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

by Robert F. Kennedy Jr.

“The first step is to give up the illusion that the primary purpose of modern medical research is to improve Americans’ health most effectively and efficiently. In our opinion, the primary purpose of commercially funded clinical research is to maximize financial return on investment, not health.” —John Abramson, M.D., Harvard Medical School

The CDC, for example, owns 57 vaccine patents1 and spends $4.9 of its $12.0 billion-dollar annual budget (as of 2019) buying and distributing vaccines.2,3 NIH owns hundreds of vaccine patents and often profits from the sale of products it supposedly regulates. High level officials, including Dr. Fauci, receive yearly emoluments of up to $150,000 in royalty payments on products that they help develop and then usher through the approval process.4 The FDA receives 45 percent of its budget from the pharmaceutical industry, through what are euphemistically called “user fees.”

Anthony Fauci seems to have not considered that his unprecedented quarantine of the healthy would kill far more people than COVID, obliterate the global economy, plunge millions into poverty and bankruptcy, and grievously wound constitutional democracy globally.

Under Dr. Fauci’s leadership, the allergic, autoimmune, and chronic illnesses which Congress specifically charged NIAID to investigate and prevent, have mushroomed to afflict 54 percent of children, up from 12.8 percent when he took over NIAID in 1984.59

By this decade’s end, obesity, diabetes, and pre-diabetes are on track to debilitate 85 percent of America’s citizens.

He regularly expressed his belief that post-infection immunity was highly likely (with occasional waffling on this topic) although he took the public position that natural immunity did not contribute to protecting the population. He supported COVID jabs for previously infected Americans, defying overwhelming scientific evidence that post-COVID inoculations were both unnecessary and dangerous.16,17 Under questioning on September 9, 2021, Dr. Fauci conceded he could cite no scientific justification for this policy.

CDC later admitted that only 6 percent of COVID deaths occurred in entirely healthy individuals. The remaining 94 percent suffered from an average of 3.8 potentially fatal comorbidities.24 Regulators misused PCR tests that CDC belatedly admitted in August 2021 were incapable of distinguishing COVID from other viral illnesses.

HHS’s own studies indicate that VAERS may be understating vaccine injuries by OVER 99 percent.29

Successive Gallup polling showed that the average Democrat believed that 50 percent of COVID infections resulted in hospitalizations. The real number was less than one percent.30

We could have easily defanged COVID-19 so that it was less lethal than a seasonal flu. We could have done this very quickly. We could have saved hundreds of thousands of lives.”

McCullough observes that, “We could have dramatically reduced COVID fatalities and hospitalizations using early treatment protocols and repurposed drugs including ivermectin and hydroxychloroquine and many, many others.”

Pulmonary and critical care specialist Dr. Pierre Kory agrees with McCullough’s estimate. “The efficacy of some of these drugs as prophylaxis is almost miraculous, plus early intervention in the week after exposure stops viral replication and prevents development of cytokine storm and entrance into the pulmonary phase,” says Dr. Kory. “We could have stopped the pandemic in its tracks in the spring of 2020.”

They point out that natural immunity, in all known cases, is superior to vaccine-induced immunity, being both more durable (it often lasts a lifetime) and broader spectrum—meaning it provides a shield against subsequent variants. “Vaccinating citizens with natural immunity should never have been our public health policy,” says Dr. Kory.

Risch, McCullough, and Kory are also among the hundreds of scientists and physicians who express shock that Dr. Fauci made no effort to identify repurposed medicines. Says Kory, “I find it appalling that there was no consultation process with treating physicians. Medicine is about consultation. You had Birx, Fauci, and Redfield doing press conferences every day and handing down these arbitrary diktats and not one of them ever treated a COVID patient or worked in an emergency room or ICU. They knew nothing.”

It’s difficult to identify anything they did that was right,” says McCullough.

“If this had been any other form of pneumonia, a respiratory illness, or any other infectious illness in the human body, we know that if we start early, we can actually treat much more easily than wait until patients are very sick.” McCullough says that the rule holds true for COVID-19:

results. By July 1, McCullough and his team had developed the first protocol based on signals of benefit and acceptable safety. They submitted the protocol to the American Journal of Medicine. That study, titled “The Pathophysiologic Basis and Clinical Rationale for Early Ambulatory Treatment of COVID-19,”51 quickly became the world’s most-downloaded paper to help doctors treat COVID-19. “It is extraordinary that Dr. Fauci never published a single treatment protocol before that,” says McCullough, “and that ‘America’s Doctor’ has never, to date, published anything on how to treat a COVID patient. It shocks the conscience that there is still no official protocol.

