Fauci’s Inquisition Against Safe and Effective Anti-COVID-19 Drugs
By Richard Gale and Dr. Gary Null | Global Research | April 6, 2024
A question needs to be asked. Were the novel experimental drug treatments for SARS-CoV-2 viral infections that Anthony Fauci, the CDC and FDA advocated for and funded responsible for worsening the contagion and countless deaths?
However, at that time there were plenty of studies confirming there were pre-existing safe, inexpensive medications known to have highly effective antiviral properties to treat Covid-19 patients. Among these were ivermectin and hydroxychloroquine (HCQ).
There were also specific nutrients such as vitamin D and zinc, known to strengthen the immune system against viral infection and yet there was no recommendation from the government about the benefits of proper nutrition. So why did Fauci along with other federal health officials choose to intentionally ignore the scientific evidence and rather condemn these repurposed drugs? In Fauci’s case, over a year and half into the pandemic, he continued to lie outright on CNN that “there is no clinical evidence whatsoever that [ivermectin] works.”[1] And could millions have been saved if these generic medications were prescribed rather than the feds doing nothing but recommending social isolation and quarantines as the world awaited an experimental Covid-19 vaccine to enter the market?
To date, between ivermectin and HCQ alone, there have been 670 published studies, analyses and papers involving over 9,800 scientists and over 682,000 patients supporting the use of these drugs over and beyond those the FDA has approved under Emergency Use Authorization (EUA) statutes. Despite this, four years later, the FDA continues to fiercely deny ivermectin’s and HCQ’s efficacy and safety under proper administration. Why this blatant cover-up?
Every CDC effort to approve a novel drug treatment for SARS-CoV-2 infections has been a dismal failure. Aside from monoclonal antibody therapy, only three anti-Covid-19 drugs have been approved under an EUA in the United States. None met their promised expectations from either the manufacturer or our federal health agencies. With their poor efficacy rates, safety profiles and a black box warning slapped upon Pfizer’s anti-Covid-19 drug Paxlovid, the CDC is scrambling to find new viable alternatives in the pharmaceutical pipeline. Bloomberg amplifies the fake Covid-19 treatment crisis by lamenting that repurposed drugs such as ivermectin are gaining global popularity as “the world needs effective Covid drugs.”[2]
Shortly after the pandemic was formally announced, the FDA recommended the cheap over the counter anti-malarial drug hydroxychloroquine but then quickly reversed its decision after Fauci publicly announced the future arrival of Gilead Sciences’ novel intravenous drug Remdesivir. The FDA’s and European Union’s approvals of Remdesivir baffled many scientists, according to the journal Science, who questioned its therapeutic value and kept a close watch on the drug’s clinical reports about a “disproportionally high number of reports of liver and kidney problems.”[3] Even an earlier Chinese study published in The Lancet found that remdesivir had no impact on the coronavirus. The Science article notes that the “FDA never consulted a group of outside experts that it has at the ready to weigh in on complicated antiviral drug issues.”[4] Six months before remdesivir received EUA approval, Anthony Fauci had already hailed the drug as a major breakthrough that would establish a new “standard of care” in Covid-19 treatment.[5]
Today, remdesivir is being increasingly recognized as a debacle in antiviral therapeutic care. Even the WHO released a “conditional recommendation against the use of remdesivir in hospitalized patients, regardless of disease severity, as there is currently no evidence that remdesivir improves survival and other outcomes in these patients.” An Italian study observed a 416 percent increase in hepatocellular injuries among hospitalized Covid-19 patients treated with Remdesivir.[6] And a smaller Taiwanese study of hospitalized unvaccinated patients reported a 185 percent higher mortality during late remdesivir treatment.[7]
Earlier this year, Pfizer’s novel oral Covid-19 medication Paxlovid was given an FDA black box warning for clinically significant adverse reactions that can potentially be fatal. Because the company does not permit independent random-controlled trials to investigate its drug, other than retrospective studies, we only have Pfizer’s own data to rely upon. Nevertheless, The Lancet published a study by a team of Chinese scientists at Shanghai Jiao Tong School of Medicine that managed to look at Paxlovid’s use among critically ill patients hospitalized with Covid-19. The study reported a 27 percent higher risk of the infection progressing, a 67 percent increased risk in requiring ventilation, and 10 percent longer stays in ICU facilities.[8]
Paxlovid is a combination of a novel SARS-CoV-2 protease inhibitor and the HIV protease inhibitor ritonavir. The FDA approved Paxlovid under a EUA with the claim it was safe. However, on the government’s HIV.gov website for ritonavir it is clearly stated that the drug “can cause serious life-threatening side effects. These include inflammation of the pancreas (pancreatitis), heart rhythm problems, severe skin rash and allergic reactions, liver problems and drug interactions.”[9] Perhaps due to the drug’s serious side effects, it is no longer used solely against HIV, but rather is given in smaller doses as a booster for AZT-related drugs. Being highly toxic, ritonavir is also not recommended for pregnant women and has been shown to interfere with hormone-based birth control efficacy.
Paxlovid only received FDA EUA approval in May 2023. At that time, the agency claimed there was no evidence that patients who were treated with the drug rebounded and came down with Covid. However, shortly thereafter this was determined to be untrue.[10] A Harvard analysis found that 21 percent of Paxlovid recipients will remain contagious and likely succumb to a viral rebound compared to only 1.8 percent who did not take the drug.
Merck’s anti-Covid-19 drug molnupiravir (Lagevrio) also has an FDA black box warning for potential fetal harm when administered to pregnant women. Why the drug was ever approved under an EUA seems to be an enigma. The drug’s antiviral activity is based upon a metabolite known as NHC, which for many years has been known to create havoc in an enzyme crucial for viral replication by inserting errors into the virus’ genetic code. The theory is: produce enough errors and the virus kills itself off. However, molnupiravir can cause hundreds of mutations thereby “supercharging” the manufacturing of new Covid-19 viral strains. Moreover, according to a Forbes article, the drug’s mutagenic powers may also interfere with our own body’s enzymes and DNA.[11] Another Forbes article points out that Merck’s clinical trial only enrolled around 1,500 participants, which is far too “small to pick up on rare mutagenic events.”[12]
Molnupiravir has a poor efficacy rate across the board including viral clearance, recovery, and hospitalizations/death (68 percent).[13] One trial, funded by Merck, concluded the drug had no clinical benefit.[14] More worrisome, the drug also has life-threatening adverse effects including mutagenic risks to human DNA and mitochondria, carcinogenic activity and embryonic death.[15]
Each of these drugs have been outrageous cash cows for their manufacturers. Remdesivir is priced at $3,120 per treatment and earned Gilead $5.6 billion in sales for 2021.
Pfizer’s Paxlovid is priced at $1,390 per treatment. Last year, the company’s revenues for its Covid products—Paxlovid and the Comirnaty vaccine—came in at $12.5 billion, and, according to Fierce Pharma, Pfizer wrote off an additional $4.7 billion on its overstocked Paxlovid inventory.[16] Merck’s molnupiravir’s sales for 2022 cashed in almost $5.7 billion. Despite their profits, none of these drugs have been shown convincingly to have measurably lessened the pandemic nor the spread of SARS-CoV-2.
