay men and minorities, who were often stigmatized or discriminated against.

He was patient with AIDS activists, and worked to convince others that the fields of public health and human rights were inseparable.

"It is a fundamental public health strategy, in general, to try to bring them in," he said in 1992. "Convince them, bring them in -- don't push them out, exclude them, discriminate against them, fight them."

Wife contributed to development of vaccines

Dr. Clements-Mann

Mary Lou Clements-Mann made her mark in vaccine development for diseases including AIDS, influenza and hepatitis B.

"If a vaccine will prevent AIDS by reducing the amount of virus in an infected person and controlling that infection, it may also have the public benefit of reducing the transmission to others."

She met Mann while working on her AIDS vaccine projects. They married a year and a half ago.

The couple was flying Wednesday to a U.N. AIDS vaccine conference in Geneva. Friends and colleagues gathered there Thursday for a memorial service.

Another Tool of Eugenics: Fluoride

2008-01-11T21:33:00.000+01:00

"any person who drinks artificially fluoridated water for a period of one year or more will never again be the same person mentally or physically."
-Charles E. Perkins, Chemist.

Water Fluoridation has hit the main stream media after decades being brushed aside. Scientific American had an article about the dangers of fluoride if its overused, revealing that its almost impossible not to overuse it. Many people don't think twice about the toxic waste that we are drowning in. Fluoride is not what you think, and the deceit is painfully obvious, you just have to look.

Calcium Fluoride is what is usually found naturally in water but the cheaper, Hexafluorosilicic Acid, is dumped in our drinking water and its not even similar to "calcium fluoride". Hexafluorosilicic Acid is a highly toxic chemical, that has a laundry list of ailments and diseases to go along with it. According to DR. Hardy Limeback's research, most American cities are purchasing an industrial grade source of fluoride to fluoridate drinking water. It comes from smokestack scrubbers that produce phosphate fertilizer, its cheaper than the pharmaceutical grade. He explains, "Tragically,that means we're not just dumping toxic fluoride into our drinking water. We're also exposing innocent, unsuspecting people to deadly elements of lead, arsenic and radium, all of them carcinogenic. Because of the cumulative properties of toxins, the detrimental effects on human health are catastrophic." But we drink it, bathe in it, wash our clothes and dishes in it without hesitation. Artificially fluoridated water is not beneficial to our health and naturally occurring fluoride is not essential for ANY living thing, and that should be common knowledge.

Acceptable amounts of fluoride to ingest is 1 part per million of water. More than 2 PPM has been ruled toxic. Acceptable levels allowed in our tap water have been rising, and more than 90 percent of our public water is fluoridated, so our food is grown with it, soda, soup, all canned with it, we are being bombarded with fluoride. Unfortunately, we have no way of knowing how much of the toxic fluoride we have stored in our bodies, it stays in your body, for unknown period's of time. "Half of all ingested fluoride remains in the skeletal system and accumulates with age" Dr. Hardy Limeback

Last year the National Research Council released the report: "Fluoride in Drinking Water: A Scientific Review of EPA's Standards." The report said too much fluoride for babies is toxic. It advised parents feeding babies powdered formula to prepare it with un-fluoridated bottled water. Yet on our grocery store shelves we have "nursery water" a brand aimed at formula fed babies, loaded with fluoride. The report was released, with little or no mention. This is INCREDIBLY dangerous, yet, the public draws a blank. Its no surprise we are being misled, the whole operation is confusing. Seven months after that report the FDA gave manufacturers of bottled water permission to print claims on their labels that drinking fluoridated water may reduce the risk of dental caries or tooth decay. Instead of the DANGER warning fluoridated water should have gotten, artificial water fluoridation gets the FDA golden seal of greatness. Currently bottled water remains virtually unregulated. "43 of 50 states have the equivalent of fewer than a single staff person dedicated to regulating bottled water."

The lawmakers are not looking to protect, but to harm, and they are preying on your inability to stay informed, drowning out the necessary information we need to make decisions. We just file in as complacent as the fluoride will get us, believing that no one would ever harm us...the government would never allow it. Do the research, WE are allowing it. In 1992, three counties of New Jersey had almost seven times the osteosarcoma (bone cancer) rate in males in the fluoridated communities compared to the non-fluoridated communities. It's a proven carcinogen...still they fluoridate.

In 1931 ALCOA, the worlds largest aluminum producer, was polluting the water with sodium fuoride, children's teeth were turning yellow, because of the high levels found in the water supply. Sodium fluoride is a toxic pollutant, an aluminum by product, the same type of fluoride that is found in toothpaste. Look a little closer at the tube of toothpaste, you will find the phone number for poison control, "toothpaste overdose" can cause convulsions, and a break down of your nervous and digestive systems, along with difficulty breathing. The amounts we pollute our bodies with everyday are harmful, and we feel the effects of the poison, without recognition, fluoride lowers your IQ and it is a main component of anti-psychotic drugs, extremely dangerous for our children. We are drugged, like patients in a sanatorium, with little resistance.

Fluoridated water is a tool of control, the benefits to the the masses are non existent, the benefits to a government trying to CONTROL the masses are endless. In the 1930's Hitler created his plan of control, and force alone was not going to be enough. The plan involved what they called "water medication" (we call it "water fluoridation"). The Nazi's would contaminate the water supply to make the people docile (and sterilize them as well).

Most of Europe does not (openly) fluoridate their water. The UK, however has unknown amounts of Prozac in their water, and its basic ingredient is fluoride, so basically they are being medicated by the government as well. We have been conned. Water Fluoridation is destroying the will of the people. It is just one of the tools that is being used against the population, it's slowing us down. In order to Fight the tyranny, first we must remove the fluoride, how can you willing ingest something that will make you less smart? You can't, its suicide. Filter your water. Don't go willingly.

http://noonehastodie.blogspot.com/2008/01/tools-of-eugenics-fluoride.html

The Merchants of AIDS - full article

2008-01-10T17:41:00.000+01:00

by Clark Henderson

The entry into the age of aids was quiet. Perhaps in 1976 the virus, carried by some foreigner, arrived in America. It is not my purpose to discuss the spread of the AIDS epidemic; that has already been done in books like And the Band Played On by Randy Shilts and History of AIDS by Mirko Grmek. My focus is the hidden side of AIDS, which has not been exposed in any book to my knowledge.

PREPARING FOR AN EPIDEMIC

There is documented evidence that a disease which could be recognized as AIDS has been worked on for years. Testimony before a sub-committee of the House Appropriations Committee, in Washington, D.C., in 1969, for Department of Defense appropriations for 1970, stated:

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. (R. Harris and J. Paxman, A Higher Form of Killing, 1982, p. 241)

The money was approved! By 1972, this potential new micro-organism was described so clearly that there is little doubt that it is AIDS:

An attempt should be made to ascertain whether viruses can in fact exert selective effects on immune function, e.g., by . . . affecting T cell function as opposed to B cell function. The possibility should also be looked into that the immune response to the virus itself may also be impaired if the infecting virus damages more or less selectively the cells responding to the viral antigens.

This is beyond question a clinical description of the function of the AIDS virus! But it appeared, of all places, in the Bulletin of the World Health Organization, Vol. 47, pp. 257-74, in 1972.

DELIBERATE MISINFORMATION

The ground was carefully prepared beforehand. Sexual promiscuity was encouraged by slogans, such as "There is nothing to be afraid of; there never was," meaning that all sexually transmitted diseases (STDs) could now be cured. The effectiveness of this propaganda can be judged by Michael Callen's remark in Surviving AIDS: ". . . Gee! Every time I get the clap [gonorrhea] I'm striking a blow for the sexual revolution!"

WITHHOLDING INFORMATION ON THE NEW DISEASE

This policy would prove the most effective of all in facilitating the spread of AIDS. Even when people began to come down with AIDS, nothing was done! The Center for Disease Control (CDC) alone reacted, but was hampered in its efforts to realize that an entirely new disease had appeared on the scene.

This should be contrasted with the reaction to another disease which occurred in the same time frame: Legionaire's Disease. When the first outbreak of this happened in a Philadelphia hotel, nobody had the faintest idea what it was. There were even speculations that it was caused by a poisonous gas. But in six months, the disease was found to be caused by a bacterium.

Does anyone suppose that AIDS could not have been determined earlier? Granted, it is far more difficult to identify a virus, but there have been several outbreaks of tropical hemorrhagic fevers in this country which were isolated and identified quickly.

THE PROPAGANDA OF HOPELESSNESS

This has been well described by Michael Callen in Surviving AIDS. All this propaganda is based on the claim that AIDS has a 100% mortality rate. Granted, it has a high mortality rate, about 85-90%. But a "Guaranteed-to-Die-or-Your-Money-Back" policy was pursued. A formula, AIDS = Death, was used, and the media used it to spread the gloom and doom scenario. Also, one might speculate on the connection of the immune system and the mental state; those who are convinced they are going to die may well die more easily.

LIES AND RIDICULE OF THOSE AFFLICTED

Again, this is well covered by Michael Callen. People who developed symptoms of AIDS were subjected to endless distortion in the press. One headline about a female doctor who had AIDS was: "Dying AIDS Doc's Agony," although the woman concerned, a Dr. Veronica Prego, seemed quite healthy.

According to Callen, the words "dying," and "deadly" appeared five times in the brief article! Why the overkill? Why is it so important that people with AIDS must be depicted as being in agony when they are not? Can one imagine a cancer patient being treated in this manner? Those taking photographs of people with AIDS would refuse to take them if the person did not have the lesions of Kaposi's sarcoma visible enough, or if the person was not considered wasted away enough! Does not this suggest a covert propaganda campaign that AIDS = Death?

DELIBERATE REFUSAL OF DRUGS IN GOVERNMENT AIDS STUDIES

The best example of this is the refusal to provide prophylaxis against pneumocystis carinii pneumonia (PCP) of people who had AIDS. The drug sulfamethoxazole (Bactrim) can prevent PCP appearing in immunocompromised individuals, but as of early 1989, more than 30,000 Americans died of AIDS-associated PCP. More importantly, in May 1987, when AIDS activists met with Dr. Anthony Fauci to beg him to issue interim guidelines to physicians for patients at high risk for PCP, he refused. Why? His reason-no data. At that time some 13,600 people had died of PCP; subsequently, another 17,000 died by February 1989. And no doubt many more have died since.

I do not have to look too hard to see the signs of a deliberate extermination policy.

CHARACTER ASSASSINATION OF PEOPLE WITH AIDS

This was done partly by ignoring such people, so that they could not be heard by the public, and partly by ridiculing them. Michael Callen relates the tale of what happened when People With AIDS (PWA) tried to set up an organization apart from the Gay Men's Health Crisis (GMHC): "Ultimately, GMHC succeeded in destroying the first organized incarnation of PWA self-empowerment in New York through a two-pronged strategy of alternately ignoring us and ridiculing us." He observes that GMHC failed to put a person with AIDS on its board of directors until 1987, until the disease was really widespread. Why?

COPING UP DR. KOOP

In the United States of America, there is one man designated to inform the public of the presence of infectious diseases: the Surgeon General. Working under the Secretary of Health, his job is to issue reports on epidemics, particularly new epidemics that affect the public health. In this way, no new disease can arise in the United States without the Surgeon General being aware of it and alerting the public in news conferences.

Thus the public should have been informed about AIDS in 1981 by Surgeon General C. Everett Koop, M.D., who was fearless, outspoken, and honest. Koop was originally chosen by the Reagan administration because he was opposed to abortion; much too late that administration realized that he was an honest man who would not fail to speak out on AIDS just because it was then regarded as a "gay disease."

What they did to prevent him speaking out is best told in Koop's own words:

By August 1981, I and others who were paying attention to the unusual news from the CDC (Center for Disease Control) learned that there were 108 cases of AIDS reported with 43 dead. I knew we were in big trouble. And there was nothing I could do about it. I was not yet the Surgeon General, and all through the summer and autumn of 1981 I was preoccupied by my long struggle to win confirmation. But I realized that if ever there was a disease made for a Surgeon General, it was AIDS. The Surgeon General is mandated by Congress to inform the American people about the prevention of disease and the promotion of health. If ever there was a public in need of education and straight talk about AIDS, it was the American people.

