In a significant development within the U.S. Department of Health and Human Services (HHS), Secretary Robert F. Kennedy Jr. (RFK Jr.) has dismissed two senior officials following the unauthorized approval of Moderna’s mRNA COVID-19 vaccine (Spikevax) for high-risk children aged 6 months to 11 years. The decision, made while RFK Jr. was on vacation, has sparked debate about internal oversight, vaccine policy reforms, and potential conflicts of interest. This report examines the timeline, key players, public reactions, and broader implications, drawing on recent news reports and social media discussions.
Background on the Vaccine Approval
On July 10, 2025, the FDA granted full approval for Moderna’s COVID-19 vaccine for use in vulnerable children, a move that contrasted with RFK Jr.’s ongoing efforts to restrict mRNA vaccine recommendations for healthy youth and pregnant women.
RFK Jr., a vocal critic of certain vaccine practices, had previously removed COVID-19 vaccines from routine schedules for healthy children in May 2025 and dismissed the entire CDC Advisory Committee on Immunization Practices (ACIP) in June 2025. According to sources close to the matter, including vaccine researcher Dr. Robert Malone, the approval was expedited by HHS Chief of Staff Heather Flick Melanson and Deputy Chief of Staff for Policy Hannah Anderson without consulting RFK Jr. or his deputy.
This occurred during RFK Jr.’s absence on a working vacation, leading to accusations of bureaucratic overreach and possible influence from pharmaceutical lobbies. The move initially fueled public speculation that RFK Jr. had softened his stance, prompting backlash from supporters who viewed it as a betrayal of his “Make America Healthy Again” agenda.
The Firings and Immediate Aftermath
Upon returning, RFK Jr. acted swiftly, firing Melanson and Anderson on July 16, 2025, as part of a larger HHS leadership restructuring. Reports indicate the dismissals were directly linked to the unauthorized approval, with one deputy allegedly reacting dramatically by crashing into RFK Jr.’s vehicle in a fit of privileged rage.
RFK Jr. has also reportedly referred the officials for criminal investigation, citing potential misconduct. This action aligns with RFK Jr.’s pattern of overhauling public health institutions, including replacing fired ACIP members with allies and vaccine skeptics. About time! It’s past time to address perceived corruption in regulatory processes.
Public and Media Reactions
The incident has generated widespread discussion on social media and in the press. Supporters praised the firings as a step toward accountability, with calls for further investigations into pharmaceutical ties. Detractors, including public health groups, have expressed concerns over the politicization of health decisions and potential disruptions to vaccine policy.
Implications for Health Policy
This event starkly exposes the relentless undermining of RFK Jr.’s leadership at HHS, where he is besieged by aggressive legal assaults on his bold reforms, such as a federal judge’s outright blockade of critical workforce reductions. Pharmaceutical powerhouses like BIO are waging an all-out lobbying war against him, funneling millions in a blatant bid to derail his agenda and preserve the status quo. Though the approval narrowly survives, it glaringly illuminates the formidable barriers to enforcing genuine transparency and reform amid a bitterly fractured regulatory arena. As RFK Jr. battles on to overhaul vaccine oversight, entrenched stakeholders from every corner clamor for “caution,” ostensibly to safeguard innovation, safety, and public trust—but in reality, often to thwart meaningful change. This saga is far from over, poised for intensified scrutiny, deeper probes, and seismic policy upheavals.
I am expert in influenza, and have consulted with the WHO over the past two decades on the topic of flu vaccines. This is one subject matter I am extremely knowledgeable about. This goes back to my medical school days, when I worked with Robert Lamb, one of the top influenza virus specialists in the world. It extended through much of my career, including my serving as Director of Clinical Influenza Vaccine Research for Solvay Biologicals, in which I oversaw over $200 million in federal (BARDA) alternative (cell-based) influenza vaccine research funding.
What is happening now with “Bird flu” is another psyops campaign being conducted by the administrative/deep state, apparently in partnership with Pharma, against the American people. They know and we know that the “vaccines” being produced will be somewhat ineffective, as all flu “vaccines” are. The government is chasing a rapidly evolving RNA virus with a syringe, just like they did with HIV and Covid-19.
Generally, the currently circulating avian influenza strain in the US does not include any cases of human-to-human transmission. And the current mortality, with over 60 cases identified, is 0%. NOT 50%.
All the while they are getting prepared to roll out masks, lockdowns, quarantines, etc.
All the while getting ready to roll out mRNA vaccines for poultry and livestock, as well as for all of us.
The more they test, the more “Bird flu” (H5N1) they will find. This “pandemic” is nothing more than an artifact of their newly developed protocols to test cattle, poultry, pets, people, and wildlife on a massive scale for avian influenza. In years past, this was not even considered. In the past, the USG did fund a massive testing and surveillance program called “Biowatch.” That program was a colossal failure and a massive waste of money. Billions of dollars.
