COVID mRNA Vaccines Should Be Pulled Off the Market, Oncologist Says

Medical commentator John Campbell, Ph.D., used a recent U.S. Senate hearing on COVID-19 vaccines, cancer and scientific censorship to spotlight concerns he says have been ignored for years — and to argue that the issue demands a public reckoning.

In a series of videos following the June 3 hearing, Campbell described the proceedings as a “massively under-discussed and under-publicized” examination of “possible links between COVID vaccines and cancer and also the active suppression of medical and scientific information.”

“It really couldn’t be more serious for science,” Campbell said in a June 4 video. “Lies are told, lies have been told and things have been ignored. This has resulted in a greatly reduced trust in mainstream media and institutions.”

Campbell devoted a June 7 video to testimony from oncologist Dr. Angus Dalgleish, whose observations of unusual cancer relapses after COVID-19 booster shots led him to question whether vaccine safety was receiving adequate scientific scrutiny.

Last week’s Senate hearing brought those concerns before lawmakers and examined claims that researchers who raise such questions have faced professional and institutional pushback.

The June 3 hearing, “Plausible Mechanisms of COVID-19 Injections Causing Cancer and Attacks on Scientific Publications,” was held by the Senate Permanent Subcommittee on Investigations, chaired by Sen. Ron Johnson (R-Wis.).

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36 Illegal Alien Commercial Truck Drivers Busted in Yuma Border Patrol Sector in 5 Days

During a five-day targeted enforcement operation, Yuma Sector Border Patrol agents arrested 52 illegal aliens during immigration stops on major Arizona highways. Of those, 36 were found to be operating commercial vehicles with licenses issued by states with sanctuary policies.

Yuma Sector agents carried out a five-day enforcement operation in mid-May, according to a social media post by sector officials. A spokesman for the U.S. Department of Transportation praised the efforts of the Yuma Sector agents this week in a message to Breitbart Texas, saying, “This is another reminder of how the Biden-Buttigieg administration failed American truckers and made our roads less safe for families.”

Officials reported that the illegal alien truck drivers were nationals of El Salvador, India, Mexico, Turkey, and Russia. Many of the individuals were working under expired work authorizations that were issued during the Biden administration. These are no longer valid, officials stated.

“USDOT is proud to support Border Patrol operations to take these dangerous foreign drivers off of our roads.” the spokesperson told Breitbart. “We need our state and local law enforcement partners to work with DHS and neutralize this threat before more innocent people die.”

This week, Yuma Sector officials announced the arrest of another Indian national, Magandeep Singh. After making contact with Singh during a traffic stop and immigration inspection, the Blythe Station agents uncovered that the illegal alien from India has an international alert and is wanted for homicide. The agents confirmed the arrest notice and processed the man for deportation.

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Legal Notice Filed to Force EPA to Set Water Standards for Atrazine, a Pesticide Linked to Cancer

Conservation and public health groups filed a formal notice on Thursday, May 28, with Environmental Protection Agency (EPA) Administrator Lee Zeldin to force the agency to develop water-quality standards for atrazine, a pesticide linked to cancer, according to the groups.

According to the notice, atrazine has been found at dangerous levels in thousands of U.S. waterways and in drinking-water supplies. The filing is a required step before the groups can sue the EPA under the Clean Water Act. [1][2]

Atrazine is the second most widely used pesticide in the United States, with tens of millions of pounds applied annually on corn and other crops. The World Health Organization’s International Agency for Research on Cancer in 2025 classified atrazine as “probably carcinogenic to humans,” according to a report from NaturalNews.com[2] Since 1999, cancer has been the leading cause of premature death in the United States for those under age 85, according to the book “Taking Action, Saving Lives” by Kristin Shrader-Frechette. [3]

The herbicide is banned in more than 60 countries due to links to birth defects, cancers and fertility problems, reported Children’s Health Defense. [4] Atrazine has been shown to disrupt endocrine systems and cause reproductive abnormalities in wildlife, including turning male frogs into hermaphrodites, according to a 2007 report from NaturalNews.com. [5]

The 1972 Clean Water Act regulates discharges into U.S. waterways, but toxic runoff from agriculture continues to pollute, according to a Frontline report cited by Mercola.com[6] The act requires the EPA to develop water-quality criteria for pollutants; the agency initiated that step in 1999 but never completed it, according to the groups.

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Exposing The Great Acid Reflux Scam

Many commonly prescribed medications are given to patients despite the risks often outweighing the benefits.

•Acid-suppressing drugs are among the worst offenders, with their overuse fueled by a lack of understanding about the crucial role of stomach acid throughout the body or that acid reflux is due to too little stomach acid (as the stomach acid of digestion gives the stomach’s opening a signal to seal and not let any more food in).

