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BREAKING: 2.9 Million-Person Study Finds mRNA Shots Increase Risk of Death, Kidney Failure (Dialysis), and Kidney Injury

Enormous vaccinated vs. unvaccinated study reveals progressively worsening kidney damage over time with no sign of stopping — and a striking mortality signal among Pfizer recipients.

This paper will SHOCK the world: Unveiling hidden biases that inflated COVID-19 vaccine effectiveness and safety

How misclassification of early post-vaccination deaths distorts mortality rates and public health assessments

BREAKING: 51 Million-Person Study Finds COVID-19 “Vaccines” Increase Risk of Respiratory Infections by up to 559%

Landmark study of the entire South Korean population uncovers a VAIDS signal — a dose-dependent rise in the common cold, upper-respiratory infections, pneumonia, and tuberculosis among the vaccinated.

The headline that wasn’t: Vaccination increased myocarditis risk from covid

Analysis of latest Lancet paper promoted by media

A new Lancet Child & Adolescent Health paper has drawn headlines suggesting that COVID-19 poses a greater myocarditis risk to children than vaccination. A closer look at the data, however, raises serious questions about how those conclusions were reached.

The headlines were that covid was a greater risk for myocarditis in children than the vaccines. There is solid evidence and from multiple sources that this is not true, so how did this reversal happen?
Comparing risks from infection and vaccination is of no relevance when vaccination did not prevent infection. The risks become additive.

The key lesson, that vaccination primes the immune system such that exposure to the virus is riskier has not been learned.

Before we begin there are three key points that mean this kind of analysis based on diagnostic codes in the medical records – even if done honestly – is not a good measure.

3% of teenage boys after their boosters had evidence of dead heart cells measured with raised troponin levels in the blood and a third had symptoms.

It is wrong to focus on only one adverse event to the exclusion of others.

The vaccines did not prevent infection so it is not an either or sum. Vaccinated children were exposed to more risk.

buried deep in Andrew Webster’s 2023 biography The Wolf You Feed, Australia’s most successful rugby league coach reveals an admission so raw, so devastating, that it challenges everything we’re told about childhood vaccine injury and genetic disease. Bennett, a man who has spent half a century perfecting the art of emotional concealment, revealed that his son Justin was brain-damaged by a routine vaccination at four months old. The real tragedy isn’t just what happened to Justin Bennett in 1977—it’s how a clear case of vaccine poisoning has been retrospectively repackaged as a genetic condition called Dravet syndrome, shifting blame from the injection that destroyed a baby’s brain to the parents who supposedly passed on defective genes.

After 40+ years, the victims were further mocked by claiming a “rare genetic mutation” was responsible:

The psychological burden placed on parents by genetic diagnoses cannot be overstated. Wayne and Trish Bennett went from knowing their son was vaccine-injured—an external harm inflicted upon their healthy child—to being told they had passed on defective genes that doomed Justin from conception. This isn’t just a change in medical classification; it’s a fundamental rewriting of moral responsibility. The perpetrator becomes fate, the crime becomes heredity, and the parents become unwitting accomplices in their child’s destruction.

As the author correctly points out “genetic diseases” is another science fraud-omat, where vaccine injury and other iatrogenic harms get repackaged:

Wayne Bennett’s personal testimony about his son’s vaccine injury gains profound scientific support from Jonathan Latham and Allison Wilson’s comprehensive analysis in “The Great DNA Data Deficit.” Their research provides the empirical foundation for understanding how genetic determinism has become what could be described as “at least 70% fraud, possibly as high as 90%” - a fraudulent edifice that serves as cover for mass poisoning and industrial pollution.

Justin Bennet was poisoned by DTP vaccine at 4 months old, suffering seizures that irreversibly destroyed his brain, and for over 40 years his family had to provide round the clock care. In 2019 his parents were blamed for passing on defective genes for “rare genetic epilepsy/Dravet syndrome” claimed by “geneticists” to affect 1:15,000 to 1:40,000.

That was in 2019.

