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antivax

The belief that vaccines are dangerous and related anti-vax views

COVID-19

British Media Report Confirms Skyrocketing Excess Deaths in All Highly COVID-19 Vaccinated Countries

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The post British Media Report Confirms Skyrocketing Excess Deaths in All Highly COVID-19 Vaccinated Countries appeared first on Global Research.

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COVID-19

Scientists acknowledge COVID vaccines and containment protocols may have boosted excess mortality

Dutch researchers indicated in a new peer-reviewed study that COVID-19 vaccines and governmental containment policies may have boosted excess mortality in the West.

The study, published Monday in the peer-reviewed journal
BMJ Public Health, explored excess all-cause deaths in 47 Western countries from 2020 to 2022. It indicated that during this period, there were 3,098,456 excess deaths: 87% of the countries under review suffered excess mortality in 2020; 89% in 2021; and 91% in 2022.

The researchers made clear that excess mortality “includes not only deaths from SARS-CoV-2 infection but also deaths related to the indirect effects of the health strategies to address the virus spread and infection.”

What caught the researchers’ attention was not only the persistence of high excess mortality following the pandemic but that “the highest number of excess deaths [1,256,942] was recorded” in 2021 — the year containment measures were coupled with experimental vaccination.

In 2020, when Western citizens largely only had to contend with the virus, government-limited mobility rights and shuttered schools, churches, workplaces, restaurants, and parks, there were 1,033,122 excess deaths.

In 2022, when most containment protocols had been lifted and uptake of COVID-19 vaccines was in fast decline, researchers indicated there were 808,392 excess deaths.

‘This is unprecedented and raises serious concerns.’

These massive figures reflect the difference in the number of reported deaths in a country in a given year and the expected number of deaths under normal conditions. For a baseline, the Dutch researchers used Ariel Karlinsky and Dmitry Kobak’s linear regression estimate model, which draws on “historical death data in a country from 2015 until 2019 and accounts for seasonal variation in mortality and year-to-year trends due to changing population structure or socioeconomic factors.”

“Excess mortality has remained high in the Western World for three consecutive years, despite the implementation of COVID-19 containment measures and COVID-19 vaccines,” wrote the researchers. “This is unprecedented and raises serious concerns.”

“During the pandemic, it was emphasized by politicians and the media on a daily basis that every COVID-19 death mattered and every life deserved protection through containment measures and COVID-19 vaccines,” continued the researchers. “In the aftermath of the pandemic, the same morale should apply.”

The Dutch researchers noted at the outset of their study that while experimental COVID-19 vaccines and draconian containment measures may have been effective in protecting segments of the population — particularly those with comorbidities and the elderly — they nevertheless had “detrimental effects that cause inferior outcomes as well.”

“Although COVID-19 vaccines were provided to guard civilians from suffering morbidity and mortality by the COVID-19 virus, suspected adverse events have been documented as well,” wrote the researchers.

The secondary analysis of the placebo-controlled, phase III randomized clinical trials of mRNA COVID-19 vaccines showed that the Pfizer trial had a 36% higher risk of serious adverse events in the vaccine group. The risk difference was 18.0 per 10000 vaccinated (95% CI 1.2 to 34.9), and the risk ratio was 1.36 (95% CI 1.02 to 1.83). The Moderna trial had a 6% higher risk of serious adverse events among vaccine recipients. The risk difference was 7.1 per 10,000 vaccinated (95% CI −23.2 to 37.4), and the risk ratio was 1.06 (95% CI 0.84 to 1.33).39. By definition, these serious adverse events lead to either death, are life-threatening, require inpatient (prolongation of) hospitalization, cause persistent/significant disability/incapacity, concern a congenital anomaly/birth defect or include a medically important event according to medical judgement.

Previous comparisons of established flu vaccines to the novel mRNA vaccines — which the Dutch researchers indicated have been classed in multiple French studies as “gene therapy products requiring long-term stringent adverse events monitoring” — have revealed the latter to carry a far higher risk of serious adverse reactions.

‘Both medical professionals and citizens have reported serious injuries and deaths following vaccination.’

COVID-19 vaccines have also been linked to various ailments, including heart disease, blood clots, hemorrhages, gut issues, thromboses, myocarditis, pericarditis, and autoimmune diseases. A number of these linkages have been well-demonstrated and even admitted by pharmaceutical giants,
as in the case of AstraZeneca.