“We didn’t have a single academic institution come up with a single protocol,” said Dr. McCullough. “They didn’t even try. Harvard, Johns Hopkins, Duke, you name it. Not a single medical center set up even a tent to try to treat patients and prevent hospitalization and death. There wasn’t an ounce of original research coming out of America available to fight COVID—other than vaccines.” All of these universities are deeply dependent on billions of dollars that they receive from NIH.

Dr. Fauci’s challenge—to prove that HCQ is dangerous—was daunting because hydroxychloroquine is a 65-year-old formula that regulators around the globe long ago approved as both safe and effective against a variety of illnesses. HCQ is an analog of the quinine found in the bark of the cinchona tree that George Washington used to protect his troops from malaria. For decades, WHO has listed HCQ as an “essential medicine,” proven effective against a long list of ailments.8 It is a generally benign prescription medicine, far safer—according to the manufacturer’s package inserts9—than many popular over-the-counter drugs.

That study concludes: “We report . . . that chloroquine has strong antiviral effects on SARS-Coronavirus infection of primate cells . . . [both] before or after exposure to the virus, suggesting both prophylactic and therapeutic advantage.”15 This conclusion was particularly threatening to vaccine makers since it implies that chloroquine functions both as a preventive “vaccine” as well as a cure for SARS coronavirus. Common sense would presume it to be effective against other coronavirus strains. Worse still for Dr. Fauci and his vaccine-making friends, a NIAID study16 and a Dutch paper,17 both in 2014, confirmed chloroquine was effective against MERS—still another coronavirus.

The prospect of an existing therapeutic drug (with an expired patent) that could outperform any vaccine in the war against COVID posed a momentous threat to the pharmaceutical cartel. Among the features pharma companies most detest is low cost, and HCQ is about $10 per course.41 Compare that to more than $3000 per course for Dr. Fauci’s beloved remdesivir.42

By March, front-line doctors around the world were spontaneously reporting miraculous results following early treatment with HCQ, and this prompted growing anxiety for Pharma. On March 13, a Michigan doctor and trader, Dr. James Todaro, M.D., tweeted his review of HCQ as an effective COVID treatment, including a link to a public Google doc.48,49 Google quietly scrubbed Dr. Todaro’s memo. This was six days before the President endorsed HCQ.

Google has a long history of suppressing information that challenges vaccine industry profits. Google’s parent company Alphabet owns several vaccine companies, including Verily, as well as Vaccitech, a company banking on flu, prostate cancer, and COVID vaccines.50,51 Google has lucrative partnerships with all the large vaccine manufacturers, including a $715 million partnership with GlaxoSmithKline.52 Verily also owns a business that tests for COVID infection.53

In the midst of a deadly pandemic, somebody very powerful wanted a medication that had been available over the counter for decades, and known to be effective against coronaviruses, to be suddenly but silently pulled from the shelves—from Canada to Zambia.

After widespread use of the drug for 65 years, without warning, FDA somehow felt the need to send out an alert on June 15, 2020 that HCQ is dangerous, and that it required a level of monitoring only available at hospitals.59 In a bit of twisted logic, Federal officials continued to encourage doctors to use the suddenly-dangerous drug without restriction for lupus, rheumatoid arthritis, Lyme and malaria. Just not for COVID. With the encouragement of Dr. Fauci and other HHS officials, many states simultaneously imposed restrictions on HCQ’s use.

Prior to COVID-19, not a single study had provided evidence against the use of HCQ based on safety concerns.

Dr. Fauci, Bill Gates, and WHO financed a cadre of research mercenaries to concoct a series of nearly twenty studies—all employing fraudulent protocols deliberately designed to discredit HCQ as unsafe. Instead of using the standard treatment dose of 400 mg/day, the 17 WHO studies administered a borderline lethal daily dose starting with 2,400 mg.61 on Day 1, and using 800 mg/day thereafter.

This was a brassy enterprise to “prove” chloroquine dangerous, and sure enough, it proved that elderly patients can die from deadly overdoses. “The purpose seemed, very clearly, to poison the patients and blame the deaths on HCQ,” says Dr. Meryl Nass, a physician, medical historian, and biowarfare expert.

The report acknowledges that, “The BMGF developed a model of chloroquine penetration into tissues for malaria.”69 BMGF’s unique dosing model for the studies deliberately overestimated the amount of HCQ that is necessary to achieve adequate lung tissue concentrations. The WHO report confesses that, “This model is however not validated.” Gates’s deadly deception allowed FDA to wrongly declare that HCQ would be ineffective at safe levels.

