This book was very eye-opening. If only 10% of what I read was true, I am convinced there are people in the medical / pharma world who should be in prison. It was THAT compelling. I'm not going to try to summarize a detailed review of the book, other than to say these are the main points I took away:
- Big pharma's priority is to make money more so than cure diseases and they collude with media and government to do so.
- Media receives considerable revenue from pharma advertisements, and therefore, they are reluctant to report stories that reflect negatively on their cash cows.
- Some studies about the efficacy and risks of COVID vaccines were poorly done and biased in FAVOR of the vaccines.
- Some studies about the efficacy and risks of other COVID treatments (using existing medicines) were poorly done and biased AGAINST the alternative therapies.
- We have been, and are being, lied to.
- Censorship of doctors and other medical professionals who merely questioned COVID protocols was rampant.
- Fauci has been involved in the "healthcare" of our country for many more years than just the COVID ones.
- There is a lot of legal liability immunity provided for most of the vaccines available.
- RFK, Jr. is not anti-vax. He's anti-vax for vaccines that have not been thoroughly vetted related to long-term side effects.
- Children are given over 70 vaccines now (it was 69 at the time of this book), as compared to only a handful when I was a child in the 60's. Meanwhile, childhood health issues such as autism have skyrocketed during that same period.
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“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
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His obsequious subservience to the Big Ag, Big Food, and pharmaceutical companies has left our children drowning in a toxic soup of pesticide residues, corn syrup, and processed foods, while also serving as pincushions for 69 mandated vaccine doses by age 18—none of them properly safety tested.
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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 Dr. Fauci has offered no explanation as to why allergic diseases like asthma, eczema, food allergies, allergic rhinitis, and anaphylaxis suddenly exploded beginning in 1989, five years after he came to power. On its website, NIAID boasts that autoimmune disease is one of the agency’s top priorities. Some 80 autoimmune diseases, including juvenile diabetes and rheumatoid arthritis, Graves’ disease, and Crohn’s disease, which were practically unknown prior to 1984, suddenly became epidemic under his watch.
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The manufacturer’s inserts of the 69 vaccine doses list each of the now-common illnesses—some 170 in total—as vaccine side effects.70
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Dr. Fauci’s failure to achieve public health goals during the COVID pandemic are not anomalous errors, but consistent with a recurrent pattern of sacrificing public health and safety on the altar of pharmaceutical profits and self-interest.
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As discussed above, Dr. Fauci and other officials made no inquiry or claims as to whether lockdowns would cause more harm and death than they averted. Subsequent studies have strongly suggested that lockdowns had no impact in reducing infection rates. There is no convincing difference in COVID infections and deaths between laissez-faire jurisdictions and those that enforced rigid lockdowns and masks.
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Dr. Fauci explained to the New York Times that he had upgraded his estimate of the vaccine coverage needed to insure “herd immunity” from 70 percent in March to 80–90 percent in September not based on science, but rather in response to polling that indicated rising rates of vaccine acceptance.
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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.
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In September 2021, in a statement justifying COVID vaccine mandates to school children, Dr. Fauci dreamily recounted his own grade school measles and mumps vaccines—an unlikely memory, since those vaccines weren’t available until 1963 and 1967, and Dr. Fauci attended grade school in the 1940s.
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As America’s COVID czar, Dr. Fauci never complained about CDC’s decision to skip autopsies from deaths attributed to vaccines. This practice allowed CDC to persistently claim that all deaths following vaccination were “unrelated to vaccination.”
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Dr. Fauci’s aficionados, including President Biden and the cable and network news anchors, counseled Americans to “trust the experts.” Such advice is both anti-democratic and anti-science. Science is dynamic. “Experts” frequently differ on scientific questions and their opinions can vary in accordance with and demands of politics, power, and financial self-interest. Nearly every lawsuit I have ever litigated pitted highly credentialed experts from opposite sides against each other, with all of them swearing under oath to diametrically antithetical positions based on the same set of facts. Telling people to “trust the experts” is either naive or manipulative—or both.
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was struck, during COVID-19’s early months, that America’s Doctor, apparently preoccupied with his single vaccine solution, did little in the way of telling Americans how to bolster their immune response. He never took time during his daily White House briefings from March to May 2020 to instruct Americans to avoid tobacco (smoking and e-cigarettes/vaping double death rates from COVID);31 to get plenty of sunlight and to maintain adequate vitamin D levels (“Nearly 60 percent of patients with COVID-19 were vitamin D deficient upon hospitalization, with men in the advanced stages of COVID-19 pneumonia showing the greatest deficit”);32 or to diet, exercise, and lose weight (78 percent of Americans hospitalized for COVID-19 were overweight or obese).33 Quite the contrary, Dr. Fauci’s lockdowns caused Americans to gain an average of two pounds per month and to reduce their daily steps by 27 percent.34 He didn’t recommend avoiding sugar and soft drinks, processed foods, and chemical residues, all of which amplify inflammation, compromise immune response, and disrupt the gut biome which governs the immune system. During the centuries that science has fruitlessly sought remedies against coronavirus (aka the common cold), only zinc has repeatedly proven its efficacy in peer-reviewed studies. Zinc impedes viral replication, prophylaxing against colds and abbreviating their duration.35 The groaning shelves that commercial pharmacies devote to zinc-based cold remedies attest to its extraordinary efficacy. Yet Anthony Fauci never advised Americans to increase zinc uptake following exposure to infection.
