The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health

by Robert F. Kennedy Jr.

When the pandemic started, most of the other medical practices in the Detroit area shut down, Dr. David Brownstein told me. “I had a meeting with my staff and my six partners. I told them, ‘We are going to stay open and treat COVID.’ They wanted to know how. I said, ‘We’ve been treating viral diseases here for twenty-five years. COVID can’t be any different.’ In all that time, our office had never lost a single patient to flu or flu-like illness. We treated people in their cars with oral vitamins A, C, and D, and iodine. We administered IV solution outside all winter with IV hydrogen peroxide and vitamin C. We’d have them put their butts out the car window and shot them up with intramuscular ozone. We nebulized them with hydrogen peroxide and Lugol’s iodine. We only rarely used ivermectin and hydroxychloroquine. We treated 715 patients and had ten hospitalizations and no deaths. Early treatment was the key. We weren’t allowed to talk about it. The whole medical establishment was trying to shut down early treatment and silence all the doctors who talked about successes. A whole generation of doctors just stopped practicing medicine. When we talked about it, the whole cartel came for us. I’ve been in litigation with the Medical Board for a year. When we posted videos from some of our recovered patients, they went viral. One of the videos had a million views. FTC filed a motion against us, and we had to take everything down.” In July 2020, Brownstein and his seven colleagues ...

Suppression and censorship of early treatment cost lives. COVID is treatable, regardless of vaccines.

Leading doctors and scientists, including some of the nation’s most highly published and experienced physicians and front-line COVID specialists like McCullough, Kory, Ryan Cole, David Brownstein, and Risch believe that Dr. Fauci’s suppression of early treatment and off-patent remedies was responsible for up to 80 percent of the deaths attributed to COVID. All five doctors independently told me the same thing. The relentless malpractice of deliberately withholding early effective COVID treatments, of forcing the use of toxic remdesivir, may have unnecessarily killed up to 500,000 Americans in hospitals. Dr. Kory says so plainly: “Dr. Fauci’s suppression of early treatments will go down in history as having caused the death of a half a million Americans in the ICU.”

Cole points out that, “If you are under 70 years of age and have no severe preexisting illness, you can hardly die [from SARS-CoV-2 infection]. So, there is no fatality rate that can be reduced. . . . And for people who are elderly and have preexisting illness,” he adds, “as we know from Dr. Peter McCullough and his colleagues’ work, there are miraculously effective medicines to treat this virus so that the fatality rates go down another 70 to 80 percent, which means there is no ground for emergency use whatsoever. That’s a huge threat to the vaccine cartel and to remdesivir.”

illness.13 Since March 2020, when doctors first used IVM against COVID-19, more than 20 randomized clinical trials (RCTs) have confirmed its miraculous efficacy against COVID for both inpatient and outpatient treatment. Six of seven meta-analyses of IVM treatment RCTs completed in 2021 found notable reductions in COVID-19 mortality. The relevant studies “all showed significant benefit for high-risk outpatients,” says the eminent Yale epidemiologist Dr. Harvey Risch. The only studies where its performance was anything short of stellar were those that investigated its efficacy in patients in very late stages of COVID.

Vera Sharav points out that in a rational universe, a poison like remdesivir would have no hope of winning regulatory approval—unless, of course, the company could somehow distract attention from the overwhelmingly catastrophic scientific evidence by getting the world’s most powerful health official—the man who conducted the clinical trial—to pronounce the drug a “miracle cure” at a globally attended press conference while lounging on an Oval Office divan beside the president of the United States. Says Sharav, “What better free advertisement?”59 Sharav adds, “Dr. Fauci had a vested interest in remdesivir. He sponsored the clinical trial whose detailed results were not subject to the peer review he demanded for the drugs he regarded as rivals, like hydroxychloroquine and ivermectin. Instead of showing transparent data and convincing results, he did ‘science’ by fiat. He simply declared the disappointing results to be ‘highly significant,’ and pronounced remdesivir to be the new ‘standard of care.’ Fauci made the promotional pronouncement while sitting on a couch in the White House, without providing a detailed news release, without a briefing at a medical meeting, or peer review for publication in a scientific journal—as is the norm and practice, to allow scientists and researchers to review the data.”

Pfizer’s six-month clinical data for its COVID vaccine trials suggested that, while the vaccine would avert a single death from COVID-19, the vaccinated group suffered 4x the number of lethal heart attacks as the unvaccinated. In other words, there was no mortality benefit from the vaccines; for every life saved from COVID, there were four excess heart attack fatalities.34 Twenty people died of “all-cause mortality” among the 22,000 recipients in Pfizer’s vaccine group, versus only fourteen in the numerically comparable placebo group. (Pfizer was evidently so alarmed by the total number of deaths in its vaccine cohort that it omitted five of them from table S4, and only disclosed them in fine print buried in the body of its report.) That means there were 42.8 percent more deaths in the vaccine than in the placebo groups. Under FDA guidelines, researchers must attribute all injuries and deaths among the study group during clinical trials to the intervention (the vaccine) unless proven otherwise.35 Under this rule, the FDA must assume people who take the vaccine have a 42.8 percent increased risk of dying.

Dr. Fauci and President Biden, presumably with Dr. Fauci’s prompting, told Americans that 98 percent of serious cases, hospitalizations, and deaths were among the unvaccinated. This was a lie. Real-world data from nations with high COVID jab rates show the complete converse of this narrative; the resumption of infections in all those countries accompanied an explosion of hospitalizations, severe cases and deaths among the vaccinated! Mortalities across the globe, in fact, have tracked Pfizer’s deadly clinical trial results, with the vaccinated dying in higher numbers than the non-vaccinated. These data cemented suspicions that the feared phenomenon of pathogenic priming has arrived, and is now wreaking havoc.

