Archive for the ‘vaccines’ Category

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.

According to the Wall Street Journalthe 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!

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

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:

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

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.

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.

Whistleblower Lawsuit Against Pfizer Dismissed

https://lionessofjudah.substack.com/p/trump-sides-with-pfizer-trumps-doj?

DOJ Has Dismissed Lawsuit Against Pfizer Concerning Its Fraudulent COVID Jab “Clinical Trial”

Pfizer Whistleblower Brook Jackson explains how Trump’s DOJ has dismissed her lawsuit against Pfizer concerning its fraudulent COVID-jab “clinical trial.”

What Has To Happen Before Shots Are Pulled & Yet Another Reason to ‘Stop the Shots’: Microscopic & Biochemical Analysis of White Clots &

https://popularrationalism.substack.com/p/what-has-to-happen-before-mrna-vaccines?

What Has to Happen Before mRNA Vaccines Are Pulled: Why RFK Jr. Hasn’t—and Why He Might Soon

Legal and regulatory options and requirements point to the pathway to freedom

 

The continued use of mRNA vaccines in the United States remains one of the most politically and medically contentious issues of our time. As public awareness grows around adverse event profiles and the questionable regulatory processes that ushered these products into global use, many are now asking an urgent question: why hasn’t HHS Secretary Robert F. Kennedy Jr. acted to revoke them?

To the untrained observer, Kennedy’s hesitation might appear as political caution or betrayal of his vaccine-critical roots. But the reality is far more complex. Pulling a product authorized under Emergency Use Authorization (EUA) or granted full Biologics License Application (BLA) approval is not a matter of executive decree. It requires a coordinated, multi-agency reckoning with evidence, policy, and law. And the legal scaffolding built to protect vaccine manufacturers—particularly under the Public Readiness and Emergency Preparedness (PREP) Act—was designed precisely to prevent the kind of abrupt retraction the public is demanding.

Yet the fortress is beginning to crumble.

The Nature of the Authorizations

Most Americans believe the mRNA vaccines are “approved.” In fact, the vaccines administered to the majority of the population have remained under EUA, not full licensure. The FDA granted BLAs to Comirnaty (Pfizer) and Spikevax (Moderna), but those exact products are often not available in the U.S. commercial supply chain. This bait-and-switch has significant legal implications, particularly around informed consent and product liability.

Under 21 U.S.C. § 360bbb-3, EUA requires that the Secretary of HHS determine that there is a public health emergency, that no adequate approved alternatives exist, and that the known and potential benefits outweigh the known and potential risks. But what happens when emerging data calls that balance into question?

What It Has Taken to Pull Vaccines Before

History tells us that only under grave circumstances does the FDA pull a vaccine. The Cutter Incident in 1955, in which live polio virus in inactivated vaccine batches caused paralytic disease and death, is one example. RotaShield, pulled in 1999 after being linked to intussusception in infants, is another. Pandemrix, used during the 2009 H1N1 pandemic, was withdrawn in Europe after post-vaccine narcolepsy cases.

But unlike those cases, mRNA vaccine injuries are statistically diffuse, often delayed, and obscured by passive surveillance systems with notorious underreporting.  (See link for article)

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Important quote:

The regulators knew. The manufacturers knew. And, in time, the record will show who acted—and who remained silent. ~ Dr. James Lyons Weiler

The article discusses the sweeping liability protection to ‘vaccine’ manufacturers called The Prep Act and that The Supreme Court could soon be asked whether HHS may revoke these immunities if the product’s risk-benefit profile is no longer defensible.  It also discusses the replacement of Peter Marks, who remained resistant to transparency to the bitter end, with Vinay Prasad, who is known for his rigorous critique of Pharma-captured science and his opposition to the inclusion of the COVID shots on the routine childhood schedule.

It was enjoyable to watch Prasad become more and more vocal after he swallowed the red pill.  At the end, he was stating,

Do not test, do not report cases, do not wear masks, do not take the shots. 

Quite a turnaround.  

He also had no trouble taking Walensky down, pointing out her repeated LIES, and stating the CDC abandoned science It was actually fun watching him go from a short-haired, square cornered, believe the ‘experts’ type doctor to a long haired, beard wearing, bloody honest doctor who in the end despises what public health has become.  Bravo!

The Prep Act needs to go.

https://www.thefocalpoints.com/p/microscopic-and-biochemical-analysis?

Microscopic and Biochemical Analysis of Anomalous White Fibrous Clots from Deceased mRNA Injection Recipients

Gold-standard analytical techniques reveal a potential novel infectious amyloid pathology associated with Spike protein exposure.

In this eye-opening interview, I sit down with embalmer Richard Hirschman and industrial chemist Greg Harrison to investigate the emergence of large, white fibrous clots in deceased individuals who received COVID-19 mRNA injections.

Hirschman, a seasoned embalmer with over 20 years of experience, first began noticing these unusual white, rubbery clots in early 2021. Found in both veins and arteries—a rarity in embalming practice—their frequency and composition were unlike anything he had encountered in two decades of work.

To better understand what they were made of, he partnered with Greg Harrison, an industrial organic chemist with deep expertise in polymer analysis. Harrison subjected the clots to rigorous biochemical testing using techniques like ICP-MS, HPLC, Raman spectroscopy, and RT-QuIC.

What they uncovered is nothing short of shocking: these are not ordinary post-mortem clots. The structures are composed of misfolded fibrin proteins with amyloid characteristics—including signs of infectious amyloid behavior, capable of triggering misfolding in other proteins. These findings raise grave concerns about a novel, systemic disease process that may be silently affecting millions.  (See link for article and video)

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**Comment**

These clots were first seen in 2021, after the shot rollout but are now seen in 30-50% of all bodies Hirschman embalms. Similar clots have been removed from living patients during surgery and catheterization.  Multiple independent embalmers and pathologists globally are now reporting the same thing and 83% of embalmers have observed these unique clots.

Standard lab panels cannot detect the clots, only specialized imaging using Thioflavin T fluorescence or similar markers can reveal them.

Their discovery that these misfolded fibrin proteins with amyloid characteristics including signs of infectious behavior and triggering misfolding in other proteins is extremely frightening indeed as it raises concerns of a novel, systemic disease process.

The rigorous testing revealed:

  • Extremely high levels of phosphorus — up to 4,900 ppm, compared to a normal blood range of 100–1,500 ppm.
  • Deficiency of essential blood elements, including iron, zinc, and magnesium — all typically abundant in red blood.
  • Dominant presence of fibrinogen beta chain — accounting for over 35% of protein content, while the fibrinogen alpha and gamma chains were severely underrepresented or nearly absent.
  • No complete fibrils detected — only monomers, indicating incomplete or dysfunctional polymerization of clotting proteins.
  • High concentrations of proline, an amino acid known to kink and misfold proteins — consistent with the presence of amyloidogenic material and potentially linked to modified codons in mRNA vaccines.

The experts believe there are three possible causes of these clots: synthetic spike protein, lipid nanoparticles, and/or modified codons and proline substitutions.

Some doctors are regretting pushing the clot shots. There are now more than 1,000 peer-reviewed articles on shot injuries and never forget that the shots don’t do diddly to protect you from anything but actually set you up for becoming infected.  The Cleveland Clinic (CC) study and the second CC study showed the shots increase your risk of contracting COVID. Other studies found the same effect: hereherehereherehereherehere.

Science that departs from the narrative apparently doesn’t matter anymore.
Unfortunately, more time is needed before these shots are halted , but it’s long overdue.

This website has posted about the unique white, rubbery clots from the beginning.