Despite all the attention and medical hype about novel experimental antiviral drugs to treat Covid-19, Anthony Fauci and other federal officials had full knowledge that other FDA-approved drugs existed that could have been quickly repurposed at minimal expense to effectively treat Covid-19 infections. Repurposing existing drugs to treat illness is a common occurrence. The antiparasitic and antiviral drug Ivermectin best stands out. Its effectiveness was observed to be so remarkable and multifaceted that researchers started to investigate its potential.
The mainstream media, including many liberal news sources who pride themselves on their independence, continue to channel the voices of Anthony Fauci, the CDC and FDA to demonize ivermectin and other generic drugs for treating Covid-19 and to reduce hospitalization and deaths. This propaganda campaign, however, has completely ignored the large body of medical literature that shows ivermectin’s statistically significant efficacy against symptomatic and asymptomatic SARS-2 infections.
Originally developed for veterinarian use, in 1987, the FDA approved ivermectin for treating two parasitic diseases, river blindness and stronglyoidiasis, in humans. Since then an enormous body of medical research has grown showing ivermectin’s effectiveness for treating other diseases. Its broad range of antiviral properties has shown efficacy against many RNA viruses such avian influenza, zika, dengue, HIV, West Nile, yellow fever, chikungunya and earlier severe respiratory coronaviruses. It has also been shown to be effective against DNA viruses such as herpes, polyomavirus, and circovirus-2.[17]
Unsurprisingly, ivermectin’s inventors Drs. William Campbell and Satoshi Omura were awarded the 2015 Nobel Prize in Physiology and Medicine.
It has been prescribed to hundreds of millions of people worldwide. Given its decades’ long record of in vitro efficacy, it should have been self-evident for Fauci’s NIAID, the CDC and the WHO to rapidly conduct in vivo trials to usher ivermectin as a first line of defense for early stage Covid-19 infections and for use as a safe prophylaxis.
For example, if funding were devoted for the rapid development of a micro-based pulmonary delivery system, mortality rates would have been miniscule and the pandemic would have been lessened greatly.[18] Repurposing ivermectin could have been achieved very quickly at a minor expense.[19] However, despite all the medical evidence confirming ivermectin’s strong antiviral properties and its impeccable safety record when administered properly, we instead witnessed a sophisticated government-orchestrated campaign to declare war against ivermectin and another antiviral drug, hydroxychloroquine (HCQ), in favor of far more expensive and EUA approved experimental drugs. Unlike the US, other nations were eager to find older drugs to repurpose against Covid-19 and protect their populations. A Johns Hopkins University analysis offered the theory that a reason why many African countries had very few to near zero Covid-19 fatalities was because of widespread deployment of ivermectin. In February 2020, the National Health Commission of China, for example, was the first to include hydroxychloroquine in its guidelines for treating mild, moderate and severe SARS-2 cases. Eight Latin American nations distribute home Covid-19 treatment kits that include ivermectin.[20] Why did the US and most European countries swayed by the US and the WHO fail to follow suit?
Early in the pandemic, physicians in other nations where treatment was less restricted, such as Spain and Italy, shared data with American physicians about effective treatments against the SARS-2 virus. In addition, there was a large corpus of medical research indicating that older antiviral drugs could be repurposed. Doctors who started to prescribe drugs such as ivermectin and HCQ, along with Vitamin D and zinc supplementation, observed remarkable results. Unlike the dismal recovery and high mortality rates reported in hospitals and large clinics that relied upon strict isolation, quarantine, and ventilator interventions, this small fringe group of physicians reported very few deaths among their large patient loads. Even reported deaths were more often than not compounded by patients’ comorbidities, poor medical facilities and other anomalies.
Very early into the pandemic, medical papers indicated ivermectin was a highly effective drug to treat SARS-2 infections.
In April 2020, less than a month after the WHO declared Covid-19 as a global pandemic, Australian researchers at the Peter Doherty Institute of Infection and Immunity published a paper demonstrating that a single ivermectin dose can control SARS-CoV-2 viral replication within 24-48 hours.[21] Monash University’s Biomedicine Discovery Institute in Australia had also published an early study that ivermectin destroyed SARS-2 infected cell cultures by 99.8 percent within 48 hours. But no American federal health official paid any attention.
As of March 2024, a database for all studies and trials investigating ivermectin against Covid-19 infections records a total of 248 studies, 195 peer-reviewed, and 102 involving controlled groups reporting an average 61 percent improvement for early infections, a 39 percent success rate in treating late infections, and an 85 percent average success rate for use as a preventative prophylaxis.[22] Moreover, prescribing ivermectin reduced mortality by 49 percent, compared to remdesivir’s 4 percent, Pfizer’s Paxlovid’s 31 percent, and molnupiravir’s 22 percent. Even hydroxychloroquine well outperforms these drugs mortality risk for early treatment at 66 percent.
A noteworthy study conducted in Brazil and published in the Cureus Journal of Medical Science prescribed ivermectin in a citywide prophylaxis program in a town of 223,000 residents. 133,000 took ivermectin. The results for a population of this size are indisputable in concluding that ivermectin is a safe first line of defense to confront the pandemic. Covid mortality was reduced 90 percent. There was also a 67 percent lower risk of hospitalization and a 44 percent decrease in Covid cases. Garcia-Aquilar et al reports a Mexican in vitro analysis showing a definitive interaction between ivermectin and the SAR-CoV-2 spike protein, which would account for its high efficacy in Covid-19 cases.[23]
The All India Institute for Medical Science (AIIMS) and the Indian Council of Medical Research (ICMR), two of India’s most prestigious institutions, acted against the WHO and launched an ivermectin treatment campaign in several states. In Uttar Pradesh there was a 95 percent decrease in morality (a decline from 37,944 to 2,014). The Indian capital of New Delhi witnessed a 97 percent reduction. During the same time period, the state of Tamil Nadu, which followed the WHO’s ban on ivermectin, had a 173 percent increase in deaths (from 10,986 to 30,016 deaths).
There have been many concerted efforts to discredit ivermectin and other repurposed drugs’ effectiveness. Most notable is the large TOGETHER Trial Brazil study published in the New England Journal of Medicine (NEJM) that concluded both ivermectin and another repurposed drug fluvoxamine showed no beneficial signs for treating Covid-19 patients. The study was widely reported in the mainstream media. However, a Cato Institute analysis discovered the study in fact showed its benefits and the results were in agreement with 87 percent of other clinical trials investigating ivermectin. The Cato analysis identifies many odd anomalies in how the trial was conducted including an unspecified placebo—although it is suspected it was Vitamin C, which has itself been shown to be mildly effective against the SARS-CoV-2 virus, and protocol changes as the study was underway including inclusion/exclusion criteria. By his own admission the TOGETHER Trial’s principal investigator Dr. Ed Mills at McMaster University in Ontario “designs clinical trials, predominantly for the Bill and Melinda Gates Foundation.”[24] In a McMaster University press release, the Gates foundation is listed as a funder for the study to debunk ivermectin and fluvoxamine.[25] Oddly, Gates is nowhere listed among the several funders in the NEJM study’s disclosure. In addition, TOGETHER Trials is owned by the Canadian for profit startup Purpose Life Sciences, founded by Mills; legal documents showed Mills’ PLS is largely funded and controlled by Sam Bankman Fried’s FTX who invested $53 million into the project. Administrators of FTX’s bankruptcy are suing PLS for fraud.[26]
In short, the ivermectin/fluvoxamine TOGETHER Trial was a complete medical sham and intentionally designed for one single purpose: to fuel media disinformation in order to undermine ivermectin’s superior efficacy and safety profile to Big Pharma’s more profitable designer drugs.
