Tag: coronavirus

Ghost Shot: Pfizer quietly admits it will never manufacture original FDA approved COVID vaccines

The August 23, 2021 FDA approval of Pfizer’s Comirnaty vaccine was a cause for celebration. Marked as a turning point in the battle against COVID19, the announcement was highly publicized by the Biden Administration with the clear intention to extinguish “vaccine hesitancy” and boost uptake.

It was celebrated as a cause for national relief, and many Americans arrived at their local pharmacies under the impression, via government and pharmaceutical propaganda, that they were receiving an FDA-approved COVID vaccine. Yet that legally distinct product, as we know it, never existed. And now we know, via Pfizer, that it will never exist.

For the uninitiated:

Comirnaty is a legally distinct product from the emergency use authorization (EUA) shots, and It has never made its way to market. For months on end, no such vaccine has ever become available. Those who received the “Pfizer shot(s)” have been injected with the emergency use authorization (EUA) version of the shots.

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3 New Plaintiffs Ask to Join COVID Vaccine Injury Lawsuit Against Bill Gates

Three COVID-19 vaccine injury victims are asking to join a Dutch lawsuit against Bill Gates, Pfizer CEO Albert Bourla and 15 other defendants, alleging they misled the public about the safety of the COVID-19 vaccines.

The lawsuit was filed last year by seven COVID-19 vaccine injury victims, one of whom has since died.

According to a filing by the plaintiffs’ attorney, Peter Stassen, the three new victims “were healthy people” who began experiencing health problems after receiving mRNA COVID-19 vaccines.

“The applicants are of the opinion that the serious side effects that occurred after having the Covid-19 (mRNA) injections are the direct result of the content / composition of these Covid-19 (mRNA) injections,” the filing states.

Doctors have repeatedly refused to diagnose a link between vaccination and their injuries, Stassen said.

During a hearing today at the District Court of North Netherlands in Leeuwarden, Stassen also asked the court to approve five expert witnesses who will testify about the risks and dangers of the COVID-19 shots:

  • Catherine Austin Fitts, founder and publisher of the Solari Report and former U.S. assistant secretary of Housing and Urban Development.
  • Sasha Latypova, a former pharmaceutical research and development executive.
  • Joseph Sansone, Ph.D., a psychotherapist who is litigating to prohibit mRNA vaccines in Florida.
  • Katherine Watt, a researcher and paralegal.
  • Mike Yeadon, Ph.D., a pharmacologist and former vice-president of Pfizer’s allergy and respiratory research unit.

Another proposed witness, Francis Boyle, J.D., Ph.D., who agreed in January to testify on behalf of the plaintiffs, has since died. Boyle was a professor of international law at the University of Illinois and a bioweapons expert who drafted the Biological Weapons Anti-Terrorism Act of 1989.

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FDA Rejects Moderna Jab for Healthy Children

For years, it’s been common practice at the FDA to routinely approve upgraded versions of existing vaccines with an oversight process best described as rubber stamping.

But the days of the FDA quietly approving vaccines may be over – bright news for activists from the Medical Freedom Movement.

Earlier this week, Dr. Vinay Prasad, the man who replaced Peter Marks, the FDA’s controversial vaccine official, boldly overruled FDA regulators who had recommended all three COVID vaccines for all age groups, including healthy children.

While the approval process for vaccines gives regulatory bodies the opportunity to scrutinize products before they hit the market, in reality, this hardly ever happened. Today, however, FDA leadership is empowered to scrutinize vaccines to insure their safety.

More importantly, the current FDA is challenging the past orthodoxy of a “one-size-fits-all” approach. In its place: the empirical “gold standard” scientific analysis that HHS Secretary Robert F. Kennedy Jr. had been promising.

Dr. Prasad, the new head of the FDA’s Center for Biologics Evaluation and Research (CBER) – which regulates vaccines, blood products and more – explained this new approach both online and in a detailed memorandum.