Health workers have administered many billions of vaccines during the past thirty-two years, yet in just eight months, the COVID vaccines have injured and killed far more Americans than all other vaccines combined over three decades. VAERS data show the huge spikes—69.84 percent65—of deaths occurring during the two weeks after vaccination, 39.48 percent within 24 hours of the injections.66 According to CDC’s fatality data, a COVID vaccine is 98 times more likely to kill than a flu vaccine.67

A recent peer-reviewed study in the high-gravitas Elsevier journal Toxicology Reports found that COVID-19 vaccines kill more people in each age group than they save. According to that study the “best-case scenario” is five times the number of deaths attributable to each vaccination vs. those attributable to COVID-19 in the most vulnerable 65+ demographic.68 Similarly, a September 2021 analysis by a team of prominent scientists and mathematicians convened by Silicon Valley entrepreneur Steve Kirsch—of half a dozen population and surveillance system databases, including VAERS—using eight different independent methods, attributes 150,000 deaths to COVID vaccines in the United States since January 2020. Kirsch has offered a million-dollar reward for anyone who finds an error in this calculation.69,70 Kirsch’s study which found that the vaccines kill more people than they save in every age range was consistent with Pfizer’s six-month clinical trial finding that people who took the vaccine were more likely to die than people who didn’t take the vaccine (there were a total of twenty deaths in the people who took the vaccine vs. fourteen deaths in the people who didn’t take the vaccine).71

One of CDC’s bold deceptions is to hide vaccine mortalities in US data by counting all people as “unvaccinated” unless their deaths occur more than two weeks AFTER the second vaccine.75 (Ironically, CDC doubles down on this fraud by counting many of these vaccine deaths as COVID deaths.) In this way, CDC captures that wave of deaths that occurs after vaccination and attributes them all to “unvaccinated.” This is only one of many statistical chicaneries that the CDC employs to hide vaccine injuries and to stoke public fears of COVID.

The CDC utilized an even brassier canard to support President Joe Biden’s claim that 98 percent of vaccine hospitalizations and deaths were among the unvaccinated. In an August 5 video statement, CDC director Dr. Rochelle Walensky inadvertently revealed the agency’s principal gimmick for fabricating that statistic. Walensky sheepishly admitted that CDC included hospitalization and mortality data from January through June 2021 in its calculation.76 The vast majority of the US population were, of course, unvaccinated during that time frame, so it makes sense that almost all hospitalizations would therefore be only among the unvaccinated. This is simply because there were almost no vaccinated Americans during that time period! By January 1, only 0.4 percent of the US population had received a COVID shot.77 By mid-April, an estimated 37 percent had received one or more shots78 and as of June 15, only 43.34 percent were fully “vaccinated.”79 Using these data was therefore pretty blatant fraud. Of course, CDC never let on that it was foisting eight-month-old data on Americans, allowing us instead to believe that these were current hospitalization rates as of August. To compound this flimflam, CDC perpetuated an even more audacious hustle. CDC omitted the current (as of August) data related to hospitalizations from the Delta variant, which disproportionately hospitalized vaccinated individuals in those other countries for which we have more reliable data.

Pfizer’s clinical data predicted potentially fatal myocarditis in one in every 318 teens. Post-marketing data confirm astronomically high rates of myocarditis injuries. On October 1, 2021, a team of medical researchers and statisticians found that myocarditis rates reported in VAERS were significantly higher in teens than Pfizer had reported in its clinical data. According to the Vaccine Adverse Event Reporting System, there have been 7,537 cases of myocarditis and pericarditis reported following COVID vaccines,85 with 5,602 cases attributed to Pfizer.86 Some 476 of these reports occurred in children from 12 to 17 years old.87 According to an article in Current Trends in Cardiology, “Within eight weeks of the public offering of COVID-19 products to the 12–15-year-old age group, we found 19 times the expected number of myocarditis cases in the vaccination volunteers over background myocarditis rates for this age group.”88

before I published this book, in late October 2021, FDA made an extraordinary admission in a letter to Pfizer92 to explain the chronic underreporting of serious but common vaccine-induced injuries and deaths. FDA, at last, admitted that VAERS is worthless for detecting vaccine injuries. We have determined that an analysis of spontaneous postmarketing adverse events [VAERS reports] reported under section 505(k)(1) of the FDCA [Federal Food, Drug and Cosmetic Act] will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis. Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks. At best, this letter is a shocking acknowledgement that regulators have no way to assess whether their vaccines are killing and injuring more humans than they are helping. In any rational regulatory environment, FDA’s alarming admission would demand an instantaneous cessation of the vaccine rollout. Only Dr. Anthony Fauci can answer the question, “Why—given FDA’s stunning confession that America has no functional surveillance system—did HHS not immediately stop the COVID vaccine rollout?” The answer, of course, is that Dr. Fauci knows that America’s bought, brain-dead, and scientifically illiterate media will never force him to answer this query.

and Pfizer was scarcely better.96 The study appearing in The Lancet confirms that vaccine effectiveness against infection disappears so fast that it is ephemeral. The heavily powered study involved 3,436,957 Kaiser Permanente Southern California customers and compared infections and COVID-19-related hospital admissions of fully vaccinated to unvaccinated people over the age of twelve for up to six months.97 The researchers found that vaccine effectiveness against infection plummeted from 88 percent during the first month after double vaccination to 47 percent after five months. The researchers found vaccine effectiveness against Delta infection was 93 percent during the first month after double vaccination but dropped to 53 percent after four months.98 This information should sicken every doctor who has ever given one of these jabs to a trusting patient. It means that these products confer no benefits to individuals or society and their long-term costs are foreboding and largely unknown. How could this have happened?

