Only two years ago numerous alternative media sources including Zero Hedge were accused of spreading “conspiracy theories” and false information relating to the origins of the Covid-19 virus. Specifically, anyone who dared to suggest that the Level 4 virology lab in Wuhan, China (right across town from covid ground zero) might be the source of the outbreak, faced outright censorship on social media. The question many people should have been asking is: “Why?” – Why was the censorship so aggressive over clearly reasonable investigations into Wuhan lab operations?
Not only that, but why were the denials and spin from officials like Anthony Fauci so swift? Why not simply examine the evidence instead of dismissing it out of hand?
The real reason for the campaign to silence discussion on the Wuhan lab becomes evident as the connections between Fauci, the NIH and the lab are revealed. Elements of the US government including Fauci were in fact bankrolling gain of function research on coronaviruses at Wuhan, and shielding it from government oversight. It is undeniable. If one accepts that the most likely source for the covid pandemic was the Wuhan laboratory then one must also accept that Fauci and his associates helped to create the pandemic.
Fauci lied about these connections incessantly under oath. Here is Anthony Fauci defending his initial lie to Congress using further lies during questioning by Sen. Rand Paul:
Evidence of the research includes documents from the Department of Defense (obtained by Project Veritas ) which confirm that EcoHealth Alliance approached DARPA in 2018 about gain of function research on bat borne coronaviruses under a proposal called Project Defuse. DARPA rejected the proposal on the grounds that it did not outline the risks of such experimentation and violated a moratorium on gain on function research. EcoHealth then went to Fauci and the NIH for funding, and Fauci was quick to support it using the labs in Wuhan.
Documents from the NIH itself also show that the group engaged in gain of function research at Wuhan focusing on developing coronaviruses that could be transferred from animals to humans. Fauci was aware of this research by at least 2021 (and was likely involved from the very beginning) and yet continued to lie about NIH involvement.
Meanwhile, the National Pulse– which has done multiple deep-dive investigations on the topic, uncovered in May of 2001 that the WIV scrubbed all mention of its partnership with the NIH from their website.
Scrutiny over Fauci’s disinformation campaign may be too little too late, and we have to wonder if the man will ever face consequences for his actions. However, the exposure of Fauci and the NIH is so overwhelming that the former Director of National Intelligence now admits that Fauci misled Congress and the American public.
The former Director of National Intelligence agrees with the former CDC Director that Dr. Anthony Fauci lied to Congress under oath about funding gain-of-function research at the Wuhan lab:
"Some of Dr. Fauci's testimony is inconsistent with some of the intelligence that we have… pic.twitter.com/raoVCBQdyR
Hopefully, this revelation will help to discourage people from blindly following the claims of government bureaucrats during the next manufactured global crisis.
Robert F. Kennedy, Jr. and Children’s Health Defense (CHD) on Friday filed a class action lawsuit against President Biden, Dr. Anthony Fauci and other top administration officials and federal agencies, alleging they “waged a systematic, concerted campaign” to compel the nation’s three largest social media companies to censor constitutionally protected speech.
Kennedy, CHD and Connie Sampognaro filed the complaint in the U.S. District Court for the Western District of Louisiana, Monroe Division, on behalf of all the more than 80% of Americans who access news from online news aggregators and social media companies, principally Facebook, YouTube and Twitter.
The plaintiffs allege top-ranking government officials, along with an “ever-growing army of federal officers, at every level of the government” from the White House to the FBI, the CIA and the U.S. Department of Homeland Security (DHS) to lesser-well-known federal agencies of inducing those companies:
“to stifle viewpoints that the government disfavors, to suppress facts that the government does not want the public to hear, and to silence specific speakers — in every case critics of federal policy — whom the government has targeted by name.”
Kennedy, chairman and chief litigation counsel of CHD, said American Democracy itself is at stake in this case:
“U.S. Supreme Court Justice Potter Stewart said, ‘Censorship reflects a society’s lack of confidence in itself. It is a hallmark of an authoritarian regime.’ It also violates the Constitution.
“The collaboration between the White House and health and intelligence agency bureaucrats to silence criticism of presidential policies is an assault on the most fundamental foundation stone of American Democracy.”
The lawsuit’s argument rests on the Norwood Principle, an “axiomatic,” or self-evident, principle of constitutional law that says the government “may not induce, encourage, or promote private persons to accomplish what it is constitutionally forbidden to accomplish.”
According to the plaintiffs, the U.S. government used the social media companies as a proxy to illegally censor free speech.
The complaint cites the now-weekly, ongoing disclosures of secret communications between social media companies and federal officials — in the “Twitter files,” other lawsuits and news reports — which revealed threats by Biden and other top officials against social media companies if they failed to aggressively censor.
The suit points to examples where the censorship campaign allegedly trampled First Amendment freedoms, such as the Hunter Biden laptop story, the COVID-19 Wuhan lab-leak theory and the suppression of facts and opinions about the COVID-19 vaccines.
The plaintiffs do not seek financial damages. Instead, they seek a declaration that these practices by federal agents violate the First Amendment and a nationwide injunction against the federal government’s effort to censor constitutionally protected online speech.
The complaint points to a Supreme Court decision that said social media platforms are “the modern public square” and argues that all Americans who access news online have a First Amendment right against censorship of protected speech in that public square.
Jed Rubenfeld, one of the attorneys arguing the case filed Friday, explained why the lawsuit was filed as a class action:
“Social media platforms are the modern public square. For years, the government has been pressuring, promoting, and inducing the companies that control that square to impose the same kind of censorship that the First Amendment prohibits.
“This lawsuit challenges that censorship campaign, and we hope to bring it to an end. The real victim is the public, which is why we’ve brought this suit as a class action on behalf of everyone who accesses news from social media.”
According to the complaint, when the administration violates the First Amendment of an entire class of people, the judiciary must step in to protect American’s constitutional rights:
“Apart from the Judiciary, no branch of our Government, and no other institution, can stop the current Administration’s systematic efforts to suppress speech through the conduit of social-media companies.
“Congress can’t, the Executive won’t, and States lack the power to do so. The fate of American free speech, as it has so often before, lies once again in the hands of the courts.”
The lawsuit also names Surgeon General Dr. Vivek H. Murthy, U.S. Department of Health and Human Services Secretary Xavier Becerra, the National Institute of Allergy and Infectious Diseases, the Centers for Disease Control and Prevention (CDC), the U.S. Census Bureau, the U.S. Department of Commerce, DHS, the Cybersecurity and Infrastructure Security Agency (CISA), and other individuals and agencies — 106 defendants in total.
‘The largest federally sanctioned censorship operation’ ever seen
According to the lawsuit, efforts by federal officials to induce social media platforms to censor speech began in 2020 with the suppression of the COVID-19 lab leak theory and reporting on Hunter Biden’s laptop.
Once President Biden took office in January 2021, senior White House officials reported the Biden team began “direct engagement” with social media companies to “clamp down” on speech the White House disfavored, which officials called “misinformation.”
Revelations would later prove the administration was asking social media companies to suppress not only putatively false speech but also speech it knew to be “wholly accurate” along with expressions of opinion.
This practice, it alleges, spread from the administration and through the entire government, becoming “a government-wide campaign to achieve through the intermediation of social media companies exactly the kind of content-based and viewpoint-based censorship of dissident political speech that the First Amendment prohibits.”
Similar allegations about this massive federal censorship campaign also so were alleged by the plaintiffs in the Missouri. v. Biden case, but this case introduces many new allegations.
Some, but not all, examples of government-coordinated suppression of free speech on social media cited in the complaint include the following:
Substantial evidence of coordinated efforts by Fauci and others to suppress the lab-leak theory, which remains plausible and supported by evidence.
Extensive email communication between Fauci and Mark Zuckerberg, Facebook CEO, demonstrating Facebook and other social media companies adopted policies that identified any claims about the lab-leak hypothesis to be “false” and “debunked.”
Facebook’s admission that its censorship of COVID-19-related speech, on supposed grounds of falsity, is based on what “public health experts have advised us.”
Public statements by Zuckerberg on Joe Rogan’s podcast that Facebook suppressed the Hunter Biden laptop story as a result of communications from the FBI.
“Twitter files” documents demonstrating weekly meetings between agents from the FBI’s 80-agent social media task force and Twitter to discuss content suppression along with direct payments from the FBI to Twitter for compliance with requests.
CISA’s work with the Center for Internet Security, a third-party group, to flag content, including particular individuals, for censorship on social media.
“Twitter files” evidence about the Election Integrity Partnership (EIP), a vast network of high-level interactions with the federal government and social media platforms — which included proposals, ultimately adopted, for the U.S. government to establish its own “disinformation” board. One free-speech advocate described the EIP as “the largest federally-sanctioned censorship operation” he had ever seen.
Documents demonstrating after the election, the EIP was transformed into the “Virality Project,” which was dedicated to “take action even against ‘stories of true vaccine side effects’ and ‘true posts which could fuel hesitancy.’”
Census Bureau documents describing work by its “Trust & Safety” team with social media platforms to “counter false information.”
“Twitter files” documents, news reports, and documents received through Freedom of Information Act requests that demonstrated myriad, consistent communications with Facebook, Twitter and Google (YouTube) and numerous Biden administration officials named as defendants in the lawsuit including Murthy, former White House Press Secretary Jen Psaki, officials from the CDC, DHS, the U.S. Food and Drug Administration, CISA, the U.S. State Department, the White House — including White House Counsel — and other agencies about how to take action against “misinformation” related to COVID-19.
This last set of communications included action against the so-called “Disinformation Dozen,” which includes Kennedy. According to the complaint, “Facebook itself has stated that the infamous ‘disinformation dozen’ claim has no factual support.”
The complaint alleges that the collusion between the administration, federal agencies and social media companies to suppress constitutionally protected free speech now also extends beyond the election and COVID-19-related commentary to include suppression of speech on topics such as climate change, “clean energy,” “gendered disinformation,” pro-life pregnancy resource centers and other topics.
It also alleges, based on research from the Media Research Center that identified hundreds of instances of censored critiques of Biden, that social media companies “have achieved astonishing success in muzzling public criticism of Joe Biden.”
It argues that the defendants’ power over social media gives them a “historically unprecedented power over public discourse in America — a power to control what hundreds of millions of people in this county can say, see, and hear.”
CHD President Mary Holland, who also serves as CHD general counsel, told The Defender :
“If Government can censor its critics, there is no atrocity it cannot commit. The public has been deprived of truthful, life-and-death information over the last three years. This lawsuit aims to have government censorship end, as it must, because it is unlawful under our constitution.”
The lawsuit asks the court to permanently enjoin them from, “taking any steps to demand, urge, pressure, or otherwise induce any social-media platform to censor, suppress, de-platform, suspend, shadow-ban, de-boost, restrict access to constitutionally protected speech, or take any other adverse action against any speaker, protected content or viewpoint expressed on social media.”
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.
Way back in the spring of 2020, the provocative title of an article caught my eye. Upon reading it, I learned that researchers were rushing to create a vaccine before the COVID-19 virus mutated, which would render the vaccine nugatory and destroy all hopes of creating a blockbuster panacea. Curious at the time, such a warning can be viewed today as having been prophetic. (Note: That article, which offered a business slant on the historic vaccine competition, is no longer available through Google—“some results have been removed,” and are seemingly irretrievable—but here’s one with a similar title from April 2020: “Coronavirus mutation could threaten the race to develop vaccine.”)
“Viruses that replicate in the human respiratory mucosa without infecting systemically, including influenza A, SARS-CoV-2, endemic coronaviruses, RSV, and many other “common cold” viruses, cause significant mortality and morbidity and are important public health concerns. Because these viruses generally do not elicit complete and durable protective immunity by themselves, they have not to date been effectively controlled by licensed or experimental vaccines.”
Accustomed as everyone is by now to a relentless barrage of contradictory proclamations and retaliatory responses to them, the claim that mRNA was never fit to purpose for rapidly mutating coronaviruses might be written off by the usual suspects as the ravings of yet another antivaxxer conspiracy theorist. Except that this paper was co-authored by Dr. Anthony Fauci, the most visible and persistent pusher of the newfangled COVID-19 vaccines throughout 2021 and 2022. So what happened?
