Vaccine Jab Quotes

People had been scammed by their own politicians, mainstream media, and Big Pharma. Not for money this time, but for their health, and perhaps their souls.

Vaccines are one of the rare commercial products that multiply profits by failing. Each new booster doubles the revenues from the initial jab.

In 2019, nearly a decade after Coburn’s remonstrance, and only a few months before the COVID-19 pandemic, Dr. Fauci made a surprise announcement: he finally had a working HIV vaccine. While the inoculation had demonstrated a bare-bones 30 percent efficacy in human trials in Thailand, data from the Phase III trial in South Africa looked promising, and NIAID was getting teed up to test the vaccine on Americans.4 Dr. Fauci added some deflating caveats: While his new vaccine didn’t prevent transmission of AIDS, the nimble technocrat jauntily predicted that intrepid souls who took the jab would find that when they did get AIDS, the symptoms would seem to be much reduced. So confident was Dr. Fauci of the media’s slavish credulity that he assumed, correctly, that he’d never need to answer the many questions raised by this feverish gibberish.

To overcome such meddling from India’s prying medical community, in 2005 Gates funded, through GAVI, a four-year, $37 million study of mass vaccination with Hib jabs in Bangladesh intending to showcase the vaccine’s benefits.184,185 GAVI’s Bangladesh study backfired, showing no advantage from Hib vaccination.

critics would complain if he spent billions on vaccines and nothing on therapeutics. However, any licensed, repurposed antiviral that was effective against COVID for prevention or early treatment (like IVM or HCQ) could kill his entire vaccine program because FDA wouldn’t be able to grant his jabs Emergency Use Authorization. Remdesivir, however, was an IV remedy, appropriate only for use on hospitalized patients in the late stages of illness. It would therefore not compete with vaccines, allowing Dr. Fauci to support it without compromising his core business. Furthermore, while HCQ and IVM were off-patent and available generically, remdesivir was in the sweet spot of still being on patent. The potential profit upside was impressive. 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.

The 1976 swine flu vaccine was so fraught with problems that HHS discontinued the jab after vaccinating 49 million Americans. According to news accounts, the incidence of flu was seven times greater among the vaccinated than the unvaccinated. Furthermore, the vaccine caused some 500 cases of the degenerative nerve disease Guillain-Barré Syndrome, 32 deaths,14 more than 400 paralyzations, and as many as 4,000 other injuries.15

yet another of his African HIV vaccine experiments. A large trial on 2,600 African girls of a Johnson & Johnson HIV jab— funded jointly by NIAID and the Bill and Melinda Gates Foundation—had failed to demonstrate a beneficial effect.120

The Rockefeller Foundation launched a “public-private partnership” with pharmaceutical companies called the International Health Commission, which set about feverishly inoculating the hapless populations of the colonized tropics with a yellow fever jab.56 The vaccine killed its beneficiaries in droves and failed to prevent yellow fever. The Rockefeller Foundation quietly dropped the useless vaccine after the foundation’s star researcher, the yellow fever vaccine’s inventor, Hideyo Noguchi, succumbed to the disease, likely contracted through careless laboratory exposure.

While his new vaccine didn’t prevent transmission of AIDS, the nimble technocrat jauntily predicted that intrepid souls who took the jab would find that when they did get AIDS, the symptoms would seem to be much reduced.

Contemporary news accounts identify Dr. Fauci as the chief proponent of the multibillion-dollar fast-track H1N1 flu vaccine given that year to millions of Americans. Dr. Fauci is “more responsible than any other single person for the fast-track development of this new flu vaccine,” according to a contemporary report by National Public Radio’s Richard Knox.73, 74 As usual, the fawning US media obediently spread fear and lies to promote Dr. Fauci’s H1N1 jabs.