In 2004, the US Congress passed an amendment to the Federal Food, Drug and Cosmetic Act known as Emergency Use Authorization (EUA). This piece of legislature legalized an anti-regulatory pathway to allow experimental medical interventions to be expedited and bypass standard FDA safety evaluations in the event of bioterrorist threats and national health emergencies such as pandemics. At the time, passage of the EUA amendment made sense because it was partially in response to the 2001 anthrax attacks and the US’s entry into an age of international terrorism. However, the amendment raises some serious considerations. Before the Covid-19 pandemic, EUAs had only been authorized on four occasions: the 2005 avian H5N1 and 2009 H1N1 swine flu threats, the 2014 Ebola and the 2016 Zikra viruses. Each of these pathogen scares proved to be false alarms that posed no threat of pandemic proportions to Americans. The fifth time EUAs were invoked was in 2020 during the Covid-19 pandemic, which at the time seemed far more plausible.
Before the government can authorize an EUA to deploy an experimental diagnostic product, drug or vaccine, certain requirements must be fulfilled. First, the Secretary of the Department of Health and Human Services (HHS) must have sufficient proof that the nation is being confronted with a serious life-threatening health emergency. Second, the drug(s) and/or vaccine(s) under consideration must have sufficient scientific evidence to suggest they will likely be effective against the medical threat. The evidence must at least include preclinical and observational data showing the product targets the organism, disease or condition. Third, although the drug or vaccine does not undergo a rigorous evaluation, it must at least show that its potential and known benefits outweigh its potential and known risks. In addition, the product must be manufactured in complete accordance with standard quality control and safety assurances.
When we look back at the government’s many debacles during the Covid-19 pandemic, other EUA requirements warrant the spotlight. On the one hand, an EUA cannot be authorized for any product or intervention if there is an FDA alternative approved product already available, unless the experimental product is clearly proven to have a significant advantage. Moreover, and perhaps more important, EUAs demand informed consent. Every individual who receives the drug or vaccine must be thoroughly informed about its experimental status and its potential risks and benefits. Recipients must also be properly informed about the alternatives to the experimental product and nobody should be forced to take it.
Finally, an EUA requires robust safety monitoring and reporting of adverse events, injuries and deaths potentially due to the drug or vaccine. This is the responsibility not only of the private pharmaceutical manufacturers but also the FDA, physicians, hospitals, clinics and other healthcare professionals.
Obviously important cautions must be considered after approving a medical intervention under the EUA requirements. Foremost are the inherent health risks of any rapid response of experimental medical interventions, especially novel drugs and vaccines. As we observed during the FDA approval process and roll out of Pfizer’s and Moderna’s mRNA Covid-19 jabs, no long-term human trials were conducted to even estimate a reliable baseline of their relative efficacy and safety. The American public has blindly placed its trust in our federal health authorities decision-making. It is expected that under a national health emergency, the authorities would be completely transparent and act only by the highest ethical standards. However our institutions betrayed public trust and either ignored or transgressed cautions underlying EUA approved medical interventions in every conceivable way. Moreover, conflicts of interests have been discovered to have plagued the entire EUA review process.
Although the EUA amendment provides some protections to authorized drug and vaccine manufacturers, it was the Public Readiness and Emergency Preparedness Act (PREP) in 2005 that expanded liability protections. In addition to protecting private corporations, PREP also shields company executives and employees from claims of personal injury or death resulting from the administration of authorized countermeasures. The only exceptions for liability are if the company or its executive offices are proven to have engaged in intentional and/or criminal misconduct with conscious disregard for the rights and safety of those taking their drugs and vaccines.
During the pandemic, the FDA issued widespread EUAs with liability immunity for the PCR diagnostic kits for SARS-2, the mRNA vaccines and the anti-Covid-19 drugs. Curiously, the Secretary of the Department of Health and Human Services invoked the PREP Act on February 4, 2020 giving liability protections; this was over a month before the pandemic was officially announced, which raises serious questions about prior-planning before the viral outbreak in Wuhan, China.
From the pandemic’s outset, Fauci embarked on the media circuit to promise Americans that federal health agencies were doing everything within their means to get a vaccine on the market because there was no available drug to clear the SARS-2 virus. As we have seen with respect to ivermectin alone, this was patently false. Rather the government placed an overriding emphasis on vaccination with a near total disregard for implementing very simple preventative measures to inhibit viral progression. Once mass vaccinations were underway, we were promised that the SARS-2 virus would be defeated and life would return to normal. In retrospect, we can look back and state with a degree of certainty that American health authorities and these products’ corporate manufacturers may have violated almost every EUA requirement. Everything that went wrong with the PCR kits, the experimental mRNA vaccines and novel drugs could have been avoided if the government had diligently repurposed effective and safe measures as pandemic countermeasures. Very likely, hundreds of thousands of lives, perhaps millions, would have been saved.
Similarly the FDA issued a warning statement against the use of ivermectin. Even ivermectin’s manufacturer Merck discredited its own product. Shortly after ridiculing its drug, the Alliance for Natural Health reported, “Merck announced positive results from a clinical trial on a new drug called molnupiravir in eliminating the virus in infected patients.”[27]
And still the FDA considers these novel patented drugs to be superior to ivermectin. Favoring a vaccine regime and government-controlled surveillance measures to track every American’s movements, American health officials blatantly neglected their own pandemic policies’ severe health consequences. Ineffective lockdowns, masks, social isolation, unsound critical care interventions such as relying upon ventilators, and the sole EUA approvals of the costly and insufficiently effective drugs brought about nightmares for tens of millions of adults and children. This was all undertaken under Fauci’s watch and the heads of the US health agencies in direct violation of the EUA requirements to only authorize drugs and medical interventions when no other safe and effective alternative is available. Alternatives were available.
The 4-year history of the pandemic highlights a sharp distinction between dependable medical research and pseudoscientific fraud. The CDC adopted a common Soviet era practice to redefine the very definition of a vaccine and the parameters of vaccine efficacy in order to fit economic and ideological agendas. This explains Washington’s aggressive public relations endeavors to silence medical opponents. According to cardiologist Dr. Michael Goodkin’s private investigations, several of the most cited studies discrediting ivermectin’s antiviral benefits were intentionally manipulated in order to produce “fake” results.[28] These studies were then widely distributed to the AMA, American College of Physicians and across mainstream media to author “hit pieces” to demonize ivermectin and other repurposed drugs. The government’s belligerent and reactive diatribes, brazenly or casually advocating for censorship, were direct violations of scientific and medical integrity and contributed nothing towards developing constructive policies for handling a pandemic with a minimal cost to life. The consequence has been a less informed and grossly naïve public, which was gaslighted into believing lies.
The FDA’s EUAs for the Covid-19 vaccines and novel experimental drugs were in fact an attack on the amendments and PREP directives. Neither the vaccines nor drugs warranted emergency authorization because effective and safe alternatives were readily available. No doubt a Congressional investigation would uncover criminal misconduct and conscious fraud. Moreover, these violations of the PREP Act may have the potential to lead directly into medical crimes against humanity as outlined in the Nuremberg Code.