Against all conventional wisdom on the ethical practice of medicine, Fauci did everything in his power to achieve maximal uptake of an experimental treatment by human beings across all cohorts, without regard to patient health, age, or any other identifying factor beyond their possession of an arm into which to inject a novel product granted Emergency Use Authorization (EUA) after an accelerated review by the Food & Drug Administration (FDA). Not only did Fauci ignore the vast disparities in vulnerability to severe illness and death between healthy infants and frail nonagenarians, but he also conducted himself for two years as though natural immunity through previous infection were somehow irrelevant to the question of whether a patient should roll up his sleeve.
Now, in the light of Fauci’s own published scientific findings, it would appear that he was right, in a sense, about natural immunity all along, albeit in an unexpectedly perverse way. First of all, as we already witnessed in real time, coronaviruses as a class, including SARS-CoV-2 (COVID-19), mutate rapidly in order to propagate themselves. This “discovery” served as the basis for the development of “boosters,” which, it was claimed, became necessary when “fully vaccinated” persons continued to become infected with COVID-19. Major outbreak-inducing strains such as Delta and Omicron, which arise through mutation, will always be one step ahead of last year’s vaccines, having survived precisely by evading the antibodies induced by injection into the body of the previous virus generation’s mRNA.
According to Fauci’s own findings, however, there is a second, even more compelling reason for denying that either vaccine or natural immunity to COVID-19 can ever be permanent. The primary difference between diseases such as measles, for which vaccines work, and the seasonal flu or SARS-CoV-2, for which they do not, is that the body’s natural immune response rises only to the level of the severity of the pathogen. Since most people can survive coronaviruses, the minimal response needed to defeat the invader is rather mild, which is why immunity dissipates rapidly over time and people can become reinfected again and again, even if they have recovered from natural infection, and whether or not they have undergone vaccination.
There are of course people who die of the flu or COVID-19, but they nearly always have comorbidities, infirmities or weaknesses, rendering them vulnerable to a pathogen which healthy bodies are capable of defeating. Notwithstanding the massive propaganda campaign for universal vaccination, most healthy young persons would have survived COVID-19, and would not have been hospitalized, with or without vaccination. Given the abundance of statistical evidence, there is simply no sense in which it can be truthfully asserted that healthy young persons with no comorbidities were “saved” by the shots. On the other hand, extremely frail and elderly persons can indeed be killed by the virus, regardless of how many “vaccines” they have taken. When it comes to the mercurial class of coronaviruses—instantiated by not only the common cold and the seasonal flu, but also COVID-19—so-called vaccines will never transcend their pedestrian identity as mere shots, for they are constitutionally incapable of offering longterm protection, not only because these viruses rapidly mutate, but also, and more fundamentally, because the body’s natural response to infection by such transitory viruses is never robust enough to be permanent. Just as having survived the flu one year has nearly no bearing on whether one will contract another case of the flu, from a different variant, in the future, no so-called vaccine solution to COVID-19 can confer longlasting protection.
Take as many boosters as you like, until the end of time, but having done so may or may not prevent you from contracting the latest iteration of the virus—or protect anyone else—since every booster or flu shot is the result of researchers’ “best guess” of what the specific properties of the next generation of viruses will be. It appears, then, that the widely celebrated and aggressively marketed, and in some cases mandated, COVID-19 vaccines, paid for thrice by the recipients of “free” shots, were in fact launched on a wing and a prayer. There was really no hope all along that the shots would or could offer longterm protection, although it was claimed for marketing purposes that they were highly effective and would save millions of lives. That those selling points were in fact lies may explain why they were supplemented all along the way with such eerily self-contradictory slogans as: “The vaccinated need to be protected from the unvaccinated!”
Dr. Fauci’s surprising publication reveals that the abundant optimism exuded by him and others in attempting to maximize vaccine uptake was scientifically unfounded from the beginning. Neither the mRNA technology nor the traditional vaccines (which introduce a small amount of the live or dead pathogen into the body to elicit an immune response) can be effective for rapidly evolving pathogens such as coronaviruses to which the highly efficient human body mounts the weakest possible effective response. But this is hardly news, for we already knew long before 2020 that, despite assiduous efforts spanning decades, no one ever managed to develop a vaccine against the common cold. Likewise, the widely touted flu shots, marketed in very public ad campaigns only slightly less aggressive than those for the COVID-19 treatments, are in fact mediocre at best, as Fauci himself has averred.
If vaccine technology, whether vector- or mRNA-based, is simply a mismatch for the nature of rapidly mutating viruses, and this is a matter of common knowledge, readily accessible to anyone working in virology, then how are we to understand Fauci’s comportment throughout the Coronapocalypse? And why did he and his coauthors boldly reaffirm in January 2023 what many other researchers have been saying for years, including a few brave souls who were silenced when they tried to suggest the same from 2020 to 2022?
Fauci faces something of a “Charybdis or Scylla” dilemma here, for if he was ignorant of basic truths of immunology known by competent and knowledgeable scientists before 2020, then he had no business serving as the nation’s fount of public health wisdom. Double-masked Fauci devotees, in the aftermath of what was empirically indistinguishable from a full-scale psyop spanning more than two years, will no doubt remain reluctant to renounce their allegiance to the person who, they believe, “guided” us through the pandemic. Confronted with the revelations of Fauci et al.’s January 2023 publication, such followers may most charitably conclude that the object of their reverence did genuinely believe in the mRNA vaccines and continues to follow “The Science” where it leads, in this case, to finally acknowledge failure.
That Fauci honestly did not know that the mRNA shots would never work has also been the conclusion of a few of his most vociferous critics, including Alex Berenson, who somewhat ironically was spurned as “The Pandemic’s Wrongest Man” by The Atlantic back in April 2021. (Morally speaking, that title surely belongs to Dr. Anthony Fauci himself, for the sheer brazenness with which he defied all known principles of medical ethics in pushing for universal vaccination across all cohorts.) Berenson was banned from social media under pressure by no less a power than the U.S. government itself when he dared to question the Fauci script at the height of the Coronapocalyptic hysteria. (Berenson’s lawsuit alleging the government’s violation of his First Amendment right to free speech is pending.)
Notwithstanding the superficial appeal (and attendant Schadenfreude) of the “Fauci was ignorant and is now eating crow” hypothesis, the Scylla horn of the interpretive dilemma would seem to cohere far better with the character of a man who remarkably responded to his critics on national television that “You’re really attacking not only Dr. Anthony Fauci, you’re attacking science.” Certainly such a person is not someone whom we would ordinarily regard as endowed with the humility needed to admit either ignorance or error. To my mind (and others, such as Dr. Robert Malone, agree) Fauci’s recent publication is yet another gambit perfectly consistent with his comportment throughout the pandemic. While Fauci’s admission that the mRNA technology is not fit to purpose for coronaviruses may on its face seem surprising, in fact, it is entirely true to form.
Yes, Fauci’s gambit is most plausibly interpreted as the latest chapter in his time-tested “fail forward” playbook: to use the outcome of the COVID-19 shot experiment to rally for yet more funding for the pharmaceutical industry. Like all good bureaucrats, Fauci uses government fiascos as a springboard to increase the reach and budget of his domain. In other words, Fauci, having quite effectively painted the COVID-19 virus as the most evil bogey man of them all, is simply continuing his efforts to impel politicians to dole out even more billions of dollars to the government-boosted industry which he has loyally supported throughout his entire career, as has been ably documented by Robert F. Kennedy, Jr. In addition to being consistent with Fauci’s dismissive, smug, and seemingly shameless character, this interpretation coheres well with the general modus operandi of the pharmaceutical industry, which has displayed in recent decades an uncanny capacity to “fail forward” by pivoting and innovating so as to be able to reap massive profits even when their products generate consequences worse than the conditions which they were intended to address.
Note that slippery snake-oil salesmen such as Pfizer’s CEO, Albert Bourla, carefully calibrated their pitches from the beginning so as to protect themselves from future allegations of fraud by equivocating about the “efficacy” of their COVID-19 treatments. When directly questioned in December 2020 about the vaccine’s ability to limit transmission of the virus, Bourla offered casual, off-the-cuff replies such as, “I think that’s something that needs to be examined. We’re not certain about that right now.” His colleague, Ugur Sahin (co-founder and CEO of BioNTech), cagily couched his anticipatory optimism in these terms: “The first interim analysis of our global Phase 3 study provides evidence that a vaccine may effectively prevent COVID-19.” [my emphasis]The rest is history. When it later emerged, to the surprise of everyone whose understanding of the crisis was shaped exclusively by the Pfizer-sponsored mainstream media, that the company never even tested the shots for their ability to prevent transmission, gaslighting fact-checkers rushed to the defense of the executives. Why in the world would anyone ever have believed that the new vaccines would prevent transmission and infection?
The government-subsidized pharma giants succeeded in profiting enormously from the politically amplified crisis by persistently touting the efficacy of their products against a virus which 99+% of people were perfectly capable of surviving on their own. The shot salesmen claimed victory when injected persons did not die, when in reality most of them would have survived even if they had declined the treatment or been injected with an inert placebo instead. But the scheme ultimately worked because marketers (including public health authorities such as Anthony Fauci and Rochelle Walensky) unerringly referred to the shots as “vaccines,” a piece of sleight of hand made possible by the CDC’s own diluted redefinition of the term in 2021 to mean “a preparation that is used to stimulate the body’s immune response against diseases.” This linguistic legerdemain worked wonders to promote the new shots, when in fact the new definition is so broad and open-ended as to make it possible to label as a vaccine anything that strengthens the immune system, including leafy green vegetables, vitamins C and D, etc.
In retrospect, there can be no doubt that the populace and the politicians crafting policy all assumed that the labeling of the mRNA treatment as vaccines implied that the shots stopped transmission and infection, even while the savviest of the snake-oil salesmen evinced ignorance from the start about the most important question of all: whether these “vaccines” were indeed like all of the other vaccines, capable not just of “stimulating” the immune system, but of producing dependable and durable immunity.
Given the statistics now available, even the more modest claim, continually chanted by pharma marketers and their lackeys in the media, that the mRNA treatment greatly diminished severe illness and hospitalization, may have been false. For the death toll of COVID-19 victims increased rather than decreased in the year after the “vaccine” launch, and the countries with the worst vaccine uptake had some of the best outcomes. On top of the virus deaths, thousands of people were diagnosed with post-vaccine injuries of a variety of sorts, believed by many of them, their families, and at least some of their doctors to have been caused by the shots. Some of the vaccine injured ended up dying long before their time, and excess deaths were also caused by the disastrous political response to the virus, with fatal drug overdoses reaching record levels. Millions of persons missed vital health screenings, having been terrorized into believing that they could not leave their homes (much less enter COVID-19–infested health facilities!) without contracting something akin to the Black Plague. Among those who sought help for their ailments, some were flat-out denied treatment for acute illnesses, either because they were not dying specifically of COVID-19, or because they had refused the experimental treatment.
In coming to terms with what transpired over the past three years, it is helpful to bear in mind pre-2020 history. When the pharmaceutical industry’s newfangled psychotropic medications did not work as advertised, they created and blitz-marketed “add-on” drugs to increase the efficacy of antidepressants now known to have exhibited success in clinical trials on a par with placebos, but with far worse longterm adverse effects, up to and including addiction and suicidal ideation. Similarly, the slick pivot of the industry in response to the opioid catastrophe (caused by itself) was to launch and market drugs which could help people in the throes of narcotics addiction.
The flu shots marketed in collaboration with and subsidized by governments have been demonstrated in clinical trials to succeed on a par with placebos, while post-flu shot deaths are invariably written off as “coincidental.” Nonetheless, the industry capitalizes on the fact that they are starting anew each year—the previous year’s flu shot results being irrelevant to the next year’s projected success. As a result, when heavily lobbied and propagandized authorities impose mandates in some places (such as the State of Massachusetts), this may lead others to follow suit. Crony capitalist windfall profits ensure the ever-augmenting marketing budget of pharma firms, with the result that each subsequent year’s sales will exceed the previous year’s tally.
