Archive for the ‘Viruses’ Category

Japanese Researchers: COVID Shot Spike Protein Damages Blood Vessels for up to 17 Months & WHO States ‘Monkeypox’ is a ‘Side Effect’ of COVID Shot

https://www.sciencedirect.com/science/article/pii/S096758682500195X?

Expression of SARS-CoV-2 spike protein in cerebral Arteries: Implications for hemorrhagic stroke Post-mRNA vaccination

https://doi.org/10.1016/j.jocn.2025.111223Get rights and content
Under a Creative Commons license
Received 31 January 2025, Accepted 31 March 2025, Available online 3 April 2025, Version of Record 3 April 2025.
Open access

Highlights

  • •Spike protein expression was detected in 43.8% of vaccinated patients.
  • •SARS-CoV-2 spike protein persists in cerebral arteries up to 17 months post-vaccination.
  • •Spike protein was expressed in the intima of the cerebral arteries.
  • •In situ hybridization confirmed vaccine- and virus-derived spike protein mRNA.
  • •Findings highlight concerns about mRNA vaccine biodistribution and long-term safety.

Abstract

Background

The rapid deployment of mRNA vaccines for SARS-CoV-2, such as BNT162b2 (BioNTech-Pfizer) and mRNA-1273 (Moderna), provided a critical tool in combating the COVID-19 pandemic. While their short-term safety and efficacy were demonstrated in clinical trials, rare adverse events, including hemorrhagic strokes, have been reported after widespread use. However, the long-term biodistribution and effects of mRNA vaccines remain underexplored.
This study aimed to investigate the long-term presence of SARS-CoV-2 spike protein in brain tissues of patients with hemorrhagic strokes, examining its potential association with mRNA vaccination.

Methods

A total of 19 cases of hemorrhagic stroke from 2023 to 2024 were retrospectively analyzed. Immunohistochemical staining for SARS-CoV-2 spike protein and nucleocapsid protein was performed on tissue samples. In situ hybridization was conducted in selected cases to confirm the origin of spike protein expression (vaccine or viral infection). Vaccination history and SARS-CoV-2 infection status were documented for all cases.

Results

Spike protein expression was detected in 43.8 % of vaccinated patients, predominantly localized to the intima of cerebral arteries, even up to 17 months post-vaccination. While no active inflammatory changes were identified, infiltration of CD4-, CD8- and CD68- positive cells was observed in the spike protein positive vessels. In situ hybridization confirmed the presence of both vaccine-derived mRNA and SARS-CoV-2 virus-derived mRNA, which encode the spike protein, in select cases. Notably, spike protein positivity was observed exclusively in female patients (P = 0.015). None of the cases showed nucleocapsid protein positivity, supporting the absence of active viral infection.

Conclusion

Although the possibility of spike protein expression due to asymptomatic SARS-CoV-2 infection cannot be entirely excluded, this study demonstrated prolonged presence of SARS-CoV-2 spike protein in the cerebral arteries following mRNA vaccination. Additionally, some inflammatory cell infiltration was observed in spike-positive vessels. These findings raise significant concerns regarding the biodistribution of lipid nanoparticle-based vaccines and their long-term safety. Global replication studies are urgently required to validate these findings and ensure comprehensive safety evaluations of mRNA vaccines.
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**Comment**
While the authors insist that the clot shots provided a critical tool in combating the COVID-19 pandemic, data, a systemic review and reality show otherwise.  In fact in November 2024, a peer-reviewed study called for immediate global moratorium on these experimental gene therapy injections due to unprecedented adverse reactions including death.
They weren’t even tested for reduction in hospitalization, death, or transmission, rather they were tested for reduction in severe symptoms – which is not the proper endpoint for “vaccine” efficacy. To make matters even worse, they dropped the 50% efficacy requirement for Emergency use Authorization (EUA).  Then, they authorized boosters without consulting its vax panel.  Rubberstamping these shots is their modus operandi.

https://slaynews.com/news/who-monkeypox-side-effect-covid-mrna-vaccines/

WHO: ‘Monkeypox’ Is a ‘Side Effect’ of Covid mRNA ‘Vaccines’

Frank Bergman

The World Health Organization (WHO) has admitted that so-called “monkeypox” is actually a side effect of Covid mRNA “vaccines.”

