Archive for the ‘vaccines’ Category

Magic Trick Reveal: How To Get Perfect Efficacy From a ‘Vaccine’ That Doesn’t Work. Two White Papers Call to Halt COVID Shots, But FDA Approves Non-mRNA COVID Shot

https://kirschsubstack.com/p/the-big-magic-trick-revealed?

The big magic trick revealed!

How can you get near perfect efficacy from a vaccine that doesn’t work? Thanks to Professor Jeffrey Morris, I now know the magic trick too! This one had me fooled me for years.

Steve Kirsch
May 16, 2025
The Secret Truth Behind Penn & Teller: Fool Us

I like Penn and Teller. But they don’t know jack about vaccines. Check out this video they did. They should apologize and re-do the video to tell the truth. YouTube will ban it though.

Executive Summary

If you have a policy of COVID testing where it is mandatory to test the unvaccinated 2x/week but the vaccinated can totally skip testing, this can massively skew all studies based on that data.

I just found out this was the case in the Czech Republic which is the only country where we have record level data.

That explains a lot, doesn’t it? A testing policy like that can make an ineffective vaccine close to perfect.

Bottom line: the only honest way to see if the vaccine worked is to compare the whole period all-cause mortality between those who got the shots and those who did not. Then you learn the truth.

Guess what? There isn’t a single study that does this.Zero. Zip. Nada.

So I calculated it for the Czech Republic. It shows that the vaccines should be stopped. But you already knew that, didn’t you?

And if you can’t get COVID, you can’t die from COVID!

BAM! The magic trick has been revealed. The next time you want to make a vaccine super effective, there is nothing like deploying a differential testing policy like this.

Therefore, in Czechia, you get a near perfect vaccine and can write papers about it and nobody is the wiser.  (See link for article)

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**Comment**

These tactics need to be continually exposed for what they are: false and misleading – constituting scientific fraud.  Those in public health should be reviewing these things before they roll out a drug or medical product of any kind.

Hirsch then shows a table (to access, click top link) that shows when you actually compare whole period all-cause mortality between the injected and the non-injected you discover the shots are killing people.  But, reality is already showing this for those paying attention.

For more:

People have been shouting about these death shots for years.  There’s plenty of published science showing the myriad of problems.

Two White Papers Call For COVID Shot Halt

The IPAK-EDU White Paper 2025-ENDEUA states that when corrected efficacy curves and suppressed risks are taken into account, the mRNA covid shots fail the EUA standard.  The shots were based upon interim data from large-scale Phase III trials. The legal standard under §564 of the Federal Food, Drug, and Cosmetic Act requires that a product may be authorized for emergency use only if it is “reasonable to believe” that the product “may be effective” against a life-threatening condition, that the known and potential benefits outweigh the known and potential risks, and that no adequate alternatives are available. This report  demonstrates, through a rigorous retrospective analysis, that these criteria were never met.  

Go here to listen to Dr. Jeyanthi Kunadhasan, an Australian anesthesiologist and perioperative physician who was terminated from her hospital position after questioning the risk-benefit profile of COVID-19 vaccines in healthy individuals. Following her dismissal, she joined a group of international medical volunteers tasked with reviewing the 500,000+ pages of internal Pfizer documents released as part of a court-ordered FOIA request. This effort was coordinated by DailyClout and Dr. Naomi Wolf. As a result of that work, Dr. Kunadhasan has become one of the foremost experts on Pfizer’s pivotal mRNA vaccine trial, focusing specifically on discrepancies in reported deaths and adverse events.

What Dr. Kunadhasan uncovers raises grave questions about data integrity, regulatory failure, fraud, and the validity of the FDA’s EUA for the Pfizer-BioNTech COVID-19 shot.

And yet another White Paper is calling for an urgent halt on self-amplifying RNA ‘vaccine’ deployment until comprehensive safety studies are done to address contagiousness risks.  The paper discusses the significant theoretical risk including contagiousness through shedding, sexual transmission, and recombination with wild-type viruses.

FDA Commissioner Dr. Marty Makary and head of FDA’s Center for Biologics Evaluation and Research, Dr. Vinay Prasad, note that a number of other countries such as Australia and Germany only recommend the clot shots to certain populations while the U.S. has taken a ‘one size fits all’ approach because experts have argued Americans are too stupid to understand age-and risk-based recommendations.

But, even this approach ignores the elephant in the room: there are treatments for COVID which means a ‘vaccine’ isn’t even needed.  Then, there’s the fact they have negative efficacy.

What more is it going to take?