But for an astonishing five and a half years I was completely cut off from AIDS. I was told by the Assistant Secretary for Health, my immediate boss, that I would not be assigned to cover AIDS. The department took its cue from him. Even though the Centers for Disease Control commissioned the first AIDS task force as early as June 1981, I, as Surgeon General, was not allowed to speak about AIDS publicly until the second Reagan term. Whenever I spoke on a health issue at a press conference or on a network morning TV show, the government public affairs people told the media in advance that I would not answer questions on AIDS, and I was not to be asked any questions on the subject. I have never understood why these peculiar restraints were placed on me. And although I have sought to find the explanation, I still don't know the answer. (C. Everett Koop, The Memoirs of America's Family Doctor, pp 195-96)

SQUELCHING DR. LOGAN

One other person who might have stopped the spread of AIDS was also effectively dealt with. He had rediscovered hyperthermia, a technique of heating a person's blood to temperatures produced by tropical fevers such as malaria. The technique was employed early in the twentieth century to treat syphilis and cancer, but later in the century fell into disuse. Hyperthermia works by fooling the body into thinking it is faced with a deadly tropical fever, and under those circumstances it will produce substances that will combat such diseases and also effectively work on cancer cells. More recently in the 1990s, hyperthermia has been used as a treatment for Lyme disease.

In the first half of 1990 Dr. William Logan, a heart surgeon at Atlanta Hospital in Georgia, treated two AIDS patients with hyperthermia; one of them had visible improvement in his condition and proclaimed himself cured of AIDS; the other one was largely unchanged following the treatment. Dr. Logan heated the blood to 108°F for five hours in these two cases and proposed to treat fifty other patients with AIDS, using hyperthermia.

But when Dr. Logan told the Georgia AIDS Task Force in August 1990 of his plans, and indicated that two university medical centers were in negotiations to test fifty people with AIDS, he was "sat on." Investigators from the National Institute for Allergy and Infectious Diseases (NIAID)-a leading government AIDS research agency-blasted his ideas. They said that hyperthermia "appears to have offered no clinical, immunologic or virological benefits." They implied that the one person wasn't suffering from Kaposi's sarcoma, and that there was no reason "for further human experimentation in this area at this time."

Dr. Anthony Fauci, director of NIAID, accused Dr. Logan of raising false hopes in AIDS-infected individuals. Dr. Logan could scarcely hide his anger: "I am totally flabbergasted," he said, adding that the report would almost certainly prevent any more work in the field of hyperthermia. He added, "This is why I am so terribly upset . . . I'm going to fight this every way I can, but I don't know what we're going to do."

If Dr. Logan had been allowed to go ahead with his proposed tests, we might have a treatment for AIDS, a treatment that is simple and does not require high technology. But Dr. Logan had been squelched, firmly and completely.

The American government's lack of action concerning AIDS is incomprehensible-unless it is a deliberate policy to spread the disease. I suspect that is the case because of information that came to me quite accidentally many years ago. Here is the story:

COVERT AGENCY RESEARCH

In the summer of 1955 I was invited to spend an evening with "Raymond," a French mining engineer who had spent his entire professional life in Africa. At that time he was about 63-65 years old.

During the course of the evening's discussion, Raymond suddenly asked me if I believed in the stories of "germ warfare" in Korea during that conflict. When I asked for proof, he showed me a 1/4 inch thick, typed manuscript, part of which had been copied from the original source, and part abstracted. At the end of that manuscript was a few pages of work on the "skinny disease" from which people wasted away and died. A table of hyperthermia tests indicated that heating the blood to 110° for 4 hours would arrest the disease.

"Where did this material come from," I asked. Raymond answered that he had worked in West Africa when young, then moved to South Africa and spent at least 25 years working in a gold mine there. In 1950, after the British lost political control in South Africa, he moved to take a consulting job in Kolwezi, a copper-mining town in what is now Zaire.

Shortly after arriving there he was approached by two people. The first person, an American of German descent (very likely Dr. Sidney Gottlieb, the CIA's resident expert on toxins, poisons, and diseases) did almost all of the talking. The other fellow said very little at the time. The first person said he wanted Raymond to translate medical scientific research papers into English, using as an inducement, fees well above normal and payable in advance-highly unusual. Raymond spoke English and French perfectly and also knew German as well as other languages, including African. Although he did not like this person of German descent (this was only 5 years after WW II), Raymond agreed to do the work. All of it was done well in advance of the deadline, neatly typed. He did not see the person who assigned him his work again. New papers, brought three times a year by the second person, were so processed, paid for each time in advance. All of them were from European medical publications.

This continued for five years until early in 1955. At that time the courier made an unexpected visit. He was upset and distraught, and did not stay long. He just picked up the metal box with translated papers, put another down, and left in a hurry. When Raymond opened the metal box, he found the new medical research papers to be translated, but he also found other things too. One in particular, about two centimeters thick, contained what can best be described as a proposal for the "cold war," written or printed between February and June, 1948. The other important material was a "progress report," apparently written late in 1954.

Raymond realized that these were highly classified materials, and disliking both people associated with them, decided to copy them out. Some of it he typed out in full, and some of it he condensed. The copies he showed me contained many sections of the proposal, but the very last one contained a hypothetical scenario on what would happen if a new type of venereal disease were to be introduced into modern society. Drawing mainly on syphilis as a model, it argued that such a disease would spread preferentially among the more promiscuous sections of society, namely "left-wing" types. There was no mention of homosexuality, no doubt because of the time it was written. The study did mention, however, that in such an eventuality "there would be large numbers of innocent victims."

Right after this section was a short paper, apparently written in late 1954 or early 1955. The first paragraph contained a description of both the mental and physical symptoms of the "skinny disease," spread by con-tamined blood, from which people wasted away and died. The main feature of this progress report was some tests that had been carried out on what was clearly AIDS-infected blood. Whoever carried out these tests was thinking even in 1954 of a cancer-causing virus. It is well known that cancer cells are more susceptible to heat than normal ones.

What got my attention was a figure showing a plot of tests done; time was plotted on the horizontal axis, and temperature on the vertical one, in steps of 5° F. From this it was clear that after heating the blood to a temperature of 110° F for 4 hours, those so treated were not infectious. That is, their blood would no longer transmit this disease. Was Dr. Logan so far off track then, 35 years later, when he wanted to test hyperthermia as a treatment for AIDS? Did NAID and Dr. Anthony Fauci know that this treatment had shown promising results decades earlier when a secret government agency was working on it? In 1956 Raymond, who was very interested in witch doctors and what they could do, told me a tale about an African courtesan who cast a magic spell on her sexual partners, protecting them from ever suffering from the "skinny disease." Updated into this decade, it would appear she had Simian Immunodeficiency Virus (SIV), which apparently immunizes against AIDS. By sleeping with each of them for a week, she transmitted it to her clients. Mirko Grmek, in his History of Aids, confirms that this disease was known in parts of Africa at that time (the 1950s).

MODERN RESEARCH

In our time, Myron Essex and his team at the Harvard School of Public Health has confirmed that prostitutes in parts of West Africa, though infected with AIDS, remain healthy, apparently because they already had SIV. Essex and his group have been studying 4,300 people living in West Africa, where a large proportion of the population is infected with the SIV virus. He has already demonstrated two things (my inference is in parentheses after each):

1. The lifespans of people in that region who are infected with the SIV virus and those who are not infected, are the same. (Hence SIV is harmless to humans.)

2. People infected with the SIV virus do not develop AIDS. (Because they are immune to it.)

Then another piece of work by Essex and his team was published recently. In this latest work, Essex has concentrated upon a group of prostitutes in the West African nation of Senegal, who are infected with the SIV virus. Now these women have multiple sexual partners each night, and as AIDS has spread to that country now, obviously some of their clients must have the early states of AIDS. But according to the article, "During the 18 months that the women have been studied . . . they have not shown even subtle signs of immune suppression, which would be detectable in individuals infected with [AIDS] itself for that long." They are immune to AIDS and presumably transmit the immunity agent-SIV virus-to their clients.

TEST THE THEORY The theory could be easily tested to see if inoculating people with SIV virus would work the same way as cowpox did for smallpox: confer immunity against it without harming people. References to the beneficial properties of cowpox in England can be traced back to the 1300s and certainly by the early 1700s every milkmaid in England knew what no doctor did, that cowpox protected against smallpox.

Here is a method of testing whether SIV virus confers immunity against AIDS;

1. Select large group of sexually active people, male and female; include both heterosexuals and homosexuals.

2. Test the blood of all the volunteers for AIDS. Reject those testing positive. Request all test subjects to have no sexual partners until told otherwise.

3. Wait six months. Again test blood of all remaining volunteers for AIDS. Again, reject any who test positive at this stage.

4. Inject all remaining volunteers with blood containing SIV virus obtained from people in West Africa. Again instruct participants to have no sexual partners until told otherwise.

5. Wait 6 months, then test blood of all volunteers to confirm that they have produced antibodies to the SIV virus.

6. Instruct all volunteers to resume normal sexual behavior, the same as they were doing before being selected.

7. Periodically monitor the blood of participants to see if there is any sign of immune system suppression.

8. Follow up with repeated tests until it becomes clear whether these people are immune to AIDS. The official position of the U.S. government indicates that nothing is going to be done for those who have AIDS. The National Research Council of the National Academy of Sciences, a private organization which provides scientific advice to the federal government, in February 1993 said, "Despite thousands of deaths and an aura of national health emergency, the AIDS epidemic will have little impact on the lives of most Americans or the way society functions" because AIDS is concentrated "among socially marginalized groups who have little economic, political and social power."

Now we know what it feels like to be a Jew in Nazi Germany!

REFERENCES:
Max Essex and Phyllis J. Kanki, "Origins of the AIDS Virus," Scientific American, October 1988, pp. 64-71. P.J. Kanki, M. F. McLane, N.W. King, Jr., N.

L. Levin, R.D. Hunt, P. Sehgal, M.D. Daniel, R. C. Desrosiers, and M. Essex, "Serologic Identification and Characterization of a Macaque T-Lymphotropic Retrovirus Closely Related to Human HTLV-III," Science, Vol. 228, No. 4707, June 7, 1985, pp. 1199-1201.

P.J. Kanki, J. Alroy, and M. Essex, "Isolation of T-Lymphotropic Retrovirus Related to HTLV-III/LAV from Wild-Caught African Green Monkeys," Science, Vol. 230, No. 4728, November 22, 1985, pp. 951-954.

F. Barin, S. M'Boup, F. Denis, P. Kanki, J.S. Allen, T.H. Lee, and M. Essex, "Serologic Evidence for Virus Related to Simian T-Lymphotropic Retrovirus III in Residents of West Africa," The Lancet, Vol 2 for 1985, December 21/28, 1985, pp. 1387-89.

Phyllis J. Kanki and others, "Human T-Lymphotropic Virus Type 4 and the Human Immunodeficiency Virus in West Africa," Science, Vol. 236, No. 4803, May 15, 1987, pp. 827-831.

Richard G. Marlink and others, "Clinical, Hematologic, and Immunologic Cross-Sectional Evaluation of Individuals Exposed to Human Immunodeficiency Virus Type 2 (HIV-2)," in Aids Research and Human Retroviruses, Vol. 4, No. 2,
April 1988, pp. 137-148.

