For over 200 years neurological damage from vaccines has been noted and documented

Neurological injuries from vaccination have been documented since the smallpox vaccine over two centuries ago, with severe injuries reported throughout medical literature.  The medical profession concealed these injuries, believing public vaccination benefits justified hiding information that might create vaccine hesitancy.

Historical injuries like spreading paralysis mirror current “one in a million” vaccine injuries, but toxicity documentation was erased to preserve the “safe and effective” narrative.

In the past, these injuries were widely reported, but now research into them is widely censored.  Many of these forgotten reports are critical for understanding modern “inexplicable” conditions like autism, A Midwestern Doctor writes.

Author’s Note: In the US, the requirement to vaccinate is largely based on the Advisory Committee on Immunisation Practices’ (“ACIP’s”) assessment (and the CDC’s) that the vaccine’s benefits outweigh its risks. Due to the dogmatic faith surrounding vaccination and ACIP’s members having massive conflicts of interest favouring vaccination, virtually every vaccine put before them ends up on the schedule and as a result, each generation of (sicker) children gets even more of them.

A key reason for this is because only a small set of injuries are tested for (typically those that are minor or very rare) and hence officially “exist,” while the much broader gamut of vaccine injuries are swept under the rug. Today, due to Robert F. Kennedy Jr.’s (“RFK’s”) bold action to replace ACIP’s members, a very different committee will have its first meeting today. For that reason, I felt it was important to highlight one major complication of vaccines: the widespread neurological injuries they cause.

From birth, we are taught that vaccines were one of the most remarkable discoveries in history, and were so safe and effective that many now unimaginable plagues vanished with few to no side effects occurring in the process. In truth, give or take, every part of that mythology is false, and remarkably similar vaccine disasters occur every few decades.

Much of this results from the fact that it is very difficult to produce safe vaccines due to both their mode of action and the methods used in their production. As such, the best “solution” which could be found to this problem was to insist in lockstep that vaccines were safe and erase any memory that vaccine disasters had in fact occurred, thereby making it possible to gaslight anyone who was severely injured by a vaccine and claim their injury was just anecdotal or a product of anti-vaccine hysteria.

For example, recently I discussed how vaccines cause autism and focused on a central argument used to debunk the link between the two – that the only reason people believe vaccines cause autism is because a disgraced British doctor published a fraudulent 1998 study claiming they did and then made everyone start hallucinating that vaccine injuries were occurring.

This mythology, however, ignores that brain injuries were a longstanding problem of vaccination. For example, a 1982 NBC news programme revealed that many parents were having children develop “post-pertussis encephalopathy” after taking the DPT vaccine for diphtheria, pertussis (whooping cough) and tetanus, and that most doctors refused to report this.

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WA Health issues urgent warning after reports wrong vaccine jabs given to patients by medical staff

Medical staff in Western Australia have been warned after reports of the wrong immunisations being given to patients.

The West Australian reports a vaccine update was sent to medical offices in the western state on Thursday reminding staff to make sure they are giving patients the right jab for respiratory syncytial virus (RSV).

“It is essential to check the correct RSV immunisation product is being given prior to administration,” WA Health said.

“Recent reporting to the Australian Immunisation Register and Western Australia Vaccine Safety Surveillance System has indicated that some Respiratory Syncytial Virus immunisation products have been administered incorrectly.”

In the alert, WA Health urged staff to use the correct products according to the Australian Immunisation Handbook

NewsWire has contacted WA Health for further comment.

There are different types of RSV jabs for particular demographics.

Beyfortus (nirsevimab) can be given to children aged up to two-years-old, while Abrysvo is a vaccine registered for women who are 28-36 weeks pregnant and for adults over the age of 60.

Another vaccine, Arexvy, is registered for adults over 60, or adults over 50 with increased risk.

