And ask yourself, and Secretary Kennedy, why he’s approving more and more of them. Safe for whom? Effective at what?
On September 22, President Trump and HHS Secretary Kennedy announce made the long-awaited announcement on autism that was the bold departure from previous failures to look squarely at the issue and speak boldly and honestly about it. And these two publicly funded officials boldly managed to ignore the entire herd of elephants in the room with them. Every. Single. One.
We have three bold new initiatives that sidestep the real issue as a means to “restore trust” and help families. ‘wanna buy a bridge?
But reality is rolling out, whether Kennedy and Trump want it to or not. Science is pumping out important, often very large-scale studies showing that mRNA vaccines are perhaps the greatest threat to humanity that we have ever faced.
There is good science emerging, but there is little good news in the remarkable document that follows here. The news, although mostly not good, is information nonetheless that you urgently need. CMN News, the Credible Medical News Network, provides a compendium and compilation of peer reviewed studies and authoritative opinion pieces which is, taken together, extremely worthwhile.
But the bad news is that the mRNA news is very, very bad. Not hopeless, but bad. Turbo cancer bad. VAIDS bad. Post injection DNA modification bad. Neurodegenerative and cardiovascular and immune function bad.
If you know people who are beginning to take in data to counter their blind faith in “safe and effective” magic words, there is a good deal here for them. Read on.
In case you needed something else to cement your conviction that mRNA vaccines are not good for living things (are any vaccines good for living things?), please take a look at this very large South Korean study.
What it underscores, yet again, is that no sane person will willingly accept an mRNA vaccine in their body, or that of their child/pet/loved one.
But isn’t Secretary Kennedy, our man on the Hill, protecting us from mRNA and other vaccines?
Among the “vaccines” approved since Secretary Kennedy took office on February 13, 2025, are more mRNA jabs, including a replicon one. And that is, indeed, very, very bad.
Here’s the list of approvals since then (mRNA jabs are in BOLD)
Penmenvy (GSK) was Approved on February 14, 2025. Nuvaxovid (Novavax) was approved May 19, 2025 mNexSpike (Moderna) was approved on May 30, 2025.2 This is a self-amplifying mRNA (replicon) vaccine which uses a self-replicating RNA platform that amplifies antigen expression inside cells. mResvia (Moderna) was approved June 12, 2025 Imovax (Sanofi) was approved on July 24, 2025 Ixchiq (Valneva Austria GmbH) was approved on August 6, 2025 Updated 2025-21026 COVID-19 formulations (Comirnaty by Prizer, Spikevax by Moderna and nNexSpike by Moderna) were approved August 27, 2025
Frankly, when you look at the other vaccines in this list, their lack of safety and dangerous profiles are appalling as well, but mRNA vaccines, especially the horrifying replicon platform ones, are an especial threat to the continued existence of humanity. Which makes sense, after all, since they are, in fact, bioweapons.
They are absolutely safe and effective,just not the way you think: safe for the people who developed them and hide behind the clever cover story of the weapons as vaccines and effective in incapacitating and killing people (that is what weapons are supposed to do, after all).
Not safe as in harmless and effective in preventing disease. Nope. Safe from prosecution and effective as destroying the population.
But, c’mon! We don’t have nearly enough of these Safe and Effective biological Molotov cocktails. We need more, lots more! We are in luck! Coming right up!
Here is a chart showing the jabs currently in the pipeline for FDA approval or recently approved. Note that we now have both “Conventional” mRNA and “Replicon mRNA” “vaccines” coming at us:
Secretary Kennedy and President Trump chose to focus on Tylenol (acetaminophen) as the convenient autism boogey man of the moment. Aside from a few dropped hints by the NOT Secretary of Health and Human Services, vaccines pretty much got a free pass despite Secretary Kennedy’s prior research, campaigns, statements, documentaries, law suites and speeches. Poof! Just like that!
It’s Tylenol! Secretary Kennedy’s research, campaigns, statements, documentaries, law suites and speeches, like the morning mist, seem to have vanished into our fondest memories of yesteryear.