Of course, these facilities producing the tests have been repurposed from the Covid-19 testing facilities.
Key questions include:
Will we all comply?
Will we be forced to comply?
Will President Trump go along with the PsyWar/psyops campaign again?
We will know soon enough.
As the United States is testing everyone who has even the mildest symptoms for the H5N1 (avian) influenza, guess what – they are finding it! This is what we call in the lab, a “sampling bias.”
Globally, from 1997 until the present, there have been 907 reported cases of H5N1. And in fact, this particular outbreak was not the worst – and it is the only one where a massive testing campaign has occurred. It appears that this is partly due to the new diagnostic capabilities developed and deployed during Covid-19. The more you test, the more you find. But is it clinically significant?
The Case Study of Tetanus: Supply Chain Issues.
The CDC recommends a booster for the tetanus vaccine every 10 years for adults.
However, research published almost a decade ago suggests that the protection from tetanus and diphtheria vaccination lasts at least 30 years after completing the standard childhood vaccination series.
“We have always been told to get a tetanus shot every 10 years, but actually, there is very little data to prove or disprove that timeline. When we looked at the levels of immunity among 546 adults, we realized that antibody titers against tetanus and diphtheria lasted much longer then previously believed.”
-Mark K. Slifka, Ph.D, study author
This research, published in a highly reputable journal, suggests that a revised vaccination schedule with boosters occurring at ages 30 and 60 would be sufficient. As this was published in early 2016, the US government, at the very least, could have commissioned easily designed prospective and retrospective studies to confirm these results. And those results would have been published by now, with the tetanus adult schedule revised to reflect what is now known about the durable immunity of tetanus and diphtheria vaccines. Reducing the boosters to just two shots would save the government vast sums of money.
Not only that, but both the tetanus and diphtheria vaccines carry risks for adults. It is estimated that 50%–85% of patients experience injection site pain or tenderness, 25%–30% experience edema and erythema. Higher preexisting anti-tetanus antibody levels are also associated with a higher reactogenicity rate and greater severity (reference).
Anaphylaxis after tetanus vaccination represents a rare but potentially serious adverse event, with an incidence of 1.6 cases per million doses. That means if 100 million adults receive the booster every ten years, 320 cases of anaphylaxis will be avoided over the 30-year period – from those two boosters being eliminated. Tetanus has always been a “rare” disease, spread through a skin wound contaminated by Clostridium tetani bacteria, commonly found in soil, dust, and manure. Before vaccines were available, there were about 500 cases a year, with most resulting in death. Concerns about vaccine-associated adverse events when immunizations were performed at short intervals led to a revision of the tetanus/diphtheria vaccination schedule in 1966 to once every 10 years for patients >6 years of age.
It has recently come to my attention that the traditional stand-alone tetanus vaccine (TT) that one used to receive as an adult has been discontinued due to WHO recommendations. Their reasoning being:
Use of TTCV combinations with diphtheria toxoid are strongly encouraged and single-antigen vaccines should be discontinued whenever feasible to help maintain both high diphtheria and high tetanus immunity throughout the life course.
The CDC blames the shuttering of the only plant producing TT for the current lack of a stand-alone TT vaccine.
Now, in order to get a booster tetanus shot, an adult must take the following.
Td: Sanofi’s Tenivacprotects against tetanus and diphtheria. Given to people 7 years and older as a booster every 10 years. *A version also includes pertussis (eg DPT), but due to the risk of encephalitis, it is not recommended as a booster.
Why is the DPT combination vaccine discouraged in adults due to encephalitis risk, but is it recommended for children? Another one of those inconvenient issues that plague the CDC-recommended childhood vaccine schedule.
While supplies of diphtheria, tetanus, and pertussis (Tdap) vaccines (Sanofi’s Adacel and GSK’s Boostrix) aren’t limited, they are more expensive, and a very small fraction of patients can develop encephalopathy (brain damage) from the pertussis component.
In the United States, diphtheria is virtually non-existent, with only 14 cases reported between 1996 and 2018. Of those cases reported, most were from international travelers or immigrants.
The market for a stand-alone TT vaccine vanished worldwide due to WHO recommendations to stop the sales of the TT vaccine. Which was due to the relatively few, economically stressed countries where diphtheria is still an issue. So, therefore, the only facility manufacturing the TT vaccine was shut down within the last year.
The blowback from the WHO recommendations is that now there is a shortage of tetanus and diphtheria (Td) vaccine in the United States, according to the Centers for Disease Control and Prevention (CDC) website.
This all comes down to poor planning. And illustrates why supply chain issues and infectious disease countermeasure stockpiles are essential considerations for governments.
The good news is that unless one is immunosuppressed, most of us have almost lifelong immunity against tetanus and diphtheria.