The Dutch researchers indicated that some of the risks these experimental vaccines carry were realized overtime outside of clinical trials: “Both medical professionals and citizens have reported serious injuries and deaths following vaccination to various official databases in the Western World, such as VAERS in the USA, EudraVigilance in the European Union and Yellow Card Scheme in the UK.”

The researchers framed the dangers posed by the vaccines as even more troubling given the understanding that the threat posed by the virus was overblown.

The pre-vaccination infection fatality rate for persons over 60 was reportedly 0.03% and the rate was 0.07% for those over 70. It posed virtually no threat to people ages 19 and younger, who alternatively faced an infection fatality rate of 0.0003%.

Gordon Wishart, chief medical officer at Check4Cancer,
told the Telegraph, “The authors are correct to point out that many vaccine-related serious adverse events may have been unreported, and point to the fact that the simultaneous onset of excess mortality and Covid vaccination in Germany is worthy of further investigation on its own.”

Just as the vaccines were nowhere near as “safe and effective” as promised, the supposed health safety protocols appear to have had an inverse effect.

The study acknowledged that it is challenging to differentiate between the various causes of excess mortality, particularly because national mortality registries “not only vary in quality and thoroughness but may also not accurately document the cause of death,” and there was a lack of consensus in the medical community on whether to label deaths of persons infected with COVID-19 but not caused by the disease as COVID-19 fatalities.

However, they appeared confident enough to assert that “indirect effects of containment measures have likely altered the scale and nature of disease burden for numerous causes of death since the pandemic,” citing a study that indicated there was a “substantial increase” in American deaths attributed to non-COVID causes in the first two years of the pandemic.

American heart disease deaths were apparently 6% above baseline in 2020 and 2021. Diabetes deaths were 17% over baseline in 2020 and 13% over in 2021. Alzheimers disease mortality was up 19% in 2020 and 15% in 2021. Alcohol-related deaths were 28% over baseline in 2020 and up 33% in 2021. Drug-related deaths were 33% over baseline in 2020 and up 54% in 2022.

The study noted that “lockdowns, school closures, physical distancing, travel restructions, business closures, stay-at-home orders, curfews, and quarantine measures with contract tracing” had numerous adverse indirect effects such as “economic damage, limited access to education, food insecurity, child abuse, limited access to healthcare, disrupted health programmes and mental health challenges” that increased morbidity and mortality from other causes.

The researchers concluded by recommending policymakers and government officials to “thoroughly investigate underlying causes of persistent excess mortality and evaluate their health crisis policies.”

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Conspiracy

It’s going to be a new CoV, not the avian flu virus

Submitted by JN Guest Post by Geert Vanden Bossche Is the bird flu panzootic expediting the end of the SARS-CoV-2 immune escape pandemic? SUMMARY Scientifically speaking, it cannot be ruled out that the bird flu panzootic is currently accelerating the evolutionary dynamics of the SARS-CoV-2 (SC-2) immune escape pandemic and expediting its final hyperacute stage. … Continue reading “It’s going to be a new CoV, not the avian flu virus”

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COVID-19

Tidal Waves Don’t Discriminate

Guest Post by Lori Weintz From a Russell Brand video posted May 28, 2024: Quote from former CDC Director Robert Redfield: “[The Covid vaccines] really aren’t that critical for those that are under 50 or younger, but those vaccines saved a lot of lives…To be honest, some people got significant side effects from the vaccine. I … Continue reading “Tidal Waves Don’t Discriminate”

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COVID-19

FDA approves new Moderna mRNA vaccine without bothering with independent advisers

The U.S. Food and Drug Administration has
approved Moderna’s mRNA-1345 vaccine, which allegedly protects adults aged 60 and older from respiratory syncytial virus infection-caused lower respiratory tract disease.

The agency’s
breakthrough therapy designation approval for the drug, which will be marketed as mResvia, is only the second Moderna drug the FDA has approved. More significantly, it is the first mRNA vaccine to have been approved to address a disease other than COVID-19.

‘We did not refer your application to the Vaccines and Related Biological Products Advisory Committee.’

Even though that amounts to a big step, it appears the regulator was keen to jump past additional levels of scrutiny.

The FDA
noted in its Friday approval letter, “We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your [biologics license application], including the clinical study design and trial results, did not raise concerns or controversial issues that would have benefited from an advisory committee discussion.”

The advisory committee’s job is to review and evaluate data concerning the “safety, effectiveness, and appropriate use of vaccines and related biological products,” then provide independent expert advice to the agency.