The United Nations “health” buried the admission on the WHO’s VigiAccess website.

The website contains a database that lists all known side effects of all drugs and vaccines that have been approved for public use.

Under “potential side effects” for the Pfizer BioNTech COVID-19 vaccine, the WHO lists “monkeypox,” “smallpox,” and “cow pox” among hundreds of other disorders.

They are listed under “infections and infestations” that emerge as “side effects” of the Pfizer mRNA vaccine.  (See link for article)

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**Comment**

A new study of WHO data shows that ‘COVID deaths’ skyrocketed among the ‘vaccinated,’ and a study of 9 million also reveals brain damage.

Similarly to COVID, a Monkeypox outbreak followed a ‘Germ-Game’ preparation. A renowned German doctor has already spoken out to warn the public that the monkeypox “outbreak” is a hoax and the “symptoms” are actually side effects of Covid clot shots.  Another doctor states monkeypox is psychological bioterrorism being pushed by ‘evil.’

Take home: these shots are worthless and dangerous.
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Activism, research, vaccines, Viruses

Cleveland Clinic Study Confirms Flu Vaccine Ineffective, Warns of Harms

https://www.medrxiv.org/content/10.1101/2025.01.30.25321421v3

Effectiveness of the Influenza Vaccine During the 2024-2025 Respiratory Viral Season

Nabin K. Shrestha, Patrick C. Burke, Amy S. Nowacki, Steven M. Gordon
doi: https://doi.org/10.1101/2025.01.30.25321421

This article is a preprint and has not been certified by peer review [what does this mean?]. It reports new medical research that has yet to be evaluated and so should not be used to guide clinical practice.

ABSTRACT

Background The purpose of this study was to evaluate the effectiveness of the influenza vaccine during the 2024-2025 respiratory viral season.

Methods Employees of Cleveland Clinic in employment in Ohio on October 1, 2024, were included. The cumulative incidence of influenza among those in the vaccinated and unvaccinated states was compared over the following 25 weeks. Protection provided by vaccination (analyzed as a time-dependent covariate) was evaluated using Cox proportional hazards regression.

Results Among 53402 employees, 43857 (82.1%) had received the influenza vaccine by the end of the study. Influenza occurred in 1079 (2.02%) during the study. The cumulative incidence of influenza was similar for the vaccinated and unvaccinated states early, but over the course of the study the cumulative incidence of influenza increased more rapidly among the vaccinated than the unvaccinated. In an analysis adjusted for age, sex, clinical nursing job, and employment location, the risk of influenza was significantly higher for the vaccinated compared to the unvaccinated state (HR, 1.27; 95% C.I., 1.07 – 1.51; P = 0.007), yielding a calculated vaccine effectiveness of −26.9% (95% C.I., −55.0 to −6.6%).

Conclusions This study found that influenza vaccination of working-aged adults was associated with a higher risk of influenza during the 2024-2025 respiratory viral season, suggesting that the vaccine has not been effective in preventing influenza this season.

Summary Among 53402 working-aged Cleveland Clinic employees, we were unable to find that the influenza vaccine has been effective in preventing infection during the 2024-2025 respiratory viral season.

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SUMMARY:

    1. THE FLU VACCINE INCREASES THE RISK OF CONTRACTING A NON-FLU RESPIRATORY ILLNESS BY 65%.
    2. THE FLU VACCINE DOESN’T REDUCE DEMAND ON HOSPITALS.
    3. THE FLU VACCINE DOESN’T PREVENT THE SPREAD OF THE FLU.
    4. THE FLU VACCINE FAILS TO PREVENT THE FLU ABOUT 65% OF THE TIME.
    5. REPEAT DOSES OF THE FLU VACCINE MAY INCREASE THE RISK OF FLU VACCINE FAILURE.
    6. DEATH FROM INFLUENZA IS RARE IN CHILDREN.
    7. THE FLU VACCINE DOESN’T REDUCE DEATHS FROM PNEUMONIA AND FLU.
    8. PATIENTS DON’T BENEFIT FROM THE VACCINATION OF HEALTHCARE WORKERS.
    9. FLU VACCINE MANDATES ARE NOT SCIENCE-BASED.