My recommendation is that unless one gets a very deep and dirty puncture wound and has not had a tetanus shot in over ten years or longer, avoid that booster.
Here is the ugly secret about influenza vaccines. They are given to protect one group of vulnerable people. Those who are immunosuppressed, and that cohort includes the very elderly.
If those influenza vaccine manufacturing plants only make enough vaccines for those susceptible to a severe case of the flu, there would not be enough of a market to sustain their production costs. Furthermore, if there were a pandemic of some sort of highly pathogenic influenza, there would not be sufficient capacity to make enough vaccines to meet demand.
Egg-based influenza vaccine production requires super “clean” eggs; about 100 million “clean” fertilized eggs are needed annually for vaccine production in the US alone. Candidate vaccine viruses are injected into the eggs. If the process is shuttered, the whole production comes to a screeching halt. Many vaccines can be stored for long periods. Even as long as a decade. This stockpiling system works well for DNA viruses with a low mutation rate. Stockpiling is rarely a solution for vaccines developed for RNA viruses that mutate rapidly.
Therefore, the influenza vaccine is pushed on the American people year after year. As a way to maintain “warm base manufacturing” and ensure sufficient market size to support industrial operations.
I have spoken on this subject at the WHO and US government agencies, as well as many, many conferences. Unfortunately, because the mRNA and RNA vaccine platforms require a lot of freezer space (commonly -20°C) to stockpile for even short periods, this limits the ability to stockpile. Furthermore, the frozen storage requirements are only for up to 6 months. That means stockpiling for more extended storage is not currently done, and it is back to square one on the supply chain issue.
The issue with freezer space and mRNA vaccines is one that most likely won’t be solved. This benefits the manufacturers of this vaccine technology – the US government has an endless need for new vaccines as the old ones expire.
My small hope is that the mRNA platform will be too costly to justify its continued use, as appeals concerning safety (or lack of) seem to fall on deaf FDA ears.
In the meantime, don’t believe the hype generated by ex-officials from the Biden and Trump administrations.
Both Dr. Lena Wen, CNN correspondent, and Dr. Redfield, ex-director of the CDC, have gone on to mainstream media shows and promoted the narrative that the case fatality rate for avian influenza is over 50 percent. This, frankly, is a lie that the WHO is promoting. Bird flu generally is not tested for when someone has flu symptoms. When an outbreak of avian flu occurs on a poultry farm, testing of farm workers who are seriously ill will commence. This has led to the generation of the 890 case reports since 2003. Of those seriously ill patients reported to the WHO, over 50 percent died.
This is not an actual case fatality rate of avian flu around the world. It is, again, a sampling error due to a tiny data set derived from those who are at greatest risk due to general health. And just like the WHO reported on an exaggerated case fatality rate for mPOX, which was also based on a sampling error, or for Covid-19, again a sampling error, it is now used to justify psychological bioterrorism on the world population. Please don’t fall for it.
El Gato Malo on X succinctly points out that Dr. Leana Wen and her public health ilk are advancing:
1. Do more of the same lousy testing used in Covid-19 to overstate a disease and cause panic.
2. Develop another non-sterilizing non-vaccine that does not work to be pushed on “the vulnerable.”
3. Doing it “right now” under EUA, so whoever makes these tests and jabs can cash in and be shielded from liability.
4. Claiming that proxies like “triggers antibody production” demonstrate clinical clinical efficacy.
It’s just one last smash-and-grab for cash before the Brandon administration ends. Anyone who falls for this one will truly fall for anything.
Question: what are Leana’s conflicts of interest? Who is paying her or giving her grants?
For those that haven’t viewed Dr. Redfield speaking of the avian flu case fatality rate, have a watch below. It is genuinely shocking. This fear-mongering comes from an ex-director of the CDC. Shame on him.
Frankly, it reminds me of the 51 intelligence officials claiming that Hunter Biden’s laptop was fake.
One has to wonder what conflict of interest motivated him to say this on national TV?
Remember in the US, there have been 62 cases of avian influenza discovered, and all but one case were very mild.
This deep dive into the supply chain issues is meant to show that public health has put itself into a groupthink situation that it can’t escape.
Many solutions to this quandary do not involve an evermore expanding schedule of vaccinations, stockpiled for some future use. I have some general thoughts before I sign off.
The use of early treatments via safe, proven drugs is a good solution.
We now have many antibiotics to treat bacterial infections. Vaccines do not always need to be our first defense.
Our medical system is very good at treating infectious diseases. The risks from such diseases are much less than it once was. People do not have to live in fear of infectious disease. I like to ask people, how many people do you know have died of flu? If you know of any (I don’t), how old were they?
The need to scare people into more and more vaccines is a dangerous trend.
And yes, the more vaccinations one receives, the more likely an adverse event.
