Tag: safety

HORROR: Illegal Alien Semi-Truck Driver Who Entered US Under Joe Biden Kills Amish Family in Head-On Crash

An illegal alien semi-truck driver killed four Americans in a head-on crash in Jay County, Indiana, this week.

The driver, 30-year-old Bekzhan Beishekeev, is an illegal alien from Kyrgyzstan who entered the US on Joe Biden’s open border invitation in December 2023.

The Amish victims were identified as 50-year-old Henry Eicher, 25-year-old Menno Eicher, 19-year-old Paul Eicher and 23-year-old Simon Girod.

Per ICE:

On February 3rd, criminal illegal alien Bekzhan Beishekeev of Kyrgyzstan allegedly swerved and drove his eighteen-wheeler head-on into a van killing four innocent Americans: 50-year-old Henry Eicher, 25-year-old Menno Eicher, 19-year-old Paul Eicher and 23-year-old Simon Girod.

Beishekeev entered the U.S. using the Biden admin’s disastrous CBP One App and was issued his CDL by Pennsylvania Governor Josh Shapiro’s Department of Transportation.

ICE’s 287(g) partners at the Indiana State Police arrested Beishekeev, and he’ll remain in ICE Fort Wayne’s custody pending immigration proceedings.

This tragedy and loss of American lives could have been prevented had PA not issued a CDL to an illegal alien.

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Ozempic’s HIDDEN DANGERS: Weight Loss Jabs Linked To HIGHER Risks of Cancer, Heart Issues, And Chronic Disease

Big Pharma’s miracle injections are under fire again as new research uncovers how Ozempic and similar GLP-1 drugs could be setting users up for severe long-term health traps. 

A new study suggests that slamming the brakes on appetite, these medications risk starving the body of essential nutrients, paving the way for elevated dangers of heart problems, chronic illnesses, and even certain cancers. 

It’s another stark reminder of how the medical-industrial complex prioritizes profits over genuine wellness, leaving Americans to pay the price.

In a landscape where synthetic fixes are pushed over real food and lifestyle reforms, this revelation is stark. With millions hooked on these jabs, the findings demand scrutiny—especially as the media downplays the risks while pushing the hype.

A recent review by Australia’s Hunter Medical Research Institute and the University of Newcastle analyzed 41 randomized controlled trials on popular GLP-1/GIP medications spanning the last 17 years. 

Shockingly, only two studies tracked dietary intake among adults, and one remains unpublished. This glaring “blind spot” highlights how little we know about the nutritional impacts of these drugs, despite their skyrocketing use.

The core issue is appetite suppression. While users shed weight, they often consume far fewer calories and nutrients, leading to deficiencies that can trigger inflammation, metabolic chaos, and heightened vulnerability to serious conditions. 

As the researchers warn, inadequate nutrition “can increase the risk of cardiovascular disease, metabolic complications, inflammation and long-term chronic conditions, including some cancers.”

At least half a million Australians are jabbing these drugs monthly, amid ongoing shortages. In the U.S., the numbers are even higher, with Ozempic and its cousins like Mounjaro becoming go-to prescriptions for obesity and diabetes.

Separate studies have already flagged mixed signals on direct cancer links. A 2025 JAMA Oncology paper found GLP-1 drugs associated with an overall 17% lower cancer risk, but with a potential uptick in kidney cancer. 

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Scuba school told instructors they were allowed to KILL two students a year, shocking lawsuit from family of girl, 12, who died there alleges

A scuba school told its instructors they were allowed to kill two students a year, according to a lawsuit filed by heartbroken parents whose daughter died while taking lessons there. 

The astonishing claim comes after 12-year-old Dylan Harrison tragically drowned on August 16, 2025, while attending a class at The Scuba Ranch in Terrell, Texas, about 40 minutes outside of Dallas. 

Harrison, who was also known as ‘Dillie Picklez’ by her loved ones, was eager to get her National Association of Underwater Instructors (NAUI) Open Water diving certification so she could join her family members in the underwater activity. 

But sadly, her dreams never came true after she vanished during her training class that summer day. She was found dead about 45ft underwater, approximately 35ft away from the platform. 

Now, a new lawsuit filed on January 30 by Harrison’s mother and father, Heather and Mitchell, detailed the disturbing guidelines the scuba school owner told his employees before being entrusted with students in the water. 

Joseph Johnson, the owner of Scubatoys, a dive and certification shop that the family was using for Harrison, was ‘seen bragging to a roomful of Scubatoys Instructors’ that two students were allowed to die each year and the business would ‘still be fine,’ the documents allege. 

The unearthed footage, filmed in 2017 by an employee, captured a worker telling Johnson not to take lawsuits lightly. 

Stunningly, Johnson appeared to have very little compassion over the statement, shrugging and telling his workers: ‘All I know is we’ve killed what, four people, five people, and we’ve never even done a deposition. 