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Dr. Fauci’s neglect of natural immune response was consistent with the pervasive hostility towards any non-vaccine intervention that characterized the federal regulatory gestalt. On April 30, 2021, Canadian Ontario College of Physicians and Surgeons threatened to delicense any doctor who prescribed non-vaccine health strategies including Vitamin D.36 “They are trying to erase any notion of natural immunity,” says Canadian vaccine researcher Dr. Jessica Rose, Ph.D., MSc, BSc. “Pretty soon the incessant lies and propaganda will have successfully instilled in the masses that the only hope for staying alive is via injection, pill-popping, so in sum, no natural immunity.”
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“The Best Practices for defeating an infectious disease epidemic,” says Yale epidemiologist Harvey Risch, “dictate that you quarantine and treat the sick, protect the most vulnerable, and aggressively develop repurposed therapeutic drugs, and use early treatment protocols to avoid hospitalizations.”
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“The strategy from the outset should have been implementing protocols to stop hospitalizations through early treatment of Americans who tested positive for COVID but were still asymptomatic. If we had done that, we could have pushed case fatality rates below those we see with seasonal flu, and ended the bottlenecks in our hospitals. We should have rapidly deployed off-the-shelf medications with proven safety records and subjected them to rigorous risk/benefit decision-making,” McCullough continues. “Using repurposed drugs, we could have ended this pandemic by May 2020 and saved 500,000 American lives, but for Dr. Fauci’s hard-headed, tunnel vision on new vaccines and remdesivir.”
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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.
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Risch points out that, “Half the deaths, in New York, and one-third nationally,45 were among elder care facility residents.”
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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 published a peer-reviewed article describing their stellar success with early treatment. FTC sent him a letter warning him to take it down. “No one wanted Americans to know that you didn’t have to die from COVID. It’s 100 percent treatable,” says Dr. Brownstein. “We proved it. No one had to die.” “Meanwhile,” adds Dr. Brownstein, “we’ve seen lots of really bad vaccine side effects in our patients. We’ve had seven strokes—some ending in severe paralysis. We had three cases of pulmonary embolism, two blood clots, two cases of Graves’ disease, and one death.”
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McCullough’s findings may be conservative. Early in the pandemic, two Spanish nursing homes simultaneously experimented with early treatment with cheap, available repurposed drugs and achieved 100 percent survival among infected residents and staff. Between March and April 2020, COVID-19 struck two elder care facilities in Yepes, Toledo, Spain. The mean age of residents in those locations was 85, and 48 percent were over 80 years old. Within three months, 100 percent of the residents at both locations had caught the virus. By the end of June, 100 percent of residents and half the workers were seropositive for COVID, meaning they had endured infection and recovered. None of them went to the hospital and none died. None had adverse drug effects. Local doctors rapidly discovered early treatment with the same sort of remedies that McCullough was championing: antihistamines, steroids, antibiotics, anti-inflammatories, aspirin, nasal washes, bronchodilators, and blood thinners. In pooled data, 28 percent of the residents in similar nursing homes in the same region over the same time period died. That study supports the experience of front-line physicians that cheap available, repurposed drugs can easily prevent hospitalizations and deaths.
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Dr. Kory told me that he was deeply troubled that the extremely successful efforts by scores of front-line doctors to develop repurposed medicines to treat COVID received no support from any government in the entire world—only hostility—much of it orchestrated by Dr. Fauci and the US health agencies. The large universities that rely on hundreds of millions in annual funding from NIH were also antagonistic. “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. As we shall see, these institutions live in terror of offending Anthony Fauci, and that fear paralyzed them in the midst of the pandemic. “Dr. Fauci refused to promote any of these interventions,” says Kory. “It’s not just that he made no effort to find effective off-the-shelf cures—he aggressively suppressed them.”
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Instead of supporting McCullough’s work, NIH and the other federal regulators began actively censoring information on this range of effective remedies. Doctors who attempted merely to open discussion about the potential benefits of early treatments for COVID found themselves heavily and inexplicably censored. Dr. Fauci worked with Facebook’s Mark Zuckerberg and other social media sites to muzzle discussion of any remedies. FDA sent a letter of warning that N-acetyle-L-cysteine (NAC) cannot be lawfully marketed as a dietary supplement, after decades of free access on health food shelves, and suppressed IV vitamin C, which the Chinese were using with extreme effectiveness. In September, Dr. McCullough used his own money to create a YouTube video showing four slides from his peer-reviewed American Medical Association articles to teach doctors the miraculous benefits of early treatment with HCQ and other remedies. His video went viral, with hundreds of thousands of downloads; YouTube pulled it two days later. 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.”
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President Trump’s endorsement of HCQ on March 19, 20207 hyper-politicized the debate and gave Dr. Fauci’s defamation campaign against HCQ a soft landing among Democrats and the media.
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Generations have used HCQ billions of times throughout the world, practically without restriction. During my many childhood trips to Africa, I took HCQ daily as a preventive against malaria, a ritual that millions of other African visitors and residents embrace. Long use has thoroughly established HCQ’s safety and efficacy such that most African countries authorize HCQ as an over-the-counter medication. Africans call the drug “Sunday-Sunday”10 because millions of them take it religiously, once a week, as a malaria prophylaxis. It’s probably not a coincidence that these nations enjoyed some of the world’s lowest mortality rates from COVID. HCQ is the #1 most used medication in India, the second-most populous nation on the planet, with 1.3 billion people.
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In the United States, the FDA has approved HCQ without limitation for 65 years, meaning that physicians can prescribe it for any off-label use.
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Since its recommended protocol as a remedy for COVID requires only one week’s use, Dr. Fauci’s sudden revelation that the drug is dangerous was specious at best.
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Some 200 peer-reviewed studies (C19Study.com) by government and independent researchers deem HCQ safe and effective against Coronavirus, especially when taken prophylactically or when taken in the initial stages of illness along with zinc and Zithromax.
