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HEALTH ALERTS

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Patricia N.
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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.

https://www.thegatewaypundit.com/2025/07/fda-announces-new-safety-warning-all-mrna-covid/   


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Patricia N.
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Australian government races to destroy evidence of covid vaccine harms:

The Australian Government is planning to destroy irreplaceable clinical data and biological samples from the QoVAX study, which investigated the safety and efficacy of various covid vaccines in over 10,000 people in Queensland.

The Government’s decision to destroy the globally important data and samples has raised concerns about a cover-up, as it comes after a series of actions that indicate it wants to bury the truth about covid vaccine harms.

It looks like the Government does not want to know the awful facts. No public analysis will be done – the public, who paid for the study, will not get the results. It looks like the Government knows the truth. We need to demand this data.

The Government cover-up continues ………. what a disgrace. Watch this space. I’m sure this is not the end of the story. We must hold the Government to account.

https://expose-news.com/2025/07/02/australian-gov-races-to-destroy-evidence/


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Heidi
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@patrician no liability shield from the wrath of God.


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Heidi
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Patricia N.
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@heidi 

Great!  I eat a lot of these foods regularly.


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Patricia N.
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Sex-changing frogs and infertile humans: Will MAHA target infamous herbicide contaminating America's water?

Atrazine is one of the most extensively used herbicides in the United States. On average, well over 70 million pounds of atrazine is sprayed every year on agricultural crops like corn and sugarcane.

This chlorotriazine herbicide — reportedly the most commonly detected herbicide in American tap water — is a potent endocrine and metabolic disruptor linked to numerous adverse health effects including birth defects, cancer, reduced sperm counts, and infertility.

The U.S. Environmental Protection Agency has recognized atrazine as "a surface water and groundwater contaminant that can enter waterways in agricultural runoff from row crops" and "cause human health problems if present in public or private water supplies in amounts greater than the drinking water standard set by EPA."

Atrazine, first registered for use in 1958 and banned by the European Union in 2004, enjoys continued support stateside by the agricultural industry despite having contaminated thousands of American communities' water supplies.

Despite years of pushback from concerned citizen and activist groups — including a class action lawsuit against agrichemical giant Syngenta, for instance, which resulted in a $105 million settlement with a number of impacted communities — the chemical compound continues to be sprayed, continues to adversely impact wildlife, and continues to leak into water systems.

That could soon change.

Robert F. Kennedy Jr. has repeatedly raised alarm about the herbicide, its ubiquity, and its adverse impacts on various forms of life. While campaigning for president last year, he promised he would ban the chemical outright if given the chance.

In September 2024, Kennedy tweeted, "We need to ban atrazine now."

"It's banned in Europe, banned all over the world, but we use it here. It's in 63% of our drinking water," Kennedy told Jordan Peterson in a September 2024 interview.

"We don't know what impact it's having on our children."

https://www.theblaze.com/news/will-maha-target-infamous-herbicide-contaminating-us-drinking-water-and-sex-changing-frogs   


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Patricia N.
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FDA approval process is broken: Hundreds of drugs do not work, some have dangerous adverse effects:

Most FDA-Approved Drugs Did Not Meet the Agency’s Basic Criteria

A two-year investigation conducted by The Lever and the McGraw Centre for Business Journalism uncovered a disturbing pattern within the FDA: In nearly a decade, the agency approved hundreds of prescription drugs without requiring substantial and robust proof of their effectiveness.2

These findings were based on various evidence, including “government reports, internal FDA documents, investigators’ notes, congressional testimony, court records and more than 100 interviews with researchers, federal officials and patients,” the Children’s Health Defence (“CHD”) reports.3

• The FDA relied on four essential standards to assess a drug’s effectiveness and safety.  According to the authors of the report, while these criteria don’t confirm “sound scientific evidence,” they do provide the minimum standard that determines drug manufacturers have given “substantial” evidence to back up their claims. These include:

  • Control group.  Patients were tested versus a control group that received a placebo treatment or a comparator drug.
  • Replication. There must be at least two “well-controlled” trials that also prove the drugs work as they should.
  • Blinding.  The subjects and their physicians must not be aware which among the participants are receiving the drug and which ones are in the control group.
  • Clinical endpoint.  Instead of relying on surrogate markers like lab results, the studies must show a significant effect on the patients’ survival or function.