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Industry lobbies Congress to weaken protections against toxic chemicals

Months after a federal judge ordered the Environmental Protection Agency (EPA) to regulate fluoride over risks to children’s brains, industry-backed lawmakers are pushing legislation that would weaken the nation’s primary law governing toxic chemicals.

The proposed changes would overhaul the Toxic Substances Control Act (TSCA), a law first passed in 1976. Legal experts say the effort would block future citizen petitions, shield the EPA from court scrutiny, and dismantle the legal tools that made the fluoride case possible.

Citizen petitions allow the public to ask the EPA to regulate chemicals it has failed to address and to sue the agency if those petitions are denied. It was a citizen petition filed in 2016 that led to a landmark federal court ruling in September 2025, when a judge found that current levels of fluoride in drinking water pose an “unreasonable risk” to children’s health.

The judge ordered the EPA to take regulatory action. The agency is appealing the ruling.

Former EPA deputy administrator Robert Sussman said the proposed TSCA changes appear designed to prevent courts from intervening as they did in the fluoride case.

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FDA Requires Vaccine Makers to Include Febrile Seizure Warning on Flu Shot Labels

The U.S. Food and Drug Administration (FDA) notified six influenza vaccine manufacturers on Jan. 9, 2026 that they must add a warning about the risk of febrile (fever) seizures to their product information labels, citing newly identified postmarketing safety data. The notices, issued under the FDA’s statutory authority to mandate safety labeling changes, were sent to Sanofi, AstraZeneca, GlaxoSmithKline (GSK), and CSL Seqirus.1

According to the FDA, observational analyses conducted during the 2023–2024 and 2024–2025 influenza seasons identified a statistically significant increase in seizures caused by fevers occurring within one day of vaccination among children aged six months through four years, prompting the agency to conclude the findings constitute “new safety information” requiring disclosure in product labeling. In its notification letter, the FDA stated that the results of the analyses “suggest a causal relationship”—language the agency typically avoids unless compelled by evidence.2

The data suggested an “estimated attributable risk of 21.2 excess febrile seizure episodes per million standard-dose quadrivalent influenza vaccinations” and “an attributable risk of 44.2 excess febrile seizure episodes per million standard doses of trivalent [influenza] vaccinations.”

Risk of Febrile Seizures May Increase After Childhood Vaccinations

The Mayo Clinic website states that in some infants and young children fevers can cause convulsions (seizures). Doctors generally describe “simple” febrile seizures as associated with fevers over 100 F, short-lived and typically harmless, although “complex” febrile seizures can last longer than 15 minutes and occur more than once in a 24-hour period.3

It has been acknowledged in the medical literature that convulsions can include an increased risk of future epilepsy (uncontrolled seizure disorder).4 5 Febrile seizures have also been associated with a spectrum of brain dysfunction and rarely, severe brain injury or death.6 7

Bioengineer Brian Hooker, PhD said he disagrees with febrile seizures being characterized as harmless. He said:

Any seizure is bad, period. Mild’ febrile seizures can double a child’s chance of an epilepsy diagnosis and ‘complex’ febrile seizures—lasting more than 15 minutes —can increase that risk up to 10 times.8

On the topic of febrile seizures and childhood vaccines, Mayo Clinic states:

The risk of febrile seizures may increase after some childhood vaccinations. These include the diphtheria, tetanus and pertussis vaccine and the measles-mumps-rubella vaccine. A child can develop a low-grade fever after a vaccination. The fever, not the vaccine, causes the seizure.9

The U.S. Centers for Disease Control and Prevention (CDC) acknowledges that some vaccines are associated with a higher risk of febrile seizures than others, particularly in infants and young children, and that the risk increases when certain vaccines—such as the influenza, pneumococcal (PCV13), and DTaP vaccines—are administered during the same visit.

The agency also notes that measles-containing vaccines, especially the MMRV (measles, mumps, rubella, and varicella) combination, are associated with a higher risk of febrile seizures than their single-component counterparts, and that these events tend to occur within specific post-vaccination time windows. Still, CDC guidance emphasizes that the overall risk is small, that febrile seizures are typically short-lived and without lasting harm, and that vaccination should continue according to the recommended schedule.10

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Scientists want to use self-amplifying mRNA to vaccinate those who do not want to be vaccinated

Newly published research papers demonstrate that gain-of-function research designed to investigate the effects of deadly pathogens is still continuing. In the course of research, live mice are being exposed to deadly doses of laboratory-built recombinant synthetic H5N1 viruses with codon optimisation, which boosts expression in human cells and cleavage site enhancement linked to viral virulence.  Lethal doses of synthetic viral material containing artificial DNA sequences are being forced into animals using lipid nanoparticles (“LNPs”) and electrical pulses. The aim of the research is to develop replicon mRNA vaccines and treatment strategies but alarmingly, the work is being partially funded by the US defence establishment and there are ties to multinational pharmaceutical companies.

