Moderna Has Found Another Virus to Monetize

Moderna is back at the public trough with another experimental mRNA vaccine, this time targeting the Bundibugyo strain of Ebola. CBC reports that Health Canada has authorized a Phase 1 trial of mRNA-1469 at three Canadian sites involving about 80 adults. Canada has never recorded a single Ebola case, and its government admits the risk to the general population is low, yet healthy Canadians will supply the human data for a product intended primarily for a third-world African nation.

As of August 1, there were 3,748 confirmed cases and 1,657 deaths in the Democratic Republic of Congo. There is no approved vaccine specifically targeting Bundibugyo Ebola, but Moderna is not financing this humanitarian venture alone. The Coalition for Epidemic Preparedness Innovations has pledged up to $50 million for preclinical research, Phase 1 testing, and manufacturing doses before the early trial is even complete.

This is public risk and private reward dressed up as charity. If the product fails, outside funding absorbs much of the loss. If it succeeds, Moderna gains another proprietary vaccine and governments or international organizations will purchase the doses. Moderna promises to make at least 500,000 doses available to poorer countries at “access pricing,” but it has not told the public what that price will be, or who will ultimately pay the bill.

COVID was perhaps the most profitable virus in pharmaceutical history. Moderna and Pfizer-BioNTech were once projected to generate between $93.2 billion and $124 billion in combined vaccine sales during 2022. Taxpayers helped finance development, governments guaranteed purchases, mandates manufactured customers, and Big Tech silenced those who questioned the arrangement. The corporations kept the profits while politicians treated the population like an obedient herd.

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NIH Used Aborted Babies for Coronavirus Research Under Fauci’s Leadership

The left is incapable of owning abortion and the results of it despite championing it, Shawn Carney, President of 40 Days For Life, said during an appearance on Breitbart News Daily, discussing the gruesome reality of aborted babies being used for coronavirus research.

Host Mike Slater played a clip of Sen. Joni Erst (R-IA) laying out the grueling reality of what happened during the coronavirus as the National Institutes of Health (NIH) used aborted babies for research.

“Researchers also used aborted baby body parts in mice research, and taxpayers paid for them to do that. NIH-funded coronavirus researcher Dr. Ralph Baric and his colleagues at UNC put parts of livers, thymuses, and chunks of human fetal lung that they got from aborted, almost five-month-old human babies. They put those parts in their research mice,” Ernst said during Fauci’s hearing before the Senate Committee on Homeland Security and Governmental Affairs last week.

“They disgustingly named them BLTL mice and wrote they had created a quote sandwich of aborted body parts in the mice. Get it, folks? BLT. A BLT sandwich. Your RML lab employees in Montana also ordered and used aborted baby body parts in their taxpayer-funded research, and emails show how they plan to use those mice for post-COVID work,” she continued.

“NIH funded putting aborted babies’ fingers and scalps off the heads of aborted babies and putting them into the backs of research mice. The scalps later grew fine baby hair in the mice. They even included those disgusting photos in their research paper that you funded. Not all of those were research on coronaviruses, but some were. Thankfully, the current NIH director has said no more of this,” she said.

“Trump banned aborted medical research using aborted babies. Dr. Fauci, yes or no? Do you think that human aborted parts should be put into mice for coronavirus research?” Ernst asked, as Fauci refused to answer.

“It is so much wrong,” Carney said, noting that President Trump banned the use of aborted babies in medical research earlier this year.

“So the HHS did that. … I was at their press conference, and not only did they cite how immoral it is, obviously, but they also cited that it’s not even needed with the medical advancement that that we have today. So Trump, you know, banned this sort of behind the scenes, but it was definitely going on, you know, in this context. And God bless Joni for you know holding Fauci’s feet to the fire,” he said, observing that the left is absolutely incapable of embracing the reality of what they support.

“This is the problem with the left. Why doesn’t he just say, “Look, abortion kills a baby, and yeah, we use the the body parts for research, for the common good. You know, why don’t think just own it?” he asked. “The left will never just own abortion, and you know they clearly didn’t in this case, and it’s hard to watch.”

When asked for the justification for this barbaric practice, Carney said they cite “vaccine use.”

“…which is where we got the flu shot from an aborted baby in the late 1930s,” he said. “It’s that it has cells that only we have, and they can be used and harvested to advance either a vaccine or some kind of medication. But back then, it was – the baby was already aborted. It wasn’t aborted for this purpose. That’s sort of like an end of the weeds, you know, argument. But yeah, that’s what it was used for. And now we don’t need those, you know, sort of human cells in certain vaccines.”