Although the Nuremberg Code has not been officially adopted in its entirety as law by any nation or major medical association, other international treaties, such as the Universal Declaration of Human Rights, the World Medical Association Declaration of Helsinki (which is not legally binding), the International Covenant on Civil and Political Rights (ICCPR) and the International Ethical Guidelines for Biomedical Research on Human Subjects incorporate some of Nuremberg’s main principles that aim to protect people from unethical and forced medical research. Although the US signed the ICCPR as an intentional party, the US Senate never ratified it. The ICCPR’s Article 7 clearly states, “No one shall be subject to torture or cruel, inhuman or degrading treatment or punishment,” which can legally be interpreted to include forced medical experimentation implied as cruel, inhuman treatment. Other ICCPR articles, 6 and 17, are also applicable to medical experimentation to ensure ethical conduct, obtaining proper informed consent and the right to life and privacy. For a moment, consider the numerous senior citizens in nursing homes and hospitals who were simply administered experimental Covid-19 vaccines without full knowledge about what they were receiving. And now how many children are being coerced by the pseudoscience of health officials’ lies to be vaccinated without any knowledge of these mRNA products’ risk-benefit ratio?
The US is also a signatory to the Helsinki Declaration, which, although not directly aligned with Nuremberg, shares much in common. The Declaration shares some common features with the EUA amendment and PREP Act. These include voluntary informed consent—which is universally accepted, adequate risk and benefit information about medical interventions, and an emphasis on the principle of medical beneficence (promoting well-being and the Hippocratic rule of doing no harm). It also guarantees protections for vulnerable groups, especially pregnant women and children, which the US government and vaccine makers directly violated by conducting trials on these groups with full knowledge about these vaccines’ adverse events in adults. In addition, weighing the scientific evidence to assess the risk-benefit ratios between prescribing ivermectin and HCQ over the new generation of novel experimental drugs conclusively favors the former. This alone directly violates the ethical medical principles noted above.
However, the failure to repurpose life-saving drugs is less criminal than the questionable unethical motivations to usher a new generation of genetically engineered vaccines that have never before been adequately researched in human trials for long term safety. This mass experimentation, which continues to threaten the health and well-being of millions of people, is global and can legally be interpreted as a genocidal attack on humanity.
If the emerging data for increasing injuries and deaths due to the Covid-19 vaccines is reliable—and we believe it is—the handling of the pandemic can be regarded as the largest medical crime in human history. In time, and with shifting political allegiances and public demands to hold our leaders in government and private industry accountable, the architects of this medical war against civilization will be brought to justice.
*
Richard Gale is the Executive Producer of the Progressive Radio Network and a former Senior Research Analyst in the biotechnology and genomic industries.
Dr. Gary Null is host of the nation’s longest running public radio program on alternative and nutritional health and a multi-award-winning documentary film director, including his recent Last Call to Tomorrow.
Notes
[1] https://www.cnn.com/videos/health/2021/08/29/dr-anthony-fauci-ivermectin-covid-19-sotu-vpx.cnn
[4] https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)31022-9/fulltext
[6] https://www.dldjournalonline.com/article/S1590-8658(21)00923-3/fulltext
[8] https://www.thelancet.com/action/showPdf?pii=S2666-6065%25252823%25252900012-3
[9] https://clinicalinfo.hiv.gov/en/drugs/ritonavir/patient
[10] https://www.yalemedicine.org/news/13-things-to-know-paxlovid-covid-19
[13] https://www.medrxiv.org/content/10.1101/2023.01.20.23284849v1.full.pdf
[14] https://evidence.nejm.org/doi/pdf/10.1056/EVIDoa2100044
[15] https://c19early.org/waters.html
[17] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290143/
[18] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539925/
[19] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564151/
[21] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129059/
[22] https://c19ivermectin.com
[23] https://www.mdpi.com/1422-0067/24/22/16392
[25] https://www.eurekalert.org/news-releases/855535
[26] https://c19ivm.org/tallaksen.html
[27] https://anh-usa.org/fda-ensures-pharma-profits-on-covid/
[28] https://www.trialsitenews.com/a/are-major-ivermectin-studies-designed-for-failure
New Studies: Pfizer’s Paxlovid doesn’t actually work, ‘rebound’ symptoms occur 25x more often than advertised
Failed drug cost U.S. taxpayers $12.6 billion
By Jordan Schachtel | The Dossier | April 5, 2024
Pfizer first scammed the world with its “100% safe and effective” Covid mRNA vaccines, and as it turns out, that was just the opening salvo from a pharmaceutical cartel that is inundated with corruption and deceit.
I wanted to turn your attention to two significant recent studies on Paxlovid, the Covid-19 oral pill that the U.S. government spent $12.6 billion taxpayer dollars on subsidizing for Pfizer.
The first study, which is brought to you by Pfizer funds (though they noticeably don’t use the brand name Paxlovid in the study), finds that Paxlovid does not actually work. They’ve known this since July, 2022, but for reasons unknown, waited two years to publish the results.
“The time to sustained alleviation of all signs and symptoms of Covid-19 did not differ significantly between participants who received nirmatrelvir–ritonavir (Paxlovid) and those who received placebo,” the authors write in this New England Journal of Medicine study, which was published on April 3rd.
That’s right. It doesn’t work at all.
In rolling out Paxlovid, Pfizer claimed in a press release that its preliminary data showed an 89% reduction in hospitalization and death for patients who took the pill.
Curiously, the Pfizer-funded study concluded in July 2022, just months after Paxlovid became available, but this seems to be the first time that results have been public.
Now, hundreds of millions of manufactured doses later, the most sophisticated apples to apples comparison shows that it isn’t effective whatsoever.
But it gets worse.
Remember “Paxlovid rebound”?
That’s short for people’s symptoms coming back after taking a course of Paxlovid.
When Paxlovid first hit pharmacy shelves, Pfizer claimed that Paxlovid rebound was inconsequential, amounting to 1 or 2 percent of patients who were prescribed the drug.
But a late March study published in The Journal of the American Medical Association (JAMA) found that about 1 in 4 patients on Paxlovid suffered from “Paxlovid rebound.” This study didn’t just analyze the presence of viral fragments. It found that 24.5 percent of enrolled patients on Paxlovid suffered from *symptomatic* rebound.
Now it makes sense why so many high profile figures, such as Joe Biden and Anthony Fauci, had bouts of “Paxlovid rebound.” It isn’t rare whatsoever.
Now imagine if Pfizer told the truth about its failed Covid-19 drug from the beginning. That truth would’ve resulted in Pfizer taking a massive financial hit, given that they relied on Paxlovid to sustain their multi billion dollar profit margins.
Meanwhile, Pfizer’s market value has continued to crash over the past year. Fewer and fewer people are buying what Pfizer is selling.
Now who will be held accountable for the greatest pharmaceutical fraud and swindle operation of all time?
Fraud Revealed in German Covid Response
Minutes of Robert Koch Institute crisis meetings reveal undue influence of “external actor”
By John Leake | Courageous Discourse™ | April 3, 2024
As a conspiracy theorist, I am batting .400. Over the last four years, I have examined many official representations of reality and posited the theory that they are the fraudulent misrepresentations of two or more persons in positions of power or undue influence. By definition, two or more persons committing an act of fraud are participating in a criminal conspiracy.
At the risk of sounding boastful, ALL of my conspiracy theories have been confirmed by the subsequent discovery of factual evidence to be actual conspiracies.
