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How Fauci ignored ethics and the law as he barbarically experimented on babies and children

By Sally Beck | TCW Defending Fredom | October 21, 2022

Yesterday we published the first part of our extract from Robert F Kennedy Jnr’s book, The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Healtha critical look at Anthony Fauci, chief medical adviser to President Joe Biden. This second part continues to report on horrific drug trials carried out on children.

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Warning: Some of the following details are distressing.

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Two years later, [investigative reporter Celia] Farber would follow the trail of child casualties left by Dr Fauci’s Aids branch, DAIDS, in Uganda, exposing the pattern of abusing African mothers and children.

After the BBC documentary aired, AP reporter John Solomon made his own efforts to calculate the number of children who died in Dr Fauci’s Aids drug experiments. Solomon’s May 2005 AP investigation revealed that at least 465 New York City foster children were subjects in NIAID’s [US National Institute of Allergy and Infectious Diseases] trials and that Dr Fauci’s agency provided fewer than one-third (142) of those children with an advocate – the minimum legally mandated protection.

A March 2004 letter from Vera Sharav to Dr David Horowitz, director of FDA’s [Food and Drink Administration] Office of Compliance, charged Dr Fauci’s HIV drug trials with numerous violations of federal law, including NIAID’s failure to protect the rights and safety of foster children, particularly during the perilous Phase 1 stages in which drug companies determine toxicity effects by exploring maximum tolerance levels. Sharav accused Dr Fauci’s team of illegally failing to provide state wards and orphans with independent guardians to represent their interests and protect their rights during brutal, dangerous, and often agonizingly painful experiments.

The 2004 FDA investigation of Dr Fauci’s AIDS research division urged the head of NIH to insist on better management from NIAID. ‘The overall management of this Division requires careful review,’ the report said. A May 2005 Congressional hearing also concluded that NIAID’s experiments had violated federal statutes.

In testimony before Congress, NIAID and its local partner – New York City’s Administration for Children’s Services (ACS) – sought to justify the unethical research practices by claiming they were providing first-class, cutting-edge treatments to HIV-infected children who could otherwise not afford expensive medicines.

However, AHRP’s [Alliance for Human Research Protection] investigation revealed that many of the children NIAID subjected to Dr Fauci’s experiments were perfectly healthy and may not even have been HIV-infected. Those investigations focused on thirty-six of the trials. For obvious reasons, clinical trials virtually always occur in hospital settings with trained medical personnel, doctors and nurses, in attendance. However, ICC [Incarnation Children’s Center] was a non-medical facility. The decision to allow experiments with highly toxic drugs at an orphanage devoid of medical personnel was, itself, a stunning act of malpractice. Subsequent events suggest that the decision was deliberate, calculated to avoid scientific and ethical objections that might have put Pharma PIs [principal investigators] at odds with trained medical professionals. Publicly, NIAID pretended it would permit pharmaceutical companies to conduct their dangerous dose tolerance experiments only on children who had terminal Aids and were therefore likely to die anyhow. However, AHRP found that NIAID was quietly allowing its Pharma partners to experiment not only on children with laboratory-confirmed HIV infection, but also those ‘presumed’ to be infected. In other words, NIAID required no proof that these children actually had HIV. AHRP accused NIAID of exposing children who might never have developed Aids to lethal risks and the horrific adverse effects of highly toxic drugs for purposes that were not therapeutic, but purely experimental.

On March 8, 2004, NIH [National Institutes of Health, of which Fauci’s NIAID is a division] rejected a Freedom of Information Act (FOIA) request for the adverse event reports from NIAID’s trials conducted at ICC, citing FOIA’s ‘trade secrets’ and ‘privacy’ exemptions. AHRP then filed a complaint on March 10 with the FDA and the Office of Human Research Protections (OHRP), charging that NIAID was depriving foster children of legally mandated federal protections against research risks. Two subsequent investigations validated AHRP’s complaint.

John Solomon’s AP investigation finally brought Dr Fauci’s experiments to national prominence. AP identified at least forty-eight Aids experiments NIAID conducted on foster children in seven states – mostly in violation of the federal requirement that NIAID provide those children with an advocate. In addition to the Dapsone trial that killed at least ten children, NIAID sponsored another study testing a combination of adult antiretroviral drugs. AP reported that of the fifty-two children in the trial, there were twenty-six moderate to severe reactions – nearly all in infants. The side effects included rash, fever, and dangerous drops in infection-fighting white blood cells.

From the outset, Dr Fauci’s experiments served his vain obsession to develop an HIV vaccine. (Despite these expenditures of tens of billions of dollars, he has failed – for forty years – to develop an HIV vaccine that was safe or effective for human use.) Medical records that NIAID ultimately and reluctantly released proved that Dr Fauci’s PIs were testing his dangerous vaccines on children from one month to eighteen years old. AP writer John Solomon confirmed that despite contrary requirements in official NIAID protocols, NIAID was knowingly allowing its Pharma partners to violate NIAID’s written study protocols by conducting these experiments on children with and without proof of HIV infection.

For example, published reports acknowledge that NIAID, Genentech, and Micro-Genesys co-sponsored a vaccine trial code-named ACTG #218. The ACTG #218 protocol states ‘Patients must have: Documented asymptomatic HIV infection,’ and the ‘Expected Total Enrolment’ was seventy-two. However, an internal report acknowledges that NIAID was allowing the companies to openly violate those requirements: ‘125 immunized children proved to be HIV uninfected’. Another report stated: ‘A total of 126 children were not infected’. NIAID’s final analysis acknowledged that ACTG #218 ‘showed no clinical benefit to vaccine recipients’.

Another HIV Phase 1 vaccine trial, ACTG #230, tested two experimental vaccines, one by Genentech, another by Chiron/Biocine. This time, the protocol openly declared: ‘Accepts Healthy Volunteers’. As Solomon discovered, the ‘volunteer’ subjects of that unethical experiment were newborns aged three days or less. NIAID randomized these infants to one of three doses of either experimental HIV vaccine or placebo. These reports validate AHRP’s concerns that Dr Fauci experimented on infants and children who were never at risk of Aids, and that he exposed them to deadly risks and agonizing discomforts in a speculative drug and vaccine exercise that offered absolutely no potential benefit for them.

Dr Fauci was certainly aware of the peril to which he was subjecting his gallant infant ‘volunteers’. Most of the drugs that his PIs tested on these children were previously approved for adults with Aids and carried Black Box warnings of potentially lethal side effects: Aldesleukin, Dapsone, Didanosine, Lamivudine, Nevirapine, Ritonavir, Stavudine, and Zidovudine.

Finally, even in cases when the children were genuinely ill, Dr Fauci’s pretence that his experiments were compassionate gestures to impoverished orphans was always a sham. NIAID’s claim that their experiments were the only opportunity for those children to receive ‘life-saving’ drugs was a canard from the outset. New York State law requires that physicians provide ‘life-saving’ treatment to wards of the state, if need be, to provide treatment ‘off-label’.

Furthermore, drug companies do not primarily design clinical trials to benefit the individual subjects. Their purpose is to gain safety and efficacy information that may prove helpful for subsequent patients and be profitable for their bottom line. Finally, not all subjects get the ‘most promising’ drug in a trial; some get placebos.

Liam Scheff’s January 2004 article, The House that AIDS Built, ignited an outraged internet controversy, prompting the New York Press to publish a follow-up article by Scheff,Inside Incarnation. Scheff’s detailed descriptions are worth reading if only to understand the sacrifices that Dr Fauci demanded from his venturesome ‘volunteer’ babies for ‘the greater good’.

Scheff’s chronicle suggests that Dr Fauci and his PIs purposefully took advantage of Incarnation Children’s Center’s status as a non-medical facility. The PIs had free rein to engage in conduct that experienced professional nurses and doctors would have flagged as unethical and illegal.

When children declined to take the toxic drugs, NIAID and its Pharma partners arranged to surgically implant feeding tubes in their bellies to force obedience. Scheff wrote, ‘When Mimi [a staff member with no medical background] started at ICC, the tubes were used infrequently. “But when the kids got older, a lot of them started to refuse the medication,” she recalled. “Then they started coming in with the tubes more and more. Kids who refused too much, or threw up too much, they’d get a tube. First it was through the nose. But then it was more and more through the stomach. You’d see a certain child refusing over and over, and one day they’d come back from the hospital from surgery, and they had a tube coming right out of their stomach. If you asked why, the doctors said it was for ‘compliance’ – the regimen. Got to keep up the regimen,” said Mimi. “Those were the rules”.’

Mimi describes how children suffered – and how some died: ‘One girl, a six-year-old, Shyanne . . . She was the most delicate little flower – beautiful, polite, full of life. Her family never gave her meds. So, Administration for Children’s Services brought her into ICC . . . she came in and started the meds. And it was three months, maybe three months. And she had a stroke. She could not see. She was this normal girl, singing, jumping, playing. Then, poof, stroked out. Blind. We were freaked out. Then, in a few months, she was gone – dead.’

Between 1985 and 2005, NIAID and its Pharma partners conscripted at least 532 infants and children from foster care in New York City as human subjects of clinical trials testing NIAID’s experimental Aids drugs and vaccines. ICC and the medical research centers that conducted the trials received substantial payments for hosting the experiments, from both the National Institutes of Health and the manufacturers of the drugs. Among those companies were Merck, Bristol Myers Squibb, Micro-Genesys, Biocine, Glaxo, Wellcome, and Pfizer.

Further reading: https://www.conservativewoman.co.uk/exclusive-an-interview-with-faucis-nemesis/

October 31, 2022 Posted by | Corruption, Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , | Leave a comment

Exposed: How Anthony Fauci tortured vulnerable children in his obsessive hunt for an HIV vaccine

By Sally Beck | TCW Defending Freedom | October 20, 2022

Anthony Fauci, chief medical adviser to President Biden and director of the US National Institute of Allergy and Infectious Diseases (NIAID) for 38 years, has resigned and is leaving his post in December. He also steps down as director of the National Institutes for Health (NIH); both organisations are government-funded.

The 81-year-old virologist, who has served seven presidents, is quitting not because (as he says) he wants ‘new challenges’, but because of two books Robert F Kennedy Jnr (RFK) has written exposing him as a liar and a fraud, says Tony Lyons, President at Skyhorse Publishing, the independent publisher of both books.

Lyons said: ‘He used every available form of censorship to protect himself about the allegations in the first book and he doesn’t have any tools left to combat the likely congressional hearings in January.

‘Censorship as a government weapon against dissent has grown to unprecedented levels in the US. It’s a danger to the future of real science, real freedom, and real democracy.’

RFK’s first book, The Real Anthony Fauci, sold one million copies and topped the New York Times best-seller list despite extreme mainstream media censorship. It exposed Fauci’s role in the Covid pandemic and in the disastrous response to the HIV/Aids crisis in the 1980s and 1990s.

In a second book called The Wuhan Cover Up – How US Health Officials Conspired with the Chinese Military to Hide the Origins of COVID-19’ due to be released next year, RFK uncovers the complex web of control and censorship at the heart of this story. Kennedy accuses Fauci of being the architect of the pandemic by funding ‘gain-of-function’ research – or bioweapon research, in plain English – in China’s Wuhan lab, the source of the SARS-CoV-2 virus.

If the books were not enough to send Fauci running for cover, this week RFK released a free-to-view documentary The Real Anthony Fauci Documentary (salsalabs.org) based on his first book’s findings.

Here is an extract from The Real Anthony Fauci, which details experiments he sanctioned on vulnerable American children during his HIV research.

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Warning: Some of the following details are distressing.

In 2004, investigative journalist Liam Scheff chronicled Dr Fauci’s secretive experiments on hundreds of HIV-positive foster children at Incarnation Children’s Center (ICC) in New York City and numerous sister facilities in New York and six other states between 1988 and 2002. Those experiments were the core of Dr Fauci’s career-defining effort to develop a second generation of profitable AIDS drugs as an encore to AZT.

Scheff described how Dr Fauci’s NIAID and his Big Pharma partners turned black and Hispanic foster kids into lab rats, subjecting them to torture and abuse in a grim parade of unsupervised drug and vaccine studies: “This former convent houses a revolving stable of children who’ve been removed from their own homes by the Agency for Child Services [ACS]. These children are black, Hispanic, and poor. Many of their mothers had a history of drug abuse and have died. Once taken into ICC, the children become subjects of drug trials sponsored by [Dr Fauci’s] NIAID (a division of the National Institutes of Health), NICHD (the National Institute of Child Health and Human Development) in conjunction with some of the world’s largest pharmaceutical companies – GlaxoSmithKline, Pfizer, Genentech, Chiron/Biocine and others.”

NIAID’s Pharma partners remunerated Incarnation Children’s Center (ICC) for supplying children for the tests. As usual, Dr Fauci had the safety oversight board rigged with his loyal principal investigators (PIs), foremost of whom was Dr Stephen Nicholas, a generously funded NIAID AIDS drug researcher. “Stephen Nicholas was not only director of the ICC until 2002; he also simultaneously sat on the Paediatric Medical Advisory Panel, which was supposed to oversee the tests—which signifies a serious conflict of interest,” criticizes [Holocaust survivor and medical abuse investigator] Vera Sharav, president of the Alliance for Human Research Protection (AHRP), a medical industry watchdog organization.

