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COVID-19

Lab wars: Inside one Democrat’s 20-year crusade to save the world from Anthony Fauci — Part 1: 2001-2014

The evidence continues to mount that the most likely source of the outbreak of SARS-CoV-2, the virus that causes COVID-19, was not a wet market as was originally claimed. The evidence likewise continues to mount that the research involved in the leak was likely gain-of-function research that was funded, at least in part, with our own tax dollars.

While much of the world has only recently woken up to this reality, one man, Dr. Richard Ebright, has been warning us for 20 years that this day was coming.

For 20 years, his warnings have largely been ignored, primarily thanks to Dr. Anthony Fauci.

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To most Americans, even those who follow the news closely, Fauci was helicoptered into their consciousness out of total obscurity in early 2020, when he became the public face of the government’s pandemic response. In many ways, though, Fauci could have been yanked out of central casting to play the role of television family doctor for the whole country — an image he carefully cultivated to project an air of competence and confidence to a shaken nation.

What most people did not know, though, was that for years, Fauci had been dogged by a very different sort of doctor — a researcher from Rutgers University who shunned the camera and preferred to keep his opinions in print. A man who made it clear with his appearance and his mannerisms that he never wanted to be an activist. A registered Democrat who supported Biden to the point of putting a Biden sign in his front yard, Ebright had always been convinced of one simple thing that he viewed to be above the petty fray of partisan politics: the government should not be spending our tax dollars to fund dangerous research on making viruses more deadly.

For years, Ebright and Fauci carried out a silent war, waged in print, visible mostly only to members of the small community of research scientists who conduct serious chemical and biological research. Over and over again the same refrain played out: Ebright warned the public that this research was making the public less safe, and Fauci insisted it was making the public more safe.

As we know now, Ebright was almost certainly right. However, it has taken four years — thanks to the concerted efforts of Fauci and his team — for the public to slowly come around to that realization.

But to understand where we are, it is first necessary to understand how we got here.

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Countless ink, both real and digital, has been spent examining Fauci’s every move taken since those fateful early days in 2020. Relatively little has been spent examining Fauci’s actions prior to 2020.

“[Dick Cheney] found one agency and one person willing to take that role… he found Anthony Fauci.”

Those actions, which are still largely shrouded in obscurity, may turn out to have been far more consequential than anything Fauci has done since he first appeared at the infamous press conference with former President Trump. You see, for the last two decades, Fauci has been by far the most important defender of what might be fairly called a bioweapons research program that the public now knows — albeit imperfectly — as “gain-of-function” research.

The U.S. government started the ball rolling on this dangerous research in the waning days of 2001. As you may recall, the al-Qaeda attacks of 9/11 were followed almost immediately by a series of high-profile anthrax attacks, in which prominent individuals in the U.S. were mailed envelopes with suspicious white powder that later tested positive for anthrax.

The Bush administration, led by then-Vice President Dick Cheney, became convinced that the government’s readiness to face bioweapons threats was weak and responded by prevailing upon Congress to pass a massive funding increase to research on both anthrax and new, “designer” viruses that did not yet exist but might potentially be created by enemies of the United States.

“Cheney, even before the anthrax mailings, felt that the U.S. biodefense posture was weak and was convinced that it could only be improved by carrying out an aggressive and assertive program of biodefense research that would include components that walked right up to the red line and, arguably, crossed the red line set by the biological weapons convention,” Ebright told Blaze News.

According to Ebright, Cheney became deeply frustrated that the Department of Defense maintained a biological weapons convention compliance office that reviewed every research proposal with bioweapons agencies by the Department of Defense. This biological weapons compliance office repeatedly thwarted dangerous research projects that Cheney wanted to see come to fruition.

And so, Cheney set out in 2003 to find an agency that would not have a biological weapons conventions compliance office that could take the lead and carry out these dangerous and legally questionable projects.

“He found one agency and one person willing to take that role, and the agency was the National Institute of Allergy and Infectious Diseases… and he found Anthony Fauci. And the resources that had been part of the Department of Defense moved almost in toto to NIAID, and the authority for all U.S. biodefense research went to the new biodefense research czar, Anthony Fauci, who then received a very large salary increase, making him the highest-compensated government employee,” Ebright said.

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Fauci was an enthusiastic and frequent champion of the program under his supervision. In NIH press releases dating back to its inception, Fauci regularly asked Congress for more money for the program and defended diverting millions of dollars from other programs.

Not all scientists, however, were convinced. As even the NIH concedes, the decision to divert money from other programs infuriated many in the scientific community — not only because the money was needed elsewhere but also because the money was being hastily thrown at many scientists who had little or no experience researching priority pathogens.

Ebright, for his part, raised yet another issue. “This drove a massive increase in the number of institutions and individuals with access to bioweapons agents,” Ebright told Blaze News. “This increased, rather than decreased, the risk of release of those agents.”

Ebright told everyone who would listen that it was a mistake to continue expanding funding that had the effect of increasing the number of people who handled dangerous pathogens — a refrain that made him unpopular both with the Bush administration and within the halls of NIAID.

Unfortunately, it would not be the last time that Ebright’s warnings in that 2004 article would prove to be prophetic.

In fact, Ebright was such a persistent antagonist to the Bush administration’s bioresearch program that the New York Times ran a positive profile on him in 2004 titled, “I BEG TO DIFFER: In a Lonely Stand, a Scientist Takes On National Security Dogma.” In the piece, Ebright specifically noted that the substantial majority of persons who had conducted germ attacks in recent history were not terrorists but were rather scientists who had gained access to the pathogens as part of their work.

Ebright’s concern would be wholly vindicated when the perpetrator of the anthrax attacks was discovered to be a biodefense researcher at Fort Detrick who had authorized access to the anthrax samples.

Unfortunately, it would not be the last time that Ebright’s warnings in that 2004 article would prove to be prophetic. Among other objections raised by Ebright to the proliferation of laboratories doing research on dangerous pathogens, Ebright specifically warned that laboratories “could leak” and that one day a dangerous pathogen could accidentally escape from one of these labs and cause havoc.

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Fauci and the NIH, meanwhile, were not listening to Ebright or anyone else’s objections. The scientific community as a whole, however, was growing sufficiently concerned that the National Academy of Sciences established a committee to review research that was being done on so-called “dual use” pathogens that had potential civilian use but also potential bioweapon use.

The committee issued a report in 2004 that identified seven ongoing studies of concern and recommended stringent federal oversight of these projects. These experiments today would be called “gain-of-function” research but were then known as “dual use” research of concern.

Fauci claimed that the research was necessary to improve the public health community’s response to the spread of the H5N1 avian flu in Asia.

The stringent federal oversight never materialized, but Ebright and fellow skeptics finally began to gain traction both with the public and with the government when Fauci’s NIAID and the CDC finally let their hubris get the better of them and bragged to the world that they had done something that imperiled the future of mankind.

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In October 2005, scientists from the CDC and NIAID proudly announced that they had reconstituted the H1N1 influenza virus, the same flu that was estimated to have killed 1% of the world’s population in 1918. Adjusted to today’s population, the death figures might well have topped 80 million.

Worse, because H1N1 has not been circulating in decades, the current world population has absolutely no immunity to this deadly strain of flu, meaning that it might well have been much more deadly in 2005 than it was in 1918.

The scientists responsible for the research, no doubt impressed by their own cleverness, bragged that they had reconstituted the virus by, in part, examining tissue samples from flu victims who were frozen in the tundra of Alaska.

Fauci himself personally vouched for the need for the research and defended its necessity. To explain why anyone would knowingly reconstitute a deadly virus thought to have perished from the earth, Fauci claimed that the research was necessary to improve the public health community’s response to the spread of the H5N1 avian flu in Asia. According to Fauci, “The new studies could have an immediate impact by helping scientists focus on detecting changes in the evolving H5N1 virus that might make widespread transmission among humans more likely.”

But then, in an instant, the partisan impressions of Fauci instantaneously turned a complete 180 degrees. Ebright watched it happen on live television.

Ebright disagreed. As noted in a Nature article at the time, Ebright blasted Fauci and the CDC for having “constructed, and provided procedures for others to construct, a virus that represents perhaps the most effective bioweapons agent now known.”

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These days, almost all discussion about Anthony Fauci is viewed exclusively through a partisan lens. If you criticize Fauci, you must be a Republican, and probably one of those crazy right wingers to boot. If you support Fauci, you must be a Democrat. To those who have watched Fauci’s career closely, the remarkable phenomenon is how thoroughly partisan perception of Fauci flipped, suddenly and instantaneously, in the early days of the pandemic.

Prior to 2020, Fauci was the subject of frequent and strident criticism from many of the liberal institutions that have since ruled any criticism of his actions out of bounds. In fact, if anything, Fauci (who was appointed to his post during the Reagan administration) was often seen as a creature of the Bush/Cheney administration and thus was extremely fair game for criticism by both Democrats and the media.

Ebright himself fits solidly in this camp. During Tuesday’s hearing before the Senate Homeland Security and Governmental Affairs Committee, Ebright flatly stated, “I’m a registered Democrat. I voted for Biden. I had a Biden sign on my lawn.”

In fact, if anything, prior to February of 2020, Fauci was probably more well liked, to the extent that he was known at all, among Republicans than Democrats.

But then, in an instant, the partisan impressions of Fauci instantaneously turned a complete 180 degrees. Ebright watched it happen on live television.

“When he had the good fortune to share screen with Trump and facepalmed Trump when Trump was making an ignorant statement, he became a progressive icon and progressive saint,” Ebright noted.

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But back in 2005, as the public was starting to sour on the Iraq war and on the Bush administration’s conduct in the war on terror in general, Fauci and his research were getting the attention of many critics, particularly on the left. And thus the New York Times, which has largely forgotten that it is possible to criticize Fauci, ran an unflattering profile on this research titled “Why Revive a Deadly Flu Virus?”

According to Ebright, if the government had acted on the recommendations of the National Academy of Sciences report, this experiment would never have taken place. “The experiments produced a new agent that had not been present on the planet in decades, that the population had no immunity to, and that, had it accidentally been released, would likely have caused a large-scale pandemic with significant, major loss of life,” Ebright told Blaze News.

In a remarkable exchange, Fauci admitted that neither the military nor the public at large was in actual, serious danger of a biological attack and that the larger danger was the freak-out over the possibility of an attack.