Back in 2020, as I watched with dismay as many of my old German friends lost their minds under the pressure of daily propaganda, I posited the theory that the Robert Koch Institute—Germany’s official infectious disease institute—had been hijacked by political interests.
My hunch was that IF unbiased scientific assessments were being conducted at the Robert Koch Institute, these were being distorted or ignored by the German government.
Now comes the news that the German independent magazine, Multipolar, has successfully sued the Robert Koch Institute to release the minutes of its Covid Crisis deliberations in 2020. Though heavily redacted, the documents reveal that pressure was indeed exerted on the Institute’s scientists to go along with public policies not supported by scientific research. For example, the Institute expressed the opinion that masking and lockdowns were of doubtful value.
Of special note was the following revelation:
As Multipolar has already reported based on the previously secret papers, the tightening of the risk assessment from “moderate” to “high” announced by the RKI in March 2020 – based on all lockdown measures and court rulings on them – was, contrary to what has previously been claimed, not based on a professional assessment of the institute, but on the political instructions of an external actor – whose name is blacked out in the minutes.
In New Bird Flu Scare Comes Tacit Admission Coronavirus Was Not a Big Deal
By Adam Dick | Peace and Prosperity Blog | April 5, 2024
“Bird flu pandemic could be ‘100 times worse’ than COVID, scientists warn.” That is the headline at the New York Post for one of many media reports out Thursday spreading the latest pandemic scare.
Note the “100 times worse” comparison. Why not “nearly as bad,” “as bad,” or even “twice as bad” as coronavirus? The answer is that the fearmongers know that most people are on to the coronavirus hoax whereby a run-of-the-mill health threat was exaggerated to justify tyrannical measures including forcing termination of a vast amount of in-person interaction, mandating mask wearing, and even pushing and mandating experimental “vaccine” shots marketed as safe and effective despite being both dangerous and ineffective. All the while, good early treatment options were suppressed, resulting in greater sickness and death as well as expansive use of dangerous medical procedures and pharmaceuticals for people whose serious illness could have been prevented.
The world could be turned upside down over coronavirus because of a concerted effort of government and media to paint coronavirus as both extremely dangerous to everyone and something for which there were not already available good medical countermeasures. Both of those assertions were false. But, at the time, many people bought into the charade and trusted that “the science” propounded by the government and media selected “experts” required radical changes in human behavior, widespread participation on novel medical experimentation, and extreme restraints on liberty.
But now it is a new day. Looking back on the coronavirus scare, increasingly people realize, including some who are ashamed to discuss the matter, that they were duped. And they don’t want to be duped again. “Fool me once, shame on you; fool me twice, shame on me,” the saying goes.
Yet, trickery is a go-to tactic for expanding power. The government and its business allies in medical and other fields aren’t about to give up on that tactic that reaped such huge gains during the coronavirus scare. Thus the ploy of tacitly admitting what has become common knowledge — that coronavirus was way overblown — so that the repression and profit process can be repeated anew to deal with a threat that, trust us, is this time really, really, really bad.
And what scientist does the New York Post article quote to support the claim that scientists say the bird flu is “100 times worse than COVID” declared in the article’s title? His name is John Fulton, described in the article as “a pharmaceutical industry consultant for vaccines.”
Oh brother: Here we go again. Or do we? If enough people stand up and say “no you don’t this time,” this new dangerous charade can be stopped in its tracks.
Does the Meningococcal Vaccine Used in the U.S. Stop Infection and Transmission of Meningococcal Bacteria?
Your bite-size dose of immunity against vaccine misinformation. Spread the truth.
Injecting Freedom by Aaron Siri | April 2, 2024
Does the meningococcal vaccine (MenACWY) used in the United States stop infection and transmission of meningococcal bacteria?
“Yes” or “No”?
When picking an answer, keep in mind that MenACWY is one of the vaccines mandated to attend secondary school in most U.S. states (and to attend university/college in many states), and the justification for these rights-crushing mandates is to prevent transmission of meningococcal bacteria in the school setting.
According to the CDC, “Rates of meningococcal disease have declined in the United States since the 1990s and remain low today. Much of the decline occurred before the routine use of MenACWY vaccines. … [D]ata suggest MenACWY vaccines have provided protection to those vaccinated, but probably not to the larger, unvaccinated community (population or herd immunity).”
Also consider that according to the CDC, “Protection from MenACWY vaccination wanes in most adolescents within 5 years,” and the CDC does not recommend routine administration of this vaccine for adults. And as for the claimed protection from this vaccine, its clinical trial did not prove it prevented a single case of meningococcal disease (relying instead on antibody levels, not clinical findings).
Screenshots of the relevant portions of the websites linked above (in case they change).
‘Shocking Cover-up’: DOJ Lawyers Committed Fraud in Vaccine Injury Case, CHD Attorney Alleges in Motion Filed Today
By Brenda Baletti, Ph.D. | The Defender | April 2, 2024
Rolf Hazlehurst, a Children’s Health Defense (CHD) staff attorney and father of a son with autism, today filed a motion in federal court alleging lawyers representing the U.S. Department of Health and Human Services (HHS) fraudulently concealed evidence that vaccines can cause autism.
In a motion filed in the U.S. Court of Federal Claims, Hazlehurst alleged that U.S. Department of Justice (DOJ) lawyers who represented HHS in vaccine injury cases repeatedly defrauded the judicial system — from the National Vaccine Injury Compensation Program (NVICP) to the U.S. Supreme Court.
That fraud led to thousands of families of vaccine-injured children being denied the right to compensation and the right to have their cases heard, according to the motion.
“This motion makes very serious and well-substantiated allegations of a massive scheme of fraud on the courts,” said Kim Mack Rosenberg, CHD general counsel who also is of counsel to Hazlehurst in the federal case.
“The evidence submitted in support of the motion clearly shows that attorneys from the Department of Justice concealed and misrepresented highly relevant information from the special masters in the Vaccine Injury Compensation Program and the judges in the courts,” Mack Rosenberg told The Defender.
Hazlehurst’s son Yates regressed into autism after being vaccinated as an infant. In the early 2000s, his family and thousands of others filed cases seeking compensation for vaccine-induced autism through the NVICP.
The program consolidated all of the petitions into the Omnibus Autism Proceeding (OAP) and selected six representative “test cases” — of which Yates’ was the second — as the basis for determining the outcome of the remaining 5,400 cases.
Unbeknownst at the time to the petitioners and the NVICP special masters, the DOJ’s star expert medical witness, Dr. Andrew Zimmerman informed DOJ attorneys during the ongoing omnibus proceedings that he had reversed his original opinion and determined that vaccines can and do cause autism in some cases.
In what Hazlehurst alleges was “a shocking cover-up,” instead of allowing Zimmerman to share his revised opinion, the DOJ attorneys relieved Zimmerman of his duties as a witness.
However, they continued to use excerpts from his unamended written opinion to make their case that vaccines did not cause autism — misrepresenting his position and committing “fraud on the court.”
According to the motion, the DOJ’s first act of fraud snowballed into a scheme of deception with far-reaching implications in which DOJ attorneys repeatedly misrepresented Zimmerman’s opinion and concealed other evidence that emerged during the test case hearings in the OAP in subsequent cases before multiple courts.