Scheff continued, “The drugs being given to the children are toxic – they’re known to cause genetic mutation, organ failure, bone marrow death, bodily deformations, brain damage, and fatal skin disorders.

“If the children refuse the drugs, they’re held down and force fed. If the children continue to resist, they’re taken to Columbia Presbyterian hospital, where a surgeon puts a plastic tube through their abdominal wall into their stomachs. From then on, the drugs are injected directly into their intestines.

“In 2003, two children, ages six and twelve, had debilitating strokes due to drug toxicities. The six-year-old went blind. They both died shortly after. Another fourteen-year-old died recently. An eight-year-old boy had two plastic surgeries to remove large, fatty, drug-induced lumps from his neck.

“This isn’t science fiction. This is AIDS research.”

Even the foster children who survived Fauci’s experiments reported dire side effects, ranging from skin outbreaks and hives, nausea, and vomiting, to sharp drops in immune response and fevers—all common adverse reactions associated with the drugs he was targeting for development.

During one of his trials involving the drug Dapsone, at least ten children died. A May 2005 Associated Press investigation reported that those “children died from a variety of causes, including four from blood poisoning.” Researchers complained they were unable to determine a safe, useful dosage. Their guessing game cost those children their lives.

“An unexpected finding in our study,” the researchers pitilessly observed, “was that overall mortality while receiving the study drug was significantly higher in the daily Dapsone group.” NIAID researchers shrugged off the deaths as a mystery: “This finding remains unexplained.”

Vera Sharav spent years investigating Dr Fauci’s torture chambers as part of her lifelong mission to end cruel medical experimentation on children. Sharav told me, “Fauci just brushed all those dead babies under the rug. They were collateral damage in his career ambitions. They were throw-away children.” Sharav said that at least eighty children died in Dr Fauci’s Manhattan concentration camp and accused NIAID and its partners of disposing of children’s remains in mass graves.

The BBC’s heart-breaking 2004 documentaryGuinea Pig Kids, chronicles the savage barbarity of Dr Fauci’s science projects from the perspective of the affected children. That year, the BBC hired investigative reporter Celia Farber to conduct field research for the film, which exposes the dark underside of Big Pharma’s stampede to develop lucrative new AIDS remedies. “I found the mass grave at Gate of Heaven cemetery in Hawthorne, New York,” she told me. “I couldn’t believe my eyes. It was a very large pit with AstroTurf thrown over it, which you could actually lift up. Under it one could see dozens of plain wooden coffins, haphazardly stacked. There may have been 100 of them. I learned there was more than one child’s body in each. Around the pit was a semi-circle of several large tombstones on which upward of one thousand children’s names had been engraved. I wrote down every name. I’m still wondering who the rest of those kids were. As far as I know, nobody has ever asked Dr Fauci that haunting question.

“I remember the teddy bears and hearts in piles around the pit and I recall the flies buzzing around. The job of recording all those names took all day. NIAID, New York, and all the hospital PIs were stonewalling us. We couldn’t get any accurate estimate of the number of children who died in the NIAID experiments, or who they were. I went to check the gravestone names against death certificates at the NYC Department of Health, which you could still do at that time. The BBC wanted to match these coffins to the names of children who were known to have been at ICC. It was a very slow, byzantine project with tremendous institutional resistance, but we did turn up a few names. We learned the story of a father who had come out of prison looking for his son. He was told his son had died at ICC of AIDS and there were no medical records, as they’d all been ‘lost in a fire.’ He was devastated. This story ran in the NY Post, believe it or not. But one after the other, every media outlet that touched this story got cold feet. Even then, the medical cartel had this power to kill this kind of story. Dr Fauci has built his career on that attitude. Nobody even asks him a follow-up question. NIAID’s narrative, at that time, was that these children were among the doomed as they ‘had AIDS,’ so supposedly they were all going to die anyway. When people died, in large numbers, gruesome deaths, NIAID’s medical researchers called it ‘lessons learned.’”

Further reading: https://www.conservativewoman.co.uk/exclusive-an-interview-with-faucis-nemesis/

In Part 2: How Fauci ignored ethics and regulations in his experiments on babies and children.

October 30, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , | Leave a comment

New Study Blames COVID on NIH, University of North Carolina — Finds Fauci and Baric’s Fingerprints on Pandemic Bug

By Robert F. Kennedy, Jr., J. Jay Couey, Ph.D., and Charles Rixey | The Defender | October 21, 2022

Critics have long questioned why the National Institutes of Health (NIH) would fund experiments by University of North Carolina of Chapel Hill (UNC) professor Ralph Baric to develop a technique for hiding evidence of human tampering in laboratory-created super viruses.

Aided by some $220.5 million in National Institute of Allergy and Infectious Diseases (NIAID) funding, Baric developed a so-called “Seamless Ligation” technique, which he boasted could perfectly conceal all evidence of human tampering in laboratory-created viruses. Baric nicknamed his invention the “no-see’m” method.

Now a new study, “Endonuclease fingerprint indicates a synthetic origin of SARS-CoV2,” published on the preprint server bioRxiv, shows that — apparently unbeknownst to Baric — the “seamless ligation” concealment gimmick leaves its own minute but legible signature.

Most momentously, these same researchers have discovered that damning signature in the genome of the virus that causes COVID-19.

Baric’s technique has long been controversial. “It’s the artist that doesn’t sign his name to the painting; the virologist that doesn’t put his signature into the virus to let us know whether or not it is emerging naturally or whether it is produced in a laboratory,” said Jeffrey Sachs, chair of The Lancet COVID-19 Commission, a task force that investigated the origins of COVID-19.

“All of it says, my God, there was really a big, very risky research agenda underway.”

This month, Sachs published the results of his 22-month investigation in The Lancet, including the damaging conclusion that COVID-19 was probably laboratory-generated and that the technology probably came from NIH-funded science.

Referring to Baric’s seamless ligation methodology, evolutionary biologist Bret Weinstein observed:

“It’s the exact opposite of what you would do if your interest was public health. Public health scientists would be marking their enhancements with red flags — not devising ways to hide them. The only reason you would want a concealer is to advance a sinister purpose — such as illegal bioweapons development — some mischief that the scientist didn’t want traceable back to his lab.”

Baric taught his “no-see’m” method to the Wuhan Institute of Virology’s (WIV) “Bat Lady” Shi Zhengli in 2016. In return, Baric received Chinese coronaviruses collected by Shi from bats in Yunnan province. (Scientists have linked the COVID-19 genome’s pedigree to closely related bats.)

Shi and her colleagues at the Wuhan Institute subsequently demonstrated their mastery of Baric’s high-risk technique in a series of published — and highly controversial — gain-of-function experiments at the Wuhan lab. It has been even more puzzling to his critics that Baric, again with NIAID funding, chose to share this dangerous technique for weaponizing pathogens with Chinese scientists who have clear links to the Chinese military.

Experts say that the implications of this new study could be far-reaching. By pointing the finger at Baric, the study raises the possibility of potentially devastating liability for the NIAID and the University of North Carolina and other parties.

Scientists, including those close to Dr. Anthony Fauci, have repeatedly pointed out that SARS-CoV-2, the virus that causes COVID-19, has genomic sequences that appear inconsistent with natural evolution: The COVID-19 virus is no longer infectious in bats, and its spiked protein feature — which is unknown in this family of coronavirus — includes numerous mutations that make it ideally infectious in humans.

The closest known coronavirus relative — a coronavirus from the Wuhan lab — is 96.2% identical to SARS-CoV-2. The peculiar spike accounts almost completely for the entire 3.8% difference. Oddly, there are multiple novel mutations in the spike and almost none in the rest of the genome.

Natural evolution would be expected to leave mutations distributed evenly across the genome. The fact that virtually all the mutations occur on the spike led these scientists to suspect that that particular Wuhan lab coronavirus collected by Shi Zhengli is the direct progenitor of SARS-CoV-2 and that its new spike was implanted through engineering.

However, the unmistakable fingerprints of lab engineering were absent — leaving many experts wondering whether Baric’s technique was used to assemble a novel coronavirus with the engineered spike while removing the evidence of lab generation.

This new study connects the biological breadcrumbs that link federally funded research to a global pandemic. That trail leads directly to UNC and NIAID.

The authors of the study — a team of researchers from Duke University, University Clinics of Würzburg and an industry group — identified a characteristic signature in the amino acid code. That indelible artifact could only have emerged from Baric’s “no-see’m” methodology.

In an interview last spring, Baric himself confessed, that at the time the pandemic began, only two or three labs in the world were using his protocol – including his UNC lab and the WIV.

The study’s authors’ conclusions rest on the presence of unique sites in the COVID-19 virus. These sites allow special enzymes called “restriction enzymes” to cut the DNA into building blocks of unique size that then can be “stitched together in the correct order of the viral genome,” according to the study’s authors.

Essentially, Baric’s technique leaves behind unique spellings in the “genetic vocabulary.” The new words include “odd spelling choices” subtly distinguishing them from typical viral vocabulary.

The magic of Baric’s “no-see’m” technique is to invisibly weave these telltale “spelling” changes into the viral sequence between relevant genes without altering the viral protein. This is like changing the “spelling” of the word without changing its meaning; the casual listener will never notice the difference.

The research team used forensic tools to drill down on minute “spelling differences” in the SARS-CoV2 genome that betray laboratory tampering using the “no-see’m” technique.

Consider how a Brit would spell “colour,” “manoeuvre” or “paediatric.” The choice to spell a word in a certain way can reveal your nation of origin. Similarly, these nearly imperceptible changes in the viral sequence give away the laboratory origins of this virus.

In sharing his seamless ligation technique with Shi Zhengli, Baric assured that the WIV possessed all the required elements of the assembly process. EcoHealth Alliance’s infamous DEFUSE proposal describes the same techniques in detail. (submitted to The Defense Advanced Research Projects Agency, or DARPA, in 2018).

The world now has proof positive that SARS-CoV2 is an engineered laboratory creation generated with technology developed by Ralph Baric with U.S. government funding.

Prosecutors and private attorneys representing clients injured by the COVID-19 pandemic now have a smoking gun. The gun points at humanity. Forensic scientists have now successfully lifted faint but precise fingerprints from the lethal pistol’s grip and trigger. Those fingerprints belong to the NIAID and the University of North Carolina.

Baric is Fauci’s favorite gain-of-function scientist. The cascade of NIAID funding to Baric and his UNC lab has financed 152 studies approaching a quarter-billion dollars.

Those federal grants have made Baric the global kingpin of gain-of-function science. In conformance with standard practice, it is probable that UNC pockets one-quarter to one-half of NIH’s financial felicities to Baric for “administrative costs.”

These monumental payments have probably incentivized UNC to turn a blind eye to Baric’s reckless experiments and to his controversial decision to transfer his dangerous technologies to a Chinese military laboratory known to suffer from deficient safety protocols and shoddy construction that make it, in the words of Congressional investigators, less secure than a “dentist’s office.”

UNC’s role in enabling the questionable conduct may have precipitated a global pandemic that could easily give rise to liability for negligence.

UNC and NIAID’s liability is now clear. But do we have positive proof that the Wuhan lab created the monstrosity that caused COVID-19?

The cumulative evidence strongly suggests that the Wuhan lab used Baric’s methodologies to cobble together the chimeric virus that caused the COVID-19 pandemic. But a few missing puzzle pieces still prevent us from definitively proving that this dangerous construction project occurred at the Wuhan lab.

As The Lancet Commission report concluded, the released emails show that NIH’s Dr. Francis Collins, NIAID’s Fauci and EcoHealth Alliance’s Peter Daszak, and others are continuing to collaborate with Shi Zhengli and Chinese officials to suppress the public release of information that would allow us to complete this picture. Stay tuned!

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

October 22, 2022 Posted by | Timeless or most popular, War Crimes | , , , , , , | 2 Comments

Scientists Have Recreated World’s Deadliest Flu Virus

By Dr. Joseph Mercola | September 8, 2022

Evidence points to SARS-CoV-2 being the product of gain-of-function (GoF) research. Indeed, attorney Tom Renz will soon release the results of a major legal investigation, which he claims will demonstrate — beyond a reasonable doubt — that SARS-CoV-2 was created as part of a GoF project.1

Whether the outbreak was accidental, intentional or the result of negligence, the end result is the same — devastation of health, commerce, finance and civil life worldwide for years on end.

Now imagine what might happen if something like the Spanish flu got out — or worse, a turbo-charged, genetically engineered version of it. Incomprehensible as it may seem to the average person, scientists in the U.S. and Canada have resurrected this devastatingly lethal virus and, not surprisingly, the National Institutes of Health (NIH) and Dr. Anthony Fauci’s National Institute of Allergy and Infectious Diseases (NIAID) are involved.

Mad Scientists Are Testing Recreated Spanish Flu on Monkeys

As reported by Tom Renz, August 19, 2022:2

“… this is so absurd that I am just starting with the reference document because I am concerned no one will believe it. Here it is: ‘Spanish Flu GoF.’3 Yes, that is right, Fauci and crew are now actively performing gain-of-function (GoF) work and infecting primates with the Spanish Flu … Here is a quote from the document:

‘… Influenza virus A/South Carolina/1918 (H1N1) was generated by reverse genetics and handled in biosafety level 4 (BSL-4) containment at the National Microbiology Laboratory (NML).