In his memo, Dr. Prasad writes that in considering the approval of Moderna’s updated mRNA COVID vaccine (“SPIKEVAX”), the FDA must weigh the benefits of the product against its risks. Only then can a specific approval process result in a scientifically sound recommendation. “FDA has a statutory mandate to only approve products when we have substantial certainty that benefits outweigh harms,” Prasad writes in his memo. Referring to Moderna’s submission, he adds, “We do not have substantial certainty [that] benefits outweigh risks of healthy children.”

Dr. Prasad elaborates: “First, consider that COVID-19 severe disease, hospitalization, and death are extremely low at pediatric ages and have fallen, according to US CDC data from 2021-22 to the present.”

Dr. Prasad continues, “These rates are lower in healthy children than in children with risk factors. Notably, the applicant has agreed to a revised submission that focuses on children with risk factors, and FDA CBER has granted this approval.”

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Canada’s COVID jab injury payouts triple in two years, reaching $18 million

Payments to COVID jab-injured Canadians have tripled in the past three years.

According to information recently published by Canada’s Vaccine Injury Support Program (VISP), payments to COVID-injured Canadians have totaled $18,140,998, nearly triple the $6,695,716 paid in 2023.

The statistics, which reflect numbers from when the program was launched in 2020 until June 1, 2024, showed that only 234 out of 3317 claims have been approved.

However, the claims do not represent the total number of Canadians injured by the allegedly “safe and effective” COVID shots, as inside memos have revealed that the Public Health Agency of Canada (PHAC) officials neglected to report all adverse effects from COVID shots and even went as far as telling staff not to report all events.

The PHAC’s downplaying of jab injuries is of little surprise to Canadians, as a 2023 secret memo revealed that the federal government purposefully hid adverse effect so as not to alarm Canadians.

Canada’s VISP was launched in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.

To date, the health department does not have an estimate on how many compensation claims will be filed.  Officially, in Canada, there have been 442 deaths linked to the COVID shot, and Canada’s Public Health Agency data claims that 98.2 million jab doses have been administered.

Earlier this week, Conservatives demanded an official investigation into the Liberal-run vaccine injury program, which has given more to VISP administrators than injured Canadians. Notably, there have been no press releases regarding the contracts on the Government of Canada website nor from Carney’s official office.

An explosive Global News report found that Oxaro Inc., the company contracted for $50 million to run the program, misallocated taxpayer funds and disregarded many jab-injured Canadians.

Of the $50.6 million that Oxaro Inc., has received, $33.7 million has been spent on administrative costs, compared to only $18.1 million going to jab-injured Canadians.

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The Telegraph alters headline to note that the harms caused by covid injections have been catastrophic

On Sunday, The Telegraph published an article describing their interview with Dr. Aseem Malhotra. By Tuesday, the paper had changed its headline to highlight Dr. Malhotra’s statement that the covid vaccines had caused catastrophic harms. This could be an indication that the noose controlling the “safe and effective” narrative is loosening further.

As well as the newly appointed chief medical adviser to the US’s MAHA Institute, Dr. Malhotra is a consultant at the HUM2N longevity clinic, which offers biohacking services.

On Tuesday, Dr. Aseem Malhotra alerted the public to a change in one of The Telegraph’s headlines to read: ‘Aseem Malhotra: ”The harm caused by covid vaccine has been catastrophic”’.

We couldn’t establish when the headline was changed because The Telegraph only shows an uploaded date and time for their articles and not a “last edited” date and time.  However, below are screenshots of the two headlines that were archived on 13 July (the day the article was published) and 15 July.

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COVID-19 mRNA Shots Destroy 8.4% of Non-Renewable Eye Cells in Just 75 Days

A new peer-reviewed study in Ophthalmic Epidemiology titled, Evaluation of the Effects of mRNA-COVID 19 Vaccines on Corneal Endothelium, has uncovered alarming evidence that Pfizer’s COVID-19 mRNA injection (BNT162b2) causes significant structural damage to the eye’s non-renewable corneal endothelium — the critical layer of cells responsible for maintaining corneal transparency and hydration.

