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.
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.
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 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.
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.
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.
https://panagispolykretis.substack.com/ ... -unveilingBREAKING: 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.
https://www.thefocalpoints.com/p/breaki ... rson-studyThis 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.
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