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FDA Announces New Safety Warning on All mRNA COVID Vaccines — Cites “Extremely High” Risk of Myocarditis and Long-Term Heart Damage in Young Men

The U.S. Food and Drug Administration (FDA) under the Trump administration has formally updated the safety labeling on all mRNA COVID-19 vaccines to reflect what many Americans have been warning about for years: a disturbingly high risk of myocarditis—particularly in young men—and the possibility of long-term, irreversible heart damage.

The revised warnings apply to both Pfizer’s Comirnaty and Moderna’s Spikevax vaccines and follow months of mounting pressure over transparency and accountability regarding the true risks of these experimental injections.

The update stems from new studies and data showing persistent cardiac abnormalities months after vaccination—especially among males aged 12 to 24.

During a presentation of the new FDA safety data on Tuesday, Dr. Vinay Prasad, Director, Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, walked the public through the harrowing evidence behind the label change.

Prasad detailed how FDA data reveals a myocarditis rate of 27 per million in young men—a figure that experts say is significantly underreported due to passive surveillance methods and political suppression of adverse event reports.

More troubling, Dr. Prasad cited late gadolinium enhancement (LGE) on cardiac MRIs as proof of sustained, potentially irreversible myocardial injury. According to Prasad, in one FDA-funded study, 60% of patients who suffered post-vaccine myocarditis still showed signs of LGE five months later.

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Pfizer’s Delayed Myocarditis Study

This headline has garnered so much attention on social media that I was asked to participate in an interview last night to discuss the topic. First, I had to clarify that I cannot be interviewed about ACIP issues without prior clearance from HHS Communications. Once that was understood, at 6:00 PM (dinner time!) I dialed in via Zoom, and we talked on the record. No, I do not know if or when the interview will be aired. Before the interview, as usual, I did the necessary diligence to avoid embarrassing myself due to ignorance, keeping in mind the first rule of social media.

It is often better to stay quiet and have people wonder if you are ignorant than to tweet and remove all doubt.

Let’s dive into the details. I think that this particular situation provides a great example of how bias, combined with insufficient background and subject matter experience, can lead to unjustified clickbait headlines. This is a chronic problem on both sides of the mRNA “vaccine” safety debate, one which makes it so, so much harder to get to the bottom of all of this.

I will try to explain so that most can understand, but it may get a little technical. The nuances of clinical research study design and implementation are complicated. Please try to stick it out, if for no other reason than it does lead back to some statements from CDC’s Captain Dr. Sarah Meyer (CDC/NCEZID) during her recent presentation titled “COVID-19 safety update” regarding long-term outcomes from COVID-19 mRNA product myocarditis. Consider that an embedded easter egg.

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Moderna To Ask For Clearance For Combination COVID-Influenza Vaccine

Moderna is going to ask regulators to approve its combination vaccine against COVID-19 and influenza, the company said on June 30.

The company said a phase 3 study evaluating its influenza vaccine candidate, mRNA-1010—which utilizes the same messenger ribonucleic acid (mRNA) platform as its COVID-19 vaccine—showed positive effectiveness.

In the trial, which featured 40,805 participants and compared mRNA-1010 to an existing seasonal flu vaccine in adults aged 50 and up, the relative protection from the candidate was 26.6 percent better. In a subgroup analysis among participants aged at least 65, the relative efficacy was 27.4 percent.

Today’s strong Phase 3 efficacy results are a significant milestone in our effort to reduce the burden of influenza in older adults,” Stéphane Bancel, Moderna’s CEO, said in a statement.

Several companies, including Moderna, have been planning to introduce combination shots against COVID-19 and influenza.

Moderna, however, in May withdrew its application for approval for its combination vaccine, a move the company said came after consulting with the Food and Drug Administration.

Moderna at the time said it planned to resubmit the application before the end of 2025 after it received efficacy data from the phase 3 trial for mRNA 1010.

“An mRNA-based flu vaccine has the potential advantage to more precisely match circulating strains, support rapid response in a future influenza pandemic, and pave the way for COVID-19 combination vaccines,” Bancel said on Monday.