Given such precedents, no one should be surprised if the failure of the COVID-19 shots to prevent infection and transmission, or even to diminish the number of persons who died from the virus, does indeed end up serving as the pretext for governments to infuse even more money into research and development of new and what are promised once again to be “miraculous” cures to be used in the future. Not long after the launch of the COVID-19 vaccines, auxiliary treatments such as Pfizer’s Paxlovid and Merck’s Lagevrio were developed to treat people who became infected with the virus despite having been “fully” vaccinated. As clear evidence that many people’s capacity for critical thought continues to be compromised by fear, when legislation to rescind the utterly illogical and unscientific COVID-19 vaccine mandate on foreigners entering the United States made it to the floor of the House of Representatives, 201 Democratic congresspersons voted to keep the executive order in place.
The ongoing support of the official government pro-pharma narrative by the president, the press secretary, the defense secretary, and most Democratic members of Congress, even in the face of ample evidence (including post-vaccination positive COVID-19 tests) demonstrating that the shots did not diminish the incidence of infection is best explained by the fact that policymakers prefer not to own up to their mistakes. Ordinarily, individuals base their future actions on what they have learned from past experience. The question arises in the present circumstance: Why is there still a push for vaccine passports when the COVID-19 vaccines do not in fact confer immunity? The assumptions funding the push for universal vaccination continue to be embraced, as though the vaccines worked resplendently, despite an accumulation of scientific evidence to the contrary.
Now that Fauci himself has clearly explained why the mRNA technology will never offer a lasting solution to COVID-19, why would anyone, including Joe Biden and other advocates for the WHO (World Health Organization), still be in favor of implementing a universal health passport system regulating the movement of persons throughout the world? The current crop of shots do not offer longterm protection and do not moderate illness except in the case of persons in a very narrow cohort. Why require anyone to demonstrate that they participated in the experimental mRNA trial more than two years ago in order to be able to enter a country where the circulating variants bear little resemblance to the strain used to determine the formula of the first crop of vaccines?
There is no plausible health pretext available to explain why political leaders around the world would be keen to impose such a restrictive health passport program on free people, preventing them from traveling unless they first demonstrate their willingness to comply with future possible arbitrary orders decreed by public health authorities. That anyone not holding pharma stocks would support at this point the adoption of a health passport is best explained, again, by the politically induced trauma which appears to have psychologically scarred some persons for life. But just as the failure of the lockdowns to “stop the spread!” impelled leaders at every level of government—local, state, and federal—to prolong and intensify the lockdowns, those who pushed vaccine mandates will continue to press for universal vaccination passport requirements under the flatly false assumption that the reason why so many people died of COVID-19 was because of the evil antivaxxers who refused to comply.
What we are witnessing, the strangely intransigent push for vaccine passports, is entirely consistent with the comportment of the very persons who just succeeded in selling billions of shots. They will continue to insist that what we need to do is provide even more government funding to the pharmaceutical industry so that they can develop more and better cures for our ills. As disturbing as this may be, the most plausible explanation for the vigorous attempt to impose a health credential system on the people of the world is to provide the pharmaceutical industry with a limitless supply of not only customers, but also future experimental subjects.
As we have seen, the addition of the COVID-19 shot to the CDC’s immunization schedule for children—whose chances of dying from the virus are minuscule—serves only industry interests, by ensuring an endless crop of healthy young arms into which to inject the latest and greatest snake oils claimed to be panaceas (until it emerges that they are not). Likewise, the implementation of a universal health passport scheme restricting the motion of persons who opt not to undergo medical treatments of which they have no need would not only reap massive profits to the pharmaceutical industry but also represent the dawning of the pharma-techno state, in which citizens are subjects whose bodies are owned by their government.
The upshot here is that all of the pro-mRNA treatment propaganda and the incredibly vicious efforts to denounce and blame the noncompliant as the reason for the lengthy duration of the COVID-19 pandemic were nothing more than marketing ploys. That those who work behind the scenes of this well-oiled marketing machine were willing to destroy people’s relationships, their livelihoods, and in some cases even their very lives, reveals that their true motives were never to save the world from the virus but, instead, to profit from it. This is why we must resist any and all attempts by these same people and their toadies to foist upon us legal requirements to serve as guinea pigs in their future experimental trials, which is precisely what “health passports” would bring.
Laurie Calhoun is the Senior Fellow for The Libertarian Institute. She is the author of We Kill Because We Can: From Soldiering to Assassination in the Drone Age, War and Delusion: A Critical Examination, Theodicy: A Metaphilosophical Investigation, You Can Leave, Laminated Souls, and Philosophy Unmasked: A Skeptic’s Critique, in addition to many essays and book chapters. Questioning the COVID Company Line: Critical Thinking in Hysterical Times will be published by the Libertarian Institute in 2023.
The mask is slipping (pun fully intended), all over the place – regarding the Big Tech/Big Government collusion. Now it’s time to pay close attention to the role played by the Centers for Disease Control and Prevention (CDC).
We’ve already been awed – just by the magnitude of the whole thing – if not exactly “shocked” by the Twitter Files.
But – what in the world was happening at Facebook, around the same time? After all, Facebook is an almost orders of magnitude bigger and more influential social network than Twitter.
For the time being, we don’t have the same “direct line” to internal documents as is the case with Twitter, which was made possible by the dedication to transparency by the new owner himself.
However, what could be dubbed as the “Facebook Files” are based on credible sources, too – Reason is coming out with a story based on confidential emails that emerged thanks to a court case – the state of Missouri suing the Biden administration.
The emails show that Facebook (and by extension Instagram) representatives and the CDC not only kept in touch at all times, but that the tech giant also “routinely asked government health officials to vet claims relating to the virus, mitigation efforts such as masks, and vaccines.”
In turn, the CDC kept a watchful eye on what speech was allowed on Facebook, what policies toward censorship of “inconvenient” Covid topics applied, and this government agency had no problem instructing the social network behemoth how to behave in these instances.
Robbie Soave, a senior editor for Reason, revealed some examples of what was happening in a series of tweets citing the emails and providing screenshots. One shows that in May 2021, CDC started to get involved in “vetting” content on Facebook that concerns Covid vaccines. And CDC had the last word on what was allowed to remain online as “accurate.”
Other emails show that Facebook (Meta) made sure the CDC was given de facto power to police Covid “misinformation,” while at the same time flagging content for the CDC, consulting with it on claims that could “contribute to vaccine refusals.”
At the same time, Reason is acknowledging that this was by no means the only federal agency to engage in similar activities, all aimed at pressuring some of the world’s biggest social platforms to allow only a certain narrative, and discredit any skepticism, even that coming from medical professionals and scientists.
Even President Biden made sure to “contribute” to this effort, when he in June 2021 bizarrely accused Facebook of “killing people.”
This was really meant to say that the giant had better not dare allow any Covid content the White House failed to “vet” behind the scenes – one way or another.
And the giant obliged, sometimes probably even exceeding the level of compliance expected from the administration. An internal email now reveals that Facebook went as far as to “snitch” on its own users making fun of Anthony Fauci, apparently in a bid to defend his reputation – again, at the expense of free speech.
“One email warned the CDC that Facebook users were mocking Fauci for changing his mind about masking and double-masking. The CDC replied that this information was ‘very helpful’,” Soave, the magazine’s senior editor and host on The Hill TV channel, tweeted.
The upcoming, March issue of Reason delves into how the CDC turned into the speech police when it came to pressuring social media to block content that the government agency decided was Covid “misinformation.”
And this was online speech that this, and other government agencies, have no constitutional way of directly suppressing without breaking the law.
“There is a word for government officials using the threat of punishment to extort desired behaviors from private actors. That word is: jawboning,” Soave remarked in one of the tweets.
And one can imagine – and the emails now show – just how gun-shy and ready to please those in power Facebook had become, after years of public vilification, and who knows what kind of pressure behind the scenes in the wake of the 2016 US election.
Warning: Some of the following details are distressing.
***
Two years later, [investigative reporter Celia] Farber would follow the trail of child casualties left by Dr Fauci’s Aids branch, DAIDS, in Uganda, exposing the pattern of abusing African mothers and children.
After the BBC documentary aired, AP reporter John Solomon made his own efforts to calculate the number of children who died in Dr Fauci’s Aids drug experiments. Solomon’s May 2005 AP investigation revealed that at least 465 New York City foster children were subjects in NIAID’s [US National Institute of Allergy and Infectious Diseases] trials and that Dr Fauci’s agency provided fewer than one-third (142) of those children with an advocate – the minimum legally mandated protection.
A March 2004 letter from Vera Sharav to Dr David Horowitz, director of FDA’s [Food and Drink Administration] Office of Compliance, charged Dr Fauci’s HIV drug trials with numerous violations of federal law, including NIAID’s failure to protect the rights and safety of foster children, particularly during the perilous Phase 1 stages in which drug companies determine toxicity effects by exploring maximum tolerance levels. Sharav accused Dr Fauci’s team of illegally failing to provide state wards and orphans with independent guardians to represent their interests and protect their rights during brutal, dangerous, and often agonizingly painful experiments.
The 2004 FDA investigation of Dr Fauci’s AIDS research division urged the head of NIH to insist on better management from NIAID. ‘The overall management of this Division requires careful review,’ the report said. A May 2005 Congressional hearing also concluded that NIAID’s experiments had violated federal statutes.
In testimony before Congress, NIAID and its local partner – New York City’s Administration for Children’s Services (ACS) – sought to justify the unethical research practices by claiming they were providing first-class, cutting-edge treatments to HIV-infected children who could otherwise not afford expensive medicines.
However, AHRP’s [Alliance for Human Research Protection] investigation revealed that many of the children NIAID subjected to Dr Fauci’s experiments were perfectly healthy and may not even have been HIV-infected. Those investigations focused on thirty-six of the trials. For obvious reasons, clinical trials virtually always occur in hospital settings with trained medical personnel, doctors and nurses, in attendance. However, ICC [Incarnation Children’s Center] was a non-medical facility. The decision to allow experiments with highly toxic drugs at an orphanage devoid of medical personnel was, itself, a stunning act of malpractice. Subsequent events suggest that the decision was deliberate, calculated to avoid scientific and ethical objections that might have put Pharma PIs [principal investigators] at odds with trained medical professionals. Publicly, NIAID pretended it would permit pharmaceutical companies to conduct their dangerous dose tolerance experiments only on children who had terminal Aids and were therefore likely to die anyhow. However, AHRP found that NIAID was quietly allowing its Pharma partners to experiment not only on children with laboratory-confirmed HIV infection, but also those ‘presumed’ to be infected. In other words, NIAID required no proof that these children actually had HIV. AHRP accused NIAID of exposing children who might never have developed Aids to lethal risks and the horrific adverse effects of highly toxic drugs for purposes that were not therapeutic, but purely experimental.
On March 8, 2004, NIH [National Institutes of Health, of which Fauci’s NIAID is a division] rejected a Freedom of Information Act (FOIA) request for the adverse event reports from NIAID’s trials conducted at ICC, citing FOIA’s ‘trade secrets’ and ‘privacy’ exemptions. AHRP then filed a complaint on March 10 with the FDA and the Office of Human Research Protections (OHRP), charging that NIAID was depriving foster children of legally mandated federal protections against research risks. Two subsequent investigations validated AHRP’s complaint.
John Solomon’s AP investigation finally brought Dr Fauci’s experiments to national prominence. AP identified at least forty-eight Aids experiments NIAID conducted on foster children in seven states – mostly in violation of the federal requirement that NIAID provide those children with an advocate. In addition to the Dapsone trial that killed at least ten children, NIAID sponsored another study testing a combination of adult antiretroviral drugs. AP reported that of the fifty-two children in the trial, there were twenty-six moderate to severe reactions – nearly all in infants. The side effects included rash, fever, and dangerous drops in infection-fighting white blood cells.