Sequences of the 1918 influenza viral segments were based on data reported under GenBank accession numbers DQ208309, DQ208310, DQ208311, AF117241, AY744935, AF250356, AY130766, and AF333238.

1918 influenza virus was cultured using Madin-Darby canine kidney … cells. MDCK cells were grown in minimum essential medium … supplemented with 5% fetal bovine serum … and 1 L-glutamine …

A passage 2 (P2) virus stock was prepared using MEM supplemented with 0.1% bovine serum albumin (BSA) … 1 L-glutamine, and 1 mg/mL N-tosyl-L-phenylalanine chloromethyl ketone (TPCK)-treated trypsin …

This stock was used for animal inoculation. The mouse 50% lethal dose (MLD50) for this stock was determined previously to be 103.2 PFU; this value was confirmed prior to the use of the stock for macaque infection.’

I frankly do not care to debate the nuance of whether the recreation of generally extinct virus ‘generated by reverse genetics’ using pieces and parts of other animals qualifies as GoF; what I care about is that we have recreated the Spanish Flu and are experimenting with it on other animals.”

Spanish Flu ‘Not Lethal Enough’

As noted by Renz, the scientists appear frustrated by the fact that their reverse engineered Spanish flu virus — even at the highest doses tested — was not lethal enough to kill the two macaque species selected for the experiment.

Macaques were therefore deemed “not ideal for the development and testing of novel pandemic influenza-specific vaccines and therapies,” necessitating “other physiologically relevant nonhuman primate models.” Renz continues:4

“… given the result of the previous coronavirus GoF, can ANYONE possibly argue GoF work on the Spanish Flu is a good idea? Even the simple recreation of the disease demonstrates an incredible lack of respect for the disaster created by the coronavirus GoF.

So you may be asking, what moron could possibly be oblivious enough to support GoF work on the Spanish Flu while the world is still dealing with the nightmare that is COVID? The answer should not be surprising … NIH and NIAID are involved.

Apparently Fauci does not mind what he did with funding the creation of COVID and is at it again. You might also note the vaccine development crew’s involvement. A foundational point in this article is that the newly recreated Spanish Flu is not dangerous enough. Here is a pull-quote:

‘However, 1918 influenza was uniformly nonlethal in these two species, demonstrating that this isolate is insufficiently pathogenic in rhesus and Mauritian cynomolgus macaques to support testing novel prophylactic influenza approaches where protection from severe disease combined with a lethal outcome is desired as a highly stringent indication of vaccine efficacy.’

This means that these people are arguing that we need to make a more dangerous version of the Spanish Flu so they can make ‘better’ vaccines for it … despite the fact that until they recreated it, it likely no longer existed in nature.”

As noted by Renz, elected officials really need to answer the question, “Why is this kind of research allowed to continue on your watch?” Why are we reverse engineering the most lethal viruses the world has ever seen — after they’ve already been eradicated?

The argument that we need to create dangerous viruses “just in case” Nature comes up with something similar, so we can create vaccines for said viruses in advance, simply doesn’t hold water. Stop creating these monstrosities, and we won’t need the vaccines! This is science gone mad, and it must be stopped.

Besides, what are the chances that a virus would emerge naturally that just so happens to perfectly match the virus we now have a vaccine against? The entire premise is irrational from start to finish. It’s biowarfare research and nothing else.

The Intentional Cover-Up of SARS-CoV-2’s Origin

Fauci, former NIH chief Dr. Francis Collins, EcoHealth Alliance president Peter Daszak and other members of the scientific community have spent the last two and a half years actively stifling debate about the genesis of SARS-CoV-2.

And, coincidentally, most of them have clear-cut connections to bat coronavirus GoF research and/or the Wuhan Institute of Virology (WIV), which appears to be the lab from which the virus somehow escaped.

So, it appears those who insist SARS-CoV-2 is of natural origin, despite all the evidence to the contrary, are doing so because they don’t want risky virological research to be blamed for the COVID pandemic. That would “blow their cover” and raise questions about the sanity of funding such research.

Some may be so enamored with their chosen careers, they cannot imagine doing anything other than tinkering with pathogens. For them, pulled funding is a threat to their livelihood. But for others, the underlying incentive may be more nefarious. Like I already said, there’s really no reason for this kind of research other than the creation of weapons of mass destruction.

Whatever incentive any given player may have had, what’s clear is that Fauci, Collins, Daszak and many others intentionally undermined efforts to get to the bottom of where SARS-CoV-2 came from.

Corrupted Science

Video Link

Attesting to this corruption of science is Jeffrey Sachs, Ph.D., professor of economy at Columbia University, a senior United Nations adviser and chair of The Lancet COVID-19 Commission, convened in June 2020.

Sachs originally assigned Daszak to lead and organize the COVID-19 Commission’s task force to investigate the virus’s genesis (one of 11 task forces under the COVID Commission). Sachs ended up dismissing Daszak from the task force in June 2021, after he realized just how serious Daszak’s conflicts of interest were,5 and that Daszak was lying to him.6

Eventually, he realized Daszak wasn’t the only rotten apple in the bunch. Other members of The Lancet Commission’s COVID Origins task force were also working against their mandate to investigate the pandemic’s origin. The final straw came when Sachs sacked Daszak and several task force members suddenly attacked him for being “antiscience.”

Shortly thereafter, a Freedom of Information Act (FOIA) request brought previously hidden NIH documents to light, and Sachs realized that those who were attacking him also had undisclosed ties that made their ability to get to the truth doubtful at best. At that point, in September 2021, he disbanded the whole task force.

Lack of Transparency Breeds Mistrust

In mid-May 2022, Sachs published a frank opinion piece in the journal PNAS,7 together with Neil Harrison, calling for a truly independent inquiry into the origin of SARS-CoV-2.

In their article, Sachs and Harrison argued that while transparency on the part of Chinese authorities would be “enormously helpful,” much may be gleaned from information found in U.S.-based research institutions that were working with Wuhan-based institutions, including the WIV. Yet such material has not been disclosed for independent analysis. Here’s an excerpt:8

“This lack of an independent and transparent US-based scientific investigation has had four highly adverse consequences. First, public trust in the ability of US scientific institutions to govern the activities of US science in a responsible manner has been shaken.

Second, the investigation of the origin of SARS-CoV-2 has become politicized within the US Congress; as a result, the inception of an independent and transparent investigation has been obstructed and delayed.

Third, US researchers with deep knowledge of the possibilities of a laboratory-associated incident have not been enabled to share their expertise effectively. Fourth, the failure of NIH, one of the main funders of the US–China collaborative work, to facilitate the investigation into the origins of SARS-CoV-2 has fostered distrust regarding US biodefense research activities.

Much of the work on SARS-like CoVs performed in Wuhan was part of an active and highly collaborative US–China scientific research program funded by the US Government (NIH, Defense Threat Reduction Agency [DTRA], and US Agency for International Development [USAID]), coordinated by researchers at EcoHealth Alliance (EHA), but involving researchers at several other US institutions.

For this reason, it is important that US institutions be transparent about any knowledge of the detailed activities that were underway in Wuhan and in the United States. The evidence may also suggest that research institutions in other countries were involved, and those too should be asked to submit relevant information …”

Sachs and Harrison go on to name a number of U.S. institutions that need to come clean about their work, including the EcoHealth Alliance (EHA), the University of North Carolina (UNC), the University of California at Davis (UCD), the NIH, NIAID and the U.S. Agency for International Development (USAID).

All of these agencies and institutions have conducted and/or collaborated on research that may be able to solve the mystery, but instead of transparently sharing their data, they’ve merely declared that they’ve “not been involved in any experiments that could have resulted in the emergence of SARS-CoV-2.”

Blanket Denials Are Not Good Enough

As noted by Sachs, before we can believe such claims, we need to be able to confirm their veracity, and that requires independent analysis of all the data.

“Blanket denials from the NIH are no longer good enough. Although the NIH and USAID have strenuously resisted full disclosure of the details of the EHA-WIV-UNC work program, several documents leaked to the public or released through the Freedom of Information Act (FOIA) have raised concerns,” Sachs and Harrison wrote.9

“These research proposals make clear that the EHA-WIV-UNC collaboration was involved in the collection of a large number of so-far undocumented SARS-like viruses and was engaged in their manipulation within biological safety level (BSL)-2 and BSL-3 laboratory facilities, raising concerns that an airborne virus might have infected a laboratory worker.

A variety of scenarios have been discussed by others, including an infection that involved a natural virus collected from the field or perhaps an engineered virus manipulated in one of the laboratories.”

Suspicious ‘Coincidences’ Abound

Sachs and Harrison go on to discuss the problem of an unusual furin cleavage site (FCS) in SARS-CoV-2 that makes it more transmissible and pathogenic than related viruses.

While it’s not yet known how this feature came to be within SARS-CoV-2, whether by natural evolution or intentional insertion, “We do know that the insertion of such FCS sequences into SARS-like viruses was a specific goal of work proposed by the EHA-WIV-UNC partnership within a 2018 grant proposal (‘DEFUSE’) that was submitted to the U.S. Defense Advanced Research Projects Agency (DARPA),” Sachs wrote.

That particular DARPA proposal was never funded, but as noted by Sachs, “we do not know whether some of the proposed work was subsequently carried out in 2018 or 2019, perhaps using another source of funding.”

“Information now held by the research team headed by EHA, as well as the communications of that research team with US research funding agencies, including NIH, USAID, DARPA, DTRA, and the Department of Homeland Security, could shed considerable light on the experiments undertaken by the US-funded research team and on the possible relationship, if any, between those experiments and the emergence of SARS-CoV-2,” Sachs and Harrison wrote.10

“We do not assert that laboratory manipulation was involved in the emergence of SARS-CoV-2, although it is apparent that it could have been. However, we do assert that there has been no independent and transparent scientific scrutiny to date of the full scope of the US-based evidence.”

In an August 2, 2022, Current Affairs interview,11 Sachs again reiterated that he believes the NIH and allied scientists colluded to impede The Lancet Commission’s investigation, for the simple reason that the virus was the result of U.S. research.

Indeed, aside from what Sachs brought up in his PNAS article, there are patents spanning decades to suggest that’s true (see “Patents Prove SARS-CoV-2 Is a Manufactured Virus“).

Sachs also opened up about his concerns and misgivings in an August 20, 2022, interview with Robert F. Kennedy Jr. (video above). He admits believing in the zoonotic spillover theory early on, only to, over time, come to change his mind as he realized he was being lied to, over and over again.

Today, he believes the lab-leak theory is the most likely explanation for the pandemic — and that the U.S. government, the NIH, the NIAID and the rest are suppressing the truth for the simple reason that they’re responsible for its creation, even if only in part.

Final Thoughts

To circle back to where we started, is it really prudent to reverse engineer the Spanish flu virus, and further tinker with it to make it even more lethal — all in the name of vaccine development?

Think back over the past few years. Mull over the deaths — an estimated 18 million from COVID-19 alone12 — the suicides (deaths of despair), the lost businesses, lost education years, the loss of freedoms and Constitutional rights, the COVID jab injuries, and the massive wealth transfer that has occurred.

All of that may have been because of this kind of mad science. Do we really want to repeat it in the future, but with a far more lethal pathogen? Most sane persons would say no. It’s time for legislators to take definitive steps to ensure mankind is not wiped out by scientific hubris.

Sources and References

September 9, 2022 Posted by | Timeless or most popular, War Crimes | , , , , , , | 1 Comment

Senators demand NIH, HHS preserve all related documents, communications, promise ‘full-throated investigation’ of Fauci

By Suzanne Burdick, Ph.D. | The Defender | August 24, 2022

Two U.S. senators on Tuesday — the day after Dr. Anthony Fauci announced plans to leave his government posts in December — formally requested the National Institutes of Health (NIH) and the U.S. Department of Health and Human Services (HHS) preserve all documents and communications related to Fauci.

Fauci on Monday said he will retire as director of the National Institute of Allergy and Infectious Diseases (NIAID) and as chief medical adviser to President Joe Biden in December to pursue “the next chapter” of his career.

In a letter to HHS Secretary Xavier Becerra, Sen. Roger Marshall (R-Kan.) demanded Becerra “immediately confirm” that HHS is preserving all records related to Fauci and  Dr. Francis Collins, who was director of the NIH from August 2009 to December 2021.

“This request applies to all documents, records, memoranda, research, correspondence, or other communication or any portion thereof relevant to any involvement of Dr. Fauci or Dr. Collins,” the letter stated.

Sen. Rand Paul (R-Ky.), in a letter to Lawrence Tabak, D.D.S., Ph.D., acting director of the NIH, asked Tabak to “ensure the preservation of all documents and communications within Dr. Fauci’s possession related to his tenure at the National Institutes of Health (NIH).”

Marshall stressed that it is “imperative” that all HHS workers are made aware of their “legal responsibilities to collect, retain, and preserve all documents, communications, and other records in accordance with federal law.”

