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COVID-19

Canadian Health Organizations Unite to Demand Truth on Vaccine Safety

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15 minute read

News release from the World Council of Health Canada

Canadian Health Authorities Served Over Childhood Vaccine Information

Children’s Health Defense, Canada Health Alliance, Vaccine Choice Canada, and WCH Canada joined this week to serve health officers and ministers of health across the country.

The Canada Health AllianceChildren’s Health Defense CanadaVaccine Choice Canada, and the World Council For Health Canada united this week to put Fraser Health and other health authorities across Canada on notice regarding dangerous information being provided to parents and families about vaccinations. Fraser Health, one of five regional health authorities in British Columbia, Canada, is responsible for delivering health care services to a population of over 2 million people in Metro Vancouver and the Fraser Valley. Fraser Health is currently promoting COVID-19 genetic “vaccines”  and various traditional vaccines for children and youth. The information that Fraser Health is providing is inaccurate and dangerous. Like many governmental agencies in Canada and elsewhere, Fraser Health is promoting misleading claims of safety and efficacy for DNA-contaminated, modified-RNA, genetic “vaccines” for COVID-19, as well as various traditional vaccines for other infections. Children’s health and lives are at risk.

On October 28, 2024, four major Canadian health organizations together sent a registered open letter to all medical health officers in Fraser Health, as well as mailed copies to all other district medical health officers in BC; all provincial, territorial, and federal chief medical officers of health; and all provincial, territorial, and federal health ministers. Appropriate cover letters were included for each recipient.

The intent of these letters is to reach the heart of the recipients, inspiring them to take corrective action on dangerous misinformation regarding childhood vaccines.

October 25, 2024

Re: Open Letter to Fraser Health Authority

We are writing in response to the information currently being disseminated by various public health officers at the request of Fraser Health Authority utilizing the ‘Healthy Schools Communications Toolkit’. (Source)

The broader medical community, the public, and especially parents look to health authorities such as Fraser Health Authority to provide accurate, up-to-date information to assist in making informed decisions regarding the health and safety of children.

Statements in the ‘Healthy Schools Communication Toolkit’ issued by Fraser Health Authority in recent weeks claim, with no conditions or qualifiers, that vaccines are ‘safe, effective and necessary’ for the health and safety of children.

These statements are inaccurate and misleading.

Of particular note for being misleading and outright dishonest are the following:

  • Tdap-IPV: protects against diphtheria, tetanus, pertussis (whooping cough) and polio.
  • “Vaccines are safe and are your child’s best protection.”
  • Repeatedly misrepresenting “vaccination” as “immunization” (Source)
  • “The COVID-19 vaccines . . . are safe, effective and will save lives.”
  • “Vaccines do more than protect the people getting vaccinated, they also protect everyone around them. The more people in a community who are immunized and protected from COVID-19, the harder it is for COVID-19 to spread.”
  • “The best way to protect others and reduce the risk of getting sick with the flu and COVID-19 is to get immunized. The flu and COVID-19 vaccines are safe, effective and available for free to anyone aged six months and older. It is much safer to get the vaccines than to get the illnesses.” (Source)

These statements are especially disconcerting given recent disclosures related to the lack of evidence of the safety of childhood vaccines and the COVID ‘vaccine’ in particular.

The COVID ‘Vaccine’

The claim of safety of the COVID ‘vaccine’ cannot be made in the face of the May 29, 2024 admission by the Public Health Agency of Canada (PHAC) in response to an order paper question from Conservative MP Cathay Wagantall. (Source) The Public Health Agency of Canada acknowledged that booster recipients have higher death numbers than the unvaccinated. The report states: “Across all weeks in the time period of interest, the number of deaths were highest among those with a primary series and 1 additional dose.”

Despite PHAC urging caution in interpreting the data, they fail to address their own misleading definitions when they identify vaccine recipients as “unvaccinated” during the first 14 days following vaccination, the period of high lethality after the injections. The misleading use of the term “unvaccinated” renders all information from the PHAC and Health Canada unreliable and validates the safety and efficacy concerns surrounding these products.