Here is a question for Secretary Kennedy: now that we’ve got autism out of the way by just avoiding a simple OTC drug in pregnancy (which hardly explains the normally developing child who gets an MMR shot at 18 months and develops regressive autism over the next 24 hours, especially if they did not get Tylenol, but, never mind – we’re sticking to the Tylenol story), could we turn to the excess deaths, myocarditis, turbo cancers, the fertility cataclysm, clotting disorders (in life and in death), autoimmune diseases, neurodegenerative disorders and the host of other horrifying consequences of “Conventional” mRNA, the disastrous “Replicon” mRNA and the ordinary disaster that “ordinary” vaccines are and have been? Or do we get to focus on another major candidate making America unhealthy, like FDA Red Dye #3 or Tylenol?
Pentagon-funded study confirms scientists deliberately created airborne hantavirus particles and carried out stabilization trials to prolong their survival.
The U.S. military has funded research, published in July in the journal Pathogens, in which scientists deliberately aerosolized Sin Nombre virus (SNV)—the hantavirus that kills roughly 30% of those infected—in order to study how long the virus can survive in the air and under what conditions it remains infectious.
Why is the Pentagon commissioning experiments that turn a rodent-borne virus with a 30% kill rate into an airborne particle?
Why are U.S. defense labs probing how to stabilize lethal aerosols?
The study would say it aerosolized hantavirus because “gaining insight into the SNV bioaerosol decay profile is fundamental to the prevention of SNV infections,” but the deeper concern is whether such work risks accidental release or could be harnessed intentionally for pandemic potential.
This new study fits the same disturbing pattern: taxpayer-funded projects that blur the line between “biodefense” and the step-by-step recipe for a future bioweapon.
Dr. Richard Bartlett didn’t mince words as he raised alarm over Pentagon-backed hantavirus aerosol experiments:
“How much longer will We the People tolerate our government using our tax dollars to do deadly experiments in our homeland? Has anyone heard that the COVID pandemic might have been caused by a lab leak? We have no guarantee that another lab leak might happen on our own soil. Remember: Dr. Anthony Fauci and a 2016 NIH-led biosecurity report identified insider leaks as the “most probable” risk in gain-of-function research.”
A Lethal Virus
The authors admit the severity of the pathogen upfront:
“Later symptoms involve respiratory distress that requires immediate medical attention and has a 30% fatality rate.”
In other words, this is not a mild virus.
If contracted, nearly one in three patients will die, and there is no approved treatment or vaccine.
The Pentagon’s Involvement
This wasn’t purely academic work.
The study declares its sponsor:
“This research was funded by the Defense Threat Reduction Agency (DTRA), under grant number DTRA/CBS-NSRI CB1099.”
That means the Pentagon’s weapons division paid for scientists to aerosolize and study the airborne stability of a lethal hantavirus—a clear overlap with bioweapons research.
Aerosolizing a Killer
The researchers describe how they turned the virus into an aerosol:
“Suspensions were aerosolized via a 120 kHz ultrasonic nozzle… with 3 lpm of carrier air.”
Put plainly, they deliberately converted liquid hantavirus into airborne particles small enough to reach deep into human lungs.
This step—aerosolization—is the foundation of making a respiratory bioweapon.
Measuring Airborne Survival
They then tracked how long these particles remained infectious under different conditions:
“At 49.1 ± 0.8% RH, the addition of 1.0 ppm ozone caused a significant increase in the amount of SNV decay at 2.6 ± 0.1 log/min.”
In other words, in normal humidity, the virus survives in the air unless destroyed by ozone.
Sunlight weakened it but did not fully eliminate infectivity.
This proves SNV is stable enough to persist airborne indoors—such as in barns, sheds, or attics—precisely where human infections are known to occur.
Comparison to Other Pandemic Viruses
The researchers themselves compared SNV to avian influenza and Lassa virus:
“This transmission route is similar to other viruses that have an environmental transmission route, such as avian influenza (e.g., H5N1) and Lassa virus.”
