Shedding Light on the Dishonorable Record of Dr. Anthony Fauci – A Real Mengele

- By F. William Engdahl - August 11, 2020

Dramatic political and social decisions are being made across the United States and around the world on what emergency quarantine measures and other steps must be taken. In many cases the radical and severe measures, such as shutting down the world economy, are being justified by COVID-19 case projections of morbidity into the future. If there is one person who is the face of the current strategy of dealing with the coronavirus in Washington it is the Director of the US National Institute for Allergy and Infectious Diseases (NIAID) of the NIH, Dr. Tony Fauci. What major media conveniently leave out in discussing Fauci’s role is his highly controversial and conflicted history since he first joined NIAID in 1984 during the beginnings of the AIDS panic. His role then sheds valuable light on his remarkable and highly controversial actions today.

Tony Fauci, a leading member of the White House Coronavirus Task Force, is being promoted by major US media such as CNN, MSNBC or the New York Times as the great expert on all related to the Covid19 outbreak. He had dismissed the President’s efforts to promote a known malaria medication as treatment for severe corona patients as “anecdotal,” even though seven years before he backed the same drug. He has publicly taken projections from an institute created in Washington State by the Gates Foundation, the same foundation that virtually owns the WHO and owns major stakes in the leading vaccine makers, to claim that up to 200,000 Americans could die from COVID19. Fauci stated that COVID19 is “probably about 10 times more lethal than the seasonal flu,” which would mean 300-600,000 coronavirus deaths this year, at the same time in a respected medical journal he compared Covid-19 as similar to seasonal flu in morbidity. When questioned how long the shutdown of much of the US economy must last, Fauci replied only when there is zero new covid19 positive tested cases, something impossible given the defective testing. He has also backed direct human tests of novel vaccines with no prior animal tests, including with radical non-tested mRNA gene-edited vaccines.

Fauci has more influence over US national policy on the unprecedented Covid-19 pandemic than anyone, including the President. Much of media treats him with awe as an unimpeachable scientist, one of the world’s finest. A closer look at Anthony Fauci’s career gives a starkly different picture, a very alarming one in fact.

America’s AIDS Czar

Tony Fauci has held the top post at the NIAID in Washington for an astonishing 36 years. Today he is well past retirement age at 79, and holds the funds to determine which drug companies or university researchers will get precious government funds or not from NIAID’s annual $5 billion budget.

Let’s go back to 1984 when Fauci was named head of NIAID during the Reagan era. That year an AIDS researcher, Robert Gallo, working under Fauci, held a press conference to announce that he had “discovered” the AIDS virus. He said it was HIV- human immunodeficiency virus. The shocking announcement which went around the world, was in complete disregard of scientific procedures of prior peer-reviewed published scientific evidence, including the required electron microscope analyses. It was a case of “science by press conference” as a critical scientist, Prof. Peter H. Duesberg described it. Duesberg was an award-winning researcher at Berkeley who isolated the first cancer gene through his work on retroviruses in 1970, and mapped the genetic structure of these viruses.

For Gallo and Fauci, that was unimportant as millions in research funds flowed into NIAID to research the new virus, HIV. Fauci and Gallo claimed that AIDS was highly contagious, also by sexual transmission, especially among homosexual men. Notably, before the Gallo claim to have found the HIV AIDS virus, NIAID had been doing research on the role of drugs, poppers or nitrites, proven immune-suppressants, in the deaths of the earliest AIDS patients. That was quickly dropped in favor of researching a “cure” for AIDS. Media was told that AIDS was the “public health threat of the Century.” Gallo went on to make millions on his patented blood test for HIV, despite the fact that the test was often giving false positives and did not test directly for the alleged virus but for active antibodies, something immunology practice said was not valid, as antibodies merely suggested a past infection response and not necessarily presence of AHIV. At this time in the 1980’S Fauci was responsible for AIDS research at NIAID, a post he still holds.

False Tests?

The issue of HIV/AIDS tests is central. While a frightened world was clamoring for a test, Gallo and Fauci promoted their deeply flawed tests of antibodies. In 2006 Gallo claimed, “HIV tests were highly accurate from the time they were developed in 1984 and have become much more accurate over time…” Highly accurate in 1984 but more accurate than highly over time? Gallo added in response to criticism, “A PCR test for the presence of the virus itself can accurately determine a child’s HIV status.”