Researchers investigating the safety and effectiveness of Pfizer’s vaccine in fully vaccinated, partially vaccinated, and unvaccinated children and teens found cases of myocarditis and pericarditis only in vaccinated children. (Source) The study also found that initial protection by BNT162b2 vaccination against positive SARS-CoV-2 tests in adolescents aged 12-15 had waned by 14 weeks after vaccination. Brian Hooker, Ph.D., chief scientific officer of Children’s Health Defense states: “This study clearly shows that Pfizer’s COVID vaccine provides almost no benefit to children and adolescents but does increase their risk of myocarditis and pericarditis. It begs the question: Why does the CDC continue to recommend these unlicensed shots for kids? Where is the data they use to support their statement that the benefits of these vaccines outweigh the risks?”

On October 7,2024, Florida State Surgeon General Dr. Joseph A. Ladapo announced new guidance regarding mRNA vaccines. (Source) The Florida Department of Health conducted an analysis to evaluate vaccine safety. This analysis found that there is an 84% increase in the relative incidence of cardiac-related death among males 18-39 years old within 28 days following mRNA vaccination. Non-mRNA vaccines were not found to have these increased risks. As such, the State Surgeon General recommends against males aged 18 to 39 from receiving mRNA COVID-19 vaccines.

The Department continues to stand by its Guidance for Pediatric COVID-19 Vaccines, issued March 2022, which recommends against use in healthy children and adolescents 5 years old to 17 years old. This now includes recommendations against COVID-19 vaccination among infants and children under 5 years old.

The following is beyond medical debate and considered accepted medical knowledge:

  • The COVID injections do not stop COVID infection or transmission.
  • Healthy young people have essentially zero risk of serious illness and death from COVID.
  • Since the COVID mRNA “vaccines” were given to the public, over 1.6 million adverse events and over 38,000 deaths related to these injections have been reported to the CDC’s Vaccine Adverse Events Reporting System (VAERS) in the US. Among these toxicities, increased rates of myocarditis—sometimes fatal—in young people, especially boys, have been demonstrated in recipients of the mRNA injections.
  • Additionally laboratory analysis has found high levels of DNA adulteration, and multiple undeclared genetic sequences in both Moderna and Pfizer Covid-19 genetic “vaccines”.
  • The Pfizer and Moderna COVID mRNA injections, while commonly called vaccines, are not true vaccines, but a type of mRNA-based gene therapy. In effect, they are ‘vaccines-in-name-only’.

There is no legitimate medical justification for healthy children or young adults to receive the COVID mRNA injections. Any institution continuing to refer to these injections as ‘vaccines’ and declaring them to be “safe and effective” is intentionally misinforming the public and health practitioners alike. This demonstrates a blatant disregard for scientific evidence and the health of our children and youth.

Lack of Proven Safety of Childhood Vaccines

In August 2024 Vaccine Choice Canada sent personalized letters (Source) to all provincial Health Ministers and chief public health officers, including Dr. Bonnie Henry, on the lack of proper safety testing of childhood vaccines. In that letter VCC stated:

In the July 6, 2024 publication of the New England Journal of Medicine, Dr. Stanley Plotkin et al. (Source) admitted “the need for more rigorous science” pertaining to the safety of vaccines. They noted that “In 234 reviews of various vaccines and health outcomes conducted from 1991 to 2012, the Institute of Medicine (IOM) found inadequate evidence to prove or disprove causation in 179 (76%) of the relationships it explored.”

What Plotkin and his fellow authors acknowledged is that the science to conclude vaccine safety is inadequate. (Source) Additionally, in 2023 the Informed Consent Action Network confirmed that “none of the vaccine doses the CDC recommends for routine injection into children were licensed based on a long-term placebo-controlled trial.” (Source) This is also true for Health Canada.

Further, five studies comparing unvaccinated children with vaccinated children provide compelling evidence that the current vaccination schedule is harming our children and a significant contributor to the epidemic of chronic disease in children today. (A New Parents Guide to Understanding Vaccination)

There is no substantive evidence to claim that the following vaccines prevent infection or transmission:

  • Pertussis
  • Polio
  • Tetanus
  • COVID
  • Influenza
  • Diphtheria

These vaccine products are designed to minimize symptoms, and do not prevent infection or transmission. Referring to these products as “immunizations” is misleading and dishonest. With these critical disclosures, it is no longer honest, responsible, or ethical for Public Health authorities to claim that “vaccines have been proven to be safe and effective”.

Fraser Health has no scientific basis to assure parents that giving their children vaccines is “your child’s best protection” when none of the vaccines on the childhood schedule have been tested for safety and effectiveness against a true placebo. That claim is scientifically unsupported and contradicts what is medically known.