This places hantavirus in the same category as pathogens with known pandemic potential.
The implication is clear: if SNV ever adapted to spread person-to-person, as Andes virus already does, the results would be catastrophic.
Particle Sizes Optimized for Lung Infection
The team also measured the size of the particles they created:
“The results indicated a bimodal distribution… with a peak at under a micron in size and a second peak under two microns.”
Translated, these are exactly the particle sizes most dangerous to humans, capable of bypassing upper airways and embedding deep inside the lungs.
This is a specialized flow-through system designed to expose bioaerosols to controlled conditions such as simulated sunlight, ozone, and humidity.
Institutional Affiliations
The authors are affiliated with the following institutions:
Department of Pathology, Microbiology, and Immunology, University of Nebraska Medical Center (UNMC), Omaha, NE
The Global Center for Health Security, University of Nebraska Medical Center (UNMC), Omaha, NE
National Strategic Research Institute (NSRI), Omaha, NE
Center for Global Health, Department of Internal Medicine, University of New Mexico, Albuquerque, NM
Full List of Scientists
Elizabeth A. Klug
Danielle N. Rivera
Vicki L. Herrera
Ashley R. Ravnholdt
Daniel N. Ackerman
Yangsheng Yu
Chunyan Ye
Steven B. Bradfute
St. Patrick Reid
Joshua L. Santarpia
Bottom Line
The Pentagon has funded scientists to take a hantavirus with a 30% fatality rate, aerosolize it into tiny lung-penetrating particles, and measure how long it stays infectious in the air.
This kind of research, while framed as biodefense, is indistinguishable from steps needed to weaponize a virus.
With no vaccine or treatment available, the knowledge produced here doesn’t just help “protect”—it creates a blueprint for how to turn hantavirus into a bioweapon.
Shot hijacks human cells to churn out “heterotrimeric” hybrid spikes—Frankenstein chimeras made of Wuhan and Omicron parts never found in nature.
A new preprint published August 19, 2025, in bioRxiv reveals that a Gates Foundation–funded team at Caltech, Gladstone Institutes, and Acuitas Therapeutics has engineered a self-amplifying mRNA vaccine platform that doesn’t just code for spike protein—it forces human cells to self-replicate the RNA instructions and churn out entire enveloped coronavirus-like particles (eVLPs).
Who & Where
The study was conducted by Chengcheng Fan, Alexander A. Cohen, Kim-Marie A. Dam, Annie V. Rorick, Ange-Célia I. Priso Fils, Zhi Yang, Priyanthi N. P. Gnanapragasam, Luisa N. Segovia, Kathryn E. Huey-Tubman, Woohyun J. Moon, Paulo J.C. Lin, Pamela J. Bjorkman, and Magnus A. G. Hoffmann, with affiliations at Caltech, Gladstone Institutes (UCSF), University of Washington, UC Berkeley, and Acuitas Therapeutics in Vancouver.
Funding disclosures make it explicit:
“These studies were funded by … Gates Foundation INV-034638 (P.J.B.) and INV-056219 (M.A.G.H.).”
That means Bill Gates’ foundation bankrolled this self-amplifying virus-factory vaccine.
Self-Amplifying & Whole Virus Design
Unlike first-generation COVID shots, this platform is designed to keep copying itself inside the cell—leading to higher, longer-lasting output.
Self-amplifying vaccines not only instruct the body’s cells to make the coronavirus spike protein—like the original mRNA COVID vaccines do—but they also instruct cells to make an enzyme that makes “copies of the original strand of RNA.”
This process leads to the production of even more spike protein within the body than first-generation mRNA COVID jabs produce.
Purported “benefits” of samRNA include extended duration (time) and magnitude (amount) of spike protein creation, a “strong” immune response, and requiring a smaller dose than original mRNA jabs.