“There was much congressional interest at the time in why the NIH had performed this research with no risk-benefit analysis. The response from the NIH director at the time and in particular from the NIAID director at the time, Anthony Fauci, was to double down on the idea that this research was essential and that had the NIH not funded it, that would have been the mistake,” Ebright continued.

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In a fascinating twist, during this time period when Fauci was publicly defending to members of Congress the vital need for funding for this kind of risky research, he gave an interview to Margot Fromer of Oncology Today in which he struck a very different note.

There, in a publication directed at scientists, Fauci all but stated that the research he was defending to members of Congress was not really necessary at all but was merely the function of public panic. Discussing the anthrax attacks that had provided the genesis for the whole gain-of-function program, Fauci agreed with the interviewer that the attacks were a “nonevent” and further stated that “the biological impact was trivial — more people died of influenza during that period — compared with the psychological impact.”

In a remarkable exchange, Fauci admitted that neither the military nor the public at large was in actual, serious danger of a biological attack and that the larger danger was the freak-out over the possibility of an attack. According to Fromer’s summary of Fauci’s remarks, which were not directly quoted, Fauci believed that the “civilian population is more vulnerable, but judging from the reaction to the anthrax situation, they are more in danger of scaring themselves into immobility than dying from an attack that will probably never come.”

And then in 2011, scientists attempted to publish a pair of studies that were so dangerous that the resultant outcry from the scientific community forced Congress to take note again.

Why, then, was the NIH continuing this research? Well, according to Fauci, the NIAID had been obligated by Congress to prepare for the worst, even though he personally made it clear that he felt NIAID was mostly wasting its time: “It is prudent to be prepared, but as a matter of practicality, it would be almost impossible to inoculate everyone in the highly unlikely event of a smallpox attack,” Fauci said.

In other words, to Congress, Fauci was claiming that the science was vital and in desperate need of additional funding. To scientists who likely knew better, he claimed that it was Congress’ fault that his agency was doing this research.

Soon, Fauci would be forced to choose a unified public posture, and when he did, he came down solidly on the side of continuing this risky research.

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From 2005 through 2011, the issue largely lay dormant in the public’s mind. The nation had other fish to fry. The Iraq war was going poorly, the 2008 election happened, and then the financial collapse of 2008 led to a severe recession. Life moved on, and the public largely forgot that scientists were working behind closed doors to make viruses more deadly and transmissible for reasons that were not really comprehensible to most ordinary people.

And then in 2011, scientists attempted to publish a pair of studies that were so dangerous that the resultant outcry from the scientific community forced Congress to take note again. Two different groups, with NIH funding, genetically modified a version of the extremely dangerous H5N1 avian flu, which had demonstrated a 60% fatality rate in humanized mice.

The scientists genetically modified this deadly version of the flu to make it transmissible via respiratory droplets among ferrets, which were the best simulation for human transmissibility. It was the first time this deadly bird flu was able to cause airborne infections in mammals.

When the study was submitted for peer review, the results were so obviously dangerous that one of the peer reviewers immediately sought out officials in the Obama administration in an attempt to prevent the study results from being published, raising concerns that publishing the research would provide a recipe for terrorists to create what would likely have been the most deadly bioweapon known to mankind.

The internal pushback was so significant that newly installed NIH director Francis Collins submitted the results of the research to the NIH’s biosecurity board to finally — after the research was already done — assess the risk from these experiments.

The New York Times editors thundered, “We nearly always champion unfettered scientific research and open publication of the results. In this case it looks like the research should never have been undertaken because the potential harm is so catastrophic and the potential benefits from studying the virus so speculative.”

The board unanimously recommended that only the “general conclusions” of the research should be published without “details that could enable replication of the experiments by those who would seek to do harm.”

Unbelievably, Fauci and Collins rejected even this modest imposition of oversight on their research, as well as growing anger and frustration from Congress over what was widely perceived in Congress as disregard for the safety of the public in conducting these experiments. They instead began a public relations campaign to defend their research, co-authoring an op-ed with NIAID colleague Gary Nabel entitled, “A flu virus risk worth taking,” which ran in the Washington Post on December 30, 2011.

Their op-ed, in retrospect and in light of everything that has happened since, is laughably unpersuasive. Fauci and his co-authors conceded at the outset that the mutant virus they had created “does not exist in nature” and furthermore that “we cannot predict whether it or something similar will arise naturally, nor when or where it might appear.” However, the authors asserted, there was “concern” that such a mutation “could evolve naturally.”

In other words, to guard against the admittedly remote or at least unknown possibility that such a deadly virus could come into existence on accident, these scientists had created it on purpose.

In a refreshing moment of honesty, Fauci and his co-authors included a vital paragraph that should have been a fatal blow to the program entirely, admitting, “The question is whether benefits of such research outweigh risks. The answer is not simple. A highly pathogenic bird flu virus transmissible in humans could arise in ways not predicted by laboratory studies. And it is not clear whether this laboratory virus would behave in humans as it does in ferrets.”

Nonetheless, the authors insisted that creating these mutant viruses would help them identify the “Achilles’ heel” of these viruses in the event that they did break out into the public and further proclaimed that “safeguarding against the potential accidental release or deliberate misuse of laboratory pathogens is imperative. The engineered viruses developed in the ferret experiments are maintained in high-security laboratories.”

Having thus satisfied themselves (and apparently Congress and the public) that they were doing everything they could to ensure safety, they persuaded the review board, incredibly, to publish the entirety of this dangerous study without any redactions at all and went back to work on their risky experiments.

Unfortunately for Fauci and Collins, the glaring danger inherent in their work was too large to be ignored, and the Obama administration was beginning to take notice of the growing chorus of voices in the scientific community who were raising the alarm about gain-of-function research. Even the New York Times published a blaring editorial entitled “An Engineered Doomsday” in January 2012 condemning the “frightening” ferrets experiments and summarily rejecting the weak arguments mustered by Fauci and Collins in favor of their continuation and publication.

Speaking probably for everyone who was not directly receiving research funding to conduct this work, the New York Times editors thundered, “We nearly always champion unfettered scientific research and open publication of the results. In this case it looks like the research should never have been undertaken because the potential harm is so catastrophic and the potential benefits from studying the virus so speculative.

“Unless the scientific community and health officials can provide more persuasive justifications than they have so far, the new virus, which is in the Netherlands, ought to be destroyed.”

Although the editorial did not single out Fauci or Collins by name, it likewise blasted their failure to exercise oversight over the program before its details came to light. “In the future, it is imperative that any such experiments be rigorously analyzed for potential dangers … not after the fact, as is happening in this case,” the editors wrote.

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Finally in 2013, the Department of Health and Human Services began to impose at least some half-hearted attempts at oversight over Fauci’s and the NIAID’s work. That year, HHS established an oversight committee that was supposed, in theory, to have imposed a before-the-fact review of risky research like the ferret experiments.

The report also found, astoundingly, that “select agent materials” had been transported throughout the building using, of all things, Ziploc bags.

The oversight program, such as it was, was immediately subverted by both Fauci and Collins, who demonstrated their contempt for the committee’s work by dismissively dubbing it the “Ferrets Committee.”

According to Ebright, whose contention is supported by multiple scientists who spoke anonymously to the Washington Post in 2021, Fauci and Collins subverted the committee’s oversight work by essentially defining “gain-of-function” out of existence. If you have ever found yourself wondering how Fauci has been able to repeatedly tell Rand Paul with a straight face that his agency does not fund gain-of-function research, it is because he has over a decade of experience doing it.

This might have continued forever, had a series of embarrassing accidents in 2014 not made it abundantly clear that Fauci’s and Collins’ protestations regarding “rigorous safety precautions” were wholly and completely empty.

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The first major accident to embarrass the small community that had been defending these experiments occurred in June 2014, when dozens of workers at the CDC were exposed to live anthrax in a debacle so thorough that then-CDC director Tom Frieden was forced to admit, “I will say that I’m just astonished that this could have happened here.”

A shamefaced Frieden was dragged before Congress, where he admitted that he was “angry” and “upset” and promised that he was working “around the clock” to make sure it would never happen again.

If anything, Frieden was understating the extent of embarrassment the incident brought on the CDC and in particular on its bioterrorism laboratory. A USDA inspector investigating the leak found a number of grievous and obvious violations of protocol that dated back to 2011, back when Fauci and Collins were confidently assuring the public that risky virus research was only happening in the very safest of facilities.

Instead, the USDA found, among other things, that some anthrax containers were summarily missing. Others were found stored in unlocked refrigerators in an “unregistered hallway” that was accessible to anyone in the building. The report also found, astoundingly, that “select agent materials” had been transported throughout the building using, of all things, Ziploc bags.

The USDA’s report found that the exposure had occurred because the researchers “failed to follow a scientifically derived and reviewed protocol that would have assured the anthrax was deactivated,” leading a number of scientists to work on anthrax without any protective equipment at all. The researchers could perhaps be forgiven for not following proper protocol, however, because the inspector found that the researchers had “limited knowledge” of what the protocol was even supposed to be and further stated that the label “did not have a standard operating procedure that would make sure the transfer of the material would be safe.”

It is worth remembering at this point that three short years earlier, Fauci and Collins had assured the public that research on a virus that killed 60% of humanized mice was safe because it was being conducted in laboratories they assured the public were safe.

By way of explanation for how one of the agency’s scientists could accidentally have mailed a package that might have released one of the deadliest viruses known to man into the general public and then failed to report it for over six weeks, the CDC’s own report condemned many of its own employees for “a lack of sound professional judgment.”

A shamefaced Frieden was dragged before Congress, where he admitted that he was “angry” and “upset” and promised that he was working “around the clock” to make sure it would never happen again.

Almost immediately, it happened again.

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In July 2014 it was revealed that a worker for the CDC had “rushed through” safety procedures in order to get to a meeting in a timely fashion and had inadvertently sent samples of a highly deadly strain of avian flu to the U.S. Department of Agriculture.

USDA researchers only realized something was wrong when the strain, which was supposed to be mild and non-lethal, promptly killed an entire flock of chickens. The USDA researchers sequenced the virus and discovered to their very great surprise that it was not the mild H9N2 strain of avian flu, as it was labeled, but instead was the deadly H5N1 strain.

The time was finally ripe for the Obama administration to attempt to rein in Fauci and Collins

Worse, subsequent investigation revealed that the incident had happened in March, had been reported to the CDC in May, but had not been reported to the public or to anyone else until July.

Ebright and others were incensed. In a quote to Reuters at the time, Ebright said, “The matter needs to be referred for civil and/or criminal investigation.”