Evidently, a lot more……

The Food and Drug Administration issued an approval for Novavax’s Covid-19 ‘vaccine.’ This is the only non-mRNA vaccine.

The vaccine was approved for adults aged 65 and older and individuals aged 12 to 64 with at least one underlying health condition that increases their risk for severe COVID-19 outcomes. Reading the clinical trials prompts serious questions.

The trials included populations that had a single dose and populations that had two doses. The trials showed a reduction in symptomatic Covid 7 days after the second dose. But the FDA didn’t approve two doses. They only approved one. So is one dose even effective at all at preventing Covid? We don’t know, that wasn’t tested.  (Is this sounding familiar yet?)

There is also a noted risk of myocarditis and heart inflammation. There was also at least one vaccine recipient with “a serious event of Guillain Barré syndrome reported 9 days following the shot.  The FDA notes that Novavax has to follow up on any further cases if they observe it.

The FDA is also supposed to follow up on how the vaccine does when it is shipped to patients. They must submit a study called “Shipping Evaluation of SARS-CoV-2 rS (JN.1 Vaccine) Drug Product in Pre-Filled Syringe (PFS) Finished Good Presentation” by July of this year.

They approve vaccines not knowing how they will fare once they are shipped to doctor’s offices. They test it on us.

Don’t forget the low prevalence of Covid.

There is good news: there are at least 16 states with pending bills seeking to ban the clot shot mandates, establish a ‘vaccine’ bill of rights, or prohibit any immunization containing mRNA material.  Some bills would require manufacturers to label foods containing mRNA, according to data compiled by Bloomberg Government.

More than 2,500 ‘vaccine’-related bills have been introduced since 2021.

And top FDA official just disclosed she never got the clot shot due to her concerns about biodistribution.  She was concerned about excretion in breast milk since she was pregnant during the COVID ‘pandemic.’  When asked if information has emerged that validates her choice, said she thinks it does, but wanted to go on record that she was not speaking on behalf of the FDA.  

Researchers reported in a 2022 paper that messenger ribonucleic acid, which is in the Pfizer and Moderna COVID-19 shots, was detected in human breast milk. Another paper, in 2023, detailed similar findings.

Pfizer and Moderna did not return requests for comment.

And ‘Dilbert’ comic strip creator, Scott Adams, just admitted to having the same aggressive turbo cancer as former President Biden.

“The smartest, happiest people are the ones who didn’t get the vaccination, and they’re still alive.” ~ Scott Adams, Dilbert creator

It’s getting hot in the kitchen, folks.

Category:

Activism, research, vaccines

‘Must Hear’ Dr. Hatfill Interview

http://  Approx. 1 Hour

Dr. Steven Hatfill Blows Whistle on COVID Treatments, Gene Therapy Injections, and Research Fraud

“They lied!”

Podcast by Dana Parish

May, 2025

This is one of the most shocking interviews I’ve ever done. Dr. Steven Hatfill, renowned virologist, bioweapons expert, author, and senior scientific adviser to HHS, joins me to reveal the debacle behind COVID, the ‘vaccine,’ early treatments, and what really happened behind the scenes during the pandemic.

Hatfill was wrongfully accused of the anthrax attacks in the early 2000s and later exonerated, earning a multi-million dollar settlement from the US Government. But that didn’t stop him from stepping back into the fire. During the first Trump administration, he became a fierce advocate for early COVID treatment while the mainstream medical establishment tried to silence him.

In this episode, he lays out the evidence on how COVID was bioengineered, early treatments were suppressed, the vaccines were entirely misrepresented, and much more.

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**Comment**

No, you are not losing your mind.  I’ve posted this podcast before here:  https://madisonarealymesupportgroup.com/2025/05/14/study-confirms-covid-shots-laced-with-cancer-causing-dna/

I just felt it important enough to repost as some might have missed it.

And you don’t want to miss this one.

Dr. Hatfill answers all of Parish’s questions humbly and honestly.  I’m happy to report that everything posted on this website on the COVID chapter aligns with what Dr. Hatfill says in this interview.  I am indebted to doctors and researchers who shared prolifically on Linkedin early on.  Many of these experts are retired or not employed by the government and could speak freely.  Unfortunately, one by one, Linked in kicked these truth-tellers off the platform until one day I too was ‘disappeared.’  

Shame on platforms for censoring experts sharing information that could have saved lives.

The entire COVID chapter was mishandled from the start and there’s many people and organizations who need to be brought to justice over the fraud, deceit, and damage done in virtually every area.