It is time to cease the unqualified claim that “vaccines are safe, effective and necessary”.

Canada has consumer protection laws which prohibits engaging in any act or practice that is otherwise misleading, false, or deceptive to the consumer. Because parents rely on Health Canada and our Public Health Officers when they make health care decisions, children are harmed by the misleading and deceptive claims of health agencies such as Fraser Health Authority. These consumer protection laws need to be enforced.

Conclusion

  • Public Health agencies such as Fraser Health Authority continue to mislead and deceive the public by maintaining the unsubstantiated claim that vaccines are safe, effective and necessary. That claim requires immediate retraction and correction.
  • Public Health undermines their credibility in making such unsubstantiated statements and puts the credibility of the entire health care system at risk.
  • We appeal to your moral and legal responsibility to be fully transparent regarding the limitations on the evidence of vaccine safety, effectiveness and necessity.

We expect you will address this matter with the same seriousness that we are and we look forward to receiving your response.

Sincerely,

Ted Kuntz, President, Vaccine Choice Canada

Dr. Bill Code, President, Canada Health Alliance

Dr. Mark Trozzi, President, World Council for Health Canada

Christine Colebeck, President, Children’s Health Defence Canada


Organizations

The Canada Health AllianceChildren’s Health Defense CanadaVaccine Choice CanadaWorld Council For Health Canada, and the World Council For Health International.

Related Material

  • Here is honest, concise information about vaccines and genetic injections in the form of a 6-minute video. Please share this liberally with parents, teachers, and families (Click Here)
  • Vaccine Choice Canada’s New Parents’ Guide to Understanding Vaccinations (Click Here)
  • Children’s Health Defense Canada. A Parents’ Guide to Healthy Children. (Click Here)
  • World Council For Health International 2022 Alert to Parents Regarding Children and Covid-19 Genetic “Vaccines”. English, Spanish, and German. (Click Here)
  • Children Should Be Freed Now and Never COVID-Injected. Children are by nature very resistant to coronavirus infection for multiple reasons that we will concisely discuss below. (Click Here)
  • COVID Injections: Unveiling the Mechanisms of Harm. New pathology, a new wave of disease, and 44 common examples of injection-induced illnesses supported by over 930 scientific publications linking these diseases with the injections. (Click Here)
  • Canada Health Alliance. Why Do Vaccines Continually Fail to Live Up to Their Promises? (Click Here)

Brownstone Institute

The Deplorable Ethics of a Preemptive Pardon for Fauci

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From the Brownstone Institute

By Alex Washburne 

Anthony “I represent science” Fauci can now stand beside Richard “I am not a crook” Nixon in the history books as someone who received the poison pill of a preemptive pardon.

While Nixon was pardoned for specific charges related to Watergate, the exact crimes for which Fauci was pardoned are not specified. Rather, the pardon specifies:

Baseless and politically motivated investigations wreak havoc on the lives, safety, and financial security of targeted individuals and their families. Even when individuals have done nothing wrong – and in fact have done the right things – and will ultimately be exonerated, the mere fact of being investigated and prosecuted can irreparably damage reputations and finances.

In other words, the dying breath of the Biden administration appears to be pardoning Fauci for crimes he didn’t commit, which would seem to make a pardon null and void. The pardon goes further than simply granting clemency for crimes. Clemency usually alleviates the punishment associated with a crime, but here Biden attempts to alleviate the burden of investigations and prosecutions, the likes of which our justice system uses to uncover crimes.

It’s one thing to pardon someone who has been subjected to a fair trial and convicted, to say they have already paid their dues. Gerald Ford, in his pardon of Richard Nixon, admitted that Nixon had already paid the high cost of resigning from the highest office in the land. Nixon’s resignation came as the final chapter of prolonged investigations into his illegal and unpresidential conduct during Watergate, and those investigations provided us the truth we needed to know that Nixon was a crook and move on content that his ignominious reputation was carve d into stone for all of history.

