Archive for the ‘Activism’ Category

COVID Shot Stroke Cover-Up And A Public Message to Anthony Fauci

https://sayerji.substack.com/p/breaking-biden-white-house-covid?

BREAKING: Biden White House COVID Stroke Cover-Up Exposed

A Pattern of Institutional Deception Finally Revealed in Stunning New Email Revelations

Newly released government documents confirm that Biden White House officials directly edited CDC messaging on COVID-19 vaccine safety in January 2023 — changing the description of a stroke risk signal in elderly Americans from “moderately elevated” to “slightly elevated,” removing the words “potential risk” entirely, and instructing health officials they “don’t want to see this document again.”

All of this happened while the same administration was aggressively pushing booster uptake in the very age group affected, and while its Surgeon General was publicly accusing independent health researchers of spreading harmful disinformation for raising the exact safety questions officials were quietly suppressing internally.

This is not a hypothetical scandal. It is documented. And for those of us who lived through the coordinated destruction of our platforms, our reputations, and our livelihoods for asking these questions in public, it is a confirmation that arrives with the full weight of vindication — and the full fury of unresolved injustice.

I was one of those researchers. And this story lands differently when you have been named a public enemy for telling the truth the government was simultaneously editing into silence.  (See link for Ji’s exposé on a purposeful bureaucratic editorial operation)

https://substack.com/home/post/p-192014160

A Public Message to Anthony Fauci

Let Me Help You Remember What Went Wrong.

In what can only be described as a New York Times public image rehabilitation attempt, former NIAID Director Anthony Fauci comes across as a Pontius Pilate – his hands washed of any responsibility for his central role as a, if not the primary, driver of public health policies that nearly destroyed the United States of America.

Dr. Fauci, we remember. We ALL remember. Here is my message to help YOU remember. Let’s start with how you helped the Biden administration threaten ALL of our jobs, but the article does not mention that. It does not mention your central role in the lockdown – in fact,

you flatly deny that your actions or policies led to any school closings or factories shut down. How is it that governors across the U.S. decided “essential” and “non-essential” businesses, and you stood by and never protested?

In August 2020 you said publicly: “If someone refuses the vaccine in the general public, then there’s nothing you can do about that. You cannot force someone to take a vaccine.” Then on September 10, 2021 — the day after Biden announced the OSHA Emergency Temporary Standard covering ~80–100 million workers — you told PBS: “I myself am quite favorably impressed by that and feel strongly that that is what we should be doing.” On November 4, 2021, testifying before the Senate HELP Committee, when Sen. Romney asked directly whether mandates would save lives, you said: “We know that vaccines absolutely save lives. And we know that mandates work.”

Also on record in a Michael Specter audiobook, Summer 2021: “It’s been proven that when you make it difficult for people in their lives, they lose their ideological bullshit, and they get vaccinated. It was played back to you at the June 2024 hearing. You did not retract it.

The mandate had no testing option for federal workers or healthcare workers — it was vaccinate or lose your job. You were the Chief Medical Advisor sitting in the White House at the time. You did not object.

We all remember, also, your key role as a driver of the lockdown.

  • You sent Dr. Clifford Lane — your NIAID deputy — to China with the WHO Joint Mission in February 2020
  • Lane returned and wrote: “China has demonstrated this infection can be controlled, albeit at great cost. This is the bottom line.”
  • Lane told you directly: “From what I saw in China, we may have to go to as extreme a degree of social distancing to help bring our outbreak under control”
  • You testified he had “every reason to believe” Lane’s evaluation
  • You then admitted: social distancing “even by somewhat difficult means” involving “essentially the entire community” was possible in the U.S.

Your methodological problems:

  1. Lane visited after China had already locked down — he could only observe what was happening, not whether the lockdown caused the decline
  2. Chinese data was demonstrably unreliable — WHO had tailored confidentiality forms “to China’s terms” (FOIA-obtained emails, Judicial Watch, March 2021) and a January 2020 WHO epidemiological analysis was marked “strictly confidential”
  3. The WHO-China Joint Mission report itself was controlled: all activities were “arranged by the Chinese Government’s National Health Commission” (per a Feb. 15, 2020 internal WHO email)

(See link for Weiler’s chronology all things fraudulently Fauci)

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**Comment**

It’s beyond time for vindication of those who were right all along, and accountability for those who pushed unscientific, fraudulent, and dangerous COVID measures that were ineffective and even deadly.