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When all the studies are collected together, despite having different outcome measures, the average benefit is 64 percent. This means that subjects who received hydroxychloroquine were only 36 percent as likely to reach the negative outcomes as subjects in the control groups.
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In May 2020, Dr. Harvey Risch, M.D., Ph.D. published the most comprehensive study, to date, on HCQ’s efficacy against COVID. Risch is Yale University’s super-eminent Professor of Epidemiology, an illustrious world authority on the analysis of aggregate clinical data. Dr. Risch concluded that evidence is unequivocal for early and safe use of the HCQ cocktail. Dr. Risch published his work—a meta-analysis reviewing five outpatient studies—in affiliation with the Johns Hopkins Bloomberg School of Public Health in the American Journal of Epidemiology, under the urgent title, “Early Outpatient Treatment of Symptomatic, High-Risk COVID-19 Patients that Should be Ramped-Up Immediately as Key to Pandemic Crisis.”30 He further demonstrated, with specificity, how HCQ’s critics—largely funded by Bill Gates and Dr. Tony Fauci31—had misinterpreted, misstated, and misreported negative results by employing faulty protocols, most of which showed HCQ efficacy administered without zinc and Zithromax which were known to be helpful. But their main trick for ensuring the protocols failed was to wait until late in the disease process before administering HCQ—when it is known to be ineffective. Dr. Risch noted that evidence against HCQ used late in the course of the disease is irrelevant.
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So, against all that I’ve shared here, Dr. Fauci offered up one answer: hydroxychloroquine should not be used because we don’t understand the mechanism it uses to defeat COVID—another shibboleth transparently invoked to defeat common sense. Regulators do not understand the mechanism of action of many drugs, but they nonetheless license those that are effective and safe. The fact is that we know more about how HCQ beats COVID than we know about the actions of many other medicines, including—notably—Dr. Fauci’s darlings, mRNA vaccines and remdesivir.
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A national study in Finland in May 2021 showed a 5x efficacy.39 And national studies in Canada and Saudi Arabia showed 3x efficacy.40 I’ll stop gilding the lily here and ask the reader: Was hydroxychloroquine some crazy baseless idea, or ought regulators to have honestly investigated it as a potential remedy during a raging pandemic?
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Pharma’s War on HCQ 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.
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No surprise, pharmaceutical interests launched their multinational preemptive crusade to restrict and discredit HCQ starting way back in January 2020, months before the WHO declared a pandemic and even longer before President Trump’s controversial March 19 endorsement. On January 13, when rumors of Wuhan flu COVID-19 began to circulate, the French government took the bizarre, inexplicable, unprecedented, and highly suspicious step of reassigning HCQ from an over-the-counter to a prescription medicine.
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A physician from Zambia reported to Dr. Harvey Risch that in some villages and cities, organized groups of buyers emptied drugstores of HCQ and then burned the medication in bonfires outside the towns. South Africa destroyed two tons of life-saving hydroxychloroquine in late 2020, supposedly due to violation of an import regulation.46 The US government in 2021 ordered the destruction of more than a thousand pounds of HCQ, because it was improperly imported.
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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 Google was not the only social media platform to ban content that contradicts the official HCQ narrative. Facebook, Pinterest, Instagram, YouTube, MailChimp, and virtually every other Big Tech platform began scrubbing information demonstrating HCQ’s efficacy, replacing it with industry propaganda generated by one of the Dr. Fauci/Gates-controlled public health agencies: HHS, NIH and WHO. When President Trump later suggested that Dr. Fauci was not being truthful about hydroxychloroquine, social media responded by removing his posts.
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In March, at HHS’s request, several large pharmaceutical companies—Novartis, Bayer, Sanofi, and others—donated their inventory, a total of 63 million doses of hydroxychloroquine and 2 million of chloroquine, to the Strategic National Stockpile, managed by BARDA, an agency under the DHHS Assistant Secretary for Preparedness and Response.56 BARDA’s Director, Dr. Rick Bright, later claimed the chloroquine drugs were deadly, and he needed to protect the American public from them.57 Bright colluded with FDA to restrict use of the donated pills to hospitalized patients. FDA publicized the authorization using language that led most physicians to believe that prescribing the drug for any purpose was off-limits.
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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.
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Gates and his cabal used an arsenal of other deceptive gimmickry to assure that HCQ would appear not just deadly, but ineffective. Each of the studies that Gates funded failed to incorporate Zithromax and zinc—important components of HCQ protocols. All of the Fauci, Gates, WHO, Solidarity, Recovery and Remap-COVID studies administered HCQ at late stages of COVID infection, in contravention of the prevailing recommendations that deem HCQ effective only when doctors administer it early.73,74 Viewing this orchestrated sabotage with frustration, critics accused the Gates grantees of purposefully designing these studies, at best, to fail and, at worst, to murder.75 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.
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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.
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Even after the FDA withdrew its Emergency Use Authorization and posted the fraudulent warning on its website,103 many front-line doctors across the country continued to prescribe and report strong benefits with appropriate doses of HCQ. In response, Dr. Fauci took even more unprecedented steps to derail doctors from prescribing HCQ.
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In March, while people were dying at the rate of 10,000 patients a week, Dr. Fauci declared that hydroxychloroquine should only be used as part of a clinical trial.104 For the first time in American history, a government official was overruling the medical judgment of thousands of treating physicians, and ordering doctors to stop practicing medicine as they saw fit.
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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.
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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.
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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. He added, “In Venezuela, HCQ is available over the counter without a prescription, while in the United States, pharmacists are prevented from filling prescriptions for HCQ.”
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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.