Original article: http://www.sonic.net/~doretk/ArchiveARCHIVE/Aids/TheMerchantsofAIDS.html

DEPARTMENT OF DEFENSE APPROPRIATIONS FOR 1970 : The funding of the Bio-terrorism AIDS virus

2008-01-10T17:26:00.000+01:00

DEPARTMENT OF DEFENSE APPROPRIATIONS FOR 1970

HEARINGS BEFORE A SUBCOMMITTEE OF THE COMMITTEE ON APPROPRIATIONS HOUSE OF REPRESENTATIVES
NINETY-FIRST CONGRESS
FIRST SESSION
SUBCOMMITTEE ON DEPARTMENT OF DEFENSE APPROPRIATIONS

H.B. 15090

PART 5
RESEARCH, DEVELOPMENT, TEST, AND EVALUATION

Department of the Army
Statement of Director, Advanced Research Project Agency
Statement of Director, Defense Research and Engineering

Printed for the use of the Committee on Appropriations
U.S. GOVERNMENT PRINTING OFFICE
WASHINGTON : 1969
UNITED STATES SENATE LIBRARY

[pg.] 129 TUESDAY, JULY 1, 1969

SYNTHETIC BIOLOGICAL AGENTS

There are two things about the biological agent field I would like to mention. One is the possibility of technological surprise. Molecular biology is a field that is advancing very rapidly and eminent biologists believe that within a period of 5 to 10 years it would be possible to produce a synthetic biological agent, an agent that does not naturally exist and for which no natural immunity could have been acquired.
MR. SIKES. Are we doing any work in that field?
DR. MACARTHUR. We are not.
MR. SIKES. Why not? Lack of money or lack of interest?
DR. MACARTHUR. Certainly not lack of interest.
MR. SIKES. Would you provide for our records information on what would be required, what the advantages of such a program would be, the time and the cost involved?
DR. MACARTHUR. We will be very happy to.
(The information follows:)

The dramatic progress being made in the field of molecular biology led us to investigate the relevance of this field of science to biological warfare. A small group of experts considered this matter and provided the following observations:

1. All biological agents up the the present time are representatives of naturally occurring disease, and are thus known by scientists throughout the world. They are easily available to qualified scientists for research, either for offensive or defensive purposes.

2. Within the next 5 to 10 years, it would probably be possible to make a new infective microorganism which could differ in certain important aspects 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.

3. A research program to explore the feasibility of this could be completed in approximately 5 years at a total cost of $10 million.

4. It would be very difficult to establish such a program. Molecular biology is a relatively new science. There are not many highly competent scientists in the field. Almost all are in university laboratories, and they are generally adequately supported from sources other than DOD. However, it was considered possible to initiate an adequate program through the National Academy of Sciences - National Research Council (NAS-NRC).

The matter was discussed with the NAS-NRC, and tentative plans were plans were made to initiate the program. However decreasing funds in CB, growing criticism of the CB program, and our reluctance to involve the NAS-NRC in such a controversial endeavor have led us to postpone it for the past 2 years.

It is a highly controversial issue and there are many who believe such research should not be undertaken lest it lead to yet another method of massive killing of large populations. On the other hand, without the sure scientific knowledge that such a weapon is possible, and an understanding of the ways it could be done, there is little that can be done to devise defensive measures. Should an enemy develop it, there is little doubt that this is an important area of potential military technological inferiority in which there is no adequate research program.

Funded for $10,000 000
12/8/69 (306 yes votes 330-no votes 33)

United States Patent 4,647,773 Gallo -Continuous production of retroviruses

2008-01-10T16:34:00.000+01:00

United States Patent 4,647,773
Gallo , et al. March 3, 1987
________________________________________
Method of continuous production of retroviruses (HTLV-III) from patients with AIDS and pre-AIDS
Abstract
A cell system is disclosed for the reproducible detection and isolation of human T-lymphotropic retroviruses (HTLV-family) with cytopathic effects (HTLV-III) from patients with the acquired immune deficiency syndrome (AIDS), pre-AIDS and in healthy carriers. One neoplastic aneuploid T-cell line derived from an adult with lymphoid leukemia, and termed HT, was susceptible to infection with the new variants of HTLV, which are transformed and providing T-cell populations which are highly susceptible and permissive from HTLV-III, and convenience for large scale production, isolation and biological detection of the virus.
________________________________________
Inventors: Gallo; Robert C. (Bethesda, MD), Popovic; Mikulas (Bethesda, MD)
Assignee: The United States of America as represented by the Department of Health (Washington, DC)
[*] Notice: The portion of the term of this patent subsequent to May 28, 2002 has been disclaimed.
Appl. No.: 06/602,946
Filed: April 23, 1984
________________________________________
Current U.S. Class: 435/239 ; 424/208.1; 435/235.1; 435/372.3; 435/948
Current International Class: C12N 5/06 (20060101); C12N 7/00 (20060101); C12N 007/02 (); C12N 007/00 (); C12N 005/00 (); C12R 001/91 ()
Field of Search: 435/235,239,240,948,5,29 424/89 128/1T
________________________________________
References Cited [Referenced By]
________________________________________
U.S. Patent Documents

4464465
August 1984 Lostrom et al.
4520113
May 1985 Gallo et al.

Other References

Popovic et al, Science, 224(4648):497-500, May 4, 1984. .
Gallo et al, "Isolation of Human T-Cell Leukemia Virus in Acquired Immune Deficiency Syndrome (AIDS)", Science, 220, pp. 865-867 (5-1983). .
Barre-Sinoussi et al, "Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for AIDS", Science, 220, pp. 868-871 (5-1983). .
Marx, "Strong New Candidate for AIDS Agent", Science, 224, pp. 475-477 (5-1984)..

Primary Examiner: Warren; Charles F.
Assistant Examiner: Tarcza; John Edward
Attorney, Agent or Firm: Roberts, Jr.; John S.
________________________________________
Claims
________________________________________

We claim:

1. A method for continuous production of HTLV-III virus which comprises infecting in cell culture highly susceptible, permissive cells consisting of a neoplastic aneuploid HT-cell line with said virus, said cells preserve the capacity for permanent growth after the infection with said virus, growing said cells under conditions suitable for cell growth and recovering said virus produced by said cells.

2. The method of claim 1, wherein said virus consists of cytopathic variants of HTLV.

3. The method of claim 1 wherein said infecting comprises cocultivating said virus with said cells to produce a cell line and recovering said cell line.

4. The method of claim 1 wherein said infecting comprises cell-free infection of said cells with said virus.

5. The method of claim 1 wherein said cells are neoplastic aneuploid T-cells derived from an adult with lymphoid leukemia.

6. A process for the continuous production of HTLV-III virus which comprises cocultivating said virus with a target HT-cell to produce an infected cell line, growing said cell line and recovering said virus from supernatants produced by said cell line.

7. The process of claim 6 wherein said target T-cell is a neoplastic aneuploid T-cell susceptible to infection with HTLV-III.

8. A process for the continual production of HTLV-III by infecting T-cells in cultures which comprises cocultivating HTLV-III virus with an HT-clone to produce an infected cell line, said clone being an aneuploid T-cell line derived from lymphoid leukemia, growing said cell line and recovering said virus from supernatants produced by said cell line.

9. The process in claim 8 wherein said clone is a mature T-cell phenotype of OKT3.sup.+ (62%), OKT4.sup.+ (39%) and OKT8.sup.-.

10. A method of producing a cell line containing an antigen of HTLV-III which comprises infecting an HT-cell line derived from lymphoid leukemia and susceptible to infection with HTLV-III, said cell line is capable of continuous large-scale production of HTLV-III, and growing the infected cell line under conditions suitable for growth.

11. The method of claim 10 wherein said cell line is a neoplastic aneuploid T-cell line.

12. The method of claim 10 wherein said HTLV-III are variants of human T-lymphotropic retrovirus, exhibit cytopathic effects and are non-transforming.

13. A cell line containing HTLV-III designated H9/HTLV-III.sub.B, ATCC Accession CRL 8543.

14. A process for producing a cell line H9/HTLV-III.sub.B which comprises infecting a target T-cell with HTLV-III virus to produce a cell line and recovering same, said infecting process overcomes the normal cytopathic effect of HTLV-III and preserves the immortal growth capacity of the target cell.

15. An HT cell line permanently infected with HTLV-III virus, wherein said cell line continually produces said virus.
________________________________________
Description
________________________________________

The present invention describes a cell system for the reproducible detection and isolation of human T-lymphotropic retroviruses (HTLV-family) with cytopathic or cell killing effects (HTLV-III) from patients with the acquired immune deficiency syndrome (AIDS), pre-AIDS and in healthy carriers. One neoplastic aneuploid T-cell line derived from an adult with lymphoid leukemia, and termed HT, was susceptible to infection with the new variants of HTLV, providing T-cell populations which are highly susceptible and permissive for HTLV-III, and convenience for large scale production, isolation, and biological detection of the virus.

BACKGROUND OF THE INVENTION

The disclosure of this invention is contained in the following journal articles: Gallo et al., "Detection, Isolation, and Continuous Production of Cytopathic Human T-Lymphotropic Retroviruses (HTLV-III) from Patients with AIDS and pre-AIDS," Science, in press; and Gallo et al., "Human T-Lymphotropic Retrovirus, HTLV-III, Isolated from AIDS Patients and Donors at Risk for AIDS," in press.

Epidemiologic data strongly suggest that acquired immune deficiency syndrome (AIDS) is caused by an infectious agent which is apparently horizontally transmitted by intimate contact or blood products. Though the disease is manifested by opportunistic infections, predominantly Pneumocystis carcinii pneumonia and Kaposi's sarcoma, the underlying disorder affects the patient's cell-mediated immunity with absolute lymphopenia and reduced helper T-lymphocyte (OKT4.sup.+) subpopulation(s). Moreover, before a complete clinical manifestation of the disease occurs, its prodrome, pre-AIDS, is frequently characterized by unexplained chronical lymphadenopathy and/or leukopenia involving a helper T cell subset. This leads to the severe immune deficiency of the patient, suggesting that a specific subset of T-cells is the primary target for an infectious agent. Although patients with AIDS or pre-AIDS are often chronically infected with cytomegalovirus or hepatitis B virus, for various reasons these appear to be opportunistic or coincidental infections apparently not linked to the immunological response deficiency. It is believed that the cause of AIDS may be a virus from the family of human T-cell lymphotropic retroviruses (HTLV) which, prior to the present invention, comprised two major well characterized subgroups of human retroviruses, called human T-cell leukemia/lymphoma viruses, HTLV-I and HTLV-II. The most common isolate, HTLV-I, is mainly obtained from patients with mature T-cell malignancies. Seroepidemiological studies, in vitro biological effects, and nucleic acid hybridization data indicate that HTLV-I is etiologically associated with these malignancies, affecting adults primarily in the south of Japan, the Caribbean and Africa. HTLV of subgroup II (HTLV-II) was first isolated from a patient with a T-cell variant of hairy cell leukemia. To date, this is the only reported isolate of HTLV-II from a patient with a neoplastic disease. Virus isolation and seroepidemiological data show that HTLV of both subgroups can sometimes be found in patients with AIDS.

Evidence suggests that the retrovirus(es) of the HTLV family is an etiological agent of AIDS based on the following: (1) there is precedence for an animal retrovirus cause of immune deficiency (feline leukemia virus in cats); (2) retroviruses of the HTLV family are T-cell tropic; (3) they preferentially infect "helper" T-cells (OKT4.sup.+); (4) they have cytopathic effects on various human and mammalian cells as demonstrated by their induction of cell syncytia formation; (5) they can alter some T-cell functions; (6) in some cases infection may result in selective T-cell killing; and (7) they are transmitted by intimate contact or through blood products. The presence of antibodies directed to cell membrane antigens of HTLV infected cells has been shown in sera of more than 40% of patients with AIDS [Essex et al., Science, 220:859 (1983)]. This antigen has since been defined as part of the envelope of HTLV [Schupbach, et al., Science, in press; and Lee, et al., Proc. Nat. Acad. Sci. U.S.A., in press].

The original detection and isolation of the various HTLV isolates were made possible by two earlier developments: the discovery of T-cell growth factor (TCGF), also called Interleukin 2 (Il-2), which enabled the routine selective growth of different subsets of normal and neoplastic mature T-cells [Ruscetti, et al., J. Immunol., 119:131 (1977); and Poiesz, et al., Proc. Nat. Acad. Sci. U.S.A, 77:6134 (1980)] and the development of sensitive assays for detection of retroviruses based on reverse transcriptase assays. The methods of HTLV isolation and transmission involved a cocultivation procedure using permissive T-cells for the virus. The use of normal human T-cells in cocultivation experiments preferentially yielded HTLV of both subgroups with immortalizing (transforming) capability for some of the target T-cells.

