A 1972 report (Bulletin 47) issued by the World Health Organization referred to an immune virus requested which would selectively destroy the Human T Cell System, to be distributed in conjunction with a Nationwide vaccination program “to observe the results”. This coincided precisely with the extensive Small Pox vaccination program in central Africa & Hepatitis B program (Africa & throughout the Americas etc)– shortly preceding the outbreak of Aids in Africa, America & elsewhere.

Note: The determining factor most common in Aids victims is the breakdown of the T Cell System in the body.  Just another disturbing coincidence.

Memoranda 47 – Virus-associated immunopathology: animal models and implications for human disease (Part 1)

Memoranda 47 – Virus-associated immunopathology: animal models and implications for human disease (Part 2)

“There is a blueprint, the 1971 research logic of the US Special (HIV) Virus program…a virus that only targets certain persons – as is evidenced by the epidemiology. Here is the final phase, the clinical trials. It was placed in the Small Pox vaccines that went to Africa. Every epidemiology that we have regarding the beginning of HIV & Aids shows that as Small Pox ended,

HIV & Aids began in mass in Africa. HIV and Aids began in mass in the late 1970’s as a result of the US Special Virus program and the complementation of that vaccine (Small Pox vaccine program in Africa) with this special virus (T-Cell disruptor component – authorized by Henry Kissinger) that shows the development of HIV over a period from 1962-1978.

How dare you have a Federal Virus program that precedes the greatest onslaught of murder in the history of the world, and you don’t want to acknowledge the program, and you certainly don’t want to review it. The people demand it. This Federal program lies at the heart of HIV & Aids and it needs to be reviewed.” Dr. Boyd Graves – formal testimony given shortly before his premature death

The Smoking gun of Aids: 1971 Flowchart / Federal Virus Program Commission – coordinates over 20,000 scientific papers and fifteen years of progress reports of a secret federal virus development program. * The epidemiology of Aids is an identical match to ‘research logic’ identified in the five section foldout. The joint US/USSR Project was run by Dr. Robert Galio.

“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.

A research program to explore the feasibility of this could be completed in approximately 5 years at a total cost of $10 million. It is a highly controversial issue  and there are many who believe such research should not be undertaken lest it lead to another method of massive killing of large populations.” Dr. Donald MacArthur: Department of Defense Appropriation Hearings/1970

‘The same technique that you make human T-cell leukemia virus from bovine leukemia virus is how you make human AIDS virus from bovine visna virus. And you take that virus and grow it in human tissue.

In 1978 a paper was published in which they were growing bovine visna virus in human tissue.And of course, that’s how you adopt that virus in human.

In that paper in 1978, which was published in The Journal of General Virology, for anybody who’s interested, said, “Is it possible, might it be, could it be that this virus is capable of producing either malignancy or a slow-virus disease of humans?”
 
And of course, what is the malignancy? The malignancy is Kaposi’s sarcoma, and of course the slow-virus disease of humans is AIDS.’ Dr. Robert Strecker, M.D.

Dr. Leonard Horowitz, one of the world’s preeminant vaccine researchers has just laid out a damning report implicating the CDC, WHO, numerous Vaccine manufacturers along with Government Agencies in collusion with The Rockefeller Trust, Rupert Murdoch & other Media, Real Estate & Medical Industry moguls – in a genocidal plot to use vaccines, in particular the H1N1 flu vaccine as a bio-weapon to deliberately sicken & depopulate the planet.

Excerpts from Affidafit: Dr. Len Horowitz Files Pandemic Charges Against Rockefeller Trust –

The Special Virus Cancer Program (SVCP) is undoubtedly linked to the origin of HIV/AIDS as evidenced by its documentation revealing HIV co-discoverer, Dr. Robert Gallo, and his employment with the National Cancer Institute overseeing Litton Bionetics’s contract (71-2025) “Investigation of Viral Carcinogenesis in Primates,” as “Project Officer.” This document relates to the Merck company SVCP contract (71-2059) “Oncogenic Virus Research and Vaccine Development,” directed by Dr. Maurice Hilleman.