And now, the IPAK-EDU White Paper 2025-ENDEUA states that when corrected efficacy curves and suppressed risks are taken into account, the mRNA covid shots fail the EUA standard.  The shots were based upon interim data from large-scale Phase III trials. The legal standard under §564 of the Federal Food, Drug, and Cosmetic Act requires that a product may be authorized for emergency use only if it is “reasonable to believe” that the product “may be effective” against a life-threatening condition, that the known and potential benefits outweigh the known and potential risks, and that no adequate alternatives are available. This report demonstrates, through a rigorous retrospective analysis, that these criteria were never met.

Trust me when I say, you need to hear this interview.  Please also share this widely, particularly to those who are still in the dark or need to hear it from an ‘expert.’  Hatfill knows his stuff.

For articles on the many topics Hatfill covers:

COVID is lab made:

Suppression of early, successful treatment:

How spike protein behaves in the body:

Is the shot gene therapy?  YES

Why was mRNA the government choice for COVID?

    • There are 9,613 patents licensed to giants in biotech and the US government
    • BARDA and DARPA have had a torrid love affair with mRNA for decades
    • A retrospective cohort study found the US government invested at least $31.9B to develop, produce, and purchase mRNA covid-19 shots, including sizable investments in the three decades before the pandemic through March 2022. 
    • While the study claims “millions of lives were saved,” the truth is the experimental, COVID gene therapy injections saved ZERO lives.

Links between COVID shots & Cancer

Nasal sprays to prevent COVID:

Persecution of doctors & health professionals who defied the global narrative:

Category:

Activism, research, Treatment, vaccines, Viruses

HHS to End COVID Shot Recommendations for Kids & Pregnant Women

https://www.thefocalpoints.com/p/breaking-hhs-to-end-covid-19-vaccine

BREAKING: HHS to END COVID-19 Vaccine Recommendations for Kids & Pregnant Women

With over 600,000 estimated COVID shot deaths in the U.S., HHS moves to roll back CDC guidance—amid mounting criminal referrals, legislative efforts, and growing calls for a complete moratorium.

May 15, 2025

According to the Wall Street Journal, the Trump administration—under the leadership of HHS Secretary Robert F. Kennedy Jr.—is preparing to end routine CDC recommendations that pregnant women, teenagers, and children receive COVID-19 vaccines. This decision, expected to be announced in the coming days, represents a long-overdue departure from current ill-advised CDC guidance, which still urges vaccination for everyone aged six months and older, including during pregnancy.

This is a critical first step—but the work is far from over.

We must continue pressing for the removal of all COVID-19 vaccine recommendations. No one is spared from the deadly effects of these injections. Healthy young adults, seniors, athletes, mothers, and children alike have suffered devastating injuries—many of them irreversible. A truly ethical public health system does not tolerate collateral damage in exchange for failed mass vaccination strategies. It’s time to stop pretending these shots are safe and effective for anyone.  (See link for article and graphics)

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For more:

I could go onto infinity with this.

It’s time to stop the shots!

Category:

Activism, Pregnancy, vaccines

FDA’s War on America’s Health

https://www.midwesterndoctor.com/p/the-fdas-war-on-americas-health?

The FDA’s War On America’s Health

Why do so many innovative therapies never see the light of day

A Midwestern Doctor
Apr 17, 2025
Story at a Glance:

•The FDA was established in 1906 in response to public concern over unsafe food and drugs, such as spoiled food and counterfeit products. However, food industry lobbyists gradually gained influence, leading to the removal of the agency’s original leader. As a result, numerous harmful food additives were granted “generally recognized as safe” (GRAS) status and continue to be used today.

•In 1962, the FDA was given broad powers to oversee drug safety following the thalidomide incident. Unfortunately, the new regulations created strict standards for drug efficacy that were often selectively enforced, benefiting the pharmaceutical industry. Unfortunately, the FDA increasingly targeted natural therapies, which led to many being erased from history.

•Despite numerous attempts to reform the agency, issues of inefficiency and bias within the FDA persist. This article examines these challenges and suggests potential reforms to improve the agency’s role in safeguarding public health.

For most of my life, I’ve observed the FDA belligerently suppress natural treatments and any unorthodox therapy which threatens the medical monopoly while simultaneously railroading through a variety of unsafe and ineffective drugs regardless of how much public protest the agency meets.

(See link for article and videos)

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**Comment**

Please share and record this important history or it will be scrubbed and lost forever.

Like most government agencies, the FDA began well and good in the 1800’s due to unscrupulous food producers as well as medicines with secret ingredients like opium and alcohol.  But, even from the get-go, the food and pharmaceutical industries were powerful and fought as lobbyists using legal tactics. The first Director of the Bureau of Chemistry, and thus the fist head of the FDA, actually resigned realizing he could do more as a private citizen than within government.  