However, HTLV variants (now termed HTLV-III), lack immortalizing properties for normal T-cells and mainly exhibit cytopathic effects on the T-cells and is now believed to be the cause of AIDS. In fact, such variants were frequently but only transiently detected using these normal T-cells as targets in cocultivation or cell-free transmission experiments. The cytopathic effect was overcome by finding a highly susceptible, permissive cell for cytopathic variants of HTLV, thus preserving the capacity for permanent growth after infection with the virus. The present invention discloses the identification and characterization of this new immortalized T-cell population and its use in the isolation and continuous high- level production of such viruses from patients with AIDS and pre-AIDS.

Early experiments identified one neoplastic aneuploid T-cell line, termed HT, derived from an adult with lymphoid leukemia, that was susceptible to infection with the new cytopathic virus isolates.

This cell line is a sensitive target for transmission of these virus isolates (HTLV-III) and it allows continuous large-scale virus production and development of specific immunologic reagents and nucleic acid probes useful for comparison of these new isolates among themselves and with HTLV-I and HTLV-II. In addition to their differences in biological effects that distinguish them from HTLV-I and HTLV-II, HTLV-III also differs from these known HTLV subgroups in several immunological assays and in morphology. However, these new retroviruses are T4 lymphotropic and exhibit many properties similar to HTLV-I and II, including similar properties of the reverse transcriptase, cross reactivity of structural proteins as determined by heterologous competition radioimmune assays with patients' sera and with animal hyperimmune sera, and induction of syncytia. These new retrovirus isolates are collectively designated HTLV-III, together with detectable differences in some of their proteins and genetic information, HTLV-III's ability to kill T-cells clearly separates these variants from other members of the HTLV family.

STATEMENT OF DEPOSIT

A cell line corresponding to the present invention, and denoted H9/HTLV-III.sub.B, has been deposited in the ATCC (under ATCC No. CRL 8543) on April 19, 1984, prior to the filing of this patent application. This deposit assures permanence of the deposit and ready accessibility thereto by the public. H9 is a representative and preferred cell line in accordance with the invention.

UTILITY STATEMENT

The cell line which is a product of the present invention (H9/HTLV-III.sub.B) is presently useful for the production of vaccines for the relief of AIDS and for the detection of antibodies to the virus in blood samples.

GENERAL DESCRIPTION

A susceptible cell line HT was tested for HTLV before in vitro infection and it was negative by all criteria, including lack of proviral sequences. Continuous production of HTLV-III is obtained after repeated exposure of parental HT cells (3.times.10.sup.6 cells pretreated with polybrene) to concentrated culture fluids containing HTLV-III harvested from short term cultured T-cells (grown with TCGF) which originated from patients with pre-AIDS or AIDS. The concentrated fluids were first shown to contain particle associated reverse transcriptase (RT). When cell proliferation declined, usually 10 to 20 days after exposure to the culture fluids, the fresh (uninfected) HT parental cells are added to cultures. Culture fluids from the infected parental cell line was positive for particulate RT activity and about 20% of the infected cell population was positive in an indirect immune fluorescent assay (IFA) using serum from a hemophilia patient with pre-AIDS (patient E.T.). Serum from E.T. also contained antibodies to proteins of disrupted HTLV-III but did not react with proteins of HTLV-I or HTLV-II infected cells.

SPECIFIC DISCLOSURE

As has been mentioned above, an aneuploid HT-cell line exhibited the desired prerequisites for the continuous propagation of HTLV-III. This cell line is a neoplastic aneuploid T-cell line derived from an adult patient with lymphoid leukemia, selected for its mature T-cell phenotype [OKT3.sup.+ (62%), OKT.sup.4 + (39%) and OKT8.sup.- ], as determined by cytofluorometry using a fluorescence-activated cell sorter. Cultures of these cells are routinely maintained in RPMI/1640 with 20% fetal calf serum and antibiotics. These cultures are shown in Example 1, Table 1. Clone H9 is preferred, with Clone H4 being secondarily preferred.

HTLV-III culture fluids are isolated from cultured cells of patients with acquired immune deficiency syndrome (AIDS). Peripheral blood leukocytes from these patients are banded in Ficoll-Hypaque, incubated in growth media (RPMI 1640, 20% fetal bovine serum 0.29 mg/ml glutamine) containing 5 .mu.g/ml phytohemagglutinin (PHA-P) for 48 hours, at 37.degree. C. in a 5% CO.sub.2 atmosphere. The leukocytes are then refed with growth medium containing 10% purified T cell growth factor (TCGF); optionally, some of the cells also received rabbit antibody to alpha interferon. Cells and growth media from these lymphocytes are then assayed for the presence of HTLV subgroups I-III. Samples exhibiting more than one of the following were considered positive: repeated detection of a Mg.sup.++ dependent reverse transcriptase activity in supernatant fluids; virus observed by electron microscopy; intracellular expression of virus-related antigens detected with antibodies from sero-positive donors or with hyperimmune serum; or transmission of particles, detected by reverse transcriptase assays or by electron microscopic observation, to fresh human cord blood, bone marrow, or peripheral blood T-lymphocytes. All isolates not classified as either HTLV-I or HTLV-II by immunological or nucleic acid analysis were classified as HTLV-III. The cells in the HTLV-III producing cell cultures, characterized using established immunological procedures, are predominantly T-lymphocytes (E rosette receptor, OKT/3 and Leu/1 positive, with a T4 phenotype (OKT4, leu 3a positive). This process is also described by Gallo, et al., in Science, 220:865-867 (1983).

The infection of parental HT cells as well as other cloned cell populations occurs by exposure of these cells to concentrated or nonconcentrated culture fluids (cell-free infection) from T-cell cultures from AIDS or pre-AIDS patients, or by cocultivation; that is, HT cells are infected by exposure to HTLV-III containing cultures. The usual cell-free infection procedure is as follows: 2 to 5.times.10.sup.6 cells are treated with polybrene (2 .mu.g/ml) or DEAE dextran for 30 minutes in CO.sub.2 incubator at 37.degree. C., and then exposed to the virus inoculum (0.1 to 1 ml) for one hour in the incubator (CO.sub.2 /37.degree. C.). The cells are kept in suspension by shaking at regular intervals. After one hour of incubation a regular growth medium is added. The positivity of infected cultures for HTLV-III is assessed after one, two, and three weeks of cultivation.

The infection of HT cells (clones) is also obtained by cocultivation procedure--HT cells are mixed in various proportions (usually 1:5) with short- term cultured T-cells (about 5 to 20 days) from AIDS or pre-AIDS patients. The positivity for HTLV-III was scored by the detection of viral antigens or viral nucleic acid sequences in the infected recipient cells at various intervals (7, 14, 21 days, etc.) after cocultivation. The mixed cultures are maintained in growth medium for several months.

EXAMPLE 1

As shown in Table 1 below, single cell HT clones were isolated as described by Popovic, et al., in Neoplasma, 18:257 (1971), and Bach, et al., Immunol. Rev., 54:5 (1981) from a long-term cultured aneuploid HT-cell line exhibiting mature T-cell phenotype (OKT3.sup.+ [62%], OKT4.sup.+ [39%] and OKT8.sup.-) as determined by cytofluorometry using a fluorescence-activated cell sorter. The cultures were routinely maintained in RPMI/1640 with 20% fetal calf serum and antibiotics. The terminal cell density of the parental cell culture, seeded at a concentration of 2.times.10.sup.5 cells/milliliter of culture media, was in the range 10.sup.6 -1.5.times.10.sup.6 cells/ml after 5 days of culture.

For detection of multinucleated cells, cell smears were prepared from cultures 6 and 14 days after infection and stained with Wright-Giemsa. Cells having more than 5 nuclei were considered as multi-nucleated cells. Cloned cells from uninfected cultures also contained some multi-nucleated giant cells as well; however, the arrangement of multiple nuclei in a characteristic ring formation was lacking and the number of these cells was much less (0.7% to 10%).

Immunofluorescence positive cells were washed with phosphate-buffered saline (PBS) and resuspended in the same buffer at concentration 10.sup.6 cells per milliliter. Approximately 50 .lambda. of cell suspension were spotted on slides, air dried, and fixed in acetone for 10 min. at room temperature. Slides were stored at -20.degree. C. until use. Twenty microliters of either hyperimmune rabbit antiserum to HTLV-III (diluted 1/2000 in PBS) or serum from the patient (E.T.) diluted 1/8 in PBS was applied to cells and incubated for 50 min. at 37.degree. C. The fluorescein-conjugated antiserum to rabbit or human immunogloblin G was diluted and applied to the fixed cells for 30 min. at room temperature. Slides then were washed extensively before microscopic examinations. The uninfected parental cell line as well as the clones were consistently negative in these assays.

To determine reverse transcriptase activity, virus particles were precipitated from cell-free supernatant as follows: 0.4 ml of 4M NaCl and 3.6 ml of 30% (wt/vol.) polyethylene glycol (Carbowax 6000) were added to 8 ml of harvested culture fluids and the suspension was placed on ice overnight. The suspension was centrifuged in a Sorvall RC-3 centrifuge at 2000 rpm at 4.degree. C. for 30 min. The precipitate was resuspended in 300 .mu.l at 50% (vol/vol) glycerol (25 mM Tris-HCl, pH 7.5/5 mM dithiothreitol/150 mM KCl/0.025% Triton X-100. Particles were disrupted by addition of 100 .mu.l of 0.9% Triton X-100/1.5M KCl. Reverse transcriptase (RT) assays were performed as described by Poiesz, et al., Proc Nat. Acad. Sci. U.S.A., 77:7415 (1980) and expressed in cpm per milliliter culture medium.

TABLE 1 __________________________________________________________________________ Response of Cloned T-Cell Populations to HTLV-III Infection Clones Characteristics H3 H4 H6 H9 H17 H31 H35 H38 __________________________________________________________________________ Total cell number (.times. 10.sup.6) 6 days after infection 1 1.5 1.5 0.3 0.4 0.3 0.5 1.8 14 days after infection 2.2 7.3 7.5 10.0 4.7 5.0 4.5 3.2 Multinucleated cells (%) 6 days after infection 24 42 32 7 13 14 30 45 14 days after infection 45 48 45 30 22 45 60 60 Immunofluorescence positive cells (%) 6 days after infection Rabbit antiserum to HTLV-III 55 56 32 32 39 21 10 87 Patient serum (E.T.) 56 29 21 ND ND ND ND 73 14 days after infection Rabbit antiserum to HTLV-III 50 74 60 97 71 40 20 80 Patient serum 45 47 56 78 61 43 22 89 Reverse transcriptase activity (.times. 10.sup.4 cpm/ml) 6 days after infection 2.4 1.8 2.1 4.1 2.6 1.4 1.7 2.5 14 days after infection 16.2 18.1 16.1 20.2 17.1 13.4 15.1 18.2 __________________________________________________________________________ ND = not done

EXAMPLE 2

As shown in Table 2 below, cocultivation with H4 recipient T-cell clone was performed with fresh mononuclear cells from peripheral blood of patients RF and SN, respectively. In the case of patients BK and LS cocultivation was performed with T-cells grown in the presence of exogenous TCGF (10% V/V) for 10 days. The ratio recipient/donor (patients') cells was 1:5. The mixed cultures were maintained in RPMI/1640 (20% FCS and antibiotics) in the absence of exogenous TCGF. Cell-free infection of H9 T-cell clone was performed using concentrated culture fluids harvested from T-cell cultures of the patient WT. The T-cell cultures were grown in the presence of exogenous TCGF for two weeks before the culture fluids were harvested and concentrated. Cells of H9 clones were pretreated with polybrene (2 .mu.g/ml) for 20 min. and 2.times.10.sup.6 cells were exposed for one hr. to 0.5 ml of 100-fold concentrated culture fluids positive for particulate RT activity.