He also reminded Tabak of his obligation, as the head of HHS, to ensure the preservation of all records and that any employee “who conceals, destroys, or attempts to conceal or destroy a federal record may be subject to fine and imprisonment for up to three years.”

Marshall pointed out that HHS previously refused to provide information to Congress:

“HHS and component agencies, including NIH in particular, continue to obstruct numerous congressional investigations through refusal to provide responsive information.

“In addition to withholding information from Congress, private parties note that NIH refuses to comply with Freedom of Information Act (FOIA) requests until forced to do so by court order.”

Marshall went on to list “recent egregious examples” of NIH’s failure to meet record-keeping requirements and said that “even one” such example “should instigate immediate oversight action by HHS.”

Marshall’s letter outlined four “notable recent concerns” with NIH’s record-keeping, including past accusations that NIH destroyed records, potential conflicts of interest within the HHS Office of Inspector General, NIH’s practice of “self-policing” and NIH’s failure to ensure required reporting of clinical trial results.

‘Fauci’s resignation will not prevent full-throated investigation into origins of pandemic’ — Rand Paul

Paul, in his letter to Tabak, also emphasized the need to preserve NIH documents for investigation purposes.

Paul wrote:

“This information is critical to ensure that Congress has access to information necessary to conduct proper oversight regarding events that took place during Dr. Fauci’s tenure with the agency.

“Specifically, I request you preserve all records, e-mail, electronic documents, and data created by or shared with Dr. Fauci during his tenure at NIH that relate to COVID-19 including, but not limited to, NIAID-funded coronavirus research.”

In an email today, Paul told The Defender :

“Dr. Fauci misled the American people on public health guidance throughout the pandemic, lied to Congress under oath, and funneled tax dollars to fund dangerous research in communist China.

“The American people deserve transparency and accountability from the NIH regarding the COVID-19 pandemic regardless of Dr. Fauci’s future employment plans.”

On Monday, Paul tweeted, “Fauci’s resignation will not prevent a full-throated investigation into the origins of the pandemic. He will be asked to testify under oath regarding any discussions he participated in concerning the lab leak.”

For more than a year, Paul has advocated for a thorough investigation into the origins of COVID-19 and pushed for a criminal investigation of Fauci, whose NIAID research at the Wuhan Institute of Virology in China Paul suggested may have been involved in creating the virus.

Following up on a threat he made in mid-July of 2021, Rand sent an official criminal referral on Fauci to the U.S. Department of Justice on July 26, 2021.

Paul asked Attorney General Merrick Garland to investigate Fauci for allegedly lying to Congress when he said the NIH “has not ever and does not now fund gain-of-function research in the Wuhan Institute of Virology.”

The week before he sent the official criminal referral, Paul asked Fauci if he wanted to retract the statement he made to Congress during a May 11 hearing. Paul said, “Dr. Fauci, knowing that it is a crime to lie to Congress, do you wish to retract your statement of May 11, where you claimed the NIH never funded gain-of-function research and move on?”

Fauci replied he would not retract the statement and was adamant he never lied before Congress.

However, Fox News commentator Tucker Carlson said on June 2, 2021, that evidence showed Fauci was “implicated in the very pandemic he had been charged with fighting.”

Emails obtained by BuzzFeed via the Freedom of Information Act show “Fauci supported the grotesque and dangerous experiments that appeared to have made COVID possible,” Carlson said.

The emails, which date back to the early winter of 2020, show Fauci was worried the public would think COVID-19 originated at the Wuhan lab. Why?

“Possibly because Tony Fauci knew perfectly well he had funded gain-of-function experiments at that very same laboratory,” Carlson said.

The emails showed Fauci and other top virologists shared an article from ZeroHedge suggesting COVID-19 was a man-made bioweapon. Despite it being a “plausible explanation,” said Carlson, ZeroHedge was banned from social media.

Carlson said:

“Until recently, you were not allowed to suggest that COVID might be man-made. Why couldn’t you suggest that? The fact checkers wouldn’t allow it. Why wouldn’t they? Because Tony Fauci assured the tech monopolies that the coronavirus could not have been manmade. And so the tech monopolies shut down the topic.”

NIAID has, for years, provided grants to the EcoHealth Alliance and others to conduct gain-of-function research on coronaviruses, as The Defender previously reported.

In March 2021, the Wuhan lab deleted mentions of its collaboration with the NIAID/NIH and other American research partners from its website. It also deleted descriptions of gain-of-function experiments on the SARS virus, according to Dr. Joseph Mercola.

“The NIH/NIAID has funded GOF [gain-of-function] research to the tune of at least $41.7 million,” Mercola said. “Up until 2014, this research was conducted by Ralph Baric at the University of North Carolina.”

After 2014, when federal funding of gain-of-function research was banned, the research was funneled to the Wuhan lab via the EcoHealth Alliance.

Mercola added:

“In August 2020, the NIAID announced a five-year, $82-million investment in a new global network of Centers for Research in Emerging Infectious Diseases that will conduct GOF experiments to ‘determine what genetic or other changes make [animal] pathogens capable of infecting humans.’”


Suzanne Burdick, Ph.D., is an independent journalist and researcher based in Fairfield, Iowa.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

Download for Free: Robert F. Kennedy’s New Book — ‘A Letter to Liberals’

August 25, 2022 Posted by | Aletho News | , , , , | 1 Comment

Fauci is Now Performing Gain-of-Function on the Spanish Flu

By Tom Renz | Tom’s Newsletter | August 19, 2022

This will be short because it really does not need much comment. In fact, this is so absurd that I am just starting with the reference document because I am concerned no one will believe it. Here it is:

Spanish Flu Gof
2.12MB ∙ PDF File – Read now

Yes, that is right, Fauci and crew are now actively performing gain-of-function (GoF) work and infecting primates with the Spanish Flu. For those of you that are unaware, GoF does not have a single agreed upon definition but, as it relates here, is essentially the modification of the Spanish Flu virus to make “more functional.” In this case, as with COVID, I have little doubt the GoF supporters will argue that this is not GoF but the article actually notes that this disease was created in canine kidneys with supplemental bovine serum. Here is a quote from the document:

Virus and cells. Influenza virus A/South Carolina/1918 (H1N1) was generated by reverse genetics (9) and handled in biosafety level 4 (BSL-4) containment at the National Microbiology Laboratory (NML). Sequences of the 1918 influenza viral segments were based on data reported under GenBank accession numbers DQ208309, DQ208310, DQ208311, AF117241, AY744935, AF250356, AY130766, and AF333238. 1918 influenza virus was cultured usingMadin-Darby canine kidney (MDCK; ATCC, Manassas, VA, USA) cells. MDCK cells were grown in minimum essential medium (MEM; HyClone) supplemented with 5% fetal bovine serum (FBS; HyClone) and 1 L-glutamine (L-Glu; Gibco, Life Technologies, Grand Island, NY, USA).

A passage 2 (P2) virus stock was prepared using MEM supplemented with 0.1% bovine serum albumin (BSA) (fraction V; HyClone), 1 L-glutamine, and 1 mg/mL N-tosyl-L-phenylalanine chloromethyl ketone (TPCK)-treated trypsin (Sigma-Aldrich). This stock was used for animal inoculation. The mouse 50% lethal dose (MLD50) for this stock was determined previously to be 103.2 PFU (9); this value was confirmed prior to the use of the stock for macaque infection.

I frankly do not care to debate the nuance of whether the recreation of generally extinct virus “generated by reverse genetics” using pieces and parts of other animals qualifies as GoF; what I care about is that we have recreated the Spanish Flu and are experimenting with it on other animals. I also care that one focus of this article is the fact that scientists are frustrated that the recreated Spanish Flu is not dangerous enough. We do not have to get far in this to see this frustration. At the beginning of the article in the summary of its importance this statement is made:

Here, we demonstrate that even at the highest doses tested, 1918 influenza was not lethal in these two macaque species, suggesting that they are not ideal for the development and testing of novel pandemic influenza-specific vaccines and therapies. Therefore, other physiologically relevant nonhuman primate models of pandemic influenza are needed.

At this point I am preparing to release the results of a major investigation we have been undertaking at Renz Law that will demonstrate that SARS-COV2 was in fact created in the Wuhan labs as part of a GoF project. We believe the investigation demonstrates this in a way that far exceeds a preponderance of the evidence standard and probably exceeds reasonable doubt. With that in mind, and given the result of the the previous coronavirus GoF, can ANYONE possibly argue GoF work on the Spanish Flu is a good idea? Even the simple recreation of the disease demonstrates an incredible lack of respect for the disaster created by the coronavirus GoF.

So you may be asking, what moron could possibly be oblivious enough to support GoF work on the Spanish Flu while the world is still dealing with the nightmare that is COVID? The answer should not be surprising and is here:

Mable Chan,ᵃ Meenakshi Tiwary,ᵇ,ᶜ Helen L. Wu,ᵇ,ᶜ Nikesh Tailor,ᵃ Robert Vendramelli,ᵃ Jonathan Audet,ᵃ Bryce M. Warner,ᵃ Kevin Tierney,ᵃ Alix Albietz,ᵃ Thang Truong,ᵃ Kaylie Doan,ᵃ Alexander Bello,ᵃ Marnie Willman,ᵃ Bryan D. Griffin,ᵃ,ᵈ Patrick W. Hanley,ᵉ Jamie Lovaglio,ᵉ David Safronetz,ᵃ,ᶠ Jim Strong,ᵃ,ᶠ Jonah B. Sacha,ᵇ,ᶜ Darwyn Kobasaᵃ,ᶠ

a. Special Pathogens, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada

b. Vaccine and Gene Therapy Institute, Oregon Health & Science University, Portland,

c. Oregon, USA Oregon National Primate Research Center, Oregon Health & Science University, Portland, Oregon, USA

d. Vaccine Safety Surveillance, Immunization Branch, Public Health Agency of Canada, Ottawa, Ontario, Canada

e. Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA

f. Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada

So, NIH and NIAID are involved. Apparently Fauci does not mind what he did with funding the creation of COVID and is at it again. You might also note the vaccine development crew’s involvement. A foundational point in this article is that the newly recreated Spanish Flu is not dangerous enough. Here is a pull-quote:

However, 1918 influenza was uniformly nonlethal in these two species, demonstrating that this isolate is insufficiently pathogenic in rhesus and Mauritian cynomolgus macaques to support testing novel prophylactic influenza approaches where protection from severe disease combined with a lethal outcome is desired as a highly stringent indication of vaccine efficacy.

This means that these people are arguing that we need to make a more dangerous version of the Spanish Flu so they can make “better” vaccines for it… despite the fact that until they recreated it, it likely no longer existed in nature. Much like with COVID, these snake oil salesmen create the disease and then create the cure. Given the complete failure and innumerable dangers of the COVID jabs, the real question is whether the cure will be worse than the disease?

For my part I find the fact that I am even writing this article to be incredible. In this election year I sincerely hope that this article is put in front of every elected official in Washington and they are asked to explain how this is continuing on their watch.

August 20, 2022 Posted by | Timeless or most popular, War Crimes | , , , , | 4 Comments

Head of the Lancet COVID-19 Commission discusses the likely Lab Origins of SARS-CoV-2

The Naked Emperor’s Newsletter | August 6, 2022

Professor Jeffrey Sachs is an American academic with specialities in economics, global poverty, human-induced climate change and financial crises. Jeffrey is University Professor at Columbia University and before this was professor at Harvard University. He has worked as Special Advisor to UN Secretaries-General Kofi Annan, Ban Ki-moon and Antonio Guterres.

The mini résumé above is to show that Professor Sachs is pretty mainstream. So mainstream in fact, that he was appointed, early in the pandemic, as the Chair of the Lancet Covid-19 Commission. So mainstream, that he appointed Peter Daszak of EcoHealth Alliance to chair the Lancet’s task force on the origins of SARS-CoV-2.

A few weeks ago, Professor Sachs said a few ‘controversial’ statements about the origins of Covid. Now, a more detailed interview with him, in Current Affairs, has revealed some important facts. Most of us have read much of this information for a few years now but coming from the head of the Lancet Commission, these statements are quite extraordinary.

Click on the link above to read the whole interview but I have included some fascinating quotations below.

When asked about his recent statement about being pretty convinced about a lab leak he said:

[Scientists are] creating a narrative. And they’re denying the alternative hypothesis without looking closely at it. That’s the basic point.

Now, what is the alternative hypothesis? The alternative hypothesis is quite straightforward. And that is that there was a lot of research underway in the United States and China on taking SARS-like viruses, manipulating them in the laboratory, and creating potentially far more dangerous viruses. And the particular virus that causes COVID-19, called SARS-Cov-2, is notable because it has a piece of its genetic makeup that makes the virus more dangerous. And that piece of the genome is called the “furin cleavage site.” Now, what’s interesting, and concerning if I may say so, is that the research that was underway very actively and being promoted, was to insert furin cleavage sites into SARS-like viruses to see what would happen. Oops!

Professor Sachs was asked to distinguish between facts and speculation; do we actually know gain of function research was actually ongoing somewhere?