The new study comes on top of Yale University School of Medicine’s discovery that spike protein from the original jabs can linger in the body for 709 days—when, earlier in the COVID pandemic, health authorities told us the spike protein only stays in the body “up to a few weeks.”
The authors of the new Gates-funded preprint describe their work this way:
“We recently developed the ESCRT- and ALIX-binding region (EABR) mRNA vaccine platform, which encodes engineered immunogens that induce budding of enveloped virus-like particles (eVLPs) from the plasma membrane, thereby resulting in presentation of immunogens on cell surfaces and eVLPs.”
This means the injected RNA doesn’t just make spike once—it replicates, keeps instructing, and drives cells to bud off whole coronavirus-like shells.
Far more viral material is created inside the body compared to regular mRNA jabs.
The implication: If standard mRNA already triggered spike toxicity and DNA contamination concerns, self-copying versions exponentially magnify those risks.
Cells Turned Into Virus Factories
The experiments confirmed that mammalian cells, when hit with this design, shed whole synthetic viral particles:
“To verify that the designed constructs induce eVLP budding, HEK293T were transiently transfected … After 48 hours, transfected cell supernatants were harvested, and eVLPs were purified by ultracentrifugation.”
Translation: In the lab, the vaccine instructions reprogrammed cells to manufacture and release entire pseudo-coronaviruses.
Novel Hybrid Spikes Created
Even more alarming, when two versions of spike were included (Wuhan + Omicron), they fused into brand-new hybrid proteins:
“Co-expression of ancestral Wu1 and Omicron S in the same cell could result in the formation of S heterotrimers consisting of Wu1 and Omicron S protomers.”
That means the vaccine doesn’t just make past spikes—it fabricates chimeric coronavirus spikes never seen before in nature.
Confirmed by Cryo-EM
This wasn’t theoretical modeling.
Cryo-electron microscopy reportedly directly showed the new synthetic hybrids:
“Single-particle cryo-EM analysis confirmed … trimerized HT2 and HT3 S proteins … These data demonstrate heterotrimeric S formation for soluble forms of SARS-CoV-2 S proteins.”
In other words, scientists actually imaged the new hybrid coronavirus spikes generated by the vaccine platform.
The Bigger Picture
This Gates-funded research is not isolated.
As my previous investigations have shown, governments and global foundations are already bankrolling self-amplifying mRNA (sa-mRNA) platforms worldwide.
Japan has already approved one (ARCT-154), and the Biden administration handed Gritstone Bio a $433-million contract to advance its own self-copying jab.
These vaccines are said to be “more efficient.”
But the reality is they extend duration and magnitude of spike production inside the body.
Cambridge University scientists already warned that first-gen mRNA is misread 10% of the time, producing rogue proteins in one-third of recipients.
If self-amplifying vaccines magnify those errors, the risks grow exponentially.
Bottom Line
Gates Foundation money funded an mRNA vaccine that self-replicates and programs cells to manufacture entire coronavirus-like particles.
This goes far beyond spike: cells become virus factories, producing synthetic hybrid spikes never found in nature.
Combined with the self-amplifying mechanism, the body isn’t just briefly making spike—it’s pushed into prolonged production of whole pseudo-viruses.
Bill Gates’ fingerprints are now on a technology that forces the body to churn out entire synthetic coronaviruses, amplified from within.
A new peer-reviewed study published today in Autoimmunityhas confirmed that both Pfizer-BioNTech and Moderna’s mRNA COVID-19 injections are contaminated with enormous quantities of DNA fragments—billions to hundreds of billions per dose—with Pfizer’s product uniquely containing the SV40 promoter-enhancer, a viral genetic element long associated with cancer concerns.
The study was authored by Dr. David J. Speicher, Dr. Jessica Rose, and Dr. Kevin McKernan.
The startling findings come as Pfizer’s own confidential safety data show serious injuries clustering in blood, immune, and neurological systems—the exact three human DNA fragments built into its vaccine plasmid, raising the possibility that plasmid integration is driving the very harms now dominating the safety signal.Subscribe
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Residual DNA Found in Every Vial Tested
The contamination was not limited to a few batches.