•Deficient stomach acid causes many chronic health problems (e.g., macular degeneration, a myriad of autoimmune disorders such as asthma, and less overt forms of reflux that cause many common diseases of the ears, nose, and throat such as allergies, coughs, and sinusitis).

•Acid blocking medications cause a variety of severe side effects, including a 19% increased risk of death and a comparable increase in cardiac events, kidney or liver disease, numerous infections, and bone damage.

•Thankfully, many safe natural treatments can effectively address acid reflux and many of the complications of a chronic stomach acid deficiency.

In the U.S., 66% of adults are estimated to have at least one prescription, and the average person has nine filled annually. As an awake physician, one of the most depressing aspects of my work is seeing patients, especially the elderly, weighed down by numerous prescriptions that frequently do more harm than good.

For example, as I showed here, statins provide a negligible benefit (e.g., at best, taking them for five years extends one’s lifespan by 3-4 days) but create significant side effects such as severe muscle pain and cognitive impairment for 20% of users.

This tragic situation is best demonstrated by a 2007 study which showed that simply discontinuing the least necessary prescriptions resulted in a 23% reduction in the death rate and an 18.2% decrease in hospital referrals. Sadly, since the trend in medicine is always to have people on more drugs, data like this has had no effect on the practice of the overprescription of medications.

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CDC Sued for Pushing Illegal 72-Dose Childhood Vaccine Schedule

First reported by The Defender, a new federal lawsuit is challenging the CDC’s entire childhood vaccine program.

Filed by Dr. Paul Thomas, Dr. Kenneth P. Stoller, and Stand for Health Freedom, the lawsuit accuses the CDC of recommending 72+ vaccine doses for American children without ever testing the cumulative schedule for safety.

Both doctors previously paid a heavy price for questioning the hyper-vaccination program:

  • Dr. Thomas had his license suspended five days after publishing a vaccinated vs. unvaccinated study.
  • Dr. Stoller lost his license for granting exemptions based on genetic vulnerabilities.

What the Lawsuit Alleges

  • No safety testing: Neither the CDC nor FDA has ever studied the long-term, combined effects of the full childhood schedule — despite two decades of warnings from the Institute of Medicine (2002, 2013).
  • 27 years of silence: By law, HHS must file biennial reports to Congress on vaccine safety efforts. Not a single report has been issued since 1998.
  • Constitutional violations: The suit charges the CDC with violating the First Amendment (silencing dissenting doctors), the Fifth Amendment (due process & bodily integrity), and the Administrative Procedure Act (arbitrary and capricious rulemaking).

What Plaintiffs Seek

  • Reclassify all childhood vaccines to Category B — shifting to shared decision-making, which would make medical exemptions far easier to obtain.
  • Require rigorous safety studies comparing fully vaccinated vs. unvaccinated children before any return to a mandated schedule.
  • End retaliation against doctors — protecting physicians who issue exemptions based on individualized medical judgment.

If successful, this lawsuit wouldn’t just expose the unlawful CDC hyper-vaccination program — it would mark a major victory for families seeking vaccine exemptions and for physicians fighting to practice real individualized medicine.

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‘Forever Chemicals’ in Drinking Water? What Is the EPA Up To?

Much controversy has surrounded the May 18 announcement by the U.S. Environmental Protection Agency (EPA) of proposed rule changes to Biden administration regulations that direct the cleanup of perfluoroalkyl and polyfluoroalkyl substances, or PFAS, in Americans’ drinking water.

Health & Human Services Secretary Robert F. Kennedy, Jr., said he strongly supports the EPA’s new tack. “I’ve read a couple of articles in the corporate media that suggest that EPA is trying to roll back PFAS regulations. It’s not true. I’ve met repeatedly with Lee and his staff, and they’re completely committed to end the exposures in a way that’s legal and practical.”

Kennedy continued, “As Lee pointed out, the Biden administration passed a [regulation] very hastily in which they ignored a Clean Water Act mandate for a public comment period . . . I can tell you, that was a fatal flaw.”

The HHS Secretary added that the Biden regulation wouldn’t withstand a court challenge and would be thrown out. “We’re doing it in a way that maintains the … maximum contaminant Safe Drinking Act levels, and gives maximum protection as quickly as possible for the American public.”

Despite widespread criticism from the legacy media and many in the MAHA base, I agree with Secretary Kennedy: the recent EPA policy shift signals an acceleration of PFAS cleanup, not a dangerous step backward.