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Fauci’s Diary-Uh: ‘Science’s’ Biggest COVID-Era Lies Thus Far

The diary of Dr. Anthony Fauci, former director of the National Institute of Allergy and Infectious Diseases (NIAID), might be the best thing to happen to us filthy, unvaxxed, granny-killing conspiracy wackadoos who took grenades from weak, terror-stricken Democrats during the COVID era.

In the days since “the Fauch’s” diary was released, We the People have learned what many of us have already kinda, sorta known: Fauci is an evil, lying Keebler elf of death who wrought unspeakable peccancies on the world for fame and fortune, and every day brings another pack of lies Fauci told the world to keep those good times rolling.

Here are some of the greatest lies (thus far) to emerge from Fauci’s demonic diary:

COVID origins: Wuhan lab of bat sandwich?

Fauci maintained for years that COVID was the result of some guy in Wuhan, China, eating a delicious bat salad he bought from a “wet market.” In his diary, dated January 26, 2020, page 676, Fauci admits, “Now we know the market was not the source, it was the amplifier.”

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Trump and Fauci: The Nefarious Tag Team Executing the Genetic Kill Switch on Humanity

The Genetic Kill Switch Introduction

We are living through the final act of a planned global genocide. According to my research findings, Donald Trump and Anthony Fauci are not adversaries — they are tag-team partners in a depopulation agenda that uses a binary weapon to trigger a genetic meltdown of the human race. (I’ll explain more below…)

The first component of this weapon is the spike protein contamination from mRNA injections, which Fauci orchestrated through gain-of-function bioweapons research at the Wuhan lab and laundered into so-called vaccines via Operation Warp Speed (pushed by Trump).

The second component is nuclear war, which Trump is likely to invoke to “finish the job” in Iran. The fallout of radioisotopes causes double-strand DNA breaks in human cells, and the spike protein has already suppressed DNA repair by 85–90%. Together, they form a kill switch that will melt down the genetic integrity of billions of humans and end humanity as we know it.

Here is how this unspeakable plan was set in motion, why the government lies about radiation risks, and what you can do to survive.

The Spike Protein Bio-Weapon: Fauci’s Contribution to Mass Genetic Contamination

Let’s trace the chain of command. Fauci, through the National Institute of Allergy and Infectious Diseases, funneled millions of taxpayer dollars to the Wuhan Institute of Virology via Peter Daszak’s EcoHealth Alliance. Newly released documents show Fauci actively protected Daszak from federal scrutiny while suppressing evidence that SARS-CoV-2 was a lab leak [1]. The result was a gain-of-function spike protein toxin.

As I have previously reported, the spike protein’s modified cleavage site was engineered into the mRNA, and that same synthetic spike is now being produced inside billions of human bodies via the so-called vaccines [2].

The genetic damage from these mRNA injections is catastrophic. A ground-breaking Swedish-Chinese study showed that the SARS-CoV-2 spike protein impairs DNA damage repair and inhibits the BRCA1 and 53BP1 pathways [3]. In plain English, this means the spike protein suppresses the cell’s ability to fix broken DNA by 85 to 90 percent.

The result is turbo cancers, immune failure, and accelerated aging. On top of that, the mRNA shots are contaminated with bacterial DNA plasmids that can integrate into the human genome and trigger cancer [4][5]. This is not a vaccine, in other words — it’s a genetic bioweapon designed to contaminate the entire population and prepare every injected person for the nuclear “genetic meltdown” kill switch.

Trump’s Complicity: From Operation Warp Speed to Nuclear War

Trump cannot pretend to be innocent. He authorized emergency use of the mRNA injections, bragged about Operation Warp Speed, and repeatedly protected Fauci from prosecution. Emails have now revealed that Fauci and then-NIH director Francis Collins agreed to suppress the lab-leak theory for political reasons, and Trump’s administration did nothing to stop it [6]. In fact, Trump’s own FDA commissioner, Marty Makary, recently stated that Fauci was “100% involved” in a “massive” COVID origins cover-up [7]. Yet Trump never held Fauci accountable. Why?

Because they are co-conspirators. They answer to the same boss.