In a sharp rebuttal of the Gallo claims, claims endorsed by Fauci and the NIAID as well as CDC, Roberto A. Giraldo, MD and Etienne de Harven, MD, the scientist who produced the first electron micrograph of a retrovirus, pointed out that both the ELISA and Western blot, and a genetic test, the PCR or ‘Viral Load’ test,” the two major tests used to determine if one has AIDS, are invalid. “None of these tests detect the HIV virus itself, nor do they detect HIV particles.” They add that there are “more than 70 different documented conditions that can cause the antibody tests to react positive without an HIV infection.” Among the false positive cases are influenza, the common cold, leprosy or the existence of pregnancy. The same tests are used today to determine SARS-CoV-2-positive.

They concluded,

“The fact that after 25 years of intense research HIV has been neither isolated nor purified in terms of classical virology indicates to us that the infectious view of AIDS as a contagious viral disease is based on an apparently non-existent microbe!”

Giraldo and de Harven declared, “The alleged existence of HIV was asserted from the study of proteins, reverse transcriptase activity (RT), and RNA fragments that were found in culture supernatants, not from the direct analysis of purified viral particles.” The CDC requires a positive antibody test for HIV to determine AIDS in the USA. Yet in Africa since 1985 the WHO requires no HIV test or any other laboratory test. Merely the patient’s symptoms that can include weight loss, chronic diarrhea, prolonged fever, persistent cough and such, symptoms endemic to chronic poverty, malnutrition and lack of sanitation.

Yet this fraud has shaped the career of Tony Fauci for more than 35 years. Fauci as head of NIAID has taken millions from the Bill & Melinda Gates Foundation as well as the Clinton Foundation along with tens of billions from US taxpayers for this bogus research. Suspiciously, the 2006 article by Giraldo and de Harven was suddenly retracted by the journal in 2019 just before the coronavirus Wuhan outbreak.

Despite the fact that he knew the established rules of virology, Fauci, as head of NIAID, recommended the Burroughs Wellcome chemotherapy drug, AZT as a “preventive drug” for HIV diagnosed patients even without symptoms! Burroughs Wellcome gave NIAID the study that was deliberately biased for AZT. Fauci even backed AZT for pregnant women despite the grave risk to the fetus. One mark of pregnancy in all women is a higher level of antigens as the natural immune system fights any infection to protect the fetus. AZT or Retrovir, a failed leukemia drug, has been proven to be a highly toxic drug. It was approved for AIDS testing in a record 5 days by Fauci and the US Government in 1987. Today despite more than thirty years funded research and billions of dollars, no effective vaccine for HIV/AIDS exists.

Fauci and Gilead

According to people who have studied the role of Tony Fauci as head of NIAID, his focus has been what is called scientific reductivism, described as “a 19 Century-style, single-germ theory for a complex web of factors that collapsed the immune systems of a subset of gay men in the early 1980s.” He has refused to explore the documentation that a variety of lethal drugs and other toxins such as nitrites could play a role. As a result he has wasted tens of billions of taxpayer dollars since 1984 on dead end experiments. One of his most nefarious was his collaboration with Gilead Sciences.

Not satisfied with having developed a false positive test for AIDS and having gained FDA fast-track approval for AZT to treat HIV-positive patients with serious illness symptoms, Fauci decided to collaborate with Gilead (as in the Biblical “balm of Gilead”) on what came to be called PrEP experiments.

Fauci promoted Truvada (AZT) as a prophylactic to the AIDS virus

Fauci in 2007 began to finance clinical trials of the AZT drugs in HIV “negatives,” on the theory the chemotherapy would “protect” them from becoming “positive.” That is, testing toxic HIV drugs on otherwise healthy persons to “insure” they never got AIDS. If it sounds mad, it was. Gilead supplied the drug, Truvada, to NIAID between 2007-2012 for Phase III human tests on HIV negative subjects. Four tests of at least 2,000 and up to 5,000 test subjects each, were done. The project was called “pre-exposure prophylaxis” or “PrEP.” Healthy subjects were given doses of chemotherapy drug Truvada on the thesis it could prevent them from one day getting HIV-positive. CDC, in its May 2014 recommendation urged physicians to prescribe Truvada for negatives in the so-called “risk groups,” an official government imprimatur for an extremely profitable drug.

The FDA ignored two of the four Truvada tests that had failed and been halted. Despite that and owing to data manipulation by Fauci’s NIAID and Gilead, the FDA approved the dangerous Truvada for PrEP. Today Gilead lists the side effects of Truvada: Kidney problems, including kidney failure; worsening Hepatitis B; too much lactic acid in your blood (lactic acidosis), which can lead to death; severe liver problems, which can lead to death; bone problems. They state that Truvada “can help reduce the risk of getting HIV-1 through sex, when taken every day and used together with safer sex practices.”

The Fauci-Gilead scam of promoting Truvada for healthy people to “reduce risk” of HIV is a marker for the level of medical malpractice and in some cases evident criminal abuse of human health that the current White House coronavirus guru, A. Fauci, represents.