According to the pharmaceutical company, the approval was based on “positive data from the Phase 3 clinical trial ConquerRSV, a global study conducted in approximately 37,000 adults ages 60 or older in 22 countries.”

Nearly 20,000 of the trial participants were based in the United States. There are at least 11 other studies under way examining the impact of the novel drug on other demographics.

The company claimed in a Feb. 29
overview of its trial data that the vaccine “continued to be efficacious through median 8.6 months follow-up” and was shown to prevent severe RSV disease “base on analysis of shortness of breath and medically attended RSV-[lower respiratory tract disease].”

The vaccine’s efficacy is allegedly 83.7%. Reuters noted, however, that the label indicates the shot is only 79% effective at preventing at least two symptoms of RSV, such as fever and cough.

While the overview insisted that the vaccine was relatively effective and safe, it nevertheless highlighted a number of “systemic reactions” reported within seven days of vaccination, such as headache, fatigue, myalgia, arthralgia, and chills, besides customary injection site pain.

A Moderna-funded
study published in the New England Journal of Medicine similarly alleged that a single dose of the vaccine “resulted in no evident safety concerns.”

Despite similarly having been presented as a safe vaccine, Moderna’s COVID-19 vaccine was
linked in various studies, including in an FDA-funded study, to an increased risk of myocarditis and pericarditis, particularly in men ages 18-25.

Extra to heart inflammation, the Global COVID Vaccine Safety Project — a Global Vaccine Data Network initiative supported by both the CDC and the Department of Health and Human Services —
revealed in a February study in the esteemed journal Vaccine that “Bell’s palsy had an increased [observed to expected] ratio after a first dose of [Pfizer’s] BNT162b2 and [Moderna’s] mRNA-1273.”

The study also noted that “there were also increased OE ratios for febrile seizures following a first and second dose of mRNA-1273 … and for generalized seizures following first mRNA-1273 dose and fourth BNT162b2 dose.”

Blaze News previously reported that the University of Auckland, which hosts the Global Vaccine Data Network, noted that there were safety signals for “acute disseminated encephalomyelitis (inflammation and swelling in the brain and spinal cord) after viral vector and mRNA vaccines.”

Despite outstanding concerns about its only other approved vaccine, Moderna appears confident in its product and has evidently secured the FDA’s confidence as well. Its next stop is the Centers for Disease Control and Prevention, whose Advisory Committee on Immunization Practices will review the vaccine during its June 26-27 meeting.

Analysts estimate Moderna will do roughly $340 million in RSV vaccine sales this year and possibly $830.5 million in 2025, reported Reuters.

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COVID-19

Flashback: Why did Moderna sign a government contract for its vaccines before COVID-19?

When Dr. Fauci testified before a House subcommittee on the origins of COVID-19, many thought the time had finally come for tough questions.

While the questions asked made it clear that he lied about six-foot distancing and masking — Glenn Beck knows it could, and should, have been a lot worse.

“I find this incredible that we’ve missed this,” Glenn says, noting that the government signed a contract with Moderna on December 12, 2019, that ensured the pharmaceutical company would not be held liable for its vaccines.

The contract was originally proposed in 2015.

“I’ve been through many, many high level negotiations, but I’ve never seen anything that started four years before. Coincidentally, once they find the Frankenstein virus and then they negotiate for four years, and what a coincidence, they sign it just before the breakout of COVID,” Glenn says.

Not only was the pharmaceutical company ready far before the outbreak, but Dr. Fauci had been funding gain-of-function research — which he has continuously lied about.

“There’s lie number one. Then this strange, ‘Hey let’s partner with Moderna.’ I don’t think this is normal,” Glenn continues, noting that the gain-of-function research was paid for by American taxpayers.

“Where’s the money, where’s it going? My feeling is it’s going to fund more of this,” he predicts, adding, “We already know Fauci was funding the Wuhan lab. We also recently found out that he was funding experiments that killed puppies in a gruesome way. So, what else was getting funded through government and private funds?”

After following the money trail as well as endless incriminating emails, Glenn has come to a conclusion.

“Is there any other way to describe it other than Fauci and the president’s science advisor colluding behind the president’s back, withholding information from him?” he asks.

“Fauci has already been brought in front of Congress and Rand Paul caught him in a bold-faced lie. Fauci will testify again, but it’s probably time to bring in the former president’s science advisor as well.”

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