The article goes into life-saving treatments vilified by the FDA as well as ‘vaccine’ cover-ups, and disastrous drug approvals.

For more:

Category:

Activism, Treatment, vaccines

German Study Confirms COVID Shots Laced With Cancer-Causing DNA & Japanese Study Demonstrates Regulatory Failure: Autopsy-Proof ‘Vaccine’ Deaths Clearly Being Systemically Ignored

https://slaynews.com/news/major-investigation-confirms-covid-vaccines-laced-cancer-causing-dna/

Major Investigation Confirms Covid ‘Vaccines’ Laced with Cancer-Causing DNA

Frank Bergman

A major investigation by a group of renowned German researchers has confirmed that Pfizer’s Covid mRNA “vaccines” are laced with dangerous levels of DNA contaminants.

While the presence of DNA contamination in Covid injections is not a new discovery, this latest study uses advanced techniques for more reliable quantification, making it the most significant investigation to date.

As Slay News has previously reported, leading scientists have been warning for some time that surges in deadly cancers among the Covid-vaccinated were caused by DNA fragments in the mRNA injections.

The study was led by Jürgen O. Kirchner, an Independent Researcher in Hamburg, and Professor Brigitte König of the University of Leipzig.

The results of the study were published in the Preprints journal.  (See link for article)

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Important excerpt:

The researchers confirm that their findings reveal that DNA contaminations exceeded safe levels by approximately 300 to 500 times.

Kevin McKernan, a former director of the Human Genome Project, described the findings as a “bombshell.”

“Chronic activation of the cGAS-STING pathway could paradoxically fuel cancer growth,” McKernan warned.

“Repeated exposure to foreign DNA through COVID-19 boosters may amplify this risk over time, creating conditions conducive to cancer development.”

While the authors concluded that these fragments were “non-replication-competent” meaning they cannot replicate in humans, McKernan disagreed.

“To assert that the DNA fragments are non-functional, they would need to transfect mammalian cells and perform sequencing, which wasn’t done here,” McKernan stated.

“Moreover, the methods used in this study don’t effectively capture the full length of DNA fragments,” he added.

“We’re in the stage where we’re scanning through tumors to look for integration events and looking for evidence of this in cancer biopsies,” McKernan said.

“And we can find them now.

“They found one that had really high spike [protein] sent to us for sequencing.

“And we can find components of Pfizer’s vaccines inside this thing a year after vaccination.”

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Dr. Steven Hatfill, senior medical advisor at HHS, just gave an explosive interview with Dana Parish.  You will recognize Parish’s name as she’s a patient which has done numerous podcasts with Lyme literate doctor Steven Phillips.

Hatfill is a virologist and biodefense expert, serving as a special advisor in the Administration for Strategic Preparedness and Response (ASPR) under HHS Secretary Robert F. Kennedy Jr. since early this month. He also worked in the first Trump administration who has seen the cover-ups firsthand, and he’s calling out the mRNA vaccines for what they are: a dangerous experiment.

The interview focuses on the mRNA shots causing cancer.  You can tell Parish is having a hard time accepting that the ‘vaccine,’ vs the virus, is what is behind the explosion in cancer as it is my understanding she took the jab herself as many well-known Lyme literate doctors unfortunately promoted the hastily made experimental gene therapy injections.  (I could be wrong on this but I feel I read it somewhere) She also is a proponent of ‘Long COVID’ despite the unfortunate truth that the shot itself is most probably behind a majority of these cases.  While she wants to be non-polarizing, it’s imperative that each ‘long covid’ case is monitored for ‘vaccine’ involvement to properly determine causality.  Thankfully, she is reporting on the devastating effects of the shots now.

https://worldcouncilforhealth.substack.com/p/sensational-new-study-demands-urgent?

Sensational New Study Demands Urgent Re-evaluation of mRNA Vaccines

Immunodeficiency, excess deaths, and Japan’s dangerous replicon experiment.

May 14, 2025

A groundbreaking commentary published in Discover Medicine has exposed critical flaws in global vaccination programs, particularly concerning mRNA COVID-19 vaccines and their long-term immunological consequences. The peer-reviewed, open-access study (Yamamoto, 2025) highlights alarming trends:

  • Vaccine-induced immunodeficiency is linked to repeated mRNA dosing
  • Japan is the only country still aggressively promoting boosters—including self-amplifying RNA (replicon) vaccines
  • Excess deaths now surpass 600,000 in Japan post-vaccination, with no clear explanation beyond aging demographics
  • Three infant deaths within 24 hours of routine vaccination have been dismissed as “unable to evaluate” by regulators

Here’s what you need to know about Yamamoto’s findings and their urgent implications for public health policy.