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300 Studies Link This Neurotoxic Pesticide to Multi-Organ Damage, Chronic Disease

For decades, regulators viewed chlorpyrifos — a pesticide widely used in the U.S. and around the world — primarily as a neurotoxin that disrupts signaling in the brain and nervous system.

But as the U.S. Environmental Protection Agency (EPA) reconsiders whether to continue to allow its use on foods like apples and soybeans, a new review indicates other insidious harms.

Published in April in the International Journal of Molecular Sciences, the review synthesizes findings from nearly 300 studies worldwide published up to this year. These include laboratory experiments, animal studies, epidemiological research, regulatory documents and risk assessments.

Growing evidence suggests chlorpyrifos may damage the brain, hormones, liver, gut microbiome, muscles, reproductive organs and bones. Studies also link the pesticide to DNA damage and lasting changes in gene activity that may increase the risk of chronic disease.

Together, the findings portray chlorpyrifos as what the reviewers call a “multi-system toxicant” that poses a more significant threat to public health than previously understood.

It suggests the pesticide acts on the body in ways far beyond disrupted nerve signaling or obvious poisoning. Pregnancy and early childhood are especially sensitive periods for chemical exposure.

“What has genuinely evolved over time is our understanding that chlorpyrifos causes harm in ways that go beyond its effects on the nervous system including damage to DNA, changes in how genes are switched on or off, interference with hormones, and disruption of the healthy bacteria that live in the gut,” said Dana Boyd Barr, Ph.D., a professor at Emory University’s Rollins School of Public Health and past president of the International Society of Exposure Science.

The authors warn that current regulatory systems may not fully capture the complexity of chlorpyrifos’ dangers to the body. Many occur at levels too low to be detected by current safety testing, which looks for the disruption of an enzyme involved in nerve cell communication.

The review links chlorpyrifos exposure to:

  • Biological changes associated with inflammation, chronic disease and cancer.
  • Brain and nervous system damage, including lower IQ and developmental harms in children, neurodegenerative disease, and disrupted cell growth, survival and communication.
  • DNA damage and altered gene regulation that hinders normal cell repair and changes how genes are switched on and off during development (epigenetics).
  • Hormone disruption involving thyroid, estrogen and testosterone pathways.
  • Liver injury, gut bacteria disruption and metabolic dysfunction are linked to obesity and Type 2 diabetes.
  • Reproductive, muscular and skeletal harm, including reduced sperm quality and bone loss.

Industry pushback despite reported harms

The review comes as the EPA reassesses whether the pesticide’s remaining uses meet the statutory standard of “no unreasonable adverse effects.” The action follows years of official stalling, prior bans, policy reversals and legal challenges.

Meanwhile, agrichemical companies are lobbying federal and state lawmakers to shield pesticide manufacturers, including Bayer and its subsidiary Monsanto, from some lawsuits involving Roundup weedkiller. The suits allege their products cause non-Hodgkin lymphoma, among other cancers.

In February 2020, Corteva Agriscience — then the world’s largest producer of chlorpyrifos — announced it would stop production, citing declining demand.

But existing stocks continued to be used. The chemical remains approved for several major crops in the U.S., including apples, strawberries, soybeans, citrus, wheat and peaches.

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Raw Milk: The Wrong Lesson

New York distillers poisoned thousands of infants with filthy milk, and the politicians paid to stop them took bribes instead. Then the government drew exactly the wrong lesson. Rather than remove the conditions that caused the disaster, it treated the symptom, protected the system, and taught generations of Americans that the cow was the problem.

She was not.

In the spring of 1858, a New York publisher named Frank Leslie received milk at his door that was blue, watery, and contaminated with pus. He ordered an analysis, disliked what he found, and sent reporters and illustrators to trace the milk to its source. What they uncovered was not a quality control failure. It was an industrial scandal that had become a business model.

The distilleries of Manhattan and Brooklyn produced enormous quantities of spent grain mash. Disposing of it cost money. Feeding it to cattle produced profit. Distillers built cow sheds against their whiskey operations and packed them with animals standing in filth, tethered over troughs and fed steaming waste from the stills. The diet destroyed the animals. Teeth loosened. Sores opened. Udders became diseased. Cows too weak to stand were suspended in slings and milked until they died.

That milk was sold to the public.

Because it was thin and blue, it was adulterated first. Chalk and plaster for color. Flour and starch for body. Molasses for appearance. Water for volume. Wagons labeled “Pure Country Milk” carried it through the city while families believed they were buying fresh milk from the country. Contemporary estimates attributed thousands of infant deaths a year to it.

The corruption that protected the trade should sound familiar.