The SVCP was speciously investigated in 2002 by the United States General Accounting Office (GAO-02-809R Origin of AIDS Virus), that concluded its fraudulent study in June 17, 2002. The investigation was forced by persecuted, and later incarcerated, Honorable Ohio Congressman, James A. Traficant, Jr.

Before his death, Dr. Hilleman, Merck’s vaccine division chief, stated that he brought the AIDS virus into North America in contaminated monkeys destined for vaccine research at Merck. This suppressed interview was posted by this affiant on You Tube where it is currently viewable. 

Litton Bionetics also exclusively administered the NCI’s facilities at Fort Detrick, Maryland at the time Litton supplied chimpanzees were used by the CDC, FDA, NIAID, and the Merck drug company to produce four subtypes of hepatitis B virus vaccines for testing on at least three known populations: 1. homosexual men in New York City, 2. African villagers in Zaire/Congo/Uganda, and 3. Willowbrook State School for mentally retarded children on Staten Island in New York. The latter studies were conducted under U.S Army contract with the New York University Medical Center’s Dr. Saul Krugman.

Thus, the leading HIV/AIDS institute in the US, the NIAID, directed by the leading American infectious disease official, HIV/AIDS czar, and leading swine flu vaccination proponent, Dr. Anthony Fauci, has grossly and criminally neglected compelling documents and solid science that indicts Merck, the FDA, CDC, and his own NIAID. The suppressed and neglected evidence proves the origin of the world’s deadliest plague, AIDS, was triggered by hepatitis B vaccinations advanced by this alliance between these defendants’ public and private enterprises.

Additional analysis of published genetic analyses concordant with this suppressed thesis and documented history of the SVCP, and related HIV activity, will prove to any reasonable person the NIAID played a central role in the aforementioned hepatitis B vaccine studies. (See: USDHEW Virology: Volume 4 — Control of Viral Infections. NIAID Task Force Report. Bethesda, MD: Public Health Service, NIH, 79-1834, 1979, p. 20; 65-78)’

‘Dr. Fauci is also co-patent holder on  ‘Immunologic enhancement with intermittent interleukin-2 therapy‘ described as being central to gene therapies and the future of “geneto-pharmaceuticals.” The Assignee on this patent is: The United States of America as represented by the Department of Health (Washington, D.C.)

“We might not ever get a vaccine for HIV.” Anthony Fauci, Director of NIAID/New England Journal Of Medicine

Regarding the history of IL-2, now in vaccine adjuvant, on Monday, Oct. 6, 2008, Dr. John Niederhuber, the director of the NCI, told Lawrence K. Altman of the New York Times that Dr. Gallo “was instrumental in every major aspect of the discovery of the AIDS virus.” He added: “Dr. Gallo discovered interleukein-2 (Il-2), an immune system signaling molecule, which was necessary for the discovery of the AIDS virus, serving as a coculture factor that allowed the virus to grow.” Dr. Fauci added to this,”There’s no doubt that Bob Gallo made enormous contributions to AIDS research, and if the Nobel rules allowed four recipients, Bob would belong in the group”.

‘I am aware that IL-2 is the “common denominator” among immune system functions, and can cause severe side effects. IL-2 has been recommended for adjuvants.  New research on Dr. Fauci’s IL-2 in the “proprietary” formula of swine flu vaccine adjuvants show IL-2 caused no benefit whatsoever stimulating the immune systems of 5,800 subjects at a cost of $85 million. CHIRON and taxpayers paid the tab. Yet, more money and time will be spent researching Drs. Fauci and Gallo’s darling drug.’ Dr. Leonard Horowitz

“In 1969 US Defense Dep’t requested and got $10 million to make the AIDS virus in labs as a political/ethnic weapon to be used mainly against Blacks. The World Health Organization started to inject AIDS-laced smallpox vaccine into over 100 million Africans (population reduction) in 1977. And over 2000 young white male homosexuals in 1978 with the hepatitis B vaccine through the Centers for Disease Control/New York Blood Center.” Dr. Robert Strecker M.D., Ph.D.