HTLV-III virus expression in both cocultured and cell-free infected cell cultures were assayed approximately one month after in vitro cultivation. There was considerable fluctuation in HTLV-III expression (see Table 2). For details of both reverse transcriptase (RT) assays and indirect immunofluorescence assays (IFA) see Example 1.

TABLE 2 __________________________________________________________________________ Isolation of HTLV-III from Patients with Pre-AIDS and AIDS Virus Expression IFA with RT Activity Rabbit Serum Human Serum (ET) Patient Diagnosis Origin (.times. 10 cpm) (% Positive) (% Positive) EM __________________________________________________________________________ RF AIDS Haiti 0.25 80 33 ND (heterosexual) SN Hemophiliac U.S. 6.3 10 ND + (lymphadenopathy) BK AIDS U.S. 0.24 44 5 + (homosexual) LS AIDS U.S. 0.13 64 19 + (homosexual) WT Hemophiliac U.S. 3.2 69 ND ND (lymphadenopathy) __________________________________________________________________________ RT = reverse transcriptase IFA = immunofluorescence assays EM = electron microscopy ND = not done

EXAMPLE 3

To select for high permissiveness for HTLV-III and to preserve permanent growth and continuous production of virus, extensive cloning of the HT parental T-cell population was performed. A total of 51 single-cell clones was obtained by both capillary and limited dilution techniques using irradiated mononuclear cells from peripheral blood of a healthy donor as a feeder. The growth of these cell clones was compared after HTLV-III infection. A representative example of response to virus infection of 8 T-cell clones which are susceptible to and permissive for HTLV-III is shown in Table 1. In parallel experiments, 2.times.10.sup.6 cells of each T-cell clone were exposed to 0.1 ml of concentrated virus. Then cell growth and morphology, expression of cellular viral antigen(s), and RT activity in culture fluids were assessed 6 and 14 days after infection. Although all 8 clones were susceptible to and permissive for the virus, there were considerable differences in their ability to proliferate after infection. The cell number decreased by 10% to 90% from the initial cell count within 6 days after infection, and a high proportion of multinucleated (giant) cells were consistently found in all 8 infected clones. The percentage of T-cells positive for viral antigen(s) determined by immunofluorescent assays with serum from AIDS patient (E.T.) and with hyperimmune rabbit serum raised against the whole disrupted HTLV-III ranged from 10% to over 80%. Fourteen days after infection, the total cell number and the proportion of HTLV-III positive cells increased in all 8 clones. The virus positive cultures consistently showed round giant cells which contained numerous nuclei. These multinucleataed giant cells are similar to those induced by HTLV-I and HTLV-II except that the nuclei exhibit a characteristic ring formation. Electron microscopic examinations showed that the cells released considerable amounts of virus.

EXAMPLE 4

To determine whether HTLV-III is continuously produced by the infected T-cells in long-term cultures, both virus production and cell viability of the infected clone, H4, were followed for several months. Although the virus production fluctuated, culture fluids harvested from the H4/HTLV-III cell cultures at approximately 14-day intervals consistently exhibited particulate RT activity which has been followed for over 5 months. The viability of the cells ranged from 65% to 85% and doubling time of the cell population, which is called H4/HTLV-III, was approximately 30-40 hours. Thus, this permanently growing T-cell population can continuously produce HTLV-III.

The yield of virus produced by H4/HTLV-III cells was assessed by purification of concentrated culture fluids through a sucrose density gradient and assays of particulate RT activity in each fraction collected from the gradient. The highest RT activity was found at density 1.16 g/ml, similar to other retroviruses.

The Strecker Memorandum video

2008-01-10T00:36:00.000+01:00

Some of this information is outdated and no longer valid, but it gives enough information so everyone can get the picture. This video is 20 or so years old.

One thing is for certain. The Governments of the world have completely ignored this information over the last 20 years so one must assume they know about it and they are using this man made virus to cull the world population.

This is why all alternative therapies will be suppressed until enough people or dead. Then someone will announce a marvelous cure.

The origin of the thesis that it is necessary to control world population by murdering of millions of people by murder is still a mystery. But rest assured that Henry Kissinger was somehow involved.

RNDr. Antonín Holý D.Sc., Dr.h.c., Faculty of Sciences, Prague

2008-01-05T08:16:00.000+01:00

Recognition of key scientists in the world that are helping persons of the HIV virus to live.

RNDr. Antonín Holý D.Sc., Dr.h.c.

Born September 1, 1936 in Prague

1954 - 1959 Faculty of Sciences, Charles University, Prague, graduated in organic chemistry.
1960 - 1963 Ph.D. study at the Institute of Organic Chemistry and Biochemistry, in organic chemistry. Dissertation: "Application of Vilsmeier-Haack reaction in Aliphatic Chemistry".
1963 - now research scientist, Institute of Organic Chemistry and Biochemistry, Prague
1967 senior scientist
1983 Head of nucleic acid chemistry group
1984 Doctor of Sciences (D.Sc.), dissertation: "Nucleoside and Nucleotide Analogs: Synthesis and Biological Activity".
1987 Head of department Bioorganic Chemistry
1988 elected Corresponding Member of Czechoslovak Academy of Sciences (which was dissolved by Jan.1, 1993).
1990 Member of the Scientific Council of the Czech Academy of Sciences.
1992 - 1994 Deputy Director for Research
1994 - 2002 Director of the Institute

Honors and Prizes:

1986 Czechoslovak National Prize for Chemistry "Acyclic Nucleoside and Nucleotide Analogs".
1998 Honor plaque: Nucleic Acids Chemistry journal.
1999 Honor medal, Czech Chemical Society
Doctor honoris causa, Palacký University, Olomouc
2001 Descartes Prize, European Union
2002 Elion Award of International Society for Antiviral Research
2002 State Medal "Pour merit"

Membership in Editorial Boards:
Nucleic Acids Chemistry (finished)
Nucleosides and Nucleotides
Antiviral Research
International Journal of Purine and Pyrimidine Research
Antiviral Chemistry and Chemotherapy
ChemBioChem
Elected scientific functions:
Vice-Chairman, Scientific Council of the Academy of Sciences of the Czech Republic,
Member of Scientific Board, Faculty of Sciences, Charles University Prague

Publications:
>450 original papers, 60 patent applications.
Books: coauthorship in:
Synthetic Procedures in Nucleic Acid Chemistry (W.W.Zorbach, R.S.Tipson,Eds.), Interscience 1968.
Nucleic Acid Chemistry (L.B.Townsend, R.S.Tipson,Eds.), Wiley-Interscience 1978.
Approaches to Antiviral Agents (M.R.Harnden,Ed.), Macmillan, 1985.
Nucleotide Analogues as Antiviral Agents (J.C.Martin,Ed.), ACS 1989.
Advances in Antiviral Drug Research (E.De Clercq, Ed.), JAI Press 1993.
Antibiotics and Antiviral Compounds (K.Krohn Ed.), Verlag Chemie 1993.
Recent Advances in Nucleosides: Chemistry and Chemotherapy (C.K.Chu, Ed.), Elsevier, 2002.

Areas of scientific interest:
nucleic acid chemistry - sugar-modified nucleoside analogs, phosphorus-modified nucleotide analogs; enzymes of nucleic acids metabolism: specificity & inhibitors of enzymes, virus-specific enzymes; biological applications of modified nucleic acids components: antivirals, cytostatics, antiparasitic drugs; anti-AIDS drugs; drug development.

Scientific organisatory activity:
organizer of a serial "Symposium on the Chemistry of Nucleic Acids Components" which is taking place from 1969 in three-year-intervals in Czechoslovakia/Czech Republic (12th symposium of this series took place in 2002).

Educational activity:
During the scientific career 7 Ph.D.'s, two long-term students, nine long-term visiting scientists (USA, Canada, Germany, Japan, Russia, Poland, Bulgaria), four diploma students. At present, three Ph.D. students, 1 diploma student.
Teaching: special lecture "Principles of antimetabolites for design of cytostatics and antivirals" (full-term lecture, 22 hours): Faculty of Science, Charles University Prague (from 1998), dtto Faculty of Science, Palacký University Olomouc (from 1999). Lectures on antivirals in Faculty of Medicine, Charles University, Prague, School of Pharmacy, Brno, Faculty of Medicine, Olomouc.

Realization of Research Results:

Duviragel™ (antiherpeticum), marketed by Léčiva Praha (Czech Republic) (1984)
original procedures for preparation of azidothymidine (anti-AIDS drug), produced in LACHEMA Brno (Czech Republic)
original antiviral drugs developed in USA by Gilead Sciences
Vistide™ (cidofovir) approved and marketed in USA a EU (1996) against CMV retinitis, also used fo treatment of malignizing papillomatoses, anogenital herpes, active against smallpox, monkeypox, etc.
Viread™ (tenofovir disoproxil) - novel anti-AIDS drug, approved 2001
Hepsera™ (adefovir dipivoxil) - novel drug against hepatitis B, approved 2002

International response:
Research in the field of acyclic nucleoside and nucleotide analogues opened new field in the development of antivirals and cytostatics. Adopted by numerous academical and industrial research laboratories: during the last 15 years 1140 original scientific papers.

International collaboration:
joint research with groups in USA, Belgium, Germany, Switzerland.

Languages:
English, German, Russian.
Selected scientific papers:
1998-2002

Present research projects:
structure-activity relationship in the field of acyclic nucleotide phosphonates (ANP); search for novel base- and chain-modified antiviral and anticancer ANP derivatives & their mode of action, novel synthetic methods for ANP preparation
ring-open ANP - synthetic approaches, mechanism of action
ANP prodrugs, effect of increased cellular drug uptake
immunomodulatory activity of ANP - effect of substitution upon stimulation of cytokines and activity of macrophages
metal complex formation of base-modified ANP

Present project funding:
Programme of targeted projects, Academy of Sciences of the Czech Republic
grants of the State Grant Agency (three shared grants)
two COST projects (# 13.40, # 20.002)
Descartes Prize (2002-2004)

United States Patent 5,676,977 Filed my Marvin S. Antelman - Method of Curing AIDS

2008-01-01T10:37:00.000+01:00

United States Patent 5,676,977
October 14, 1997 ~ Cl. 424/618
Method of Curing AIDS with Tetrasilver Tetroxide Molecular Crystal Devices

Marvin S. Antelman

Abstract ~

The diamagnetic semiconducting molecular crystal tetrasilver tetroxide ( Ag4O4 ) is utilized for destroying the AIDS virus, destroying AIDS synergistic pathogens and immunity suppressing moieties (ISM) in humans. A single intravenous injection of the devices is all that is required for efficacy at levels of about 40 PPM of human blood. The device molecular crystal contains two mono and two trivalent silver ions capable of "firing" electrons capable of electrocuting the AIDS virus, pathogens and ISM. When administered into the bloodstream, the device electrons will be triggered by pathogens, a proliferating virus and ISM, and when fired will simultaneously trigger a redox chelation mechanism resulting in divalent silver moieties which chelate and bind active sites of the entities destroying them. The devices are completely non-toxic. However, they put stress on the liver causing hepatomegaly, but there is no loss of liver function.

References Cited ~
U.S. Patent Documents:

4415565 ~ Nov., 1983 ~ Wysor ~ 424/618
4915955 ~ Apr., 1990 ~ Gomori~ 424/618
4952411 ~ Aug., 1990 ~ Fox, Jr. et al.~ 424/618
5073382 ~ Dec., 1991 ~ Antelman~ 424/618
5078902 ~ Jan., 1992 ~ Antelman ~ 424/618
5089275 ~ Feb., 1992 ~ Antelman ~ 424/618
5211855 ~ May, 1993 ~ Antelman ~ 424/618
5223149 ~ Jun., 1993 ~ Antelman ~ 424/618
5336499 ~ Aug., 1994 ~ Antelman ~ 424/618
5571520 ~ Nov., 1996 ~ Antelman ~ 424/618

Other References ~

"Is The AIDS Virus A Science Fiction?" by Peter H. Duesberg and Bryan J. Ellison: Policy Review (Summer 1990), pp. 40-51.