In 2025, a cabal of witches that goes by the name of Philadelphia Children’s Hospital (CHOP) said “hold my beer”, and went for the gold. Enter “Baby KJ” with a rarest genetic diseases of all genetic diseases out there… Now we get to my main story:

“Baby KJ”’s personalized CRISPR therapy for an “ultra-rare genetic disorder”
If you don’t know what CRISPR means, you can read the sci-fi nonsense about it on Wikipedia. Or ask your favorite “genomics expert” in the “health freedom” and they will talk your ear off about it. This Substack does not deal in fraudulent science porn. My personal informed opinion about CRISPR - it’s poison in lipid nanoparticles. I will discuss baby KJ’s specific concoction below, I promise you - it is a very-very exciting bullshit.

As pharma industry and science press breathlessly reported back in May: An infant known publicly as KJ (KJ Muldoon) became the first person to receive a bespoke, patient-specific in-vivo CRISPR gene-editing therapy to treat a life-threatening, ultra-rare metabolic disorder (severe CPS1 — carbamoyl phosphate synthetase 1 — deficiency). The case and clinical details were reported in a peer-reviewed paper and institutional releases in May 2025:

CPS1 deficiency is a urea-cycle disorder that prevents the liver from clearing ammonia produced during protein metabolism; untreated, it causes dangerous hyperammonemia that can lead to neurological injury or death. Standard management often requires strict dietary protein restriction, nitrogen-scavenger drugs, and in severe cases liver transplantation.

What are the chances for a baby to be born with this “ultra-rare genetic disorder”? It’s 1 in 1,300,000, says $cience, without blushing. One in 1.3 million! Gosh, genetic science is amazing isn’t it? 1:15K was bad enough. And that number is made up, mind you, to begin with. However, those Aussies were amateurs. With the “multidisciplinary CHOP-[chop] team” we are in the big leagues. The “team” included illustrious names coming not only from major academia but from places such as Danaher corp, Acuitas (the owner of the LNP weapons platform) and who else, but AmplifyBio, JD Vance’s company!

I had a hunch and went to look it up in VAERS data. I searched for only one of the symptoms of baby KJ’s supposed “ultra-rare genetic disease” - increased ammonia in the blood. I found approximately 80 reports, about half in babies and young children after Rotavirus and TDP shot (the one that crippled Justin Bennet in Australia), and the other half - adults after covid shots. The cases were a spectrum of liver injury, from elevated markers to hepatitis, to seizures and permanent brain damage, just like Justin Bennet’s.

The CHOP-chop team, of course, blamed what is highly likely a vaccine injury (either baby KJ’s DTP shot or the mother’s vaccination during pregnancy), on “ultra-rare” mutation and elegantly pinned it on KJ’s dad being a “genetic mutant”:

The team chose to target the Q335X mutation (from Dad), which required converting a stop codon back to a functional amino acid by changing an adenine (A) to a guanine (G).

They then set out to make a miracle injection juice and called it “kayjayguran abengcemeran, or k-abe”. I don’t know about you, but it sounds too close to “Kayfabe” in pro wrestling to me. Here is the description of the product from the 4500 pages (!!! I am not kidding) of the NEJM paper + full protocol that I purchased. Thank you, paid subscribers, for giving me fascinating things to read before bed to cause functional nightmares:

The drug product (DP) is a liver-targeted, lipid nanoparticle (LNP) base editing therapeutic comprising a messenger RNA (mRNA) drug substance (DS) encoding an adenine base editor (ABE), a single guide RNA (gRNA) DS to engage with the ABE once expressed within the target cells, and lipid excipients that provide the LNP delivery system for the nucleic acid DSs. The DP will be administered intravenously.

Wait… let’s rewind… what? mRNA in LNP is a GENE THERAPY??? As in we are “correcting” the “incorrect” ultra-rare genes with it? And it’s not a vaccine? Hello, FDA… Bueller… Bueller… Buellerrrrr….

This “CRISPR” therapy is nearly identical to the covid shots, down to uridine substitution and a similar molecular weight:

The mRNA comprises the 5’ cap, the 5’ untranslated region (UTR), the ABE coding sequence, the 3’ UTR, and the 3’ polyadenylate tail. The ABE coding sequence, 4818 nucleotides in length, is codon optimized with uridine minimization and has substitution of all uridines with the modified nucleotide N1- methylpseudouridine.

Why Isn't There a Cure for Alzheimer's Disease?

Exposing the Great Amyloid Scam and The Cures They Buried for Billions

Story at a Glance:

• Alzheimer’s disease is commonly thought to result from abnormal plaque buildup in the brain that gradually destroys brain tissue.