Brazilian prosecutors have accused the authors of the study of committing homicide by purposefully poisoning the elderly subjects in their study with high doses of chloroquine.76

Gates warned that: “Leaders can help by not stoking rumors or panic buying. Long before the drug hydroxychloroquine was approved as an emergency treatment for COVID-19, people started hoarding it, making it hard for lupus patients who need it to survive.”78 This, of course, was a lie. The only ones hoarding HCQ were Dr. Fauci and Rick Bright, who had padlocked 63 million doses in the Strategic National Stockpile79—more than enough to supply virtually every gerontology-ward patient in America. Despite such efforts to create a shortage, none existed. HCQ is cheap, quick, and easy to manufacture, and since its patent is expired, dozens of manufacturers around the world can quickly ramp up production to meet escalating demand.

Asked by Bloomberg News in mid-August about how the Trump White House had promoted HCQ “despite its repeatedly being shown to be ineffective and, in fact, to cause heart problems in some patients,” Gates happily responded: “This is an age of science, but sometimes it doesn’t feel that way. In the test tube, hydroxychloroquine looked good. On the other hand, there are lots of good therapeutic drugs coming that are proven to work without the severe side effects.”82 Gates went on to promote Gilead’s remdesivir as the best alternative, despite its lackluster track record compared to HCQ. He didn’t mention having a large stake in Gilead,83 which stood to make billions if Dr. Fauci was able to run remdesivir through the regulatory traps.

The capacity of their Pharma overlords to strong-arm the world’s top two medical journals, the NEJM and The Lancet, into condoning deadly research95,96 and to simultaneously publish blatantly fraudulent articles in the middle of a pandemic, attests to the cartel’s breathtaking power and ruthlessness. It is no longer controversial to acknowledge that drug makers rigorously control medical publishing and that The Lancet, NEJM, and JAMA are utterly corrupted instruments of Pharma.

The Lancet editor, Richard Horton, confirms, “Journals have devolved into information laundering operations for the pharmaceutical industry.”97 Dr. Marcia Angell, who served as an NEJM editor for 20 years, says journals are “primarily a marketing machine.”98 Pharma, she says, has co-opted “every institution that might stand in its way.”99,100

Referring to the Lancet Surgisphere study during a May 27 CNN interview, Dr. Fauci stated on CNN about hydroxychloroquine, “The scientific data is really quite evident now about the lack of efficacy.”101 And even after the scandal lay exposed and the journals retracted their articles, Dr. Fauci let his lie stand. Instead of launching an investigation of this momentous and enormously consequential fraud by the world’s two leading medical journals and publicly apologizing, Dr. Fauci and the medical establishment simply ignored the wrongful conduct and persevered in their plan to deny global populations access to lifesaving HCQ.

On June 17, the WHO—for which Mr. Gates is the largest funder after the US, and over which Mr. Gates and Dr. Fauci exercise tight control—called for the halt of HCQ trials in hundreds of hospitals across the world.

In compliance with the WHO recommendation, Switzerland banned the use of HCQ; however, about 2 weeks into the ban, Switzerland’s death rates tripled, for about 15 days, until Switzerland reintroduced HCQ. COVID deaths then fell back to their baseline.118 Switzerland’s “natural experiment” had provided yet another potent argument for HCQ.

Similarly, Panamanian physician and government advisor Sanchez Cardenas notes that when Panama banned HCQ, deaths shot up, until the government relented, at which point deaths dropped back to baseline.119

Many countries with underdeveloped health care systems were using HCQ early and achieving far lower mortalities than in the United States, where HHS and the FDA impede access to HCQ.120 AAPS General Counsel Andrew Schlafly observed that “Citizens of the Philippines, Poland, Israel, and Turkey all have greater access to HCQ than American citizens do,” and they have superior morbidity outcomes.

Other foreign studies support strong claims for HCQ. A study by Nova demonstrated that nations using HCQ have death rates 80 percent lower than those that banned it.122

Country by country, data consistently links broader access to HCQ to lower mortality. The very poorest countries—if they used HCQ—had far lower case fatality rates than wealthy countries that did not. Even impoverished African nations, where “experts” like Bill Gates predicted the highest death rates, had drastically lower mortalities than in nations that banned HCQ. Senegal and Nigeria, for example, both use hydroxychloroquine and had COVID fatality rates that were significantly lower than those experienced in the United States.126 Similarly, despite the fact that hygiene in those countries is often far inferior, in Ethiopia,127 Mozambique,128 Niger,129 Congo,130 and Ivory Coast,131 there are far fewer per capita deaths than in the US. In those nations, death rates vary between 8 and 47.2 deaths per million inhabitants as of September 24, 2021. In contrast, western countries that denied access to HCQ experienced numbers of coronavirus deaths per million inhabitants between 220 per million in Holland,132 2,000 per million in the US, and 850 deaths per million in Belgium.133 Dr. Meryl Nass observed, “If people in these malaria countries would boost their immune system with zinc, vitamin C and vitamin D, the coronavirus death toll would even further decrease.”