A paper was published on 13 January 2026 in Nature Communications is entitled ‘Intranasal replicon vaccine establishes mucosal immunity and protects against H5N1 and H7N9 influenza’. It reports the development of a self-replicating mRNA vaccine targeted at H5N1 and H7N9 viruses – so-called avian or bird flu viruses. The vaccine is administered with an intranasal spray, which is designed to attach itself to the nasal mucosa via a nanostructured lipid carrier and then replicate itself like a virus in the human body. The research was funded by the Department of Defence of the US government. One of the stated aims of the research is to develop proof of concept for an mRNA vaccine delivery system, which will overcome vaccine hesitancy and reach whole populations rapidly.

In a parallel development, an international team of researchers from USA, Canada and the EU have used so-called gain-of-function methods to design, engineer and test synthetic versions of the H5N1 bird flu virus’s hemagglutinin protein – one of the key components that allows the virus to infect cells. Their results are reported in a Nature paper entitled ‘Electroporation and LNP-mediated delivery of plasmid DNA-encoded H5N1 influenza virus hemagglutinin support protection against highly pathogenic avian influenza’. In summary, the paper reports that researchers have produced synthetic versions of a dangerous flu component and injected them into mice. They then exposed the animals to very deadly strains of the H5N1 virus to see how well their synthetic constructs functioned. Their research was funded by a US federal vaccine-development initiative said to be designed to prepare for future influenza outbreaks using rapidly adaptable genetic platforms. 

Scientists are creating novel genetic viral pathogenic sequences and then saying we need to be protected from them. In other words, they are posing as saviours when they are the ultimate sinners.

The senior scientist involved, David B. Weiner, disclosed paid relationships with Pfizer, AstraZeneca, Sanofi, Inovio, Flagship and other commercial biotechnology and/or pharmaceutical companies.

These reports demonstrate how the type of dangerous research which likely created covid-19 is still being conducted in laboratories around the world. If New Zealand were to pass the Gene Technology Bill, it is likely that our laboratories will be co-opted by the lure of lucrative funding to participate in such collaborative research projects, despite the fact that the FBI, CIA, MI6, BND and other international intelligence organisations have confirmed that the covid pandemic was likely the result of laboratory-engineered pathogen manipulation.

Make your feelings known. Our voice is more powerful than we realise. Do not get distracted by the injustices of the past to the extent of ignoring the very real threats that are being developed around us. We need a better future than the one that is currently being planned, created and curated for us. 

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Powdered whole milk may be culprit in botulism outbreak that sickened dozens of babies

Powdered whole milk used to make ByHeart infant formula could be the source of contamination that led to an outbreak of botulism that sickened dozens of babies.

The Centers for Disease Control and Prevention (CDC) reported the details on Friday.

Powdered whole milk may be culprit in botulism outbreak

What we know:

Testing by the U.S. Food and Drug Administration (FDA) found that bacteria in an unopened can of formula matched a sample from a sick baby — and it also matched contamination detected in samples of organic whole milk powder used to make ByHeart formula and collected and tested by the company, officials said. 

FDA testing also found contamination in a sample of whole milk powder supplied to ByHeart — and it matched the germ in a finished sample of the company’s formula.

What they’re saying:

A ByHeart official said the finding helps shed light on what has become a “watershed moment” for the company.

“We are focused on the root cause and our responsibility to act on what we’ve learned to help create a safer future for ByHeart and infant formula,” said Dr. Devon Kuehn, ByHeart’s chief scientific and medical officer.

What we don’t know:

While these results advance the agency’s understanding of the outbreak, the FDA said the findings are not conclusive, and the investigation continues “to determine the source of the contamination.”

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Supreme Court Poised to Grant Chemical Warfare Immunity: How Glyphosate Legal Shield Would Poison American Justice

Introduction: The Supreme Court’s Glyphosate Gamble: Corporate Immunity Over Human Life

The U.S. Supreme Court has stepped onto a dangerous precipice, agreeing to hear a case that could grant chemical manufacturers a staggering new power: blanket immunity from lawsuits for poisoning the American people. Agro-chemical giant Bayer, owner of Monsanto, is appealing a $1.25 million Missouri jury verdict, arguing that because federal regulators claim its flagship weedkiller Roundup is safe, the company should be shielded from all state-level failure-to-warn lawsuits brought by cancer victims. A ruling in Bayer’s favor would dismantle legal recourse for thousands of citizens and establish a perilous precedent where captured federal agencies, not independent science or juries, dictate corporate accountability for public harm. This case represents nothing less than a corporate coup against the constitutional right to a trial by jury, placing profits above the sanctity of human life.

