Japanese oncologist: I didn’t have a covid vaccine because I thought the genetic vaccines were foolish from the beginning

On 19 April 2024, Commissione Medico Scientifica Indipendente (“CMSi”) held an online conference titled ‘Perspectives of the World Health Organisation: from advisory body to world government?’.  One of the experts giving a presentation was Prof. Masanori Fukushima. 

Prof. Fukushima is a Professor Emeritus of Kyoto University, Director of the Translational Research Centre for Medical Innovation and the Foundation for Biomedical Research and Innovation, President of the Foundation of Learning Health Society Institute and former Director of the Outpatient Oncology Unit of Kyoto University Hospital. He is the author of more than 290 scientific publications.

During his presentation, hosted by Italian biologist Dr. Panagis Polykretis, Prof. Fukushima said:

 “Genetic vaccines are totally unacceptable. The introduction of transgenes into the human body is gene therapy.   How can this be considered acceptable for creating vaccines?

“If you encapsulate mRNA in nanoparticles and administer it you only get off-target effects starting from the ovaries, to the brain, liver, spleen and bone marrow. The biggest problem is going to the bone marrow, the reproductive organs like the ovaries and then every possible organ.

“The fact that spike proteins are still detected in the rash after more than a year makes it obvious that mRNA is producing spike proteins. There is no way for a year-old spike protein to remain in the rash and be detected.

“I didn’t choose to get vaccinated because I think it was a foolish decision from the beginning.  I haven’t even opted for the flu shot because I consider it an unwise choice.”

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‘Vast Majority’ of Pandemic Employee Retention Credit Claims Are Likely Scams, Says IRS

You can add the Internal Revenue Service to the ranks of federal agencies conceding that raining taxpayer money on all and sundry to offset the negative effects of pandemic-era closures didn’t go as well as intended. Not only was a program meant to offset the cost of paying workers during lockdowns and voluntary social-distancing prone to being gamed, but the “vast majority” of claims submitted to the program show evidence of being fraudulent.

In the course of a detailed review of the Employee Retention Credit, “the IRS identified between 10% and 20% of claims fall into what the agency has determined to be the highest-risk group, which show clear signs of being erroneous claims for the pandemic-era credit,” the IRS announced June 20. “In addition to this highest risk group, the IRS analysis also estimates between 60% and 70% of the claims show an unacceptable level of risk.”

The Employee Retention Credit was offered to businesses that were shut down by government COVID-19 orders in 2020 or the first three quarters of 2021, experienced a required decline in gross receipts during that period, or qualified as a recovery startup business at the end of 2021. But it was clear early on that scammers were taking advantage of giveaways of taxpayer money, either to claim it for themselves or to pose as middlemen helping unwitting business owners file claims.

In March of 2023, the tax agency warned of “blatant attempts by promoters to con ineligible people to claim the credit.” In September of that year, it stopped processing claims amidst growing evidence that vast numbers of applications were “improper,” as the IRS delicately puts it. In March 2024, the agency announced that its Voluntary Disclosure Program had recovered $1 billion (since raised to over $2 billion) in improper payouts from participants who got to keep 20 percent of the take.

Ultimately, only “between 10% and 20% of the ERC claims show a low risk” for fraud, even by generous federal standards for throwing other people’s money at problems largely of government creation.

“We will now use this information to deny billions of dollars in clearly improper claims and begin additional work to issue payments to help taxpayers without any red flags on their claims,” commented IRS Commissioner Danny Werfel.

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Lancet Autopsy Paper Finally Published After Being Censored

In 2023, The LANCET censored & CANCELLED a ground-breaking COVID-19 Vaccine Injury & Autopsy paper within 24 hours following over 100,000 downloads. It has just passed peer review & is now published

The rapid development of COVID-19 ‘vaccines’, combined with a high number of adverse event reports, has led to concerns over possible mechanisms of injury, including systemic lipid nanoparticle (LNP) and mRNA distribution, Spike protein-associated tissue damage, thrombogenicity, immune system dysfunction, and carcinogenicity.