Now Trump is set to launch nuclear weapons in his desperate escalation of war with Iran or Russia. As of early 2026, Trump has escalated rhetoric against Russia, shortening a “50-day” warning to “10 to 12 days” and threatening strikes deep into Russian territory. This is a deliberate provocation designed to trigger a nuclear response that could kill up to 200 million Americans from the initial strikes alone.

The radiation from those bombs will circulate globally and cause double-strand DNA breaks, but the spike protein has already disabled the body’s repair machinery in billions of people. That means billions of human beings will die from genetic damage that could have otherwise been self-repaired if not for the presence of the spike protein, an engineered toxic and part of a binary weapon system targeting human genetic integrity.

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Pfizer Freezes Air Traffic Control Funds in Poland and Romania Over COVID Vaccine Contract Dispute

Pfizer has frozen funds owed to air traffic control agencies in Poland and Romania as part of a contract dispute over COVID-19 vaccine deliveries, according to a report published July 31 by Children’s Health Defense [1]. The freeze followed an April 1 ruling by a court in Brussels that ordered Poland to pay about $1.5 billion and Romania about $640 million, plus interest and fees, for vaccine doses ordered under a 2021 European Union contract.

Polish and Romanian authorities stopped accepting further deliveries in 2022, citing falling demand. Both governments have said they will appeal the ruling. The enforcement action has raised questions about the financial stability of the two countries’ air navigation agencies, which rely on the funds.

Contract Origins and Refused Deliveries

The contract was signed between the European Commission and Pfizer in 2021, and it obligated participating member states to purchase additional doses. By 2022, Poland and Romania refused scheduled deliveries as demand declined. Poland cited financial pressure from hosting refugees fleeing Ukraine. Romanian political scientist Dragos Moldoveanu said Romania ordered 120 million doses despite a population below 20 million and had one of the European Union’s lowest vaccination rates.

Pfizer filed suit in 2023 after the countries did not pay for doses they declined to accept. Earlier contract terms had already drawn criticism. The Bureau of Investigative Journalism reported in February 2021 that Pfizer was demanding countries put up sovereign assets as collateral for expected vaccine injury lawsuits [2].

Legal Enforcement and Appeals

Because the contract is governed by Belgian law, the case is being heard in Brussels. Polish public broadcaster TVP World reported that Poland asked the Belgian court to delay enforcement while it appeals, but the request was rejected.

Dutch attorney Meike Terhorst called the action “outrageous and unethical” and said it could endanger flights. Lukasz Wojdyga of the Warsaw Enterprise Institute said the creditor has a legal right to enforce the judgment but called targeting air-safety funding “disproportionate and irresponsible.” Both governments have said they will protect the financial stability of the agencies and keep services running.

Transparency and Contract Scrutiny

The dispute has revived scrutiny of the EU vaccine procurement. Brussels Signal reported the EU-Pfizer contract was worth 35 billion euros ($40 billion), one of the largest contract awards in EU history. Governments and Pfizer have declined to release contract terms, saying the information is commercially confidential [3].

The European Court of Justice ruled in 2024 that the European Commission violated EU law when it denied The New York Times’ request to review text messages between Commission President Ursula von der Leyen and Pfizer CEO Albert Bourla [4]. In 2025, a court ordered the disclosure of concealed texts related to the deal [5]. European Parliament member Gheorghe Piperea said the contract “ought never to have existed” because the EU exceeded its treaty powers. Transparency activist Frederic Baldan said von der Leyen negotiated directly with Bourla through self-destructing Signal messages, and that a Belgian Federal Police anti-corruption report found sufficient elements to establish offenses. Baldan said the European Public Prosecutor’s Office moved to have the investigation annulled.

The scale of the purchases also drew criticism from public health writers. Michel Chossudovsky questioned how a vaccine that normally takes years to develop was launched within months [6]. Joseph Mercola and Ronnie Cummins noted that the trials’ only criterion of success was a reduction of moderate to severe symptoms, not prevention of infection [7].

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‘We Won Completely’: Weinstein Says COVID ‘Conspiracy Theorists’ Were Totally Vindicated

Not so long ago, everything below was a bannable offense – usually based on the vapid logic of some 24-year-old “trust & safety” associate. In a clip circulating Thursday, evolutionary biologist Bret Weinstein takes stock of what the dissidents actually won for their trouble, Vigilant Fox reports.

WEINSTEIN: “We live in two worlds simultaneously at the moment. I remember conversations that I had with people I cared deeply about at the beginning of COVID right as the lab leak story was beginning to crack.”