LITTON BIONETICS & THE BIRTH OF AIDS VIRUS: “During the past year [1970] macaques were inoculated at birth or in utero with the Mason-Pfizer monkey mammary virus, Epstein-Barr virus (EBV), Herpesvirus saimiri, and Marek’s disease virus. EB virus was given with immuno-stimulation and immuno-suppression (ALS, prednisone, imuran). Australian antigen [HB virus] was given to newborn African green monkeys.”

“[B]reeding and holding colonies were surveyed for antibody to EBV. All breeders were positive and their offspring contain maternal antibody for several months… [Moreover,] An RNA-dependent DNA polymerase, [the primary AIDS-linked enzyme] similar to that associated with RNA tumor viruses, was detected in human leukemic cells but not in normal cells stimulated by phytohemagglutinin. The enzyme was isolated, purified and concentrated 200-fold, making possible its further characterization and study in relation to the leukemic process in man.” Special Virus Cancer Program: Report

Dr. Robert Gallo, credited for co-discovering HIV in 1984, actually served as “Project Officer” for the NCI, overseeing Litton’s development and testing of various cancer-causing viruses. All of the money for this program was also administered by BIONETICS, the U.S. Army’s 6th top biological weapons developer at that time, and the NCI’s chief SVCP contractor and supplier of viruses, viral cell lines, monkeys and chimpanzees, used to generate carcinogenic infections, and then experiment with various vaccines in efforts to prevent and reverse the cancers these researchers created in their lab cultures and infected animals.

‘I thought it was just a coincidence until we studied the latest findings about the reactions which can be caused by Vaccinia. Now I believe the smallpox vaccine theory is the explanation to the explosion of Aids. In obliterating one disease, another was transformed.‘ Adviser to WHO, London Times interview, 05/11/87

“The link between the WHO program and the (Smallpox) epidemic is an interesting and important hypothesis. I cannot say that it actually happened, but I have been saying for some years that the use of live vaccines such as that used for smallpox can activate a dormant infection such as HIV.” Dr. Robert Gallo, M,D

“The (AIDS) epidemic did not begin in Africa. The first AIDS cases were uncovered in Manhattan in 1979. At that time there were no reported African cases. In fact, the AIDS epidemic in Africa did not begin until the autumn of 1982 at the earliest. There was no AIDS in America until the exact year the government began experimenting with gay men.” Dr. Alan Cantwell, MD

‘There is a close connection between the rise of genetic engineering & mixing of viruses in the early 1970s and the outbreak of HIV in the late 1970s. This connection persists in the form of the many unprecedented “emerging diseases” caused by “new viruses” that continue up to the present time. In 1970 the discovery of a cell enzyme, called “reverse transcriptase” by Howard Temin and David Baltimore, allowed molecular biologists to detect so-called retroviruses in some animal cancers. It was soon recognised that retroviruses could be found normally in the genes of many animal cells, and that scientists could manipulate these viruses to produce detrimental effects on the immune system.

In “species jumping” laboratory experiments, many viruses were transferred between different animal species and were also adapted to human cells.

The earliest AIDS cases in America can be clearly traced back to the time period when the hepatitis B experiment began at the New York Blood Centre. The Centre began injecting gay men with multiple doses of the experimental vaccine in November 1978. The inoculations ended in October 1979, less than two years before the official start of the epidemic. Most importantly, the vaccine was developed in chimpanzees – the primate now thought to contain the “ancestor” virus of HIV. Also downplayed is the Centre’s pre-AIDS connection to primate research in Africa and also to a primate centre in the New York City area. The final experimental vaccine was also made by Merck and the NIH from the pooled serum specimens of countless gay men who carried the hepatitis B virus in their blood.