Vaccinating pregnant women and babies should always be a last resort.
It is time for Congress to rethink the vaccine liability laws.
The House Oversight Select Subcommittee on the Coronavirus Pandemic released a 520-page report yesterday, detailing the findings of the subcommittee’s investigation concluded after its two-year investigation into the COVID-19 pandemic. It is the most thorough review of the pandemic conducted to date. This report ensures COVID-19 accountability and serves as a roadmap for the U.S. to prepare for and respond to future pandemics.
It is beyond damning, names names and references criminal acts. People are calling for a Nuremberg-type trial to prosecute the main players for crimes against humanity.
The final report is titled, “After Action Review of the COVID-19 Pandemic: The Lessons Learned and a Path Forward.” (Below)
This final report will serve as a road map for Congress, the Executive Branch, and the private sector to prepare for and respond to future pandemics. Since February 2023, the Select Subcommittee has sent more than 100 investigative letters, conducted more than 30 transcribed interviews and depositions, held 25 hearings and meetings, and reviewed more than one million pages of documents. Members and staff have exposed high-level corruption in America’s public health system, confirmed the most likely origin of the pandemic, held COVID-19 bad actors publicly accountable, fostered bipartisan consensus on consequential pandemic-era issues, and more. This 520-page final report details all findings of the Select Subcommittee’s investigation.
“This work will help the United States, and the world, predict the next pandemic, prepare for the next pandemic, protect ourselves from the next pandemic, and hopefully prevent the next pandemic. Members of the 119th Congress should continue and build off this work, there is more information to find and honest actions to be taken,” wrote Chairman Wenstrup in a letter to Congress. “The COVID-19 pandemic highlighted a distrust in leadership. Trust is earned. Accountability, transparency, honesty, and integrity will regain this trust. A future pandemic requires a whole of America response managed by those without personal benefit or bias. We can always do better, and for the sake of future generations of Americans, we must. It can be done.”
On Wednesday, December 4, 2024, at 10:30am, the Select Subcommittee will hold a markup of the final report and officially submit the report to the Congressional record. Ahead of the markup, the Select Subcommittee will also release additional supporting materials and recommendations.
The full, 520-page final report can be found here and below. Here’s a summary of the staggering information contained within:
The Origins of the Coronavirus Pandemic, Including but Not Limited to the Federal Government’s Funding of Gain-of-Function Research
COVID-19 ORIGIN: COVID-19 most likely emerged from a laboratory in Wuhan, China. The FIVE strongest arguments in favor of the “lab leak” theory include:
The virus possesses a biological characteristic that is not found in nature.
Data shows that all COVID-19 cases stem from a single introduction into humans. This runs contrary to previous pandemics where there were multiple spillover events.
Wuhan is home to China’s foremost SARS research lab, which has a history of conducting gain-of-function research at inadequate biosafety levels.
Wuhan Institute of Virology (WIV) researchers were sick with a COVID-like virus in the fall of 2019, months before COVID-19 was discovered at the wet market.
By nearly all measures of science, if there was evidence of a natural origin it would have already surfaced.
PROXIMAL ORIGIN PUBLICATION: “The Proximal Origin of SARS-CoV-2” publication — which was used repeatedly by public health officials and the media to discredit the lab leak theory — was prompted by Dr. Fauci to push the preferred narrative that COVID-19 originated in nature.
GAIN-OF-FUNCTION RESEARCH: A lab-related incident involving gain-of-function research is most likely the origin of COVID-19. Current government mechanisms for overseeing this dangerous gain-of-function research are incomplete, severely convoluted, and lack global applicability.
ECOHEALTH ALLIANCE INC. (ECOHEALTH): EcoHealth — under the leadership of Dr. Peter Daszak — used U.S. taxpayer dollars to facilitate dangerous gain-of-function research in Wuhan, China. After the Select Subcommittee released evidence of EcoHealth violating the terms of its National Institutes of Health (NIH) grant, the U.S. Department of Health and Human Services (HHS) commenced official debarment proceedings and suspended all funding to EcoHealth.
New evidence also shows that the Department of Justice (DOJ) has opened an investigation into EcoHealth’s pandemic-era activities.
NIH FAILURES: NIH’s procedures for funding and overseeing potentially dangerous research are deficient, unreliable, and pose a serious threat to both public health and national security. Further, NIH fostered an environment that promoted evading federal record keeping laws — as seen through the actions of Dr. David Morens and “FOIA Lady” Marge Moore.
The Efficacy, Effectiveness, and Transparency of the Use of Taxpayer Funds and Relief Programs to Address the Coronavirus Pandemic, Including Any Reports of Waste, Fraud, or Abuse
COVID-19 RELIEF FUNDING: Federal and state governments had significant lapses in coordination, were unprepared to oversee the allocation of COVID-19 relief funds, and failed to sufficiently identify waste, fraud, and abuse of taxpayer dollars during the pandemic.