This real-world evidence suggests that over the summer, the vaccines killed nine times as many 15- to 19-year-olds as COVID did—eighty-one versus nine. “If not,” asks Jones, “what are the other possible explanations, and how likely are they?” Teen deaths among 15- to 19-year-olds have increased by 47 percent in the UK since they started getting the COVID-19

As part of a broad propaganda agenda, they report—with seeming glee—the occasional COVID death among the unvaccinated. Illustratively, on September 10, 2021, an ABC affiliate in Detroit solicited stories on its Facebook page about unvaccinated people who had died from COVID. Instead, the network got something they did not want: more than 230,000 messages containing heartbreaking stories of injuries and deaths from vaccines. None of these communications were reporting deaths among the unvaccinated. Readers shared the post over two hundred thousand times in ten days.103

In July 2021, the CDC found that fully vaccinated individuals who contract the infection have as high a viral load in their nasal passages as unvaccinated individuals who get infected. This means the vaccinated are just as infectious as the unvaccinated. Another study from Indonesia supported this observation, noting that vaccinated individuals carry 251x the viral loads of Delta and other mutant variants than they did in the pre-vaccine era. Simply put, as Dr. Peter McCullough observed, “each vaccinated person is now a kind of Typhoid Mary for COVID, spreading concentrated viral loads of vaccine resistant mutants to vaccinated and unvaccinated alike.”104 CDC acknowledges that vaccinated individuals carry at least as many COVID germs in their noses as the unvaccinated.105 CDC cited this revelation to justify its August 2021 mask mandate.

“Of all tyrannies, a tyranny sincerely exercised for the good of its victims may be the most oppressive. It would be better to live under robber barons than under omnipotent moral busybodies. The robber baron’s cruelty may sometimes sleep, his cupidity may at some point be satiated; but those who torment us for our own good will torment us without end for they do so with the approval of their own conscience.” —C. S. Lewis

Spot on.

Eight US patents list Dr. Anthony Fauci as an inventor. However, NIAID, NIH, and GAO do not list any of them in their reports of active licensing despite the fact that Dr. Fauci has acknowledged collecting patent royalties on his interleukin-2 “invention.”22

How big is Dr. Fauci’s drug development enterprise? Since Dr. Fauci arrived at NIH, the agency has spent approximately $856.90 billion.24,25 Between 2010 and 2016, every single drug that won approval from the FDA—210 different pharmaceuticals— originated, at least in part, from research funded by the NIH.26 Following drug approval, Dr. Fauci continues to collaborate with his pharmaceutical partners on promoting and pricing and profiting from their new product. Over the decades since Dr. Fauci took over NIAID, the agency has formalized an elaborate process of negotiating against US taxpayers to allow Pharma to extract maximum profits back from NIAID’s germinated drugs. With NIAID’s help, the lucky pharmaceutical company walks the new drug through accelerated FDA approval. The CDC then sets obscene retail prices for these collaborative products in secretive negotiations. Such sweetheart deals—at taxpayer and consumer expense—and accelerated approvals can yield direct financial benefits to NIAID, to Dr. Fauci’s favored employees, and even to Dr. Fauci himself.27

The disparate treatment of patented versus less expensive off-patent COVID-19 drug treatments by federal health agencies clearly exposes Dr. Fauci’s historic bias for high-ticket patent medicines that favor extravagant pharmaceutical industry profits over public health.32

Under Dr. Fauci’s leadership, the commercial features of this partnership have eclipsed his agency’s mission to advance science. At NIAID, the Pharma tail now wags the public health dog. Dr. Fauci has done almost nothing to advance NIAID’s core obligation of researching the causes of the devastating explosions in epidemics of chronic allergic and autoimmune diseases that, under his tenure, have mushroomed to afflict 54 percent of children,35 up from 12.8 percent when he took charge of NIAID in 1984.36 While ignoring the explosion of allergic conditions, Dr. Fauci has instead reshaped NIAID into the leading incubator for new pharmaceutical products, many of which, ironically, profit from the cascading chronic disease pandemic.

Over the last fifty years at NIH, Dr. Fauci has played a leading role in Big Pharma’s engineered demolition of American health and democracy, working hand in glove with pharmaceutical companies to overcome federal regulatory obstacles and transform the NIH and NIAID into a single-minded vehicle for development, promotion, and marketing of patented pharmaceutical products, including vaccines and vaccine-like products. Most of us would like “America’s Doctor” to properly diagnose our illnesses using the best science, and then instruct us on how to get healthy. What if, instead of spending their entire budgets developing profitable pharmaceutical products, Dr. Fauci and the heads of other NIH institutes deployed researchers to explore the links between glyphosate in food and the explosion of gluten allergies, the link between pesticide residues and the epidemic of neurological diseases and cancers, the causal connections between aluminum and Alzheimer’s disease, between mercury from coal plants and escalating autism rates, and the association of airborne particulates with the asthma epidemic? What if NIH financed research to explore the association between childhood vaccines and the explosion of juvenile diabetes, asthma, and rheumatoid arthritis, and the links between aluminum vaccine adjuvants and the epidemics of food allergies and allergic rhinitis? What if they studied the impacts of sugar and soft drinks on obesity and diabetes, and the association between endocrine dis...