Researchers from two Turkish university hospitals conducted a prospective study on 64 healthy, COVID-naive volunteers. Using advanced imaging tools (Sirius corneal topography and Tomey EM-4000 specular microscopy), they evaluated 128 eyes before vaccination and approximately 75 days after the second Pfizer dose.

The corneal endothelium does not regenerate. Once these cells are lost, they cannot be replaced — damage is considered irreversible. Sustained injury to this layer may result in blurred vision, chronic corneal swelling, or even blindness in severe cases.

This study provides objective, measurable evidence of structural and functional eye damage shortly after mRNA COVID-19 injection — even in young, healthy adults with no prior ocular pathology.

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New Study Stokes Debate: Did Mass Vaccination Fuel New COVID Variants?

Researchers who set out to examine how SARS-CoV-2, the virus responsible for COVID-19, evolved to evade the human immune system have inadvertently added fuel to the debate over whether mass vaccination may have prolonged the pandemic.

A peer-reviewed study, published this month in the journal Scientific Reports, hypothesized that SARS-CoV-2’s pathway to infecting humans shifted over time. Understanding that process will help scientists develop treatments for all future variants of the virus, the authors said.

Using public datasets consisting of blood and nasal samples from over 500 people, split into COVID-positive and control groups, the researchers found that the original strain of the SARS-CoV-2 and early variants “primarily affected pathways related to viral replication” — the process through which viruses insert their genetic material into host cells, co-opting those cells to create new viral particles.

These earlier strains of the virus led to more changes in gene expression — the process through which cells convert instructions in our DNA into a functional product, such as a protein. This, in turn, led to more severe COVID-19 infections.

However, later strains of SARS-CoV-2, such as Beta and Omicron, “showed a strategic shift toward modulating and evading the host immune response,” but also resulted in milder infections for most people.

According to TrialSite News, this is a “striking evolutionary shift in how SARS-CoV-2 interacts with the human body,” suggesting that newer variants “may be optimized for immune evasion.”

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Doctor Reveals What COVID Vaccines Do to the Lungs in Just One Week

A vaccine-injured doctor just came forward with an alarming statistic that should concern every COVID-vaccinated person.

Speaking at a Senate committee hearing hosted by Senator Ron Johnson on Tuesday, Dr. Robert Sullivan, an anesthesiologist, delivered a raw and heartbreaking testimony about what the shot did to him.

But he also shared a disturbing finding from a peer-reviewed study that paints a grim picture of what these COVID vaccines can do to the lungs.

During his testimony, he revealed COVID boosters AGE lung capacity in athletes by “five to ten YEARS in just ONE WEEK.”

For Dr. Sullivan, the damage was much worse. He says his lung capacity was slashed by HALF after taking the COVID shots the government recommended.

After a period of being unsure if the damage was in his head or not, Dr. Sullivan was diagnosed with pulmonary hypertension, a dangerous condition that elevates blood pressure and forces the heart to work much harder to pump blood to the lungs.

“On the outside, I look fine… I’ve lost half my lung capacity. If I can look this normal while carrying that much damage, how many others are out there suffering silently?” Dr. Sullivan asked.

The peer-reviewed study he referenced was conducted in 2022 and found that 19% of athletes with a mean age of 37 experienced an 8.6% drop in VO₂max just one week after receiving the Pfizer-BioNTech mRNA booster. That’s equivalent to aging about ten years in terms of aerobic capacity.

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 Johnson & Johnson Lead Scientist Confesses J&J COVID-19 Vaccine Was ‘Not Safe and Effective,’ Reveals “Lack of Research” From Rushing to Release Vaccine: “People Wanted It, We Gave It to Them”

“We didn’t do the typical tests,” said Joshua Rys, a Lead Scientist in Regulatory Affairs for Johnson & Johnson (J&J), revealed on hidden camera that the typical clinical process was abandoned for the COVID-19 vaccine, knowingly bypassing standard testing protocols under pressure from the U.S. government and public demand. He added, “This was just, ‘let’s test it on some lab models… and just throw it to the wind and see what happens.’”