PAYCHECK PROTECTION PROGRAM: The Paycheck Protection Program — which offered essential relief to Americans in the form of loans that could be forgiven if the funds were used to offset pandemic-era hardships — was rife with fraudulent claims resulting in at least $64 billion of taxpayers’ dollars lost to fraudsters and criminals.
FRADULENT UNEMPLOYMENT CLAIMS: Fraudsters cost the American taxpayer more than $191 billion dollars by taking advantage of the federal government’s unemployment system and exploiting individuals’ personally identifiable information.
SMALL BUSINESS ADMINISTRATION (SBA) FAILURES: $200 million of taxpayers’ dollars were lost as a result of the SBA’s inability to conduct proper oversight, implement internal controls, and ensure fraud protection measures were enacted.
TRANSNATIONAL FRAUD: At least half of the taxpayer dollars lost in COVID-19 relief programs were stolen by international fraudsters.
COVID-19 RELIEF FUNDING OVERSIGHT: Expanding relief programs that lacked proper oversight functions exposed severe vulnerabilities in the system and paved the way for fraudsters, international criminals, and foreign adversaries to take advantage of taxpayers.
The Implementation or Effectiveness of Any Federal Law or Regulation Applied, Enacted, or Under Consideration to Address the Coronavirus Pandemic and Prepare for Future Pandemics
WORLD HEALTH ORGANIZATION (WHO): The WHO’s response to the COVID-19 pandemic was an abject failure because it caved to pressure from the Chinese Communist Party and placed China’s political interests ahead of its international duties. Further, the WHO’s newest effort to solve the problems exacerbated by the COVID-19 pandemic — via a “Pandemic Treaty” — may harm the United States.
SOCIAL DISTANCING: The “6 feet apart” social distancing recommendation — which shut down schools and small business across the country — was arbitrary and not based on science. During closed door testimony, Dr. Fauci testified that the guidance, “sort of just appeared.”
MASK MANDATES: There was no conclusive evidence that masks effectively protected Americans from COVID-19. Public health officials flipped-flopped on the efficacy of masks without providing Americans scientific data — causing a massive uptick in public distrust.
LOCKDOWNS: Prolonged lockdowns caused immeasurable harm to not only the American economy, but also to the mental and physical health of Americans, with a particularly negative effect on younger citizens. Rather than prioritizing the protection of the most vulnerable populations, federal and state government policies forced millions of Americans to forgo crucial elements of a healthy and financially sound life.
NEW YORK PANDEMIC FAILURES: Former New York Governor Andrew Cuomo’s March 25 Order — which forced nursing homes to accept COVID-19 positive patients — was medical malpractice. Evidence shows that Mr. Cuomo and his Administration worked to cover up the tragic aftermath of their policy decisions in an apparent effort to shield themselves from accountability.
Evidence suggests Mr. Cuomo knowingly and willfully made false statements to the Select Subcommittee on numerous occasions about material aspects of New York’s COVID-19 nursing home disaster and the ensuing cover-up. The Select Subcommittee referred Mr. Cuomo to the DOJ for criminal prosecution.
TRAVEL RESTRICTIONS: President Trump’s rapidly implemented travel restrictions saved lives. During Dr. Fauci’s transcribed interview, he unequivocally agreed with every travel restriction issued by the Trump Administration. This testimony runs counter to the public narrative that the Trump Administration’s travel restrictions were xenophobic.
COVID-19 MISINFORMATION: Public health officials often spread misinformation through conflicting messaging, kneejerk reactions, and a lack of transparency. In the most egregious examples of pervasive misinformation campaigns, off-label drug use and the lab leak theory were unjustly demonized by the federal government.
The Biden Administration even employed undemocratic and likely unconstitutional methods — including pressuring social media companies to censor certain COVID-19 content — to fight what it deemed misinformation.
The Development of Vaccines and Treatments, and the Development and Implementation of Vaccination Policies for Federal Employees and Members of the Armed Forces
OPERATION WARP SPEED: President-elect Trump’s Operation Warp Speed — which encouraged the rapid development and authorization of the COVID-19 vaccine — was highly successful and helped save millions of lives.
COVID-19 VACCINE: Contrary to what was promised, the COVID-19 vaccine did not stop the spread or transmission of the virus.
RUSHED COVID-19 VACCINE APPROVAL: The FDA rushed approval of the COVID-19 vaccine in order to meet the Biden Administration’s arbitrary mandate timeline. Two leading FDA scientists warned their colleagues about the dangers of rushing the vaccine approval process and the likelihood of adverse events. They were ignored, and days later, the Biden Administration mandated the vaccine.