Great summary of the damage of his 50 year career at NIH/NIAID

Today CDC and NIAID promote the popular orthodoxy: that intrepid public health regulators, armed with innovative vaccines, played the key role in abolishing mortalities from these contagious illnesses. Both science and history dismiss this self-serving mythology as baseless. As it turns out, the pills, potions, powders, surgeries, and syringes of modern medicine played only a minor role in the historic abolition of infectious disease mortalities. An exhaustive 2000 study by CDC and Johns Hopkins scientists published in Pediatrics, the official journal of the American Academy of Pediatrics, concluded, “Thus vaccination does not account for the impressive declines in [infectious disease] mortality seen in the first half of the [20th] century . . . nearly 90 percent of the decline in infectious disease mortality among US children occurred before 1940, when few antibiotics or vaccines were available.”16 Similarly, a comprehensive 1977 study by McKinlay and McKinlay, formerly required reading in almost all American medical schools, found that all medical interventions, including vaccines, surgeries, and antibiotics, contributed only about 1 percent of the decline and at most 3.5 percent.17 Both CDC and the McKinlays attributed the disappearance of infectious disease mortalities not to doctors and health officials, but to improved nutrition and sanitation—the latter credited to strict regulation of food preparation, electric refrigerators, sewage treatment, and chlorinated water...

Vaccines and other interventions DID NOT cause the dramatic decrease in mortality from infectious diseases in the first half of the 20th century -- sanitation and nutrition did.

“The CDC increasingly needed a major epidemic” to justify its existence.23 According to Peter Duesberg, author of Inventing the AIDS Virus, the HIV/AIDS theory was salvation for American epidemic authorities.24 James Curran, the Chief of the CDC’s Sexually Transmitted Diseases unit, described the desperation among the public health corps in the early 1980s: “There was double-digit inflation, very high unemployment, a rapid military buildup and a threat to decrease all domestic programs, and this led to workforce cuts at the Public Health Service, and particularly CDC.”25 Nobel Laureate Kary Mullis similarly recalled the institutional desperation during the Reagan administration era. He said of the CDC: “They were hoping for a new plague. Polio was over. There were memos going around the agency saying, ‘We need to find the new plague’; ‘We need to find something to scare the American people so they will give us more money.’”26 NIH scientist Dr. Robert Gallo—who would become Dr. Fauci’s partner, coconspirator, and confidant—offered a similar assessment: “The CDC in Atlanta was under threat for reductions and even theoretically for closure.”27

Desperation at the CDC. HIV/AIDS was its savior

NIAID Director, Richard M. Krause, helped pioneer this new strategy in 1976, during Dr. Fauci’s first year at the agency. Krause was a champion of what he called “The Return of the Microbes” strategy,28 which sought to reinstate microbes to their former status as the feared progenitors of deadly diseases.

Prior to 1997, the FDA forbade pharmaceutical advertising on television, and the drug companies had not yet transformed television reporters into pharmaceutical reps. Journalists, in short, were still permitted to do journalism. Sixty Minutes aired a scathing segment in which Mike Wallace mercilessly exposed the corruption, incompetence, and cover-ups at HHS that led to the phony swine flu pandemic and the wave of casualties from NIH’s experimental vaccine.37 The scandal forced the resignation of CDC Director David Sencer for his role in concocting the phony pandemic and pushing the dangerous vaccine.38 NIAID chief Richard Krause quietly resigned in 1984, deeding his seat to his faithful deputy, Tony Fauci.39 In a poignant emblem of the ascending power of the pharmaceutical paradigm under Dr. Fauci’s stewardship, the Sixty Minutes report on the 1976 pandemic scandal is now largely scrubbed from the Internet. You can still view it on the Children’s Health Defense website.

Swine flu pandemic scam, bad vaccine, Guillan-Barre syndrome, Mike Wallace excoriates HHS and CDC over it on 60 Minutes

Fauci helped terrify millions into wrongly believing they were at risk of getting AIDS when they were not; emphasis in his statement is added to highlight the caveats and conditional language: The long incubation period of this disease, we may be starting to see, as we’re seeing virtually, as the months go by, other groups that can be involved, and seeing it in children is really quite disturbing. If the close contact of the child is a household contact, perhaps there will be a certain number of individuals who are just living with and in close contact with someone with AIDS or at risk of AIDS who does not necessarily have to have intimate sexual contact or share a needle, but just the ordinary close contact that one sees in normal interpersonal relationships. Now that may be farfetched in a sense that there have been no cases recognized as yet in which individuals have had merely casual contact, close or albeit with an individual with AIDS who for example have gotten AIDS. For example, there have been no cases yet reported of hospital personnel, who have fairly close contact with patients with AIDS. There have been no case reports of them getting AIDS; but the jury is still out on that because the situation is constantly evolving and the incubation period is so long, as you know. It’s a mean of about fourteen months, ranging from six to eighteen months. So what medical researchers and public health service officials will be—are concerned with is what we felt were the conf...

Fauci incorrrectly fearmongering about AIDS transmission

“Teflon Tony” The AIDS crisis’s best-known activist—and the most vocal critic of the NIH response—playwright Larry Kramer, may have been the first to make the cold assessment about Dr. Fauci’s winning capacity for combining charm and flattery with evasion, misdirection, and misinformation to bedazzle the media into suspending skepticism and overlooking his reliable incompetence. “The main reason that Fauci has gotten away with so much,” Kramer observed in 1987, “is that he’s attractive and handsome and dapper and extremely well spoken and he never answers your question.”68 Historians Torsten Engelbrecht, author of Virus Mania, and Konstantin Demeter call Fauci “Dr. Baron of Lies.”69