Fauci, meanwhile, has evaded investigations on matters far more serious than Watergate. In 2017, DARPA organized a grant call – the PREEMPT call – aiming to preempt pathogen spillover from wildlife to people. In 2018 a newly formed collaborative group of scientists from the US, Singapore, and Wuhan wrote a grant – the DEFUSE grant – proposing to modify a bat sarbecovirus in Wuhan in a very unusual way. DARPA did not fund the team because their work was too risky for the Department of Defense, but in 2019 Fauci’s NIAID funded this exact set of scientists who never wrote a paper together prior or since. In late 2019, SARS-CoV-2 emerged in Wuhan with the precise modifications proposed in the DEFUSE grant submitted to PREEMPT.

It’s reasonable to be concerned that this line of research funded by Fauci’s NIAID may have caused the pandemic. In fact, if we’re sharp-penciled and honest with our probabilities, it’s likely beyond reasonable doubt that SARS-CoV-2 emerged as a consequence of research proposed in DEFUSE. What we don’t know, however, is whether the research proceeded with US involvement or not.

Congress used its constitutionally-granted investigation and oversight responsibilities to investigate and oversee NIAID in search of answers. In the process of these investigations, they found endless pages of emails with unjustified redactions, evidence that Fauci’s FOIA lady could “make emails disappear,” Fauci’s right-hand-man David Morens aided the DEFUSE authors as they navigated disciplinary measures at NIH and NIAID, and there were significant concerns that NIAID sought to obstruct investigations and destroy federal records.

Such obstructive actions did not inspire confidence in the innocence of Anthony Fauci or the US scientists he funded in 2019. On the contrary, Fauci testified twice under oath saying NIAID did not fund gain-of-function research of concern in Wuhan…but then we discovered a 2018 progress report of research NIAID funded in Wuhan revealing research they funded had enhanced the transmissibility of a bat SARS-related coronavirus 10,000 times higher than the wild virus. That is, indisputably, gain-of-function research of concern. Fauci thus lied to the American public and perjured himself in his testimony to Congress, and Senator Rand Paul (R-KY) has referred Fauci’s perjury charges to the Department of Justice.

What was NIAID trying to preempt with their obstruction of Congressional investigations? What is Biden trying to preempt with his pardon of Fauci? Why do we not have the 2019 NIAID progress report from the PI’s who submitted DEFUSE to PREEMPT and later received funding from NIAID?

It is deplorable for Biden to preemptively pardon Fauci on his last day in office, with so little known about the research NIAID funded in 2019 and voters so clearly eager to learn more. With Nixon’s preemptive pardon, the truth of his wrongdoing was known and all that was left was punishment. With Fauci’s preemptive pardon, the truth is not yet known, NIAID officials in Fauci’s orbit violated federal records laws in their effort to avoid the truth from being known, and Biden didn’t preemptively pardon Fauci to grant clemency and alleviate punishment, but to stop investigations and prosecutions the likes of which could uncover the truth.

I’m not a Constitutional scholar prepared to argue the legality of this maneuver, but I am an ethical human being, a scientist who contributed another grant to the PREEMPT call, and a scientist who helped uncover some of the evidence consistent with a lab origin and quantify the likelihood of a lab origin from research proposed in the DEFUSE grant. Any ethical human being knows that we need to know what caused the pandemic, and to deprive the citizenry of such information from open investigations of NIAID research in 2019 would be to deprive us of critical information we need to self-govern and elect people who manage scientific risks in ways we see fit. As a scientist, there are critical questions about bioattribution that require testing, and the way to test our hypotheses is to uncover the redacted and withheld documents from Fauci’s NIAID in 2019.

The Biden administration’s dying breath was to pardon Anthony Fauci not for the convictions for crimes he didn’t commit (?) but to avoid investigations that could be a reputational and financial burden for Anthony Fauci. A pardon to preempt an investigation is not a pardon; it is obstruction. The Biden administration’s dying breath is to obstruct our pursuit of truth and reconciliation on the ultimate cause of 1 million Americans’ dying breaths.

To remind everyone what we still need to know, it helps to look through the peephole of what we’ve already found to inspire curiosity about what else we’d find if only the peephole could be widened. Below is one of the precious few emails investigative journalists pursuing FOIAs against NIAID have managed to obtain from the critical period when SARS-CoV-2 is believed to have emerged. The email connects DEFUSE PI’s Peter Daszak (EcoHealth Alliance), Ralph Baric (UNC), Linfa Wang (Duke-NUS), Ben Hu (Wuhan Institute of Virology), Shi ZhengLi (Wuhan Institute of Virology) and others in October 2019. The subject line “NIAID SARS-CoV Call – October 30/31” connects these authors to NIAID.