His anger, if anything, was understated. By way of explanation for how one of the agency’s scientists could accidentally have mailed a package that might have released one of the deadliest viruses known to man into the general public and then failed to report it for over six weeks, the CDC’s own report condemned many of its own employees for “a lack of sound professional judgment.”

As noted by Reuters at the time, the CDC’s own report further found that “there was no approved procedure for what the scientist was doing, colleagues who might have noticed a breach were frantically rushing to finish experiments ahead of a February scientific meeting, and the lab director had a ‘heavy work load’.”

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Not to be outdone, Fauci and Collins’ NIH joined the party in July 2014, when a worker who was cleaning out an unsecured storage room in a joint FDA/NIH facility discovered six vials of smallpox, as well as several other vials filled with dangerous and exotic pathogens.

Workers in the facility were not even notified of the discovery of these pathogens that had apparently been lying about for decades until reports surfaced in the media. As noted by the Washington Post at the time, “One scientist, who works in the building and spoke on the condition of anonymity for fear of retaliation, said he learned about it Tuesday when his supervisor read a media report.”

Unbelievably, rather than promptly destroying the vials, the FDA and NIH turned the vials over to the CDC, which, according to Nature, “confirmed that powder contained in the vials contained variola (smallpox) virus DNA. They are now attempting to grow the virus in cell culture under the highest level of containment to determine whether it is still viable, and expect results in two weeks.” (Emphasis added). The samples, which were indeed viable, were later allegedly destroyed in front of inspectors from the World Health Organization.

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The time was finally ripe for the Obama administration to attempt to rein in Fauci and Collins. Faced with a string of public embarrassments that demonstrated in the most graphic way that the supposedly safe laboratories that conducted risky virus research were anything but, a working group was formed featuring Ebright and other scientists, who prevailed upon Obama administration officials to institute a moratorium, or “pause,” on funding for gain-of-function research.

I asked Ebright how he was finally able to convince policymakers that Fauci’s program needed to be curtailed.

“Something you need to keep in mind is that there was a change in administration, from the Bush-Cheney administration to the Obama administration. Which meant that the policies we were talking about were not Obama’s policies, and that made them politically addressable. It was possible to interface with the Obama administration and make the case that this research was not providing public health benefit and was actually degrading rather than enhancing national security,” Ebright told Blaze News.

Given this reality, and given the cavalcade of embarrassments befalling the biodefense sector, it was possible in that time period to “gain the Obama administration’s attention through their Office of Science and Technology Policy.” Finally, Ebright and his colleagues were able to get a “pause” on the research put in place and thus end this risky research, or at least temporarily stop it.

Or so everyone thought.

The reality, of course, was that neither Fauci nor Collins had any intention of letting bureaucrats stand in the way of their work, as they would soon demonstrate to the world.

Read More
COVID-19

Prominent scientists demand retractions from journals that published ‘unsound’ articles downplaying possible COVID-19 lab origins

Former National Institute of Allergies and Infectious Diseases director Anthony Fauci, EcoHealth Alliance boss Peter Daszak, and
elements of their inner circle were far from the only people in the Western medical establishment who actively downplayed the possibility that COVID-19 leaked from a lab where the likely patients zero executed dangerous experiments on coronaviruses with American taxpayer dollars.

Early in the pandemic, multiple scientific publications ran articles decrying “conspiracy theories” that suggested the virus may have originated in the Wuhan Institute of Virology. Various authors argued, instead, that it was more likely that the virus made a cross-species leap into humans, possibly at a Chinese wet market.

Now that it’s abundantly clear that the lab origin theory was all along the
most likely explanation, molecular biologist Dr. Richard H. Ebright of Rutgers University and dozens of other scientists are seeking accountability for perceived efforts to cure the origins narrative. They have sent open letters to the editors of the journals Science, Emerging Microbes & Infections, and Nature Medicine, requesting the retraction of “scientifically unsound papers” concerning the origins of the virus.

“Scientists have a responsibility to science and the public to point out scientific misconduct, particularly scientific fraud, when they discover it,” Dr. Ebright told Blaze News. “This is especially true for scientific misconduct on matters of high public importance, like the origin of COVID-19.”

Emerging Microbes & Infections

The first of the four papers of interest was published online in Emerging Microbes & Infections on Feb. 26, 2020, and authored by
Shan-Lu Liu and Linda Saif of Ohio State University; Susan Weiss of the University of Pennsylvania; and Lishan Su of the University of Maryland.

The paper, entitled, “No credible evidence supporting claims of the laboratory engineering of SARS-CoV-2,” stated, “There are speculations, rumours and conspiracy theories that SARS-CoV-2 is of laboratory origin. Some people have alleged that the human SARS-CoV-2 was leaked directly from a laboratory in Wuhan where a bat CoV (RaTG13) was recently reported, which shared ∼96% homology with the SARS-CoV-2.”

After downplaying a number of possible lab-made culprits, including a
chimeric coronavirus that could replicate in human airway cells and possibly transmit to humans, the authors concluded, “There is currently no credible evidence to support the claim that SARS-CoV-2 originated from a laboratory-engineered CoV.”

The
June 14 open letter to the editors of the journal stated, “The authors’ and editor’s private email communications, obtained through an Ohio Public Records Act request, provide compelling evidence that there is clear basis to infer the paper may be the product of scientific misconduct, up to and including fraud.”

When Weiss, for instance, expressed uncertainty about how the
furin cleavage site could possibly end up in the virus naturally, her colleague Liu “completely agree[d]” but signaled a greater eagerness to dispel the notion that the “furin site may be engineered.”

Despite publicly suggesting there was no credible evidence of a lab origin, Weiss noted days before the publication of her paper:

Henry and I have been speculating- how can that site have appeared at S1/S2 border- I hate to think it was engineered- among the MHV strains, the cleavage site does not increaser (sic) pathogenicity while it does effect entry route (surface vs endosome). so for me the only significance of this furin site is as a marker for where the virus came from- frightening to think it may have been engineered.

Concealed doubts and persuasive counterpoints were not the only things said to have compromised the integrity of the paper.

University of North Carolina virus expert
Ralph Baric has long toyed with coronaviruses. Years ahead of the pandemic, he expressed an interest in continuing to experiment with a chimeric virus that could infect human lung cells. He even shared transgenic mice with the Wuhan lab where Chinese virologist Zhengli Shi was executing radical experiments.

In violation of publisher Taylor and Francis’ authorship policies, “Ralph Baric and Shi Zhengli, despite clear conflicts of interest, made substantial contributions to the manuscript but were not credited as authors or acknowledged,” said the letter.

Besides secretly involving people with potential conflicts, Su, Liu and the journal’s editor-in-chief Shan Lu reportedly also had “privileged information about a SARS-CoV-2 infection in a Beijing lab in 2020,” but decided to keep this under wraps.

Su wrote to Lieu on Feb. 14, 2020: “Your former colleague was infected with sars2 in the lab?”

“Yes,” responded Liu. “He was infected in the lab!”

“I actually am very concerned for the possibility of SARS-2 infection by lab people. It is much more contagious than SARS-1. Now every lab is interested in get a vial of virus to do drug discovery. This can potentially [be] a big issue. I don’t think most people have a clue,” wrote Shan Lu.

Despite weighing in heavily on the paper, Lu elected not to be included in the coauthorship, stating in a Feb. 12, 2020, message, “I definitely will not be an author as you guys did everything. It can also keep things somewhat independent as the editor.”

Extra to collapsing the distance between author and editor, Lu subsequently admitted he accepted the paper with “basically no review.”

“Taken together, the authors’ and editor’s private communications indicate the paper is a product of scientific misconduct, up to and including fraud, by the authors and by the Editor-in-Chief of
Emerging Microbes & Infections, Shan Lu,” said the open letter. “Now that these documents have come to light, we urge Emerging Microbes & Infections to issue an Expression of Editorial Concern for this paper and to initiate a retraction process.”

Taylor and Francis, the publisher of the journal, said in a statement to Blaze News, “We can confirm that the Editor of the journal forwarded the open letter to Taylor & Francis on 14th June and that our Publishing Ethics & Integrity team are investigating the concerns raised, in accordance with the Committee on Publication Ethics guidelines and our Editorial Policies.”

Nature Medicine

The journal Nature Medicine published the controversial paper “The Proximal Origin of SARS-CoV-2” on March 17, 2020, which Fauci used on multiple occasions to suggest to the American public that COVID-19 was not a lab leak but rather an animal virus that jumped to a human.

Blaze News
previously reported that despite privately discussing the prospect that the natural-origins theory was rubbish, the paper’s four official authors — Kristian Andersen, W. Ian Lipkin, Edward Holmes, and Robert Garry — concluded, “We do not believe that any type of laboratory-based scenario is plausible.”

Andersen, a Danish evolutionary biologist and Scripps Research Institute immunology professor, was especially doubtful in private about the conclusion he gave his name to.

On Jan. 31, 2020, Andersen
wrote to Fauci, “You have to look very closely at the genome to see features that are potentially engineered. … I should mention that after discussions earlier today, Eddie [Holmes], Bob [Garry], Mike [Farzan], and myself all find the genome to be inconsistent with expectations from evolutionary theory.”

On Feb. 8, Andersen
stated, “Passage of SARS-like CoVs have been ongoing for several years, and more specifically in Wuhan under BSL-2 conditions. … The fact that Wuhan became the epicenter of the ongoing epidemic caused by nCoV is likely an unfortunate coincidence, but it raises questions that would be wrong to dismiss out of hand. Our main work over the last couple of weeks has been focused on trying to disprove any type of lab theory, but we are at a crossroad where the scientific evidence isn’t conclusive enough to say that we have high confidence in any of the three main theories considered.”

Andersen also
expressed concern about a paper penned by Ralph Baric and Zhengli Shi concerning the apparent insertion of furin cleavage sites into SARS, which he and his colleagues figured for a “how-to-manual for building the Wuhan coronavirus in a laboratory.”

Last month, Ebright and five others
wrote to Joao Montiero, the chief editor of Nature Medicine, requesting a retraction. They noted that documentation obtained through public records requests along with congressional testimony from Andersen and Garry “provide conclusive evidence of misconduct.”

The letter does not mention Fauci’s
alleged involvement in the development of the paper but instead World Health Organization scientist Jeremy Farrar’s unacknowledged role in the “paper’s development, including its prompting, organizing, editing, and approval.”

‘It is imperative that this misleading and damaging product of scientific misconduct be removed from the scientific literature.’