Claims ~

What is claimed is:

1. A method of treating AIDS-afflicted humans comprising injecting a multitude of tetrasilver tetroxide molecular crystals into the bloodstream of the human subject.

2. A method for increasing white blood cell counts in AIDS-afflicted humans comprising injecting a multitude of tetrasilver tetroxide molecular crystals into the bloodstream of the human subject.

3. Methods of treating AIDS-affilicted humans according to claims 1-2 where the concentration of said molecular crystals is approximately 40 PPM of the total blood weight of the human subject.

Description ~

BACKGROUND OF THE INVENTION

The present invention relates to the employment of molecular crystals as anti-AIDS devices, but more particularly to the molecular crystal semiconductor tetrasilver tetroxide Ag4O4 which has two monovalent and two trivalent silver ions per molecule, and which through this structural configuration enables intermolecular electron transfer capable of killing viruses and binding them to the resulting silver entity so that a single intravenous injection will completely obliterate acquired immune deficiency syndrome (AIDS) in humans. Furthermore, said devices are capable of killing pathogens and purging the bloodstream of immune suppressing moieties (ISM) whether or not created by the AIDS virus (HIV); so as to restore the immune system.

The present invention is based on concepts previously elucidated in applicant's U.S. Pat. No. 5,336,499 which discloses the destruction and inhibition of bacteria, algae and the AIDS virus in nutrient life supporting systems by using said silver oxide devices. Example 3 of said patent discloses that 18 PPM of said crystal devices could totally suppress the AIDS virus (page 6, line 5). Subsequent to the filing of the aforementioned patent, further testing revealed complete 100% destruction of the AIDS virus in vitro at 20 PPM, and the fact that said devices were harmless when ingested and inhaled, being non-toxic.

Encouraged by these evaluations and successes, applicant obtained permission to evaluate the crystals in vitro against murine acquired immune deficiency syndrome (MAIDS). Only one facility in the State of Israel is licensed for these evaluations, namely, the Kaplan Hospital in Rehovot, Israel, which is affiliated with the Hebrew University-Hadassah Medical School where said evaluations were done.

The initial evaluations entailed experimenting with various silver moieties cited in applicant's aforementioned patent, concentrations, non-reactive buffers and modes of administration. After about 18 months of judicious efforts and initial failures, success was finally achieved in destroying the MAIDS virus in C57BL mice with a single intravenous injection. The results of this test program comprise Example 5 of U.S. Pat. No. 5,336,499. After success with mice, the inventor was able to test the efficacy of said devices on two select etiological groups of terminal AIDS patients in a clinic in Tegucigalpa, Honduras, Central America.

The AIDS patients comprised the etiological subgroups, Candidiasis and Wasting Syndrome. Current indicator diseases for diagnosing AIDS which have been expanded by the CDC, fall into the following five major categories with the approximate percent distribution among AIDS patients:

______________________________________
1. P. carinii pneumonia 51%
2. Wasting syndrome 19%
3. Candidiasis 13%
4. Kaposi's sarcoma 11%
5. Dementia 6%
______________________________________

This invention concerns itself with the treatment and cure of candidiasis and wasting syndrome AIDS patients with Tetrasil*. These two groups account for approximately one third of AIDS cases.

*Trademark of Holipharm Corporation (of Israel) for Ag.sub.4 O.sub.4

Stedman's Medical Dictionary (Williams & Wilken's 26th Ed., 1995) defines wasting syndrome "as a condition of 10% weight loss in conjunction with diarrhea or fever . . . Associated with AIDS (p. 1744)."

OBJECTS OF THE INVENTION

The main object of the invention is to provide for a molecular scale device of a single tetrasilver tetroxide crystalline molecule capable of restoring the immunity of AIDS afflicted humans of the two AIDS etiological subgroups, candidiasis and wasting syndrome.

Another object of the invention is to provide for immunity restoration in said AIDS afflicted humans through a single injection.

Another object of this invention is to destroy ISM in humans manifesting AIDS diseases of said AIDS etiological subgroups irrespective as to whether said ISM was HIV induced, since it is known that humans may manifest AIDS and still be HIV negative, and thus restore the immune system in said humans.

Another object of this invention is to destroy the AIDS virus when present in the systems of said AIDS afflicted humans.

SUMMARY OF THE INVENTION

This invention relates to a molecular scale device not only capable of destroying the AIDS virus, but of purging the human bloodstream of pathogens and restoring immunity to AIDS patients of the candidiasis and wasting syndrome categories. Said molecular device consists of a single crystal of tetrasilver tetroxide (Ag4O4). The crystal lattice of this molecule has a unique structure since it is a diamagnetic semiconducting crystal containing two mono and two trivalent silver ions, which in effect are capable of "firing" electrons under certain conditions which will destroy AIDS viruses, other pathogens and immune suppressing moieties (ISM), not only through the electrocution mode, but also by a binding process which occurs simultaneously with electron firing, namely, binding and chelation of divalent silver, i.e., the resulting product of the electron transfer redox that occur when the monovalent silver ions are oxidized and the trivalent ions are reduced in the crystal. The binding/chelation effect occurs at active sites of the AIDS virus, pathogens and ISM. Because of the extremely minute size of a single molecule of this crystal, several million of these devices may be employed in concert to destroy a virus colony to purge a life support system of ISM and pathogens with the consumption of only parts per trillion of the crystal devices. Thus an optimum of 40 PPM of the devices by weight of human blood was found to be sufficient to completely obliterate AIDS. This concentration is slightly over double of the optimum concentration recommended in applicant's aforementioned U.S. patent for the destruction of the human AIDS virus in vitro. Other details concerning the structure of the crystal and its mechanism against pathogens, the AIDS virus and ISM would analogously hold here, and have already been further elucidated in said patent.

The actual destruction of pathogens, ISM and the AIDS virus is effectuated by injection of a suspension of these devices in distilled or deionized water with a non-reacting electrolyte directly, i.e. intravenously, into the bloodstream. A single injection is all that is required under these conditions. Accordingly, humans injected in this manner, upon being inspected after three weeks or more had elapsed and compared with similar humans that had been given placebos, were completely cured of AIDS. The control group still manifested AIDS. Accordingly, the tetrasilver tetroxide device performed in concert with and in full conformity with the ultimate objects of this invention. Furthermore, three out of four wasting syndrome terminal patients and four out of the five candidiasis terminal patients were still alive in 1995 after a year and a half had elapsed from their initial injection. By that time all the AIDS patients had been released from the clinic and allowed to return home.

Other objects and features of the present invention shall become apparent to those skilled in the art when the present invention is considered in view of the accompanying examples. It should, of course, be recognized that the accompanying examples illustrate preferred embodiments of the present invention and are not intended as a means of defining the limits and scope of the present invention.

EXAMPLE 1

Five patients afflicted with AIDS of the candidiasis etiological category were segregated for Tetrasil treatment. The rationale for selecting them was based on facts presented in an article by Peter H. Duesberg and Brian J. Ellison entitled "Is The AIDS Virus A Science Fiction?" (Policy Review, Summer 1990 pp. 40-51). Only the factual presentations of the article were utilized and the hypothesis of the authors was ignored. The facts presented in the article related to the method of selecting AIDS patients based on the five aforementioned etiological subgroups targeted by the CDC, and the evidence presented, that there is AIDS without HIV as well as with it so that an anti-viral agent in most instances will not necessarily restore the immunity system.

Evaluations with Tetrasil were conducted on AIDS patients at Lucha Contra el Sida, Comayaguela, Honduras. The patients two weeks prior to inoculation were removed from their AZT, AIDS therapy. Tetrasil was administered at approximately 40 PPM of blood volume per patient as a suspension in a proprietary buffer solution (pH = 6.5), supplied by Holipharm Corporation.

The results of evaluations with candidiasis are tabulated in Table I under its disease category. All patients evaluated were terminal. Some, however, were in moderate (m) condition and others in poor (p) as designated in the Table. The I and F designations refer to initial and final values as shown. WBC indicates white cell blood count. The H column, following CD 8, indicates whether hepatomegaly occurred. This was an unfortunate consequence of the treatment which resulted in enlarged livers in all patients except the second one. Despite hepatomegaly, there was no interference with liver function.

The onset of hepatomegaly was not spontaneous and varied from patient to patient, being in the range of 4-16 days.

It should also be noted that shortly after injection of Tetrasil there were indications of fever (symbolized by T in the Ag4O4 column), sometimes accompanied by fatigue (F). The body temperature was invariably 38.5.degree. C. (101.3.degree. F.). This was indicative of restoration of the immune response of the body, since normally the body will destroy pathogens when the immune system is functional by raising the temperature. The patient who died; first responded favorably to Diflucan, which previously gave no response. He was cured of his candidiasis, but unfortunately succumbed to his previous body damage. All the other candidiasis syndrome people who previously did not respond to the indicated medications subsequently responded after the Tetrasil treatment. Further evidence of the recovery of the AIDS patients manifested itself 30 days after the initial injection when white blood cell counts were taken. They are shown in Table I under the WBC column, which gives the initial and final WBC. All candidiasis patients showed a dramatic increase in their white blood cell counts, indicative of the restoration of their immunity systems.

EXAMPLE 2

The above protocol of Example 1 was repeated with AIDS patients exhibiting wasting syndrome. The results of their treatment are tabulated in Table I under the disease category of said syndrome. It should be noted that two of the four wasting syndrome patients showed improved white blood counts. The female patient, whose condition improved from poor and terminal to be among the living, showed a decrease in the WBC. However, she showed an increase in body temperature which was indicative of immune response. The test results indicate that one cannot rely on a single factor to indicate the demise of AIDS. The usual HIV marker CD 4 initial and final are irrelevant. ISM suppression appears to be more critical than the destruction of HIV. AIDS was suppressed, any permanent damage that had been done to the patients in the course of their succumbing to AIDS was not obviously cured or corrected by said crystal device treatment, rather said injury persisted and the patient was improved with respect to AIDS but still suffered from said permanent injury or impairment previously inflicted.

TABLE I
__________________________________________________________________________
Response of AIDS Patients to Single 40 PPM Ag4O4 Inoculation

_________________________________________________________________________

As this invention may be embodied in several forms without departing from the spirit or essential characteristics thereof, the present embodiments are therefore illustrative and not restrictive, since the scope of the invention is defined by the appended claims rather than by the description preceding them, and all changes that fall within the metes and bounds of the claims or that form their functional as well as conjointly cooperative equivalents, are therefore intended to be embraced by these claims.

Low dosage Naltrexone aka LDN

2008-01-01T09:47:00.000+01:00

LDN improves T-Cells

The truth about the Rockefeller drug empire

2007-12-13T12:12:00.000+01:00

The Drug Story - by Hans RueschFrom David Icke's Medical Archive:

In the 30's Morris A. Bealle, a former city editor of the old Washington Times and Herald, was running a county seat newspaper in which the local power company bought a large advertisement every week. This account took quite a lot of worry off Bealle' s shoulders when the bills came due.

But according to Bealle' s own story, one day the paper took up the cudgels for some of its readers that were being given poor service from the power company, and Morris Bealle received the dressing down of his life from the advertising agency which handled the power company' s account. They told him that any more such "stepping out of line" would result in the immediate cancellation not only of the advertising contract, but also of the gas company and the telephone company.

That' s when Bealle' s eyes were opened to the meaning of a "free press" and he decided to get out of the newspaper business. He could afford to do that because he belonged to the landed gentry of Maryland, but not all newspaper editors are that lucky.

Bealle used his professional experience to do some deep digging into the freedom-of-the-press situation and came up with two shattering exposes - "The Drug Story", and "The House of Rockefeller." The fact that in spite of his familiarity with the editorial world and many important personal contacts he couldn't get his revelations into print until he founded his own company, The Columbia Publishing House, Washington D.C., in 1949, was just a prime example of the silent but adamant censorship in force in "the Land of the Free and the Home of the Brave".