For more:

Meningitis B Vaccine: Chimeric Bioengineered Bacterial Proteins & Aluminum – 96% Adverse Reaction Rate

Predictably, 29 measles cases in the UK are being used to push this frankenshot.

https://jonfleetwood.substack.com/p/meningitis-b-vaccine-contains-chimeric?

Meningitis B Vaccine Contains Chimeric Bioengineered Bacterial Proteins and Aluminum—96% Adverse Reaction Rate, 29% Experience Severe Reaction

FDA admits jab “may not protect all vaccine recipients.”

The meningococcal B (MenB) vaccine BEXSERO contains bioengineered bacterial proteins—including chimeric (“Frankenstein”) antigens—and aluminum, while FDA regulatory documents and clinical trial data show that up to 96% of recipients experience adverse reactions and as many as 29% report reactions severe enough to interfere with normal daily activity.

These findings come from multiple primary sources, including the FDA’s full prescribing information, the manufacturer’s patient information leaflet, a large clinical study, and federal toxicology data from the CDC’s Agency for Toxic Substances and Disease Registry (ATSDR).

The FDA and manufacturer documents show that the MenB vaccine can produce fever, headache, vomiting, irritability, seizures, and neurologic events—symptom categories that overlap with the clinical presentation of meningococcal disease itself.

Meningitis B vaccinations are now being given to 15 and 16-year-olds in U.K. schools in response to a reported outbreak.  (See link for article)

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Important excerpts:

FDA Prescribing Information

individuals remain at increased risk “even if they develop antibodies following vaccination.”

Manufacturer Insert

“you remain at increased risk of disease…”

Clinical Trial Failed Key Effectiveness Benchmark

The study reports:

“the non-inferiority endpoint… was… not met because of the lower response against PorA.”

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For more:

Medicine has lost its mind.  If you haven’t found an independent doctor yet, do it NOW. An independent doctor could save your life, and how hospitals are the new ‘killing fields’ to be avoided at all costs.  These monoliths are beholden to government funding, as are doctors who take money from insurance companies  and the government for utilizing certain drugs/interventions over others.  This is a glaring conflict of interest that needs to end now.  

Go here, to learn how to download a form to print out and have to be able to take to the hospital with you, should you need to go that will protect you from getting needless vaccines.

District Judge Singlehandedly Freezes Vax Schedule & Strips CDC Director of Authority

https://childrenshealthdefense.org/defender/aap-trade-groups-federal-judge-injunction-vaccine-schedule-upsell/

Agency Capture

How a Gaggle of Vaccine Trade Groups Got a Federal Judge to Help Upsell Vaccines No State Thinks Are Necessary

On March 16, U.S. District Judge Brian Murphy in Massachusetts issued a preliminary injunction that freezes the federal childhood vaccine schedule and strips the CDC director of the authority to change who gets which vaccines. Here’s why the District Court ruling was wrong — and what we plan to do about it.

Editor’s note. Attorney Rick Jaffe is representing Children’s Health Defense (CHD) and five other plaintiffs in a lawsuit alleging the American Academy of Pediatrics (AAP) has been running a decades-long racketeering scheme to defraud American families about the safety of the childhood vaccine schedule.  Jaffe is also representing CHD in its motion to intervene in the AAP’s lawsuit against HHS and U.S. Health Secretary Robert F. Kennedy Jr.
Something happened on March 16 that Robert F. Kennedy Jr.’s people need to understand.

U.S. District Judge Brian Murphy in Massachusetts issued a preliminary injunction in AAP v. Kennedy that freezes the federal childhood vaccine schedule and strips the Centers for Disease Control and Prevention (CDC) director of the authority to change who gets which vaccines.

Not for a week. Not until the next hearing — but for the duration of this case, which could be years.

Let me explain what Judge Murphy actually did, because I don’t think the people advising Kennedy understand it.

The two holdings that shut down everything

The order from the U.S. District Court for the District of Massachusetts does two things.

