Fauci’s Fatal Mismanagement of the AIDS Epidemic

In chapters 3-6 of the The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health, Kennedy explores how Fauci fabricated and manipulated (for his own profit) the 1980s AIDS epidemic in the exact same way he has fabricated and manipulated the current plandemic. Then, as now, he promoted a faulty diagnostic test, he massively exaggerated the contagiousness and severity of AIDS, he caused tens of thousands of needless deaths by suppressing cheap and effective treatments, he aborted animal studies and Phase III human trials because “too many people were dying,” he falsified studies to promote AZT (because he owned shares in the company), and he shrewdly deflected criticism through misdirection and outright lies.

AZT was a failed (because it was far too toxic) cancer chemotherapy drug that Fauci enabled Burroughs-Wellcome to resurrect, at $10,000 per patient, to treat AIDS. Originally developed by the National Cancer Institute, AZT cost the drug company pennies per tablet to produce

Meanwhile Fauci’s agency, the National Institute of Allergy and Infectious Disease (NIAID) blocked FDA approval for cheap off-label medications for fatal AIDS complications, eg ribavirin, alpha interferon, DHPG, Peptide D, Foscarnet, Bactrim, Septra, and aerosol pentamidine.

When the study leading to FDA approval for Fauci’s drug AZT was finally published in 1987, independent analysis reveals that it was more fatal than AIDS at recommended doses.** During the study, researchers could only keep  some AZT patients alive by giving them repeated blood transfusions.

Chapters 5 and 6 mainly concern Fauci’s deliberate destruction of the career of renowned virologist and cancer researcher Dr Peter Duesberg for his extremely cogent critique of the hypothesis promoted by NIAID under Fauci’s leadership that HIV causes AIDS.

Credited as the worlds foremost retrovirologist, Duesberg found it highly improbable that a retrovirus such as HIV could be the sole cause of the total immune system breakdown found in AIDS. As Duesberg and other retrovirologists point out, retroviruses have always lived in a comfortable symbiosis with human beings. Eight to ten percent of our current DNA consists of retroviruses we have incorporated into our genetic material. Until the discovery of HIV, no retrovirus in 3 billion years ever developed the capacity to attack human cells, as HIV allegedly attacks the CD4 T-cell fundamental to cell-mediated immunity. Moreover neither Robert Gallo nor Luc Montaigner, the researchers who identified HIV as the cause of AIDS, could ever explain how a totally benign retrovirus could mysteriously mutate into a killer virus.

In my view, the two most likely alternative infectious agents Duesberg and others put forward for AIDS are the herpes virus HHV6 or some type of mycoplasma. HHV6 was first identified in 1986 the blood of AIDS patients and Chronic Fatigue Syndrome (which appeared in epidemic proportions in heterosexuals around the same time AIDS appeared in gays). Unlike HIV, HHV6 is a killer virus and attacks CD4 T-cells. Ironically even Gallo, the alleged US discoverer of HIV, acknowledged in 1988 that HHV6 could be a “co-factor” (with HIV) in causing AIDS.

A year earlier a Chinese investigator discovered a new mycoplasma (mycoplasma incognitis) in the brains, livers and spleens of AIDS patients that caused an AIDS-like illness when he injected it into monkeys. Despite wide international recognition of Dr Lo’s work, Fauci sidelined and/or disciplined every NIAID researcher who attempted to replicate his research.

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*Because the patent on these drugs had expired, the only potential funding for randomized controlled trials (RCT) was NIAID (drug companies won’t fund new RCTs on existing drugs once their patent expires). Fauci refused to authorize them.

**When the FDA halved the recommended dose, it stopped killing people.

Just to let people know I’m moving to Substack and Telegram after several readers informed me I’ve been censored from WordPress Reader feed. The link to my Substack account is https://stuartbramhall.substack.com/. The link to my Telegram channel is https://t.me/themostrevolutionaryact I’ll continue to publish on WordPress as long as I’m able, but if my blog suddenly disappears you’ll know where to find me.

Whistleblower: Vaccines, Retroviruses and Chronic Illness

A growing body of peer reviewed research suggests some link between the current childhood vaccination schedule and the development of a variety of chronic illnesses. A recent article by John P Thomas in Health Impact News discusses the various retroviruses that contaminate vaccines and human blood products and their possible role in the current epidemic of autism, chronic fatigue syndrome and other autoimmune, neuroimmune and neurodevelopmental disorders.

According to researcher Judy A. Mikovits PhD, approximately 6% of the U.S. population harbors retroviruses with the potential to develop into an acquired immune deficiency. Unlike traditional Acquired Immune Deficiency Syndrome (AIDS), these immune disorders are caused by non-HIV retroviruses.

Although 20 million Americans are likely to be infected, not everyone will develop serious illness. Retroviruses in the human body are like sleeping giants. They remain silent unless some external stress activates them. Once activated, they cause diseases such as Myalgic Encephalomyelitis, also called Chronic Fatigue Syndrome (ME/CFS), Chronic Lyme disease, Chronic Lymphocytic Leukemia, autism spectrum disorder (ASD), numerous cancers, and a wide range of other chronic disorders.

Mikovits, along with Kent Heckenlively JD, writes about the link between non-HIV retroviruses and these various disorders in their recent book Plague: One Scientist’s Intrepid Search for the Truth about Human Retroviruses and Chronic Fatigue Syndrome (ME/CFS), Autism, and Other Diseases.

The Early Link Between Polio and Yellow Fever Vaccine and Chronic Fatigue and Autism

The book reveals how the problem first began with trials of polio and yellow fever vaccines in the early 1930s. This is when the first recorded cases of Chronic Fatigue Syndrome and autism appeared. This was followed by several decades in which scientists were developing vaccines in the same laboratories that were injecting mice with different viruses to weaken their immune system. For many years they believed that human and mouse viruses couldn’t interact or travel from one part of the research facility to another. More recently, scientists have discovered that many many of these viruses and retroviruses can travel through the air and infect human beings.

The Discovery of Mouse Retroviruses in Patients with Autism and Chronic Fatigue

In 2006 Mikovits, an immunologist specializing in virology and epigenetics, was studying patients with autism and chronic fatigue syndrome when she discovered very high levels of XMRV (xenotropoic murine retrovirus) and related mouse retroviruses in their blood and tissue. She went on to discover similar elevated levels in Lou Gehrig’s Disease, treatment resistant Lyme disease, and Parkinson’s Disease.

Thomas’s excellent article, which is meticulously researched and documented, provides more detail about the various scientists who have raised concern over the years about pathogenic mouse viruses contaminating vaccines and blood products. In addition to elaborating on Mikovits’s specific research findings, it also details efforts by Big Pharma and the federal government to destroy her career in an effort to cover up the inadvertent exposure of 20 million Americans to pathogenic mouse retroviruses.*

Read more: Vaccines and Retroviruses: Whistleblower Reveals What Government is Hiding

 

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*According Mikovits, Intercept, a recent technology Cerus Corporation developed in 2014, enables vaccine makers and blood banks to cleanse pathogenic viruses and retroviruses from current vaccines and blood products. It does nothing to help the 20 million Americans who have already been infected and run the risk of transmitting pathogenic retroviruses through the exchange of bodily fluids (sex, breast milk and mother-to-infant transmission via the placenta).