The Glyphosate Deception: A Chemical Assault on Human Health

At the heart of this legal battle is glyphosate, the active ingredient in Roundup and the most heavily used herbicide in the world, with approximately 300 million pounds applied annually in the United States alone. For decades, Monsanto marketed Roundup as safe for humans and animals, a claim now exposed as a profound deception by a mountain of independent research.

Despite the Environmental Protection Agency’s (EPA) repeated assertions that glyphosate is “not likely to be carcinogenic,” science tells a horrifically different story. A major 2025 international carcinogenicity study found that low doses of glyphosate-based herbicides cause multiple types of cancer in rats, with tumors appearing in blood, skin, liver, and other organs even at levels regulators consider safe. This research adds to a substantial body of evidence linking glyphosate exposure to non-Hodgkin’s lymphoma and other chronic diseases in humans. As investigative journalist Carey Gillam notes in her book, the truth about such public health dangers often only emerges through “lawyers, lawsuits, journalists, and the occasional whistleblower” when regulators fail. The EPA’s fraudulent safety claims stand in direct contradiction to this independent science, blessing a chemical poison while natural, non-toxic agricultural solutions are suppressed and ignored.

Corporate Capture: How Regulatory Agencies Betray the Public Trust

Bayer’s legal strategy hinges on a doctrine known as federal preemption, which posits that federal regulatory approval should override state-level consumer protection laws and common-law tort claims. This argument reveals the deep and dangerous corruption of federal health agencies, which now serve as puppets for the very industries they are supposed to regulate.

This phenomenon, known as regulatory capture, is systemic. As Robert F. Kennedy Jr. explains in his work on corporate influence, agencies like the FDA become “sock puppets” for Big Pharma and chemical interests, with a significant portion of their budgets coming from the companies they oversee. The glyphosate case is a textbook example. The EPA has consistently parroted the industry line on glyphosate’s safety, ignoring robust independent evidence of carcinogenicity. This betrayal was further underscored when the Trump administration’s Solicitor General, in a December legal brief, urged the Supreme Court to take Bayer’s side, arguing that a manufacturer “should not be left subject to 50 different labeling regimes.

This move represents a blatant political manipulation of the justice system to insulate a powerful corporation from accountability. If the Court rules for Bayer, it would effectively nullify state-level consumer protections and constitutional rights, centralizing power in the hands of a corrupted federal bureaucracy. As a NaturalNews.com report on the case warns, this gambit “silences victims and overrides the rule of law,” completing the transformation of public health agencies into immunity-granting enablers of corporate malfeasance.

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Texas Air-Drops Live Virus-Containing Edible Rabies Vaccines Over Cities from Aircraft—’Leaving Persons at Risk for Vaccine Exposure and Vaccine Virus Infection’: CDC

The Texas Department of Health and Human Services (DHS) has begun its annual distribution of RABORAL V-RG®, an oral rabies vaccine (ORV) bait—dropping the live laboratory-made virus from airplanes over Texas, as well as distributing it by hand.

The $2 million annual project is funded by the State of Texas and the United States Department of Agriculture Animal and Plant Health Inspection Service/Wildlife Services.

The U.S. Centers for Disease Control and Prevention (CDC) has known for over a decade that the RABORAL edible vaccine leaves “persons at risk for vaccine exposure and vaccine virus infection.”

Yet the department still allows millions of live genetically modified virus baits to be dispersed over communities, forests, and waterways each year without public notice, informed consent, or comprehensive biosafety oversight—posing potential risks to human health, wildlife, and national biosecurity.

Americans are being involuntarily exposed to laboratory-engineered pathogens capable of infecting multiple species, with no transparent risk disclosure or opt-out mechanism.

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Vaccine Hesitancy Reflects Appropriate Concerns

The World Health Organization (WHO) considers vaccine hesitancy one of the top ten threats to global health. If that is the case, is it always a bad thing? AlterAI assisted with this analysis.

The Lancet manuscript “Profiling vaccine attitudes and subsequent uptake in 1.1 million people in England: a nationwide cohort study” (Whitaker et al, 2026) presents one of the most exhaustive longitudinal analyses of COVID‑19 vaccine hesitancy ever conducted. Using data from the Real‑time Assessment of Community Transmission (REACT) study, the researchers tracked English adults’ views and actions surrounding vaccination between January 2021 and March 2022, linking survey responses with verified NHS vaccination records.

  • Population: Over 1.1 million adults (aged ≥ 18 years; 57% female).
  • Initial hesitancy: At the beginning of 2021, 8% were hesitant about vaccination.
  • Hesitancy decline: By early 2022, the hesitant fraction dropped to roughly 1%.
  • Behavioral outcome: Among those initially hesitant, 65% later received at least one vaccine dose.

This significant attitudinal shift demonstrates that while early-stage doubts about vaccine safety and efficacy were widespread, the majority were transient and susceptible to persuasion, propaganda, and mandates.

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