He acknowledged that the public wasn’t informed about the shortcuts, asking, “Do you have any idea the lack of research that was done on those products?” Rys claimed, “People wanted it, we gave it to them.”

While public officials claimed the vaccines were “safe and effective,” Rys pushed back. “There’s no proof. None of that stuff was safe and effective,” he said, adding that the industry relies on a benefit-risk tradeoff to justify product launches.

Rys also pointed to government pressure through Operation Warp Speed. “The government is like, ‘We need help… You’re solving this problem,’” he said. “People panic, so they try to solve it in whatever way they think is good.”

According to a U.S. Department of Health and Human Services (HHS) spokesperson, “Even during a public health emergency, pharmaceutical companies are still required to follow strict protocols for clinical testing. For emergency use, companies must show that the benefits clearly outweigh the risks. Oversight doesn’t stop at approval — the FDA and other agencies also monitor products closely once they’re in use. That includes real-world safety tracking, independent advisory committees, and required reporting of any adverse events. These steps are in place to make sure public health decisions are based on solid science and strong safeguards — especially in emergencies.

Dr. Marty Makary and Dr. Vinay Prasad recently announced a new vaccine safety and transparency framework — one that’s built on gold-standard science, real-world data, and honest communication with the public and will require thorough safety testing before licensing. Their work is focused on strengthening trust, improving how we monitor safety after vaccines are in use, and making sure people have clear, accurate information to make informed decisions.

HHS remains committed to full transparency and evidence-based oversight — putting the safety of the American people first.”

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Why Are Taxpayers Still Funding These Injection Mandates?

It was nerve wracking, to say the least; having a high school student who had gotten into his dream college in mid-December 2020 but was uncertain if he could attend the following fall due to Covid-19 vaccine mandates. Those harrowing days and nights we spent focusing on little else as we scoured college websites to eventually find what we pretty much expected would come to pass. 

It started in April of 2021 when Rutgers University and then Harvard University announced their students would be required to take Covid-19 vaccines prior to enrollment. In these early days, I remember thinking that surely, they will reveal some scientific data showing these vaccines could prevent transmission and severe illness or death to justify the mandates, but alas, the wait was in vain. 

Living up to their cult behavior reputation, by the summer of 2021, over 1,000 colleges announced the exact same fear-fueled narrative and implemented some of the world’s most oppressive mandate policies. By August, millions of college students would be mandated to take primary series Covid-19 vaccines prior to enrollment, many without enough notice to get their deposits back, transfer colleges, or even file for an exemption. The directive was clear: take these novel medical treatments with zero scientific evidence to show you need them, or don’t bother showing up. 

The best and brightest minds in academia never demanded to see the scientific data to justify their colleges’ strict mandate policies and never demanded the reasoning behind their administrations summoning a 100% compliance rate, but instead elevated the propaganda in lockstep fashion. To this day, it is astounding to think of what transpired and that so few questioned the lack of supporting science either because they were aghast to consider that our federal government was responsible for perpetrating the greatest crime against humanity the world has ever seen, or just because it was easier to comply and convince others to do the same. 

Some of us could see the writing on the wall. We knew colleges and universities were going to take this global pandemic opportunity to manipulate and control their vulnerable and young healthy adult populations into compliance, and that is exactly what they did. I kept hoping I was wrong, and once more data was released, these institutions would reverse course, but I was wrong then, and I still am now.

Health science students are still being coerced to take Covid-19 vaccines either prior to enrollment in their institutional program or prior to the start of their practical training at hospitals and clinical partner programs. In fact, they are the only college students still being coerced to take Covid-19 vaccines, and most of the time, it feels as though there is no end in sight.

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