•Almost all Alzheimer’s research for decades has been directed toward eliminating amyloid, even after the basis for much of this work was shown to stem from fraudulent research.

•The billions spent on amyloid Alzheimer’s research have only produced three drugs, all of which offer minuscule benefits and severe side effects.

•In contrast, affordable and straightforward treatments that reduce dementia or the preceding cognitive impairment have been maligned and buried by the medical industry.

•DMSO for example, has incredible neuroprotective qualities that have spared many stroke and spinal cord injury victims from a life of “incurable” disability. Decades of forgotten research also show it treats cognitive impairment and dementia.

•This article will review the great amyloid scam and the simple therapies for cognitive decline we’re never told about.

Medicine is strongly biased towards adopting biochemical models of disease as this facilitates costly therapeutics being developed for each disease and hence sustains the medical industry. Unfortunately, in many cases, the biochemical approach to disease, at best can manage symptoms, and as a result, many conditions remain “incurable” while non-patentable natural therapies that can cure them languish in obscurity.

That’s why, despite spending an ever increasing amount of money on Alzheimer’s research (e.g., the NIH spent 2.9 billion in 2020 and 3.9 billion in 2024), we’ve still failed to make any real progress on the disease. This is particularly remarkable given the vast costs to the country (e.g., last year Alzheimer’s was estimated to cost the United States 360 billion dollars) and the even greater social costs that accompany it.

The Ebola Equation

Vaccine harm scaled up

When we teach children mathematics, we often use simple numbers to explain a concept before asking them to apply it to more complex situations.

For vaccines, we can do the same.

Meet Dr Sane. She is about to travel to Sierra Leone to help during an Ebola outbreak. She is nervous about the risk this poses to her own health — and her life.
Being a rational doctor, she looks up the statistics.

During the 2014–2016 outbreak, a frightening 8 % of local healthcare workers caught Ebola. Across the whole outbreak, 40 % of infected people died, and shockingly among local healthcare workers, the fatality rate was closer to 60 %.

By contrast, only a handful of Western doctors were infected, and nearly all survived. In fact, among 27 healthcare workers treated in Europe and North America, the mortality rate was 18.5 %.

Why Does Natural Medicine Caution Against Suppressing Fevers?

Exploring the link between Tylenol and Autism

Story at a Glance:

•Over-the-counter (OTC) pain and fever medications are widely used despite having marginal efficacy and significant side effects that hospitalize hundreds of thousands of Americans each year.

•While a widespread practice, using these medications to reduce fevers has long been controversial, both due to their toxicity and the notion that fevers are essential for health.

•During the 1918 Influenza pandemic, one of the most critical lessons was that avoiding fever suppression was vital for protecting patients from dying.

•While considered the “safest” option, Tylenol has a wide range of issues, including liver damage, gastrointestinal issues, blood cancers, and kidney injuries.

•An extensive body of data connects using Tylenol during pregnancy or in infancy to the development of neurological injuries (e.g., autism).

•Many of these tragic cases illustrate a longstanding observation within natural medicine—suppressing superficial reactions (e.g., fevers) can transform illnesses into chronic ailments that can cause far more issues.

Definitive Evidence of DNA Adulteration in the mRNA Vaccines

Kevin McKernan, CSO Medicinal Genomics

In 2023, McKernan’s lab discovered DNA contamination (adulteration) in the SARS-CoV-2 mRNA vaccines and has been exploring the impact of the Endocannabinoid system in vaccine injury. Medicinal Genomics has also been exploring the use of Bitcoin to decentralize Peer Review and crowd fund scientific investigation of important but controversial public health matters.

Wellbeing: Death by Flour

The hidden dangers of sugar, refined carbs, folic acid, preservatives, pesticides, and potassium bromate

Folic acid
Folic acid is added to breakfast cereals, flour, and grain as a substitute for natural folate acid. This is added so that pregnant women make adequate amounts of folate to prevent neural tube defects (Spina bifida and Anencephaly) in babies and to help meet the minimum folate standards. Of note, the U.S. FDA has mandated the enrichment of wheat flour, cornmeal, and rice flour with folic acid (140 µg per 100 g of flour) since 1998.