From the outset, Dr Fauci’s experiments served his vain obsession to develop an HIV vaccine. (Despite these expenditures of tens of billions of dollars, he has failed – for forty years – to develop an HIV vaccine that was safe or effective for human use.) Medical records that NIAID ultimately and reluctantly released proved that Dr Fauci’s PIs were testing his dangerous vaccines on children from one month to eighteen years old. AP writer John Solomon confirmed that despite contrary requirements in official NIAID protocols, NIAID was knowingly allowing its Pharma partners to violate NIAID’s written study protocols by conducting these experiments on children with and without proof of HIV infection.
For example, published reports acknowledge that NIAID, Genentech, and Micro-Genesys co-sponsored a vaccine trial code-named ACTG #218. The ACTG #218 protocol states ‘Patients must have: Documented asymptomatic HIV infection,’ and the ‘Expected Total Enrolment’ was seventy-two. However, an internal report acknowledges that NIAID was allowing the companies to openly violate those requirements: ‘125 immunized children proved to be HIV uninfected’. Another report stated: ‘A total of 126 children were not infected’. NIAID’s final analysis acknowledged that ACTG #218 ‘showed no clinical benefit to vaccine recipients’.
Another HIV Phase 1 vaccine trial, ACTG #230, tested two experimental vaccines, one by Genentech, another by Chiron/Biocine. This time, the protocol openly declared: ‘Accepts Healthy Volunteers’. As Solomon discovered, the ‘volunteer’ subjects of that unethical experiment were newborns aged three days or less. NIAID randomized these infants to one of three doses of either experimental HIV vaccine or placebo. These reports validate AHRP’s concerns that Dr Fauci experimented on infants and children who were never at risk of Aids, and that he exposed them to deadly risks and agonizing discomforts in a speculative drug and vaccine exercise that offered absolutely no potential benefit for them.
Dr Fauci was certainly aware of the peril to which he was subjecting his gallant infant ‘volunteers’. Most of the drugs that his PIs tested on these children were previously approved for adults with Aids and carried Black Box warnings of potentially lethal side effects: Aldesleukin, Dapsone, Didanosine, Lamivudine, Nevirapine, Ritonavir, Stavudine, and Zidovudine.
Finally, even in cases when the children were genuinely ill, Dr Fauci’s pretence that his experiments were compassionate gestures to impoverished orphans was always a sham. NIAID’s claim that their experiments were the only opportunity for those children to receive ‘life-saving’ drugs was a canard from the outset. New York State law requires that physicians provide ‘life-saving’ treatment to wards of the state, if need be, to provide treatment ‘off-label’.
Furthermore, drug companies do not primarily design clinical trials to benefit the individual subjects. Their purpose is to gain safety and efficacy information that may prove helpful for subsequent patients and be profitable for their bottom line. Finally, not all subjects get the ‘most promising’ drug in a trial; some get placebos.
Liam Scheff’s January 2004 article, The House that AIDS Built, ignited an outraged internet controversy, prompting the New York Press to publish a follow-up article by Scheff,Inside Incarnation. Scheff’s detailed descriptions are worth reading if only to understand the sacrifices that Dr Fauci demanded from his venturesome ‘volunteer’ babies for ‘the greater good’.
Scheff’s chronicle suggests that Dr Fauci and his PIs purposefully took advantage of Incarnation Children’s Center’s status as a non-medical facility. The PIs had free rein to engage in conduct that experienced professional nurses and doctors would have flagged as unethical and illegal.
When children declined to take the toxic drugs, NIAID and its Pharma partners arranged to surgically implant feeding tubes in their bellies to force obedience. Scheff wrote, ‘When Mimi [a staff member with no medical background] started at ICC, the tubes were used infrequently. “But when the kids got older, a lot of them started to refuse the medication,” she recalled. “Then they started coming in with the tubes more and more. Kids who refused too much, or threw up too much, they’d get a tube. First it was through the nose. But then it was more and more through the stomach. You’d see a certain child refusing over and over, and one day they’d come back from the hospital from surgery, and they had a tube coming right out of their stomach. If you asked why, the doctors said it was for ‘compliance’ – the regimen. Got to keep up the regimen,” said Mimi. “Those were the rules”.’
Mimi describes how children suffered – and how some died: ‘One girl, a six-year-old, Shyanne . . . She was the most delicate little flower – beautiful, polite, full of life. Her family never gave her meds. So, Administration for Children’s Services brought her into ICC . . . she came in and started the meds. And it was three months, maybe three months. And she had a stroke. She could not see. She was this normal girl, singing, jumping, playing. Then, poof, stroked out. Blind. We were freaked out. Then, in a few months, she was gone – dead.’
Between 1985 and 2005, NIAID and its Pharma partners conscripted at least 532 infants and children from foster care in New York City as human subjects of clinical trials testing NIAID’s experimental Aids drugs and vaccines. ICC and the medical research centers that conducted the trials received substantial payments for hosting the experiments, from both the National Institutes of Health and the manufacturers of the drugs. Among those companies were Merck, Bristol Myers Squibb, Micro-Genesys, Biocine, Glaxo, Wellcome, and Pfizer.
Critics have long questioned why the National Institutes of Health (NIH) would fund experiments by University of North Carolina of Chapel Hill (UNC) professor Ralph Baric to develop a technique for hiding evidence of human tampering in laboratory-created super viruses.
Aided by some $220.5 million in National Institute of Allergy and Infectious Diseases (NIAID) funding, Baric developed a so-called “Seamless Ligation” technique, which he boasted could perfectly conceal all evidence of human tampering in laboratory-created viruses. Baric nicknamed his invention the “no-see’m” method.
Now a new study, “Endonuclease fingerprint indicates a synthetic origin of SARS-CoV2,” published on the preprint server bioRxiv, shows that — apparently unbeknownst to Baric — the “seamless ligation” concealment gimmick leaves its own minute but legible signature.
Most momentously, these same researchers have discovered that damning signature in the genome of the virus that causes COVID-19.
Baric’s technique has long been controversial. “It’s the artist that doesn’t sign his name to the painting; the virologist that doesn’t put his signature into the virus to let us know whether or not it is emerging naturally or whether it is produced in a laboratory,” said Jeffrey Sachs, chair of The Lancet COVID-19 Commission, a task force that investigated the origins of COVID-19.
“All of it says, my God, there was really a big, very risky research agenda underway.”
This month, Sachs published the results of his 22-month investigation in The Lancet, including the damaging conclusion that COVID-19 was probably laboratory-generated and that the technology probably came from NIH-funded science.
“It’s the exact opposite of what you would do if your interest was public health. Public health scientists would be marking their enhancements with red flags — not devising ways to hide them. The only reason you would want a concealer is to advance a sinister purpose — such as illegal bioweapons development — some mischief that the scientist didn’t want traceable back to his lab.”
Baric taught his “no-see’m” method to the Wuhan Institute of Virology’s (WIV) “Bat Lady” Shi Zhengli in 2016. In return, Baric received Chinese coronaviruses collected by Shi from bats in Yunnan province. (Scientists have linked the COVID-19 genome’s pedigree to closely related bats.)
Shi and her colleagues at the Wuhan Institute subsequently demonstrated their mastery of Baric’s high-risk technique in a series of published — and highly controversial — gain-of-function experiments at the Wuhan lab. It has been even more puzzling to his critics that Baric, again with NIAID funding, chose to share this dangerous technique for weaponizing pathogens with Chinese scientists who have clear links to the Chinese military.
Experts say that the implications of this new study could be far-reaching. By pointing the finger at Baric, the study raises the possibility of potentially devastating liability for the NIAID and the University of North Carolina and other parties.
Scientists, including those close to Dr. Anthony Fauci, have repeatedly pointed out that SARS-CoV-2, the virus that causes COVID-19, has genomic sequences that appear inconsistent with natural evolution: The COVID-19 virus is no longer infectious in bats, and its spiked protein feature — which is unknown in this family of coronavirus — includes numerous mutations that make it ideally infectious in humans.
The closest known coronavirus relative — a coronavirus from the Wuhan lab — is 96.2% identical to SARS-CoV-2. The peculiar spike accounts almost completely for the entire 3.8% difference. Oddly, there are multiple novel mutations in the spike and almost none in the rest of the genome.
Natural evolution would be expected to leave mutations distributed evenly across the genome. The fact that virtually all the mutations occur on the spike led these scientists to suspect that that particular Wuhan lab coronavirus collected by Shi Zhengli is the direct progenitor of SARS-CoV-2 and that its new spike was implanted through engineering.
However, the unmistakable fingerprints of lab engineering were absent — leaving many experts wondering whether Baric’s technique was used to assemble a novel coronavirus with the engineered spike while removing the evidence of lab generation.
This new study connects the biological breadcrumbs that link federally funded research to a global pandemic. That trail leads directly to UNC and NIAID.
The authors of the study — a team of researchers from Duke University, University Clinics of Würzburg and an industry group — identified a characteristic signature in the amino acid code. That indelible artifact could only have emerged from Baric’s “no-see’m” methodology.
In an interview last spring, Baric himself confessed, that at the time the pandemic began, only two or three labs in the world were using his protocol – including his UNC lab and the WIV.
The study’s authors’ conclusions rest on the presence of unique sites in the COVID-19 virus. These sites allow special enzymes called “restriction enzymes” to cut the DNA into building blocks of unique size that then can be “stitched together in the correct order of the viral genome,” according to the study’s authors.
Essentially, Baric’s technique leaves behind unique spellings in the “genetic vocabulary.” The new words include “odd spelling choices” subtly distinguishing them from typical viral vocabulary.
The magic of Baric’s “no-see’m” technique is to invisibly weave these telltale “spelling” changes into the viral sequence between relevant genes without altering the viral protein. This is like changing the “spelling” of the word without changing its meaning; the casual listener will never notice the difference.
The research team used forensic tools to drill down on minute “spelling differences” in the SARS-CoV2 genome that betray laboratory tampering using the “no-see’m” technique.
Consider how a Brit would spell “colour,” “manoeuvre” or “paediatric.” The choice to spell a word in a certain way can reveal your nation of origin. Similarly, these nearly imperceptible changes in the viral sequence give away the laboratory origins of this virus.
In sharing his seamless ligation technique with Shi Zhengli, Baric assured that the WIV possessed all the required elements of the assembly process. EcoHealth Alliance’s infamous DEFUSE proposal describes the same techniques in detail. (submitted to The Defense Advanced Research Projects Agency, or DARPA, in 2018).
The world now has proof positive that SARS-CoV2 is an engineered laboratory creation generated with technology developed by Ralph Baric with U.S. government funding.
Prosecutors and private attorneys representing clients injured by the COVID-19 pandemic now have a smoking gun. The gun points at humanity. Forensic scientists have now successfully lifted faint but precise fingerprints from the lethal pistol’s grip and trigger. Those fingerprints belong to the NIAID and the University of North Carolina.
Baric is Fauci’s favorite gain-of-function scientist. The cascade of NIAID funding to Baric and his UNC lab has financed 152 studies approaching a quarter-billion dollars.
Those federal grants have made Baric the global kingpin of gain-of-function science. In conformance with standard practice, it is probable that UNC pockets one-quarter to one-half of NIH’s financial felicities to Baric for “administrative costs.”
These monumental payments have probably incentivized UNC to turn a blind eye to Baric’s reckless experiments and to his controversial decision to transfer his dangerous technologies to a Chinese military laboratory known to suffer from deficient safety protocols and shoddy construction that make it, in the words of Congressional investigators, less secure than a “dentist’s office.”
UNC’s role in enabling the questionable conduct may have precipitated a global pandemic that could easily give rise to liability for negligence.
UNC and NIAID’s liability is now clear. But do we have positive proof that the Wuhan lab created the monstrosity that caused COVID-19?
The cumulative evidence strongly suggests that the Wuhan lab used Baric’s methodologies to cobble together the chimeric virus that caused the COVID-19 pandemic. But a few missing puzzle pieces still prevent us from definitively proving that this dangerous construction project occurred at the Wuhan lab.