“This omission of a significant role played by the head of a funding agency, allegedly to maintain his ‘independence,’ represents a serious breach of publishing ethics that completely undermines the credibility of the journal and calls into question the motivation behind the paper,” said the letter. “The classification of the paper as an ‘opinion’ rather than a ‘research article’ further exacerbates the issue, as the authors’ intentional withholding of Farrar’s involvement damages public trust in the editorial process.”

Ebright and scores of other scientists
pressed Nature Medicine last year for a retraction as well, noting in an open letter dated July 26, 2023, “It is imperative that this misleading and damaging product of scientific misconduct be removed from the scientific literature. We, as STEM and STEM-policy professionals, call upon Nature Medicine to publish an expression of editorial concern for the paper and to begin a process of withdrawal or retraction of the paper.”

Blaze News reached out to Montiero for comment, but he did not respond by deadline.

Science

Ebright, Stanford University epidemiologist
Dr. Jay Bhattacharya, and dozens of other scientists signed another open letter on June 14 to the editors of the journal Science with regards to two papers: “The Huanan Seafood Wholesale Market in Wuhan was the early epicenter of the COVID-19 pandemic,” and “The molecular epidemiology of multiple zoonotic origins of SARS-CoV-2,” both of which named Jonathan Pekar of the University of California, San Diego, as an author along with Andersen, Holmes, Garry, evolutionary biologist Andrew Rambaut, and Michael Worobey of the University of Arizona.

Blurbs leading into the papers, which were both largely funded by Fauci’s NIAID — whose parent agency
supported and financed research at the Wuhan lab — and published on July 26, 2022, stated, “The precise events surrounding virus spillover will always be clouded, but all of the circumstantial evidence so far points to more than one zoonotic event occurring in Huanan market in Wuhan, China, likely during November–December 2019.”

According to the scientists seeking retractions, the analyses and the premises of “Worobey et al. 2022 and Pekar et al. 2022 are unsound,” and the papers may be “products of scientific misconduct, up to and including scientific fraud.”

“Phylogenomic evidence, epidemiological evidence, and documentary evidence all indicate that SARS-CoV-2 entered humans in July-November 2019,” says the letter. “Arguments based on data for the Huanan Seafood Market on or after mid- to late December 2019 — as in Worobey et al. 2022 and Pekar et al. 2022 — cannot, even in principle, shed light on spillover into humans that occurred one to five months earlier, in July-November, 2019.”

The open letter noted that Andersen, Garry, Holmes, and others knew full well that the “premises and conclusions of their paper were invalid at the time the paper was drafted.”

A spokesman for American Association for the Advancement of Science, the publisher of the Science family of journals, confirmed to Blaze News that it had received the letter.

“We follow COPE (Committee on Publication Ethics) processes to address any concerns raised on published papers and are doing so here,” said the spokesman.

The AAAS spokesman noted in a subsequent email, “We will follow up when we make a final decision.”

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Kansas sues Pfizer for claiming its vaccine was ‘safe and effective’

Kansas Attorney General Kris Kobach (R) announced Monday that the Sunflower State is suing Pfizer for “misleading claims it made related to the COVID vaccine.”

Kobach
noted at a press conference in Topeka that “Pfizer made multiple misleading statements to deceive the public about its vaccine at a time when Americans need the truth.”

“Pfizer misled the public that it had a ‘safe and effective’ COVID-19 vaccine,” claims the
lawsuit, filed in the District Court of Thomas County, Kansas. “Pfizer said its COVID-19 vaccine was safe even though it knew is COVID-19 vaccine was connected to serious adverse events, including myocarditis and pericarditis, failed pregnancies and deaths. Pfizer concealed this critical safety information from the public.”

‘Pfizer must be held accountable for falsely representing the benefits of its COVID-19 vaccine while concealing and suppressing the truth.’

The complaint further alleges the pharma giant:

  • glossed over the waning efficacy of the Pfizer-BioNTech COVID-19 Vaccine as well as its ineffectiveness against variants and the absence of evidence it curbed transmission;
  • “used FOIA denial and delay to conceal critical data relating to the safety and effectiveness of its COVID-19 vaccine”;
  • “used an extended study timeline to conceal critical data relating to the safety and effectiveness of its COVID-19 vaccine”;
  • used confidentiality agreements to hide the possible dangers and ineffectiveness of the jab;
  • covered its tracks by destroying the vaccine control group; and
  • engaged in a propaganda campaign wherein it omitted critical data about its vaccine, vilified critics, and mischaracterized its profitable product.

While reportedly making roughly $75 billion from its COVID-19 vaccine sales inside a two-year window — selling
$57 billion of COVID products in 2022 alone — the lawsuit claims the company “worked to censor speech on social media that questioned Pfizer’s claims about its COVID-19 vaccine.”

Former New York Times reporter Alex Berenson, for instance,
claimed that Scott Gottlieb, a former U.S. Food and Drug Administration commissioner who became a senior board member of Pfizer, leaned on Twitter in 2021 in an apparent effort to censor criticism of the vaccine. It appears such pressure may have been successful on numerous occasions.

The complaint accuses Pfizer of multiple violations of the Kansas Consumer Protection Act and civil conspiracy.

“Pfizer must be held accountable for falsely representing the benefits of its COVID-19 vaccine while concealing and suppressing the truth about its vaccine’s safety risks, waning effectiveness, and inability to prevent transmission,” added the lawsuit.

Pfizer, which has produced
over 366 million doses of its COVID-19 vaccine, told The Hill the case has “no merit.”

“We are proud to have developed the COVID-19 vaccine in record time in the midst of a global pandemic and saved countless lives. The representations made by Pfizer about its COVID-19 vaccine have been accurate and science-based,” said the company.

The lawsuit comes several months after Texas Attorney General Ken Paxton
filed a similar lawsuit, claiming, “Pfizer intentionally misrepresented the efficacy of its COVID-19 vaccine and censored persons who threatened to disseminate the truth in order to facilitate fast adoption of the product and expand its commercial opportunity.”

The Texas lawsuit
moved to a federal court in January.

Kansas’ legal action also follows numerous medical admissions and scientific studies confirming the vaccines were not as advertised, as well as a
class-action lawsuit against another COVID-19 vaccine manufacturer in Britain over injuries and deaths.

Blaze News
previously reported that a peer-reviewed multinational study examining data from nearly 100 million people not only affirmed the well-documented link between the COVID-19 vaccines and increased risk of heart conditions but has also highlighted troubling links between the AstraZeneca, Moderna, and Pfizer vaccines and medical conditions such as Guillain-Barré syndrome, brain and spinal cord inflammation, Bell’s palsy, and convulsions.

The study,
published in the esteemed journal Vaccine, also noted there were “significantly higher risks of myocarditis following the first, second and third doses” of Pfizer’s BNT162b2 vaccine.

Another
peer-reviewed study published Jan. 24 in the Springer Nature Group journal Cureus suggested the COVID-19 vaccines were a rushed product with an “unacceptable harm-to-reward ratio.”

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‘NIAID cannot be trusted’: Fauci’s agency planned to make monkeypox more deadly, says congressional report

The National Institute of Allergy and Infectious Diseases under Anthony Fauci funded deadly gain-of-function research on coronaviruses at the likely epicenter of the pandemic. Although millions of Americans died from COVID-19, the NIAID apparently did not learn its lesson.

According to congressional investigators, the NIAID received approval to execute radical gain-of-function experiments on MPXV, the virus that causes monkeypox.

Monkeypox is endemic in various African regions but made a global play in April 2022. The New England Journal of Medicine indicated on the basis of diagnoses in 16 countries that 98% of the persons infected with the virus were homosexual.

Those infected with monkeypox often experience a painful rash that can look like pimples or blisters, respiratory problems, exhaustion, fever, swollen lymph nodes, and chills. Like COVID-19, monkeypox can be spread via respiratory droplets, through “direct contact with a rash or sores of someone who has the virus,” and through “contact with clothing, bedding, and other items used by a person” with the virus.

While it’s unclear what nightmarish symptoms a lab-engineered version of monkeypox could produce, it’s clear that some of Fauci’s people were eager to find out.

Over the past two years, the House Committee on Energy and Commerce — which has jurisdiction over public health agencies — has been looking into a particular research project that was “planned and/or conducted” at the NIAID prior to Fauci’s retirement.

Committee members were alerted to the experiment by a Sept. 15, 2022, interview in Science magazine, in which Dr. Bernard Moss, a NIAID pox virologist, revealed that his team was working on endowing a West African variant of monkeypox responsible for the global outbreak at the time, “clade 2,” with genes from a far more deadly variant, “clade 1.”

Whereas clade 2 has roughly a 1% mortality rate, clade 2 reportedly has a mortality rate ranging from 10%-15%.

Congressional investigators noted that Moss’ admission troubled some of his peers.

Epidemiologist Thomas Inglesby, director of the Center for Health Security at the Johns Hopkins University Bloomberg School of Public Health, told the magazine the following month that if a more powerful version of the outbreak strain ever escaped the NIAID lab, it could trigger an “epidemic with substantially more lethality.”

The committee noted in an interim staff report Tuesday, “If the experiment transferred genes from clade IIb MPXV — which caused the 2022-2023 mpox epidemic — into clade I virus, the resulting chimeric virus could have a reproductive number (R₀) of 1.10 to 2.40 coupled with a case fatality rate of 10 – 15 percent in the unvaccinated.”

According to the interim report, the Department of Health and Human Services, the National Institutes of Health, and the NIAID “repeatedly obstructed and misled” the committee about the experiment referenced by Moss in Science.

‘NIAID cannot be trusted to oversee its own research of pathogens responsibly.’

Whereas HHS and the NIH denied that that the experiment(s) had been proposed, planned, approved, or conducted, the committee noted that internal NIH documents “show this experiment was formally proposed and received approval before the NIH’s Institutional Biosafety Committee (IBC) on June 30, 2015.”

HHS Assistant Secretary for Legislative Affairs Melanie Egorin confirmed in a March 19 letter to the committee that the experiment was greenlit.

The committee has been unable to confirm whether or not the dangerous experiment actually took place but indicated there was a window of time between June 2015 and May 2023 when researchers could have done so.

In the first three years, there were reportedly no requirements imposed on the experiment. In 2018, scientists were asked only to notify the NIH’s IBC when getting ready to make clade 2 more potent.

Science indicated that at the very least, part of the experiment was conducted. Researchers moved genes from clade 2 to clade 1.