Founded in 1965, LEMSIP was affiliated with New York University Medical Centre, where the first cases of AIDS-associated Kaposi’s sarcoma were discovered in 1979. NYU Medical Centre researchers were also heavily involved in the development of the experimental hepatitis B vaccine, and the Centre received government grants and contracts connected with biological warfare research beginning in 1969, according to Dr. Leonard Horowitz, author of Emerging Viruses: AIDS and Ebola (1996). In 1974 Prince, with the support of Aaron Kellner, President of the NYBC, moved the chimp hepatitis research to a new primate centre called Vilab II in Robertsfield, Liberia, in Africa. Chimps were captured from various parts of West Africa and brought to VILAB. The lab also prides itself by releasing “rehabilitated” chimps back into the wild. One cannot help but wonder if some of the purported “ancestors” of HIV in the African bush have their origin in chimpanzees held in African primate labs for vaccine and medical experimentation.

The hepatitis B experiment, which inoculated over 1,000 healthy gay men, was a huge success with 96% of the men developing antibodies again the hepatitis virus. This high rate of success could not have been achieved if the men were immunosuppressed, because immunosuppressed people do not easily form antibodies to the vaccine. The experiment was followed by similar hepatitis B experiments using gay men in Los Angeles, San Francisco, Chicago, Denver and St. Louis, beginning in March 1980 and ending in October 1981, the same year the epidemic became official. In the mid-1980s the many blood specimens donated by the gay Manhattan men during the experiment were retrospectively examined for HIV infection by researchers at the NYBC. It was determined that 6% of the specimens donated between 1978-1979 were positive for HIV. By 1984 (the end of the study period) over 40% of the men tested positive for HIV.

In 1994 it was reported that KS is actually caused by a new “herpes-8” virus. KS ((Kaposi’s sarcoma) cases were first discovered in the late nineteenth century; and before AIDS it was a rare form of cancer. Before AIDS, KS was a non-transmissible disease that was never seen in young American men. The finding of a new KS virus indicates that two different viruses (HIV & KS) were simultaneously introduced into gay men when AIDS began in the late 1970s. No rational explanation has been put forth for this bizarre occurrence; and how this “new” virus could cause a gay epidemic of KS has never been explained satisfactorily. Further complicating the “sole cause” of AIDS scenario is the recent discovery of tiny bacterial forms known as “mycoplasma.” Luc Montagnier believes these microbes are important infectious “co-factors” in the development of AIDS, although most AIDS researchers ignore mycoplasma.’ Dr. Alan Cantwell, MD

USC Sec. 1524/TITLE 50 – WAR AND NATIONAL DEFENSE: CHAPTER 32 (CHEMICAL AND BIOLOGICAL WARFARE PROGRAM)

‘The Secretary of Defense may enter into agreements with the Secretary of Health and Human Services to provide support for vaccination programs of the Secretary of Health and Human Services in the United States through use of the excess peacetime biological weapons defense capability of the Department of Defense.‘

UPDATE: A State-of-the-Art Aids Vaccine, grown in a genetically modified variant of diseased Green Monkey Simian virus SV40 is currently undergoing Clinical testing – ‘The researchers gave 24 healthy rhesus macaques a vaccine containing a genetically modified form of the virus, rhesus cytomegalovirus (CMV). In 13 of the monkeys, the vaccine appeared to offer protection against simian immunodeficiency virus (SIV), monkey equivalent of HIV. Of these 13, 12 monkeys were still protected one year on.’

Center for Comparative Medicine and Department of Medical Pathology Study, 09/02 – A recombinant rhesus cytomegalovirus expressing enhanced green fluorescent protein retains the wild-type phenotype and pathogenicity in fetal macaques:

Findings of Study: ‘To facilitate identification of rhesus cytomegalovirus (RhCMV)-infected cells, a recombinant virus expressing enhanced green fluorescent protein (EGFP), designated RhCMV-EGFP, was constructed. An expression cassette for EGFP under the control of the simian virus 40 (SV40) early promoter was inserted into the intergenic region between unique short 1 (US1) and US2 of the RhCMV genome by homologous recombination. RhCMV-EGFP exhibited comparable growth kinetics to that of wild-type virus in rhesus fibroblast cultures and retained its pathogenicity in monkey fetuses. Typical neurologic syndromes caused by CMV infection were observed in all fetuses experimentally inoculated with RhCMV-EGFP, as evidenced by sonographic and gross examinations. Systemic RhCMV infections were established in all fetuses, as viral antigen was detected in multiple organs and virus was isolated from fetal blood samples. The engineered viral genome was stable following rapid serial passages in vitro and multiple rounds of replication in vivo. Infected cells could be readily distinguished by green fluorescence both in tissue cultures and in the fetuses. In addition, EGFP (marker gene product) expression was detected in various cell types that were permissive to RhCMV infection, consistent with a broad tissue tropism of the SV40 promoter.’