This systematic review aims to investigate possible causal links between COVID-19 vaccine administration and death using autopsies and post-mortem analysis.

“We found that 73.9 percent of deaths were directly due to or significantly contributed to by COVID-19 vaccination,” said Dr. Wiliam Makis, a radiologist, oncologist, cancer researcher, and author of 100+ publications. The study examined 325 autopsy cases.

Our data suggest a high likelihood of a causal link between COVID-19 vaccination and death,”

This is a victory of SCIENCE over CENSORSHIP!!

As Makis outlines, Author Nicolas Hulscher’s Incredible perseverance first. They didn’t give up after LANCET pulled our paper within 24 hours after 100,000 downloads for no legitimate reason.

Big pharma put the squeeze on @TheLancet but surprisingly failed to stop us.

The paper was delayed by one year, and many deaths could have been prevented. This paper SHOULD be a game changer. Dr. Makis says that this is the most comprehensive medical report linking autopsies & sudden deaths to the COVID Vaccines.

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Pfizer purchased companies that produce drugs to treat the same conditions caused by covid vaccines

In 2017 a former vice president of Pfizer blew the whistle and said that pharmaceutical companies intentionally design vaccines to keep the public in a state of illness to profit from the treatments of vaccine-induced illnesses. 

Pfizer’s acquisitions of other pharmaceutical companies since the rollout of its covid vaccine seem to indicate this is indeed the case.

In 2021, Pfizer’s acquisition of Arena Pharmaceuticals raised eyebrows. The purchase price seemed disproportionate to the market size of the drug they acquired – a drug that is a potential therapy for all kinds of immuno-inflammatory diseases, including inflammation of the heart.  As we know, myocarditis began to skyrocket after the rollout of Pfizer’s mRNA vaccines.

In 2023, Pfizer purchased Seagen Pharmaceuticals, known for its cancer drugs.  Was this because of the connection between the mRNA injections and “turbo cancers”?

In 2022, Pfizer purchased Global Blood Therapeutics for its drug to treat sickle cell disease, again for an amount that seemed disproportionate to the profit the company could make off the drug considering how many people have the disease.  Does Pfizer know something we don’t? Will we see a blood cell disease epidemic as well?

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4 More U.S. States Sue Pfizer Over False COVID Vaccine Claims

Four additional states will follow Kansas’s lead by filing large-scale lawsuits against pharmaceutical giant Pfizer. These states allege that the company misled the public regarding the safety and efficacy of its COVID-19 vaccine.

Last week, Kansas Attorney General Kris Kobach announced that he is suing pharmaceutical giant Pfizer for misleading Kansas residents about the safety and efficacy of its COVID-19 vaccine.

During a press conference in Topeka, alongside Deputy Attorney General Fran Oleen and Assistant Attorneys General Kaley Schrader and Melanie Jack, Kobach detailed the allegations lodged against Pfizer.

“Kansas is filing a civil suit against the Pfizer Corporation under the Kansas Consumer Protection Act, seeking enhanced civil monetary penalties, damages, and injunctive relief for misleading and deceptive statements made in marketing its COVID-19 vaccine. Pfizer also violated previous consent judgments with the state of Kansas, in which Pfizer promised never to use deceptive information to market their products,” said Kobach.

The complaint, lodged today in Thomas County District Court, accuses Pfizer of misleading Kansans about the vaccines’ risks, including potential harm to pregnant women and the risk of myocarditis. The suit further alleges that Pfizer falsely claimed its vaccine was effective against COVID variants, despite evidence to the contrary.

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All Cause Mortality Higher in the Covid-Vaccinated — Study

study published Sunday detailed how individuals who received the Covid vaccine were more likely to die, while their booster dose did nothing to help them.

In order to view the full study one must download the PDF file.