VACCINE MANDATES: Vaccine mandates were not supported by science and caused more harm than good. The Biden Administration coerced healthy Americans into compliance with COVID-19 vaccine mandates that trampled individual freedoms, harmed military readiness, and disregarded medical freedom to force a novel vaccine on millions of Americans without sufficient evidence to support their policy decisions.
NATURAL IMMUNITY: Public health officials engaged in a coordinated effort to ignore natural immunity — which is acquired through previous COVID-19 infection — when developing vaccine guidance and mandates.
VACCINE INJURY REPORTING SYSTEM: Vaccine injury reporting systems created confusion, failed to properly inform the American public about vaccine injuries, and deteriorated public trust in vaccine safety during the COVID-19 pandemic.
VACCINE INJURY COMPENSATION: The government is failing to efficiently, fairly, and transparently adjudicate claims for the COVID-19 vaccine injured.
The Economic Impact of the Coronavirus Pandemic and Associated Government Response on Individuals, Communities, Small Businesses, Health Care Providers, States, and Local Government Entities
BUSINESS IMPACTS: Federal and state governments imposed mandatory lockdowns that were the primary cause of temporary and permanent business closures. More than 160,000 businesses closed due to the pandemic — with 60% of those closures classified as permanent. For the businesses that stayed or re-opened, the lack of supply chain diversity exacerbated pandemic-era challenges and deepened existing disparities.
HEALTHCARE IMPACTS: America’s healthcare system was severely damaged by the COVID-19 pandemic. Patients experienced a decreased quality-of-care, longer wait times, shorter medical appointments, and missed diagnoses.
WORKER IMPACTS: Unemployment rates surged to levels not seen since the Great Depression. Overly broad mitigation measures — including the now debunked “6 feet apart” guidance — disproportionately impacted sectors with low wage earners.
FEDERAL RESERVE: The Federal Reserve’s aggressive, early, and unprecedented response to the COVID-19 pandemic prevented a severe economic downturn. This continued approach also contributed to staggering inflation.
The Societal Impact of Decisions to Close Schools, How the Decisions Were Made and Whether There is Evidence of Widespread Learning Loss or Other Negative Effects as a Result of These Decisions
COVID-19 SCHOOL CLOSURES: The “science” never justified prolonged school closures. Children were unlikely to contribute to the spread of COVID-19 or suffer severe illness or mortality. Instead, as a result of school closures, children experienced historic learning loss, higher rates of psychological distress, and decreased physical well-being.
CENTERS FOR DISEASE CONTROL AND PREVENTION (CDC) INFLUENCE: The Biden Administration’s CDC broke precedent and provided a political teachers organization with access to its scientific school reopening guidance. Former CDC Director Rochelle Walensky asked the American Federation of Teachers (AFT) to provide specific language for the guidance and even went so far as to accept numerous edits made by AFT.
AFT INFLUENCE: Schools remained closed longer than necessary because of AFT’s political interference in the CDC’s school reopening guidance. AFT is a political union, not a scientific organization, that advocated for mitigation efforts that prolonged school closures — including an automatic closure “trigger.”
Testimony revealed that AFT President Weingarten had a direct telephone line to contact former CDC Director Walensky.
LONGTERM IMPACTS: Standardized test scores show that children lost decades worth of academic progress as a result of COVID-19 school closures. Mental and physical health concerns also skyrocketed — with suicide attempts by 12-17 year-aged girls rising 51%.
Cooperation By the Executive Branch and Others with Congress, the Inspectors General, the Government Accountability Office, and Others in Connection with Oversight of the Preparedness for and Response to the Coronavirus Pandemic
HHS OBSTRUCTION: The Biden Administration’s HHS engaged in a multi-year campaign of delay, confusion, and non-responsiveness in an attempt to obstruct the Select Subcommittee’s investigation and hide evidence that could incriminate or embarrass senior public health officials. It appears that HHS even intentionally under-resourced its component that responds to legislative oversight requests.
ECOHEALTH OBSTRUCTION: EcoHealth President Dr. Peter Daszak obstructed the Select Subcommittee’s investigation by providing publicly available information, instructing his staff to reduce the scope and pace of productions, and doctoring documents before releasing them to the public. Further, Dr. Daszak provided false statements to Congress.
DR. DAVID MORENS: Dr. Fauci’s Senior Advisor, Dr. David Morens, deliberately obstructed the Select Subcommittee’s investigation, likely lied to Congress on multiple occasions, unlawfully deleted federal COVID-19 records, and shared nonpublic information about NIH grant processes with EcoHealth President Dr. Peter Daszak.
NEW YORK OBSTRUCTION: New York’s Executive Chamber — led presently by Governor Kathy Hochul — redacted documents, offered numerous illegitimate privilege claims, and withheld thousands of documents without an apparent legal basis to obstruct the Select Subcommittee’s investigation into former Governor Cuomo’s pandemic-era failures.