Key points
1. mRNA vaccines cause immune dysfunction

Yamamoto notes research showing three key ways that mRNA vaccines screw up immune systems:

  • IgG4 antibody class switching. Repeated mRNA vaccination shifts immune responses toward non-inflammatory IgG4 antibodies, potentially blunting protection against infections (Irrgang et al., 2023).
  • Lymphocyte depletion. Studies report post-vaccination lymphopenia (Seban et al., 2022), raising concerns about temporary immunosuppression.
  • Vaccine-Acquired Immunodeficiency Syndrome (VAIDS). Some researchers warn that frequent boosters may erode natural immunity (Seneff et al., 2022).
2. Japan is taking more risks on this genetic tech than other nations

While most nations halted mRNA boosters by mid-2022 due to safety concerns, Japan continues administering 8th doses, including:

  • Self-amplifying mRNA (saRNA) vaccines—untested in humans until now.
  • Simultaneous administration with flu shots, obscuring adverse event causality.
  • Regulatory capture: vaccine review committees include pharma-funded members, while autopsy-confirmed deaths post-vaccination are routinely classified as “unable to evaluate” (γ).
3. Baby deaths and injuries are going unacknowledged

Yamamoto notes that three infants died within 24 hours of routine vaccinations.

While autopsies were performed, no causal link was officially acknowledged. This is symptomatic of a wider systemic failure to acknowledge vaccine harms. Japan’s compensation system has historically recognized 150+ vaccine-related deaths—but none from COVID-19 vaccines, despite 932 reported fatalities.

4. Japan’s excess mortality and hidden data

Some interesting observations from Yamamoto here:

  • The 600,000+ excess deaths in Japan since 2021 cannot be explained by COVID-19 alone.
  • Similar trends have been observed in highly vaccinated Western nations (Mostert et al., 2024).
  • Japan’s Ministry of Health (MHLW) misclassified vaccinated individuals as “unvaccinated” in early statistics, skewing efficacy data.

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**Comment**

Despite this information and a plethora of research now showing how dangerous the ineffective shots are, the new leadership supposedly in charge of MAHA (Make America Healthy Again) flip flop more than a waffle maker. The FDA will meet on May 22, 2025 to discuss and make recommendations on the selection of the 2025-2026 formula for COVID gene therapy injections for use in the U.S.

It appears that Podcaster Shannon Joy is completely correct: RFK & Trump is a ‘Deal With the Devil That Betrayed Medical Freedom.’

http:// Approx. 9 Min

MAHA FDA Chief, Marty Makary, Flip-Flops on COVID Shots

The Jimmy Dore Show

May 11, 2025

Newly minted FDA Chief Marty Makary is sending what some would consider “mixed” signals about his support for COVID boosters and mRNA technology. During a recent TV interview Makary said he wasn’t sure whether young, healthy children should be receiving booster shots. Whereas Makary has up to this point been among the most vocal critics of the COVID vaccine. Jimmy and former HUD Assistant Director Catherine Austin Fitts discuss why Makary would be changing his tune this way and whether he has been absorbed into “the box” that co-opts anti-establishment voices once they become insiders.

Even HHS Secretary Robert F. Kennedy recently supported the measles vaccine after an outbreak in Texas, despite saying in the past that US has measles outbreaks ‘every year,’ and that there are safety concerns about the live measles vaccine, saying testing was inadequate. He also raised safety concerns about the vaccine for pertussis. Just today Stanford scientists confirm a fatal case of vaccine-associated measles encephalitis in an immunocompromised child.

In this case, the vaccine measles virus hypermutated to a fatal strain that invaded the brain and killed the child.

If the child was unvaccinated, the AML would have been treated in the usual fashion, with a good chance at survival. Source

You won’t hear about this little factoid from mainstream media.

It will be interesting to see if the new FDA head of biologics, vaccines division, Dr. Vinay Prasad, waffles back and forth as well, as he was a vocal critic of all things COVID.

Sadly, much of the world will never come to grips with the COVID psyop that according to one expert had policy that is ‘completely stupid’ & unethical.’

Despite the MAHA rhetoric, until its leaders come clean, much of the public will remain shrouded in the dark, led by emotions rather than truth, and completely vulnerable to it all happening over and over.

Category:

Activism, Cancer, research, vaccines