As The Lancet Commission report concluded, the released emails show that NIH’s Dr. Francis Collins, NIAID’s Fauci and EcoHealth Alliance’s Peter Daszak, and others are continuing to collaborate with Shi Zhengli and Chinese officials to suppress the public release of information that would allow us to complete this picture. Stay tuned!
Following the announcement, numerous news stories about the study’s results focused on the fatality rate observed in the laboratory mice used in the study.
Commenting on the researchers’ announcement, Robert F. Kennedy, Jr., Children’s Health Defense chairman of the board and chief legal counsel, remarked on the potential danger of such research — and its federal funding:
“What could be more insane than Anthony Fauci funding more of his GOF [gain of function] experiments to soup up coronavirus lethality in the middle of a pandemic caused by a juiced-up coronavirus that has killed millions?
“All of horrified humanity is watching Lord Of The Flies play out at NIH [National Institutes of Health] and praying for the adults to appear.”
Rachel Lapal Cavallario, Boston University’s associate vice president for public relations and social media, told the media the research conducted was not gain-of-function research and that, “In fact, this research made the virus [replication] less dangerous.”
However, others disputed that claim.
Sen. Roger Marshall (R-Kan.), a doctor, said the research involved “lethal gain of function virus research” that creates the “potential to kill more people than any singular nuclear weapon.”
“Viruses have managed to escape even the most secure labs,” Marshall said, adding that this type of “research must stop immediately while the risks and benefits can be investigated.”
“What they have done in this work, as described by their own methods and results, is akin to madness.
“It is akin to madness because … they basically created and published a recipe for a deadly pathogen (80% mortality rate in the subjects of their experiments) of their own construction in their lab.
“By the way, this is precisely gain-of-function research. It couldn’t be more descriptive.”
Boston University today issued the following statement, downplaying the risks of the research:
“The research was reviewed and approved by the Institutional Biosafety Committee (IBC), which consists of scientists as well as local community members. The Boston Public Health Commission also approved the research.
“Furthermore, this research mirrors and reinforces the findings of other, similar research performed by other organizations, including the FDA. Ultimately, this research will provide a public benefit by leading to better, targeted therapeutic interventions to help fight against future pandemics.”
Efforts to prevent construction of NEIDL BSL-4 lab failed
NEIDL describes itself as “a Boston University Center dedicated to research on emerging and re-emerging infectious diseases and the pathogens that cause them,” and “a major step forward in advancing public health” that “provide[s] the necessary information and understanding to develop diagnostic tests, treatments, and vaccines.”
NEIDL also claims that it “will not conduct any secret or classified research” and that “the public will have access through several channels to information about any and all research before it even begins” — making NIAID’s claims that it was unaware of the spike protein research project all the more perplexing.
According to the Daily Mail, NEIDL is one of 13 biosafety level 4 (BSL-4) labs in the U.S.
However, this particular research took place under BSL-3 precautions, although according to STAT, “There is no evidence the work … was conducted improperly or unsafely,” noting that an internal biosafety review committee and the Boston Public Health Commission approved the work.
The journal Nature described the difference between BSL-3 and BSL-4 as follows:
“BSL-3 laboratories are designed so that scientists can safely work with potentially lethal and inhalable pathogens in a contained environment. Experiments are conducted in sealed workspaces in which the air is filtered and not recirculated, and the entrance to the facility is typically secured by self-closing doors.
“BSL-4 facilities, in which researchers work with fatal pathogens that can spread through aerosols, and for which vaccines or treatments are lacking or limited, require extra security measures.”
University of Illinois international law professor Francis Boyle, J.D., Ph.D., said the dangers of BSL-4 facilities have long been known, which is why he participated in efforts to stop the construction of the NEIDL facility.
“Years ago, there was a lawsuit to prevent and stop the building of this BSL-4 [facility] at Boston University that I did work on, and we failed.
“At that time we argued that the BSL-4 would engage in existentially type dangerous biological warfare research, and that was even before … gain-of-function.
So, we knew from the get-go how dangerous this lab was going to be and tried to stop it. We tried, we failed, and now this Nazi biowarfare death science dirty work is going on.”
Commenting on gain-of-function research in general, Boyle said:
“You’ll note it was funded by NIH and NIAID under Tony Fauci.
“The New York Times has pointed out that about 94% of all this Nazi biowarfare death science dirty work has been funded by NIH and NIAID since Reagan put him in charge of NIAID.”
According to Boyle, this has resulted in more than $100 billion in federal bioweapons spending since Sept. 11, 2001.
Boyle said the federal government “doesn’t rein in or prosecute” scientists working on such projects, “because the federal government is paying for this type of Nazi biowarfare death science dirty work.”
Such research, and the facilities in which it is performed, also pose a risk to surrounding communities and the world at large, Boyle said, suggesting a Wuhan-like leak could occur at any similar facility in the U.S.:
“This is another catastrophe waiting to happen, and that Boston University BSL-4 [facility] should be shut down immediately.
“They know full well how existentially dangerous this is, certainly for the metropolitan Boston area … and especially for the African American community in Dorchester surrounding that Boston University BSL-4 lab.”
For Boyle, “It’s not enough to ban gain-of-function.” He also called for BSL-3 and BSL-4 facilities, including the Boston University facility, a CDC facility in Atlanta and a new facility in Kansas where the federal Plum Island Animal Disease Center is being relocated, to be shut down.
“The only remedy here is to shut down all BSL-3s and BSL4-s in the U.S.A., immediately and effectively,” Boyle said. “Otherwise, there is going to be another leak.”
Notably, the Wuhan Institute of Virology where research involving “engineered novel bat coronaviruses” took place is said to have been performed in BSL-2 and BSL-3 facilities.
Rose questioned the lower safety conditions under which the NEIDL researchers created the hybrid strain, while also raising broader security concerns and calling for gain-of-function work to be “banned” and its products “destroyed immediately.”
She said:
“This paper reveals more than the successful creation of a deadly new virus. It [gives] this recipe in the methods to anyone with a decent lab to recreate it.
“They don’t even mention what the hell they are planning to do with this new virus! They don’t say a bloody word about the fact that they created a virus that for all intents and purposes, is a Level IV pathogen, so why the hell are they playing with it in a Level III [laboratory]?”
NIH claims it didn’t know what it was funding
According to NEIDL, grants from the NIH “provide the support for research at NEIDL.”
In September, the study’s lead author, Mohsan Saeed, Ph.D., received a five-year, $2 million grant from the NIAID, and a separate five-year, $2 million grant from the National Institute of General Medical Sciences, to “explore novel aspects of clinically important viruses and human defense mechanisms.”
Following the publication of the preprint study — and the controversy that ensued — the NIAID appeared to distance itself from the research. According to STAT, “The research team did not clear the work” with the NIAID, leading the agency to look “for some answers as to why it first learned of the work through media reports.”
Dr. Emily Erbelding, M.P.H., director of the NIAID’s Division of Microbiology and Infectious Diseases, told STAT that the research team’s “original grant applications did not specify that the scientists wanted to do this precise work. Nor did the group make clear that it was doing experiments that might involve enhancing a pathogen of pandemic potential in the progress reports it provided to NIAID.”
Erbelding said the NIAID is “going to have conversations” with the research team in the coming days, adding that “we wish that they would have” informed NIAID of the “intent of the research.”
According to Erbelding, this would have likely resulted in a committee being convened “that would assess the risks and benefits” of the research involving “enhanced pathogens of pandemic potential.”
What the NEIDL researchers did
According to STAT, the NEIDL researchers set out “to determine if the mutations in the Omicron spike protein were responsible for this variant’s increased ability to evade the immunity to SARS-2 that humans have built up, and whether the changes led to Omicron’s lower rate of severity.”
The research involved extracting the Omicron variant’s spike protein and attaching it to the original strain.
Put differently, the scientists took the deadliest COVID-19 strain and combined it with the spike protein from the most infectious strain. They then infected laboratory mice and human cells with the new hybrid strain.
The results showed that while the Omicron variant’s spike protein was responsible for the variant’s ability to evade immunity developed via infection, vaccination or both, it is not responsible for the decrease in the severity of the Omicron strain.
“The researchers looked at how mice fared against the new hybrid strain compared to the original Omicron variant.
“When a similar group of rodents were exposed to the standard Omicron strain, however, they all survived and only experienced ‘mild’ symptoms. …
“[The researchers] found the hybrid strain produced five times more viral particles than the original Omicron.”
According to the MetroUK, “The scientists also infected human cells with the hybrid variant and found it was five times more infectious than Omicron.”
In the preprint, the researchers wrote:
“We generated chimeric recombinant SARS-CoV-2 encoding the S gene of Omicron in the backbone of an ancestral SARS-CoV-2 isolate and compared this virus with the naturally circulating Omicron variant.
“The Omicron S-bearing virus robustly escapes vaccine-induced humoral immunity, mainly due to mutations in the receptor-binding motif (RBM), yet unlike naturally occurring Omicron, efficiently replicates in cell lines and primary-like distal lung cells.
“In K18-hACE2 mice, while Omicron causes mild, non-fatal infection, the Omicron S-carrying virus inflicts severe disease with a mortality rate of 80%. This indicates that while the vaccine escape of Omicron is defined by mutations in S, major determinants of viral pathogenicity reside outside of S.”
In a statement remarking on the outcome of the study, NEIDL’s Saeed, who is also an assistant professor of biochemistry at Boston University, said:
“Consistent with studies published by others, this work shows that it is not the spike protein that drives Omicron pathogenicity, but instead other viral proteins.
“Determination of those proteins will lead to better diagnostics and disease management strategies.”
Media focuses on study’s findings, but critics more concerned about the research itself
Some media outlets focused on the researchers’ findings that 100% of the mice infected with the engineered virus died.
Others, however, downplayed the study’s findings. According to Fox News, for example, one of the study’s limitations was that the specific breed of mice used may not provide an accurate model for the risk posed to humans, “as other types [of mice] are more similar to humans.”
In a blog post, commentator Alex Berenson, a former writer for The New York Times, also addressed the sensationalism surrounding the study’s findings, pointing out that while an 80% fatality rate in lab mice sounds bad, 100% of the mice that previously were infected with the wild variety of COVID-19 had died.
He wrote:
“[The research] says the Omicron/wild-type Sars-Cov-2 combination the researchers created is more lethal than Omicron.
“However, it ALSO says the Omicron/wild type virus is LESS lethal than [the] original wild type. Neither of those findings should be a surprise. Omicron is much less dangerous than the original Sars-Cov-2, so blending the two together produces a virus with intermediate lethality.
“What’s with the 80 percent mortality rate then? It’s in mice, people. And guess what? The wild-type had a 100 percent mortality rate in mice. Yes, all the mice infected with the original Sars-Cov-2 died. I think we can agree that Sars-Cov-2 does not have a 100 percent mortality rate in humans.”
Specifically addressing the probable risk to humans, Berenson added:
“Nor did the researchers provide any evidence that the blended Omicron/wild-type coronavirus is able to defeat antibodies in people who have been infected with and recovered from Omicron. Which is basically all of us. (They did show that both the original Omicron and their variant beats the mRNA vaccines, but that fact is not a surprise either.)”
Erbelding shared similar remarks, stating, “That 80% kill rate, that headline doesn’t tell the whole story, because Wuhan” — the original strain — “killed all the mice.”
In turn, behind its headline, the Daily Mail wrote, “The scientists admit the hybrid virus is unlikely to be as deadly in humans as it was in mice,” adding, “This is because the specific breed of lab mice used are very susceptible to severe COVID disease. Mice and humans also have very different immune responses to the virus.”
STAT also remarked on this point, writing:
“The fatality rate seen in this strain of mice when they were infected with these viruses raises questions about how good a model they are for what happens when people are infected with SARS-2. The Wuhan strain killed less than 1% of people who were infected.”
But Boyle and Rose and others, like David Livermore, Ph.D., a professor of microbiology at the University of East Anglia, and Shmuel Shapira, an Israeli government scientist, said the news coming out of NEIDL was less about the study’s results and more about the research itself.