First, Murphy held that the CDC director cannot change the immunization schedule unless the Advisory Committee on Immunization Practices (ACIP) originates the change.

Murphy ruled that the changes to the CDC’s vaccine recommendations, approved by the CDC’s then-acting director, Jim O’Neill, were invalid because the changes didn’t come through ACIP. (See Preliminary Injunction Opinion, page 21: “The CDC cannot simply bypass ACIP in altering the immunization schedules.”)

In other words, the CDC director can’t initiate. He can only accept or reject what ACIP gives him.

Second, Murphy’s decision stayed the appointments of all 13 ACIP members that Murphy ruled were improperly appointed (Opinion, pages 43-44). He found Kennedy violated “balance” requirements.

Therefore, ACIP cannot meet. Cannot deliberate. Cannot vote.

Read those two holdings together. The director can’t act because the District Court says only ACIP can originate. ACIP can’t act because the court shut it down.

Here is the District Court’s opinion. I’ll say it plainly:

The CDC director cannot, right now, today, change a single vaccine recommendation on the childhood schedule. Cannot reclassify a vaccine. Cannot act on new safety data about an existing vaccine. Cannot recommend a new vaccine the FDA authorizes.

The CDC’s scientists can still track diseases, run laboratories, investigate outbreaks. What they cannot do is watch their Director act on their work. If the science changes on any of the seventeen currently recommended vaccines, the director can’t respond.

If the U.S. Food and Drug Administration (FDA) authorizes a new vaccine tomorrow, the director can’t recommend it. The recommendation apparatus is frozen, and it stays frozen until this case is resolved or ACIP is reconstituted to Murphy’s satisfaction.

(See link for article)

For more:

Massachusetts Makes AGS a Reportable Illness

https://www.capeandislands.org/local-news/2026-03-23/state-will-start-tracking-cases-of-tick-borne-mammal-product-allergy

State will start tracking cases of tick-borne mammal product allergy

Governor Maura Healey (at the podium) announced that alpha-gal syndrome will become a reportable condition in Massachusetts at the Frances A. Crane Wildlife Management Area in North Falmouth. Massachusetts Public Health Commissioner Dr. Robbie Goldstein (leftmost person standing) spoke about the importance of collecting data on the emerging condition.

Gilda Geist / CAI
Governor Maura Healey (at the podium) announced that alpha-gal syndrome will become a reportable condition in Massachusetts at the Frances A. Crane Wildlife Management Area in North Falmouth. Massachusetts Public Health Commissioner Dr. Robbie Goldstein (leftmost person standing) spoke about the importance of collecting data on the emerging condition.

Starting April 1, Massachusetts health care providers and labs will be required to alert the state when they encounter cases of the tick-borne allergy alpha-gal syndrome.

Alpha-gal syndrome is an allergy to mammal products that can be caused by a lone star tick bite. It’s been on the rise on Cape Cod and the Islands, to the point where it’s caught the attention of the governor’s office.

At a press conference in North Falmouth last week, Governor Maura Healey announced that alpha-gal syndrome will be considered a reportable condition for at least the next year. The designation will make it easier for the state to collect data on alpha-gal syndrome, which at this time has no treatment.

“As the global life sciences capital of the world, I hope that somehow our data and our collection can be used with science and research right now in our state to eradicate this once and for all,” Healey said.

Massachusetts Public Health Commissioner Dr. Robbie Goldstein was also at the event. Until recently, he said, there were no lone star ticks in Massachusetts. But climate change has made Massachusetts hospitable to lone star ticks, named for the single white dot on their backs.

“Warmer temperatures, shorter winters [and] shifting ecosystems all have allowed the lone star tick to crawl—literally crawl—northward,” he said. “We’re seeing that expansion now on Cape Cod, on Martha’s Vineyard and on Nantucket. And increasingly, we’re seeing it in the mainland.”

Barnstable County has been working closely with public health partners on the Vineyard, where alpha-gal syndrome has emerged as a significant concern.

“By taking this data-driven, proactive approach, we are doing more than just simply responding to an emerging public health challenge,” Goldstein said. “We are helping people prevent alpha-gal syndrome.”