Merck maintained it had not tested either vaccine against an inert placebo in pre-approval trials, so no one could scientifically predict if the vaccines would avert more injuries or cancers than they would cause. Nevertheless, the sister FDA panel, VRBPAC, approved Gardasil—to prevent cervical cancer—without requiring proof that the vaccine prevented any sort of cancer, and despite strong evidence from Merck’s clinical trial that Gardasil could dramatically raise risks of cancer and autoimmunity in some girls.82 ACIP, nevertheless, effectively mandated both jabs. Gardasil would be the most expensive vaccine in history, costing patients $420 for the three-jab series and generating revenues of over $1 billion annually for Merck.83 That year, nine of the thirteen ACIP panel members and their institutions collectively received over $1.6 billion of grant money from NIH and NIAID. Systemic Conflicts of Interest Pharma and Dr. Fauci similarly rig virtually all the critical drug approval panels using this strategy of populating them with PIs who, bound by financial fealty to Pharma and NIAID funders, reliably approve virtually every new drug upon which they deliberate—with or without safety studies. From 1999 to 2000, Government Oversight Committee (GOC) Chairman Republican Congressman Dan Burton investigated the systemic corruption of these panels during two years of intense investigations and hearings. According to Burton, “CDC routinely allows scientists with blatant

Compare ivermectin’s safety record to Dr. Fauci’s two chosen COVID remedies, remdesivir (which hospital nurses have dubbed “Run-death-is-near”), and the COVID vaccines. Over 30 years, ivermectin has been associated with only 379 reported deaths, an impressive death/dose reporting ratio of 1/10,584,408. In contrast, over the 18 months since remdesivir received an EUA, about 1.5 million patients have received remdesivir, with 1,499 deaths reported (a dire 1/1,000 D/D ratio). Meanwhile, among recipients of COVID jabs in the US during the ten months following their rollout, some 17,000 deaths have occurred following vaccination, a reported D/D ratio of 1/13,250. Ivermectin, therefore, is thousands of times safer than remdesivir and COVID vaccines. The science also indicates that it is far more effective than either.

It is true that vaccines have in the past taken a long, long time to develop. Until 2020, a new vaccine usually took at least ten years to develop from concept to roll-out. Many took much longer. The malaria vaccine programme at the Jenner Institute has been going for twenty-five years, and research into malaria vaccines had been going on for more than a hundred years – so far, with limited success. The lab-to-jab record-holder was the mumps vaccine, developed in four years by Maurice Hilleman in the United States in the 1960s.1 But the standard lengthy timeline we were all used to was never because vaccine development required ten, fifteen or thirty years of continuous painstaking lab work, clinical trials and data analysis. For every vaccine that had ever been developed up until 2020, most of the elapsed development time was spent waiting. In 2020, there were three key factors that enabled us to cut out the waiting and crunch ten years into one: first, the work we had already done; second, changes to the way funding was given out; and third, doing in parallel things that we would normally do in sequence.

His critics argue that Dr. Fauci’s “slow the spread, flatten the curve, wait for the jab” strategy—all in support of a long-term bet on unproven vaccines—represented a profound and unprecedented departure from accepted public health practice. But most troubling were Dr. Fauci’s policies of ignoring and outright suppressing the early treatment of infected patients who were often terrified.

This could have been easily explained by medical experts skilled in helping the public weigh the pros and cons of health decisions. Many media outlets, however, seemed gripped by the fear that anything more than a passing report on possible risks would damage vaccine uptake and provide fodder for the conspiracy crowd. Except the opposite turned out to be true: without easy access to reliable, in-depth information about vaccine risks, rumors about friends of friends falling ill or dropping dead after getting “the jab” coursed through the digital grapevine. A door was left wide open for my doppelganger and other attention-economy hustlers to position themselves as fearless medical investigators, combing through raw vaccine trial data and supposedly suppressed CDC reports that people without medical degrees generally lack the expertise to interpret. Of course that didn’t stop them from cherry-picking every self-reported claim or actual negative reaction to support their incessant cries that a vaccine “genocide” was underway and being covered up by the Big Pharma–funded lackeys in the lamestream media.

still can't believe that). Babies just eight-weeks-old have a single jab against diphtheria, tetanus, pertussis, haemophilus influenzae type b and polio and another against pneumococcal disease. Then, as if that were not enough, babies of three

expecting 1-3 mass shootings in close succession to shock the public into clamoring for gun control right before the vaccine becomes available so people can’t resist it by shooting whoever is trying to jab them.

But the swine flu pandemic was a dud, and HHS’s response was a global embarrassment. Only one casualty—a soldier at Fort Dix34—succumbed to the “pandemic,” and Merck’s experimental vaccine triggered a national epidemic of Guillain-Barré syndrome, a devastating form of paralysis resembling polio, before regulators recalled the jab.