No matter how bad you think Covid policies were, they were intended to be worse.
Consider the vaccine passports alone. Six cities were locked down to include only the vaccinated in public indoor places. They were New York City, Boston, Chicago, New Orleans, Washington, D.C., and Seattle. The plan was to enforce this with a vaccine passport. It broke. Once the news leaked that the shot didn’t stop infection or transmission, the planners lost public support and the scheme collapsed.
It was undoubtedly planned to be permanent and nationwide if not worldwide. Instead, the scheme had to be dialed back.
Features of the CDC’s edicts did incredible damage. It imposed the rent moratorium. It decreed the ridiculous “six feet of distance” and mask mandates. It forced Plexiglas as the interface for commercial transactions. It implied that mail-in balloting must be the norm, which probably flipped the election. It delayed the reopening as long as possible. It was sadistic.
Even with all that, worse was planned. On July 26, 2020, with the George Floyd riots having finally settled down, the CDC issued a plan for establishing nationwide quarantine camps. People were to be isolated, given only food and some cleaning supplies. They would be banned from participating in any religious services. The plan included contingencies for preventing suicide. There were no provisions made for any legal appeals or even the right to legal counsel.
The plan’s authors were unnamed but included 26 footnotes. It was completely official. The document was only removed on about March 26, 2023. During the entire intervening time, the plan survived on the CDC’s public site with little to no public notice or controversy.
It was called “Interim Operational Considerations for Implementing the Shielding Approach to Prevent COVID-19 Infections in Humanitarian Settings.”
“This document presents considerations from the perspective of the U.S. Centers for Disease Control & Prevention (CDC) for implementing the shielding approach in humanitarian settings as outlined in guidance documents focused on camps, displaced populations and low-resource settings. This approach has never been documented and has raised questions and concerns among humanitarian partners who support response activities in these settings. The purpose of this document is to highlight potential implementation challenges of the shielding approach from CDC’s perspective and guide thinking around implementation in the absence of empirical data. Considerations are based on current evidence known about the transmission and severity of coronavirus disease 2019 (COVID-19) and may need to be revised as more information becomes available.”
By absence of empirical data, the meaning is: nothing like this has ever been tried. The point of the document was to map out how it could be possible and alert authorities to possible pitfalls to be avoided.
The meaning of “shielding” is “to reduce the number of severe Covid-19 cases by limiting contact between individuals at higher risk of developing severe disease (‘high-risk’) and the general population (‘low-risk’). High-risk individuals would be temporarily relocated to safe or ‘green zones’ established at the household, neighborhood, camp/sector, or community level depending on the context and setting. They would have minimal contact with family members and other low-risk residents.”
In other words, this is what used to be concentration camps.
Who are these people who would be rounded up? They are “older adults and people of any age who have serious underlying medical conditions.” Who determines this? Public health authorities. The purpose? The CDC explains: “physically separating high-risk individuals from the general population” allows authorities “to prioritize the use of the limited available resources.”
This sounds a lot like condemning people to death in the name of protecting them.
The model establishes three levels. First is the household level. Here high-risk people are“physically isolated from other household members.” That alone is objectionable. Elders need people to take care of them. They need love and to be surrounded by family. The CDC should never imagine that it would intervene in households to force old people into separate places.
The model jumps from households to the “neighborhood level.” Here we have the same approach: forced separation of those deemed vulnerable.
From there, the model jumps again to the “camp/sector level.” Here it is different. “A group of shelters such as schools, community buildings within a camp/sector (max 50 high-risk individuals per single green zone) where high-risk individuals are physically isolated together. One entry point is used for exchange of food, supplies, etc. A meeting area is used for residents and visitors to interact while practicing physical distancing (2 meters). No movement into or outside the green zone.”
Yes, you read that correctly. The CDC is here proposing concentration camps for the sick or anyone they deem to be in danger of medically significant consequences of infection.
Further: “to minimize external contact, each green zone should include able-bodied high-risk individuals capable of caring for residents who have disabilities or are less mobile. Otherwise, designate low-risk individuals for these tasks, preferably who have recovered from confirmed COVID-19 and are assumed to be immune.”
The plan says in passing, contradicting thousands of years of experience, “Currently, we do not know if prior infection confers immunity.” Therefore the only solution is to minimize all exposure throughout the whole population. Getting sick is criminalized.
These camps require a “dedicated staff” to “monitor each green zone. Monitoring includes both adherence to protocols and potential adverse effects or outcomes due to isolation and stigma. It may be necessary to assign someone within the green zone, if feasible, to minimize movement in/out of green zones.”
The people housed in these camps need to have good explanations of why they are denied even basic religious freedom. The report explains:
“Proactive planning ahead of time, including strong community engagement and risk communication is needed to better understand the issues and concerns of restricting individuals from participating in communal practices because they are being shielded. Failure to do so could lead to both interpersonal and communal violence.”