“The deliberate, prolonged effort to deceive the Committee is unacceptable and potentially criminal,” said the interim report. “HHS, the NIH, and NIAID continue to insist the GOFROC experiment transferring material from clade I into clade II was never conducted, despite being approved for a period of over eight years. However, HHS has repeatedly refuse to produce any documents to corroborate this claim.”

The report suggested that the refusal to cough up evidence might suggest “that the information not produced was unfavorable” and that the HHS is effectively lying.

Despite painting HHS as obstructionist, the report emphasized that the “NIAID is the agency that bears the most responsibility for misleading the Committee.”

The primary conclusion drawn at this point in the investigation is that NIAID cannot be trusted to oversee its own research of pathogens responsibly. It cannot be trusted to determine whether an experiment on a potential pandemic pathogen or enhanced potential pandemic pathogen poses unacceptable biosafety risk or a serious public health threat. Lastly, NIAID cannot be trusted to honestly communicate with Congress and the public about controversial GOFROC experiments.

Committee Chair Cathy McMorris Rodgers (R-Wash.) said of the report, “In order to start rebuilding trust in our government health agency guidance, agencies like the NIH must be honest and transparent with Congress and the American people.”

“This report demonstrates a disturbing lack of judgment and accountability from HHS, the NIH, and particularly, NIAID. It is unacceptable and demonstrates the clear need for reform,” added Rodgers.

Justin Goodman, senior vice president of the White Coat Waste Project — a watchdog that helped expose EcoHealth Alliance’s and Fauci’s ties to the gain-of-function experiments at the Wuhan Institute of Virology — told Blaze News, “These treacherous monkeypox gain-of-function experiments are the latest example of Fauci’s rampant waste, fraud, and abuse and disregard for taxpayers and lawmakers.”

“Even though Fauci is gone from government, his atrocious animal testing legacy is alive and well, and we’re working with Republicans and Democrats to cut NIH’s reckless spending,” continued Goodman. “The solution is simple: Stop the money. Stop the madness.”

An HHS spokesman said in a statement, “The committee is looking for an issue where there isn’t one. HHS and its divisions, including NIH, follow strict biosafety measures as our scientists work to better understand and protect the public from infectious diseases — like mpox.”

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Republicans remain silent as Moderna and the FDA target our seniors

Just as we begin to fully assess the dangers of the COVID mRNA shots, the FDA has approved Moderna’s next mRNA shot for the respiratory syncytial virus without any public hearing. Regulators are also in discussions with the mRNA manufacturer to concoct a shot for the bird flu.

How is it that they can so brazenly elevate their next poison jab even as we’re still discovering the extent of the calamity from their first invention? That’s easy: a feckless Republican Party.

It should be obvious by now that mRNA should be banned altogether, yet here we are green-lighting an entirely new shot made from this poison.

The Centers for Disease Control and the FDA approved GSK and Pfizer’s RSV shots last year, including Pfizer’s shot for pregnant women, despite strong signals for pre-term births and neonatal deaths. At least the CDC and FDA held advisory meetings of their “expert” panels before doing so. But Moderna’s mRNA version of the RSV shot for seniors was quietly approved last week without any public hearing. And guess what? You can trust them that the shot is 83.7% effective with “no risks”!

Even if we took the claim of 83.7% efficacy at face value, how sick do seniors even get from a virus that mainly affects infants? Moreover, if we had a public hearing, we’d be able to scrutinize the data from Moderna’s phase-three clinical trial, which seemed to detect 200 adverse events and 10 serious events per mild case of RSV supposedly avoided. Moderna’s numbers show that for each RSV infection prevented, the shot caused 200 side effects, including 10 severe side effects. Among the total participants in the trial, those receiving the vaccine incurred an extra 10,156 side effects, including 455 rated Grade 3 or higher, in return for contracting 46 fewer cases of RSV.

The efficacy is likely a mirage. Dr. Dan Stock, a functional medicine expert and family doctor from Indiana, explained to me how the RSV vaccine of the 1960s wound up becoming “negative effective” and made kids sicker, but it didn’t occur until the second season.

“The Moderna RSV vaccine will likely have even more trouble avoiding efficacy loss than all the RSV vaccines that have come before it, and its own data show that’s true,” Stock said.

“The first indication is simply what happens whenever you make a vaccine for a rapidly changing RNA virus that only causes disease in those with compromised immune systems,” he explained. “The vaccine induces a memorized response, and rapidly a slight mutation develops that learns to evade that response, which having learned to fight one way, responds the old way to new variants.”

“Eventually, one variant, usually in year two, learns to benefit from the defective immune system’s learned response, and becomes worse than being exposed to the new variant in an unvaccinated state,” Stock said.

That’s called antibody dependent enhancement, Stock explained, and it occurs by multiple mechanisms. “The other two RSV vaccines on the market are already showing dropping efficacy approximately 18 months into their studies,” he said.

This is what we saw with the COVID shots, so, naturally, the RSV shots will be at least as bad, given their history. It should be obvious by now that mRNA vaccines should be banned altogether, yet here we are green-lighting an entirely new shot made from this poison.

We already have evidence from a Swedish study that the mRNA likely converts into DNA because it was found to integrate into the DNA of liver cells within six hours. How can Republicans not only decline to defund the COVID mRNA shots but completely ignore the FDA’s foray into RSV for seniors who have already been blasted with endless COVID shots?

At Monday’s hearing of the House Oversight Subcommittee on coronavirus with Anthony Fauci, not one Republican raised the issue of the millions of vaccine-related deaths and injuries. Subcommittee Chairman Brad Wenstrup (R-Ohio) even went so far as to thank Fauci for vaccines that “saved millions of lives.”

It is widely believed that the shots protect against critical illness, but there is no evidence of this during the period when COVID was still deadly.

Every week, new studies appear showing catastrophic damage from the first batch of mRNA shots.

A new British Medical Journal study of excess deaths in 47 countries, mainly in Europe and the United States, found that excess deaths spiked in 2021 when the vaccines were released — over and above the excess deaths in 2020, which was the first year of the pandemic without any vaccines.

Perhaps Wenstrup should read up on the academic literature from the most prestigious medical institutions in his home state of Ohio. A Cleveland Clinic study found that after monitoring 47,500 of its employees during the first part of 2024, there was a 46% greater risk of the vaccinated contracting COVID than the unvaccinated. Those with three doses were 95% more likely to get infected than people who declined the shot. People with more than three doses were a whopping 151% more likely to get infected.

In case you think “the more you inject, the more you infect” dynamic during the pandemic was limited to mild cases, a new Ohio State University study found much higher mortality from COVID among those supposedly vaccinated against it. The study, published in Frontiers in Immunology, tracked mortality outcomes among 23 vaccinated and 89 unvaccinated subjects who presented to OSU with serious cases of COVID. Shockingly (or not), there was a 70% mortality rate among those vaccinated compared with a 37% in the never-vaxxed group.

Although the sample size is small, the massive divergence in outcomes gives the results a high level of marginal significance, even when accounting for the health status of those in both groups. It is widely believed that the shots protect against critical illness, but there is no evidence of this during the period when COVID was still deadly.

As a possible culprit for the increased mortality risk among the vaccinated, the study’s authors observed an increased surge IgG4 antibodies among the vaccinated cohort. Several studies have found that the vaccines cause an unnatural surge in these tolerated, rather than neutralizing, antibodies, which could be responsible for the Trojan horse effect of allowing the virus deeper access into the body behind the defenses of the immune system.

Meantime, a new preprint from Oxford researchers examined 1 million children to compare the rates of myocarditis and pericarditis among those vaccinated as compared to those unvaccinated but recovered from COVID. They found no cases among those unvaccinated, even though the spike protein of the virus itself could harm cardiovascular health. This means that when we see all the data showing excess heart attacks beginning in 2021, it’s likely that almost all of them emanated from the vaccine, not the virus.

How many more studies, data points, and government documents do we need to uncover for it to be fashionable among Republicans to fight these mRNA shots?

What is so shocking is that the South Carolina legislature, at the behest of Republican Governor Henry McMaster, is convening a special session to take up the health czar bill to consolidate the state’s health bureaucracy without addressing a single odious policy of those agency heads. To this day, the South Carolina Department of Health and Environmental Control recommends COVID shots for infants. Where is the urgency to convene special sessions in red states to take these shots off the market?

In that sense, who could blame Moderna and the FDA for proceeding to the next mRNA poison shot when the so-called opposition party refuses to recognize the human tragedy of their first experiment?

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It’s time to let go of Anthony Fauci

I lost my best friend almost exactly four years ago, in the waning days of May 2020. Although I am sure he is listed somewhere as a casualty of the pandemic, the actual story of his death is slightly more complicated.

He suffered all his life from severe Crohn’s disease. He had a bad flare-up at the worst possible time: February 2020, just as pandemic panic was nearing its peak. After a failed surgery that was intended to remove a problematic part of his small intestine, doctors determined that he needed an entirely new small intestine and ordered a small intestine transplant.

Here in 2024, three years after the fact, Fauci has ceased to be a person. He is now a totem.

The hospital that was treating him was not capable of performing this operation, so plans were made to transfer him to another facility. Unfortunately, almost immediately thereafter, my friend caught COVID while in the hospital, and his transfer to another hospital that might have helped him was forever delayed.

Because his condition was so poor at the outset, he had to go on a ventilator for respiratory support for weeks to address the COVID. By the time he recovered from the effects of COVID, his intestines had developed a fistula, and complications of the fistula eventually took his life.

Until the end, he remained conscious and was able to communicate, at least via text message. He was a very social person, and his one complaint about his time in the hospital was that he was not allowed to see anyone.

Day after day he expressed his wish to me to see an actual friendly face who was not a nurse. I wanted to go sit with him. I asked hospital staff if I would be allowed if I signed a waiver or whatever they required so that he would not have to spend what we both knew would likely be the last few weeks of his life alone.

I was refused.

The COVID-19 pandemic, combined with the hysterical protocols instituted in response to it, killed my best friend — and worse, made him die alone.

Where does the anger lead?

George Floyd died just a couple of days before my friend did. I barely noticed at the time; I was so consumed by anger and grief over what was happening. My friend’s desire, expressed frequently to anyone who knew him well, was for his ashes to be spread in California, where he always said he was happiest while in college.

As it became clear that COVID-19 protocols would also deny him this last dignity, events in the world at large began to sink in. I watched in amazement and slowly mounting anger as city after city was wracked by throngs of shouting people marching in the streets, with nary a mask in sight and no one telling them to get back inside and isolate.

