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

Pfizer’s clinical data predicted potentially fatal myocarditis in one in every 318 teens. Postmarketing data confirm astronomically high rates of myocarditis injuries. On October 1, 2021, a team of medical researchers and statisticians found that myocarditis rates reported in VAERS were significantly higher in teens than Pfizer had reported in its clinical data.

According to the Vaccine Adverse Event Reporting System, there have been 7,537 cases of myocarditis and pericarditis reported following COVID vaccines,85 with 5,602 cases attributed to Pfizer.86 Some 476 of these reports occurred in children from 12 to 17 years old.87

According to an article in Current Trends in Cardiology, “Within eight weeks of the public offering of COVID19 products to the 12–15-year-old age group, we found 19 times the expected number of myocarditis cases in the vaccination volunteers over background myocarditis rates for this age group.”88 But even these alarming numbers may underreport myocarditis injuries. Israeli data and US data presented to CDC’s advisory committee on June 23, 2021 similarly found the rate of reported cases of myocarditis in vaccinated teenage boys aged 12–17 is at least twenty-five times greater than expected, and is fifty times greater than the reported rate in vaccinated males over 65.

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.

In October 2021, Sweden, Denmark, and Finland announced that they will pause the use of Moderna’s COVID vaccine for children under 18 years of age, after increased reports of inflammatory diseases like myocarditis and pericarditis.90,91 That same week, Iceland banned Moderna’s jab outright due to heart inflammation risk.

Furthermore, the VAERS data may also be dramatically underreporting myocarditis and other injuries.

Just before I published this book, in late October 2021, FDA made an extraordinary admission in a letter to Pfizer92 to explain the chronic underreporting of serious but common vaccine-induced injuries and deaths. FDA, at last, admitted that VAERS is worthless for detecting vaccine injuries.

We have determined that an analysis of spontaneous postmarketing adverse events [VAERS reports] reported under section 505(k)(1) of the FDCA [Federal Food, Drug and Cosmetic Act] will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis. Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.



At best, this letter is a shocking acknowledgement that regulators have no way to assess whether their vaccines are killing and injuring more humans than they are helping. In any rational regulatory environment, FDA’s alarming admission would demand an instantaneous cessation of the vaccine rollout.

Only Dr. Anthony Fauci can answer the question, “Why—given FDA’s stunning confession that America has no functional surveillance system—did HHS not immediately stop the COVID vaccine rollout?” The answer, of course, is that Dr. Fauci knows that America’s bought, brain-dead, and scientifically illiterate media will never force him to answer this query.

Waning Vaccines

Compounding concerns over FDA’s confession that Americans have no way to assess the risks from COVID vaccines is the uncontestable proof that COVID vaccine efficacy drops precipitously almost immediately after vaccination.

Pfizer and FDA may have opted to end the company’s clinical trial after six months (the optional plan was a three-year trial ending in December 2023), after realizing that the vaccine was causing significant harms and that its fast-waning efficacy would make a cost/benefit analysis unsupportable if the study continued. In other words, the injury axis almost immediately crosses the benefits axis.

An October 3, 2021 study in the peer-reviewed journal BioRxiv by Stanford and Emory University scientists suggests that antibody levels generated by the Pfizer-BioNTech vaccine can suffer a ten-fold decrease seven months after the second vaccination.93 The scientists warn that the precipitous drop in antibody levels will compromise the body’s ability to defend itself against COVID19 if the individual is exposed to COVID.

A second study published the same week confirms that the immune protection offered by two doses of Pfizer’s COVID19 vaccine drops off after only two months!94

Another government-funded study in October confirms the decline in vaccine effectiveness in England95 finding that the reduction in transmission “declined over time since second vaccination, for Delta reaching similar levels to unvaccinated individuals by 12 weeks for [the AstraZeneca vaccine] and attenuating substantially for [Pfizer].” In other words, within just three months, AstraZeneca did nothing to prevent transmission, and Pfizer was scarcely better.96

The study appearing in The Lancet confirms that vaccine effectiveness against infection disappears so fast that it is ephemeral. The heavily powered study involved 3,436,957 Kaiser Permanente Southern California customers and compared infections and COVID19-related hospital admissions of fully vaccinated to unvaccinated people over the age of twelve for up to six months.97

The researchers found that vaccine effectiveness against infection plummeted from 88 percent during the first month after double vaccination to 47 percent after five months. The researchers found vaccine effectiveness against Delta infection was 93 percent during the first month after double vaccination but dropped to 53 percent after four months.98

This information should sicken every doctor who has ever given one of these jabs to a trusting patient. It means that these products confer no benefits to individuals or society and their long-term costs are foreboding and largely unknown. How could this have happened?

Vaccinating Children is Unethical

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