“What I saw was, actually, I think we’re going to win the lab leak story. We’re not yet winning the vaccine story, and we’re way behind on the repurposed drug story.

“In 2026, here’s what we see. We actually won. Completely. All of these things are now visible to anybody who wishes to see them.

Yet, while hearts and minds were won and ‘conspiracy theorists’ vindicated, we have a limp dicked government that won’t hold anyone’s feet to the fire

“And we’ve lost completely. Our capacity to do anything about this is now on full display. We have none.”

“Your ability to simply get the story clear enough and enough evidence on the table does not have an impact on what happens next.

“We’re still apparently dispensing these frickin shots. How crazy is that? Right after all that we have unearthed, after all the people who lost their careers to unearth this stuff, they’re still dispensing the frickin shots.”

WEINSTEIN: “We need to figure out now how to talk to the people who actually have goodness in their hearts, but are still so desperately confused.

“You have to figure out how to approach them with enough generosity of spirit that you can get them over the line to just seeing. You can get them to take off the blindfold.”

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Data from a large autism clinic shows 40% of sudden regression autism happened within 2 days after vaccination

Even though this is a crisis, we do not really want to know the true cause of autism.

Why? Because if we used a time proximity analysis, it would reveal that the parental decision to follow their pediatrician’s advice and vaccinate their kids is the cause.

Congress will not investigate because they will lean on large studies which use methods designed specifically not to find a signal to claim vaccines don’t cause autism. But those studies only prove that bad studies can fail to find a signal if they use the wrong methods.

The most sensitive method is simply to make a histogram of the time between a child’s most recent vaccine and the onset of rapid regressive autism. The methodology was described in my earlier Substack article.

You can do this in any autism practice anywhere in the world retrospectively. It is simple. NOBODY HAS DONE THIS. I wonder why?

It took a long time, but I finally located a large autism treatment clinic who was willing to share the statistical information that they had gathered from the parents of autistic kids in the clinic that I wrote about in an earlier Substack article.

This is new. This has never been revealed to the world before. Nobody would dare do that.

The clinic examined 182 patient records.

84 were “rapid onset autism” cases (46%).

Of those cases, a “routine vaccination” was mentioned as happening before the event in 98% of those cases.

In 40% of the cases, the regression happened within 2 days after routine vaccination.

In 76% of the cases, the regression happened within 2 weeks after routine vaccination.

These numbers cannot happen by chance.

The only explanation is vaccines cause autism. Adding acetaminophen post-vaccine makes the autism outcome more likely.

However, if you believe otherwise, please explain in the comments what you think is causing these cases.

I predict there will be no follow ups on this from any country in the world because they don’t want to know the truth that they are causing the autism epidemic.

This data is stunning. I’m arranging funding of a larger version of this study and hopefully, we can get it on a preprint server. It will likely never be published in any mainstream journal.

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Clinical Trial Results Were Clear: Pfizer’s COVID Vaccine Delivered More Risk Than Benefit

U.S. Health Secretary Robert F. Kennedy Jr.’s recent decision to terminate the COVID-19 emergency use authorization (EUA) declarations invites reconsideration of the evidence that launched this extraordinary regulatory chapter.

The U.S. Food and Drug Administration’s (FDA) first EUA for a COVID-19 vaccine rested on its determination that the known and potential benefits of the Pfizer-BioNTech vaccine outweighed its known and potential risks. Yet the pivotal trial report did not bring those benefits and risks together within a common quantitative framework.

Better late than never: more than five years later, I did — and what I found was startling.

At first glance, the famous 95% efficacy against protocol-defined, laboratory-confirmed symptomatic COVID-19 — based on eight versus 162 cases in a trial that randomized 43,548 participants — seems highly promising.

But when this finding is considered alongside the broader set of participant-relevant outcomes (dispersed across the trial publication, its Supplementary Appendix, and the contemporaneous FDA review materials), the overall clinical picture looks markedly different.

Depending on the counting period used, the vaccine group had 2-8 fewer cases of severe COVID-19, whereas the safety data showed numerical excesses of 4-101 participants across clinically consequential adverse-event categories. These categories are not directly comparable, and some may overlap.

Even so, the evidence did not establish that the vaccine’s clinically consequential benefits outweighed its potential harms. Nor did the trial establish that vaccination reduced the overall burden of COVID-19-like symptoms, let alone that it reduced person-to-person transmission.

Crucially, this conclusion does not rest on hindsight: the relevant evidence was already before the FDA when it issued the EUA.