Excerpts:

Originally, the flu vaccine was a measure to protect the elderly, but go here for a blast from the past when four scientists researching the Flu vaccine during the 1960s found it to be ineffective and refused to give it to their own families.  The scientists state they were prevented from publishing their negative findings.

Despite this, the ineffective and dangerous vaccine has increasingly been pushed on everyone 6 months old and up, including pregnant women despite the fact the flu vaccine is linked to increased risk of miscarriage.

Now a recent Japanese study shows NO BENEFIT on hard outcomes: hospitalization and death. Another perfect example of how the massive push to vaccinate people for the flu has been a waste of time and effort.  Do not expect to read about this in the news.

Further demonstrating the diabolical history behind vaccines, the military mandated the Adenovirus vaccine for ‘cold-like symptoms’:

”…when it was shown that the vaccine contained a contaminant which caused cancer in laboratory animals, it was taken off the market, but that was 3 years after the division’s scientists have pointed out the danger…”

The Adenovirus vaccine (which contains live adenovirus Type 4 and type 7 can be shed in stool and and breast milk and infect contacts – particularly children, pregnant women, and those with immune system problems, as well as harming the unborn) is still available for United States military personnel.  It is not available to the general public.

Category:

Activism, vaccines, Viruses

The History of Howard Alliger – Pioneer of Chlorine Dioxide Therapies

https://pierrekorymedicalmusings.com/p/the-history-of-howard-alliger-pioneer?

The History Of Howard Alliger – Pioneer Of Chlorine Dioxide Therapies

In the 1970’s, Howard Alliger, a scientist, inventor, and entrepreneur recognized the therapeutic potential of chlorine dioxide to treat human skin, nasal, and oral diseases (among many other uses).

Pierre Kory, MD, MPA
Apr 01, 2025

Although I am going ever deeper into the “rabbit hole” of chlorine dioxide, I again want to emphasize that I am not writing as a doctor recommending a treatment. I consider this work to be in the vein of an amateur investigative science journalist trying to compile all the evidence necessary to guide and promote the research needed to establish chlorine dioxide as a viable therapy for all. Subscribe now to not miss critical upcoming posts on this topic.

HISTORY OF THE MODERN CHLORINE DIOXIDE PIONEERS

To recap, although chlorine dioxide has been widely used since the 1940’s in multiple industries such as water purification and as a disinfectant and bleaching agent, it was not until 1985 that oral ingestion was discovered to have therapeutic properties at much lower and safely tolerated concentrations.

The 1985 water treatment incident in Nigeria was relayed to me by an anonymous translational scientist with high-level security clearances (now 85 years old), who, in that post, I identified only by his old nickname, “Colonel Mondragon (CM).”

To be fair, I would say we don’t really know when its therapeutic potential as an orally ingested therapeutic was first discovered because CM found that soon after his discovery of its efficacy against malaria in Nigeria, he learned of Mexican and Central American doctors that were using it to cure other diseases as well (but not malaria).

Soon after the Nigeria incident, CM was assigned to support the aid teams sent by Ronald Reagan to assist the Russians in their response to the Chernobyl nuclear accident. In that follow-up post, I provided granular details about that mission and how it led to CM meeting Vladimir Pasechnik, a Soviet scientist who later became an international whistleblower on the Russian Bioweapons program. It was Pasechnik who informed CM that chlorine dioxide was a “universal antidote against bioweapons.” Pasechnik also told CM that the Soviets had been studying it in the treatment of disease and that he was curing TB with it. That was in 1985. And that information has, as far as I know, been classified by the Russians to this day. Here is a timeline of the oral and topical chlorine dioxide pioneers…. (See link for article)

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**Comment**

Kory goes through Alliger’s contributions to the science and development of numerous therapeutic applications of CD.