Livermore told the Daily Mail, “Given the strong likelihood that the COVID pandemic originated from the escape of a lab-manipulated coronavirus in Wuhan, these experiments seem profoundly unwise.”
Shapira also condemned the research. “This should be totally forbidden, it’s playing with fire,” he said.
Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”
Twenty years ago, the “Cheney-Bush junta” — as Gore Vidal called it — launched its propaganda campaign to invade Iraq, effectively casting the dye for much of the historic period since.
The same day, then Vice President Dick Cheney appeared on Meet the Press with Tim Russert, hyping the New York Times story as evidence that Hussein was attempting to acquire “the kinds of tubes that are necessary to build a centrifuge and the centrifuge is required to take low-grade uranium and enhance it into highly-enriched uranium which is what you have to have in order to build a bomb.” Colin Powell and Condoleezza Rice followed Cheney’s lead on other shows.
In 2005, I confronted Miller about her reporting, asking her at if she would name the anonymous lying source who she allegedly relied on to falsely report “the best technical experts and nuclear scientists at laboratories like Oak Ridge supported” the CIA claim that the tubes were for a nuclear weapons program. In fact, it would later be established, the nuclear scientists did not support such an assessment and were effectively muzzled. When I questioned her, Miller refused to name the source that fed her this false information and Marvin Kalb, the moderator of the event, see video, ran interference, stopping further follow-ups. (See my piece “Should Media Expose Sources Who Lied to Them?”)
Many serious analysts early on deduced that the source was Cheney himself, likely through his chief of staff, Scooter Libby.
Even the mainstream Bob Simon of CBS would later remark to Bill Moyers about Cheney: “You leak a story, and then you quote the story. I mean, that’s a remarkable thing to do.”
Remarkable is actually an understatement. It’s engaging in a de facto conspiracy to deceive the U.S. public into war.
In April of 2020, a journalist asked at the daily White House press briefing: “Mr. President, I wanted to ask Dr. Fauci: Could you address these suggestions or concerns that this virus was somehow manmade, possibly came out of a laboratory in China?”
Anthony Fauci replied: “There was a study recently that we can make available to you, where a group of highly qualified evolutionary virologists looked at the sequences there and the sequences in bats as they evolve. And the mutations that it took to get to the point where it is now is totally consistent with a jump of a species from an animal to a human.”
That article was widely accepted by the major media as eviscerating the possibility of lab origin of Covid, shutting down debate at that critical time and continuing to hinder it to this day.
The thing is, Fauci seems to have had a serious role in that article’s appearing.
In 2021, limited Freedom of Information Act findings showed that Fauci had at minimum effectively coordinated with the named authors of the Nature Medicine article. See Nass’ write-up and subsequent reporting by some mainstream outlets such as USA Today.
Thus, this insidious tactic of helping to plant a story pushing the line you want in a media outlet and then citing it as evidence for your case was employed by both longtime creatures of Washington at historic junctures.
There are other notable parallels. Both Fauci and Cheney have also both been leading beneficiaries of Trumpwashing.
Ashley Rindsberg makes some serious arguments in his piece, “How Dick Cheney created Anthony Fauci,” including about the buildup of US bio“defense” after 9/11 (actually the anthrax attacks) — a trend several observers have noted. Alexis Baden-Mayer traces such arguments back to 1976, when Cheney and Donald Rumsfeld apparently pressured President Ford to order massive inoculations in the Swine Flu scare, which he would be widely mocked for.
While the antiwar forces and “left” criticism of the Iraq WMD propaganda were wholly inadequate, they at least manifested themselves on the national stage to some extent. Covid origins has hardly been recognized as an antiwar issue by most and the “left” at times has actually played a detrimental role, explicitly doing the establishment’s bidding in irrationally denying or minimizing the possibility of lab origin of the pandemic.
One thing that should be kept in mind as one parses through the claims and “exposés” is that some are de facto cover stories.
The Bush administration ramped up their propaganda campaign for the Iraq invasion, as noted at the beginning of this article, in September of 2002.
Why then? Sophisticates at the time would quote Andrew Card: “From a marketing point of view, you don’t introduce new products in August” said Bush’s chief of staff.
With the Bush administration cynically using the one year anniversary of 9/11 as a backdrop to launch their push for invading Iraq, the rationale articulated by Card was actually a remarkably benign motivation, a likely cover, in comparison to the war makers actual thinking.
Evidence points to SARS-CoV-2 being the product of gain-of-function (GoF) research. Indeed, attorney Tom Renz will soon release the results of a major legal investigation, which he claims will demonstrate — beyond a reasonable doubt — that SARS-CoV-2 was created as part of a GoF project.1
Whether the outbreak was accidental, intentional or the result of negligence, the end result is the same — devastation of health, commerce, finance and civil life worldwide for years on end.
Now imagine what might happen if something like the Spanish flu got out — or worse, a turbo-charged, genetically engineered version of it. Incomprehensible as it may seem to the average person, scientists in the U.S. and Canada have resurrected this devastatingly lethal virus and, not surprisingly, the National Institutes of Health (NIH) and Dr. Anthony Fauci’s National Institute of Allergy and Infectious Diseases (NIAID) are involved.
Mad Scientists Are Testing Recreated Spanish Flu on Monkeys
As reported by Tom Renz, August 19, 2022:2
“… this is so absurd that I am just starting with the reference document because I am concerned no one will believe it. Here it is: ‘Spanish Flu GoF.’3 Yes, that is right, Fauci and crew are now actively performing gain-of-function (GoF) work and infecting primates with the Spanish Flu … Here is a quote from the document:
‘… Influenza virus A/South Carolina/1918 (H1N1) was generated by reverse genetics and handled in biosafety level 4 (BSL-4) containment at the National Microbiology Laboratory (NML).
Sequences of the 1918 influenza viral segments were based on data reported under GenBank accession numbers DQ208309, DQ208310, DQ208311, AF117241, AY744935, AF250356, AY130766, and AF333238.
1918 influenza virus was cultured using Madin-Darby canine kidney … cells. MDCK cells were grown in minimum essential medium … supplemented with 5% fetal bovine serum … and 1 L-glutamine …
A passage 2 (P2) virus stock was prepared using MEM supplemented with 0.1% bovine serum albumin (BSA) … 1 L-glutamine, and 1 mg/mL N-tosyl-L-phenylalanine chloromethyl ketone (TPCK)-treated trypsin …
This stock was used for animal inoculation. The mouse 50% lethal dose (MLD50) for this stock was determined previously to be 103.2 PFU; this value was confirmed prior to the use of the stock for macaque infection.’
I frankly do not care to debate the nuance of whether the recreation of generally extinct virus ‘generated by reverse genetics’ using pieces and parts of other animals qualifies as GoF; what I care about is that we have recreated the Spanish Flu and are experimenting with it on other animals.”
Spanish Flu ‘Not Lethal Enough’
As noted by Renz, the scientists appear frustrated by the fact that their reverse engineered Spanish flu virus — even at the highest doses tested — was not lethal enough to kill the two macaque species selected for the experiment.
Macaques were therefore deemed “not ideal for the development and testing of novel pandemic influenza-specific vaccines and therapies,” necessitating “other physiologically relevant nonhuman primate models.” Renz continues:4
“… given the result of the previous coronavirus GoF, can ANYONE possibly argue GoF work on the Spanish Flu is a good idea? Even the simple recreation of the disease demonstrates an incredible lack of respect for the disaster created by the coronavirus GoF.
So you may be asking, what moron could possibly be oblivious enough to support GoF work on the Spanish Flu while the world is still dealing with the nightmare that is COVID? The answer should not be surprising … NIH and NIAID are involved.
Apparently Fauci does not mind what he did with funding the creation of COVID and is at it again. You might also note the vaccine development crew’s involvement. A foundational point in this article is that the newly recreated Spanish Flu is not dangerous enough. Here is a pull-quote:
‘However, 1918 influenza was uniformly nonlethal in these two species, demonstrating that this isolate is insufficiently pathogenic in rhesus and Mauritian cynomolgus macaques to support testing novel prophylactic influenza approaches where protection from severe disease combined with a lethal outcome is desired as a highly stringent indication of vaccine efficacy.’
This means that these people are arguing that we need to make a more dangerous version of the Spanish Flu so they can make ‘better’ vaccines for it … despite the fact that until they recreated it, it likely no longer existed in nature.”
As noted by Renz, elected officials really need to answer the question, “Why is this kind of research allowed to continue on your watch?” Why are we reverse engineering the most lethal viruses the world has ever seen — after they’ve already been eradicated?
The argument that we need to create dangerous viruses “just in case” Nature comes up with something similar, so we can create vaccines for said viruses in advance, simply doesn’t hold water. Stop creating these monstrosities, and we won’t need the vaccines! This is science gone mad, and it must be stopped.
Besides, what are the chances that a virus would emerge naturally that just so happens to perfectly match the virus we now have a vaccine against? The entire premise is irrational from start to finish. It’s biowarfare research and nothing else.
The Intentional Cover-Up of SARS-CoV-2’s Origin
Fauci, former NIH chief Dr. Francis Collins, EcoHealth Alliance president Peter Daszak and other members of the scientific community have spent the last two and a half years actively stifling debate about the genesis of SARS-CoV-2.
And, coincidentally, most of them have clear-cut connections to bat coronavirus GoF research and/or the Wuhan Institute of Virology (WIV), which appears to be the lab from which the virus somehow escaped.
So, it appears those who insist SARS-CoV-2 is of natural origin, despite all the evidence to the contrary, are doing so because they don’t want risky virological research to be blamed for the COVID pandemic. That would “blow their cover” and raise questions about the sanity of funding such research.
Some may be so enamored with their chosen careers, they cannot imagine doing anything other than tinkering with pathogens. For them, pulled funding is a threat to their livelihood. But for others, the underlying incentive may be more nefarious. Like I already said, there’s really no reason for this kind of research other than the creation of weapons of mass destruction.
Whatever incentive any given player may have had, what’s clear is that Fauci, Collins, Daszak and many others intentionally undermined efforts to get to the bottom of where SARS-CoV-2 came from.
Attesting to this corruption of science is Jeffrey Sachs, Ph.D., professor of economy at Columbia University, a senior United Nations adviser and chair of The Lancet COVID-19 Commission, convened in June 2020.
Sachs originally assigned Daszak to lead and organize the COVID-19 Commission’s task force to investigate the virus’s genesis (one of 11 task forces under the COVID Commission). Sachs ended up dismissing Daszak from the task force in June 2021, after he realized just how serious Daszak’s conflicts of interest were,5 and that Daszak was lying to him.6
Eventually, he realized Daszak wasn’t the only rotten apple in the bunch. Other members of The Lancet Commission’s COVID Origins task force were also working against their mandate to investigate the pandemic’s origin. The final straw came when Sachs sacked Daszak and several task force members suddenly attacked him for being “antiscience.”
Shortly thereafter, a Freedom of Information Act (FOIA) request brought previously hidden NIH documents to light, and Sachs realized that those who were attacking him also had undisclosed ties that made their ability to get to the truth doubtful at best. At that point, in September 2021, he disbanded the whole task force.
Lack of Transparency Breeds Mistrust
In mid-May 2022, Sachs published a frank opinion piece in the journal PNAS,7 together with Neil Harrison, calling for a truly independent inquiry into the origin of SARS-CoV-2.
In their article, Sachs and Harrison argued that while transparency on the part of Chinese authorities would be “enormously helpful,” much may be gleaned from information found in U.S.-based research institutions that were working with Wuhan-based institutions, including the WIV. Yet such material has not been disclosed for independent analysis. Here’s an excerpt:8
“This lack of an independent and transparent US-based scientific investigation has had four highly adverse consequences. First, public trust in the ability of US scientific institutions to govern the activities of US science in a responsible manner has been shaken.
Second, the investigation of the origin of SARS-CoV-2 has become politicized within the US Congress; as a result, the inception of an independent and transparent investigation has been obstructed and delayed.
Third, US researchers with deep knowledge of the possibilities of a laboratory-associated incident have not been enabled to share their expertise effectively. Fourth, the failure of NIH, one of the main funders of the US–China collaborative work, to facilitate the investigation into the origins of SARS-CoV-2 has fostered distrust regarding US biodefense research activities.