Why he is Teflon Tony

An elite cancer virologist brought over from Germany’s Max Planck Institute whose credentials are so outstanding, who was well on his way to solving cancer’s genetics . . . felled suddenly by a fatwah, issued by this . . . Mufti? Who was he to issue a fatwah against America’s top cancer virologist? Well, he did. He blocked every federal research dollar to Duesberg after 1987, because Duesberg repudiated the woke ideology Fauci’s HIV empire, in a few paragraphs of a scientific paper that was about something else. He sustained the economic and reputational attack/vendetta for the next 3 decades. Without blinking. It’s really an unbelievable story. It would make Americans’ blood boil if they knew about it—because almost all have lost somebody in their family to cancer. Fauci had, by 1987, when Duesberg wrote the Cancer Research paper that sealed his scientific fate, an apparatus that included mass media, psychological operations, public health—this octopus that just straight-up throttled the entire scientific tradition of Western civilization. Evidence based science and the discourse culture that goes with it— gone. That’s what he did. It’s no small feat. He destroyed American science by snuffing out its spirit, the spirit of open inquiry, proof and standards. The reason so many outstanding scientists lent their names to opposing Fauci’s vendetta on Duesberg was not that they cared, necessarily, about the cause of AIDS; This was, for them, a battle over the very soul of scien...

Fauci's vendetta against Duesberg and his destruction of science and research

That 2006 ACIP panel recommended two new blockbuster Merck shots: the Gardasil HPV vaccine for all girls ages nine through twenty-six,76 and three doses of a Merck rotavirus vaccine, Rotateq, for infants at ages two, four, and six months.77 Both Bill Gates78 and Tony Fauci (via NIAID)79 had provided seed and clinical trial funding for the development of both Gardasil and the rotavirus vaccine.80,81 Merck maintained it had not tested either vaccine against an inert placebo in pre-approval trials, so no one could scientifically predict if the vaccines would avert more injuries or cancers than they would cause. Nevertheless, the sister FDA panel, VRBPAC, approved Gardasil—to prevent cervical cancer—without requiring proof that the vaccine prevented any sort of cancer, and despite strong evidence from Merck’s clinical trial that Gardasil could dramatically raise risks of cancer and autoimmunity in some girls.82 ACIP, nevertheless, effectively mandated both jabs. Gardasil would be the most expensive vaccine in history, costing patients $420 for the three-jab series and generating revenues of over $1 billion annually for Merck.83 That year, nine of the thirteen ACIP panel members and their institutions collectively received over $1.6 billion of grant money from NIH and NIAID.

Gardasil HPV and rotavirus not cleared as safe yet deemed mandatory for young girls, and followed by huge research grants

Dr. Offit counsels his fellow PIs that lying is part of their job. He justifies any whopper that maximizes vaccine uptake. In 2017, Offit coached a group of fellow PIs, “You can never really say that MMR doesn’t cause autism but frankly when you get in front of the media you better get used to saying it because otherwise people hear a door being left open when a door shouldn’t be left open.”96 In his 2008 book, Autism’s False Prophets, Offit fabricated a conversation claiming that a vaccine safety advocate, J. B. Handley—a prominent Portland, Oregon, businessman with a severely autistic son—threatened one of Offit’s acolytes. Handley sued Offit for libel,97 forcing him to retract the statement, to publicly apologize for the fabrication, and to make a humiliating $5,000 donation to Jenny McCarthy’s autism charity.98 Despite such embarrassments, the mainstream media treat Offit’s most outlandish statements as gospel. Physicians rely upon the veracity of his pronouncements in making treatment decisions. Dr. Offit serves on the board of various pharma front groups99 and astroturf organizations100 and commands a vast network of bloggers and trolls, each of them directly or indirectly paid by the pharmaceutical companies to stifle debate, propagate lies, bully and intimidate the mothers of intellectually disabled children, silence scientific and medical dissent, and root out heresy. In 1998, Offit sat on the CDC’s ACIP Committee and participated in the debate that added rotaviru...

Dr Offitt the liar and shill for Pharma abou vaxx safety

From 1985 to 1991, prior to the introduction of the rotavirus vaccine, the rotavirus disease caused only 20–60 deaths per year nationwide, mainly due to dehydration associated with diarrhea.109,110 Since dehydration is easily treated, virtually all deaths from rotavirus are avoidable with timely and appropriate medical care. Reported adverse reactions from Dr. Offit’s RotaTeq vaccine range from 953 to 1,689 per year. These included fever, diarrhea, vomiting, irritability, intussusception, SIDS, severe combined immunodeficiency, otitis media, nasopharyngitis, broncho-spasm, urinary tract infection, hematochezia, seizures, Kawasaki disease, bronchiolitis, urticaria, angioedema, gastroenteritis, pneumonia, and death.111 The best evidence indicates that Dr. Offit’s rotavirus vaccine causes negative net public health impacts; in other words, Dr. Offit’s vaccine almost certainly kills and injures more children in the United States than the rotavirus disease killed and injured prior to the vaccine’s introduction. Finally, in 2010, after its introduction, NIH learned that Offit’s vaccine, RotaTeq, also contained the porcine retrovirus that causes an HIV-like syndrome called “wasting disease” in pigs.112 Neither Dr. Fauci nor any other agency has ever funded a study to establish the safety of injecting their dangerous pig retroviruses into babies. Millions of American children have now been inoculated with the virus, thanks to Offit. In 2006, ACIP added Offit’s vaccine to the sched...