However, after an intensive analysis, the reporters found that the majority of the FDA-approved medications failed to meet these basic criteria.

• Nearly 3 out of 4 new drug approvals did not comply with these criteria.  Among all the drugs approved by the FDA between 2013 and 2022, 73% failed to meet these foundational standards that prove the drugs work as expected.4 “Fifty-five of the approved drugs met only one of those four standards, and 39 met none of them,” the CHD notes.

• Drugs were green-lit despite insufficient data presented by manufacturers.  The Lever found that more than half of approvals were based on preliminary data – without considering sound evidence, such as whether the patient experienced fewer symptoms, had improved function, or lived.

• Particularly concerning are cancer drugs.  Based on their findings, of the 123 FDA-approved cancer medications, only 2.4% met all four of the FDA’s scientific criteria. On the other hand, 29 of these drugs tested (23%) did not meet a single criterion.

https://expose-news.com/2025/07/09/fda-approval-process-is-broken/   


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Patricia N.
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FDA expresses scepticism of the science that demonised saturated fats as causing heart disease:

For decades, defending saturated fat was considered scientific heresy. Suggesting that butter might be better than margarine – or that full-fat cheese wouldn’t clog your arteries – was enough to get you labelled as fringe, irresponsible, even dangerous.

The medical dogma was firmly entrenched: saturated fat raised cholesterol and cholesterol caused heart disease.

But the science behind it was shaky – built on cherry-picked data and upheld more by consensus than by critical evaluation.

And in 2013, The BMJ published a commentary by cardiologist Dr. Aseem Malhotra titled ‘Saturated fat is not the major issue’, attacking decades of flawed advice and warning that the obsession with lowering cholesterol may have worsened heart disease.

Researchers like Christopher Ramsden and colleagues added more data.  ...They showed that replacing saturated fat with linoleic acid (from vegetable oils) did indeed lower cholesterol – but paradoxically increased mortality, particularly from heart disease.

It’s taken decades. The cholesterol hypothesis wasn’t just a scientific claim – it became a professional litmus test. To challenge it was to risk your funding, your career, your credibility.  Many of us paid that price.

Even now, entrenched interests remain.  The US dietary guidelines committee – particularly the saturated fat subcommittee – has been heavily criticised for its conflicts of interest. Many members have ties to plant-based advocacy groups or have built careers promoting low-fat diets. Independent voices remain marginalised.  But the tide may be turning.

US Health Secretary Robert F. Kennedy Jr. has also raised concerns about industry influence over dietary guidelines and hinted that upcoming revisions may elevate full-fat dairy and remove the saturated fat cap altogether.  If those changes come to pass, it would mark a historic course correction – one rooted in evidence rather than ideology.

The point is that we may finally be seeing the collapse of one of the most destructive public health myths in modern history.  And if Makary and Kennedy stay true to their word, the next generation of dietary guidelines may reflect the science – and not the politics.

https://expose-news.com/2025/07/28/fda-sceptical-about-saturated-fats/  


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Patricia N.
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Are ‘conspiracy theorists’ right about organ donation?

A recent investigation conducted by the HRSA revealed that hospitals have allowed the organ procurement process to begin while the donor showed signs of life.

“Conspiracy theorists” have been sounding the alarm about organ donation and the practice's potentially shady incentives for decades, only to have their concerns brushed aside as crazy or even selfish — until now.

Secretary of Health and Human Services Robert F. Kennedy Jr. has announced a major initiative to begin reforming the organ transplant system following an investigation that revealed horrific practices by a major organ procurement organization.