The trial results have been fully published or peer reviewed. Moderna said it plans to submit the results to a peer-reviewed journal.

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Judge Awards $4 Million to St. Louis Public School Employees Who Sued Over Vaccine Mandate

A jury ruled on Thursday in favor of 13 employees with the St. Louis Public Schools System who were forced to take the COVID vaccine despite religious objections.

The court awarded the 13 employees $4 million for the injustice.

According to Schrag on Law, the plaintiffs Wanda Brandon and over a dozen other current and former employees in the St. Louis Public Schools system,  sued the Board of Education of the City of St. Louis, Superintendent Kelvin Adams, and Chief Human Resources Officer Charles Burton in the Eastern District of Missouri raising claims of violations of the First Amendment’s Free Exercise Clause, the Fourteenth Amendment’s Equal Protection Clause, Title VII religious discrimination, and the Missouri Human Rights Act.

In fall of 2021 during the height of the COVID pandemic, the St. Louis Board of Education adopted Policy 4624, requiring all employees to be fully vaccinated against COVID-19 by October 15, 2021, or obtain an approved exemption.

The sixteen original plaintiffs submitted religious exemption forms to their employer. The employees cited their Christian, Islamic and Pentacostal beliefs that conflicted with the vaccine that was developed from fetal cell lines.

The St. Louis Board denied all 189 of the religious exemption requests and forced the employees to take the experimental vaccine.

The Board then suspended or terminated the employees who refused to take the COVID vaccine.

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VICTORY! After Four Years and Two Months British Nursing Council Drops Charges Against Dr. Niall McCrae for Publishing His Completely Factual Report on COVID Vaccine Risks on The Gateway Pundit in 2021

In the covid debacle, health professions played a major role in enforcing the official narrative. I can now reveal my experience with the UK Nursing & Midwifery Council (NMC), who charged me with contradicting government guidance on vaccination and risking patients’ lives, after writing an entirely factual article on Gateway Pundit.

As a senior lecturer in psychiatric nursing at King’s College London, the NMC was my professional regulator.

When covid vaccines were introduced, I feared that blind faith and propaganda about an oxymoronic ‘miracle of science’ would lead to less impressive and harmful outcomes.

On 4th March 2021, Gateway Pundit published my article ‘British government study confirms Covid-19 vaccine risk’.  The article is linked below. This related to a Public Health England report showing increased infections soon after vaccination, which I attributed to a known phenomenon of temporary depletion in immunity.

Although factually accurate, a fact-check website labeled my article as ‘misleading’. On 8th March I was notified by the NMC of a referral by a ‘Dr Byrne’, who had seen my writing and found me on the register. The NMC began an investigation of my fitness to practise, alleging ‘failure to uphold your position as a registered nurse – in that you promoted health advice contrary to official health advice in the context of a global pandemic’.

From the outset, I was confident that the NMC had no reasonable case against me. I submitted my statement, supported by three experts (physician Helen Westwood, biostatistician Paul Cuddin, and nursing professor Roger Watson.  Cuddin wrote: ‘on the basis that there is consistent, increasing real-world and clinical evidence of increased infections in the two weeks after vaccination, the points raised by Dr Niall McCrae need to be addressed as a matter of urgency.’

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Supreme Court Declines to Hear Children’s Health Defense Case Alleging Meta-Government Collusion to Censor Vaccine Speech

The Supreme Court has turned down a petition from Children’s Health Defense (CHD), leaving unexamined the group’s challenge to what it describes as collusion between Meta and federal agencies aimed at suppressing constitutionally protected speech.

The case, which dates back to 2020, centered on CHD’s allegations that Facebook, under government influence, targeted and silenced its views on vaccines and COVID-19.

CHD filed its initial complaint against Meta in August 2020 and later amended it, arguing that government officials worked alongside the tech giant to stifle dissenting opinions that the public had every right to hear.