Fauci and COVID-19

In October, 2019 Fauci and his NIAID got $100 million from the Gates Foundation to develop “gene-based” therapies for HIV and sickle cell disease. That means at the time of the first claims of novel coronavirus in Wuhan China, Fauci was still promoting a 35-year fraud around HIV. Fauci is also part of the Gates Foundation cabal. In 2012 Fauci was named one of the five Leadership Council of the Gates Foundation-created Global Vaccine Action Plan.

This is highly relevant to his role today as the Trump Administration coronavirus “pope.” Has his NIAID or any other laboratory in the world rigorously, with electron microscopy, isolated and purified samples of patients tested SARS-CoV-2 positive for Covid-19? Or are the virus proofs as faulty as Fauci and the AIDS clique have made for HIV?

In addition NIAID is working with Gilead to conduct Phase II human trials on Gilead’s drug, remdesivir, as a potential treatment for hospitalized adult patients diagnosed with COVID-19.

A Coincidence?

Relevant also is the fact that all top scientific advisers to the US President’s Task Force on COVID-19 are tied since decades to the bogus and destructive HIV/AIDS research and propagation of false theories. Alongside Tony Fauci of NIAID stands Deborah L. Birx, M.D., Obama appointee as US Global AIDS Coordinator who worked under Tony Fauci at NIAID from 1983-1986.
Dr. Deborah Birx

Robert Redfield is the current Director of the Centers for Disease Control and Prevention, center of the recent coronavirus testing scandal. Redfield cofounded with the discredited Robert Gallo, former Fauci colleague in the AIDS scandals of the early 1980’s at NIH, the Institute of Human Virology based at University of Maryland. Redfield and Birx also coauthored numerous scientific articles on purported HIV vaccines, none of which have been effective.

Dr. Robert Redfield, director of the Centers for Disease Control and Prevention

Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history.

F. William Engdahl is strategic risk consultant and lecturer, he holds a degree in politics from Princeton University and is a best-selling author on oil and geopolitics, exclusively for the online magazine “New Eastern Outlook.”



AIDS Can't be Sexually Transmited - David-Rasnick-PhD (AIDS-HIV Hoax)

The phrase "Acquired Immune Deficiency Syndrome (AIDS)" was coined by the U.S. Military referring to highly malnutrition people suffering from lack of proper nutrition, not having good enough foods to eat in war zones, during banker's wars for profit.

AIDS is and has always been a hoax, a big lie to kill people for profit to make billions by the corrupt, commission collecting doctors in private practice, the evil pharmaceutical companies executives, staff doctors and scientists, in close cooperation with U.S. terrorist Government officials; known as the "shadowy and or deep state, warmongering evil people".

There are many fabricated mythical diseases; AIDS is the most profitable of them all. The other highly profitable disease, but easily curable using fresh, green cannabis is cancer.

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Beauty To Die For: Health Hazards of Cosmetics And Skin Care Products

Health Hazards of Cosmetics And Skin Care Products

- By Leigh Erin Connealy, M.D.

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Your medicine cabinet is one of the most dangerous areas of your house, and not for the reasons you may think. Lurking just behind your bathroom mirror, where all of your favorite beauty products are housed, is a virtual toxic nightmare. The growing list of synthetic ingredients manufacturers add to their products is turning the most innocent-looking shampoos and moisturizers into cocktails of toxins that could cause cancer or reproductive damage over years of sustained use. Modern cosmetics contain a host of dangerous ingredients, which would be more at home in a test tube than in our bodies.

Like most people, you probably assume that the ingredients found in beauty products have been thoroughly tested for safety well before they land on your grocery store's shelves. After all, the government has regulations in place for the water we drink, the food we eat and the air we breathe. One would assume that the FDA would also be overseeing the cosmetic industry to ensure the health and safety of consumers. Unfortunately, the FDA has little power when it comes to regulating the ingredients found in your beauty products. In fact, the only people ensuring the safety of personal care products are the very people who govern the industry: The Cosmetic Toiletry and Fragrance Association (CTFA). Scientists paid by the CTFA make up the Cosmetic Ingredient Review panel (CIR) and are charged with regulating the safety of the industry's products.

In 2004, the Environmental Working Group (EWG) released the findings of a study it conducted regarding the safety of beauty care products. Comparing approximately 10,000 ingredients found in 7,500 different products against lists of known and suspected chemical health hazards, the research revealed that the CIR was falling tragically short of ensuring consumer safety.

Of the 7,500 products tested by the EWG, a mere 28 had been evaluated for safety by the CIR. The EWG found that one in every 120 products analyzed contained ingredients certified by the government as known or probable carcinogens and that nearly one-third of the products contained ingredients classified as possible carcinogens. Astoundingly, 54 products even violated recommendations for safe use that the CIR had put in place, yet these products are still available for sale today.