The authors make it plain:
“Residual DNA was detected in all 32 vaccine vials surveyed.”
Every single dose they tested had measurable DNA contamination.
Levels Exceed FDA & WHO Limits by Up to 627-Fold
The FDA and WHO set a maximum limit of 10 ng of DNA per dose.
These vaccines blew through that ceiling:
“Using fluorometry coupled with RNase A digestion, all products tested exceeded the guidelines for residual DNA set by the FDA and WHO of 10 ng/dose by 36–627-fold.”
Translation: These vaccines didn’t just skirt the limit—they shattered it, with up to 627 times more DNA than allowed.
Pfizer Contains SV40 Promoter—Linked to Gene Activation & Cancer
One of the most alarming discoveries: only Pfizer vials contained the SV40 promoter-enhancer, a sequence designed to push DNA into cell nuclei and drive gene expression.
“The SV40 promoter-enhancer-ori (0.25–23.72 ng/dose) was only detected in Pfizer vials.”
The SV40 promoter is not an inert bystander—it’s a nuclear targeting element used in gene therapy and flagged in past studies as tumorigenic.
This means Pfizer doses deliver cancer-linked viral DNA elements directly into patients’ cells, wrapped in lipid nanoparticles.
Billions to Hundreds of Billions of DNA Fragments Per Dose
This isn’t just a little DNA dust.
We’re talking staggering numbers:
“These data demonstrate the presence of 1.23 × 10^8 to 1.60 × 10^11 plasmid DNA fragments per dose encapsulated in lipid nanoparticles.”
That’s hundreds of billions of DNA molecules in each injection, not floating free but packaged in lipid nanoparticles designed to deliver genetic material into human cells.
Pfizer’s DNA Exceeds Limits in Multiple Lots
While Moderna’s DNA fragments stayed within FDA limits by qPCR, Pfizer repeatedly broke through:
“When tested by qPCR, all Moderna vials were within the regulatory limit, but 2/6 Pfizer lots (3 vials) exceeded the regulatory limit for the SV40 promoter-enhancer-ori by 2-fold.”
So Pfizer’s contamination isn’t hypothetical—it’s verified above-regulatory limits.
DNA Fragments Are Protected, Not Degradable
If these were just naked DNA fragments, they’d be destroyed quickly.
But because they’re wrapped inside lipid nanoparticles, they’re shielded from breakdown and can enter cells efficiently.
The authors stress:
“This study emphasizes the importance of methodological considerations when quantifying residual plasmid DNA in modRNA products, considering increased LNP transfection efficiency, and cumulative dosing presents significant and unquantified risks to human health.”
Layman’s terms: these DNA fragments are protected, designed to get into your cells, and regulators never accounted for that risk.
Authors’ Warning
In their conclusion, the authors reaffirm the data “demonstrate the presence of billions to hundreds of billions of DNA molecules per dose in the modRNA COVID-19 products tested.”
They warn that current safety guidelines are outdated and must be revised, urging replication of their findings under strict forensic conditions.
“Our findings extend existing concerns about vaccine safety and call into question the relevance of guidelines conceived before the introduction of efficient transfection using LNPs. With several obvious limitations, we urge that our work is replicated under forensic conditions and that guidelines be revised to account for highly efficient DNA transfection and cumulative dosing.”
The scientists stress that regulators must follow the precautionary principle, prove safety with transparency, and fully disclose how these products are made.
“This work highlights the need for regulators and industry to adhere to the precautionary principle and provide sufficient and transparent evidence that products are safe and effective, and disclose the details of their composition and method of manufacture.”
Bottom Line
Pfizer and Moderna’s COVID-19 vaccines were found to contain massive amounts of residual DNA—far above regulatory thresholds—with Pfizer uniquely contaminated by SV40 promoter-enhancer sequences.
These DNA molecules are packaged in lipid nanoparticles that maximize cell entry, raising the specter of genome integration, cancer risk, and long-term genetic damage.