Wealthier democracies or countries with especially restrictive HCQ protocols—Ireland, Canada, Spain, the Netherlands, UK, Belgium, and France—are comparatively deadly environments. Andrew Schlafly observed that, “The mortality rate from COVID-19 in countries that allow access to HCQ is only one-tenth the mortality rate in countries where there is interference with this medication, such as the United States. . . . In some areas of Central America, officials are even going door to door to distribute HCQ. . . . These countries have been successful in limiting the mortality from COVID-19 to only a fraction of what it is in wealthier countries.”135

In his early AIDS days, Dr. Fauci had thrashed FDA as inhumane for demanding randomized double-blind placebo studies at the height of the pandemic. Now, here he was doing what he had condemned by blocking an effective treatment simply because it would compete with his expensive patent-protected pharmaceutical, remdesivir, and vaccines.

The COVID vaccines that qualified for Emergency Use Authorization include novel platforms like mRNA and DNA with no known safety profile. Others use toxic adjuvants like squalene and aluminum or novel adjuvants, with proven risks and potentially high rates of serious injuries. The two-month randomized clinical trials that justified the EUAs for COVID vaccines were far too brief to detect injuries with longer incubation periods.151,152,153 The vaccines are so risky that the insurance industry has refused to underwrite them,154 and the manufacturers refuse to produce them without blanket immunity from liability.155 Bill Gates, who is the principal investor in many of these new COVID vaccines, stipulated that their risk is so great that he would not provide them to people unless every government shielded him from lawsuits.

Dr. Fauci’s on-again-off-again interest in drug safety is situational and self-interested. He claimed on July 31 about HCQ that “If that randomized placebo-controlled trial shows efficacy, I would be the first to admit it and to promote it, but I have not… So I just have to go with the data. I don’t have any horse in the game one way or the other; I just look at the data.”157 In fact, Dr. Fauci always had a stable of horses in the game. One of them is remdesivir, even after the WHO’s randomized placebo trial showed remdesivir ineffective against COVID.158 Furthermore, remdesivir has a catastrophic safety profile.159

His second nag is the Moderna vaccine, in which he invested years and six billion taxpayer dollars. He was thrilled to sponsor a human trial of a Moderna COVID vaccine (partly owned by his agency), before there were any safety and efficacy data from animal studies, which goes against FDA regulations. He then pushed for hundreds of millions of people to get EUA vaccines before the randomized placebo-controlled trials were complete. So much for Dr. Fauci’s requirement for having high-quality evidence before risking use of drugs and vaccines in humans.

Kory testified that “IVM could reduce hospitalizations by almost 90 percent and deaths by almost 75 percent.” Kory is one of a multitude of leading front-line physicians, including McCullough, Florida’s Surgeon General Joe Ladopo, Professor Paul Marik, Dr. Joseph Varone, and mRNA vaccine inventor, Dr. Robert Malone, and many, many others, who believe that early treatment with ivermectin would have avoided 75 percent-80 percent of deaths and saved our country a trillion dollars in treasure. “COVID resulted in ~6 million hospitalizations and 700,000+ deaths in America,” says Dr. Kory. “If HCQ and IVM had been widely used instead of systematically suppressed, we could have prevented 75 percent, or at least 500,000 deaths, and 80 percent of hospitalizations, or 4.8 million. We could have spared the states hundreds of billions of dollars.”

NIH’s neutral January 14, 202130 “non-recommendation,”31 issued in the face of strong evidence of ivermectin’s safety and efficacy for COVID-19, was the first obvious signal of the agency’s determination to suppress IVM. NIH claimed that there was “Insufficient evidence . . . to recommend either for or against the use of ivermectin for the treatment of COVID-19.” NIH shrouded its process for reaching that non-recommendation in secrecy, refusing to disclose the panel members who took part in the ivermectin deliberations, and redacting their names from the documents that various Freedom of Information Act requests compelled the agency to produce. For a time, only Dr. Fauci, Francis Collins, and the panelists themselves knew their identities. NIH took extreme measures to keep the names secret, fighting all the way into federal court to shield the proceedings from transparency.32,33

Nations whose residents have easy access to ivermectin invariably see immediate and dramatic declines in COVID deaths.

A December 2020 study showed that African and Asian countries that widely used ivermectin to treat and prevent various parasitic diseases enjoy some of the world’s lowest-reported COVID case and mortality rates.