Important quote:

We found that the chlorine dioxide in our products kills all bacteria, virus, spores, yeast, all microorganisms within a minute in vitro, which is hard to believe, but it does that. And we put it on a wound, it did something even more than that. It oxidized free radicals and cytokines. ~ Howard Alliger, Founder of Frontier Pharma

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Category:

Activism, Treatment, Viruses

Despite Peddling MMR Shots, Texas Has More Measles Than the Entire US Had in 2024 – But a Four Year Old Given Budesonide Goes Home in 36 Hours

https://www.zerohedge.com/medical/texas-gave-15000-more-mmr-shots-year-now-it-has-more-measles-cases-entire-us-had-2024

Texas Gave 15,000 More MMR Shots This Year – Now It Has More Measles Cases Than the Entire US Had In 2024

by Tyler Durden
Friday, Mar 28, 2025 – 07:05 PM

Authored by Jon Fleetwood

Texas administered 15,000 more measles vaccinations this year compared to 2024—and now there’s a growing measles outbreak that has surpassed the total number of cases reported across the entire United States last year.

The news follows this website’s February report that measles cases in Gaines County, Texas, had jumped 242% following a health district campaign to hand out free measles vaccines.

A measles outbreak after higher vaccination rates in Texas calls into question the shot’s claimed effectiveness and underlying design.

Timeline & Numbers

Between January 1 and March 16 last year, 158,000 measles vaccines were administered in the state, according to CBS News.

During the same time this year, 173,000 measles doses were given.

There are now more measles cases in Texas than there were across the United States in all of 2024.

On Friday, the Texas Department of State Health Services reported 309 cases have been identified in the state since late January.

That’s compared to only 285 cases nationwide last year, according to Centers for Disease Control and Prevention (CDC) data.

What’s worse, measles cases in West Texas are “still on the rise” and “local public health officials say they expect the virus to keep spreading for at least several more months and that the official case number is likely an undercount,” according to CBS.

The numbers don’t lie—Texas is witnessing a record-breaking measles outbreak in the wake of increased vaccination efforts.

Measles Vaccine Virus Is Product of Gain-of-Function & Can Shed Onto Unvaccinated

U.S. military biodefense experts confirm in a May 2016 publication in The Journal of Infectious Diseases that the live virus inside the measles (MMR) vaccine is engineered using “a technique that could be considered, by current definitions, GOF research.”

GOF (gain-of-function) experiments can cause viruses to become more infectious. (See link for article)

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https://childrenshealthdefense.org/defender/4-year-old-measles-home-hospital-36-hours-budesonide-treatment/

4-Year-Old Hospitalized Post Measles Infection Goes Home 36 Hours After Budesonide Treatment

Lyla was admitted to the emergency room of Covenant Children’s Hospital in Lubbock on Feb. 28 due to breathing difficulty. Two days earlier at the same hospital, a 6-year-old girl who also had pneumonia following a measles infection died. The deceased child did not receive any breathing treatment before her death.

by Suzanne Burdick, Ph.D.
April 1, 2025

A 4-year-old West Texas girl who developed secondary pneumonia following a measles infection spent over four days in a hospital before she was given budesonide, a steroid used to relieve inflammation affecting the airways.

Budesonide is one of the treatments Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. has promoted during the Texas measles outbreak, according to The Hill.

Lyla was admitted to the emergency room of Covenant Children’s Hospital in Lubbock on Feb. 28 due to breathing difficulty.

Two days earlier at the same hospital, a 6-year-old girl who also had pneumonia following a measles infection died. The deceased child did not receive budesonide or any similar breathing treatment before her death. The hospital also administered the wrong antibioticfor the 6-year-old’s community-acquired pneumonia, according to experts who reviewed the medical records.

According to Lyla’s mother, MaryAnn, budesonide helped Lyla make a strong and fast turnaround from her illness. Within hours of receiving the treatment, Lyla was “starting to walk around. She’s eating, she’s talking, she’s acting more and more like herself, and we’re just like, ‘whoa,’” MaryAnn said.

Within 36 hours of Lyla’s first budesonide treatment on March 3 in Covenant Children’s Hospital’s intensive care unit (ICU), she was released straight to home.  (See link for article)

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**Comment**

Meanwhile, 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.

I’m telling you, this is COVID 2.0, and instead of being refused ivermectin and oxygen, patients with measles are being refused a simple steroid and vitamins and the vaccine is pushed at all costs.

We live in a mad world where health officials reject logic.

Avoid hospitals like the plague.