The authors—Speicher, Rose, and McKernan—are clear: regulators need to reassess DNA safety limits in light of lipid nanoparticle delivery and cumulative dosing, something never done before these products were unleashed globally.
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.
In late 2019, the FBI came into possession of Hunter Biden‘s laptop. The laptop contained damning evidence that directly implicated the Biden family and Joe Biden himself. Specifically, it proved a pattern of influence-peddling, where political access was traded for personal and familial gain involving various international players. However, instead of revealing this information, or even preparing for a legitimate disclosure, the FBI chose a different route. Over the course of 2020, they embarked on a campaign with Big Tech to ensure this story—the truth—would be buried before it ever came to light. The FBI, aided by Big Tech companies, successfully suppressed the Hunter Biden laptop story in an effort that ultimately constituted interference in the 2020 presidential election—and according to polling changed the outcome of the election.
The timeline of the Hunter Biden laptop story—from its initial acquisition by the FBI to the New York Post’s publication of the details, and the ensuing censorship by Big Tech—reveals the depth of coordination that was at play. The FBI’s actions went beyond mere incompetence or negligence; it was a preemptive strategy to condition influential social media platforms to dismiss any forthcoming stories about Hunter Biden as Russian disinformation. This “prebunking” approach—preemptively discrediting real information—ensured that when the truth finally emerged, it was met with skepticism, censorship and suppression.
The Timeline of Interference
The first significant event in this saga occurred in late 2019, when the FBI acquired Hunter Biden’s laptop. By this point, the FBI had verified its authenticity—a verification that took place before any public reporting on the laptop’s contents. The laptop, abandoned by Hunter Biden at a Delaware repair shop, contained emails, photos and documents detailing the Biden family’s involvement in foreign business dealings, with the former Vice President allegedly benefiting from these ventures. The laptop was, without a doubt, real, and the FBI knew it.
Despite this knowledge, the FBI took a questionable next step. In early 2020, they began meeting with Big Tech companies, such as Facebook, Twitter and Microsoft, ostensibly to prepare them for potential Russian disinformation campaigns targeting the upcoming election. During these meetings, the FBI set the narrative. They warned that foreign actors—most notably Russia—might attempt a “hack-and-leak” operation intended to discredit the Biden family. The FBI specified that this operation would likely involve claims about the Biden family’s ties to Ukraine—a detail very close to the information that was already present on Hunter Biden’s laptop.
These meetings between the FBI and Big Tech were not casual conversations. Over the course of 2020, the FBI held more than 30 such meetings with major social media platforms, consistently hammering home the point about an impending “October Surprise” in the form of leaked information about the Bidens. Not only did this position social media companies to expect an attack, but it also primed them to act as gatekeepers, ready to filter or suppress anything that matched the FBI’s predicted narrative.
Big Tech’s Role in Suppression
The turning point came in October 2020 when the New York Post published its explosive story on the Hunter Biden laptop. The timing—just weeks before the presidential election—made the story incredibly significant. Almost immediately after publication, Big Tech companies took action to limit its spread. Twitter outright banned users from sharing links to the story, even locking accounts that tried, including that of the New York Post itself. Facebook, for its part, suppressed the story’s reach on its platform, reducing its visibility to users and ensuring it would not gain traction in the crucial days leading up to the election.
This coordinated suppression did not happen in a vacuum. Internal communications from Facebook reveal that they were acting based on information from the FBI. In one chat, Facebook employees openly discussed how the FBI had warned them about an imminent leak related to Burisma—the Ukrainian energy company with ties to Hunter Biden. These conversations happened only a week before the New York Post story broke. The alignment between what the FBI had “warned” about and what actually happened was notable.
Even more noteworthy are the internal communications from Facebook and Microsoft employees, who acknowledged that the FBI had effectively “tipped them off” about the story. One Microsoft employee noted that the FBI’s warning had specifically mentioned a potential Burisma story, adding that the timing matched exactly with the New York Post release. Such specificity raises serious questions about whether the FBI’s intention was ever about safeguarding the election from disinformation—or if it was about managing the narrative to protect one candidate from a damaging story.