“Our findings show that hospitals allowed the organ procurement process to begin when patients showed signs of life, and this is horrifying,” Kennedy said, explaining that these organ procurement organizations must be held accountable.

This particular organ procurement organization that’s been under investigation was operating in Kentucky, Southwest Ohio, and part of West Virginia, and they were found to be taking organs from patients that were showing signs of life.

One man, T.J. Hoover in Kentucky, was admitted to Baptist Health’s emergency room in 2021. He was unresponsive for two days before his family agreed to donate his organs. However, while he was being prepped for organ donation surgery, he began thrashing, crying, resisting, and showing signs of life.

And according to the HRSA investigation, Hoover’s case is far from the only one.

“HRSA examined 351 cases where organ donation was authorized but not completed, identifying issues — 103 cases. Of those, 73 patients showed neurological signs incompatible with organ donation, and 28 may not have been deceased when procurement began,” Stuckey says.

...there can be confusion as to whether or not their neurologic function is nonexistent or if it’s simply being “clouded by drugs.”

Not only that, but the family of the deceased donor will receive no compensation, and instead, the organ procurement organization pays the hospital for time and resources used. So some of the fees they collect are used to fund their activities.

“Is it reasonable to wonder if there would be more of an incentive, then, to allow a patient to die so that their organs could be harvested than it would be to keep them alive? Because there would be no reimbursement if that patient survives,” Stuckey comments.

https://www.theblaze.com/shows/relatable/are-conspiracy-theorists-right-about-organ-donation


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Patricia N.
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RFK Jr. Bans Mercury in Vaccines After Two-Decade Battle: ‘No More Poisoning Pregnant Women and Children’:

Robert F. Kennedy Jr., who led the push for more than 20 years, confirmed the move on Saturday, blasting federal health agencies for allowing a known neurotoxin to be injected into pregnant women and children for decades.

In a detailed video statement, Robert F. Kennedy Jr. announced that thimerosal, a mercury based preservative still found in flu shots given to children and pregnant women, has now been fully banned in the United States.

Thimerosal, a compound whose main ingredient is ethylmercury, had been used for decades as a preservative in multi-dose vaccine vials. According to Kennedy, the CDC shockingly continued to permit its use in flu shots given to pregnant women and children, despite overwhelming evidence of its neurotoxicity.  “The amount of ethylmercury in the flu shot that CDC just banned under my order is 25,000 times the EPA’s safety level for drinking water,” he said.

Kennedy also slammed federal agencies, accusing them of turning a blind eye to the science for decades. He pointed to a 2001 admission by FDA official William Egan, who testified under oath before Congress that thimerosal’s safety had never been studied in humans. 

A subsequent study found that this highly toxic mercury remains in the brain for over 27 years. Kennedy cited a CDC-funded 2017 study linking flu shots during pregnancy to miscarriage, which found the odds of miscarriage within 28 days were 7.7 times higher for women who received the vaccine. He also referenced a 2017 study published in JAMA that reported an elevated risk of autism spectrum disorders in children whose mothers received a flu shot during the first trimester.

Kennedy stressed that flu shots will remain available in mercury-free, single-dose formats.

“This decision sends a clear message,” Kennedy concluded. “The days of ignoring the science are over. The days of putting profits ahead of people are over.”

https://www.breitbart.com/politics/2025/08/02/rfk-jr-bans-mercury-in-vaccines-after-two-decade-battle-no-more-poisoning-pregnant-women-and-children/   


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Patricia N.
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Exclusive — Poll: Ninety-Two Percent of Trump Voters Want FDA to Protect Americans from Unsafe Chinese Drugs:

Ninety-two percent of Trump voters want the Food and Drug Administration (FDA) to do more to protect Americans from unsafe prescription drugs, a poll obtained exclusively by Breitbart News found.

A poll conducted by Fabrizio Ward, one of President Donald Trump’s favored polling firms, revealed that Trump voters remain highly concerned about the growing threat of unsafe, foreign-made drugs entering the country through online pharmacies and rogue compounders.