Alpha-gal is a sugar molecule that is in most mammals, but not humans. It’s also in the saliva of lone star ticks. When someone is bitten by a lone star tick, the alpha-gal in the tick’s saliva can get into the person’s bloodstream. The body’s immune system can see the presence of alpha-gal as a threat, causing an allergic reaction that is triggered when people are exposed to alpha-gal in the future by consuming mammal products. That can include meat and dairy, as well as non-food products, such as some medications that contain mammal additives or stabilizers. (See link for article)

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**Comment**

I will refrain from my regular diatribe, but ticks are impervious to weather:

Researchers and the Media are beholden to Big Pharma and government – pretty much their main funders.  They understand who butters their bread and that they must toe the lie to get those hotly contested research dollars. This requires them to regurgitate the accepted narrative, even though it’s been proven wrong, again and again.

It’s now been exposed that billionaires under the guise of philanthropy have financed research portals to control scientific discourse and that a carefully planned 20 year architecture is behind ‘pandemics’ as a business model.

Big money is behind the faulty climate change narrative and it seems researchers care more about their paychecks than facts.

Just as it’s far more likely that geoengineering is behind deleterious weather conditions, not to mention health issues, it’s also far more likely that the government’s deployment of radioactive lone star ticks in Virginia have more to do with tick dispersement than the weather.

Lone star ticks have been found in Minnesota, Wisconsin and up into Maine.

Then, there’s the very real issue that ticks are not the sole perp in this drama:

More on AGS:

Pfizer’s Former Chief Toxicologist: COVID Jab “Should Never Have Been Approved”

This should be spread FAR AND WIDE…..

http://  Approx. 5 Min

Former Pfizer Chief Toxicologist

Dr. Helmut Sterz

3/22/26

Virologist and former Pfizer toxicology chief Dr. Helmut Sterz speaks at German Covid inquiry on the COVID mRNA injections.

Important points:

  • Underreporting puts the death toll from the Comirnaty (Pfizer) COVID shots from between 20,000 to 60,000 Germans.  This number does not include COVID shots produced by other manufacturers.
  • Carcinogenic risk was not studied for ‘time reasons’ and no alternative studies have been conducted.
  • The rat reproduction study was defective so no reliable results of the effect of the shots on pregnancy or subsequent development could be given
    • This recent rat study shows pregnant rats that received the COVID-19 mRNA BNT162b2 vaccine during gestation had offspring with autism-like behaviors, decreased neuronal counts, and impaired motor performance. 
  • Essential toxicology studies were sacrificed to speed without acceptable reasons.
  • Robert Koch Institute (RKI) noted that side effects and adverse effects should be checked only after market launch.
  • Pfizer’s post marketing report gave over 1,200 suspected deaths within only two months after approval.
  • The Paul Elriche institute received so far 2,133 reports of death after Comirnaty.
  • There is a high number of unreported cases due to under reporting so deaths are likely much higher.
  • Pfizer’s documentation does not reveal a positive risk benefit ratio.
  • Mathematician Robert Rockenfeller from the University of Koblenz states that for every severe case of COVID allegedly prevented, there were 25 serious side effects.
  • Mortality increased from 2021 and 2022 compared to 2020.  If the vaccine was effective mortality would have decreased.
  • Vaccine purity was too expensive for mass production so the population received a shot with the help of a bacterium Escherichia coli (E. coli) and the result was significant impurities with bacteria of the DNA and the consequence could be a considerably increased cancer risk.

https://dailytelegraph.co.nz/news/pfizers-former-chief-toxicologist-says-covid-jab-should-never-have-been-approved/

Pfizer’s former chief toxicologist says COVID jab “should never have been approved”

A hearing in the German Bundestag has triggered fresh controversy over the approval and safety of COVID-19 mRNA ‘vaccines’, after a former chief Pfizer toxicologist confirmed that critical safety testing was bypassed during development.

March 24, 2026 Daily Telegraph NZ

Speaking at the Corona Investigation session on March 19, 2026, Dr Helmut Sterz said “essential toxicity studies were sacrificed to speed, without acceptable reasons,” adding that the vaccine’s approval effectively resulted in “prohibited human trials.”

The claims were presented during a session organised by an opposition-led committee, with reports indicating the testimony was limited to a brief five-minute window.  (See link for article)