PI Offit and his dangerous Rotateq vaxx that made him rich

All that changed in 2005, after I published an article, “Deadly Immunity,” about corruption in CDC’s vaccine branch, simultaneously in Rolling Stone and Salon. Newspapers thereafter generally refused to publish my articles on vaccine safety and ultimately banned me from publishing on any issues. In 2008, without consulting me or citing a specific reason, Salon retracted and removed my 2005 article. Salon’s founder, David Talbot, faulted Salon for caving in to Pharma. Rolling Stone finally removed the article without explanation in February 2021, and HuffPost purged all half-dozen of my vaccine articles. The editors of those online journals had thoroughly fact-checked my pieces prior to publication. They removed them without notice to me, and without ever explaining their decisions. It was the beginning of the mass censorship of any vaccine information that departs from official narratives. That year, universities and corporate hosts and municipal speakers’ forums suddenly cancelled my scheduled speeches in droves. My bookings dropped from sixty paid speeches per year down to one or two. My speakers’ bureau told me that floods of telephone calls from powerful members of the medical community had prompted the cancellations.

Censorship of vaxx safety problems begins for Kennedy and others

On May 31, 1988, Kramer wrote his famous “Open Letter to Tony Fauci” in the Village Voice. Kramer’s diatribe compared NIAID to the fraternity of miscreants, delinquents, and dimwitted knuckleheads in the comedy film Animal House. He called Dr. Fauci an “idiot” and a “murderer.” He described Fauci sweating and squirming under Representative Ted Weiss’s questioning: “You were pummeled into admitting publicly what some have been claiming since you took over some three years ago. You have admitted that you are an incompetent idiot.”62 Said Kramer, “You expect us to buy this bullshit and feel sorry for you? YOU FUCKING SON OF A BITCH OF A DUMB IDIOT, YOU HAVE HAD $374 MILLION AND YOU EXPECT US TO BUY THIS GARBAGE OF EXCUSES!”

Dr. Fauci’s Strategic Pivot Anthony Fauci needed a makeover, and this master of bureaucratic survival responded to his existential crisis with a breathtaking pivot. Suddenly, Dr. Fauci turned to embrace the AIDS activists he had previously reviled. In the summer of 1989, he accosted Larry Kramer on a Montreal street during an international AIDS conference, took him for a walk, effectively begged forgiveness, and proposed a working partnership.70 He began testing AIDS community drugs in parallel trials, as Senator Kennedy and amfAR had long requested. Dr. Fauci partnered with the AIDS doctors—the contemporary equivalents of Front Line COVID-19 healers Dr. Pierre Kory, Dr. Peter McCullough, Dr. Richard Urso, and Dr. Ryan Cole (among others)—giving them authority and millions of dollars to launch local Community Research Initiative (CRI) programs that allowed community AIDS clinics to test promising drugs outside the formal clinical trial programs dominated by Dr. Fauci’s Pharma PIs, and to quickly win federal approvals. “Fauci himself was now trying to build a system that consisted of greater access to drugs at a much earlier stage in the testing game,”71 said Nussbaum. In a gesture of reconciliation with his biggest critics, Dr. Fauci named the parallel track program after Senator Kennedy’s aide, Terry Beirn, and he gave Larry Kramer a seat at the table.

Most ironically, in light of his successful campaign to sabotage hydroxychloroquine and ivermectin during the COVID crisis, Dr. Fauci suddenly dropped his knee-jerk insistence that every drug needed randomized placebo-controlled testing prior to approval. In an extraordinary volte-face, he fiercely argued that if a drug looked promising for alleviating potentially lethal illness during pandemics, patients ought to be able to get access to it, even if it hadn’t been through a double-blind placebo trial. In a brassy display of chutzpah and brazenly hypocritical misdirection, he questioned the ethics of FDA regulators who insisted on placebo testing of beneficial drugs during a global pandemic when people were dying. He seemed to have forgotten that this was precisely his posture until just a few weeks before. Dr. Fauci accused the FDA of foot-dragging and overmanaging drug development. He openly attacked NIAID’s sister agency for its cruel and rigid insistence on randomized double-blind placebo testing for DHPG, a promising remedy for retinal herpes. In order to quiet the AIDS community, Tony Fauci even put AL 721 into trials. Dr. Fauci became a vocal cheerleader of “parallel track” approval of the retinue of popular buyers’ club drugs: “It doesn’t make any sense to deprive those people of the choice of whether or not they want to take a chance on a drug that has proven to be effective, as long as it doesn’t interfere with clinical trials. As a scientist, I think it’s an app...

AIDS activists afterward learned that at the same time Dr. Fauci was telling them and Senator Kennedy’s office that he was finally testing AL 721, Teflon Tony was confiding to his Pharma PIs that he had rigged the AL 721 studies to fail: “I wanted to debunk it,” he reassured them.76 Just as he would do with hydroxychloroquine during the COVID crisis thirty years later, he designed his AL 721 clinical trials in a way that would ensure their failure and thus discredit the unpatentable medicine. Dr. Fauci told the Burroughs Wellcome PIs who dominated his “independent” committee, “Let’s put the thing into trial and get it over with once and for all.”77 Nussbaum’s verdict: “If there was any chance for a fair test for AL 721, it wasn’t going to come from Tony Fauci’s clinical trials system.”78 At first, his devious plan backfired. Instead of debunking AL 721, the NIAID study confirmed that AL 721 stopped viral replication. When those promising results began emerging, Dr. Fauci and his PIs cancelled the trial, making sure that AL 721 never went to Phase 2. Dr. Fauci told skeptical activists that he could not get any volunteers to enroll in the study. (In 2021, he would invoke the same bunko to kill NIAID’s ivermectin trials.)

