Trump Admin Is Prosecuting One of the Few Doctors Who Honored his Hippocratic Oath to ‘Do No Harm’ during Covid Madness

A Utah surgeon, Dr. Kirk Moore, is facing the prospect of 35 years in federal prison for alleged criminal acts.

His crime?

The doctor destroyed thousands of vials of mRNA COVID vaccines, giving his patients vaccine cards without taking the shots, and injecting saline into children whose parents wanted them to believe they got vaccinated without risking the deadly side effects.

The 58-year-old Dr. Michael Kirk Moore Jr. operates Plastic Surgery Institute of Utah in Salt Lake County. He began his trial on Monday, July 7, at the federal courthouse in Salt Lake City.

A rally took place Monday at the courthouse steps, organized by We Are The People Utah, in support of the doctor. Among those in attendance were veterans of the health freedom movement, including vaccine safety activist Robert Scott Bell, as well as the team that produced the documentary film Died Suddenly.

Countless other prominent figures in the Make America Healthy Again (MAHA) movement, including Dr. Mary Talley Bowden, joined online to stand with Dr. Moore.

According to Zero Hedge, the charges against him were filed in 2023 by the Department of Justice under Joe Bidenand have not been dropped yet by President Trump’s Attorney General Pam Bondi.

Health and Human Services Secretary Robert F. Kennedy Jr. has not intervened in the case, but did publicly expressed his support in April of this year, saying on his government verified X account, “Dr. Moore deserves a medal for his courage and commitment to healing.

The charges against Dr. Moore include conspiracy to defraud the United States; conspiracy to convert, sell, convey, and dispose of government property; and conversion, sale, conveyance, and disposal of government property and aiding and abetting.

The government property being referred to is $28,000 worth of government-provided COVID-19 vaccines, also referred to by Pfizer as “government prototypes” due to their experimental, untested, and dangerous nature.

Dr. Moore is also accused of distributing at least 1,937 “fraudulently completed vaccination record cards” to his patients, none of which are testifying for or against him in court. He also allegedly administered saline shots to some of his patients’ kids, admitted by the DOJ to have been carried out with the full knowledge and consent of their parents, so their children would actually believe and act as if they were vaccinated, and not have to lie to live a normal life with their friends amidst the pandemic mandates and madness.

This is a bizarre case. And it’s quite sad that the Trump administration is continuing to prosecute it against one of the few doctors who actually honored his Hippocratic oath, to do no harm.

As of Monday, a ‘GiveSendGo’ donation campaign for him is at just under $140,000.

Zero Hedge reports that Dr. Moore was arrested when the charges were made official in 2023 under the Biden regime.

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New York Supreme Court reinstates all employees fired for being unvaccinated, orders backpay

A New York state Supreme Court ordered all New York City employees who were fired for not being vaccinated to be reinstated with back pay.

The court found Monday that “being vaccinated does not prevent an individual from contracting or transmitting COVID-19.” New York City Mayor Eric Adams claimed earlier this year that his administration would not rehire employees who had been fired over their vaccination status.

NYC fired roughly 1,700 employees for being unvaccinated earlier this year after the city adopted a vaccine mandate under former Mayor Bill de Blasio.

Many of those fired were police officers and firefighters.

FDNY-Uniformed Firefighters Association President Andrew Ansbro and FDNY-Uniformed Fire Officers Association President Lt. James McCarthy condemned Adams earlier this year after the mayor allowed an exception to the vaccine mandate for athletes and performers, even as firefighters were still being fired over their status. The pair called on the city to expand the exception to all New Yorkers.

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Vaccine advisory board votes to remove controversial mercury-based compound from flu vax

In a win for the Make America Healthy Again (MAHA) movement, the Advisory Committee on Immunization Practices (ACIP) voted 5-1 to limit flu vaccines to only those free of thimerosal. The mercury-containing preservative, largely phased out of childhood vaccines by 2001, still lingers in some multi-dose flu shots. But with 96% of U.S. flu vaccines for the 2024-2025 season already thimerosal-free, single-dose options are not hard to come by.

The committee, freshly revamped by Health and Human Services (HHS) Secretary Robert F. Kennedy Jr., also voted 5-1 to mandate thimerosal-free flu vaccines for children 18 and under and pregnant women. 

The effort to remove thimerosal began in the late 1990s, sparked by growing public and scientific scrutiny of mercury exposure. In 1997, the FDA Modernization Act prompted a review of mercury in medical products, including thimerosal, a mercury-based preservative used since the 1930s to prevent microbial contamination in multi-dose vaccine vials.

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Insidious Australian Government in full PANIC MODE destroying all evidence of the Covid CLOT SHOTS including statistics, records and clinical data

The Australian Government is under intense scrutiny following revelations that it plans to destroy vital clinical data and biological samples from the publicly funded QoVAX study, which examined the safety and effectiveness of COVID-19 vaccines.

As reported by The Exposé, this move has sparked widespread concern over a potential cover-up, especially in light of the government’s broader pattern of avoiding accountability for vaccine-related harms. Critics argue that the destruction of such irreplaceable evidence would hinder scientific transparency and obstruct justice for those seeking answers.

  • Broken Promises and Legal Evasion: The Australian Government has failed to deliver on its promise to launch a Royal Commission into COVID-19 vaccine harms and has argued in court that it holds no duty of care toward individuals injured by the vaccines.
  • Suppression of Adverse Data: Authorities have neglected to fully investigate over 1,000 reported vaccine-linked deaths, including 35 on the day of injection, and altered statistical methods to obscure a rise in non-COVID excess deaths post-vaccine rollout.
  • Destruction of Critical Evidence: The government is moving to destroy biospecimens and archive data from the QoVAX study—an extensive, taxpayer-funded trial tracking vaccine safety in over 10,000 Queenslanders—despite legal warnings to preserve the materials.
  • Allegations of a Cover-Up: Critics argue that the decision to shut down and erase QoVAX findings amid growing global scrutiny of mRNA vaccine safety reflects a coordinated effort to conceal potential harms and avoid accountability.

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‘Nothing was ready’: Inside Canada’s Vaccine Injury Support Program

A$50-million program the federal government created to help Canadians seriously injured by COVID-19 vaccines is in disarray, current and former staffers say.

The Vaccine Injury Support Program (VISP), created during the pandemic, was designed to compensate people who have been seriously and permanently injured by any Health Canada-authorized vaccine administered in Canada on or after Dec. 8, 2020.

The Public Health Agency of Canada subsequently selected a consulting firm, Oxaro Inc., to administer the program. The Ottawa-based company vowed it had the “people, processes, and tools” to run the initiative with “industry best practices.”

However, a five-month-long Global News investigation, involving more than 30 interviews with current and former Oxaro employees, injured claimants and their attorneys, has uncovered allegations that the company was unequipped to deliver fully on the program’s mission, questions about why the Public Health Agency of Canada (PHAC) chose this company over others, and internal documents that suggest poor planning from the start.

Global News also heard descriptions of a workplace that lacked the gravitas of a program meant to assist the seriously injured and chronically ill: drinking in the office, ping pong, slushies and Netflix streaming at desks.

The overall result: many claimants feel they have not received the “timely and fair” access to support that the government promised.

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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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