We have a lot of reason to believe that it was, because the scientists that were doing that research loved that research. And they explained to us publicly why it’s so important. And they wrote editorials about why this research must continue. And they made grant proposals saying that it should continue. And for those of us in the business of writing grant proposals, the fact that a particular grant proposal that’s deeply troubling was turned down doesn’t mean that it wasn’t carried out afterwards…

And the scientists like those that talk about the Huanan market, they don’t even discuss that research that was underway. That is just misdirection, to my mind. It’s like sleight of hand art. Don’t look over there. Look over here…

And yet I see NIH with its head in the ground. “Oh, no, nothing here to look at.” And then I see the scientists. “Oh, nothing here to look at. We know it’s the market. Did we find an animal? No. Do we have an explanation of where that furin cleavage site came in? No. We don’t have an explanation of the timing, which doesn’t quite look right. Oh, but don’t look over there, because there’s nothing there, they keep telling us. Well, that’s a little silly.

What I’m calling for is not the conclusion. I’m calling for the investigation. Finally, after two and a half years of this, it’s time to fess up that it might have come out of a lab and here’s the data that we need to know to find out whether it did.

He continued about Gain of Function research.

But they [champions of Gain of Function research] weren’t actually aiming to just test viruses that they were collecting in nature. They were aiming to modify those viruses. Because the scientists knew that a SARS-like virus without a furin cleavage site wouldn’t be that dangerous. But they wanted to test their drugs and vaccines and theories against dangerous viruses. Their proposal was to take hundreds, by the way—or least they talked about in one proposal more than 180 previously unreported strains—and test them for their so-called “spillover potential.” How effective would they be? And to look: do they have a furin cleavage site, or technically what’s called a proteolytic cleavage site? And if not, put them in. For heaven’s sake. My God! Are you kidding?

Jeffrey was asked about the distinction between ‘kooky theories’ and plausible ones.

The right one to look at is part of a very extensive research program that was underway from 2015 onward, funded by the NIH, by Tony Fauci, in particular NIAID [National Institute of Allergy and Infectious Diseases], and it was to examine the spillover potential of SARS-like viruses. The champions of this research explained in detail their proposals. But after the event, we’d never asked them, “So what were you actually doing? What experiments did you do? What do you know?” We somehow never asked. It was better just to sweep it under the rug, which is what Fauci and the NIH have done up until this point. Maybe they could tell us, “Oh, full exoneration,” but they haven’t told us that at all. They haven’t shown us anything.  So there’s nothing “kooky” about it, because it’s precisely what the scientists were doing…

So you saw a narrative being created. And the scientists are not acting like scientists. Because when you’re acting like a scientist, you’re pursuing alternative hypotheses. And the scientists just wrote recently an op-ed saying the only evidence that this came out of a lab that’s been put forward is that it came in a city, Wuhan, where an institute was located. Well, that’s a lie. That is not the only coincidence that leads to this theory. What leads to this alternative hypothesis is the detailed research program the NIH funded that was underway in the years leading up to the outbreak. So I see the scientists absolutely trying to create a narrative and take our eyes off of another issue.

Next, he was asked about the research being undertaken in the Wuhan Institute of Virology.

We know that at the Wuhan Institute of Virology, the scientists there had been trained by American scientists to use advanced bioengineering methodologies. And in particular, we have scientists in North Carolina, Texas, and so forth who do this kind of research, believe in it, argue for it, and say that they don’t want any regulations on it and so on. And they were in close contact with Wuhan Institute of Virology, and they were part of a joint research group that was stitched together by something called EcoHealth Alliance. And EcoHealth Alliance was the kind of marriage maker between the American scientists and the Chinese scientists. That was the vehicle for funding from the U.S. government, especially from the National Institutes of Health, and especially from Tony Fauci’s unit, the NIAID.

When asked about EcoHealth Alliance, Professor Sachs admitted that he hired Peter Daszak to head the task force on the origins of Covid.

I thought, naively at the beginning, “Well, here’s a guy who is so connected, he would know.” And then I realized he was not telling me the truth. And it took me some months, but the more I saw it, the more I resented it.

And so I told him, “Look, you have to leave.” And then the other scientists in that task force attacked me for being anti-scientific. And I asked them: “What are your connections with all of this?” They didn’t tell me. Then when the Freedom of Information Act released some of these documents that NIH had been hiding from the public, I saw that people that were attacking me were also part of this thing. So I disbanded that whole task force. So my own experience was to witness close up how they’re not talking. And they’re trying to keep our eyes on something else. And away from even asking the questions that we’re talking about…

He [Peter Daszak] could have explained to me right from the beginning that there was a big research program and that they were manipulating the viruses, and here’s how. He could have given me the research proposals. And when I asked him for one of the research proposals, he said, “No, my lawyer says I can’t give it to you.” I said, “What? You’re heading a commission. We’re a transparent commission. You’re telling me your lawyer says you can’t give me your project proposal.” I said, “Well, then you can’t be on this commission. This is not even a close call.”

But there were so many other things. He was just filled with misdirection.

He concluded that we need far more oversight over Gain of Function work.

I can tell you one thing that I’ve learned from talking to a lot of scientists in the last couple of years: the technological capacity to do dangerous things using this biotechnology is extraordinary right now. So I want to know what’s being done. I want to know what other governments are doing, too, not just ours. I want some global control over this stuff.

Furthermore, he is disappointed with the information that, even he as the head of the commission, is able to obtain.

The most interesting things that I got as chair of the Lancet commission came from Freedom of Information Act (FOIA) lawsuits and whistleblower leaks from inside the U.S. government. Isn’t that terrible? NIH was actually asked at one point: give us your research program on SARS-like viruses. And you know what they did? They released the cover page and redacted 290 pages. They gave us a cover page and 290 blank pages! That’s NIH, for heaven’s sake. That’s not some corporation. That is the U.S. government charged with keeping us healthy.

A fascinating interview which I recommend you read in full.

August 6, 2022 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , , | 4 Comments

The Fauci/ COVID-19 Dossier. The 2002 SARS-CoV Patent.

By Dr. David Martin | May 28, 2022

Background

Over the past two decades, my company – M·CAM – has been monitoring possible violations of the 1925 Protocol for the Prohibition of the Use in War of Asphyxiating, Poisonous, or other Gases, and of Bacteriological Methods of Warfare (the Geneva Protocol) 1972 Convention on the Prohibition of the Development, Production, and Stockpiling of Bacteriological and Toxin Weapons and Their Destruction (the BTWC).

In our 2003-2004 Global Technology Assessment: Vector Weaponization M·CAM highlighted China’s growing involvement in Polymerase Chain Reaction (PCR) technology with respect to joining the world stage in chimeric construction of viral vectors. Since that time, on a weekly basis, we have monitored the development of research and commercial efforts in this field, including, but not limited to, the research synergies forming between the United States Centers for Disease Control and Prevention (CDC), the National Institutes for Allergies and Infectious Diseases (NIAID), the University of North Carolina at Chapel Hill (UNC), Harvard University, Emory University, Vanderbilt University, Tsinghua University, University of Pennsylvania, many other research institutions, and their commercial affiliations.

***

The National Institute of Health’s grant AI23946-08 issued to Dr. Ralph Baric at the University of North Carolina at Chapel Hill (officially classified as affiliated with Dr. Anthony Fauci’s NIAID by at least 2003) began the work on synthetically altering the Coronaviridae (the coronavirus family) for the express purpose of general research, pathogenic enhancement, detection, manipulation, and potential therapeutic interventions targeting the same. As early as May 21, 2000, Dr. Baric and UNC sought to patent critical sections of the coronavirus family for their commercial benefit.1 In one of the several papers derived from work sponsored by this grant, Dr. Baric published what he reported to be the full length cDNA of SARS CoV in which it was clearly stated that SAR CoV was based on a composite of DNA segments.

“Using a panel of contiguous cDNAs that span the entire genome, we have assembled a full-length cDNA of the SARS-CoV Urbani strain, and have rescued molecularly cloned SARS viruses (infectious clone SARS-CoV) that contained the expected marker mutations inserted into the component clones.”2

On April 19, 2002 – the Spring before the first SARS outbreak in Asia – Christopher M. Curtis, Boyd Yount, and Ralph Baric filed an application for U.S. Patent 7,279,372 for a method of producing recombinant coronavirus. In the first public record of the claims, they sought to patent a means of producing, “an infectious, replication defective, coronavirus.” This work was supported by the NIH grant referenced above and GM63228. In short, the U.S. Department of Health and Human Services was involved in the funding of amplifying the infectious nature of coronavirus between 1999 and 2002 before SARS was ever detected in humans.

Against this backdrop, we noted the unusual patent prosecution efforts of the CDC, when on April 25, 2003 they sought to patent the SARS coronavirus isolated from humans that had reportedly transferred to humans during the 2002-2003 SARS outbreak in Asia. 35 U.S.C. §101 prohibits patenting nature.

This legality did not deter CDC in their efforts. Their application, updated in 2007, ultimately issued as U.S. Patent 7,220,852 and constrained anyone not licensed by their patent from manipulating SARS CoV, developing tests or kits to measure SARS coronavirus in humans or working with their patented virus for therapeutic use. Work associated with this virus by their select collaborators included considerable amounts of chimeric engineering, gain-of-function studies, viral characterization, detection, treatment (both vaccine and therapeutic intervention), and weaponization inquiries.

In short, with Baric’s U.S. Patent 6,593,111 (Claims 1 and 5) and CDC’s ‘852 patent (Claim 1), no research in the United States could be conducted without permission or infringement.

We noted that gain-of-function specialist, Dr. Ralph Baric, was both the recipient of millions of dollars of U.S. research grants from several federal agencies but also sat on the World Health Organization’s International Committee on Taxonomy of Viruses (ICTV) and the Coronaviridae Study Group (CSG). In this capacity, he was both responsible for determining “novelty” of clades of virus species but directly benefitted from determining declarations of novelty in the form of new research funding authorizations and associated patenting and commercial collaboration. Together with CDC, NIAID, WHO, academic and commercial parties (including Johnson & Johnson; Sanofi and their several coronavirus patent holding biotech companies; Moderna; Ridgeback; Gilead; Sherlock Biosciences; and, others), a powerful group of interests constituted what we would suggest are “interlocking directorates” under U.S. anti-trust laws.

These entities also were affiliated with the WHO’s Global Preparedness Monitoring Board (GPMB) whose members were instrumental in the Open Philanthropy-funded global coronavirus pandemic “desk-top” exercise EVENT 201 in October 2019. This event, funded by the principal investor in Sherlock Biosciences and linking interlocking funding partner, the Bill and Melinda Gates Foundation into the GPMB mandate for a respiratory disease global preparedness exercise to be completed by September 2020 alerted us to anticipate an “epidemic” scenario.

We expected to see such a scenario emerge from Wuhan or Guangdong Province, China, northern Italy, Seattle, New York or a combination thereof, as Dr. Zhengli Shi and Dr. Baric’s work on zoonotic transmission of coronavirus identified overlapping mutations in coronavirus in bat populations located in these areas.

This dossier is by no means exhaustive. It is, however, indicative of the numerous criminal violations that may be associated with the COVID-19 terrorism. All source materials are referenced herein. An additional detailed breakdown of all the of individuals, research institutions, foundations, funding sources, and commercial enterprises can be accessed upon request.

Note

This work was supported, in part, by a fund-raising effort in which approximately 330 persons contributed funds in support of the New Earth technology team and Urban Global Health Alliance.

It is released under a Creative Commons license CC- BY-NC-SA. Any derivative use of this dossier must be made public for the benefit of others. All documents, references and disclosures contained herein are subject to an AS-IS representation. The author does not bear responsibility for errors in the public record or references therein. Throughout this document, uses of terms commonly accepted in medical and scientific literature do not imply acceptance or rejection of the dogma that they represent.

Copyright © Dr. David MartinDr. David Martin, 2022

May 28, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , , | Leave a comment

Evidence of Pandemic and Bioweapon Cover-Ups

By Dr. Joseph Mercola | April 7, 2022

As evidence of a potential bioweapons cover-up has started emerging, a company called Metabiota is gaining prominence. The links between Metabiota and several key players in the COVID pandemic and/or the Ukraine labs story are manifold, so there’s no really simple way to unravel it in a logical sequence. That said, let’s start with what Metabiota does and the connections of its founder, and expand from there.

Metabiota’s Mission

Metabiota’s mission is to make the world more resilient to epidemics by providing “data, analytics, advice and training to prepare for global health threats and mitigate their impacts.”1

Through data analysis, they help “decision makers across government and industry” to estimate and mitigate pandemic risks. But they also claim to support “sustainable development,” which seems to have little to do with pandemic risk management.

That term, “sustainable development,” is one promoted by Klaus Schwab, founder of the World Economic Forum (WEF). It’s part and parcel of Schwab’s plan for a global Great Reset and transhumanist revolution (aka, the Fourth Industrial Revolution).

It’s not surprising, then, to find out that the founder of Metabiota, Nathan Wolfe, not only has close ties to the WEF, but is also a rising star there. He’s a WEF Young Global Leader graduate and was awarded the WEF’s Technology Pioneer award in 2021.

Metabiota and the Search for Pandemic Viruses

Metabiota was a core partner of a United States Agency for International Development’s (USAID) Pandemic Threat Program called PREDICT, which sought to identify viruses with pandemic potential.