The survey also detailed that there is broad bipartisan backing for more stringent FDA oversight and enforcement to boost American pharmaceutical manufacturing and reduce reliance on China.

Sen. Tom Cotton (R-AR) has proposed legislation that would bring pharmaceutical manufacturing back to America. Breitbart News detailed:

China produces an overwhelming majority of active pharmaceutical ingredients (APIs) used for drugs in America. This includes 95 percent of imports of ibuprofen, 70 percent of acetaminophen, and 40-45 percent of penicillin.

Axios reported that the coronavirus outbreak has jeopardized the American supply of roughly 150 pharmaceuticals, “including antibiotics, generics,” and brand-name drugs. Some of these drugs do not have alternatives on the market.

“The safety of American patients is under attack from unregulated foreign drug factories, shady online pharmacies, and unchecked compounders operating outside the law,” Lopez concluded in his statement. 

https://www.breitbart.com/politics/2025/08/06/exclusive-poll-ninety-two-percent-trump-voters-want-fda-protect-americans-from-unsafe-chinese-drugs/   


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Patricia N.
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Senior HHS Adviser Confirms the Worst COVID Fears Were True:

Another COVID “conspiracy theory” just came true.  A Senior HHS Adviser confirmed it, and you could see the pain written all over his face.

This explains why RFK Jr. effectively shut down all mRNA vaccine funding.

HHS Secretary RFK Jr. dropped a mega bombshell on Tuesday when he announced that BARDA will be CANCELING 22 mRNA vaccine development contracts, saving taxpayers about $500 million in the process.

He declared, “mRNA technology poses MORE risk than benefits for these respiratory viruses.”

...HHS Senior Adviser Dr. Steven Hatfill revealed that RFK Jr. pulled mRNA funding after the data showed getting vaccinated was MORE dangerous than COVID itself.  In other words, the “cure” was WORSE than the disease.  Dr. Hatfill said, “It was more dangerous to take a vaccine than it was to contract COVID-19 and be hospitalized with it.”

Dr. Hatfill added that the shots send a “sudden flood” of mRNA into the body, which overwhelms the cells and creates “BIOLOGICAL HAVOC.”  With pain written all over his face, he concluded, “IT HAD TO BE STOPPED.”  No one says something that grave unless the data is absolutely damning.

In another series of explosive statements, Dr. Hatfill attested that the vaccine manufacturers never did their due diligence to ensure their shots were safe and “essentially ran the pandemic response.”

“Nobody stood up to them. Nobody questioned them… Pfizer wanted a [75]-year moratorium on the clinical trial data, which from the start showed these never prevented infection or disease transmission,” he explained, adding, “There’s no good clinical data to ever show it reduced the severity of disease.”

Senior HHS Advisor Dr. Steven Hatfill just said mRNA shots induce “BIOCHEMICAL HAVOC.”  He’s likely referring to the new study that found mRNA shots induce severe, long-lasting genetic disruption linked to cancer and chronic disease.

Using high-resolution RNA sequencing on blood samples, they discovered that COVID-19 “vaccines” SEVERELY disrupt expression of THOUSANDS of genes—triggering mitochondrial failure, immune reprogramming, and oncogenic activation that can persist for MONTHS to YEARS post-injection.

Massive injury: heart, brain, immune system, fertility, cancer.  Harms include myocarditis, strokes, immunosuppression, infertility & aggressive tumor progression — driven by spike toxicity, LNP biodistribution & genetic contamination.  Urgent call for a global moratorium.

All modRNA products must be withdrawn immediately, given the scale of harm.

Kennedy effectively canceled future mRNA vaccines by pulling the plug on government funding. The next logical step is to yank the shots. It will come with political backlash, but it’s the right thing to do.

https://www.thegatewaypundit.com/2025/08/senior-hhs-adviser-confirms-worst-covid-fears-were/   


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