It was impossible to avoid the conclusion that people were dying alone, deprived of even funerals, for absolutely no scientific reason at all. And it was becoming equally clear around the same time that the official story about where the pandemic came from was likely bogus — or if not bogus, certainly not as scientifically settled as leading lights, including Dr. Anthony Fauci, were making it out to be.

I don’t say all this to ask for pity. My story is merely one of millions like it in America and tens of millions more throughout the world.

My only point is this: I’ve had ample time and opportunity to stew in anger toward the medical establishment in this country and toward Fauci in particular.

And as I watched the debacle unfold before the House Coronavirus Select Subcommittee on Monday, I was seized by only one thought: This is pointless, and it needs to stop.

Getting to the truth

I have my own theories and beliefs about Fauci and his motivations, particularly when it comes to his actions to obfuscate the truth about the origins of the pandemic that has now killed millions. Suffice to say, those theories and beliefs are not flattering. I would like nothing more than for some way to be found to force Fauci to tell the whole, unvarnished truth about what he knew in those early days of the pandemic.

It should be evident by now that no such truth serum exists. And even if it did exist, it would likely only confirm that Fauci was covering his own backside in the possible event that it was discovered that the Wuhan Institute of Virology was responsible for the pandemic. There’s no real way, after all, that Fauci himself could have actually known where the pandemic started.

The reality is this: We had one shot to get an honest look at the evidence, and the World Health Organization responded by sending in a team that featured all the people who stood to gain the most from concluding that the pandemic had a natural origin, including of all people the now-disgraced Dr. Peter Daszak. The chances that the WHO task group was going to reach the truth were zero from the start, just based on how the group was conducted.

But we should not deceive ourselves. Even if honest brokers had been sent to China to investigate, the Chinese government was never going to allow a real investigation, as even the compromised WHO investigatory team was forced to admit. And the Chinese government is certainly not now going to let any actual investigation occur, short of a military invasion, which no country in the world (including the United States) will undertake.

And so we must content ourselves with the evidence we have, which is not enough to reach an ironclad conclusion. It certainly looks suspicious, and I know what I believe is the most likely source of the pandemic outbreak, but I am forced to concede that if I were called upon to prove it in a criminal court, I could not do it.

Forever and always, it seems that the best we will be able to do for ourselves when it comes to asking where the pandemic came from is “probably.” I want nothing more than to know for sure. I have spent more hours looking at this question than perhaps any other question I’ve put my mind to. And “probably” is as far as I can get.

Inept and embarrassing questions

As I watched Monday’s hearings, I was not surprised to learn that I still have plenty of capacity for anger over what has been done to us by the pandemic and also by our government in response to the pandemic.

The content of the hearings, though, made clear that continued anger at Fauci is distracting us from the bigger issue at hand. It’s also pointless. Everyone already knows what they think about Fauci, and those thoughts are likely impenetrable. The only thing more exasperating than the ineptitude of most of Fauci’s Republican interlocutors was the parade of Democrats doing their best impersonation of group of besotted Taylor Swift fans while clearly striving to be Fauci’s biggest white knight for the television cameras.

That this is personal to Fauci himself could not be clearer. Two weeks ago, one of Fauci’s top advisers, David Morens, testified before this same subcommittee about email exchanges in which he clearly advised key players in the potential lab-leak cover-up to hide emails from the public. Morens was unceremoniously blistered by both Republican and Democrat alike, with no less illustrious a right-winger than former NAACP President Kweisi Mfume (D-Md.) intoning at one point, “I think you are going to be haunted by your testimony here today. And it’s all on the record.”

Yet, sitting in the same chair, Fauci was summarily excused from responsibility for Morens by the same Democrats based on the facially laughable excuse that he didn’t really get any advice from his senior adviser.

The next virus that escapes from a lab might well be ten or a hundred times more deadly than COVID-19 was.

The number of people who have any sort of nuanced, fact-based view of Fauci and his actions is so small that it might as well be nonexistent. Here in 2024, three years after the fact, Fauci has ceased to be a person. He is now a totem, and which side of the partisan divide you sit on depends on whether you think the deity he represents is evil or benign.

This is a role that Fauci is happy to play, because it obscures the question that he doesn’t want you to ask, which is: Why would Fauci be desperate to cover up a leak from a Chinese lab in the first place? Why would it be important to him that people accept the natural origin theory?

The conventional answer is that he sought to avoid personal and professional embarrassment for having potentially funded the WIV with grant money that his agency approved. That may well play a part, but I don’t think it has played the most significant part in Fauci’s calculus at all.

I think Fauci, who is 83 and was close to retirement even at the beginning of the pandemic, is and always has been much less interested in protecting his own image than he is in protecting the kind of research that may well have caused the lab leak — research that he devoutly believes in.

Research that, without exaggeration, threatens the future of humankind.

I am talking, of course, about gain-of-function research, a phrase that as yet has only pierced the consciousness of the very most online and politically committed individuals.

That is something that needs to change, and it needs to become a nonpartisan issue, because the next virus that escapes from a lab might well be ten or a hundred times more deadly than COVID-19 was.

Dangerous experiments

Fauci, of course, has been a champion of gain-of-function research since long before COVID-19 ever existed. And he has needed to champion it, because before the COVID-19 pandemic, there was bipartisan, ongoing, and constant concern about whether it should be allowed at all.

The controversy first erupted in 2011 when a team of scientists funded by the NIH intentionally created a version of the bird flu that had an astonishing 60% fatality rate and then blithely bragged about it in a paper they sought to publish.

This obviously dangerous experiment touched off a firestorm that might have been contained exclusively to the scientific community if one of the scientists involved in peer review had not flagged a concerned official in the Obama administration. Fauci responded by taking the extraordinary step of co-authoring a Washington Post op-ed defending the need for gain-of-function research.

After years of back-and-forth, the Obama administration finally announced a moratorium on gain-of-function research in 2014, and since that time, Fauci has been fighting a tireless rearguard action to revive public funding for research that makes viruses deadlier. He also, by all accounts, worked with his superior Francis Collins to ensure that researchers were able to find loopholes in the moratorium.

Finally, in 2017, Fauci prevailed upon the Trump administration to lift the moratorium. You would be forgiven for being confused at this point if you’ve followed the modern political discourse, which has suggested that only the ultra MAGAs of the world oppose gain-of-function research.

The reality is the exact opposite: The Democrats were the first to see the danger of this research, and they were right. Republicans reversed them, and they were wrong.

Most of the media is frankly not interested in knowing the particulars of the issue, but they know that Senator Rand Paul (R-Ky.) seems to be strongly against gain-of-function research, so they assume it must be great. And around and around goes the dumb discourse about the most important issue of the last century.

The real threat

I don’t think we need any more show hearings where Anthony Fauci is alternately yelled at and feted upon. Anthony Fauci is gone. He’s never coming back to government service. By all means, people should argue about his legacy, and that book is definitely not yet closed. I have no problem with heated debate over Fauci’s legacy, but the reality is that Fauci isn’t an ongoing threat.

Gain-of-function research is. And gain-of-function research continues to exist. Worse, it’s continuing to get more and more dangerous. Incredibly, the U.S. Department of Agriculture was revealed earlier this year to have begun a new study in 2021 on an even more dangerous avian flu with, incredibly, the Chinese Academy of Sciences — an institution that oversees the Wuhan Institute of Virology.

And this is exactly what Anthony Fauci wants. He truly believes in his heart that it is the right thing for humanity for these risky experiments to go forward. He might even be right. I certainly don’t begrudge him having that opinion.

But what I do begrudge him are his efforts to keep the rest of us ordinary folks out of having an informed say on what he and his colleagues are doing with our tax dollars in the name of research. I do begrudge his dishonest campaign to split hairs with Rand Paul over what his agency has been doing in clear violation of the spirit of both the Obama gain-of-function moratorium and the P3CO framework.

The best way to fight back, though, is not to haul him in front of cameras and yell at him. He seems more or less immune to that, and he certainly at this point cannot be made to say anything he has not already said. Every one of these appearances probably just serves to help some clever businessmen to sell more of those ridiculous shirts with his face on them to his liberal fans.

The best way to fight back is to turn our attention back to where it belongs: on the risky research he’s likely been hoping we’ll forget. Our survival, quite literally, might depend on it.

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COVID-19

Fauci cries while testifying before the House; feels ‘terrible’

To no one’s surprise, Dr. Anthony Fauci’s recent testimony was full of what some might call nonsense. However, it was also full of tears.

“Dr. Fauci, can you please share with us the nature of the threats you have received since the start of the COVID-19 pandemic?” he was asked.

“Yes, there have been everything from harassments by emails, texts, letters of myself, my wife, my three daughters,” Fauci responded.

“There have been credible death threats leading to the arrests of two individuals and credible death threats mean someone who clearly was on their way to kill me,” he continued, adding, “and it’s required my having protective services essentially all the time.”

“It is very troublesome to me, it is much more troublesome because they’ve involved my wife and my three daughters,” he said.

At this point, he’s asked how these moments make him “feel.”

Water begins to well up in his eyes, and his face wrinkles.

“Terrible,” he answers in a choked voice, telling the House that he gets threats “every time someone gets up and says I’m responsible for the death of people throughout the world.”

Megyn Kelly and Dave Rubin cannot believe it.

“Well, you are,” Kelly says, annoyed. “No one feels sorry for you.”

“Megyn, have you ever received a mean email or a mean text?” Rubin asks.

“You want to see my death threats? Let’s go over the past ten years,” Kelly laughs.

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COVID-19

Scientists acknowledge COVID vaccines and containment protocols may have boosted excess mortality

Dutch researchers indicated in a new peer-reviewed study that COVID-19 vaccines and governmental containment policies may have boosted excess mortality in the West.

The study, published Monday in the peer-reviewed journal
BMJ Public Health, explored excess all-cause deaths in 47 Western countries from 2020 to 2022. It indicated that during this period, there were 3,098,456 excess deaths: 87% of the countries under review suffered excess mortality in 2020; 89% in 2021; and 91% in 2022.

The researchers made clear that excess mortality “includes not only deaths from SARS-CoV-2 infection but also deaths related to the indirect effects of the health strategies to address the virus spread and infection.”

What caught the researchers’ attention was not only the persistence of high excess mortality following the pandemic but that “the highest number of excess deaths [1,256,942] was recorded” in 2021 — the year containment measures were coupled with experimental vaccination.