Further, there must be some mechanisms to prohibit suicide:
Additional stress and worry are common during any epidemic and may be more pronounced with COVID-19 due to the novelty of the disease and increased fear of infection, increased childcare responsibilities due to school closures, and loss of livelihoods. Thus, in addition to the risk of stigmatization and feeling of isolation, this shielding approach may have an important psychological impact and may lead to significant emotional distress, exacerbate existing mental illness or contribute to anxiety, depression, helplessness, grief, substance abuse, or thoughts of suicide among those who are separated or have been left behind. Shielded individuals with concurrent severe mental health conditions should not be left alone. There must be a caregiver allocated to them to prevent further protection risks such as neglect and abuse.
The biggest risk, the document explains, is as follows: “While the shielding approach is not meant to be coercive, it may appear forced or be misunderstood in humanitarian settings.”
(It should go without saying but this “shielding” approach suggested here has nothing to do with focused protection of the Great Barrington Declaration. Focused protection specifically says: “schools and universities should be open for in-person teaching. Extracurricular activities, such as sports, should be resumed. Young low-risk adults should work normally, rather than from home. Restaurants and other businesses should open. Arts, music, sport and other cultural activities should resume. People who are more at risk may participate if they wish, while society as a whole enjoys the protection conferred upon the vulnerable by those who have built up herd immunity.”)
In four years of research, and encountering truly shocking documents and evidence of what happened in the Covid years, this one certainly ranks up at the top of the list of totalitarian schemes for pathogenic control prior to vaccination. It is quite simply mind-blowing that such a scheme could ever be contemplated.
Who wrote it? What kind of deep institutional pathology exists that enabled this to be contemplated? The CDC has 10,600 full-time employees and contractors and a budget of $11.5 billion. In light of this report and everything else that has gone on there for four years, both numbers should be zero.
Back in June, there was encouraging news that the World Health Organization’s (WHO) pandemic agreement failed to pass. This agreement would have surrendered American sovereignty to unaccountable and unelected international bureaucrats operating at the behest of special interests. Thankfully, this agreement failed to pass.
But the WHO isn’t giving up. It is continuing its march for power.
The issue was brought up to members of Congress for a press conference on the Hill to raise awareness about the ongoing power grab attempt by the United Nations (UN) and the WHO.
The globalists at the UN and the WHO want power over America’s public health policy. If they are successful, their proposed pandemic agreement will irreparably harm American national sovereignty. Family Research Council Action (FRC Action) has been working on this matter and keeping you updated over the past year. Would you consider supporting our work by making a donation today?
This past weekend, the UN hosted a conference called “Summit of the Future” where certain international agreements, including the Pact for the Future, were discussed. The Pact would give the WHO power over the response to future pandemics, large-scale climate events, major events in space, and much more.
During the press conference, Rep. Eli Crane (R-Ariz.) told reporters there were “enough examples and enough reasons” listed in the Pact for the Future’s emergency platform “for them to get involved pretty much whenever and wherever they want to.”
He later said on Washington Watch, “They want authority. They want global governance. And they’ll do whatever they can to achieve that. This agreement that we’re trying to stop would give them authority, global authority, in multiple categories of catastrophic events that might happen around the world.”
Congressman Crane also pointed out that Americans will not be able to vote the WHO’s bureaucrats out of office, meaning they will not be held accountable to we the people. This would be a terrible infringement upon American sovereignty, which is why FRC Action has been sounding the alarm for quite some time.
Recently, the U.S. House passed the No WHO Pandemic Preparedness Treaty Without Senate Approval Act. This important bill would require the Senate to ratify the WHO’s pandemic agreement since it would function as a legally binding treaty. The Senate should also pass this measure to protect American sovereignty.
That’s one reason why the upcoming election is so important. Our nation needs leaders who will protect American sovereignty, not those who will hand it over to bureaucrats overseas. After all, our elected members of Congress are supposed to be the ones who represent the people of the United States.
Also discussed during the UN conference was the UN’s Global Digital Compact, which would require member states to control misinformation and disinformation. Under said Compact, even communications critical of the WHO could be characterized as “misinformation.” The UN’s Common Agenda document would provide “accountability criteria for discrimination and misleading content.”
We cannot allow this dangerous power grab to go unchallenged. I am convinced that the UN and the WHO think we are not paying attention to what they are trying to do. They would be mistaken.
Tens of thousands of you have already signed petitions to Congress urging them not to allow Washington to cede American sovereignty to the WHO.
The United States should defund the UN and the WHO, and any pandemic agreement or treaty should be submitted to the Senate for ratification.
While many ignore the WHO’s continual march for power, actions will continue sounding the alarms and work to stop it. Our members of Congress must act to protect American sovereignty from the WHO.
fox files 
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