Contractors funded through this program have included the EcoHealth Alliance, headed by Peter Daszak. The PREDICT program, directed by Dennis Carroll, appears to have served as a proof of concept for the Global Virome Project that Carroll founded.

According to a recent investigation by U.S. Right to Know (USRTK),2 Carroll appears to have diverted government funds from the PREDICT program while he was still running it, to fund this personal side project, which was set up with the intention to collect, identify and catalogue 1 million viruses from wildlife in an effort to predict which ones might cause a human epidemic.

Metabiota’s Funding

Metabiota receives funding from several interconnected organizations and agencies, including:3

Pilot Growth Management, cofounded by Neil Callahan. Callahan is also a cofounder of Rosemont Seneca Technology Partners, and he sits on Metabiota’s board of advisers

The Global Virome Project, which reportedly paid (or was planning to pay) Metabiota $341,000 to conduct a cost-benefit analysis4

In-Q-Tel, a CIA venture capital firm that specializes in high-tech investments that support or benefit the intelligence capacity of U.S. intelligence agencies

The U.S. Department of Defense’s Threat Reduction Agency (DTRA).5 Specifically, in 2014, DTRA awarded Metabiota $18.4 million in federal contracts for scientific and technical consulting services to the DTRA’s labs in Ukraine and Georgia6

By outsourcing work to private companies, DTRA is able to circumvent Congressional oversight. Russia is now accusing the U.S. of funding secret and illegal bioweapons research in these Ukraine labs, and claims this was the real reason behind its invasion

Rosemont Seneca,7 an investment fund co-managed by Hunter Biden.8 If Russia’s accusations turn out to be true, this tie may prove deeply problematic for the White House, as this means the Biden family was more or less directly involved in the funding of that research

Wolfe has also received more than $20 million in research grants from Google, the NIH and the Bill & Melinda Gates Foundation, just to name a few, and was a friend of now-deceased Jeffrey Epstein. In his 2012 book, “The Viral Storm,” Wolfe thanked friends for their support, including Epstein and Boris Nikolic. Nikolic, a biotech venture capitalist, was named “back-up executor” in Epstein’s will.9

Epstein, who besides being a convicted pedophile and accused child sex trafficker, had a robust interest in eugenics. It’s now well-known that he dreamed of creating a “superhuman” race of his own by impregnating dozens of women at a time at his New Mexico ranch.10 Epstein also managed to secure meetings with Bill Gates,11 whose family history is also marked by an interest in eugenics and population control.

Metabiota’s Founder Tied to Suspect in COVID Pandemic

In addition to having close ties to the WEF and its Great Reset agenda, Wolfe, the founder of Metabiota, has also served on the EcoHealth Alliance’s editorial board since 2004. In 2017, he even co-wrote a study on coronaviruses in bats together with EcoHealth Alliance president, Peter Daszak.

As you may recall, EcoHealth Alliance, a nonprofit organization focused on pandemic prevention, worked closely with the Wuhan Institute of Virology (WIV) in China, where SARS-CoV-2 is suspected of having originated.12

Daszak — who received funding for coronavirus research from the National Institute of Allergy and Infectious Diseases (NIAID), led by Dr. Anthony Fauci, and the U.S. State Department13 — subcontracted some of that work to Shi Zheng-li at the WIV. He was also the coauthor on research projects at the WIV.

Once rumors of SARS-CoV-2 being man-made first began, Daszak played a central role in the plot to obscure the lab origin by crafting a scientific statement condemning such inquiries as “conspiracy theory.”14,15 This manufactured “consensus” was then relied on by the media to counter anyone presenting theories and evidence to the contrary.

This, despite the fact that he, in 2015, warned that a global pandemic might occur from a laboratory incident — and that “the risks were greater with the sort of virus manipulation research being carried out in Wuhan”!16

In 2021, two investigations into the origins of the COVID pandemic were opened, one by the World Health Organization17 and another by The Lancet,18 and Daszak somehow managed to end up on both of these committees, despite having openly and repeatedly dismissed the possibility of the pandemic being the result of a lab leak.19

Editor’s note: The WHO reference has been scrubbed from both the agency’s website and internet archives, but several news stories like this one from NPR,20 published after the investigation was launched, are still live and accessible.

Interestingly, one of EcoHealth Alliance’s policy advisers is a former Fort Detrick commander named David Franz. Fort Detrick is the principal U.S. government-run “biodefense” facility, although Franz himself has publicly admitted that “in biology … everything is dual use — the people, the facilities and the equipment.”21

Metabiota and the DTRA

In late May 2016, Metabiota hired Andrew C. Weber,22 a member of the Council on Foreign Relations, to head up its Global Partnerships.23 Between 2009 and 2014, Weber served as assistant secretary of defense for Nuclear, Chemical and Biological Defense under then-president Obama.

Weber is credited with creating the Defense Threat Reduction Agency (DTRA) — a combat support agency within the U.S. DoD, specializing in countering weapons of mass destruction, including biological weapons24,25 — and as mentioned earlier, the DTRA has reportedly funded Metabiota to operate U.S.-funded biological research labs in Ukraine.

The DTRA has also issued a number of grants to the EcoHealth Alliance, totaling at least $37.5 million,26,27 including a 2017 grant for $6.5 million to “understand the risk of bat-borne zoonotic disease emergence in Western Asia.”28

According to a December 2020 report by The Defender,29 EcoHealth Alliance had tried to hide most of the Pentagon funding that it had received between 2013 and 2020, most of which came from the DTRA.

Metabiota’s Bungled Ebola Response

In 2016, CBS News published a scathing critique of Metabiota’s response to the 2014 Ebola epidemic in West Africa.30 Metabiota had been hired by the WHO and the local government of Sierra Leone to monitor the spread of the epidemic, but according to an investigation by The Associated Press, “some of the company’s actions made an already chaotic situation worse.”

In a July 17, 2014, email obtained by AP, Dr. Eric Bertherat, medical officer at the WHO’s Department of Epidemic and Pandemic Alert and Response, complained about misdiagnoses and “total confusion” at the small laboratory Metabiota shared with Tulane University in Kenema, Sierra Leone.

According to Bertherat, there was “no tracking of the samples” and “absolutely no control on what is being done.” “This is a situation that WHO can no longer endorse,” he wrote. Similarly, Sylvia Blyden, special executive assistant to the president of Sierra Leone, told AP Metabiota’s response was a disaster:31

“’They messed up the entire region,’ she said. She called Metabiota’s attempt to claim credit for its Ebola work ‘an insult for the memories of thousands of Africans who have died.’”

U.S. health official Austin Demby, who evaluated Metabiota’s and Tulane’s lab work at the request of the U.S. Centers for Disease Control and Prevention and the government of Sierra Leone, was also critical.

In one email, Demby noted used needles were left out and there was no ultraviolet light for decontamination. The space was also too small to safely process blood samples. “The cross-contamination potential is huge and quite frankly unacceptable,” he wrote.

Anja Wolz, an emergency coordinator with Doctors Without Borders, told AP she witnessed Metabiota workers entering homes of suspected Ebola patients without protective gear, and leaving high-risk areas without performing any kind of decontamination procedure. She also accused Metabiota of miscalculating the severity of the outbreak, while insisting that they had the situation under control when clearly, they didn’t.

Tulane microbiology professor Bob Garry was also critical of Metabiota’s choice to have Dr. Jean-Paul Gonzalez run the operation, as Gonzalez, in 1994, had accidentally gotten infected with a rare hemorrhagic fever while working in a Yale University lab.

He failed to notify anyone about the exposure for more than a week, a delay that put more than 100 other people at risk. Gonzalez was ordered to take a remedial safety course, but according to Garry, such carelessness was a red flag, and he didn’t think Gonzalez was the right man to teach Sierra Leoneans about Ebola.

“Do you really want the person who infected himself with hemorrhagic fever going around explaining to people how to be safe?” Garry asked in an email to a Metabiota media representative. Wolfe defended his company, saying there was no evidence they’d done anything wrong. Some of the problems he blamed on misunderstandings, and others on commercial rivalry.

Lab Accident ‘Most Likely,’ yet Least Probed Cause of COVID

In a March 28, 2022, report,32 U.S. Right to Know (USRTK) revealed the contents of a 2020 State Department memo33 obtained by the group. USRTK writes:34

“‘Origin of the outbreak: The Wuhan labs remained the most likely but least probed,’ reads the topline. The memo is written as a BLUF — ‘bottom line up front’ — a style of communication used in the military. The identity of the author or authors is unknown …

‘BLUF: There is no direct, smoking gun evidence to prove that a leak from Wuhan labs caused the pandemic, but there is circumstantial evidence to suggest such is the case,’ the memo reads. Apparently drafted in spring 2020, the memo details circumstantial evidence for the ‘lab leak’ theory — the idea that COVID-19 originated at one of the labs in Wuhan, China, the pandemic’s epicenter.

The memo raises concerns about the ‘massive amount’ of research on novel coronaviruses apparently conducted at the Wuhan Institute of Virology and the nearby Wuhan Center for Disease Control lab … The memo also flags biosafety lapses at both labs, calling the Wuhan Institute of Virology’s ‘management of deadly viruses and virus-carrying lab animals … appallingly poor and negligent.’

The memo provides an extraordinary window into behind-the-scenes concerns about a lab accident among U.S. foreign policy leaders, even as this line of inquiry was deemed a conspiracy theory by international virologists, some of whom had undisclosed conflicts of interest.

The memo also calls into question these virologists’ impartiality. Shi Zhengli, a Wuhan Institute of Virology coronavirus researcher nicknamed the ‘Bat Woman,’ has forged wide-reaching international collaborations, including with prestigious Western virologists, the memo notes.

‘Suspicion lingers that Shi holds an important and powerful position in the field in China and has extensive cooperation with many [international] virologists who might be doing her a favor,’ it reads …

The memo laments that ‘the most logical place to investigate the virus origin has been completely sealed off from inquiry by the [Chinese Communist Party]’ … The memo even suggests that other hypotheses may have served as a distraction from a probe of the city’s extensive research on novel coronaviruses. ‘All other theories are likely to be a decoy to prevent an inquiry [into] the WCDC and WIV,’ it states …

The memo cites a 2015 paper35 coauthored by Shi titled ‘A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence’ that described creating a ‘chimera,’ or engineered virus, with the spike protein of a coronavirus from a Chinese horseshoe bat.

Editors at Nature Medicine added a note in March 2020 cautioning that the article was ‘being used as the basis for unverified theories that the novel coronavirus causing COVID-19 was engineered’ … But the memo shows that the State Department indeed considered the paper relevant to the pandemic’s origins.”

NIH Retracted Gene Sequence at WIV Researcher’s Request

While we’ve yet to obtain bulletproof evidence that SARS-CoV-2 was developed as a bioweapon, there’s plenty of circumstantial evidence that points in that direction. Disturbingly, as time goes on, more and more of this circumstantial evidence seems to highlight the United States’ involvement. If one proverbial finger is pointing at China, four others are pointing back at us.

This is profoundly bad news, but it really ought to strengthen our resolve to get to the bottom of it. None of us are safe until the mad scientists responsible for this pandemic are brought to justice. It doesn’t matter who they are. In all likelihood, we’ll find that blame cannot be pinned on a single nation. At bare minimum, the U.S. and China appear to be covering for each other.

As just one example, there are the deletions of information that have occurred both at the National Institutes of Health and the WIV, either at the other’s request, or as what appears to be a favor.

As reported by Just the News,36 NIH deleted a genetic sequencing submission of SARS-CoV-2 from its Sequence Read Archive (SRA) at the request of a researcher at the WIV. Emails37 obtained via FOIA request to the NIH by Empower Oversight show a WIV researcher who had submitted two genetic sequences to the SRA, one in March 2020, and a second in June 2020, asked to have the last one retracted.

NIH initially stated that it would be better to edit or replace the submission rather than retracting it, but the researcher insisted it be removed, which they did. To be fair, the NIH also states it has retracted at least eight SRA submissions in total, most from American researchers, at their request. However, emails also show the NIH directed reporters on how to provide more favorable and less sensationalized coverage of the deletion of the Chinese sequence. Just the News writes:38

“[Empower Oversight] says one of the most disconcerting elements of the emails is evidence showing the NIH has refused to participate in a transparent process to examine data on the deleted sequences.

‘Most importantly, why has NIH refused to examine archival copies of deleted sequences in an open scientific process to determine whether any of that information might be able to shed light on the origins of the COVID-19 pandemic?’ the group asked.

However, that argument was dismissed by NIH official Steve Sherry. Although sequences are never fully deleted, according to the agency, Sherry told a researcher who asked for transparency, ‘As you know, when data sets are withdrawn from the database, that status does not permit use for further analyses.’”