Nussbaum points out that even at the height of Dr. Fauci’s “conversion,” NIAID continued to ignore hundreds of other effective drugs for opportunistic diseases because “PIs have their own scientific agenda, which is not necessarily the same as the country’s.”80 Dr. Fauci’s whole charade ended the moment the FDA approved AZT. By then, Dr. Fauci had rigged the key committees that controlled drug approvals at NIH and FDA by stacking them with academic and industry scientists and doctors from his PI system: “Scientists who . . . made their entire careers in AZT . . . sat on committees voting on potential commercial competitors. Scientists who have had financial dealings with Burroughs Wellcome or other pharmaceutical companies have come to dominate the government’s entire clinical trials network.”81 While they actively stymied clinical trials for aerosolized pentamidine and AL 721, Dr. Fauci’s insider’s cabal greased the skids, allowing Burroughs Wellcome to skip animal testing and to proceed directly to human trials. This omission was unprecedented in the history of chemotherapy drugs, but again foreshadowed the decision to allow the Pfizer/BioNTech COVID-19 vaccine to proceed to human testing without completing the usual panel of safety testing in animal models.

In 1987, Dr. Fauci’s team declared the human study a success and terminated it after four months of a proposed six-month study—a record-setting speed for chemotherapy approval. That four-month observation period was far too short for researchers to detect side effects that would occur in patients taking AZT for years, or even a lifetime. But Dr. Fauci argued that his decision to abort the study was the only ethical choice: after sixteen weeks, nineteen trial subjects in the inactive placebo group and only one participant from the AZT group had died—an outcome that could be hailed as an extraordinary 95-percent efficacy! Dr. Fauci said that those results proved AZT safe and effective against AIDS. Even more importantly for Burroughs Wellcome shareholders, Dr. Fauci cleared AZT for use on healthy HIV-positive people, meaning people with no symptoms. Following those brief clinical trials, FDA granted AZT fast-tracked Emergency Use Approval in March 1987.

Gallo had trailblazed the technique of “science by press release” four years earlier, when he had staged an HHS press event to announce that the probable cause of AIDS had been found, a retrovirus that would later be named the “Human Immunodeficiency Virus” or “HIV.” The press reported Gallo’s discovery as scientific fact, even though Gallo had not published a peer-reviewed paper supporting his enormously consequential assertion. Here was a useful innovation that allowed regulatory officials to craft and control the public narrative from inception. The science was what the regulators declared it to be. There could be no opportunity for journalists to read the ambiguous data, consider contrary expert opinion, or second-guess official pronouncements. Dr. Fauci made himself the virtuoso of this technique, displaying it, at its apogee, during his April 28, 2020, announcement of remdesivir’s miraculous performance during NIAID’s rigged and fraud-tainted clinical trials, while seated on an Oval Office couch beside President Trump. He had no peer-reviewed or published study, no authentic placebo trial, no data, and not even a handout for the press. With this vague hearsay claim, he forced through Emergency Use Authorization for his darling drug and sold Gilead’s entire inventory to the president without publishing a word or ever leaving the sofa. Under Dr. Fauci’s leadership, this practice would become a routine vehicle for extreme abuse in the COVID-19 era, when vaccine companie...

In 1991, four years later, Lauritsen filed a Freedom of Information request asking for various FDA documents pertaining to the Phase II AZT trials—most importantly, the “Establishment Inspection Report” on the Boston center, written by FDA investigator Patricia Spitzig. After months of lies, evasions, and obstructions from the FDA, a courageous female FDA whistleblower breached all the stonewalling and saw to it that Lauritsen got the Spitzig Report.97 It was a bombshell: As it turned out, the Boston Principal Investigators (PIs) cheated on almost every patient. The Burroughs Wellcome PIs had quickly realized that AZT was so reliably deadly that they were hard-pressed to keep the trial recruits alive for the full six-month study. The Boston team solved this dilemma by lying about the length of time patients were in the trials. The company incentivized this sort of fraud by paying its PIs according to how many months they kept the AZT trial subjects alive. “Simply put,” says Lauritsen, “the doctors received a great deal more money,” from longer-term enrollments. Pharma PIs know that their careers and paychecks depend on their ability to consistently produce study outcomes that will win FDA approval for the subject drug. Such perverse incentives naturally drive research bias, confirmation bias, data tampering, strategic laziness, and deliberate falsification and cheating. PIs routinely covered up adverse events, violated protocols, falsely reported AZT patients as being plac...

Of those who got AZT, all suffered from its unspeakable toxicity. “A number of them . . . would very definitely have died from anemia,” had the PIs not given the blood transfusions to keep them alive, says Lauritsen. AZT causes anemia in every animal species ever studied, including human beings. In his book, Poisoned by Prescription, Lauritsen explains how “[p]atients taking AZT became anemic, and suffered low white blood cell counts accompanied by vomiting.” FDA’s documents showed that everyone in the AZT group suffered severe toxicities and anemia, yet NIAID’s official report listed no adverse effects among AZT recipients. Some of the AZT patients suffered adverse reactions so deadly that they needed multiple blood transfusions just to keep them alive. Dr. Fauci’s crooked researchers pumped these individuals with regular blood transfusions and then neglected to record their multiplicity of health problems. In the AZT group, thirty patients—over half the total—clung to life until the end of the study only with help from multiple blood transfusions. In each case the Boston PIs checked “no adverse reactions” on the CRFs. Some 20 percent received multiple transfusions. In the placebo group, on the other hand, only five patients received transfusions. “What happens when you get a blood transfusion?” asks noted AIDS researcher and author Dr. Robert E. Willner, MD, PhD. “You look better, you feel better, and you live a little bit longer.