It is approximately in that time range – October/November 2019 – when SARS-CoV-2 is hypothesized to have entered the human population in Wuhan. When it emerged, SARS-CoV-2 was unique among sarbecoviruses in having a furin cleavage site, as proposed by these authors in their 2019 DEFUSE grant. Of all the places the furin cleavage site could be, the furin cleavage site of SARS-CoV-2 was in the S1/S2 junction of the Spike protein, precisely as proposed by these authors.

In order to insert a furin cleavage site in a SARS-CoV, however, the researchers would’ve needed to build a reverse genetic system, i.e. a DNA copy of the virus. SARS-CoV-2 is unique among coronaviruses in having exactly the fingerprint we would expect from reverse genetic systems. There is an unusual even spacing in the cutting/pasting sites for the enzymes BsaI and BsmBI and an anomalous hot-spot of silent mutations in precisely these sites, exactly as researchers at the Wuhan Institute of Virology have done for other coronavirus reverse genetic systems. The odds of such an extreme synthetic-looking pattern occurring in nature are, conservatively, about 1 in 50 billion.

The virus did not emerge in Bangkok, Hanoi, Bago, Kunming, Guangdong, or any of the myriad other places with similar animal trade networks and greater contact rates between people and sarbecovirus reservoirs. No. The virus emerged in Wuhan, the exact place and time one would expect from DEFUSE.

With all the evidence pointing the hounds towards NIAID, it is essential for global health security that we further investigate the research NIAID funded in 2019. It is imperative for our constitutional democracy, for our ability to self-govern, that we learn the truth. The only way to learn the truth is to investigate NIAID, the agency Fauci led for 38 years, the agency that funded gain-of-function research of concern, the agency named in the October 2019 call by DEFUSE PI’s, the agency that funded this exact group in 2019.

A preemptive pardon prior to the discovery of truth is a fancy name for obstruction of justice. The Biden administration’s dying breath must be challenged, and we must allow Congress and the incoming administration to investigate the possibility that Anthony Fauci’s NIAID-supported research caused the Covid-19 pandemic.

Republished from the author’s Substack

Author

Alex Washburne is a mathematical biologist and the founder and chief scientist at Selva Analytics. He studies competition in ecological, epidemiological, and economic systems research, with research on covid epidemiology, the economic impacts of pandemic policy, and stock market response to epidemiological news.

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COVID-19

BREAKING: Days before Trump Inauguration HHS fires doctor in charge of gain of function research project

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Dr. Daszak will likely be protected by the DoD & CIA from additional penalties.

By John Leake

HHS Formally Debars EcoHealth Alliance, President Peter Daszak Fired.

On January 17, 2025—just three days before President Trump is to be sworn in—Congress issued a press release with the following statement:

Today, after an eight-month investigation, the U.S. Department of Health and Human Services (HHS) cut off all funding and formally debarred EcoHealth Alliance Inc. (EcoHealth) and its former President, Dr. Peter Daszak, for five years based on evidence uncovered by the Select Subcommittee on the Coronavirus Pandemic.

As far as I can tell, the New York Times did not report this story, though the New York Post did.

More interesting than the superficial news reporting is the HHS ACTION REFERRAL MEMORANDUM  recommending that Dr. Peter Daszak be barred from participating in United States Federal Government procurement and nonprocurement programs.

The Memorandum also states:

Dr. Peter Daszak was the President and Chief Executive Officer of EHA from 2009 until his termination, effective January 6, 2025. Dr. Daszak was the Project Director (PD)/Principal Investigator (PI) for Grant Number 1R01AI110964-01.

I am not sure what to make of this document, which is written in such an arcane and convoluted style that it challenges the attention span of even the most focused reader.

I have been researching this story for four years, and I found the following paragraphs the most intriguing:

9. In a letter dated May 28, 2016, the NIAID contacted EHA concerning possible GoF research based on information submitted in its most recent Year 2 RPPR. The NIAID notified EHA that GoF research conducted under Grant Number 5R01AI110964-03 would be subject to the October 17, 2014, United States Federal Government funding pause, and that per the funding pause announcement, new United States Federal Government funding would not be released for GoF research projects that may be reasonably anticipated to confer attributes to influenza, MERS, or SARS viruses such that the virus would have enhanced pathogenicity and/or transmissibility in mammals via the respiratory route. In the letter, the NIAID requested that EHA provide a determination within 15 days of the date of the letter as to whether EHA’s research under Grant Number 5R01AI110964-03 did or did not include GoF work subject to the funding pause.