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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.” Similarly, Bangladesh CFR, Senegal, Pakistan, Serbia, Nigeria, Turkey, and Ukraine all allow unrestricted use of HCQ and all have miniscule case fatality rates compared to the countries that ban HCQ.134 Wealthier democracies or countries with especially restrictive HCQ protocols—Ireland, Canada, Spain, the Netherlands, UK, Belgium, and France—are comparatively deadly environments.
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Beginning June 27, 2020, Dr. Nass began a list of deceptive strategies that the Fauci/Pharma/Gates cartel used to control the narrative on hydroxychloroquine and deny Americans access to this effective remedy. The list has grown to 58 separate strategies.140 “It is remarkable,” she observed, how “a large series of events taking place over the past months produced a unified message about hydroxychloroquine (HCQ) and produced similar policies about the drug in the US, Canada, Australia, New Zealand and western Europe. The message is that generic, inexpensive hydroxychloroquine (costing only $1.00 to produce a full course) is dangerous.”
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Dr. Fauci’s hypocrisy about HCQ is evident to anyone who looks at his vacillating pronouncements throughout his long career. He has persistently insisted on double-blind randomized placebo trials for medicines he dislikes (those that compete with his patented remedies) and airily fixed the NIAID study of remdesivir by changing the endpoints midstream to favor the drug. Dr. Fauci did not sponsor or encourage randomized trials for masks, lockdowns, or social distancing. And in the decades since he took over NIAID, he has never demanded randomized studies to confirm safety of the combined 69 vaccine doses currently on the childhood schedule. Every one of these vaccines is regarded as so “unavoidably unsafe”—in the words of the 1986 Vaccine Act (NCVIA) and the Supreme Court—that their manufacturers have demanded—and received—immunity from liability.
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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.
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The international press initially raved that this safe, inexpensive, well-known, and readily available drug had demolished SARS-CoV-2 in cell cultures. “We found that even a single dose could essentially remove all viral RNA by 48 hours and that even at 24 hours there was a really significant reduction in it,” said lead researcher Dr. Kylie Wagstaff.7 Based on this study, on May 8, 2020, Peru—then under siege by a crushing COVID endemic— adopted ivermectin in its national guidelines. “Peruvian doctors already knew the medicine, widely prescribed it for parasites, and health authorities knew it was safe and were comfortable with it,” recalls Dr. Pierre Kory. COVID deaths dropped precipitously—by 14-fold—in the regions where the Peruvian government effectively distributed ivermectin. Reductions in deaths correlated with the extent of IVM distributions in all 25 states. In December 2020, Peru’s new president, under pressure from WHO, severely restricted IVM availability and COVID cases rebounded with deaths increasing 13-fold.
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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.
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“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.”
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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 As Collins and Dr. Fauci maneuvered to shade the process from sunlight, the Centers for Disease Control and Prevention (CDC), in response to a separate FOIA request, disclosed the group’s nine members.34 Three members of the working group, Adaora Adimora, Roger Bedimo, and David V. Glidden, had disclosed financial relationships with Merck. A fourth member of the NIH Guidelines Committee, Susanna Naggie, received a $155 million grant35 to conduct further studies of ivermectin following the NIH non-recommendation. NIAID’s windfall payoff to Naggie would have been unlikely to go forward if the committee voted to approve IVM.
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India showed that early combination therapy—budesonide, ivermectin, doxycycline, and zinc, costing between two and five dollars—made COVID symptoms disappear within three to five days. By January 2021, a country of more than 1.3 billion people and a vaccine uptake of almost 7.6 percent nationally44 had witnessed only 150,000 COVID deaths.45 By comparison, the US, with a population of 331 million, had recorded 357,000 deaths.46 Many Indian officials and doctors consider ivermectin a miracle drug for controlling the outbreak. A natural experiment involving two Indian states—Uttar Pradesh and Tamil Nadu—with opposite COVID strategies helped cement that impression. With 241 million people, Uttar Pradesh has the equivalent of two-thirds of the United States population. According to the Indian Express:47 “Uttar Pradesh was the first state in the country to introduce large-scale prophylactic and therapeutic use of ivermectin. In May-June 2020, a team at Agra [Uttar Pradesh’s fourth largest city], led by Dr. Anshul Pareek, administered ivermectin to all RRT team members in the district on an experimental basis. None of them developed Covid-19 despite being in daily contact with patients who had tested positive for the virus.48 Uttar Pradesh State Surveillance Officer Vikssendu Agrawal added that, based on the findings from Agra, the state government sanctioned the use of ivermectin as a prophylactic for all the contacts of COVID patients and began administering doses to infected persons.
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By September, the Uttar Pradesh government announced that the state’s 33 districts are virtually devoid of active cases, despite having a vaccination rate of only 5.8 percent.49 The Hindustan Times reported, “Overall, the state has a total of 199 active cases, while the positivity rate came down to less than 0.01 per cent. The recovery rate, meanwhile, has improved to 98.7 per cent.”
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Meanwhile, the Indian state of Tamil Nadu continued using Anthony Fauci’s protocol of administering remdesivir, outlawing ivermectin, and discouraging early treatment. According to the Indian Times, Tamil Nadu continues to experience cases and fatalities that perfectly match the US catastrophe.
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Gates also uses Unitaid to fund corrupt science by tame and compromised researchers like Hill that legitimizes his policy directives to the WHO. Unitaid gave $40 million to Andrew Hill’s employer, the University of Liverpool, four days before the publication of Hill’s study.
