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November 14, 2023 - May 11, 2024
DTRA was a major funder of EcoHealth Alliance, Peter Daszak’s “charity” that sought out lethal animal viruses around the world, retrieving the most deadly for the Pentagon.
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.’”
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.
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.
Bill Gates’s surrogate group GAVI asked in a press release: “How did a drug many used to treat parasites in cows come to be of interest to doctors treating humans with COVID-19?” The characterization was especially insincere. Gates’ foundation and GAVI were, at that moment, distributing millions of doses of ivermectin annually to Indian children for filariasis, and to Africans for river blindness and filariasis.
NPR, which has taken $3 million from the Bill & Melinda Gates Foundation, jumped on the dogpile and deceptively insinuated that Rogan took horse-level doses:88 Joe Rogan has told his Instagram followers he has been taking ivermectin, a deworming veterinary drug formulated for use in cows and horses, to help fight the coronavirus. The Food and Drug Administration has warned against taking the medication, saying animal doses of the drug can cause nausea, vomiting and in some cases severe hepatitis.
Rolling Stone, the onetime banner of the counterculture, had by 2021 devolved into a reliable mouthpiece for medical cartel orthodoxies.89
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.
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.
All their diabolical tricks seemed the work of winks and nods and a powerful hidden hand, with no corporation or federal agency taking clear responsibility for carrying out a deliberate policy to suppress a life-saving drug.
Why would Dr. Fauci care to undermine any medicine that might compete with remdesivir? Might it have something to do 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?3,4
six months into the Ebola study, the trial’s Safety Review Board suddenly pulled both remdesivir and ZMapp from the trial.12 Remdesivir, it turned out, was hideously dangerous.
Within 28 days, subjects taking remdesivir had lethal side effects including multiple organ failure, acute kidney failure, septic shock, and hypotension, and 54 percent of the remdesivir group died—the highest mortality rate among the four experimental drugs.13
NIAID recruited the 400 US volunteers for Dr. Fauci’s remdesivir trial.16 Dr. Fauci’s press release said only that remdesivir “has shown promise in animal models for treating Middle East Respiratory Syndrome (MERS).”17 It’s unclear, then, if NIAID informed these frightened souls that, less than a year earlier, a safety review board had deemed remdesivir unacceptably toxic.
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
In one of his many extraordinary feats of uncanny foresight, beginning in 2017, Dr. Fauci paid $6 million to his gain-of-function guru, Ralph Baric—a University of North Carolina microbiologist—to accelerate remdesivir as a coronavirus remedy at China’s biosecurity laboratory in Wuhan.23,24
Early in March 2020, the Gates Foundation bankrolled $125 million of tax-deductible grants to support drug makers to develop coronavirus treatments.30
While fewer patients receiving remdesivir died, those receiving remdesivir were also a lot less sick than the placebo subjects when they entered the trial.
Dr. Fauci had little reason to worry that insiders would complain about the corruption of the study, since his trusted deputy, Cliff Lane, chaired the NIH Treatment Guidelines panel.40 Lane was doubly conflicted, since he had personally overseen the remdesivir trials in China, and stood, potentially, to share in patent rewards and royalties for the drug.41 In addition to Lane, seven of the panel members had financial relationships with Gilead—and eight additional panel members had had financial relationships with Gilead prior to the past eleven months, for which they were required to declare a
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Based on Dr. Fauci’s representation, President Trump purchased the world’s entire stock of remdesivir for Americans.55 The European Union signed a “joint procurement agreement” with Gilead to queue up in the pipeline for 500,000 treatment courses.56 The day after Dr. Fauci’s announcement at the White House, the University of North Carolina issued a press release headlined: “Remdesivir, developed through a UNC-Chapel Hill partnership, proves effective against COVID-19 in NIAID human clinical trials.”57 Dr. Fauci’s gain-of-function wizard, Dr. Ralph Baric, called this “a game changer for the
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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
He simply declared the disappointing results to be ‘highly significant,’ and pronounced remdesivir to be the new ‘standard of care.’
Improving Gilead’s business even more, doctors and hospitals that failed to use remdesivir could now be sued for malpractice, leading some medical experts to believe that coercing the use of this worthless and dangerous drug on COVID patients almost certainly cost tens of thousands of Americans their lives.