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Category:

Activism, vaccines, Viruses

Peter Marks Gets the Boot: A Post Mortem of His FDA Legacy

Pharma Stocks tumbled after Peter Marks, M.D., Ph.D., director of the agency within the U.S. Food and Drug Administration (FDA) responsible for authorizing vaccines, resigned under pressure from his new boss, Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.

“If Peter Marks does not want to get behind restoring science to its golden standard and promoting radical transparency, then he has no place at FDA under the strong leadership of Secretary Kennedy,” an HHS official said in a statement.  Source

The Washington Post reported a sweeping purge of agencies that oversee government health programs. Top officials were put on administrative leave or offered reassignment to the Indian Health Service. (Indians should protest)

Democratic attorneys general and governors have filed a lawsuit against HHS and the HHS Secretary for the department’s sudden rollback of $12 billion in public health funding.

“The COVID-19 pandemic is over, and HHS will no longer waste billions of taxpayer dollars responding to a non-existent pandemic that Americans moved on from years ago. HHS is prioritizing funding projects that will deliver on President Trump’s mandate to address our chronic disease epidemic and Make America Healthy Again,” the US Department of Health and Human Services said in a statement Wednesday.  Source

The vaccine cabal is also shouting that ‘the sky is falling’ due to HHS canceling hundreds of vaccine grants.

https://popularrationalism.substack.com/p/a-postmortem-on-peter-marks-fda-legacy?

A Postmortem on Peter Marks’ FDA Legacy: False Positives Killed Untold Numbers of People — and Marks Was Warned

We saw his decisions. We raised concerns, issued warnings, and watched them go unheeded. Marks answered not to science, but to those who saw objectivity as optional. The tone-deafness remains obvious.

 
James Lyons-Weiler
Mar 30, 2025
 

Dr. Peter Marks, former director of the FDA’s Center for Biologics Evaluation and Research (CBER), resigned on March 28, 2025, with an overly dramatic letter (see below) citing conflicts with Health and Human Services Secretary Robert F. Kennedy Jr. over vaccine misinformation. His tenure was marked by significant controversies, particularly concerning the approval and oversight of COVID-19 diagnostics and vaccines.

The PCR Catastrophe: False Positives, Fear, and Fatal Protocols

Under Dr. Marks’ leadership, the FDA authorized the widespread use of RT-PCR tests for COVID-19 diagnosis. Concerns arose regarding their specificity and the potential for false-positive results, especially in low-prevalence settings.​ Marks oversaw the deployment of high-cycle RT-PCR testing without adequate controls or interpretive guidance.

To this day, the public largely confuses False Positive Rate (FPR) with False Discovery Rate (FDR)—a distinction crucial to understanding the magnitude of harm. While the FPR is the proportion of truly negative tested samples that test positive (usually low), the FDR is the proportion of positive results that are false. In low-prevalence settings, even a highly specific test with low FPR can yield an FDR exceeding 50%, meaning that most positive test results are wrong.

And that’s exactly what happened.  

(See link for article)

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Bulletpoint summary:

  • Marks was silent when Fauci selectively amplified HCQ results to give the predetermined outcome it was ineffective, permitting a distorted narrative that shut down scientific inquiry.
  • Under Marks, the FDA expedited approval of COVID shots despite studies showing waning immunity, breakthrough infections, negative efficacy, adverse events, and links to cancer, autoimmune disorders, and deadly kidney failure.
  • Under Marks, the FDA faced criticism for delays and redactions in releasing clinical trial data, and for the agency’s inconsistent messaging.
  • Despite failure to meet primary endpoints in phase 3 trials, under Marks, the FDA granted accelerated approval of other gene therapies.
  • In his resignation letter Marks conflates MMR data with broader vaccine safety claims which redirects and misleads the debate as not all vaccines have been studied for associations with neurodevelopmental outcomes.
  • Throughout Marks’ tenure, dissenting experts were continually sidelined.
  • Marks misled the public on Paxlovid and boosters and forced Gruber and Krause to resign when they blew the whistle on the Biden admin for insisting on the COVID booster before the agency even approved it.
  • Marks pushed unethical vaccine mandates.

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Category:

Activism, Treatment, vaccines, Viruses