WIV Deleted Mentions of US Collaborators

The WIV has also deleted information in what appears to be an effort to shield the NIH. Shortly after Fauci testified in a Senate hearing in March 2021,39 the WIV quietly deleted all mentions of its collaboration with Fauci’s NIAID, the NIH and other American research partners from its website. As reported May 15, 2021, by The National Pulse :40

“March 21st, 2021, the lab’s website listed six U.S.-based research partners: University of Alabama, University of North Texas, EcoHealth Alliance, Harvard University, the National Institutes of Health (NIH), the United States, and the National Wildlife Federation.41

One day later, the page was revised to contain just two research partners — EcoHealth Alliance and the University of Alabama.42 By March 23rd, EcoHealth Alliance was the sole partner remaining.43

EcoHealth Alliance is run by long-standing Chinese Communist Party-partner Dr. Peter Daszak, who National Pulse Editor-in-Chief Raheem Kassam has repeatedly claimed will be the first ‘fall guy’ of the Wuhan lab debacle …

Beyond establishing a working relationship between the NIH and the Wuhan Institute of Virology, now-deleted posts44 from the site also detail studies bearing the hallmarks of gain-of-function research conducted with the Wuhan-based lab.”

Indeed, a now-deleted WIV web page titled “Will SARS Come Back?” stated that:45

“Prof. Zhengli Shi and Xingyi Ge from WIV, in cooperation with researchers from University of North Carolina, Harvard Medical School, Bellinzona Institute of Microbiology … examine the disease potential of a SARS-like virus, SHC014-CoV, which is currently circulating in Chinese horseshoe bat populations.

Using the SARS-CoV reverse genetics system, the scientists generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone.

The results indicate that group 2b viruses encoding the SHC014 spike in a wild-type backbone can efficiently use multiple orthologs of the SARS receptor human angiotensin converting enzyme II (ACE2), replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV.

Evaluation of available SARS-based immune-therapeutic and prophylactic modalities revealed poor efficacy; both monoclonal antibody and vaccine approaches failed to neutralize and protect from infection with CoVs using the novel spike protein.

On the basis of these findings, they synthetically re-derived an infectious full-length SHC014 recombinant virus and demonstrate robust viral replication both in vitro and in vivo …”

The WIV’s deletions of American research partners from its website (with the exception of EcoHealth Alliance), and its deletion of the article discussing genetic research on the SARS virus only served to strengthen suspicions of a cover-up. At the time, the most surprising thing about it was that they were covering up American involvement and not just their own.

Are We the Bad Guys?

Alas, as noted by Maajid Nawaz,46 a former Islamist revolutionary who became an anti-extremism activist, if it turns out that the U.S. did in fact engage in illegal bioweapons development in Ukraine, it might just turn out that we’re the bad guys here. He writes, in part:47

“On the 24th February 2022, the very day of Russia’s invasion, some of us were already worried about the prospect of biological weapons laboratories existing in Ukraine …

The existence of bio-weapons labs on Ukraine’s border with Russia has since been confirmed by both Russia and the US (I say both because the Ukrainian government is essentially serving as a US proxy). The only remaining question is around what we were doing in those laboratories.

It is no longer in doubt that we funded bio-weapons research in the Wuhan lab in China, from where it is now believed that COVID most likely leaked from. So were we doing the same in Ukraine too? Russia has certainly made the allegation …

The official representative of the Russian Ministry of Defense, Major General Igor Konashenkov stated48 ‘In the course of a special military operation, the facts of an emergency cleansing by the Kiev regime of traces of a military biological program being implemented in Ukraine, funded by the US Department of Defense, were uncovered.’

With this, he released this document drop49 alleging … that these papers substantiated their case. If Russia’s allegations hold up, the US and her proxy Ukrainian regime would be in violation of the first article of the UN Convention on the Prohibition of Bacteriological (Biological) and Toxin Weapons.50

Russia’s announcement appears to have forced America’s hand to admit that such bio labs do indeed exist. US Undersecretary of State Victoria Nuland framed this admission by stating that these labs were for defensive research only.

Under Secretary Nuland however continued to make the case that such labs would be dangerous if they fell into Russian hands, without apparently noticing the contradiction inherent in her position that such labs are only dangerous because they can be weaponized …

Matching Russian precision strikes to a map of bio lab locations inside Ukraine certainly does suggest that Putin’s ‘special military operation’ appears to be targeting some of these dangerous labs.”

Indeed, Nawaz highlights a 2021 Ukrainian petition51,52 to president Zelensky, asking for a) the immediate closure of “American bio-laboratories in the territory of Ukraine,” b) an investigation into the activities of those labs, and c) an investigation into potential Ukrainian participation in the creation of SARS-CoV-2.

In other words, at least some Ukrainians, by 2021, were wondering whether the U.S. labs in their country might have been involved in the creation of this pandemic.

Denouncements Ring Hollow

Not surprisingly, the U.S. State Department took a hard line, denouncing all allegations with the statement that “The United States does not have chemical and biological weapons labs in Ukraine.”53 In another statement,54 the State Department “clarified” that the labs were for “biodefense,” not biological weapons, thus semantically cleansing their criminal activities.

The problem with that is that there’s no hard line between biodefense and bioweapons research. As admitted by EcoHealth Alliance’s policy advisor and former Fort Detrick commander David Franz, it’s all “dual use — the people, the facilities and the equipment.”55 Biodefense implies biowarfare, as it involves the creation of more dangerous pathogens for the alleged purpose of finding treatments against them.

Bioweapons expert Francis Boyle, who drafted the Biological Weapons Anti-Terrorism Act of 1989, has also pointed out that most BSL-4 labs are dual use: “They first develop the offensive biological warfare agent and then they develop the supposed vaccine.”56 And then, there’s the weapons proliferation agreement57 between the U.S. and Ukraine, signed at the end of August 2005.

Incidentally, former President Barrack Obama spearheaded the project to construct these Ukrainian labs back in 2005, when he was still a senator and, curiously, the online announcement of his involvement in this project has also been deleted from the web.58

According to this agreement, the U.S. Department of Defense will assist the Ministry of Health in Ukraine, at no cost, to prevent “proliferation of technology, pathogens and expertise” found in a number of Ukraine labs, that “could be used in the development of biological weapons.”

The Burning Question of Intent

So, the agreement itself clarifies that they’re working on pathogens that COULD be used as biological weapons, and Nuland’s stated concerns back this up. The only question remaining then is one of intention. What’s the intended use of these pathogens? Defense? Or offense? And is there really a difference?

As noted by Nawaz, the U.S. clinging to the defense of “biodefense” and anti-bioweapons proliferation is “the equivalent of denying that Einstein’s discovery of splitting the atom to generate energy is not also something that could be used to make nuclear weapons. After the COVID outbreak, the notion that bio labs can be weaponized should simply be presumed as a rule.”

Also, consider the network of players reviewed earlier. The Ukrainian-American collaboration to study pathogens capable of weaponization is run by the DTRA, which funds Metabiota, which is run by a WEF leader with close personal ties to the one person — Daszak — suspected of being a key player in the creation of SARS-CoV-2, a go-between of the NIH and the WIV, and a central force in the cover-up of the lab leak theory.

Interestingly, Metabiota is also financially backed by Hunter Biden’s investment company, and let’s not forget that young Biden also collected a six-figure salary from a Ukrainian gas company for doing literally nothing, other than supplying his “powerful name.”59

Circumstantial or not, it just doesn’t look good. And, by now, it should be crystal clear that any lab doing defensive work is equally capable of churning out offensive weapons. Debating that point is just silly, as it all boils down to semantics.

According to Bulgarian journalist Dilyana Gaytandzhieva, Metabiota is a key player in the Ukrainian labs. David Horowitz, a political writer, has noted that Metabiota is “a company that tracks the trajectory of outbreaks and sells pandemic insurance, but also seems to have its hand in the actual labs that … might be the source of some of these outbreaks.”60

In other words, could it be that Metabiota has been producing biological agents under diplomatic cover and then selling pandemic insurance and pandemic trackers to “help countries get ahead of what they are putting out”?61

Nawaz asks, “was ensuring that a ‘next pandemic’ doesn’t occur by taking out these bio labs, what Putin had in mind by his phrase ‘special military operation’?”62 At this point, it seems a valid question.

Sources and References

April 7, 2022 Posted by | Deception, Militarism, Timeless or most popular, War Crimes | , , , , , , , , , , | 1 Comment

Pharma now kills more Americans every year than the Axis powers did in all of World War II

This is normalized, monetized, and usually publicly-funded

By Toby Rogers | March 13, 2022

Let’s talk about the big picture of Pharma’s war against humanity. It is happening throughout the developed world but for the purposes of this article I will focus on data from the U.S.

🚩 FDA-approved drugs, when used as directed, kill about 100,000 Americans every year. (Gøtzsche, 2013, p. 259).

🚩 Hospital errors kill another 100,000 to 150,000 Americans every year. (Makary & Daniel, 2016).

🚩 Opioid overdoses killed 75,693 Americans last year (CDC, 2021).

🚩 Coronavirus shots killed an estimated 150,000 Americans in 2021 (Kirsch, Rose, and Crawford, 2021).

🚩 A gain-of-function virus created in a bioweapons lab in Wuhan, China funded by Tony Fauci killed 350,831 Americans in 2020 and another 615,387 Americans since the introduction of Covid-19 shots in Dec. 2020. About 90% of those fatalities could have been prevented with early treatment. But the regulatory agencies and the medical establishment blocked access to early treatment in order to create the market for deadly Covid-19 shots.

To put this in perspective — in World War II, the Nazis, the Royal Italian Army, and the Imperial Japanese Army killed 405,399 Americans in the space of four years.

In the last two years, Pharma, the corrupt medical establishment, and the captured regulatory agencies are killing about twice that many Americans each year.

That’s what we are up against.

So the problem is not a few bad actors (although there are plenty of those). The problem is that the entire system is rotten:

🚩 The pharmaceutical industry makes terrible products. Political capture is more profitable than innovation, so that’s what they do. The captured regulatory agencies — FDA, CDC, NIAID, NIH — engage in data laundering to make pharmaceutical products appear better than they are. Iatrogenic fatalities are just the tip of the iceberg. Pharmaceutical products also cause cancer, disability, and chronic illness.

🚩 Profit-driven hospitals with their military hierarchy and cult-like work practices are dangerous places.

🚩 The pharmaceutical industry is committing genocide via opioids in economically depressed towns throughout the rust-belt and Appalachia — because it is profitable to do so and because they see poor people as undesirable and expendable.

🚩 The pharmaceutical industry has engaged in genocide via the childhood vaccination schedule since they received liability protection in 1986 — because creating chronic illness in kids is their core business model.

🚩 Under the guise of Covid, the pharmaceutical industry has expanded the genocide to all Americans and people throughout the developed world — by blocking access to effective treatments and injecting people with dangerous genetically modified substances.

🚩 All of bourgeois society — academia, the media, the medical and scientific establishment, government, and Wall Street — conspire to cover up these crimes that now impact nearly every American family in some way.

When we take power we must dismantle this system, prosecute those who created it, and build a decentralized alternative based on actual health.

March 13, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , , , | 2 Comments

Moderna Patented Key COVID Spike Protein Sequence in 2016

By Dr. Joseph Mercola | March 7, 2022

The facts surrounding SARS-CoV-2’s origin just keep getting stranger and more disturbing as time goes on. From the start, most of the evidence seemed to point to the virus being a lab creation that somehow escaped the confines of the laboratory. We really don’t have much of anything to suggest otherwise.

Now, a study1,2 published February 21, 2022, in Frontiers in Virology claims to have discovered that a sequence of the virus’ spike protein is a 100% match to a modified messenger RNA (mmRNA) sequence patented3 by Moderna — in 2016.

Some believe this is a smoking gun, proving gain of function research is at the heart of this mystery. Of course, more research is needed to verify the findings, but if proven correct, it could be rather incriminating.

What Did Moderna Patent?

The genetic sequence patented4 by Moderna — and now found to be part of the SARS-CoV-2’s furin cleavage site in the spike protein that gives the virus access into human cells — is a 19-nucleotide sequence of a human gene called MSH3, which is a DNA repair gene.5

Nucleotides code for specific amino acids. The MSH3 gene works with the part of your immune system responsible for combating cancer by repairing damaged cells. This pathway has been identified as a potential target for new cancer treatments.

As noted in the patent application, the gene sequence has been modified “for the production of oncology-related proteins and peptides,” ostensibly for use in cancer research. The first name listed on the patent is Stéphane Bancel, a Frenchman who has been Moderna’s chief executive officer since 2011.

What’s so curious here is that the scientists of the Frontiers in Virology paper searched all viral and bacterial databases looking for matches to the furin cleavage site patented by Moderna, and SARS-CoV-2 is the only pathogen that has this sequence. It’s an absolute match — 100% identical.

What are the chances of a naturally-occurring virus having a rarely encountered furin cleavage site that is genetically identical to an engineered and patented one? As noted by the authors:6

“The absence of CTCCTCGGCGGGCACGTAG from any eukaryotic or viral genome in the BLAST database makes recombination in an intermediate host an unlikely explanation for its presence in SARS-CoV-2.”

In other words, the sequence being a natural zoonosis is extremely unlikely. According to the researchers, the chance that SARS-CoV-2 would have randomly acquired this furin cleavage site through natural evolution is 1 in 3 trillion.7 They also noted that “Recombination in an intermediate host is an unlikely explanation.” What’s more, it’s known that inserting a furin cleavage site on the spike protein of a virus will make it more infectious.