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At the conclusion of the January 14 BIRD conference, Dr. Lawrie delivered a monumental closing address that should be recorded among the most important speeches in the annals of medical history. Dr. Lawrie spoke out at considerable personal risk, since her livelihood and career largely rely on the very agencies she targeted for criticism. Dr. Lawrie began by endorsing the miraculous efficacy of IVM. Had ivermectin been employed in 2020 when medical colleagues around the world first alerted the authorities to its efficacy, millions of lives could have been saved, and the pandemic with all its associated suffering and loss brought to a rapid and timely end. Dr. Lawrie told the audience that the suppression of ivermectin was a signal that Pharma’s pervasive corruption had turned a medical cartel against patients and against humanity. The story of ivermectin has highlighted that we are at a remarkable juncture in medical history. The tools that we use to heal and our connection with our patients are being systematically undermined by relentless disinformation stemming from corporate greed. The story of ivermectin shows that we as a public have misplaced our trust in the authorities and have underestimated the extent to which money and power corrupts.
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When Dr. Kory’s explosive December 8, 2020 Senate testimony63 describing the peer-reviewed science supporting ivermectin went viral, prescriptions for ivermectin from US doctors exploded. Americans were getting legitimate prescriptions filled at pharmacies, up to 88,000 scripts in a single week. The truth of the drug’s benefits was going viral, and the last thing Dr. Fauci et al. could tolerate was an effective treatment for COVID. Something needed to be done.
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Physicians traditionally have had unlimited authority to prescribe FDA-approved medications for any purpose as long as they explain the risks and benefits to their patients. Suddenly, the AMA and its industry patrons and captive regulators moved to limit the doctor’s authority to treat patients. FDA has no authority to regulate the practice of medicine.
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In Florida and South Carolina, Blue Cross Blue Shield (BCBS) sent mass mailings to physicians notifying them that BCBS would no longer pay insurance claims for IVM, and threatened audits of any physician who wrote prescriptions for the drug.
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Gain-of-function refers to experiments that intentionally modify a pathogen to create the ability to cause or worsen disease, enhance transmissibility, and/or create novel strains with potential to cause global spread in humans.
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In June 2021, as FDA and NIAID were cranking up the medical cartel’s opposition against IVM, the HHS agreed to purchase 1.7 million 5-day treatment courses of molnupiravir from Merck for 1.2 billion dollars80—when the drug wins FDA approval, a contingency that can be virtually guaranteed while Anthony Fauci is Washington’s drug kingmaker.
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Not only was the drug developed with taxpayer money, but its $712 per dose price to the taxpayer is forty times more than Merck’s $17.64 cost of production.
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Like IVM, it is also a protease-inhibiting anti-parasitic. With these two new drugs teed up for a simultaneous FDA approval, the entire medical/media cartel launched a final coordinated coup de grâce against IVM—branding it a dangerous horse drug. Mainstream media outlets across the US and overseas obediently ran stories promoting the horse medicine propaganda scam.
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In late August 2021, NIH, FDA, and CDC launched an innovative new campaign to slander ivermectin as a “horse dewormer” that only deluded foolhardy nincompoops would consume. Picking up on those themes, The Independent asked, “Ivermectin: Why Are US Anti-Vaxxers Touting a Horse Dewormer as a Cure for COVID?”
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On August 15, the FDA instructed, on its website: “You are not a horse.” In an August 21, 2021 Twitter post,84 the FDA expanded the theme: “You are not a horse. You are not a cow. Seriously, y’all. Stop it.” The White House and CNN also urged listeners that they should avoid veterinary products. CDC joined the chorus, warning Americans to not risk their health consuming a “horse de-wormer.” Elsewhere on its website, the CDC urged black and brown human immigrants to load up on ivermectin. “All Middle Eastern, Asian, North African, Latin American, and Caribbean refugees should receive presumptive therapy with: ivermectin, two doses 200 mcg/Kg orally once a day for two days before departure to the United States.85 Whether this was intended to deworm them or to prevent COVID transmission during travel to the US is unclear.
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Only Green Med Info, a health news and information site, saw through the chicanery: “A Media Smear Campaign Timed to Clear Market for Pfizer’s Ivermectin Clone Drug, Which Will Be Hailed as a ‘Miracle.’”
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Demonizing IVM as a “horse drug” was, of course, ironic, given that NIAID initially developed Merck’s replacement therapy, molnupiravir, as a horse drug. Furthermore, calling ivermectin a horse drug is like calling antibiotics a horse drug. Many long-established basic drugs are, of course, effective in all mammals because they work on our shared biology. But facts be damned, media companies called all hands on deck to push these stories. Ivermectin’s devastating effectiveness against infections from parasites and solid 40-year history of proven safety have made it, also, the world’s most prescribed veterinary medicine—but the Nobel Prize was for those billions of times it helped humans, and the government’s silly safety warnings were, of course, specious.
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Jake Tapper, who has sounded progressively more like a pharma rep than a journalist as the lockdown dragged on, slavishly parroted Dr. Fauci’s new talking point:86 “Poison control centers are reporting that their calls are spiking in places like Mississippi and Oklahoma, because some Americans are trying to use an anti-parasite horse drug called ivermectin to treat coronavirus, to prevent contracting coronavirus.” It mattered not that both Mississippi and Oklahoma officials quickly denied that anyone in their state had been hospitalized for IVM poisoning.