“…those vaccinated with one or two doses who had significantly higher risks than the unvaccinated,” the study said in the ‘Conclusion’ section. “We found all-cause death risks to be even higher for those vaccinated with one and two doses compared to the unvaccinated and that the booster doses were ineffective. We also found a slight but statistically significant loss of life expectancy for those vaccinated with 2 or 3/4 doses.”

The researchers analyzed data from the Italian province of Pescara for their paper.

Interestingly, the researchers calculated the loss of life expectancy of those who were injected with the exotic gene therapy technology, or rather, how many days of life is lost on average per shot.

They used the ‘restricted mean survival time’ (RMST) and the ‘restricted mean time lost’ (RMTL) to articulate the data.

“…we calculated the RMST difference that represents the best index of “life expectancy” in those comparisons where the assumptions of the model were not met [12], and with the RMTL ratio that can approximate the HR in the absence of proportional hazard assumption [13]. The RMST difference represents the days of life lost by the vaccinated population compared to those of the unvaccinated one, while the RMTL ratio represents the percentage of life expectancy lost in the vaccinated population compared to in the unvaccinated one,” the study said in the ‘Discussion’ section. “The differences in RMSTs between the vaccinated and unvaccinated are significant for both the two-dose and the three-or-more-dose groups. They may appear irrelevant (in the order of a few days), but they refer to a limited period of time (739 days for those vaccinated with two doses and 579 days for those vaccinated with three or more doses). They could be compared with the entire life expectancy of an individual, which in the province of Pescara has an average value of 82.6 years [14] (corresponding to 30,149 days).”

Surprisingly, those vaccinated with two doses lost more time on this earth than those vaccinated with three or more doses, however that is likely due to the fact that those only vaccinated with two doses died before they had the opportunity to receive their third.

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The US Swine Flu Epidemic That Wasn’t

In July of 2009, amid the national swine flu panic stoked by the CDC, I got two tips from insiders: the CDC had instructed hospitals and states to stop testing for swine flu! Doctors were to presume that any patients who came in with flu-like symptoms had swine flu, or H1N1, and treat them as such without testing them to confirm it.

How strange! both of my sources told me, separately. I had to agree. Why would the CDC not want to collect the best data possible during an outbreak that the agency implied could bring America to its knees? The CDC had already green lighted emergency development and approval of what could be a very lucrative swine flu vaccine.

The CDC’s official rationale for stopping tests was that swine flu had supposedly become so widespread, it was reasonable to save money on tests and just assume everyone who caught something that looked like any sort of flu had the H1N1 variety.

My sources were suspicious.

I remember the words of one of them—a government scientist. He told me, “CDC is either trying to inflate the number of swine flu cases or downplay the number. Your job is to figure out which it is.”

I was stunned by what I discovered. And a CBS News manager short-circuited the resulting story to keep it off of the Evening News.

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Lawyer breaks media silence on Ottawa Detective’s probe into sudden infant death increase

An Ottawa police detective is facing trial for allegations of misconduct after investigating a series of unusual sudden infant deaths in the region, in 2021 and 2022.

Detective Helen Grus, who was working at the time for the sexual assault and child abuse unit (SACA) for the Ottawa Police Service (OPS), is accused of unauthorized access of an internal database while researching a potential link between the novel COVID-19 mRNA vaccines and an uptick in sudden infant deaths after their roll out.

During her tribunal defence hearing in May of this year, Grus presented evidence of a roughly 97% fatality rate among unborn babies in Pfizer’s clinical trial data. This full disclosure could not be heard because Grus was interrupted and silenced by the hearing officer, retired superintendent Chris Renwick, who has no legal training.

The defence suspects that the police and the hearing officer are politically motivated to silence and prosecute Grus, disregarding potential criminality around this alarming trend affecting the most vulnerable population.

Grus’ lawyer, Bath-Sheba van den Berg, describes the unsettling incident as unlike anything she has witnessed in proceedings before.