The removal of CHD’s Facebook and Instagram accounts in 2022 only fueled concerns about the growing threat of coordinated censorship in digital spaces.

Those accounts, once a major source of alternative information for millions, remain banned.

In a decision last year, the 9th Circuit Court of Appeals sided with Meta, holding that the company’s actions reflected private policy choices rather than government compulsion.

CHD hoped the Supreme Court would take up the case and examine whether that distinction truly shields Big Tech from accountability when it suppresses speech at the behest of public officials. But the justices declined, offering no explanation, as is typical in most of the thousands of petitions they review annually.

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RFK Jr. Unloads Disturbing Vaccine Secrets on Tucker—And Surprises Everyone on Trump

It’s not every day an active HHS Secretary sits down for 90 minutes straight with Tucker Carlson.

But that’s exactly what happened, and Kennedy instantly seized Carlson’s attention with a chilling story of CDC corruption.

He revealed that the health agency buried a 1999 internal study led by researcher Thomas Verstraten, which showed an alarming 1135% increase in autism risk from the hepatitis B vaccine.

Kennedy said the researchers were “shocked” by the findings.

So what did they do? They covered it up, according to Kennedy.

“They got rid of all the older children essentially and just had younger children who are too young to be diagnosed [with autism].”

RFK Jr. then explained the real reason why your pediatrician will kick you out of their practice for refusing vaccines.

“There’s a published article out there now that says that 50% of revenues to most pediatricians come from vaccines.”

It’s all about the money. The higher the vaccination rate, the bigger the bonus.

“And that’s why your pediatrician, if you say I want to go slow on the vaccines… will throw you out of his practice because you’re now jeopardizing that bonus structure.”

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New CDC Vaccine Panel Recommends Merck’s RSV Shot for All Newborns

Advisers to the Centers for Disease Control and Prevention (CDC) this morning voted to recommend all newborns receive Merck’s new monoclonal antibody shot, designed to protect against respiratory syncytial virus (RSV).

Two of the seven committee members, Retsef Levi, Ph.D., and Vicky Pebsworth, Ph.D., opposed the recommendation, citing safety concerns. The remaining five members supported it.

The vote marked the first — and closely watched — decision by the new members of the Advisory Committee on Immunization Practices (ACIP), appointed early this month by U.S. Secretary of Health and Human Services Robert F. Kennedy Jr. He replaced all 17 sitting members, citing long-standing conflicts of interest that he said had plagued the committee for years.

Kennedy’s decision outraged the mainstream public health industry, which feared the new committee would be more critical of vaccines. It even prompted a move by vaccine manufacturers, insurers and the professional medical organizations they support to bypass government health agencies’ recommendations by creating a nongovernmental system for recommending and purchasing vaccines.

The U.S. Food and Drug Administration earlier this month approved Merck’s RSV shot, clesrovimab, which will be marketed as Enflonsia. It joins two other recently approved RSV drugs. One is Sanofi and AstraZeneca’s monoclonal antibody shot for infants, Beyfortus (nirsevimab). The other is Pfizer’s RSV vaccine, Abrysvo, for pregnant mothers.

Data presented by the CDC during Wednesday’s ACIP meeting reassured committee members that the recently approved RSV interventions were safe and effective.

However, an analysis of the CDC’s Vaccine Safety Datalink for the 2023-2024 respiratory season revealed an association between Abrysvo and an increased risk for hypertensive disorders of pregnancy, which include gestational hypertension, preeclampsia, eclampsia and HELLP syndrome, a life-threatening pregnancy complication.

Presenters repeatedly emphasized that RSV — a common respiratory virus that usually causes mild cold-like symptoms but can be serious in infants — is the leading cause of hospitalization for infants in the U.S. There are fewer than 100 deaths per year from RSV in the U.S., according to data presented at the meeting.

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