When public outrage forced an investigation, inspectors warned the operators before arriving. The barns were cleaned. The conditions were staged. The committee toured the sanitized sheds, declared the danger exaggerated, and recommended better ventilation. One member, Charles Haswell, filed a dissent describing the fraud and warning that children were dying. He was ignored. Years of pressure passed before the state acted.

The story is usually told backward.

Nothing about the swill milk scandal shows that milk was inherently dangerous. The deaths came from confinement, diseased animals, contaminated feed, adulteration, and political corruption. The milk was dangerous because the system producing it was dangerous.

There were two ways to respond.

One was to fix the source. Take the cattle out of the distillery sheds. Clean up the conditions. Test the animals. Keep the herds healthy. Produce milk under conditions that do not cause disease.

The other was to leave the industrial system in place and try to neutralize the result after the fact.

The second path won.

Pasteurization was not the choice made in 1858. It did not yet exist as a practical milk intervention. Pasteur’s early work was on wine; milk pasteurization did not take hold in the United States until decades later. The officials who inspected the swill dairies were not choosing heat over reform. They were choosing corruption over reform.

That distinction matters.

Decades later, when the federal government did push pasteurization, it conceded that the method was not ideal, only practical under existing conditions. In plain terms, restructuring the production system was harder than heating the final product. The industry was already large, centralized, and politically connected. Heating the milk was easier than fixing the barn.

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Senate Investigation Finds FDA Officials Covered-Up 25 COVID Shot Safety Signals

A new Majority Staff Interim Report from Sen. Ron Johnson’s Permanent Subcommittee on Investigations was released today (April 29, 2026), titled Unmasked: How Biden Health Officials Purposely Turned a Blind Eye Toward COVID-19 Vaccine Safety Signals.

In early 2021 — just weeks after the COVID-19 vaccines rolled out under EUA — FDA senior medical officer Dr. Ana Szarfman (a key developer of the agency’s own data mining system) teamed up with Dr. William DuMouchel (the statistician who literally invented FDA’s “gold standard” EB data mining algorithm) to run an upgraded analysis on VAERS data.

Their new method (Regression-Adjusted Gamma Poisson Shrinker — RGPS) fixed a known flaw called “masking” — where signals for one COVID vaccine get drowned out by the sheer volume of reports from the others.

What they found was explosive:

  • 49 examples of extreme masking
  • ~25 new statistically significant safety signals that FDA’s standard MGPS method completely missed
  • Signals included: sudden cardiac death, acute myocardial infarction, pulmonary infarction, Bell’s palsy, non-site specific embolism/thrombosis, dementia, and “Death and sudden death” — for Pfizer, Moderna, and J&J shots

Dr. Szarfman repeatedly shared these findings with senior CBER officials (the very people in charge of vaccine safety), including Dr. Peter Marks, in March, April, May, and July 2021.

Their response?

  • Told her to “hold off” on creating and sending any more data mining reports
  • Called her work a “major distraction”
  • Worried it would “create erroneous conflicts that feed into anti-vaccination rhetoric”
  • Eventually ordered her to “cease and desist”

Later, FDA quietly locked down distribution of its own weekly data mining reports to CDC — right around the time FOIA requests and Sen. Johnson’s letters started coming in. One CDC official even admitted they may have asked FDA to stop sending them “because of the FOIAs.”

Even after Dr. Szarfman and DuMouchel published their findings in Drug Safety (2022) showing masking was eight times more likely with COVID vaccines, and Dr. Robert Califf replied “Thanks. These are good,” no changes were made to the methodology.

This is documented, internal FDA communication showing deliberate suppression of safety signals at the exact moment millions of Americans were being told the shots were “safe and effective.”

The cover-up continues to unravel. Accountability is urgently warranted.

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The managed decline of Cobourg parks and playgrounds

Last summer, a five-year-old boy picked up a used needle while playing at a park in Cobourg, Ontario. His mom says they’re not going back unless something changes, but Cobourg has launched a new 10-year Parks and Recreation Master Plan project that doesn’t include a plan of how to fix the squalor, but instead chooses to cede public spaces to it.

Cobourg was coined Ontario’s feel good town for it’s pristine beach, safe streets, and irresistible charm. Now, woke bureaucrats and ideologue politicians seem determined to manage its decline instead of protecting its legacy.

Case in point: families now scour every crevice of every park before letting their kids play, if they dare go at all. They must sweep public bathrooms for needles and paraphernalia before entering, while port-a-potties at local parks risk fentanyl-laced exposure.

What makes this proposed plan even more concerning is that it will be at the centre of every Cobourg kids’ childhood for the next decade.

With families avoiding parks because of encampments, discarded needles, open drug use, crime, disorder and disarray; drug fuelled criminality has turned quiet streets into hubs of chaos and it’s pulling kids away from public spaces.

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