[The Drug Story and The House of Rockefeller must have been published in 1949.]

Although "The Drug Story" is one of the most important books on health and politics ever to appear in the USA, it has never been admitted to a major bookstore nor reviewed by any establishment paper, and was sold exclusively by mail. Nevertheless, when we first got to read it, in the 1970s, it was already in its 33rd printing, under a different label - Biworld Publishers, Orem, Utah.Examples As Bealle pointed out, a business which makes 6% on its invested capital is considered a sound money maker.

Sterling Drug, Inc., the main cog and largest holding company in the Rockefeller Drug Empire and its 68 subsidiaries, showed operating profits in 1961 of $23,463,719 after taxes, on net assets of $43,108,106 - a 54% profit. Squibb, another Rockefeller-controlled company, in 1945 made not 6% but 576% on the actual value of its property.

That was during the luscious war years when the Army Surgeon General's Office and the Navy Bureau of Medicine and Surgery were not only acting as promoters for the Drug Trust, but were actually forcing drug trust poisons into the blood streams of American soldiers, sailors and marines, to the tune of over 200 million 'shots'.
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Is it any wonder, asked Bealle, that the Rockefellers and their stooges in the Food and Drug Administration, the US Public Health Service, the Federal Trade Commission, the Better Business Bureau, the Army Medical Corps, the Navy Bureau of Medicine and thousands of health officers all over the country, should combine to put out of business all forms of therapy that discourage the use of drugs."The last annual report of the Rockefeller Foundation", reported Bealle, "itemizes the gifts it has made to colleges and public agencies in the past 44 years [written in 1949?], and they total somewhat over half a billion dollars.

These colleges, of course, teach their students all the drug lore the Rockefeller pharmaceutical houses want taught. Otherwise there would be no more gifts, just as there are no gifts to any of the 30 odd colleges in the United States that don' t use therapies based on drugs."Harvard, with its well-publicized medical school, has received $8,764,433 of Rockefeller's Drug Trust money, Yale got $7,927,800, Johns Hopkins $10,418,531, Washington University in St. Louis $2,842,132, New York's Columbia University $5,424,371, Cornell University $1,709,072, etc., etc."

And while "giving away" those huge sums to drug-propagandizing colleges, the Rockefeller interests were growing to a world-wide web that no one could entirely explore. Already well over 30 years ago it was large enough for Bealle to demonstrate that the Rockefeller interests had created, built up and developed the most far reaching industrial empire ever conceived in the mind of man. Standard Oil was of course the foundation upon which all of the other Rockefeller industries have been built.

The story of Old John D., as ruthless an industrial pirate as ever came down the pike, is well known, but is being today conveniently ignored. The keystone of this mammoth industrial empire was the Chase National Bank, now renamed the Chase Manhattan Bank.Not the least of its holdings are in the drug business. The Rockefellers own the largest drug manufacturing combine in the world, and use all of their other interests to bring pressure to increase the sale of drugs. The fact that most of the 12,000 separate drug items on the market are harmful is of no concern to the Drug Trust...The Rockefeller Foundation

The Rockefeller Foundation was first set up in 1904 and called the General Education Fund. An organization called the Rockefeller Foundation, ostensibly to supplement the General Education Fund, was formed in 1910 and through long finagling and lots of Rockefeller money got the New York legislature to issue a charter on May 14, 1913.It is therefore not surprising that the House of Rockefeller has had its own "nominees" planted in all Federal agencies that have to do with health. So the stage was set for the "education" of the American public, with a view to turning it into a population of drug and medico dependents, with the early help of the parents and the schools, then with direct advertising and, last but not least, the influence the advertising revenues had on the media-makers.

A compilation of the magazine Advertising Age showed that as far back as 1948 the larger companies in America spent for advertising the sum total of $1,104,224,374, when the dollar was still worth a dollar and not half a zloty. Of this staggering sum the interlocking Rockefeller-Morgan interests (gone over entirely to Rockefeller after Morgan' s death) controlled about 80 percent, and utilized it to manipulate public information on health and drug matters - then and even more recklessly now.Censorship"Even the most independent newspapers are dependent on their press associations for their national news," Bealle pointed out, "and there is no reason for a news editor to suspect that a story coming over the wires of the Associated Press, the United Press or the International News Service is censored when it concerns health matters.

Yet this is what happens constantly."In fact in the '50s the Drug Trust had one of its directors on the directorate of the Associated Press. He was no less than Arthur Hays Sulzberger, publisher of the New York Times and as such one of the most powerful Associated Press directors.It was thus easy for the Rockefeller Trust to persuade the Associated Press Science Editor to adopt a policy which would not permit any medical news to clear that is not approved by the Drug Trust "expert", and this censor is not going to approve any item that can in any way hurt the sale of drugs.

This accounts to this day for the many fake stories of serums and medical cures and just-around-the-corner breakthrough victories over cancer, AIDS, diabetes, multiple sclerosis, which go out brazenly over the wires to all daily newspapers in America and abroad. Emanuel M. Josephson, M.D., whom the Drug Trust has been unable to intimidate despite many attempts, pointed out that the National Association of Science Writers was "persuaded" to adopt as part of its code of ethics the following chestnut: "Science editors are incapable of judging the facts of phenomena involved in medical and scientific discovery.
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Therefore, they only report 'discoveries' approved by medical authorities, or those presented before a body of scientific peers."This explains why Bantam Books, America's biggest publisher, made a colossal mistake in its initial enthusiasm and optimism sending review copies of SLAUGHTER OF THE INNOCENT to the 3,500 "science writers" on its list, instead of addressing them to the literary book reviewers who are not subject to medical censorship. One single censor decreed NO and SLAUGHTER OF THE INNOCENT sank in silence.
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Thus newspapers continue to be fed with propaganda about drugs and their alleged value, although according to the Food and Drug Administration (FDA) 1.5 million people landed in hospitals in 1978 because of medication side effects in the US alone, and despite recurrent statements by intelligent and courageous medical men that most pharmaceutical items on sale are useless at best, but more often harmful or deadly in the long run.

The truth about cures without drugs is suppressed, unless it suits the purpose of the censor to garble it. Whether these cures are effected by Chiropractors, Naturopaths, Naprapaths, Osteopaths, Faith Healers, Spiritualists, Herbalists, Christian Scientists, or MDs who use the brains they have, you never read about it in the big newspapers.
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To teach the Rockefeller drug ideology, it is necessary to teach that Nature didn't know what she was doing when she made the human body. But statistics issued by the Children's Bureau of the Federal Security Agency show that since the all-out drive of the Drug Trust for drugging, vaccinating and serumizing the human system, the health of the American nation has sharply declined, especially among children. Children are now given "shots" for this and "shots" for that, when the only safeguard known to science is a pure bloodstream, which can be obtained only with clean air and wholesome food. Meaning by natural and inexpensive means. Just what the Drug Trust most objects to.

When the FDA, whose officials have to be acceptable to Rockefeller Center before they are appointed, has to put an independent operator out of business, it goes all out to execute those orders. But the orders do not come directly from Standard Oil or a drug house director. As Morris Bealle pointed out, the American Medical Association (AMA) is the front for the Drug Trust, and furnishes the quack doctors to testify that even when they know nothing of the product involved, it is their considered opinion that it has no therapeutic value.

PersecutionWrote Bealle:
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"Financed by the taxpayers, these Drug Trust persecutions leave no stone unturned to destroy the victim. If he is a small operator, the resulting attorney's fees and court costs put him out of business. In one case, a Dr. Adolphus Hohensee of Scranton, Pa., who had stated that vitamins (he used natural ones) were vital to good health, was taken to court for 'misbranding' his product. The American Medical Association furnished ten medicos who reversed all known medical theories by testifying that 'vitamins are not necessary to the human body'. Confronted with government bulletins to the contrary, the medicos wiggled out of that one by declaring that these standard publications were outdated!"
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In addition to the FDA, Bealle listed the following agencies having to do with "health" - i.e., with the health of the Drug Trust to the detriment of the citizens - as being dependent on Rockefeller: US Public Health Service, U.S. Veterans Administration, Federal Trade Commission, Surgeon General of the Air Force, Army Surgeon General' s Office, Navy Bureau of Medicine & Surgery, National Health Research Institute, National Research Council, National Academy of Sciences.The National Academy of Sciences in Washington is considered the all-wise body which investigates everything under the sun, especially in the field of health, and gives to a palpitating public the last word in that science.

To the important post at the head of this agency, the Drug Trust had one of their own appointed. He was none other than Alfred N. Richards, one of the directors and largest stockholders of Merck & Company, which was making huge profits from its drug traffic.When Bealle revealed this fact, Richards resigned forthwith, and the Rockefellers appointed in his place the President of their own Rockefeller Institution, Detlev W. Bronk.

America's Medico-Drug Cartel

The medico-drug cartel was summed up by J.W Hodge, M.D., of Niagara Falls, N.Y., in these words:

"The medical monopoly or medical trust, euphemistically called the American Medical Association (AMA), is not merely the meanest monopoly ever organized, but the most arrogant, dangerous and despotic organisation which ever managed a free people in this or any other age. Any and all methods of healing the sick by means of safe, simple and natural remedies are sure to be assailed and denounced by the arrogant leaders of the AMA doctors' trust as fakes, frauds and humbugs."Every practitioner of the healing art who does not ally himself with the medical trust is denounced as a 'dangerous quack' and impostor by the predatory trust doctors. Every sanitarian who attempts to restore the sick to a state of health by natural means without resort to the knife or poisonous drugs, disease imparting serums, deadly toxins or vaccines, is at once pounced upon by these medical tyrants and fanatics, bitterly denounced, vilified and persecuted to the fullest extent."
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The Lincoln Chiropractic College in Indianapolis requires 4,496 hours, the Palmer Institute Chiropractic in Davenport a minimum of 4,000 60-minute classroom hours, the University of Natural Healing Arts in Denver five years of 1,000 hours each to qualify for a degree. The National College of Naprapathy in Chicago requires 4,326 classroom hours for graduation. Yet the medico-drug cartel spreads the propaganda that the practitioners of these three "heretic" sciences are poorly trained or not trained at all - the real reason being that they cure their patients without the use of drugs. In 1958, one of those "ill-trained" doctors, Nicholas P. Grimaldi, who had just graduated from the Lincoln Chiropractic College, took the basic science examination of the Connecticut State Board along with 63 medics and osteopaths. He made the highest mark (91.6) ever made by a doctor taking the Connecticut State Board examination
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Rockefeller' s various "educational" activities had proved so profitable in the U S. that in 1927 the International Educational Board was launched, as Junior' s own, personal charity, and endowed with $21,000,000 for a starter, to be lavished on foreign universities and politicos, with all the usual strings attached. This Board undertook to export the "new" Rockefeller image as a benefactor of mankind, as well as his business practises. Nobody informed the beneficiaries that every penny the Rockefellers seemed to be throwing out the window would come back, bearing substantial interest, through the front door.Rockefeller had always had a particular interest in China, where Standard Oil was almost the sole supplier of kerosene and oil "for the lamps of China". So he put up money to establish the China Medical Board and to build the Peking Union Medical College, playing the role of the Great White Father who has come to dispense knowledge on his lowly children. The Rockefeller Foundation invested up to $45,000,000 into "westernizing" (read corrupting) Chinese medicine.