10. In a letter dated June 8, 2016, EHA provided a response to the NIAID’s May 28, 2016 letter. EHA explained that the goal of its proposed work was to construct MERS and MERS-like chimeric CoVs in order to understand the potential origins of MERSCoV in bats by studying bat MERS-like CoVs in detail. EHA stated that it believed it was highly unlikely that the proposed work would have any pathogenic potential, but that should any of these recombinants show evidence of enhanced virus growth greater than certain specified benchmarks involving log growth increases, or grow more efficiently in human airway epithelial cells, EHA would immediately: (1) stop all experiments with the mutant, (2) inform the NIAID Program Officer of these results, and (3) participate in decision-making trees to decide appropriate paths forward.

11. Based on the information provided by EHA, the NIAID concluded that the proposed work was not subject to the GoF research pause. In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.

Note that various statements in the above paragraphs are inconsistent with what Baric et al. state in their 2015 paper A SARS-like cluster of circulating bat coronavirus shows potential for human emergence—a research paper funded by the NIAID EcoHealth Grant “Understanding the Risk of Bat Coronavirus Emergence.”

As the authors state in the section on Biosafety and biosecurity:

Reported studies were initiated after the University of North Carolina Institutional Biosafety Committee approved the experimental protocol (Project Title: Generating infectious clones of bat SARS-like CoVs; Lab Safety Plan ID: 20145741; Schedule G ID: 12279). These studies were initiated before the US Government Deliberative Process Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS and SARS Viruses (http://www.phe.gov/s3/dualuse/Documents/gain-of-function.pdf). This paper has been reviewed by the funding agency, the NIH. Continuation of these studies was requested, and this has been approved by the NIH.

As I noted in my series of essays titled The Great SARS-CoV-2 Charade, one of the silliest lies told by Dr. Anthony Fauci has been his insistence that NIAID did not approve Gain-of-Function work by EcoHealth.

Fauci has repeatedly asserted this in a loud and vexed tone, as though he is outraged by the mere proposition. And yet, Ralph Baric and his colleagues—including Zhengli-Li Shi at the Wuhan Institute of Virology—plainly state in their 2015 paper that their Gain-of-Function experiments, performed in Baric’s UNC lab and Zhengli-Li Shi’s lab in Wuhan, were grandfathered in, given that they were funded before the 2014 Pause.

Another statement (in paragraph 11 of the recent HHS Action Referral Memo) that deserves special scrutiny is the following:

In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.

Again, it’s tough to interpret this statement, given that Baric et al. had, by the own admission, already generated chimeras that “replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV.”

Let’s review what Baric et al. state in their Abstract about the functionality of the chimeric virus (named SHCOI4-MA15) they claimed to have generated. Using humanized mice (genetically modified to have primary human airway cells) as their experimental animals, the authors state:

Using the SARS-CoV reverse genetics system2we 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. Additionally, in vivo experiments demonstrate replication of the chimeric virus in mouse lung with notable pathogenesis.

To this day, no legal authority that I am aware of has investigated the question: What became of the the chimeras SHC014-MA15 and WIV1-MA15? The latter chimera was documented by Baric et al. in their March 2016 paper titled SARS-like WIV1-CoV poised for human emergencea chimera “that replaced the SARS spike with the WIV1 spike within the mouse-adapted backbone.”

What did the Wuhan Institute of Virology do with these chimeras? Did its researchers continue to modify and experiment with these chimeras?

Another exceedingly silly claim made by U.S. government officials—including members of Congress—is that the true origin of SARS-CoV-2 is likely to remain a mystery, given that the Chinese government and military will almost certainly never agree to perform a full and transparent investigation of their Wuhan Institute of Virology.

What did the U.S. government expect when it agreed to share cutting edge American biotechnology with the Wuhan Institute of Virology, which has long been known to be run by the Chinese military?

One grows weary of our U.S. government officials evading responsibility by pretending to be imbeciles or by revealing themselves to be true imbeciles.

If you found this post informative, please consider becoming a paid subscriber to our Substack. Penetrating the smoke and mirror show performed by the abominable U.S. government requires a great deal of time and effort.

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