“As a result, thousands of cases in the Omnibus Autism Proceeding were denied compensation and the impact beyond the OAP is enormous,” Mack Rosenberg said. “This fraud affected the Vaccine Injury Compensation Program — especially the Omnibus Autism Proceeding — the Court of Federal Claims, the Court of Appeals for the Federal Circuit and even the U.S. Supreme Court.”
Hazlehurst said he is “asking the court to give this motion the serious attention it deserves.” He added, “At a minimum, the court should allow discovery and hold a hearing on this motion.”
Overturning a ruling due to fraud on the court is an extraordinary remedy reserved for extraordinary cases but according to Hazlehurst, “This motion we filed shows that this indeed is an extraordinary case.”
The DOJ has until April 30 to respond to the motion.
CHD CEO Mary Holland told The Defender, “Vaccines most definitely do cause autism, and the government has been lying about this reality for decades.”
Holland added:
“With others, I published a law review article in 2011 showing that the government absolutely knew that vaccines cause autism — and yet they have covered it up and lied about it since the inception of the Vaccine Injury Compensation Program.
“How many hundreds of thousands of children and families would have been spared the heartaches and crushing financial burdens of autism had the government come clean?”
‘Exceptionally difficult’ to obtain compensation through NVICP
In the late 1980s, a substantial number of lawsuits for vaccine injuries related to Wyeth’s (now Pfizer) DPT vaccine, combined with “grossly insufficient compensation” for victims of vaccine injury, threatened the vaccine program’s viability.
In response, Congress passed the National Childhood Vaccine Injury Act of 1986, which established the “vaccine court.” The law gave the pharmaceutical industry broad protection from liability and proposed to compensate vaccine-injured children through the new NVICP.
The NVICP originally was designed to be a “swift, flexible, and less adversarial alternative to the often costly and lengthy civil arena of traditional tort litigation.”
To receive compensation, parents file a claim with the program.
The Court of Federal Claims (which oversees the program) appoints “special masters” — typically lawyers who previously represented the U.S. government — to manage and decide the individual claims. Attorneys may represent the petitioners, and the DOJ represents HHS.
NVICP proceedings are more informal than a typical courtroom. Unlike regular court proceedings, petitioners in the “vaccine court” have no right to discovery.
If a petitioner files a claim for a vaccine covered under the program and listed on the Vaccine Injury Table — the list of known vaccine side effects associated with certain vaccines within set time frames — it is presumed that a vaccine caused the petitioner’s injury and the petitioner is eligible for compensation without proof of causation.
However, if a petitioner experiences an “off-table injury” — an injury not listed on the table or that didn’t happen in the recognized injury time frame — the petitioner must prove by “a preponderance of evidence” that the vaccine caused the injury. Evidence includes medical records and expert witness testimony.
Claims must be filed within three years of the first symptom or two years of death.
Petitioners must provide a medical theory of the cause, a sequence of cause and effect, and show a temporal relationship between vaccine and injury.
However, the NVICP does not specify the required volume and type of evidence, so meeting the “preponderance of evidence” standard is largely at the discretion of the special master.
Petitioners can appeal NVICP cases to the Court of Federal Claims, the Court of Appeals for the Federal Circuit and ultimately to the U.S. Supreme Court.
It is “exceptionally difficult” to obtain compensation within the NVICP, Hazlehurst told The Defender. The proceedings are often turned into drawn-out, contentious expert battles and the backlog of cases is substantial.
The Vaccine Act of 1986 is unjust for petitioners, Hazlehurst alleges. And that injustice reached its zenith with the OAP, when the DOJ perpetrated fraud right under the noses of the special masters, signaling the beginning of the fraud on the courts that continues to this day.
Hazlehurst told The Defender he hopes his motion will shed light on the damage inflicted by this law and that it will ultimately help end the autism epidemic.
“The Vaccine Act of 1986 is one of the fundamental causes of the autism epidemic,” Hazlehurst said. “Understanding why this is true, and how the United States Department of Justice perpetrated fraud upon the courts, including the Supreme Court of the United States, is the key to ending the autism epidemic.”
A short history of the autism omnibus proceedings
By 2002, to address a “massive influx” of petitions alleging vaccine-induced autism, the Office of Special Masters combined over 5,000 claims into the OAP to determine whether vaccines cause autism and if so, under what conditions.
Initially, the NVICP planned to investigate causation issues and apply those general findings to individual cases. However, the program changed its strategy and instead selected six “test cases” by which it would examine the evidence for injuries caused by the measles mumps rubella (MMR) vaccine, thimerosal-containing vaccines (TCV), or a combination of both.
Then it would apply the findings of the test cases to other similar cases.
In doing so, Hazlehurst alleges, the court conflated general causation evidence with specific causation evidence from a few cases, without allowing for rules of discovery or evidence that would apply in an actual court.
This, Hazlehurst said, “was a recipe for disaster” as each test case was then used to determine the outcome for the remaining 5,000 cases.
Three cases — Cedillo v. HHS, Hazlehurst v. HHS and Poling v. HHS — are at the center of the alleged fraud by the DOJ.
Fraud #1: the Zimmerman testimony
Hearings for the first OAP test case, Cedillo v. HHS, began in 2007. Zimmerman had worked with the DOJ to prepare an expert report on behalf of HHS finding that Michelle Cedillo’s autism had likely not been caused by the MMR vaccine.
Zimmerman later wrote in a 2018 affidavit that he attended the Cedillo hearing and listened to the testimony of Dr. Marcel Kinsbourne, another world-renowned expert in pediatric neurology.
On that basis, Zimmerman stated, he decided to clarify his written expert opinion about Michelle Cedillo, concerned it would be taken out of context.
Zimmerman spoke with DOJ attorneys to clarify that his expert opinion in the Cedillo case “was not intended to be a blanket statement as to all children and all medical science,” according to the 2018 affidavit.
He specified that advances in science, medicine and his own clinical research had led him to believe there were exceptions in which vaccinations could cause autism.
He also referred the attorneys to a paper he published with colleagues in 2006, the Poling paper, describing the case of an unidentified child who suffered regressive autism following vaccine adverse reactions. The paper suggested a possible association between mitochondrial dysfunction, vaccinations and regressive autism.
After communicating this evidence to DOJ attorneys, the DOJ dismissed Zimmerman as a witness but continued to use his written opinion as general causation evidence.
The DOJ was also allowed to use that report, submitted in one test case, as general causation evidence in other test cases.
None of the petitioners in the test cases could cross-examine Zimmerman, because he was no longer a witness. This was only possible because the federal rules of evidence do not apply in NVICP proceedings.
Yates’ case, Hazlehurst v. HHS, was the second test case in the OAP. His treating neurologist, Dr. Jean-Ronel Corbier testified Yates’ autism was likely caused by a genetic predisposition combined with an environmental insult in the form of vaccinations administered when Yates was ill. (Yates was a patient of Zimmerman in 2002.)
Corbier’s theory of causation in Yates was similar to the theory developed by Zimmerman in the Poling paper and shared with DOJ attorneys.
Yet, despite knowing Zimmerman had concluded that in a subset of children like Yates, vaccines can cause autism, the DOJ “intentionally and fraudulently” misrepresented Zimmerman’s expert testimony in its closing statements in Yates’ case, Hazlehurst alleges.