For breakfast cereal fortification, a folic acid solution or powder is sprayed or mixed onto the finished cereal before packaging. It is also required for meal replacement (protein) bars and powders. Of course, it isn’t just breakfast cereals; folic acid is in all of our bread - unless it is made with organic flour.

Most people tolerate this supplement well. However, roughly 30–40% of the population carries a genetic mutation called MTHFR polymorphism, which reduces their ability to metabolize folic acid efficiently. And for 10-15% of the population, their bodies do not properly break down folic acid, leading to unmetabolized folic acid (UMFA) buildup in the blood, which may weaken immune function, including natural killer (NK) cell activity.

There can also be significant methylation-related issues in those with MTHFR polymorphisms, leading to elevated homocysteine levels despite adequate folic acid intake.

High homocysteine levels mainly increase the risk of cardiovascular and neurological disease. Chronically elevated levels can damage blood vessel linings, promote arterial plaque buildup and blood clots, and are linked to higher rates of heart attack and stroke. In the brain, excess homocysteine contributes to oxidative stress and impaired neurotransmitter function, raising the risk of cognitive decline, dementia, depression, and neuropathy, especially when folate or vitamin B12 is low.

In pregnancy, high homocysteine is associated with miscarriage, preeclampsia, and birth defects such as neural tube defects. Overall, it’s a marker of impaired methylation and B-vitamin deficiency, with vascular and neurological damage being the most common and clinically significant consequences.

There is a simple blood test widely available to analyze for MTHFR variants. The test looks for two main DNA variants (SNPs) in the MTHFR gene:

C677T (rs1801133) is the MTHFR gene most strongly linked to reduced enzyme activity and,

The A1298C (rs1801131) gene, which has milder effect, but can compound with C677T

The results of a lab report testing for the variants will report on whether an individual has the following profile:

Normal (wild type)

Heterozygous (one copy of the variant)

Homozygous (two copies, most substantial effect)

Because of the higher risk of cardiovascular disease associated with the MTHFR gene and the lack of overt symptoms, we recommend that everyone consider getting tested. However, some groups of people are more likely than others to have one of these variants.

The geographic and Ethnic Distribution of the Frequency of C677T Allele differs:

East Asian (China, Japan, Korea) - 30–40% homozygous - Among the highest prevalence globally; linked to high homocysteine levels and folate sensitivity.

Southern European (Italy, Spain, France, etc.) - 10–20% homozygous - Moderate frequency; often associated with mild enzyme reduction.

Northern European - 5–12% homozygous - Common but less than in Mediterranean regions.

African and African American - <2–3% homozygous -The 677T variant is rare; A1298C is somewhat more common.

Indigenous American (including S. Americans) - Variable (10–30%) - Reflects East Asian ancestry patterns.

South Asian (India, Pakistan)- 10–15% homozygous.

Older studies and meta-analysis studies have not been conclusive regarding the association between the C677T gene and cardiovascular disease, but more recent studies have found that, especially in Asian populations, the risk is higher:

“We observed a significant correlation between the MTHFR C677T polymorphism and the development of CHD in the recessive model (OR: 1.35, 95% CI: 1.06-1.71, P = 0.006) for the overall population.

In subgroups stratified by ethnicity and source of controls, subgroup analyses indicated similar associations in Asians and hospital-based groups, but not for Caucasians and population-based groups.” (ref).

Our findings indicated that MTRR rs1532268, MTHFR rs1801131 and MTHFR rs1801133 polymorphisms may affect the risk of CHD in Asians and Caucasians, while the MTRR rs1801394 polymorphism may only affect in risk of CHD in Asians (ref).

And yet still, no major medical group or the HHS “task force” recommends testing, not even for the Asian population, who are most at risk. Particularly if eating a high-carb (cereal/bread/etc) diet - as the amount of folic acid being ingested could be quite high in those individuals.

The real reason why folic acid supplementation is required is to prevent neural tube defects, and those numbers have decreased by 36% since folic acid was added to foods so that pregnant women can get adequate amounts. Neural tube defects have declined from around 4,100 cases per year to around 3,000 - so this truly has been a blessing for some families. This is important, but the only people being affected by this mandated supplement are pregnant women and their babies. Are the neural tube defect benefits sufficient to justify the harms done to those with MTHFR gene C677T genetic alleles? No one has done the risk/benefit analysis to the best of my knowledge. So I asked Grok to perform the analysis (see below at the end of this essay).