Facebook’s own leadership seemed aware of the stakes. In internal messages, Nick Clegg, Facebook’s Vice President of Global Affairs, admitted that their handling of this issue would influence how a “Biden administration views us.” This kind of political calculation—censoring legitimate news to curry favor with an incoming administration—is the very definition of election interference. The internal cynicism among Facebook’s staff was evident: when discussing their suppression of the New York Post story, one employee noted, “The Press is only as good to you as you are bad to Trump.”
The very employees tasked with executing these policies knew the likely impact. They joked about how, when eventually called to testify, they would say that their actions to “influence the 2020 election” had been planned with the U.S. government for years. These jokes were admissions. The censorship was not incidental; it was designed, coordinated, and executed based on direct guidance from the FBI.
The Impact on Public Perception
The FBI’s efforts did not end with Big Tech’s suppression of the story. Only days after the New York Post article was published, 51 former intelligence officials released a public statement claiming that the Hunter Biden laptop had “all the classic earmarks of a Russian information operation.” This statement, orchestrated by Secretary Antony Blinken while he was an advisor to the Biden campaign, was intended to cast further doubt on the story. The statement provided the final piece of the puzzle: a supposed expert validation that the laptop was part of a foreign disinformation effort, even though it was not. Former Vice President Joe Biden cited this letter in his defense during debates, using it to dismiss the revelations as “Russian disinformation,” even as the FBI knew it was authentic.
In the four years since the 2020 election, the truth has slowly unraveled. Mark Zuckerberg and other Big Tech leaders have admitted that their actions to suppress the New York Post story were influenced directly by the FBI. These admissions come too late. The damage—in the form of suppressed information, manipulated public opinion and election interference—has already been done. The FBI’s preemptive framing of the Hunter Biden story as a Russian plot was a calculated effort to control the narrative and protect a favored candidate.
A Pattern of Censorship
What happened with Hunter Biden’s laptop was just the beginning. Once the Biden regime took office, pressure on Big Tech to censor content only grew. In the months following the inauguration, platforms like Facebook, YouTube and Amazon began receiving explicit demands from the White House to curb speech deemed undesirable by the regime. This included not only political content but also opinions and jokes, signaling an era of broad and pervasive censorship. My own accounts on Twitter and Medium were permanently suspended.
The collaboration between the Biden-Harris regime and Big Tech took many forms, but the roots were planted in 2020 when the FBI orchestrated a plan to “prebunk” an accurate story about Joe Biden’s corruption. This prebunking effort weaponized both the media and major technology companies, effectively turning them into tools of state influence. By controlling the flow of information, the FBI ensured that voters would not learn about Hunter Biden’s dealings until it was too late to matter. This not only undermined faith in the institutions that are supposed to ensure fair elections but also demonstrated a significant level of governmental overreach.
Conclusion
The suppression of the Hunter Biden laptop story in 2020 represents one of the clearest examples of state-sponsored election interference in U.S. history. The FBI had the laptop, verified its authenticity and instead of allowing the information to reach the public, undertook a campaign to preemptively discredit it. They primed Big Tech to see the story as a foreign attack, and when the New York Post broke the news, Big Tech platforms did what they had been conditioned to do—they censored it. The result was a manipulated election where critical information about one candidate was withheld from the public.
This case is not only about Hunter Biden’s laptop. It is about the relationship between the federal government and the platforms we rely on for information. It is about the deliberate actions taken by those in power to shape what voters know and, ultimately, how they vote. The weaponization of the FBI and Big Tech to “prebunk” a true story speaks to the broader dangers of unchecked government influence over supposedly independent media channels. As the revelations continue to unfold, the American people must demand accountability, transparency, and, most importantly, a commitment to protecting the sanctity of free and fair elections.
fox files 
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