“She’s sitting there in front of me, facing me,” details van den Berg, “and she’s stating simply that, 31 out of 32 [babies died]. And as she was stating that, the hearing officer lurched forward and said ‘stop.’”

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Stroke Risk: COVID Shots 200 Times More Likely to Cause Blood Clots in Brain

The COVID-19 vaccines carry a much higher risk of blood clots in the brain compared with other vaccines, according to a new study by Dr. Peter McCullough and colleagues.

The researchers looked at reports in the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) from January 1990 through December 2023.

They counted the number of cerebral thromboembolism events — as in, blood clots of the brain’s veins or arteries — reported in people who received a COVID-19 shot compared with those who received a flu shot or other vaccines.

Blood clots that block blood flow to the brain account for roughly 87% of all strokes, according to the American Stroke Association, a division of the American Heart Association.

McCullough — a cardiologist with over 1,000 publications and over 685 citations in the National Library of Medicine — told The Defender the study showed “an unacceptable risk of catastrophic thrombotic injuries to the brain” in individuals who took one or more COVID-19 shots.

McCullough summarized the study’s results on Substack:

“Compared to influenza vaccines given over 34 years, COVID-19 vaccines in 36 months of use had over 1000-fold increased risk of most blood clot events, and compared to all vaccines combined administered over 34 years, this risk remained at over 200-times greater with COVID-19 vaccination.”

Prior research has suggested that the spike protein in both the SARS-CoV-2 virus and the COVID-19 vaccine can cause serious blood clotting, McCullough and his co-authors noted in their report.

Blood clots in the brain are difficult to treat, McCullough told The Defender, and “oftentimes leave patients with devastating disabilities.”

“This and other sources of data,” he added, “support calls to remove all COVID-19 vaccines from public use.”

The study — co-authored with Claire Rogers, Dr. James Thorp and Kirstin Cosgrove — is under peer review and available online as a preprint.

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Lawsuit On Behalf Of Vaccine-injured Seeks To Strike Down ‘Unconstitutional’ PREP Act

lawsuit filed Tuesday seeks to strike down the PREP Act — the federal law that granted legal immunity to companies such as Pfizer and Moderna for injuries caused by their COVID-19 vaccines and other COVID-19 countermeasures.

The lawsuit, filed in the U.S. District Court for the Middle District of Florida, Tampa Division, alleges the Public Readiness and Emergency Preparedness (PREP) Act violates the U.S. Constitution and the Administrative Procedure Act, which governs how federal agencies develop and issue regulations.

Plaintiffs in the suit include the nonprofit Moms for America and individual plaintiffs who were injured by a COVID-19 vaccine, or whose loved one suffered injury or death from a COVID-19 vaccine.

According to the complaint, “This case is about the government’s failure to resolve conflicts involving Americans killed or grievously harmed while receiving healthcare during the COVID-19 pandemic.”

Defendants are the U.S. Department of Health and Human Services (HHS), the U.S. Health Resources and Services Administration, HHS Secretary Xavier Becerra and President Joe Biden.

“As even The New York Times has recently acknowledged,” Jeff Childers, attorney for the plaintiffs, told The Defender, “too many Americans have been injured by the COVID vaccines and other rushed treatments, and now have no recourse, no help and no support. They can’t sue anybody, thanks to PREP.”

“PREP was poorly conceived, badly executed, and gave far too much power to unelected bureaucrats and executive agencies,” he added.

Childers wrote on Substack today that the PREP Act should “be crushed and burned to a cinder in the incinerator of history’s worst ideas.”

The lawsuit asks the court to declare the PREP Act unconstitutional and to declare that the HHS secretary’s actions in implementing the act violate the Administrative Procedure Act.

The suit also asks the court to declare that the plaintiffs can sue companies like Pfizer and Moderna in federal and state courts. It also seeks compensation for attorney fees.

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