Evasion of CD8+ T Cells Is Critical for Superinfection by Cytomegalovirus: ‘Cytomegalovirus (CMV) can superinfect persistently infected hosts despite CMV-specific humoral and cellular immunity; however, how it does so remains undefined. We have demonstrated that superinfection of rhesus CMV–infected rhesus macaques (RM) requires evasion of CD8+ T cell immunity by virally encoded inhibitors of major histocompatibility complex class I (MHC-I) antigen presentation. These findings demonstrate that US2-11 glycoproteins promote evasion of CD8+ T cells in vivo, thus supporting viral replication and dissemination during superinfection, a process that complicates the development of preventive CMV vaccines but that can be exploited for CMV-based vector development.‘

Note: Study 1 – ‘These results demonstrate that RhCMV can be successfully engineered without loss of wild-type replication and pathogenic potential. Further, the spectrum of cortical anomalies and the distribution of infected cells in the brain tissues indicated that RhCMV may have preferentially targeted immature neuronal cells.’ Study 2 – ‘Cytomegalovirus (CMV) can superinfect persistently infected hosts despite CMV-specific humoral and cellular immunity.’ Both these studies previously verified the link between viral replication of animal cell substrates & a heightened risk of resulting adventious agents (rogue neoplasms or cancer); including the inevitability of mutagenic viral strains (’pathogenic potential’).

Polio, Hepatitis & Aids
www.tetrahedron.org
www.originofaids.com

Aids Timeline
http://members.iimetro.com.au/~hubbca/aids.htm

Aids Cure: U.S. Patent #5676977 Dr. Boyd Graves discusses the origin of AIDS as well as the United States’ patented cure, all based on official government documentation.

Aids Special Virus Flow Chart
http://www.ubol.com/index_files/Page3884.htm

Aids Cover-up: In depth analysis
http://www.apfn.org/apfn/aids.htm

Professor Marco Ruggiero PhD on Aids related deaths from drug-induced cancers: Part 1

Professor Marco Ruggiero PhD on Aids related deaths from drug-induced cancers: Part 2

Professor Marco Ruggiero PhD on Aids related deaths from drug-induced cancers: Part 3

AFFADAVIT: Dr. Leonard Horowitz Files Pandemic Charges Against Rockefeller Trust
http://www.docstoc.com/docs/11851145/Affidavit-of-Leonard-G-Horowitz

Related Articles:

See VRM: The Autism Report

VRM Worldwide Autism Study
http://vaccineresistancemovement.org/?page_id=5463

VRM: The Problem With Vaccines Part 1
http://vaccineresistancemovement.org/?p=488

VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body
http://vaccineresistancemovement.org/?p=6097

VRM: Vaccine Clinic – A Concise Compendium To The Problem With Vaccines
http://vaccineresistancemovement.org/?p=6278

VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
http://vaccineresistancemovement.org/?p=6880

VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
http://vaccineresistancemovement.org/?p=7283

VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting Body
http://vaccineresistancemovement.org/?p=8787

VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body
http://vaccineresistancemovement.org/?p=8836

VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body
http://vaccineresistancemovement.org/?p=8847

VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus http://vaccineresistancemovement.org/?p=9431

VRM: The Rise of Mutagenic Viruses http://vaccineresistancemovement.org/?p=13124

VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460

VRM: The Flu Report http://vaccineresistancemovement.org/?p=9226

VRM: 5 Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642

VRM: Vaccine Ingredients
http://vaccineresistancemovement.org/?p=979

VRM: Family Charts Gradual Decline Of Daughter
http://vaccineresistancemovement.org/?p=3156