In 2020, when Western citizens largely only had to contend with the virus, government-limited mobility rights and shuttered schools, churches, workplaces, restaurants, and parks, there were 1,033,122 excess deaths.

In 2022, when most containment protocols had been lifted and uptake of COVID-19 vaccines was in fast decline, researchers indicated there were 808,392 excess deaths.

‘This is unprecedented and raises serious concerns.’

These massive figures reflect the difference in the number of reported deaths in a country in a given year and the expected number of deaths under normal conditions. For a baseline, the Dutch researchers used Ariel Karlinsky and Dmitry Kobak’s linear regression estimate model, which draws on “historical death data in a country from 2015 until 2019 and accounts for seasonal variation in mortality and year-to-year trends due to changing population structure or socioeconomic factors.”

“Excess mortality has remained high in the Western World for three consecutive years, despite the implementation of COVID-19 containment measures and COVID-19 vaccines,” wrote the researchers. “This is unprecedented and raises serious concerns.”

“During the pandemic, it was emphasized by politicians and the media on a daily basis that every COVID-19 death mattered and every life deserved protection through containment measures and COVID-19 vaccines,” continued the researchers. “In the aftermath of the pandemic, the same morale should apply.”

The Dutch researchers noted at the outset of their study that while experimental COVID-19 vaccines and draconian containment measures may have been effective in protecting segments of the population — particularly those with comorbidities and the elderly — they nevertheless had “detrimental effects that cause inferior outcomes as well.”

“Although COVID-19 vaccines were provided to guard civilians from suffering morbidity and mortality by the COVID-19 virus, suspected adverse events have been documented as well,” wrote the researchers.

The secondary analysis of the placebo-controlled, phase III randomized clinical trials of mRNA COVID-19 vaccines showed that the Pfizer trial had a 36% higher risk of serious adverse events in the vaccine group. The risk difference was 18.0 per 10000 vaccinated (95% CI 1.2 to 34.9), and the risk ratio was 1.36 (95% CI 1.02 to 1.83). The Moderna trial had a 6% higher risk of serious adverse events among vaccine recipients. The risk difference was 7.1 per 10,000 vaccinated (95% CI −23.2 to 37.4), and the risk ratio was 1.06 (95% CI 0.84 to 1.33).39. By definition, these serious adverse events lead to either death, are life-threatening, require inpatient (prolongation of) hospitalization, cause persistent/significant disability/incapacity, concern a congenital anomaly/birth defect or include a medically important event according to medical judgement.

Previous comparisons of established flu vaccines to the novel mRNA vaccines — which the Dutch researchers indicated have been classed in multiple French studies as “gene therapy products requiring long-term stringent adverse events monitoring” — have revealed the latter to carry a far higher risk of serious adverse reactions.

‘Both medical professionals and citizens have reported serious injuries and deaths following vaccination.’

COVID-19 vaccines have also been linked to various ailments, including heart disease, blood clots, hemorrhages, gut issues, thromboses, myocarditis, pericarditis, and autoimmune diseases. A number of these linkages have been well-demonstrated and even admitted by pharmaceutical giants,
as in the case of AstraZeneca.

The Dutch researchers indicated that some of the risks these experimental vaccines carry were realized overtime outside of clinical trials: “Both medical professionals and citizens have reported serious injuries and deaths following vaccination to various official databases in the Western World, such as VAERS in the USA, EudraVigilance in the European Union and Yellow Card Scheme in the UK.”

The researchers framed the dangers posed by the vaccines as even more troubling given the understanding that the threat posed by the virus was overblown.

The pre-vaccination infection fatality rate for persons over 60 was reportedly 0.03% and the rate was 0.07% for those over 70. It posed virtually no threat to people ages 19 and younger, who alternatively faced an infection fatality rate of 0.0003%.

Gordon Wishart, chief medical officer at Check4Cancer,
told the Telegraph, “The authors are correct to point out that many vaccine-related serious adverse events may have been unreported, and point to the fact that the simultaneous onset of excess mortality and Covid vaccination in Germany is worthy of further investigation on its own.”

Just as the vaccines were nowhere near as “safe and effective” as promised, the supposed health safety protocols appear to have had an inverse effect.

The study acknowledged that it is challenging to differentiate between the various causes of excess mortality, particularly because national mortality registries “not only vary in quality and thoroughness but may also not accurately document the cause of death,” and there was a lack of consensus in the medical community on whether to label deaths of persons infected with COVID-19 but not caused by the disease as COVID-19 fatalities.

However, they appeared confident enough to assert that “indirect effects of containment measures have likely altered the scale and nature of disease burden for numerous causes of death since the pandemic,” citing a study that indicated there was a “substantial increase” in American deaths attributed to non-COVID causes in the first two years of the pandemic.

American heart disease deaths were apparently 6% above baseline in 2020 and 2021. Diabetes deaths were 17% over baseline in 2020 and 13% over in 2021. Alzheimers disease mortality was up 19% in 2020 and 15% in 2021. Alcohol-related deaths were 28% over baseline in 2020 and up 33% in 2021. Drug-related deaths were 33% over baseline in 2020 and up 54% in 2022.

The study noted that “lockdowns, school closures, physical distancing, travel restructions, business closures, stay-at-home orders, curfews, and quarantine measures with contract tracing” had numerous adverse indirect effects such as “economic damage, limited access to education, food insecurity, child abuse, limited access to healthcare, disrupted health programmes and mental health challenges” that increased morbidity and mortality from other causes.

The researchers concluded by recommending policymakers and government officials to “thoroughly investigate underlying causes of persistent excess mortality and evaluate their health crisis policies.”

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COVID-19

FDA approves new Moderna mRNA vaccine without bothering with independent advisers

The U.S. Food and Drug Administration has
approved Moderna’s mRNA-1345 vaccine, which allegedly protects adults aged 60 and older from respiratory syncytial virus infection-caused lower respiratory tract disease.

The agency’s
breakthrough therapy designation approval for the drug, which will be marketed as mResvia, is only the second Moderna drug the FDA has approved. More significantly, it is the first mRNA vaccine to have been approved to address a disease other than COVID-19.

‘We did not refer your application to the Vaccines and Related Biological Products Advisory Committee.’

Even though that amounts to a big step, it appears the regulator was keen to jump past additional levels of scrutiny.

The FDA
noted in its Friday approval letter, “We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your [biologics license application], including the clinical study design and trial results, did not raise concerns or controversial issues that would have benefited from an advisory committee discussion.”

The advisory committee’s job is to review and evaluate data concerning the “safety, effectiveness, and appropriate use of vaccines and related biological products,” then provide independent expert advice to the agency.

According to the pharmaceutical company, the approval was based on “positive data from the Phase 3 clinical trial ConquerRSV, a global study conducted in approximately 37,000 adults ages 60 or older in 22 countries.”

Nearly 20,000 of the trial participants were based in the United States. There are at least 11 other studies under way examining the impact of the novel drug on other demographics.

The company claimed in a Feb. 29
overview of its trial data that the vaccine “continued to be efficacious through median 8.6 months follow-up” and was shown to prevent severe RSV disease “base on analysis of shortness of breath and medically attended RSV-[lower respiratory tract disease].”

The vaccine’s efficacy is allegedly 83.7%. Reuters noted, however, that the label indicates the shot is only 79% effective at preventing at least two symptoms of RSV, such as fever and cough.

While the overview insisted that the vaccine was relatively effective and safe, it nevertheless highlighted a number of “systemic reactions” reported within seven days of vaccination, such as headache, fatigue, myalgia, arthralgia, and chills, besides customary injection site pain.

A Moderna-funded
study published in the New England Journal of Medicine similarly alleged that a single dose of the vaccine “resulted in no evident safety concerns.”

Despite similarly having been presented as a safe vaccine, Moderna’s COVID-19 vaccine was
linked in various studies, including in an FDA-funded study, to an increased risk of myocarditis and pericarditis, particularly in men ages 18-25.

Extra to heart inflammation, the Global COVID Vaccine Safety Project — a Global Vaccine Data Network initiative supported by both the CDC and the Department of Health and Human Services —
revealed in a February study in the esteemed journal Vaccine that “Bell’s palsy had an increased [observed to expected] ratio after a first dose of [Pfizer’s] BNT162b2 and [Moderna’s] mRNA-1273.”

The study also noted that “there were also increased OE ratios for febrile seizures following a first and second dose of mRNA-1273 … and for generalized seizures following first mRNA-1273 dose and fourth BNT162b2 dose.”

Blaze News previously reported that the University of Auckland, which hosts the Global Vaccine Data Network, noted that there were safety signals for “acute disseminated encephalomyelitis (inflammation and swelling in the brain and spinal cord) after viral vector and mRNA vaccines.”

Despite outstanding concerns about its only other approved vaccine, Moderna appears confident in its product and has evidently secured the FDA’s confidence as well. Its next stop is the Centers for Disease Control and Prevention, whose Advisory Committee on Immunization Practices will review the vaccine during its June 26-27 meeting.

Analysts estimate Moderna will do roughly $340 million in RSV vaccine sales this year and possibly $830.5 million in 2025, reported Reuters.

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COVID-19

Blaze News investigates: Meet the sex-obsessed, gay ‘activist physician’ in charge of vaccines, COVID at the CDC​

Since at least the COVID-related government shutdowns of 2020, Americans have been keenly aware of the Centers for Disease Control and its role in influencing public health policy, particularly regarding vaccines. However, they may not know that the man currently tasked with overseeing the CDC’s immunization services and its coronavirus division, Dr. Demetre Daskalakis, is an LGBTQ+ “activist” with a long history of pushing vaccines and drugs to facilitate promiscuous sexual behavior, especially among gay men.

Blaze News took a look into the background of Daskalakis — the
director of the National Center for Immunization and Respiratory Diseases, a subdivision of the CDC — to better understand how a sex-obsessed physician rose to such a position of prominence within a powerful federal agency and to gauge how his work there may be affected by his personal lifestyle choices.

The “media requests”
page on the NCIRD website can no longer “be found,” so Blaze News reached out to the agency through another email address listed on the site, asking a bevy of specific questions about Daskalakis’ beliefs about gender and his approaches to medicine. We never received a response.

‘Radical gay doctor’: Daskalakis takes on meningitis in NYC

Daskalakis, described in his CDC bio as an “activist physician,”
reportedly grew up in Arlington, Virginia, in a Greek Orthodox family and attended medical school at New York University. After residency in Boston, he moved back to NYC, where he became known as a “progressive, radical gay doctor” eager to take on infectious diseases known to spread among gay men.