Of the products tested, the worst offenders were those containing the cancer-causing ingredients coal tar, alpha hydroxy acids and beta hydroxy acids, and those containing the hormone-disrupting ingredient, phthalate.

Coal Tar

Seventy-one hair dye products evaluated were found to contain ingredients derived from coal tar (listed as FD&C or D&C on ingredients labels). Several studies have linked long-time hair dye use to bladder cancer, non-Hodgkin’s lymphoma and multiple myeloma.

A research study conducted in 2001 by the USC School of Medicine found that women using permanent hair dye at least once a month more than doubled their risk of bladder cancer. The study estimates that "19 percent of bladder cancer in women in Los Angeles, California, may be attributed to permanent hair dye use."

A link between hair dye and non-Hodgkin's lymphoma was established in 1992 when a study conducted by the National Cancer Institute found that 20 percent of all cases of non-Hodgkin’s lymphoma may be linked to hair dye use.

While the FDA has not stepped in to prevent the use of coal tar in beauty products, it does advise consumers that reducing hair dye use will possibly reduce the risk of cancer.

Alpha Hydroxy Acids (AHA) & Beta Hydroxy Acids (BHA)

Alpha Hydroxy Acids and Beta Hydroxy Acids are commonly used in products advertised to remove wrinkles, blemishes, blotches and acne scars. With consumer complaints of burning, swelling and pain associated with AHA and BHA flooding into the FDA, the regulatory body began conducting its own research about 15 years ago. The findings linked the use of AHA and BHA with a doubling of UV-induced skin damage and a potential increased risk of skin cancer.

According to the Environmental Protection Agency, skin cancer has reached "epidemic proportions," with 1 million new cases occurring each year and one person dying every hour from the disease. The agency estimates that, at the current rate, one in five people will develop skin cancer over their lifetime.

The FDA's study findings were presented to the CIR, but the panel approved the continued use of AHA and BHA "in spite of serious safety questions submitted by a consumer group and a major manufacturer," according to an FDA spokesperson.

Even though one out of every 17 products analyzed by the EWG study contained either AHA or BHA (with nearly 10 percent being moisturizers and 6 percent sunscreens), the most that the FDA could do was suggest that products containing the ingredients carry a warning to use sunscreen and to limit sun exposure while using the product. A puzzling solution, since some of the products containing the dangerous ingredient are designed specifically for use in the sun.

Phthalates

Phthalates are industrial plasticizers widely used in personal care products to moisturize and soften skin, impart flexibility to nail polish after it dries and enhance the fragrances used in most products. Studies indicate that phthalates cause a wide range of birth defects and lifelong reproductive impairments, targeting every organ in the male reproductive system and causing problems ranging from low sperm count to serious genital deformities that can lead to an increased risk of cancer.

While the EWG only found four products with phthalate listed as an ingredient (all nail care products), there is no telling how many products actually contain it. The industry is not required to list fragrance ingredients or "trade secret" ingredients on products, and phthalates often fall into one of those two categories.

In September 2004, the European Union implemented a ban on all beauty products containing phthalates. California Assemblywoman Judy Chu has proposed a similar bill (AB 908) to be voted on later this year that would implement the same ban in the United States. Opponents of the bill, mainly the CTFA, argue that changing labeling processes would present a huge economic burden and could infringe on trade secrets. A similar bill failed just last year.

Four Steps of Action

1. Go to www.ewg.org and check out the health risks of your favorite products. EWG has compiled a guide of 7,500 beauty care products and has ranked them according to their ingredients' potential to cause cancer, trigger allergic reactions, interfere with the endocrine (hormonal) system, impair reproduction or damage a developing fetus.

2. Visit the FDA's website at www.fda.gov and familiarize yourself with the steps that you can take in order to file complaints or concerns about consumer products.

3. Visit www.safecosmetics.org to learn more about how you can become involved with bill AB 908 to ban phthalates in beauty products in the United States.

4. Check out my recommendations for all-natural and safe products for both you and your family at www.scmedicalcenter.com. All products mentioned have been used safely and with wonderful results by my patients for years.

Dr. Connealy, M.D., M.P.H., began private practice in 1986. In 1992, she founded South Coast Medical Center for New Medicine where she serves as medical director. Her practice is firmly based in the belief that strictly treating health problems with medications does not find the root cause of the illness. Dr. Connealy writes monthly columns for Coast and OC Health magazines, and is a bi-weekly guest on Frank Jordan's "Healthy" radio show. She routinely lectures and educates the public on health issues.

http://www.NaturalNews.com/

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