VRM: Health Matters Part 1
http://vaccineresistancemovement.org/?p=6719

VRM: Health Matters Part 2
http://vaccineresistancemovement.org/?p=6746%EF%BB%BF

VRM: Alternative Cancer Cures That Work
http://vaccineresistancemovement.org/?p=3729

VRM: Flu Death Statistics – WHO & The Big Lie http://vaccineresistancemovement.org/?p=784

VRM: Canada’s 2010-11 Flu Vaccine A Deadly Concoction http://vaccineresistancemovement.org/?p=5692

VRM: United States 2010-11 Flu Vaccine Afluria – Buyer Beware http://vaccineresistancemovement.org/?p=5271

VRM: Australian Vaccine Scandal http://vaccineresistancemovement.org/?p=3377

VRM: Pregnancy Tips
http://vaccineresistancemovement.org/?p=3270

VRM: The Vanishing Sperm Count
http://vaccineresistancemovement.org/?p=4639

VRM: Media Spin & Swine Flu Hysteria
http://vaccineresistancemovement.org/?p=2347

VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t & WHO – Cost To Taxpayers Exceeds 2.5 Billion
http://vaccineresistancemovement.org/?p=4969

VRM: Polio – United Nations & The Great Cull
http://vaccineresistancemovement.org/?p=4916

VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) http://vaccineresistancemovement.org/?p=10091

VRM: Weaponized Polio & The African Green Monkey Conundrum http://vaccineresistancemovement.org/?p=10727

VRM: Mandatory Vaccinations – How They Will Be Implemented http://vaccineresistancemovement.org/?p=11806

VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460  

VRM : Vaccine Industry Deception, Propaganda & Media Collusion
http://vaccineresistancemovement.org/?p=197

VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios
http://vaccineresistancemovement.org/?p=997

VRM: H1N1 Bio-weaponry Incorporated
http://vaccineresistancemovement.org/?p=884

VRM: Morgellons Syndrome & Chemtrails
http://vaccineresistancemovement.org/?p=839

VRM : Council On Foreign Relations 10/16/09- Major Influence on Government Vaccine Policy
http://vaccineresistancemovement.org/?p=1880

VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines
http://vaccineresistancemovement.org/?p=5935

VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario
http://vaccineresistancemovement.org/?p=5102

VRM : World Health Organization & Vaccine Manufacturers Implicated In Massive H1N1 Financial Scam Involving Kickbacks & Cover-ups
http://vaccineresistancemovement.org/?p=4610

VRM : Former Pharmaceutical Representative Gwen Olsen Exposes Systemic Industry Fraud
http://vaccineresistancemovement.org/?p=5920

VRM: Britain’s National Health Service – Criminal Syndicate Swindling Billions While Rapidly Destroying Health Care System
http://vaccineresistancemovement.org/?p=4986

VRM: UK Institutes Brand of Medical Martial Law With ‘Super-Vaccination’ Day
http://vaccineresistancemovement.org/?p=4986

VRM : The Awakening Has Begun
http://vaccineresistancemovement.org/?p=6469

VRM: Medical Martial Law In The US – Sleeping Giant Of Tyranny
http://vaccineresistancemovement.org/?p=5865

VRM : Multi-Virus Vaccine Quinvaxem Proving Deadly
http://vaccineresistancemovement.org/?p=5219

VRM: New Generation Cancer Vaccine Will Cause Infertility
http://vaccineresistancemovement.org/?p=5311

VRM: CDC-Gate Exposes A Trail of Fraud Behind Autism Studies
http://vaccineresistancemovement.org/?p=5743

VRM : Squaline – The Military Agenda Comes Home
http://vaccineresistancemovement.org/?p=1797

VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis.
http://www.blogtalkradio.com/empradio/2011/01/28/truth-to-power-thursday

VRM Live – 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk.
http://www.blogtalkradio.com/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday

VRM Live – 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis.
http://www.blogtalkradio.com/empradio/2010/09/24/truth-to-power-thursday

If you appreciate the efforts to bring this information forward do consider making a donation. Any amount, no matter how small will help enable me to carry on this invaluable research. See Paypal link on the VRM website (click on ‘Donate’ tab in upper right corner). Thank you all.