Not only might underage boys have illicitly snuck into these venues otherwise restricted to adults, but even the adults at the clubs and bathhouses may have been under the influence of drugs or alcohol.

One such disease that ravaged the LGBTQ+ populations in NYC in 2012 and 2013 was meningitis. Ostensibly in an effort to limit the spread of the disease, Daskalakis began going to gay nightclubs and bathhouses and offering meningitis vaccinations to those in attendance. He even occasionally performed those vaccinations while wearing a drag costume — “to take the edge off the injection,” NBC News said.

In a feature story on Daskalakis several years ago, the Columbia College Alumni Association, which counted Daskalakis among its membership, called this approach “innovative” and claimed it was “making healthcare accessible and easy for at-risk populations.” “Daskalakis is known for … putting convention aside and going into the community rather than waiting for people to come to him,” the
association said.

One possible concern with this “innovative” approach, however, is whether the individuals who received a vaccination from Daskalakis under these conditions were in a position to consent to it. Not only might underage boys have illicitly snuck into these venues otherwise restricted to adults, but even the adults at the clubs and bathhouses may have been under the influence of drugs or alcohol.

In our email to the NCIRD, Blaze News asked what steps Daskalakis took to ensure that his vaccination recipients were of age and sound mind to consent to the injection. Neither the NCIRD nor Dr. Daskalakis responded.

When HIV ‘prevention’ boosts Big Pharma’s bottom line

Another infectious disease known to affect gay men in particular is HIV, the virus that can cause AIDS. Though the scourge of AIDS frequently made headlines in the late 1980s and early 1990s, a time when celebrities proudly wore red ribbons to award shows in support of AIDS research, its popularity as a cause
waned by the 2000s.

Rather than attempting to curtail the unsafe behaviors, Daskalakis was, wittingly or unwittingly, facilitating promiscuity within the gay community, all under the guise of sexual ‘health.’

Dr. Daskalakis made HIV the focus of his early medical career, which likely began in the late 1990s, when HIV was beginning to fall off the national radar. Daskalakis’ CDC bio claims that at the time, he stressed the importance of HIV testing in LGBTQ+ communities as well as “prevention.”

Indeed, Daskalakis soon adopted a prevention-minded HIV treatment program known as PrEP, short for pre-exposure prophylaxis. A major component of PrEP, however, usually involves a daily dose of an expensive drug called Truvada.

While state and federal programs may have made Truvada more affordable, PrEP participants must take a dose every single day, which makes them dependent — which is not to say addicted — on a drug made necessary because of unsafe sexual practices. Rather than attempt to curtail the unsafe behaviors, Daskalakis wittingly or unwittingly attempted to inoculate against some of the consequences of those behaviors, thus facilitating promiscuity within the gay community, and all under the guise of sexual “health.”

In fairness, it appears that PrEP has helped reduce the rates of HIV infection in places like NYC, San Francisco, and Washington, D.C. According to a study cited by NBC News, between 2012 and 2017, new HIV diagnoses in NYC dropped from about 400 for every 1,000,000 people to about 250.

However, PrEP depends largely on individuals consuming Truvada or other antiretroviral drugs, and pharmaceutical companies have since apparently tried to expand the consumer base for these medicines beyond just the LGBTQ community to encourage more drug purchases. NBC News even admitted that the positive results from PrEP prompted the government to set up the
U.S. Preventive Services Task Force, which ultimately “recommended that doctors assess all Americans’ HIV risk … vastly increasing the number of people recommended to take [Truvada]” (emphasis added).

‘Sexual health clinics’: Daskalakis revamps NYC’s health agency

Because of his work with gay men, Daskalakis was eventually hired to be the assistant commissioner of the Bureau of HIV/AIDS Prevention and Control at the New York City Health Department around the time that Bill de Blasio was sworn in as mayor in January 2014. Over the next several years, Daskalakis advanced in the agency and seized the opportunity to significantly change its approach to sex and health.

For one thing, Daskalakis rebranded STD clinics to be “sexual health clinics,” even though the healthiest form of sexuality is expressed exclusively within a
monogamous marriage.

Daskalakis was also involved in devising new sex-related media campaigns in NYC. “Gone were the scare-tactic campaigns of the Bloomberg administration … . They were replaced by joyful, brightly colored ads that encouraged people to come in for STD testing,” NBC News claimed.

Such a description dodges the crudely suggestive nature of these ads, some of which are featured on NYC
subways. NBC News shared an image of an ad from 2018 that promoted a casual hookup and included emojis that reference male genitalia and ejaculation. Current NYC ads feature similarly vulgar images through strategic use of fruit.

In 2022, a year or so after Daskalakis left, the city’s health department changed its name to NYC Department of Health and Mental Hygiene. Though the name suggests the Division of Mental Hygiene encourages clean, wholesome thoughts, it actually “oversees the agency’s work on mental health, alcohol and drug use prevention, care and treatment and children youth and families,” according to its
website.

‘Leadership on health equity’: Daskalakis joins the CDC

During his years at the NYC health department, Daskalakis held several titles, including “incident commander” of the “COVID-19 public health emergency” in 2020, a position that increased his public profile considerably. In fact, he actually joined the CDC in December 2020, the tail end of the Trump administration, to be the director of the Division of HIV/AIDS Prevention in the National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, though all the while he continued to promote the COVID vaccines.

Then in August 2022, Joe Biden named Daskalakis and Robert Fenton of FEMA to spearhead the effort to combat the so-called monkeypox virus, which spread mainly among gay men. Biden first developed confidence in Fenton and Daskalakis because of their tireless efforts to promote the COVID vaccines for nearly everyone, including babies as young as
6 months old.

“Both played critical roles in making COVID vaccines more accessible for underserved communities and closing the equity gap in adult vaccination rates, through the implementation and execution of FEMA mass vaccination sites in some of the country’s most underserved communities, and working with trusted members of local communities to build vaccine confidence,” said a
statement from the White House.

Dr. Anthony Fauci — the controversial former director of the
National Institute of Allergy and Infectious Disease, a subset of the National Institutes of Health — praised the appointment of Daskalakis and Fenton.

“From Bob’s work at FEMA leading COVID-19 mass vaccination efforts and getting vaccines to underserved communities to Demetre’s extensive experience and leadership on health equity and STD and HIV prevention, this team will allow the Biden Administration to further accelerate and strengthen its monkeypox response,” Fauci said at the time.

Several months later, Daskalakis and his overtly sexual medical persona went viral on social media after users on the right began sharing a video of him from the HIV Prevention Summit in Las Vegas in 2023. In the video, Daskalakis, wearing a suit as well as some bondage-related accoutrement, struts onto a platform flanked by men in banana-boat-like attire as rainbow-colored lights flash about the stage and Madonna’s “Erotica” thunders through the speakers.

“Erotic. Erotic. Put your hands all over my body,” the lyrics repeat.

“Our country is run by clowns and pervs,” commented popular right-wing X account
I Meme Therefore I Am in reference to the video.

If users hoped sharing the video would shame the Biden administration into pulling Daskalakis’ appointment, they were wrong. In fact, after Daskalakis’ stint with the monkeypox response team, he was promoted to director of the CDC’s National Center for Immunization and Respiratory Diseases, a position that he still holds today.

Among the respiratory disease threats now under Daskalakis’ care is COVID, as the NCIRD has an entire subdivision devoted to the coronavirus and “other respiratory viruses.”

As NCIRD director, Daskalakis is also tasked with “advancing health equity.” Blaze News asked NCIRD to clarify what it means by “health equity” and whether such an approach to treatment privileges the health concerns of certain groups over others. The NCIRD did not respond.

‘Satan is waiting’: Daskalakis’ personal life

The 2023 video of Daskalakis at the HIV prevention convention in Las Vegas does not in any way exaggerate Daskalakis’ focus on his gay sexual identity. A quick glance at his personal
Instagram account reveals a man obsessed with sex and disturbing — possibly even satanic — imagery.

Most of the images on the account are selfies of himself with no shirt on, exposing his many tattoos, at least one of which includes a pentagram image. In others, he’s standing with his legal partner, Michael Macneal.

The reels on the Instagram account are even more unsettling. Several feature drag queens expounding on Daskalakis’ many contributions to the trans community.
Another post from several years ago features a Macy’s ad during June, sometimes referred to as Pride Month. In the ad, Daskalakis and Macneal cuddle and embrace in front of a rainbow-colored star. In one shot, Macneal even licks Daskalakis’ face.

“JUST A LITTLE PRIDE WITH MY BOO,” reads the attending message from Daskalakis.

Daskalakis has apparently embraced the homosexual lifestyle so completely that he has even disparaged heterosexuality. In a July 2022
post on the platform then known as Twitter, Daskalakis joked: “A white straight cis man comparing sex to bowling tells me so much about straight sex.”

Such a joke from a private citizen would hardly be worth mentioning, but Daskalakis has strong influence over national federal policy regarding immunizations. He is also a physician who ought to treat everyone — from promiscuous homosexual men at NYC bathhouses to conservative Christian heterosexual women living in faithful marriages — the same in terms of medicine and bedside manners.

Possible anti-heterosexual biases aside, Daskalakis has evinced a personal outlook that would likely stand in stark contrast to the outlook of average Americans, especially Christians. In 2014, Daskalakis and Macneal partnered with Sarah LaBier to open a spin and yoga studio called Monster Cycle, which may sound rather innocuous but offered a decidedly dark atmosphere and approach to exercise.

One
Facebook post from the studio features satanic images, including a pentagram and the number 666. Another offered “free tarot readings.” Yet another post promotes a sale of six classes for $66.66. “Satan is waiting,” the photo promo reads.

Images from a 2014
New York Post story about the studio likewise show LaBier practicing yoga in front of a pentagram and Macneal atop a spin bike wearing a costume that includes devilish horns.

Despite these images and promotions, LaBier insisted that she and her fellow co-owners were not satanists. “We don’t worship the devil, we’re not Satan followers,” she told the Post. “We’re just sort of taking that energy and making it more positive.”

When asked about his possible interest in satanism in September 2022, Daskalakis
replied, “I wish I were that interesting.”

Though the Facebook account for Monster Cycle remains active, the studio may be closed. The most recent Facebook post on the account is from March 2020, and calls to the phone number advertised on it either did not go through at all or were met with a busy signal. A
website for the studio is likewise defunct.

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