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Rolling Stone, the onetime banner of the counterculture, had by 2021 devolved into a reliable mouthpiece for medical cartel orthodoxies.89 In October 2021, Rolling Stone announced that it had removed from its website a 2005 article linking mercury in vaccines to brain injuries in children. Rolling Stone also reported that Oklahomans overdosing on ivermectin horse dewormer were causing emergency rooms to be “so backed up that gunshot victims were having hard times getting” access to health facilities. An accompanying photo purported to depict a long line of ambulatory gunshot casualties seeking hospital admission to an Oklahoma emergency room already filled to capacity with dingbats poisoned by horse wormer.90 The Rolling Stone story91 spread like wildfire among the world’s reigning media outlets, including the Daily Mail, 92 Business Insider, Newsweek,93 Yahoo News, The Guardian,94 and The Independent,95 many of which rely on Gates Foundation largesse. MSNBC’s news host, Rachel Maddow, told her audience that “Patients are overdosing on ivermectin backing up rural Oklahoma hospitals, ambulances.”96 “Ivermectin is meant for a full-size horse,” she explained. She repeated that the victims first gullibly swallowed the false claims of antivaxxers before guzzling down horse dewormer. “The ERs are so backed up that gunshot victims were having hard times getting to facilities where they can get definitive care and be treated.” The story, of course, was fraud. Days later, Oklahoma’s Sequoyah Northeastern Health System posted a categorical denial on its website, dismissing the entire story as mere fabrication. That Rolling Stone picture of the long lines was an Associated Press stock photo from the previous January, a photo of people waiting in line to get vaccines. As it turns out, not a single patient has been treated in Oklahoma for ivermectin overdose. Instead of retracting the article, Rolling Stone simply posted an attention-dodging “update” at the top of the article reporting the hospital’s denial.97 The Guardian similarly published a nondescript update at the bottom of its article.98
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On September 28, the New York Times introduced a new tactic: reporting that the demand for ivermectin among the crackpots trying to treat COVID had created a shortage for veterinary purposes, warning that—any day now—animals might begin to suffer.
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The osteopath Dr. Joseph Mercola observed,102 “This idea that ivermectin is a horse dewormer that poses a lethal risk to humans is pure horse manure, shoveled at us in an effort to dissuade people from using a safe and effective drug against COVID-19. . . . The intent is clear. What our so-called health agencies and the media are trying to do is confuse people into thinking of ivermectin as a ‘veterinary drug,’ which simply isn’t true. Ultimately, what they’re trying to do is back up the Big Pharma narrative that the only thing at your disposal is the COVID shot.”
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Anthony Fauci needed to use all his moxie and all his esoteric bureaucratic maneuvers—mastered during his half-century at NIH—to win FDA’s approval for his vanity drug, remdesivir. Remdesivir has no clinical efficacy against COVID, according to every legitimate study. Worse, it is deadly poisonous, and expensive poison at $3,000 for treatment.1 In fact, remdesivir’s wholesale cost is roughly 1,000x more costly than hydroxychloroquine and ivermectin. The challenge required Dr. Fauci to first sabotage HCQ and IVM. Under federal rules discussed earlier, FDA’s recognition of HCQ and IVM efficacy would automatically kill remdesivir’s ambitions for EUA designation. And even if Dr. Fauci somehow finagled an FDA license for remdesivir, demand for the product, which doctors were administering late in the disease, as it had to be given through an IV in the hospital, would plummet if either HCQ or IVM stopped the COVID-19 infections early.
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Why would Dr. Fauci care to undermine any medicine that might compete with remdesivir? Might it have something to with NIAID and CDC having just spent $79 million2 developing remdesivir for Gilead, a company in which the Bill & Melinda Gates Foundation owns a $6.5 million stake?
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Remdesivir cost Gilead $10 per dose to manufacture.18,19 But by granting Gilead an EUA, regulators could force private insurers, Medicare, and Medicaid to fork over around $3,120.00 per treatment—hundreds of times the cost of the drug.20,21 Gilead predicted remdesivir would bring in $3.5 billion in 2020 alone.
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For HCQ, Dr. Fauci demanded well-designed randomized double-blind placebo-controlled trials32,33 and he warned against the use of IVM for treatment.34 In contrast, Fauci green-lighted remdesivir following studies in which the control group did not receive a real placebo.
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NIAID’s remdesivir trial’s original endpoint made sense: to win approval, the drug would need to demonstrate a “reduction in COVID mortality.” However, the drug didn’t show the hoped-for benefit. While fewer patients receiving remdesivir died, those receiving remdesivir were also a lot less sick than the placebo subjects when they entered the trial. So Dr. Fauci’s team decided to move the goalposts. The researchers, in fact, had changed the trial “endpoints” twice in an effort to create a meager appearance of benefit. Dr. Fauci’s new endpoints allowed the drug to demonstrate a benefit, not by improving the chances of surviving COVID, but by achieving shorter hospital stays.38 Yet this too was a scam, because it turned out that almost twice as many remdesivir subjects as placebo subjects had to be readmitted to the hospital after discharge—suggesting that Fauci’s improved time to recovery was due, at least in part, to discharging remdesivir patients prematurely. Altering protocols in the middle of an ongoing study is an interference commonly known as “scientific fraud” or “falsification.” UCLA Epidemiology Professor Sander Greenland explains, “You’re not supposed to change your endpoint mid-course. That’s frowned upon.” Vera Sharav agrees: “Changing primary outcomes after a study has commenced is considered dubious and suspicious.”
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Before his study was completed or peer-reviewed, much less published, Dr. Fauci learned that The Lancet had just published a placebo-controlled Chinese study that showed remdesivir utterly ineffective at keeping hospitalized patients alive OR reducing the duration of hospitalizations.48 Even more importantly, remdesivir did not reduce the presence of the virus in the blood. Worst of all, the Chinese study confirmed remdesivir’s deadly toxicity. The Chinese regulators and researchers shuttered that trial because of potentially lethal side effects. Remdesivir caused serious injuries in 12 percent of the patients, compared to 5 percent of patients in the placebo group.49 Unlike Dr. Fauci’s trial, the Chinese study was a randomized, double-blind, placebo-controlled, multi-center, peer-reviewed study, published in the world’s premier scientific journal, The Lancet. All the underlying data was available to the incurious press and the uninformed public.