Potential Harms of Folic Acid supplementation are primarily associated with excessive intake (>1,000 mcg/day). At high doses, unmetabolized folic acid (UMFA) can accumulate, especially in TT carriers due to impaired conversion, potentially creating a “pseudo-MTHFR deficiency” by further suppressing enzyme activity.

Evidence for harm is mostly associative (from observational studies and meta-analyses), not causal, and focused on excess rather than standard use. No large randomized trials show definitive risks at 400 mcg.

Once again, this is a public mandate to supplement all grains for which we, the public, weren’t given a choice. And the results are that for some, the risk of cardiac heart disease, immune dysfunction, and cognitive issues may be significant. Another example of “Public Health” officials mandating a one-size-fits-all solution based on flawed utilitarian (greatest good for the greatest number) logic.

BTW- the CDC does not address the issues directly, but instead focuses on the need for folic acid supplements for pregnant women, yet there are alternatives such as methylated folate, which is a natural form of folate and more like one would eat in whole foods. The problem is that 5-MTHF (methylated folate) and folinic acid most likely will improve folate status - but until clinical trials demonstrating fewer NTDs have been conducted, the CDC will not recommend them. As the CDC finds folic acid adequate, there is little incentive for the government to fund such studies. So, guidelines continue to recommend folic acid specifically. But there are many “methylated folate” supplements on the market.

Potassium bromate
Then there is potassium bromate in bread, which some commercial bakeries use to produce bread with a higher rise and firmer texture. It helps the dough hold gas during proofing and creates a uniform crumb and white color. Perfect for mass production!

Potassium bromate is classified as a possible human carcinogen (Group 2B) by the International Agency for Research on Cancer (IARC). Animal studies have linked it to kidney and thyroid tumors. The concern is that bromate residues can remain in finished bread if baking temperatures or times are inadequate to convert it to non-toxic bromide fully.

Potassium bromate addition to food is banned or restricted in the EU, UK, Canada, Brazil, China, Japan, and many other countries, but is still allowed to be used in the USA. So, this is another ingredient to check out when reading food labels. Specifically look for “potassium bromate” or “bromated flour.

BREAKING: Bill Gates Foundation Under Federal Investigation for ‘Aiding Foreign Enemies’ — Congress Warns of Prison and Asset Seizures

The walls may finally be closing in on Bill Gates.

The walls may finally be closing in on Bill Gates.

The once untouchable billionaire “philanthropist” is now facing serious questions from Congress, as the Bill and Melinda Gates Foundation comes under federal investigation for allegedly aiding foreign adversaries under the guise of charity.

According to a letter sent Monday by Senator Chuck Grassley, Chairman of the Senate Judiciary Committee, the Foundation is accused of funnelling tens of millions of dollars through overseas programs that may have benefited hostile foreign governments and organizations — a direct violation of U.S. nonprofit law.

While the Gates Foundation claims its global network of partnerships promotes health and equality, congressional investigators say the evidence tells a different story. According to recent reports, in just one fiscal year, the Foundation directed over $20 million to entities tied to the Chinese Communist Party, including government-controlled universities and corporations identified by the Department of Defense as working with the Chinese military.

HHS Builds $37.5M Bird Flu Pandemic Hospital Network—75 Facilities to Serve as Federal 'Special Pathogen' Centers

Internal NETEC document confirms H5N1 avian influenza preparedness at the core mission of new taxpayer funded hospital network.

The U.S. Department of Health and Human Services (HHS), through its Administration for Strategic Preparedness and Response (ASPR), is funding a $37.5 million national hospital expansion to prepare for H5N1 bird flu and other high-consequence pathogens, according to a newly released internal federal document issued by the National Emerging Special Pathogens Training and Education Center (NETEC).

NIH and NIAID—which are under HHS, led by Secretary Robert F. Kennedy Jr.—are funding experiments that create brand new bird flu pathogens, raising conflict of interest worries as well as questions about the government’s motives (see list of articles below this article detailing these many experiments).

NIAID chief Dr. Jeffery Taubenberger is directing U.S. tax dollars toward bird flu reverse genetics experiments while holding a patent for the carcinogenic BPL-based bird flu jab at the center of the Trump administration’s $500 million ‘Generation Gold Standard’ program—funding both the problem and the patented solution.