Medical colleges were instructed that if they wished to benefit from the Rockefeller largesse they had better convince 500 million Chinese to throw into the ashcan the safe and useful but inexpensive herbal remedies of their barefoot doctors, which had withstood the test of centuries, in favor of the expensive carcinogenic and teratogenic "miracle" drugs Made in USA, which had to be replaced constantly with new ones, when the fatal side-effects could no longer be concealed; and if they couldn't "demonstrate" through large- scale animal experiments the effectiveness of their ancient acupuncture, this could not be recognized as having any "scientific value". Its millenarian effectiveness proven on human beings was of no concern to the Western wizards.But when the Communists came to power in China and it was no longer possible to trade, the Rockefellers suddenly lost interest in the health of the Chinese people and shifted their attention increasingly to Japan, India and Latin America.
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"No candid study of his career can lead to other conclusion than that he is victim of perhaps the ugliest of all passions, that for money, money as an end. It is not a pleasant picture.... this money-maniac secretly, patiently, eternally plotting how he may add to his wealth.... He has turned commerce to war, and honey-combed it with cruel and corrupt practices.... And he calls his great organization a benefaction, and points to his church-going and charities as proof of his righteousness. This is supreme wrong-doing cloaked by religion. There is but one name for it - hypocrisy."
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This was the description Ida Tarbell made of John D. Rockefeller in her "History of the Standard Oil Company", serialized in 1905 in the widely circulated McClure's Magazine. And that was several years before the "Ludlow Massacre", so JDR was as yet far from having reached the apex of his disrepute. But after World War II it would have been hard to read, in America or abroad, a single criticism of JDR, nor of Junior, who had followed in his father' s footsteps, nor of Junior' s four sons who all endevoured to emulate their illustrious forbears. Today's variousencyclopedias extant in public libraries of the Western world have nothing but praise for the Family. How was this achieved?Ironically, the two apparently most NEGATIVE events in the career of JDR brought about a huge POSITIVE change in his favor, to a degree that he himself could not foresee.

To wit:In the year when according to the current Encyclopaedia Britannica (long become a Rockefeller property and transferred from Oxford to Chicago), Rockefeller had "retired from active business", namely in 1911, he had been convicted by a US court of illegal practices and ordered to dissolve the Standard Oil Trust, which comprised 40 corporations. This imposed dissolution was to provide his Empire with added might, to a degree that was unprecedented in the history of modem business. Until then, the Trust had existed for all to see - an exposed target. After that, it went underground, and thereby its power was cloaked in security, and could keep expanding unseen and therefore unopposed.

The second apparently negative experience was a certain 1914 event that persuaded JDR, until then utterly contemptuous of public opinion, to gloss over his own image."The Ludlow Massacre"The United Mine Workers had asked for higher wages and better living conditions for the miners of the Colorado Fuel and Iron Company, one of the many Rockefeller-owned companies.The miners - mostly immigrants from Europe' s poorest countries - lived in shacks provided by the company at exorbitant rent. Their low wages ($1.68 a day) were paid in script redeemable only at company stores charging high prices. The churches they attended were the pastorates of company-hired ministers; their children were taught in company-controlled schools; the company libraries excluded books that the Bible-thumping Rockefellers deemed "subversive", such as "Darwin' s Origin of the Species."

The company maintained a force of detectives, mine guards, and spies whose job it was to keep the camp quarantined from the danger of unionization.When the miners struck, JDR, Jr., then officially in command of the company, and his father' s hatchet man, the Baptist Reverend Frederick T. Gates, who was a director of the Rockefeller Foundation, refused even to negotiate. They evicted the strikers from the company-owned shacks, hired a thousand strike-breakers from the Baldwin-Felts detective agency, and persuaded Governor Ammons to call out the National Guard to help break the strike.

Open warfare resulted. Guardsmen, miners, their women and children, who since their eviction were camping in tents, were ruthlessly killed, until the frightened Governor wired President Wilson for Federal Troops, who eventually crushed the strike, The New York Times, which then already could never be accused of being unfriendly to the Rockefeller interests, reported on April 21, 1914."A 14-hour battle between striking coal miners and members of the Colorado National Guard in the Ludlow district today culminated in the killing of Louis Tikas, leader of the Greek strikers, and the destruction of the Ludlow tent colony by fire."And the following day:
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"Forty-five dead (32 of them women and children), a score missing and more than a score wounded is the known result of the 14- hour battle which raged between state troops and coal miners in the Ludlow district, on the property of the Colorado Fuel and Iron Company, the Rockefeller holding. The Ludlow is a mass of charred debris, and buried beneath it is a story of horror unparalleled in the history of industrial warfare. In the holes that had been dug for their protection against rifle fire, the women and children died like trapped rats as the flames swept over them. One pit uncovered this afternoon disclosed the bodies of ten children and two women."
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The worldwide revulsion that followed was such that JDR decided to hire the most talented press agent in the country, Ivy Lee, who got the tough assignment of whitewashing the tycoon' s bloodied image.When Lee learned that the newly organized Rockefeller Foundation had $100 million lying around for promotional purposes without knowing what to do with it, he came with a plan to donate large sums - none less than a million - to well-known colleges, hospitals, churches and benevolent organizations.

The plan was accepted. So were the millions. And they made headlines all over the world, for in the days of the gold standard and the five cent cigar there was a maxim in every newspaper office that a million dollars was always news.That was the beginning of the cleverly worded medical reports on new "miracle" drugs and "just-around-the-corner breakthroughs" planted in the leading news offices and press associations that continue to this day, and the flighty public soon forgot, or forgave, the massacre of foreign immigrants for the dazzling display of generosity and philanthropyfinanced by the ballooning Rockefeller fortune and going out, with thunderous press fanfare, to various "worthy" institutions.
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The Purchase of Public Opinion:

In the following years, not only newsmen, but whole newspapers were bought, financed or founded with Rockefeller money. So Time Magazine, which Henry Luce started in 1923, had been taken over by J.P. Morgan when the magazine got into financial difficulties. When Morgan died and his financial empire crumbled, the House of Rockefeller wasted no time in taking over this lush editorial plum also, together with its sisters Fortune and Life, and built for them an expensive 14-story home of their own in Rockefeller Center - the Time & Life Building.Rockefeller was also co-owner of Time's "rival" magazine, Newsweek, which had been established in the early days of the New Deal with money put up by Rockefeller, Vincent Astor, the Harrimann family and other members and allies of the House.
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For all his innate cynicism, JDR must have been himself surprised to discover how easily the so-called intellectuals could be bought. Indeed, they turned out to be among his best investments.By founding and lavishly endowing his Education Boards at home and abroad, Rockefeller won control not only of the governments and politicos but also of the intellectual and scientific community, starting with the Medical Power - the organization that forms those priests of the New Religion that are the modern medicine men. No Pulitzer or Nobel or any similar prizeendowed with money and prestige has ever been awarded to a declared foe of the Rockefeller system.Henry Luce, officially founder and editor of Time Magazine, but constantly dependent on House advertising, also distinguished himself in his adulation of his sponsors.
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JDR's son had been responsible for the Ludlow massacre, and an obedient partner in his father' s most unsavory actions. Nonetheless, in 1956 Henry Luce put Junior on the cover of Time, and the feature story, soberly titled "The Good Man", included hyperboles like this:

"It is because John D. Rockefeller Junior's is a life of constructive social giving that he ranks as an authentic American hero, just as certainly as any general who ever won a victory for an American army or any statesman who triumphed in behalf of U.S. diplomacy."
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Clearly, Time's editorial board wasn't given the choice to change its tune even after the passing of Junior and Henry Luce, since it remained just as dependent on House of Rockefeller advertising. Thus, when in 1979 one of Junior's sons, Nelson A. Rockefeller died - who had been one of the loudest hawks in the Vietnam and other American wars, and was personally responsible for the massacre of prisoners and hostages at Atticia prison - Time said of him in it obituary, without laughing: "He was driven by a mission to serve, improve and uplift his country.

"Perhaps it was all this that Prof. Peter Singer had in mind when telling the judges in Italy that the Rockefeller Foundation was a humanitarian enterprise bent on doing good works. One of their best works seems to be sponsoring Prof. Peter Singer, the world's greatest animal friend and protector who claims that vivisection is indispensable for medical progress and for more than 20 years refuses to mention that legions of medical doctors are of the opposite view.
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Millions of Dollars Free Publicity. Another interesting revelation in the article of Time was that many years ago already Singer "was pleasantly surprised when Britannica approached him to distill in about 30,000 words the discipline that is, at its heart, the systematic study of what we ought to do." So now we touch the subject of sponsorisation and patronage. They don' t always mean immediate cash but, more important, long-term profits.Many decades ago the Encyclopedia Britannica moved from Oxford to Chicago because Rockefeller had bought it to add much needed lustre to the University of Chicago and its medical school, the first one he had founded.

Source: http://www.davidicke.net/medicalarchives/conspiracy/drugstory.html

1990: In the Fall of 1990, two medical researchers, Drs.William Lyman and Steven Kaali Patent AIDS Cure

2007-12-13T10:10:00.000+01:00

In the Fall of 1990, two medical researchers, Drs.William Lyman and Steven Kaali, working at Albert Einstein College of Medicine in New York City made an important discovery. They found that they could inactivate the HIV virus by applying a low voltage direct current electrical potential with an extremely small current flow to AIDS infected blood in a test tube. Initially, they discovered this in the lab by inserting two platinum electrodes into a glass tube filled with HIV-1 (type 1) infected blood.

They applied a direct current to the electrodes and found that a current flow in the range of 50-100 microamperes (uA) produced the most effective results. Practically all of the HIV viral particles were adversely affected while normal blood cells remained unharmed. The viral particles were not directly destroyed by the electric current, but rather the outer protein coating of the virus was affected in such a way as to prevent the virus from producing reverse transcriptase, a necessary enzyme needed by the virus to invade human cells.

Reverse transcriptase allows the virus to enter a human T cell line (called CEM-SS) and commandeer the DNA reproduction machinery. After using the host cell to reproduce itself into thousands of new virii, the swollen host cell (now called syncytia or giant cell) will burst and spew the contents into the bloodstream or lymph system. This is how the virus spreads, but lacking reverse transcriptase, the HIV virus can't invade the host cell and it becomes vulnerable to destruction by the body's immune system. (The details of this experiment can be read from Kaali's patent application.)

A brief announcement of this discovery appeared in The Houston Post (Mar 20, 1991), then in Science News (Mar. 30, 1991 pg. 207) and later in Longevity magazine: (Dec.1992 pg. 14). Following their work in the Fall of 1990, Kaali and Lyman presented their findings at the First International Symposium on Combination Therapies (an AIDS conference) in Washington DC on March 14th, 1991. Kaali outlined two methods for treating an AIDS patient with this new therapy: One method involved removing a small amount of blood, electrifying it and then returning it to the patient's body. The second method involved sewing a miniature electrifying power supply along with two tiny electrodes directly into the lumen of an artery. For long term treatment, the mini electrifying unit needed to be removed and relocated to a new artery site after 30-45 days since scar tissue and calcification forming around the implant unit would lead to artery blockage. Kaali (along with co-inventor Peter Schwolsky) filed for a patent on this implantable electrifying device on Nov 16, 1990 and nine months later was granted patent #5,139,684 on August 18, 1992.

It's interesting to note two things here:

1. In order to obtain a patent from the United States Patent Office, Kaali and Schwolsky had to prove that the device works as claimed. Lacking solid proof, US patents are simply not granted.
2. Very often it takes years to obtain a patent, yet this patent was granted in only nine months; a further indication to me of the strength of their demonstrated claims

It's also interesting to note that other than the 3 publications mentioned above and the March '91 AIDS conference, nothing again appeared in print, radio, or TV about this important discovery as a potential treatment and cure for AIDS from Kaali and company. Most knowledgeable observers feel that Kaali and Lyman's discovery was intentionally suppressed following the March '91 AIDS conference presentation.

If AIDS research was on the level and not the sham that it actually is, this should have made front page news around the world. (Around 1999, I was contacted by a woman with AIDS who had managed to reach Dr. William Lyman over the phone. She asked him about his experiments with Kaali regarding blood electrification and if she could obtain the treatment through them. Lyman denied any knowledge of any AIDS treatment or cure. He said he never heard of Dr. Kaali and he had no idea what she was talking about concerning blood electrification and then hung up on her. What does that tell about the power of the people behind the suppression of this discovery?)

Ken Adachi, http://educate-yourself.org/cn/LymanKaalibiocompatibleHIV1996report18nov06.shtml