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. This time only, the brazenness of the fraud earned Dr. Fauci some rare criticism even in mainstream science and press, and from academic institutions that customarily maintain silence about his shenanigans, given their addictions to whopping NIH and BMGF funding. On October 24, 2020, Umair Irfan noted that “The FDA is once again promoting a Covid-19 therapy based on shaky evidence.”61 The British Medical
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Eric Topol of Scripps Research Translational Institute scolded that, “This is a very, very bad look for the FDA, and the dealings between Gilead and EU make it another layer of badness.”63 Angela Rasmussen, a virologist at Columbia University Mailman School of Public Health, told a reporter: “I was really surprised when I saw that news.”64 Science Magazine said Dr. Fauci’s move had, “baffled scientists who have closely watched the clinical trials of remdesivir unfold over the past 6 months—and who have many questions about remdesivir’s worth.”65 University of Oxford Professor of Clinical
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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
On July 15, 2021, a large Johns Hopkins Study in Original Investigation | Infectious Diseases once again confirmed that “Remdesivir treatment was not associated with improved survival but was associated with longer hospital stays.”72 (Emphasis added.)
On October 2, 2020, the European Union released its own safety review of remdesivir. The study reported serious side effects.73,74
Assessing remdesivir’s impact on hospitalized COVID-19 patients is difficult, in part, because—like COVID-19—remdesivir causes extreme toxicity to lungs and kidneys,78 and mimics several of the other lethal symptoms of COVID, including multi-organ failure.79 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?”
Brazil, one of the first nations to widely use remdesivir, had the second highest death toll.80,81
Dr. McCullough gives us a stark and clear summary: “Remdesivir has two problems. First, it doesn’t work. Second, it is toxic and it kills people.”
“The only means to fight a plague is honesty.” —Albert Camus, The Plague (1947)
The first obstacle was the coronavirus’s tendency to rapidly mutate, producing vaccine-resistant variants.
As if to confirm such fears, in May of that year, Britain’s top vaccinologist, Andrew Pollard, admitted that the Oxford University’s government-funded and patriotically ballyhooed AstraZeneca vaccine had failed to achieve sterilizing immunity in monkeys; the inoculated macaques, even when asymptomatic, continued to support high viral loads in their nasal pharynxes.3 Then in August, Dr. Fauci primped up the dismaying news of similar failures by all the competing candidates with a kind of celebratory bravado. Instead of declaring defeat and retreating to the drawing board, Dr. Fauci cheerfully
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Even worse, vaccinated individuals, he warned, would become asymptomatic carriers and “mutant factories” blasting out vaccine-resistant versions of the disease that were likely to lengthen and intensify rather than abbreviate the pandemic.
Vaccines are one of the rare commercial products that multiply profits by failing. Each new booster doubles the revenues from the initial jab.
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
In October 2021, Pfizer announced that it was projecting an astonishing $26 billion in revenues from its COVID boosters.8
The even more daunting obstacle to coronavirus vaccines was their tendency to induce “pathogenic priming”—also known as “antibody-dependent enhancement” (ADE)—an overstimulation of immune system response that can cause severe injuries and death when vaccinated individuals subsequently encounter the wild viruses.
Dr. Hotez confessed to the committee that his colleagues had killed a number of children from pathogenic priming during experiments with the respiratory syncytial virus (RSV) vaccines in 1966, and recounted that during his own earlier work on coronavirus vaccines, he saw the same effect on ferrets: We started developing coronavirus vaccines and our colleagues—we noticed in laboratory animals that they started to show some of the same immune pathology. So we said, “Oh my God, this is going to be problematic.”
In an April 26, 2020 interview with Pharma troll Dr. Zubin “ZDogg” Damania, MD, Merck’s top vaccine promoter, Dr. Paul Offit, amplified these concerns:11 [B]inding antibodies can be dangerous and cause something called Antibody Dependent Enhancement. And we’ve seen that. I mean, we saw that with the [Gates-funded] dengue vaccine. But with the dengue vaccine, in children who had never been exposed to dengue before, it actually made them worse when they were then exposed to the natural virus. Much worse. Vaccinated children who were less than nine years of age, who had never been exposed to
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1) 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.
2) Second, as COVID czar, Dr. Fauci stubbornly refused to fix HHS’s designed-to-fail vaccine injury surveillance system (VAERS), which systematically suppresses reporting of most vaccine injuries.
3) 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.
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.
4) Fourth, Dr. Fauci allowed CDC to discourage autopsies in deaths following vaccination.
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5) Fifth, Dr. Fauci populated the key FDA and CDC committees with NIAID, NIH, and Gates Foundation grantees and loyalists to insure rubber-stamp approvals for his mRNA vaccines, without any long-term injury studies.
6) Sixth, by vaccinating the entire population, Dr. Fauci seems to be striving to eliminate the control group, to hide vaccine injuries.