Even in that innocent era, the United States mainstream media heavily censored journalistic criticism of Dr. Fauci and the corruption in the AZT studies. Most Americans were therefore unaware of any dissent from the AIDS orthodoxy. This was less true in Europe and the UK. On February 12, 1992, Channel 4 Television in London broadcast a documentary, “AZT: Cause for Concern.” Produced by Meditel, the film described the material from the FOIA documents, exposed the crooked AZT trials as rank fraud, and chronicled the terrible toxicities of the drug. The next day, the charity, Wellcome Foundation, divested itself of most of its stock in Wellcome Pharmaceuticals, the parent company of Burroughs Wellcome, the manufacturer of AZT. Burroughs Wellcome stocks plunged, and the company suffered a series of hostile takeovers by SmithKline Beecham and then by Glaxo. Millions around the world viewed the UK documentary, but neither it nor any of the Medical AIDS-critical documentaries have ever been broadcast in the US.102 AZT is the most toxic drug ever approved for long-term use. Molecular biologist Professor Peter Duesberg has explained AZT’s mechanism of action: It is a random terminator of DNA synthesis, the life process itself. Dr. Joseph Sonnabend stated simply: “AZT is incompatible with life.”

On January 27, 1988, NBC News broke the censorship blockade to broadcast the first of reporter Perry Peltz’s three-part exposé on the AZT Fischl trial.104,105 Peltz reported additional evidence of widespread tampering with the rules and the pervasive cheating, which she discovered had started on day one. Peltz learned that Fauci’s claim that the study was double-blind was a wholesale canard and reported that most volunteers knew who was on the drug and who wasn’t. Since everyone was desperate for the “miracle drug,” the volunteers on AZT admitted to sharing their drug with placebo group members. This practice assured that researchers would get no clean results from either cohort. Furthermore, Peltz learned both placebo and study subjects were taking other drug regimens they obtained by purchasing remedies from buyers’ clubs. Peltz was practicing understatement when she branded NIAID’s AZT experiments as “seriously flawed.”

By September of 2021, Dr. Fauci’s power to muzzle his critics had achieved a mastery over free expression unprecedented in human history. That month, with a single phrase, Dr. Fauci silenced pop icon Nicki Minaj after she questioned whether COVID vaccines might be causing problems involving testicular swelling. When CNN’s Jake Tapper asked him about Minaj’s claim, Dr. Fauci simply declared, “The answer to that, Jake, is a resounding no.”108 As usual, he cited no study to support this assertion. The vaccine manufacturers acknowledge that the products are not tested for effects on fertility.109 110 Nevertheless, based upon Dr. Fauci’s word alone, Twitter immediately evicted Minaj from its platform, censoring her communication with her 22 million followers. Pharma’s obedient attack dogs CNN, CBS, and NBC rushed on to the dog pile to defame and discredit the rapper and to assure the public that Minaj was wrong. Dr. Fauci, after all, had spoken!

By invoking the “people are dying argument” to rush through AZT’s licensing for healthy Americans, the FDA’s drug approval process was decimated. Farber told me “the idea that complying with the normal safeguards of the regulatory process and taking time to prudently study a drug for safety or efficacy was artfully conflated with murder.” In that sense, an unbroken devolution of FDA’s regulatory function leads from AZT to the fraud-fueled “Emergency use approvals” of remdesivir and the Moderna mRNA vaccine during the COVID pandemic. “The death blow to FDA’s safety function was AZT,” says Farber. “After that, any potentially deadly disease became an excuse for curtailing clinical trials. Death by medication was normalized as an inherent part of progress.” All those poisoned Americans were just unfortunate casualties in Little Napoleon’s noble war against the germs.

By 1991, Dr. Fauci had effectively abandoned testing low-profit repurposed drugs in the parallel track CRI program. But he used a parallel track to open a loophole in the FDA drug approval system, a loophole large enough to drive through truckloads of Pharma’s new high-profit patented antivirals.

The drug had so many debilitating and lethal side effects that FDA, in an uncharacteristic act of civil disobedience against NIAID’s diminutive dictator, issued a black box warning. Nevertheless, desperate HIV-infected Americans rushed like doomed lemmings to take the drug. In 2010, FDA issued a statement that ddI can cause potentially a fatal liver disease called non-cirrhotic portal hypertension.126 Even with its demonstrated toxicity, Dr. Fauci used CRI parallel-track process to bypass the usual controls, to win approval for use of ddI in pregnant mothers who test positive for HIV. A 2019 study [Hleyhel et al., Environ Mol Mutagen (2019)127] found that ddI accounted for 16 percent of prescriptions for infected mothers and 30 percent of the cancers in their children.

“On the surface of AIDS, what the public sees, is a benevolent exterior, devoted to ‘saving lives,’ of originally mostly gay men in the west, then, since they shifted the narrative, primarily Africans. A global apparatus now worth over $2 trillion and composed of more NGOs, more organizations than anybody could count, obliterates all dissent, all real language, history and truth,” says Celia Farber, author of Serious Adverse Events: An Uncensored History of AIDS. “It’s a Beast system, and Fauci created it. It’s not ‘capitalism,’ at all. It detests merit, standards, and all the values of Western Civilization. It uses the violence of the ‘woke’ economy to re-cast lies as truth, and to proudly crush and block any and all dissenting voices. It does this always in the name of ‘saving lives.’ Only now, with COVID, are Americans able to see Fauci’s cold, ruthless face behind the mask. Americans have tried to follow what that man has said for a year and a half now, and we who have been dealing with him for so long, we feel like: Welcome to our nightmare. Nothing he says makes sense, yet nobody stands over him, to reign him in. Tower of Babble. Americans are trying to make him into a benign figure, but more and more, they feel a sinking feeling. Is he a madman? Why can’t we understand what he is actually saying, what he means? This is very unsettling, when people are as afraid as people are now, since Covid.”