Vaccines Caused 17 Million Deaths During Pandemic Plus 4 More Takeaways From Largest Excess Mortality Study to Date

A major investigation by Canadian researchers into excess mortality during the COVID-19 pandemic found that patterns of excess death globally could not be explained by a pandemic respiratory virus, The Defender reported last week.

Instead, the authors concluded the major causes of death globally stemmed from the public health establishment’s response, including lockdownsharmful medical interventions and the COVID-19 vaccines.

The study by researchers from the nonprofit Correlation Research in the Public Interest analyzed excess mortality in 125 countries — about 35% of the global population — during the COVID-19 pandemic, beginning with the March 11, 2020, World Health Organization (WHO) pandemic declaration and ending on May 5, 2023, when the WHO declared the pandemic over.

The investigation concluded that “nothing special would have occurred in terms of mortality had a pandemic not been declared and had the declaration not been acted upon.”

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New Emails Reveal Big Tech-Biden Admin Collusion on COVID-19 Narratives, Involving CDC and Twitter Censorship

Trying to refute collusive practices involving major social media companies is probably not high on the agenda of the US government right this moment; nevertheless, the evidence of the highly controversial practice keeps rolling in.

America First Legal (AFL), a conservative non-profit, has disclosed a new batch of documents obtained through litigation, this time against the Centers for Disease Control and Prevention (CDC). It concerns May 2021 communications meant to set the tone online and “manage” the government agenda around topics related to Covid vaccines.

The emails were exchanged between Facebook and CDC – and the documents focus on the activities of CDC spokesperson Carol Crawford, who also “happened” to be involved with Twitter’s Partner Support Portal around the same time.

This Twitter program’s “secret superpower” was that it allowed government-affiliated individuals to participate in flagging content for censorship.

Genelle Adrien (of the Politics and Government Outreach Team over at Facebook) and Crawford “star” in the email chain obtained by AFL, with the latter being asked point blank that the CDC approve Facebook’s “COVID-19 Information Center FAQ.”

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Covid Shots Can Enlarge & Weaken the Heart — Case Study

While the association between Covid vaccination and myocarditis is well established, a recent case study documented how inflammatory dilated cardiomyopathy (another heart inflammation disorder) was induced by the Pfizer (BNT162b2) injection.

“A 78-year-old previously healthy female was referred by her family physician and admitted to our hospital for management of dyspnoea 11 days after receiving the third mRNA-1273 vaccine dose. The patient underwent a primary two-dose BNT162b2 series. On the fourth day after vaccination, the patient experienced palpitations and dyspnoea, which gradually worsened,” the case study said in the ‘Case Report’ section. “Therefore, the temporal relationship between the preceding COVID-19 immunization and the occurrence of iDCM with no other identifiable cause led to the final diagnosis of COVID-19 VAM.”

Thankfully for the patient, her condition improved with oral prednisolone treatment, which was documented via chest X-ray (CXR) and electrocardiography (ECG). One may note the reduction in size of the inflamed heart post-treatment.

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Paediatrician is alarmed at Bill Gates’ plan to inject 500 million children with harmful and unnecessary vaccines

According to a report published last week by the World Health Organisation (“WHO”) and United Nations Children’s Fund (“UNICEF”), global childhood immunisation rates have stalled, with 84% of children vaccinated in 2023, which has not improved despite efforts. According to the report, this stagnation highlights ongoing challenges in the wake of the covid-19 pandemic, including poor access to health services and fragile, conflict-ridden areas.

The report highlights the reduction in missed doses of “routine” DTP vaccines last year with 13.9 million fewer children receiving all doses in 2022. The report also laments the gaps in measles vaccinations, noting that outbreaks hit 103 countries.

GAVI’s plan aims to vaccinate 500 million children by 2030, with existing and new vaccines, claiming it will avert up to 9 million deaths. The organisation is seeking $9 billion in new pledges of the $11.9 billion needed for the strategic period.

However, Dr. Paul Thomas, who is the author of a study comparing the health outcomes of vaccinated versus unvaccinated children and others, argued that vaccination programs are unnecessary.  Additionally, he argued, success should be measured on the overall health of the population, not on vaccination rates.

“The less we vaccinate, the healthier the population,” he said.

The paediatrician’s warning highlights the potential risks and unintended consequences of mass vaccination efforts. He told The Defender that the global vaccination programmes continue to use the dangerous whole-cell DTP formulation instead of the less risky acellular version.

The whole-cell vaccine, which contains the entire Bordetella pertussis organism rather than just purified components, has since the 1930s resulted in widespread reports of neurological damage. It was phased out in the US by 1997, but the formulation has continued to be used in low- and middle-income countries, potentially killing millions of children.

Dr. Thomas also doesn’t agree with WHO’s stance on measles.