Moderna CEO Suggests Lab Leak Responsible for COVID-19

One hypothesis raised in the paper is that the matching code might have been introduced into the SARS-CoV-2 genome through infected human cells that express the MSH3 gene. The question, then, is how and when did that happen?

Interestingly, in a February 24, 2022, interview, Fox Business host Maria Bartiromo questioned Bancel about the finding. He responded saying their scientists are looking into the claim, adding:

“That it came from a lab is possible. Humans make mistakes. It’s possible that the Wuhan lab in China was working on virus enhancement or gene modification and then there was an accident where somebody was infected in the lab, which affected family and friends. It is possible. On the claim you just mentioned, scientists will look to know if it’s real or not.”

Why This Code?

Now, if SARS-CoV-2 was man-made, why would they use this particular code? As noted in the Frontiers of Virology paper, the MSH3 sequence in question has been shown to cause mismatch repair in DNA, and faulty repair of genetic damage can lead to a number of diseases, including cancer. But overexpression of MSH3 also plays a role in virology:

“Overexpression of MSH3 is known to interfere with mismatch repair … which holds virologic importance. Induction of DNA mismatch repair deficiency results in permissiveness of influenza A virus (IAV) infection of human respiratory cells and increased pathogenicity. Mismatch repair deficiency may extend shedding of SARS-CoV-2 …

A human-codon-optimized mRNA encoding a protein 100% homologous to human MSH3 could, during the course of viral research, inadvertently or intentionally induce mismatch repair deficiency in a human cell line, which would increase susceptibility to SARS-like viral infection.”

It’s interesting to note that Moderna did not have a single successful mRNA product brought to market before the COVID-19 pandemic allowed them to bypass normal regulatory requirements.

Now, all of a sudden, we’re to believe they managed to throw together a safe and effective mRNA injection against SARS-CoV-2, a virus that just so happens to contain one of its own patented components. What are the odds?

Did Dr. Anthony Fauci, a leading promoter of mRNA technology as a replacement for traditional vaccines, have anything to do with Moderna’s sudden “success”? It certainly looks that way. After all, the National Institutes of Allergy and Infectious Diseases (NIAID), an arm of the National Institutes of Health (NIH), both funded and co-developed Moderna’s COVID-19 jab.

As explained by the NIH,8 the injection “combines Moderna’s mRNA delivery platform with the stabilized SARS-CoV-2 spike immunogen (S-2P)9 developed by NIAID scientists.” In mid-November 2021, Moderna granted co-ownership of its COVID-19 mRNA “vaccine” patent to the NIH to resolve a dispute involving the naming of the inventors.10

Can the COVID Jab Trigger Cancer?

Incidentally, since the release of the mRNA COVID jab, some doctors have raised concerns about the possibility of the injections to trigger cancer, largely due to its detrimental impact on your immune function.

For clarity, this may have nothing to do with Moderna’s patented MSH3 sequence specifically, because the RNA code in the jab is not identical to the RNA code of the actual virus. The RNA in the jab has been genetically altered yet again to resist breakdown and ensure the creation of abundant copies of the spike protein.11

So far, the link to cancer post-jab seems to be related to the downregulation of toll-like receptor 4 (TLR4), which is involved in both infections and cancer. In an October 2021 article, Dr. Nicole Delépine, a French pediatric oncologist,12 discussed reports of exploding cancer cases post-jab:13

“Several months ago, we expressed at least “theoretical reservations” about vaccinating cancer patients or former patients who had been cured, because of the underlying mechanism of the gene injection on immunity.

Several geneticists had also expressed their concerns about the possible interference between active or dormant cancer cells and the activity of gene therapy on lymphocytes in particular. Months have passed, and the vaccine madness has amplified … [C]learly there seems to be three situations:

The appearance of a cancer rapidly after the injection (two weeks to a few months) and very progressive, in a person who was previously free of known carcinological pathologies.

The resumption of cancer in a patient who has been in complete remission for several months or years.

The rapid, even explosive, evolution of a cancer that is not yet controlled.

Beyond the testimonies that are pouring in from relatives and friends and on social networks, a Swiss newspaper has finally addressed the subject in a broader way. Here are some excerpts from their article and their references:

‘Can COVID vaccines cause cancer? In some cases, the answer seems to be yes … [It] has been shown that in up to 50% of vaccinees, COVID vaccines can induce temporary immunosuppression or immune dysregulation (lymphocytopenia) that can last for about a week or possibly longer.

Furthermore, COVID mRNA vaccines have shown to ‘reprogram’… adaptive and innate immune responses and, in particular, to downregulate the so-called TLR4 pathway, which is known to play an important role in the immune response to infections and cancer cells.

Thus, if there is already a tumor somewhere — known or unknown — or if there is a predisposition to a certain type of cancer, such a state of vaccine-induced immune suppression or immune dysregulation could potentially trigger sudden tumor growth and cancer within weeks of vaccination …’”

Dr. Ryan Cole, in August 2021, also reported14,15 seeing a significant increase in certain types of cancer, especially endometrial and uterine cancers, since the start of the mass injection campaign. Cole runs a large pathology laboratory in Idaho.

Other Key Components of SARS-CoV-2 Have Also Been Patented

Time will tell where this all leads, but clearly, SARS-CoV-2 does not appear to be the result of natural evolution. The evidence for it being man-made is simply overwhelming. So far, few in mainstream media have been willing to touch this story, for obvious reasons.

Finding a key gene sequence of the virus in a patent of one of the primary vaccine makers is inconvenient to say the least — and this is in addition to all the other patents relating to the virus.

As previously detailed16 by David Martin, Ph.D., SARS-CoV-2 appears to have been engineered in the 1990s, perfected in 1999 and patented in 2002. Evidence also shows that plans for mandatory vaccinations were hatched in 2015. That year, during an Academies of Science meeting, Dr. Peter Daszak, president of EcoHealth Alliance stated:

“… until an infectious disease crisis is very real, present, and at an emergency threshold, it is often largely ignored. To sustain the funding base beyond the crisis, we need to increase public understanding of the need for MCM’s [medical countermeasures] such as pan-influenza or pan-coronavirus vaccine.

A key driver is the media, and the economics follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of [the] process.”

According to Martin, “That’s admission of a felony, and the felony is domestic terrorism.” In a November 2021 Red Pill Expo speech,17 Martin reviewed the timeline of the COVID-19 jab, which began in 1990 with the first coronavirus vaccine patent for canines (dogs) filed by Pfizer.

That vaccine was an S-1 spike protein vaccine — just like the current Pfizer COVID shot, and according to Martin, that S-1 spike protein is a bioweapon, not a pathogen. Nine years later, in 1999, Fauci, as director of the NIAID, tasked the University of North Carolina Chapel Hill with the creation of “an infectious replication-defective coronavirus” specifically targeted for human lung epithelium.

The patent for that replication-defective coronavirus that attacks human lung cells, filed April 19, 2002, (Patent No. 7279327), details the gene sequencing of the resulting virus, and how the ACE receptor, the ACE2 binding domain and the S-1 spike protein were engineered and could be synthetically modified in the lab using readily available gene sequencing technologies.

Basically, computer code is turned into a manmade pathogen, or an intermediate pathogen. This technology was initially funded in order to harness the coronavirus as a vector for an HIV vaccine, but it clearly didn’t end there.

CDC Holds Patents on SARS Coronavirus

The U.S. Centers for Disease Control and Prevention also holds key patents, including an illegally obtained patent for the entire gene sequence for the SARS coronavirus (Patent No. 7220852), which Martin says is 99% identical to the sequence now identified as SARS-CoV-2.

That CDC patent also had several derivative patents associated with it, including U.S. patent 46592703P and U.S. patent 7776521, which cover the gene sequence of SARS coronavirus and the means for detecting it using RT PCR testing. With these two patents, the CDC has complete scientific control, as it owns the provenance of both the virus and its detection.

According to Martin, there’s also evidence of a criminal conspiracy involving the CDC and Sequoia Pharmaceuticals. April 28, 2003 — three days after the CDC filed its patent for the SARS coronavirus — Sequoia Pharmaceuticals filed a patent on an antiviral agent for the treatment and control of infectious coronavirus (Patent No. 7151163).

So, the CDC filed a patent on SARS coronavirus, and three days later there’s a treatment? This strongly suggests there was a working relationship behind the scenes. Sequoia Pharmaceuticals, founded in 2002, develops antiviral therapeutics with a special focus on drug-resistant viruses.18 Its lead investors include the Wellcome Trust.

But there’s yet another problem with Sequoia’s 2003 filing for an antiviral agent. It was actually issued and published before the CDC patent on SARS coronavirus had been granted, which didn’t happen until 2007, and the CDC had paid to keep the application private.

So, there is zero possibility for anyone but an insider to have that information. This is clear evidence of criminal conspiracy, racketeering and collusion, Martin notes. You cannot develop a treatment for something that you do not know exists.

Sanofi also owns a series of patents detailing what we’ve been told are novel features of SARS-CoV-2, namely the polybasic cleavage site, the spike protein and the ACE2 receptor binding domain. The first of those patents, U.S. Patent No. 9193780, was issued November 24, 2015.

Between 2008 and 2017, a series of patents were also filed by a long list of players, including Crucell, Rubeus Therapeutics, Children’s Medical Corporation, Ludwig-Maximilians-Universität in München, Protein Science Corporation, Dana-Farber Cancer Institute, University of Iowa, University of Hong Kong and the Chinese National Human Genome Center in Shanghai.

According to Martin, there are 73 patents, issued between 2008 and 2019, that describe the very elements that are said to be unique to SARS-CoV-2. It’s unclear whether Moderna’s 2016 patent filing is part of that list.

Sources and References

March 8, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular | , , , , , , | Leave a comment

Military Documents About Gain of Function Contradict Fauci Testimony Under Oath

Project Veritas | January 10, 2022

WASHINGTON, D.C. – Project Veritas has obtained startling never-before-seen documents regarding the origins of COVID-19, gain of function research, vaccines, potential treatments which have been suppressed, and the government’s effort to conceal all of this.

The documents in question stem from a report at the Defense Advanced Research Projects Agency, better known as DARPA, which were hidden in a top secret shared drive.

DARPA is an agency under the U.S. Department of Defense in charge of facilitating research in technology with potential military applications.

Project Veritas has obtained a separate report to the Inspector General of the Department of Defense written by U.S. Marine Corp Major, Joseph Murphy, a former DARPA Fellow.

The report states that EcoHealth Alliance approached DARPA in March 2018, seeking funding to conduct gain of function research of bat borne coronaviruses. The proposal, named Project Defuse, was rejected by DARPA over safety concerns and the notion that it violates the basis gain of function research moratorium.

According to the documents, NIAID, under the direction of Dr. Fauci, went ahead with the research in Wuhan, China and at several sites across the U.S.

Dr. Fauci has repeatedly maintained, under oath, that the NIH and NAIAD have not been involved in gain of function research with the EcoHealth Alliance program. But according to the documents obtained by Project Veritas which outline why EcoHealth Alliance’s proposal was rejected, DARPA certainly classified the research as gain of function.

“The proposal does not mention or assess potential risks of Gain of Function (GoF) research,” a direct quote from the DARPA rejection letter.

Major Murphy’s report goes on to detail great concern over the COVID-19 gain of function program, the concealment of documents, the suppression of potential curatives, like Ivermectin and Hydroxychloroquine, and the mRNA vaccines.

Project Veritas reached out to DARPA for comment regarding the hidden documents and spoke with the Chief of Communications, Jared Adams, who said, “It doesn’t sound normal to me,” when asked about the way the documents were shrouded in secrecy. “If something resides in a classified setting, then it should be appropriately marked,” Adams said. “I’m not at all familiar with unmarked documents that reside in a classified space, no.”

In a video breaking this story published on Monday night, Project Veritas CEO, James O’Keefe, asked a foundational question to DARPA:

“Who at DARPA made the decision to bury the original report? They could have raised red flags to the Pentagon, the White House, or Congress, which may have prevented this entire pandemic that has led to the deaths of 5.4 million people worldwide and caused much pain and suffering to many millions more.”

Dr. Anthony Fauci has not yet responded to a request for comment on this story.

READ THE DOCUMENTS

REJECTION OF DEFUSE PROJECT PROPOSAL

EXECUTIVE SUMMARY: DEFUSE

BROAD AGENCY ANNOUNCEMENT PREventing EMerging Pathogenic Threats(PREEMPT)

U.S. Marine Corp Major Joseph Murphy’s Report to Inspector General of DoD

About Project Veritas

James O’Keefe established Project Veritas in 2010 as a non-profit journalism enterprise to continue his undercover reporting work. Today, Project Veritas investigates and exposes corruption, dishonesty, self-dealing, waste, fraud, and other misconduct in both public and private institutions to achieve a more ethical and transparent society and to engage in litigation to: protect, defend and expand human and civil rights secured by law, specifically First Amendment rights including promoting the free exchange of ideas in a digital world; combat and defeat censorship of any ideology; promote truthful reporting; and defend freedom of speech and association issues including the right to anonymity.

January 11, 2022 Posted by | Deception, Timeless or most popular, Video, War Crimes | , , , | 1 Comment