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In any event, the Chinese study spelled certain doom for remdesivir. It was now D.O.A. at FDA—a poem title? But Dr. Fauci never accepted this. The inimitable maestro of regulatory combat responded to the crisis with savvy and bold action that would miraculously salvage his sinking product: He appeared at one of his regular White House press conferences, this one in the Oval Office. Seated on the couch next to Deborah Birx and opposite President Trump, Dr. Fauci made a surprise announcement. From that lofty platform, Dr. Fauci, with great fanfare, declared victory. The data from NIAID’s clinical trial for remdesivir shows “quite good news,” he said, glossing over the drug’s failure to demonstrate any mortality advantage.51 He boasted that the median time for hospitalization was eleven days for patients taking remdesivir, compared to fifteen days in the placebo group. He told the credulous press: “The data shows that remdesivir has a clear-cut, significant, positive effect in diminishing the time to recovery.” He claimed that his study had therefore proven remdesivir so remarkably beneficial to COVID patients that he had decided that it would be unethical to deny Americans benefits of this wonder drug. He was, he declared, unblinding and ending the study and giving remdesivir to the placebo group. Remdesivir would be America’s new “standard of care”52 for COVID. It was, of course, all a lie.
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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
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As we shall see, Dr. Fauci copied the choreographed script for winning remdesivir’s EUA from the worn rabbit-eared playbook that he developed during his early AIDS years, and then used repeatedly across his career to win approvals for deadly and ineffective drugs. Time and again, he has terminated clinical trials of his sweetheart drugs the moment they begin to reveal cataclysmic toxicity. He makes the absurd claim that his drug-du-jour had proven so miraculously effective that it would be unethical to deny it to the public, and then he strong-arms FDA to grant his approvals.
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Then, on October 19, 2020, three days before remdesivir’s FDA approval, the World Health Organization published a definitive study on remdesivir involving 11,266 COVID-19 patients in 405 hospitals and 30 countries.69,70 The power of this study dwarfed the Fauci/Gilead project, which had recruited 1,062 patients. In the WHO’s trial, remdesivir failed to reduce mortality, and failed to reduce the need for ventilators OR the length of hospital stays. WHO researchers found no detectable benefits from remdesivir and recommended against its use in COVID-19 patients.71 WHO published its devastating indictment of remdesivir one month after FDA issued the remdesivir EUA for children less than 12 years of age. Dr. Fauci and the FDA knew about the WHO study before the FDA issued the EUA for remdesivir, and almost certainly read the preprints and understood the findings. It appears, in fact, that Dr. Fauci once again hurried the approval through FDA so as to beat the publication of a negative study.
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“Every independent randomized controlled trial of remdesivir has shown either a lack of benefit or a clear trend to harm,” says Dr. Pierre Kory. “It’s only those two Pharma studies (with Dr. Fauci) that show any benefits and even then, the benefits are minor.”
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Many doctors believe our country’s record COVID-19 fatalities are at least in part due to widespread use of remdesivir in 2020. “We had the most deaths worldwide,” says Dr. Ryan Cole. “It’s a haunting question: How many of these Americans were remdesivir casualties?” For several months, we were the only country treating people with a drug proven to be lethal. That year, 2020, we had almost double the number of deaths per month compared to most other countries. Brazil, one of the first nations to widely use remdesivir, had the second highest death toll.
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But Tony Fauci and his partner, Bill Gates, seemed to have a strategy for neutralizing the variant threat. The two men had put billions of taxpayer and tax-deducted dollars into developing an mRNA platform for vaccines that, in theory, would allow them to quickly produce new “boosters” to combat each new “escape variant.” This scheme was Big Pharma’s holy grail. Vaccines are one of the rare commercial products that multiply profits by failing. Each new booster doubles the revenues from the initial jab. Since NIAID co-owned the mRNA patent,6 the agency stood to make billions from its coronavirus gambit by producing successive boosters for every new variant; the more, the better! The good news for Pharma was that all of humanity would be permanently dependent on biannual or even triannual booster shots. Dr. Peter McCullough warned that mass vaccination with a leaky vaccine during a pandemic “would put the world on a never-ending booster treadmill.”7 That kind of talk had Pharma popping champagne corks. In October 2021, Pfizer announced that it was projecting an astonishing $26 billion in revenues from its COVID boosters.
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Dr. Fauci’s first approach was to abort the three-year clinical trials at six months and then vaccinate the controls—a preemption that would prevent detection of long-term injuries, including pathogenic priming. Regulators initially intended the Pfizer vaccine trial to continue for three full years, until May 2, 2023.14 Because the FDA allowed Pfizer to unblind and terminate its study after six months—and to offer the vaccine to individuals in the placebo group—we will never know whether vaccinated individuals in the trial suffered long-term injuries, including pathogenic priming, that cancelled out short-term benefits. Science and experience tell us that many vaccines can cause injuries like cancers, autoimmune diseases, allergies, fertility problems, and neurological illnesses with long-term diagnostic horizons or long incubation periods. A six-month study will hide these harms.