WHO Director-General Tedros Adhanom Ghebreyesus said: “Measles outbreaks are the canary in the coal mine, exposing and exploiting gaps in immunisation and hitting the most vulnerable first.”

Dr. Thomas stated that measles is not a threat to well-nourished, healthy children and that the focus on vaccines as a solution “is destroying the immune systems” of those who are highly vaccinated.

“The focus should be on making sure children of the world have adequate nutrition and adequate support of vitamins A, D and C,” he said.

WHO’s report noted “progress” in some areas of global immunisation including HPV vaccine uptake.

Thomas called the HPV shot “the most dangerous vaccine on the planet other than COVID,” and argued that it “should have been removed from the market long ago.”

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‘Fraud, Pure and Simple’: Merck Mumps Vaccine May Contain Up to 4 Times Approved Amount of Live Virus

Drug manufacturer Merck misrepresented the efficacy of its mumps vaccine for years, “overfilling” the vaccine with live mumps virus to meet efficacy targets despite the lack of safety testing — and the practice may be continuing today.

Merck appears to have concealed the practice from public health agencies, which have taken no action to stop it.

Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense, joined “The Defender In-Depth” this week to discuss the revelations, which stem from a lawsuit two Merck whistleblowers filed in 2010 under the False Claims Act.

The 3rd Circuit U.S. Court of Appeals in Philadelphia heard oral arguments in the case on July 9.

According to Hooker, the Merck measles, mumps rubella vaccine, MMR II — the only mumps vaccine licensed in the U.S. and listed on the childhood vaccine schedule for 12- to 18-month-olds — may contain up to 4 times the approved concentration of live mumps virus.

two-part deposition by Dr. David Kessler, former head of the U.S. Food and Drug Administration (FDA), also indicates that Merck, rather than informing regulators that it was “overfilling” its MMR vaccine, relied on passive surveillance — reports from parents regarding vaccine reactions in their children — to identify possible safety signals.

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U.S. Government ‘Saddled’ With COVID Vaccine Injury ‘Mess’ — While Vaccine Makers Avoid Liability

As early as January 2022, National Institutes of Health (NIH) researchers were aware of at least 850 peer-reviewed case reports and/or research articles about COVID-19 vaccine reactions, according to emails obtained by Children’s Health Defense (CHD).

In one email (name and agency redacted), NIH researchers were told the federal government was “saddled” with the “mess” of dealing with those injured by the COVID-19 vaccines, due to the liability shield enjoyed by vaccine manufacturers.

The emails, part of a 309-page batch of documents released to CHD on June 21, originated from a U.S. Food and Drug Administration (FDA) request to NIH researchers for input on a report highlighting several injuries common among people who received the vaccines.

CHD requested the documents via a Freedom of Information Act (FOIA) request to the NIH in November 2022. When the NIH hadn’t responded by April 2023, CHD sued the agency.

In an October 2023 settlement, the NIH agreed to produce up to 7,500 pages of documents at a rate of 300 pages per month.

The batch of documents released in June — which include emails to Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research — revealed that by fall 2021, key NIH researchers were aware of scientific studies on serious adverse events, including persistent neurological symptoms, following COVID-19 vaccines.

As with prior releases of the NIH documents, June’s tranche also included several emails from vaccine-injured individuals to NIH researchers, seeking help for their symptoms — with one person asking, “Why aren’t you studying vaccine injuries?”

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Update on Antibody-Dependent Enhancement (ADE) in SARS-CoV-2 Infection and Vaccination

Antibody-Dependent Enhancement (ADE) is a complex immunological phenomenon where virus-specific antibodies, rather than neutralizing the virus, enhance its entry into host cells and amplify its replication. ADE can occur in the context of natural infections and vaccinations, leading to heightened disease severity. This phenomenon has been observed in various viral infections, including respiratory syncytial virus (RSV), dengue, and HIV, and has been a subject of intense scrutiny in the context of SARS-CoV-2, the virus responsible for COVID-19.

The historical context of ADE provides critical insights into its mechanisms and implications. One notable example is the RSV vaccine trials in the 1960s. Vaccinated children who later encountered natural RSV infection experienced more severe respiratory illness compared to unvaccinated children. This was attributed to ADE, where vaccine-induced antibodies facilitated enhanced viral entry and immune activation (Kim et al., 1969). Understanding the diverse mechanisms of ADE, its implications for vaccine development, and its potential occurrence in SARS-CoV-2 infection is crucial. This comprehensive analysis aims to elucidate the different types of ADE, evidence of ADE in SARS-CoV-2, and the risks and proposed mitigation strategies associated with ADE in COVID-19 vaccines.