DOJ attorneys selectively quoted Zimmerman’s expert report from the Cedillo case, telling the court that Zimmerman found there was “no sound evidence to support a causative relationship with exposure to both or either MMR and/or mercury,” when Zimmerman had explicitly told the DOJ that his opinion was the opposite, according to the affidavit.
Fraud #2: the Hannah Poling case
Three weeks after closing arguments in Yates’ case, the DOJ quietly conceded Hannah Poling’s case, which was on the verge of becoming the fourth test case.
Hannah regressed into autism over several months after being vaccinated against nine diseases at one doctor’s visit.
In 2003, Poling’s father, Jon, a physician and trained neurologist, and mother, Terry, an attorney and nurse, filed an autism petition against HHS under the NVICP for their daughter’s injuries.
Jon Poling was a co-author of the 2006 paper with Zimmerman that analyzed an unnamed child, later revealed as Hannah Poling, who had a mitochondrial disorder — a condition with which Yates was later diagnosed.
In 2007, just three weeks after the lead DOJ attorney misrepresented Zimmerman’s opinion during the hearing in Hazlehurst, the same DOJ attorney submitted a report to the special masters conceding that in the case of Poling v. HHS, Hannah’s “regressive encephalopathy with features of autism spectrum disorder” (i.e., regressive autism) was caused by a vaccine injury, based upon a preponderance of the evidence standard.
This was the same neurological diagnosis Zimmerman had made for Yates in 2002.
According to court documents, if HHS had not conceded Poling, Poling v. HHS would have been designated as a test case. However, because the DOJ conceded the case, it was taken out of the omnibus and the DOJ had the case records sealed —- although they were later leaked to the press and published in the Huffington Post in 2008.
In March 2008, Hannah’s parents moved to make the proceedings transparent and available to the public, but the DOJ opposed the motion and the NVICP deferred a ruling on the motion for 60 days.
During those 60 days, the DOJ filed amendments to its report conceding the Poling case. It retroactively changed the basis for compensation to say that Hannah had a “table injury.”
This meant that instead of conceding that the petitioners had proven with a preponderance of evidence that the vaccines caused her autism, they said she had a presumptive injury on the vaccine table, in which causation is presumed.
By conceding the Poling case, opposing the parents’ motion for complete transparency and changing the basis for compensation, the DOJ was able to conceal fraud and critical material evidence of how vaccines cause autism, according to Hazlehurst.
Fraud #3: appellate courts and the U.S. Supreme Court
On Feb. 12, 2009, the special masters denied compensation in the first three cases. They found the petitioners failed to establish causation between MMR or TCV vaccines and autism.
In Hazlehurst’s case, the NVICP explicitly relied on the portion of Zimmerman’s expert report that DOJ attorneys misrepresented.
The Hazlehursts appealed to the Court of Federal Claims and the Court of Appeals for the Federal Circuit, both of which upheld the special master’s decision — by relying on Zimmerman’s misrepresented opinion and knowingly fraudulent statements made by a DOJ attorney, according to Hazlehurst.
Those prior decisions directly influenced the U.S. Supreme Court’s decision in the Bruesewitz v. Wyeth.
In that case, Wyeth, now Pfizer, argued that a decision favoring the Bruesewitz family — who was attempting to sue the company for their daughter’s vaccine injury — would lead to a “flood of frivolous lawsuits,” including by the families from the omnibus.
Amicus briefs from the American Academy of Pediatrics, GlaxoSmithKline, Merck and Sanofi Pasteur on behalf of Wyeth relied on Hazlehurst v. HHS and other OAP decisions that were based on the misrepresentation of Zimmerman’s testimony that there was “no scientific basis” that vaccines cause autism.
The Supreme Court ruled that the National Childhood Vaccine Injury Act, and the NVICP it created, preempt all design-defect claims against vaccine manufacturers by individuals seeking compensation for injury or death.
In oral arguments and in their written opinions, the justices explicitly cited the portions of the amicus briefs citing Hazlehurst v. HHS and other OAP rulings that relied on the DOJ misrepresentations in their rulings.
Since that ruling, the special masters have continued to rely on the DOJ’s fraudulent claims to deny compensation to families filing complaints in the NVICP.
Robert F. Kennedy Jr., CHD chairman on leave, and Hazlehurst in September 2018 filed a complaint with the DOJ Office of Inspector General outlining what they then knew about the DOJ’s fraud during the OAP.
The DOJ Office of Professional Misconduct investigated and responded in a June 2019 letter that it found no wrongdoing.
In that letter, however, the Office of Professional Responsibility conceded the DOJ had in fact kept Zimmerman’s testimony while dismissing him as a witness in order to avoid creating the appearance that he had changed his opinion and to prevent the petitioners from cross-examining him, according to Hazlehurst.
The ‘fraud on the court’ doctrine
It has taken 17 years, Hazlehurst said, since the DOJ’s first alleged act of fraud upon the court, for him to gather all of the admissible evidence necessary to “connect the dots and reveal the DOJ’s web of deceit” to make this claim under the “fraud on the court” doctrine.
Under this doctrine, codified as Rule 60(d)(3) in the rules of the Court of Federal Claims, there is no time limit for the court to overturn a judgment made on the basis of fraud on the court.
The petitioner must demonstrate that there was fraud, intent to defraud and that the fraud affected more than one instance of litigation — putting the integrity of the judicial process at stake.
Hazlehurst alleges DOJ attorneys committed fraud by knowingly making false statements and offering evidence they knew to be false and that they did not take remedial action to disclose information they knew to be false and misleading to the court.
The special masters themselves have an obligation to consider all relevant evidence, but didn’t, in this case, Hazlehurst said. Instead, they ignored the contradictions in Zimmerman’s opinions and ignored the Poling evidence.
This is particularly problematic for NVICP cases, where petitioners can’t conduct meaningful discovery or cross-examination and the special masters’ oversight is the only meaningful safeguard to prevent the DOJ’s abuse of power, according to Hazlehurst.
“There is nothing fair about a government proceeding where the government controls the admissibility of evidence,” he said.
Hazlehurst said that by forcing people injured by vaccines into an administrative program, petitioners are deprived of the basic constitutional rights to due process and equal protection under the law. “It should be declared unconstitutional,” he said.
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Big Pharma designed WHO’s Global Health Policy from 2000-2009
Corruption and deception, not science, is the foundation of WHO health policy
By Judy Wilyman PhD | Vaccination Decisions | April 1, 2024
“The past was erased, the erasure was forgotten, the lie became truth.” – George Orwell, 1984
The history of the GAVI alliance, a board that influences the direction and design of WHO’s global health policies, illustrates how these policies have been directly influenced by industry partners from 2000-2009, and not by an objective board selected by the WHO.
This direct influence was hidden from the public in 2009 when the alliance became known as the Gavi board. At this time its composition and function changed to hide the role that industry had played from 2000-2009 in changing the direction of global health policies to a new focus on vaccine production and global implementation.
History of the Gavi Board:
In 1998 the Global Alliance for Vaccines and Immunisation (GAVI) was established by the Head of the World Bank after a meeting with pharmaceutical companies and other agencies. The GAVI alliance was established on the advice of industry because the pharmaceutical companies were claiming that there was no incentive for them to provide vaccines to the developing countries.
This meeting led to the Bill and Melinda Gates Foundation providing the seed funding of $750 million in 1999 and governments then matched this figure to establish an alliance of private-public partnerships in 2000, to fund the vaccination programmes for all countries.