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Third, Dr. Fauci’s trump card was his capacity to enlist mainstream and social media companies to make reporting of injuries and deaths disappear from the airwaves, newspapers, and the Internet, and therefore from the public consciousness. Facebook, Google, and the television networks purged doctors and scientists who reported pathogenic priming, and censored reports about the waves of other vaccine injuries. As a federal official sworn for four decades to uphold the Constitution, Dr. Fauci should have been the champion of free speech and vigorous debate during the pandemic. Instead, he worked hand in glove with Bill Gates, Mark Zuckerberg, and other Big Tech titans to censor criticism of his various mandates and suppress information about vaccine injuries, including discussions of pathogenic priming.16,17 Email traffic shows that Dr. Fauci colluded directly with Mark Zuckerberg and the social media platforms to censor doctors who reported vaccine failures, harms, and deaths, to deplatform public health advocates like myself, and to evict and muzzle patients who reported their own injuries. The science journals, utterly dependent on Pharma advertising, obligingly refused to publish studies on the rash of deadly and debilitating jab reactions. The Bill Gates-funded fact-checking organization, Politifact,18 worked with Pharma-funded fact-checkers like FactCheck, which receives, funding from the Robert Wood Johnson Foundation, and whose current CEO is Richard Besser, former acting head of the CDC, which owns $1.8 billion in Johnson & Johnson stock19,20 to “debunk” stories and studies of vaccine injuries.
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In January of 2021, baseball superstar Hank Aaron, whom I knew, died seventeen days after receiving the COVID jab at a CDC-sponsored press conference in Atlanta. I observed, in a Defender article,22 that Aaron’s death was one of a wave of deaths among the elderly following COVID jabs. This was true, but the New York Times nevertheless vilified me for spreading “misinformation” and claimed that the Fulton County Coroner had determined that Aaron’s death was “unrelated to vaccines.” USA Today, Newsweek, TIME, Daily Beast, ABC, CNN, and CBS reported the Times claim.23 But when I called to verify their claim, the Fulton County Coroner told me that the office has never seen Aaron’s body and that no autopsy was ever performed. Aaron’s family had buried the home-run hero without a postmortem. The Times’ fabrication was part of the systematic campaign of deception, propaganda, and censorship by HHS regulators in partnership with mainstream media—almost unprecedented in the American experience—that helped conceal the tsunami of vaccine injuries and fatalities.
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September 2021 Israeli study demonstrating that natural immunity provides 27x better protection against COVID than the Pfizer vaccine is just one of 29 recently published peer-reviewed studies that vouch for the superiority of natural immunity.
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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.
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Gibraltar The world’s most vaccinated nation, Gibraltar, aggressively inoculated its 34,000 inhabitants, achieving 115 percent coverage (officials also vaccinated Spanish tourists) by July 2021. In December 2020, prior to the vaccine rollout, Gibraltar’s health agency had experienced only 1,040 confirmed cases and five deaths from COVID-19. After the vaccination blitz, the number of new infections increased fivefold—to 5,314—and the number of deaths increased nineteen-fold.38 Malta Malta, another of Europe’s vaccine champions, administered 800,000 doses to its 500,000 inhabitants, achieving vaccine coverage of nearly 84 percent over six months. But beginning in July 2021, the epidemic and fatalities surged, forcing the authorities to impose new restrictions and to admit that vaccination cannot shield the population from COVID.
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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.
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England Over a period of seven months preceding October 2021, some 60 percent of those 2,542 Brits who died from COVID were double vaccinated. Of people hospitalized in the UK for COVID in the last seven months, 157,000 were double-vaccinated.52 There were more per capita deaths among the “fully” vaccinated than the unvaccinated.53 The UK government’s latest Office for National Statistics report on mortality rates by COVID vaccination status shows that for age-adjusted mortality rate, the death rate by October 2021 was higher among the vaccinated than the unvaccinated.
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Wales According to October 2021 data from public health officials in Wales, UK, vaccinated individuals accounted for shocking 87 percent of all new COVID hospitalizations.55 Only 80 percent of Welsh were then fully vaccinated. In other words, only 13 percent of severe cases that required a trip to the hospital were unvaccinated, suggesting that those who have taken the experimental vaccine are more likely to experience adverse reactions and become hospitalized from COVID-19. Scotland In Scotland, official data on hospitalizations and deaths for October 2021 showed 87 percent of those who had died from COVID-19 in the third wave that began in early July were vaccinated. Only 70 percent of Scots were, at the time, fully vaccinated.
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In 1976, US regulators pulled the swine flu vaccine after it was linked to 25 deaths.62 In contrast, between December 14, 2020 and October 1, 2021, American doctors and bereaved families have reported more than 16,000 deaths and a total of 778,685 injuries to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccination.63,64 The Europeans’ surveillance sites tallied 40,000 deaths and 2.2 million adverse reactions. Due to chronic undercounting by VAERS and its European sister system, those numbers are almost certainly only a fraction of the true injuries. To illustrate how unprecedented this harm and death is, look at this “hockey stick” effect in CDC’s own graph of the 30-year history of deaths reported to VAERS from all vaccines. 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
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In yet another effort to calculate excess deaths from vaccinations from a non-VAERS database, Ohio-based Attorney Thomas Renz used the Medicare database (Centers for Medicare & Medicaid Services) to calculate that there have been 48,465 deaths among Medicare/Medicaid beneficiaries within fourteen days of a first or second dose of a COVID-19 vaccine.72,73 There are about 59.4 million Americans covered by Medicare, representing only 18.1 percent of the population, so these staggering numbers are roughly comparable to Steve Kirsch’s population-wide estimate of 150,000.
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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. CDC’s promotion of this statistical bunko was obviously grossly misleading. Assuming President Biden wasn’t deliberately lying to the American people, it’s clear that CDC was lying to President Biden and using him to dupe the rest of us.
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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.
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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.
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These astonishing numbers mean myocarditis is far from a “rare” side effect, as Dr. Fauci and Pfizer like to claim. Nor is it harmless. A recent study suggests that myocarditis is associated with a 50 percent mortality within five years.89 A teen had effectively zero risk of dying from COVID and a substantial risk of death from vaccination.
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