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Longtime pro-jab apologist finally comes clean about lack of science proving vaccine safety

After decades of aggressively promoting vaccines of all kinds, Dr. Stanley Plotkin, the world’s leading vaccinologist, is finally coming clean about the fact that vaccine safety has never been robustly studied as he has long claimed.

A paper he co-authored that was published in The New England Journal of Medicine (NEJM) on July 6, 2024, reveals that no vaccine has ever been properly studied either before or after their release.

Aaron Siri tweeted a lengthy post about Plotkin’s new paper in the NEJM, which admits that “prelicensure clinical trials have limited sample sizes [and] follow-up durations,” as well as that “there are not resources earmarked for postauthorization safety studies.”

“That is an incredible reversal,” Siri said before unpacking the rest of the study’s damning revelations basically indicting the vaccine industry and Big Pharma for science fraud.

“For decades, the medical community insisted vaccines are the most thoroughly studied product ever; for example, Dr. Paul Offit said, ‘I think we should be proud of vaccines as arguably the safest, best tested things we put in our body,'” Siri further explained.

“For decades, parents of vaccine injured children, vaccine injured adults, and other stakeholders contested these claims only to be shunned and attacked by the medical community and health agencies.”

(Related: At the 2020 Advisory Committee on Immunization Practices [ACIP] meeting, Plotkin, often referred to as ‘the godfather of vaccines,’ promoted Donald Trump’s COVID injections before they were even released under Operation Warp Speed.)

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‘Highly Confidential’: Former FDA Chief Details Fraud in Merck’s Testing, Marketing of Mumps Vaccine

For decades, Merck misrepresented the efficacy of its mumps vaccine, marketing an “adulterated” drug without proven efficacy to millions of American children, according to a recently released expert report by Dr. David Kessler, former head of the U.S. Food and Drug Administration (FDA).

The report — posted in two documents and marked “highly confidential,” for “attorneys’ eyes only” — provides over 800 pages of Kessler’s opinion and analysis about the history and severity of Merck’s regulatory violations over decades, beginning in the late 1990s.

By 1998, regulatory labeling review had revealed that the mumps component of Merck’s measles, mumps rubella vaccine, MMRII, did not maintain the stated potency over its shelf-life, in violation of FDA regulations.

Rather than recalling the vaccine or attempting to develop a different formula, the company spent years trying to develop new and more sensitive ways to test the existing vaccine that would show high efficacy results, so it would still be in compliance with regulatory requirements and allow Merck to maintain its exclusive license.

Merck did this even though its existing data showed the vaccine was significantly less effective than claimed, Kessler wrote.

To temporarily make the drug meet Merck’s efficacy claims while the company developed tests, Merck increased the dosage of virus present in the vaccine — with the FDA’s knowledge — although the higher dosage was never tested in clinical trials for either safety or efficacy.

The company did not inform the vaccine recipients, providers or purchasers — including the Centers for Disease Control and Prevention (CDC), which purchased the drug through its Vaccines for Children Program — that its vaccine was out of compliance.

Merck’s actions, Kessler wrote, had important “public health significance.”

According to the report, starting in 2006 and recurring since then, there has been a resurgence of mumps outbreaks in the U.S. The largest outbreak in 2017 affected more than 10,000 people in 46 states.

The vast majority of the people infected in all of the outbreaks received the recommended two-dose regime of Merck’s MMR vaccine, the report says.

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Sixfold Increased Risk of Colon Cancer in Covid-Vaccinated — Study

study published in June documented how one form of colon cancer saw a sixfold increase in individuals vaccinated with the Covid injection. The researchers explained the link between the shot and the cancer.

“Microsatellite instable (deficient mismatch repair, dMMR) colon cancer is associated with hypermutability and immune infiltration-activation. COVID-19 vaccines stimulate immune-inflammation response,” the study said in the ‘Introduction’ section.

A medical doctor broke down the findings on social media.

“Pfizer vaccination conferred sixfold increased risk,” Dr. Peter McCullough said regarding the study’s findings.

The researchers discussed how the Covid injection affects the immune system in a way that is linked to the onset of this type of colon cancer.

“Immune infiltration in dMMR colon cancer may interact with COVID-19 vaccine-induced immune activation,” the study said in the ‘Conclusion’ section.

The researchers compared the vaccinated and non-vaccinated cancer patients.

“The study was a single-center case-control study. Patients diagnosed with colon cancer at least three months after the last COVID-19 vaccine (BNT162b2, CoronaVac) dose were included. Patients with dMMR and microsatellite stable (MSS) tumors were defined as cases and controls, respectively, between June 2021 and June 2023,” the study said in the ‘Methods’ section. “Baseline characteristics and vaccine status between case-control groups were compared as univariable and multivariable. Inflammation markers were compared between MSS+CoronaVac and dMMR+BNT162b2 groups.”

After analyzing the study, Dr. McCullough discussed its findings on his Substack.

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