In 2000 the alliance was launched at the World Economic Forum (WEF), not the World Health Organisation (WHO), and it established a working party to work with the WHO to design the International Health Regulations (IHR), yet it was a body established outside of the WHO’s charter.
At this time all stakeholders in the Global Alliance for Vaccines and Immunisation (GAVI) were able to directly influence the design of the WHO’s Global Health Policies through this working party (2000-2009), including the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA). They could attend meetings and present information for policy development.
Other stakeholders in the GAVI at this time included the BMGF, the Rockefeller Foundation, the World Bank and the International Monetary Fund (IMF). The influence of these stakeholders led to a new focus on vaccine production and implementation in the WHO’s global health policies.
These global policies were presented to countries in the International Health Regulations (IHR) that came into force in June 2007.
This direct influence of all stakeholders changed in 2009 when the GAVI alliance became known as the GAVI board. Its composition was changed to include only four permanent board members – UNICEF, BMGF, the World Bank and WHO – and other partners would be on a part-time basis.
This change to only four permanent board members, one of which was now the WHO, hides the fact that from 2000-2009 all stakeholders were able to directly influence the design of WHO’s global health policies.
The first recorded meeting of the Gavi board on its website is in 2009. It describes the role of the Gavi board as ‘being responsible for strategic direction and policy-making, oversees the operations of the Vaccine Alliance and monitors programme implementation’ .
This alliance of partners, many of whom profit from vaccines, make donations to the Gavi board and still influence global health policies in a more indirect fashion.
The WHO’s IHR are currently being amended with strong influence from this corporate alliance. If the amendments are approved, the draconian directives implemented during the COVID ‘pandemic’ years, will become binding on every WHO member country, whenever the director of the WHO declares another pandemic. This is removing fundamental human rights and objective scientific evidence from global health policies.
It is time for Australians to make our voices heard to ensure that Australia exits the WHO and joins the World Council for Health to protect both human health and fundamental human rights in all public health policies.
[The information above can be referenced from Ch 3 of my PhD 2015]
Important Information:
- Here is the witness statement from ex-Qantas pilot, Captain Graham Hood, describing that lack of evidence for safety and efficacy that was used by the Australian Therapeutic Goods Administration (TGA) and the Australian Prime Minister, Scott Morrison, to mandate this mRNA genetically-engineered injection (called a ‘vaccine’) in the Australian population – Ex-Qantas Pilot, Graham Hood, provides a witness statement in the Australian parliament.
- Australian Medical Professional Society (AMPS) presents ‘Too Many Dead’ in Australia, but the Australian government will not investigate and the media does not report these facts.
- Study finds the Majority of Patients with Long COVID were Vaccinated
- Epidemic of Fraud
Globalism and Disease X
By Meryl Nass | March 30, 2024
What is biowarfare? COVID was due to a biological warfare agent. It was designed in one or more laboratories to be more virulent than its natural precursors:
- to prefer to infect humans;
- to infect more organs than possible in naturally occurring strains;
- to interfere with the body’s immune responses.
I say one or more laboratories becasue many of its features had been previously discovered or created in various laboratories, and then these features were essentially grafted onto a coronavirus, one by one; or some features were achieved by passaging the virus through humanized mice, other humanized animals, human cell tissue cultures or humans themselves.
Why were these features created? In which labs?
Why were they painstakingly added to a coronavirus backbone? Where was this done and how many labs were involved?
Why was a coverup by western scientists so critical? Because claiming that pandemics come from animals living in nature, and are spread to humans due to our incursions into their territory, was needed to justify the entire biosecurity agenda that the WHO is steamrolling over us.
By the way, the newest version of the treaty (released March 7, 2024) states that part of the WHO plan is to “identify” those areas where disease “spillover” occurs. You watch: the WHO will then empty those areas of humans. It really is a great cover story, “spillover.” Except it is a total lie.
_____________________
Historically most biowarfare agents were naturally occurring viruses or bacteria. Here is one example in which whistleblowers identified the hand of the CIA.
It is “gain-of-function” research that makes them more virulent and/or more transmissible. Gain of function research was considered illegal under international law until about 2001, and then the customary norms of national behavior simply changed, after the US was caught ignoring the usual norms—as revealed in the NYT on 9/4/2001 and in the book GERMS.
The WHO suggested it should be put in charge of gain-of-function research in the pandemic treaty draft that was released on February 14, 2024. It only took 3 weeks before a new draft was issued on March 7, 2024 in which all mention of “gain-of-function” was erased. I wonder if the rapidity of release of the next draft (it usually takes about 3 months to get a new draft) had to do with cutting out the Gain-of-Function section.
But the idea of requiring nations to supply the WHO with samples of potential pandemic pathogens, and to upload their genetic sequences to publicly accessible databases asap remained, was discussed with even more details in the newest March 7 draft. The WHO and nations would be free to share biological warfare agents aka potential pandemic pathogens (essentially) with anyone they liked.
This makes no sense any way you look at it. The goal seems to be a situation where “Pandemics R Us” and they appear frequently, with no ability to tell where they came from or whether they were deliberate or an accident. By sharing them all globally the WHO has paved the way for using the alibi of accidental release for future COVIDs.
The biowarfare segment starts at about 26 minutes into the episode.
As I said, we at DoortoFreedom.org are here to help you educate your lawmakers while you urge them to question this effort publicly, introduce resolutions, and in other ways throw some boulders in front of the steamroller, just like Louisiana’s Senate did this week.
merylnass@gmail.com
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Book Review
Jeffrey Epstein: A Jewish Individual?
The Occidental Observer | February 5, 2023
One Nation Under Blackmail: The Sordid Union between Intelligence and Organized Crime that Gave Rise to Jeffrey Epstein (Volume 1 & 2) by Whitney Webb
“Far from being an anomaly, Epstein was one of several men who, over the past century, have engaged in sexual blackmail activities designed to obtain damaging information (i.e., “intelligence”) on powerful individuals with the goal of controlling their activities and securing their compliance.”[1]
Jeffrey Epstein is dead and Ghislaine Maxwell is locked away in prison, and the thought-makers of our world seem keen to let the more explosive parts of the scandal dissipate from the public consciousness. As far as the mainstream media is concerned, Epstein and Maxwell were little more than well-connected socialites who ran a sex-trafficking ring for the rich and the powerful, and the focus has shifted instead to the criminal and civil cases seeking to achieve redress for the victims of sexual abuse.
On occasion some newspaper articles will mention the hidden cameras littered across Epstein’s properties, others the reams of CDs and hard drives found within them during the FBI raids. Altogether missing from the Netflix documentaries (Jeffrey Epstein: Filthy Rich [2020] and Ghislaine Maxwell: Filthy Rich [2022]) or the articles that spend their time narrowly focusing on the links between Epstein and Bill Gates, is the acknowledgement of the true nature of Epstein himself and the ultimate purpose of this sex-trafficking of minors — a sexual blackmail operation.
Not everyone is cowardly enough to let these controversial aspects lie untouched, as the newly released two-volume book One Nation Under Blackmail by independent reporter Whitney Webb seeks to blow wide open this media-enforced blackout. Utilizing primarily open-source information (that is, publicly accessible information such as books, newspapers articles and government reports),[2] Webb’s book delves into the life and times of Jeffrey Epstein and his deep ties to Jewish billionaires and Israeli intelligence. … continue
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