Much of the work on SARS-like CoVs performed in Wuhan was part of an active and highly collaborative US–China scientific research program funded by the US Government (NIH, Defense Threat Reduction Agency [DTRA], and US Agency for International Development [USAID]), coordinated by researchers at EcoHealth Alliance (EHA), but involving researchers at several other US institutions.
For this reason, it is important that US institutions be transparent about any knowledge of the detailed activities that were underway in Wuhan and in the United States. The evidence may also suggest that research institutions in other countries were involved, and those too should be asked to submit relevant information …”
Sachs and Harrison go on to name a number of U.S. institutions that need to come clean about their work, including the EcoHealth Alliance (EHA), the University of North Carolina (UNC), the University of California at Davis (UCD), the NIH, NIAID and the U.S. Agency for International Development (USAID).
All of these agencies and institutions have conducted and/or collaborated on research that may be able to solve the mystery, but instead of transparently sharing their data, they’ve merely declared that they’ve “not been involved in any experiments that could have resulted in the emergence of SARS-CoV-2.”
Blanket Denials Are Not Good Enough
As noted by Sachs, before we can believe such claims, we need to be able to confirm their veracity, and that requires independent analysis of all the data.
“Blanket denials from the NIH are no longer good enough. Although the NIH and USAID have strenuously resisted full disclosure of the details of the EHA-WIV-UNC work program, several documents leaked to the public or released through the Freedom of Information Act (FOIA) have raised concerns,” Sachs and Harrison wrote.9
“These research proposals make clear that the EHA-WIV-UNC collaboration was involved in the collection of a large number of so-far undocumented SARS-like viruses and was engaged in their manipulation within biological safety level (BSL)-2 and BSL-3 laboratory facilities, raising concerns that an airborne virus might have infected a laboratory worker.
A variety of scenarios have been discussed by others, including an infection that involved a natural virus collected from the field or perhaps an engineered virus manipulated in one of the laboratories.”
Suspicious ‘Coincidences’ Abound
Sachs and Harrison go on to discuss the problem of an unusual furin cleavage site (FCS) in SARS-CoV-2 that makes it more transmissible and pathogenic than related viruses.
While it’s not yet known how this feature came to be within SARS-CoV-2, whether by natural evolution or intentional insertion, “We do know that the insertion of such FCS sequences into SARS-like viruses was a specific goal of work proposed by the EHA-WIV-UNC partnership within a 2018 grant proposal (‘DEFUSE’) that was submitted to the U.S. Defense Advanced Research Projects Agency (DARPA),” Sachs wrote.
That particular DARPA proposal was never funded, but as noted by Sachs, “we do not know whether some of the proposed work was subsequently carried out in 2018 or 2019, perhaps using another source of funding.”
“Information now held by the research team headed by EHA, as well as the communications of that research team with US research funding agencies, including NIH, USAID, DARPA, DTRA, and the Department of Homeland Security, could shed considerable light on the experiments undertaken by the US-funded research team and on the possible relationship, if any, between those experiments and the emergence of SARS-CoV-2,” Sachs and Harrison wrote.10
“We do not assert that laboratory manipulation was involved in the emergence of SARS-CoV-2, although it is apparent that it could have been. However, we do assert that there has been no independent and transparent scientific scrutiny to date of the full scope of the US-based evidence.”
In an August 2, 2022, Current Affairs interview,11 Sachs again reiterated that he believes the NIH and allied scientists colluded to impede The Lancet Commission’s investigation, for the simple reason that the virus was the result of U.S. research.
Sachs also opened up about his concerns and misgivings in an August 20, 2022, interview with Robert F. Kennedy Jr. (video above). He admits believing in the zoonotic spillover theory early on, only to, over time, come to change his mind as he realized he was being lied to, over and over again.
Today, he believes the lab-leak theory is the most likely explanation for the pandemic — and that the U.S. government, the NIH, the NIAID and the rest are suppressing the truth for the simple reason that they’re responsible for its creation, even if only in part.
Final Thoughts
To circle back to where we started, is it really prudent to reverse engineer the Spanish flu virus, and further tinker with it to make it even more lethal — all in the name of vaccine development?
Think back over the past few years. Mull over the deaths — an estimated 18 million from COVID-19 alone12 — the suicides (deaths of despair), the lost businesses, lost education years, the loss of freedoms and Constitutional rights, the COVID jab injuries, and the massive wealth transfer that has occurred.
All of that may have been because of this kind of mad science. Do we really want to repeat it in the future, but with a far more lethal pathogen? Most sane persons would say no. It’s time for legislators to take definitive steps to ensure mankind is not wiped out by scientific hubris.
Mr. and Mrs. Barack Obama got a $65 million advance for their joint book deals. Except, nobody sells enough books to make such a stupefying advance work. So those of an inquiring mind wondered if the book deal was a way to launder money to the former President and his family for services rendered.
Mr. Fauci earns a bureaucrat’s salary. $437,000/year. But with royalties, adding in his wife’s salary (head Ethics officer for the NIH Clinical Center) and their investments, it is said the family earned $1.7 million dollars last year.
You’d have thought he got a tidy sum on his last book, which came out only 10 months ago. But no. He only got a basket of superlatives:
Compiled from hours of interviews drawn from the eponymous National Geographic documentary, this inspiring book from world-renowned infectious disease specialist Anthony Fauci shares the lessons that have shaped the celebrated doctor’s life philosophy, offering an intimate view of one of the world’s greatest medical minds as well as universal advice to live by.
Before becoming the face of the White House Coronavirus Task Force and America’s most trusted doctor, Dr. Anthony Fauci had already devoted three decades to public service. Those looking to live a more compassionate and purposeful life will find inspiration in his unique perspective on leadership, expecting the unexpected, and finding joy in difficult times.
With more than three decades spent combating some of the most dangerous diseases to strike humankind– AIDS, Ebola, COVID-19–Dr. Fauci has worked in daunting professional conditions and shouldered great responsibility. The earnest reflections in these pages offer a universal message on how to lead in times of crisis and find resilience in the face of disappointments and obstacles.
Filled with inspiring words of wisdom, this profound book will offer readers a concrete path to a bright and hopeful future.
Editor’s Note: Dr. Anthony Fauci had no creative control over this book or the film on which it is based. He was not paid for his participation, nor does he have any financial interest in the film or book release.
Well then, since I don’t think he could legally be paid extra for a book while in office, it will be of great interest how much he gets for his next work of art. Somebody that good must be worth plenty.
Fauci’s final thoughts from STAT (he never forgets the $): “Thanks to the power of science and investments in research and innovation, the world has been able to fight deadly diseases and help save lives around the globe,” Fauci said. “I am proud to have been part of this important work and look forward to helping to continue to do so in the future.”
We the people will not necessarily benefit from Il Fauci giving up his post. What changed when Francis Collins left the NIH? Nothing. The Acting Director job was given to Lawrence A. Tabak, D.D.S., Ph.D. Dentist Tabak was one of Fauci and Collins’ co-conspirators in the COVID origins coverup. He knows where the bodies are buried and has kept the shovels locked up.
‘We need a new plague’ was the sentiment in the early 1980s in the corridors of America’s Centers for Disease Prevention and Control (CDC), because the agency was facing closure. In his book The Real Anthony Fauci Robert F Kennedy Jr cites Dr Kary Mullis recalling the institutional desperation reflected in circulating memos which said: ‘We need to find something to scare the American people into giving us more money.’
The events which followed, and the panoply of artifices used to secure this end, became a template for amassing unbridled power over the population, the institutions, and even the White House.
Kennedy recounts that in the summer of 1981 the CDC reported that approximately 50 gay men in Los Angeles, San Francisco and New York had presented with Kaposi’s sarcoma (a skin cancer associated with immune suppression) and other immune deficiency-related health problems including a rare form of pneumonia (PCP).
As cases starting appearing in other major cities in the same cohort, the hunt was on for the cause of this new disease, dubbed Acquired Immune Deficiency Syndrome (Aids).
Responsibility for it fell under the US National Cancer Institute (NCI). In 1983 the French virologist Dr Luc Montagnier identified signals of a retrovirus in some Aids patients, which he believed could be responsible for causing the disease. Dr Robert Gallo of the NCI persuaded Montagnier to send him a sample of the virus in exchange for fast-tracking the publishing of Montagnier’s work in the journal Science.
Before doing so, Gallo cultured the sample, gave it a different name, patented an antibody kit he claimed capable of detecting it, and in April 1984 called a press conference to announce to the world that the probable cause of Aids had been found in the form of a ‘known human cancer virus’, claiming the discovery as his own. Once the announcement was made, no one could review Gallo’s work which was published subsequently.
A bitter row ensued between Montagnier and Gallo, which eventually led to an ‘accommodation’, whereby the researchers agreed to share the discovery, and the virus was given the name HIV (Human Immunodeficiency Virus).
The hypothesis that HIV caused Aids, however, had not been subject to the normal processes of independent replication, verification, dissent and rebuttal. A nascent hypothesis had been seized and hurriedly converted into accepted fact. ‘Science by announcement’ was a dangerous development which has had grave repercussions to the present day.
Robert Gallo’s overt ambition to be awarded a Nobel Prize made him a natural ally of Anthony Fauci. So once the HIV story of a worldwide lethal virus was launched, claiming the highly infectious nature of it, Fauci wrested jurisdiction for the disease away from NCI and into his moribund National Institute for Allergies and Infectious Diseases (NAID), thus capturing the flood of congressional funds that would be made available to combat it.
Many eminent scientists had misgivings about the hypothesis. Foremost was Professor Peter Duesberg, a world-respected molecular biologist. Duesberg was a consummate scientist and an applied scholar. At thirty-three, having discovered the ‘oncogene’ which appeared to cause cancer, he subjected his own theory to more rigorous tests than his critics had, and became convinced his discovery had been a lab fluke. He therefore publicly abandoned his own hypothesis, at the height of his acclaim. Colleagues praised him for his ‘integrity, his genius, his kindness and his intelligence’.
Duesberg, Kary Mullis and their school of critics believed the first generation of Aids was a complex illness which had its cause in a variety of chemicals. The profusion of recreational drugs used by the homosexual community, particularly amyl nitrate (poppers) known to cause immune suppression, in combination with the constant use of antibiotics to treat infections, were strong factors in immunity collapse. But after Robert Gallo’s April 1984 press conference Fauci moved to quash all talk of toxic causation to attribute Aids uniquely to the deadly virus.
Following Gallo’s announcement, Duesberg studied every scientific publication on HIV and Aids, and in 1987 published his observations in the journal Cancer Research. He argued that retroviruses were not, by accepted definition, a life form, and HIV was not capable of causing either cancer or Aids. Referring to the supposed indeterminate incubation period of HIV he said: ‘There are no slow viruses causing Aids, only slow scientists.’ Duesberg was committed to clean functional proof at a time when electron microscopy and other technologies for detecting new viruses were making biology – particularly the study of viruses – increasingly murky. Fame and finance were driving the frenzy in viral research. With official and commercial encouragement, researchers were blaming newly discovered viruses for an assortment of ancient diseases. Duesberg argued that the apparent high incidence of HIV-Aids in Africa was a function of the now notorious PCR to produce false diagnoses of infection, and the broad definition of Aids, which captured everything in its net from malnutrition to endemic diseases.
The second generation of Aids in the early 1990s is now widely recognised to have been caused by the poisonous drug Azidothymidine (AZT) pushed by Fauci on to ‘HIV positive cases’. AZT was developed in the 1960s as a leukaemia chemotherapy drug but abandoned when government researchers deemed it too toxic even for short-term use. Described by Joseph Sonnabend as ‘incompatible with life’, AZT randomly destroys bones, kidneys, livers, muscle tissue, the brain and the central nervous system.