The full basis for this conclusion is presented in my comprehensive reassessment of the evidence, currently available as a preprint. That reassessment is necessarily detailed because the relevant data are complex, scattered across multiple documents and subject to important methodological and interpretive qualifications.

The present column is not intended to replace that analysis, but to distill several of its central findings and implications for a broader readership.

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Sen. Ron Johnson Unloads Devastating Safety Data on Fauci — Says COVID Shot Logged Nearly 7,000 Death Reports Per Year While FDA Ignored Warning Signs and Pushed Remdesivir

Sen. Ron Johnson (R-WI) dropped another bombshell during Wednesday’s explosive Senate hearing with Dr. Anthony Fauci, confronting the former COVID czar with adverse event data that he argued should have triggered urgent scrutiny years ago—but instead was ignored while federal health agencies relentlessly promoted COVID vaccines and Remdesivir.

Johnson’s latest exchange came after he previously confronted Fauci with stacks of studies on ivermectin and questioned why federal officials dismissed evidence supporting alternative treatments before Fauci invoked his Fifth Amendment right against self-incrimination during the hearing.

The Wisconsin senator displayed comparative adverse-event figures during the hearing, arguing they represented safety signals that federal regulators refused to adequately investigate.

“These are averages. Again, it doesn’t prove causation, but there’s correlation. It’s there. It’s there for a safety signal,” Johnson said.

The chart, titled “Drug Adverse Event Comparison” and labeled “FDA and CDC Data: Worldwide,” compared adverse event reports, total reported deaths, and average deaths per year across multiple products.

According to the chart presented by Johnson:

  • Ivermectin (30 years, 1996–2026): 5,127 adverse events, 518 deaths, averaging 17 deaths per year.
  • Hydroxychloroquine (HCQ) (38 years, 1988–2026): 37,270 adverse events, 5,404 deaths, averaging 142 deaths per year.
  • Flu vaccines (36 years, 1990–2026): 243,335 adverse events, 2,770 deaths, averaging 77 deaths per year.
  • Dexamethasone (57 years, 1969–2026): 143,017 adverse events, 25,589 deaths, averaging 448 deaths per year.
  • Tylenol (57 years, 1969–2026): 184,186 adverse events, 42,627 deaths, averaging 747 deaths per year.
  • Remdesivir (69 months): 10,657 adverse events, 2,751 deaths, averaging 546 deaths per year.
  • COVID-19 vaccines (68 months): 1,677,227 adverse events, 39,182 deaths, averaging 6,922 deaths per year.

The chart also highlighted that 9,342 reported deaths occurred on days 0, 1, or 2 following COVID-19 vaccination.

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HHS So Confident an Influenza Pandemic Will Be Declared It’s Developing ‘Day One’ Vaccines, SAM.gov RFI Reveals

In a June Request for Information (RFI) titled “Protection Before Day One Vaccine: Advancing Broadly Protective Seasonal Influenza Vaccines with Pandemic Coverage,” the U.S. Department of Health and Human Services (HHS) is asking the biotechnology industry to develop influenza vaccines before the next pandemic begins, reflecting a level of planning that treats another influenza pandemic as a matter of when, not if.

HHS is therefore confident that there will be a future determination by authorities that an influenza pandemic has begun.

The proposal follows a series of federal future influenza pandemic-orchestrating initiatives, including Congress seeking $3.3 billion for a future influenza pandemic, HHS funding experiments determining how to make H5 influenza more pathogenic, HHS funding the creation of never-before-seen chimeric H6Nx bird flu viruses said to carry immune-evasion traits, and DARPA/NIH-funded scientists reprogramming dormant influenza parts with new replication and competition-suppressing functions.

It also comes after U.S. taxpayers funded the research behind Moderna’s new mRNA-1010 influenza vaccine and an FDA—which is under HHS—advisory committee backed the shot despite providing less than a 1% absolute benefit.

The initiatives raise a fundamental national security question: Why is the government simultaneously investing in making influenza viruses more dangerous while preparing “Day One” vaccines for the influenza pandemic it appears to expect?

You can contact HHS here to ask why the agency is planning for another influenza pandemic while simultaneously funding research that seeks to increase the capabilities of influenza viruses (see list of many such projects at the end of this article).

The RFI lists Wendy Rehman (wendy.rehman@ati.org) as the “Primary Point of Contact” for the Protection Before Day One Vaccine project.

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