After Peter Duesberg’s compelling 1987 article, which challenged point by point the basis of the HIV-Aids hypothesis, the scientific world waited for answers to Duesberg’s probing questions, but Gallo never attempted a reply. Instead Fauci moved ruthlessly to annihilate Duesberg’s voice. His stature and the respect he commanded were an existential threat to Fauci’s plans for control and grandeur through the theory of a dangerous virus.
Marshalled by Fauci, the self-interested scientific press banished Duesberg. John Maddox, editor of the journal Nature, invited Duesberg’s colleagues to slander him without fear of response, writing an editorial stating that the virologist, by his heresy, had forfeited the standard scientific practice of ‘right of reply’.
Scientific conferences disinvited Duesberg. His graduate students were warned by their university that working with him would render them irrelevant, and the fawning mass media followed the instructions handed down from on high. As the reporter Celia Farber wrote, ‘Duesberg’s problem transcended science: It was career protection to partake in his bullying and degradation. The Fauci serf scientists were driven by fear that if they did not publicly denounce Duesberg in sufficiently disgusted tones they themselves would be punished.’
In 1994 a senior geneticist, Dr Stephen O’Brien, was dispatched by the very same editor of Nature, John Maddox, to try to persuade Duesberg to change his position, in exchange for ‘reinstatement’. O’Brien rang Duesberg on the pretext of needing to speak to him urgently and the two met at the opera in San Francisco. O’Brien pulled from his pocket a paper entitled ‘HIV Causes Aids: Koch’s Postulates Fulfilled’ with his own name and that of Duesberg printed at the bottom, and begged Duesberg to sign it. To his undying credit, Duesberg refused.
Duesberg’s remarkable lack of bitterness towards his persecutors is the sign of a man at peace with his soul. It is likely that Fauci’s rancour, and the depths to which he sank to humiliate and denigrate Duesberg, sprang from a hatred of his ability and integrity, qualities Fauci could not bear to contemplate.
Think back to July 2020. Trump and Fauci were at war with each other. Key leaders within the Trump administration, including Peter Navarro, wanted to fire Fauci. There were riots in the streets as people protested the murder of George Floyd. And new evidence shows that behind the scenes, Fauci was working to torpedo Trump’s chances for re-election.
We already knew that Fauci, the FDA, CDC, and the pharmaceutical industry went to great lengths to block safe and effective treatments including hydroxychloroquine and ivermectin in order to prolong the pandemic and create the market for Covid-19 vaccines. But a new book reveals that Fauci also forced Moderna to delay their clinical trial by three weeks — which pushed the release of their preliminary results until after the presidential election.
This key piece of information comes from The Messenger: Moderna, the Vaccine, and the Business Gamble That Changed the World published last week byHarvard Business Review Press.The author, Peter Loftus, is a reporter for the Wall Street Journal and they published his essay about the book in their Review section on Saturday. What’s astonishing is that Loftus does not even realize the enormity of the story he just stumbled upon. Cultural capture and too many shots apparently prevent one from connecting the dots, so I will do it for him.
Most people already know the broad brush strokes of the Moderna story — they had never successfully brought a product to market before Operation Warp Speed. They were grifters — they took $25 million from the Defense Advanced Research Projects Agency (DARPA) in 2013 to develop mRNA products that never worked and another $125 million from the Biomedical Advanced Research and Development Authority (BARDA) in 2015 for a vaccine for Zika that also failed. But Fauci really liked these grifters and so when the pandemic began in 2020, BARDA directed $483 million to Moderna for Covid-19 vaccine development — and Moderna cut NIH in on the patents. That gave NIH and especially Fauci control over what came next.
The key paragraphs from Loftus’ WSJ essay are here:
Dr. Zaks [Chief Medical Officer for Moderna] had wanted to use a private contract research organization to run the whole trial, but NIAID officials wanted their clinical-trial network involved. Eventually, Dr. Zaks backed off, and both entities participated. “I realized we were at an impasse, and I was the embodiment of the impasse,” Dr. Zaks said.
Next, when Moderna’s 30,000-person study began enrolling volunteers in July 2020, the subjects weren’t racially diverse enough. Moncef Slaoui, who led Warp Speed’s vaccine efforts, and Dr. Fauci began holding Saturday Zoom calls with Mr. Bancel and other Moderna leaders to “help coax and advise Moderna how to get the percentage of minorities up to a reasonable level,” Dr. Fauci recalled.
Drs. Fauci and Slaoui wanted Moderna to slow down overall enrollment, to give time to find more people of color. Moderna executives resisted at first. “That was very tense,” Dr. Slaoui said. “Voices went up, and emotions were very high.” Moderna ultimately agreed, and the effort worked, but it cost the trial about an extra three weeks. Later, Mr. Bancel called the decision to slow enrollment “one of the hardest decisions I made this year.”
The claim that Fauci cared about racial diversity in the clinical trial is a lie. How do we know this? Later “clinical trials” for Pfizer and Moderna in kids looked at antibodies in the blood, not actual health outcomes, in only about 300 study participants. The number of people of color enrolled in those undersized trials were in the single digits (literally two or three Black participants total) — so those results were not statistically significant. Yet this did not stop authorization. It appears that Fauci’s delay tactics were designed to accomplish a different goal.
Let’s do the math:
Moderna released their preliminary results — claiming 94.5% effectiveness — on November 16, 2020.
The presidential election was less than two weeks earlier — on November 3, 2020.
Trump lost by less than 1% of the vote in 4 key swing states.
Fauci’s demand to slow down enrollment in July 2020 cost Moderna 3 weeks.
If Moderna had released their results 3 weeks earlier — on October 25, 2020, Trump would have scored a major win in the final week of the campaign and won the election.
It does not matter how one feels about Trump or Biden. A massive political win in the week before the election would have convinced enough voters of Trump’s competence and thus pushed Trump’s vote total over the top.
What about Pfizer? They also could have published their preliminary results prior to the election which would have secured Trump’s re-election. According to Loftus, Pfizer “opted out of Operation Warp Speed for fear it would slow the company down.” Pfizer still took $2 billion off of the Trump administration for advance purchase orders. But Scott Gottlieb and Pfizer clearly preferred Biden and so they held their preliminary results until November 9, 2020 — just 6 days after the election. The Biden administration returned the favor by giving Pfizer a blank check and authorizing shots for additional age groups based on the worst “clinical trial” results anyone has ever seen.
The important thing to understand in all of this is that Fauci, the FDA, NIH, and CDC are political functionaries pretending to be scientists. Pandemics, vaccines, and public health are a way for the Democratic Party machine to direct billions of dollars to their base and reward large donors to the party. These companies and their bureaucratic enablers were happy to take money off of Trump. But they knew that they could get an even better deal from Biden.
As you know, the results of this criminal scheme are gruesome. The Covid-19 shots authorized right after the 2020 election have made no discernible impact on the course of the pandemic. Far more people have died of Covid-19 since the introduction of the shots under Biden than during the Trump administration when no Covid-19 shots existed. The Covid-19 shots have negative efficacy and even quadruple-dosed Biden and quadruple-dosed Fauci have contracted Covid-19, twice. These are the deadliest and most toxic shots in the history of the world.
So what started out as a grift turned into mass murder and a crime against humanity.
And now it’s happening again…
II. Pfizer and Moderna move up the release date for reformulated Covid-19 shots in the effort to help Democrats win the midterm elections
On Thursday of last week, the White House and the FDA told their favorite stenographers at the NY Times that Moderna and Pfizer are going to release their reformulated Covid-19 shots, that will completely skip clinical trials, in mid-September.
As readers of my Substack will recall, back on June 28, Pfizer said that the fastest the reformulated shots could be released was October; Moderna said “late October or November” — provided they could skip clinical trials (which of course the FDA granted because they work for Pharma). Did Pfizer and Moderna not understand their own production capabilities? How did Pfizer and Moderna suddenly speed up their production schedule by 6 weeks?
It appears that once again, the public health gatekeepers are doing politics not science. If shots go into bodies in the last two weeks of September, Democrats will claim progress against Covid during October right before the midterm elections on November 8. It’s basically the political win that these same actors denied to Trump (it’s not a public health win, as I will show below).
What’s likely driving this is that Fauci, Pfizer, Moderna, the FDA, CDC, and NIH all want Democrats to retain the House and Senate in order to prevent hearings into their bungling of the Covid-19 response. Of course they also want to keep the Covid-19 vaccine gravy train going as long as possible.
But, you’re surely saying to yourself, we know that these 5th dose reformulated shots are likely to cause catastrophic harms. We’re already seeing a 5% to 15% increase in all-cause mortality across the most heavily vaccinated countries as a result of non-specific effects from these shots. There are 29,790 VAERS reports of death following these shots and this is likely an underestimate by a factor of 41 (so actual death toll = 1,221,390). These reformulated shots are going to use a form of mRNA never tried before and skip clinical trials altogether, so the harms could be even worse. There also seem to be cumulative harms from these shots — the more doses, the more messed up the immune system, the more vulnerable one is to Covid and all sorts of other diseases including cancer.
So how exactly do they plan to get away with this, especially right before an election?
The same way they always get away with it — they own the media. Pfizer and Moderna will rush out press releases claiming that these reformulated shots are a miracle. The CDC’s in-house newsletter, MMWR, will rush out articles and janky studies claiming that these reformulated shots are a miracle. The mainstream media will dutifully report that these reformulated shots are a miracle. Meanwhile, people you know and love — coworkers, friends, neighbors, and family — will be getting injured and killed by these shots. Yet all of the stories in the news will be hosannas about the genius of Tony Fauci, Peter Marks, and the FDA. Billions of dollars of dark money from Pharma will flow into Democratic Congressional campaign coffers. If Democrats can retain the House and Senate they will reward Pfizer and Moderna by blocking any inquiry into the failed Covid-19 response. Win, win, win for Pharma. Everyone else loses.
Which brings me to my last point….
III. Republicans, you have to step up and fight for us or you will lose
Republicans thought that they could take back the House and Senate simply by not being Democrats. Most Republicans did not really fight for us, they just sat back and let Dems destroy themselves. That plan was working until the Supreme Court overturned Roe. Now the Republican advantage in the generic Congressional ballot (‘which party do you prefer’) has evaporated. Pelosi has passed a range of popular bills. Manchin has fallen in line so Biden will likely get some late legislative wins. Gas prices have declined somewhat. And now it appears that Democrats, who were left for dead just weeks ago, will retain the Senate and may retain the House.
IF REPUBLICANS WANT TO WIN THE MIDTERM ELECTIONS THEY HAVE TO MAKE IT ABOUT DEMOCRATS’ FAILED RESPONSE TO COVID!
No more sitting back. No more making warrior mamas do all of the emotional labor for our country. If Republicans want to win they have to make it clear that they will fire, arrest, and prosecute Fauci (and all of his lieutenants) as soon at Republicans take power. Fauci funded the creation of the chimera virus, blocked access to safe and effective treatments, and inflicted deadly toxic vaccines on the entire population. Over 2 million Americans are dead as a direct result of Fauci’s corruption (1 million dead from/with Covid, over 1 million dead from the shots). If Republicans cannot be bothered to sink this two-foot putt then they don’t deserve to win. If Republicans want the votes of the 18 million single-issue medical freedom voters who decide every national election these days — that’s what they have to run on: #ArrestFauci!
In retrospect it can be seen that the 1967 war, the Six Days War, was the turning point in the relationship between the Zionist state of Israel and the Jews of the world (the majority of Jews who prefer to live not in Israel but as citizens of many other nations). Until the 1967 war, and with the exception of a minority of who were politically active, most non-Israeli Jews did not have – how can I put it? – a great empathy with Zionism’s child. Israel was there and, in the sub-consciousness, a refuge of last resort; but the Jewish nationalism it represented had not generated the overtly enthusiastic support of the Jews of the world. The Jews of Israel were in their chosen place and the Jews of the world were in their chosen places. There was not, so to speak, a great feeling of togetherness. At a point David Ben-Gurion, Israel’s founding father and first prime minister, was so disillusioned by the indifference of world Jewry that he went public with his criticism – not enough Jews were coming to live in Israel.
So how and why did the 1967 war transform the relationship between the Jews of the world and Israel? … continue
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