The genetic sequence found in Pfizer’s Modified mRNA slow kill bioweapon “vaccine” integrates into the human genome, and now all future “vaccinated” generations are genetically modified, as well as their offspring.
…whereby we now have irrefutable proof that not only were the highly carcinogenic and gene altering SV40 promotor sequences deliberately added by Pfizer to their PSYOP-19 Modified mRNA slow kill bioweapon “vaccine,” but they intentionally selected an especially deadly plasmid to inflict maximal damage; to wit:
🚨🚨🚨 Breaking #plasmidgate update. If you haven't seen this conversation you should. Pfizer not only hid the SV40 elements present in the plasmid used to produce its mRNA vaccine, but it DELIBERATELY chose a plasmid KNOWN to have functional SV40 elements to drive gene expression.
That means: ▶️The EMA lied. ▶️The TGA lied. ▶️Pfizer lied.
The two SV40 cassettes (inserts derived from one of the most carcinogenic viruses known) are in that plasmid because they were DESIGNED to maximise gene expression - going all the way back to 1980.
The problem is that they MUST NOT be used in human biological products because of the risk that when the DNA is "inactivated" (chopped up by DNAases), those elements are free to enter your cells and cause havoc - cell dysregulation with a significant risk of cancer.
They used these plasmids because they could get the most product out of their vats of poo (E Coli), not caring about the impact on the population but about profit vs expenditure. [2SG: the other component is willful depopulation and generating windfall profits from severe adverse events en route to premature death.]
Not only is that criminal in itself but lying to the EMA that "there were no functional elements" compounded the crime, because it was fraud. The elements are deliberately functional - even though they don't code for a separate protein, because they drive maximal gene expression. Exactly what you don't want in human cells.
The annotations below are from the EMA document submitted by Pfizer in 2020 - knowingly hiding the functional SV40 elements. After multiple warnings from people like @Kevin_McKernan and @DJSpeicher the EMA and TGA "investigated" but then lied about the elements, declaring them non-functional.
All to protect their own interests.
This conversation traces the origins of the plasmid and identifies the dual cassettes of SV40 regulatory sequences that were deliberately chosen to keep in the plasmid.
While the SV40 sequences may not be newly introduced and represent overlapping legacy sequences, it is at this point impossible to believe that this is some kind of innocent “contamination” mistake given that the researchers and C-suites at Pfizer and BioNTech as well as their Intelligence-Industrial Complex handlers (who happen to own most of the C-19 “vaccine” patents) all must have somehow not known just how dangerous these plasmids really are to humans.
In terms of SV40 promotor sequences integrating into the human genome, it extends well past the “vaccine” recipients, and genetically alters future generations as well:
When they found RNA/DNA from vax in placenta… I knew it was only a matter of time before Kevin McCairn would find this.
Not that the nucleic acids are causing it but that they are forensic tracer molecules for where the harm is going.
And given that the “vaccine” spike protein inhibits and disrupts the function of the natural p53 tumor suppression pathway, with p53 being a critical tumor suppressor encoded by the TP53 gene on chromosome 17, often referred to as the "guardian of the genome," combined with the addition of the SV40 promotor sequence being extraordinarily carcinogenic, what we have been witnessing is a twin-pronged turbo cancer attack on anyone that was subjected to these eugenics injections:
I asked Professor Angus Dalgleish (Professor of Oncology at St. George's University of London and one of the world's leading cancer immunologists) whether he believed the COVID vaccine was creating turbo cancers. He said yes, and that after reviewing over 400 publications on the subject the mechanisms are so numerous it's surprising there aren't more cases than we're already seeing.
He walked me through several of them. The vaccine suppresses T-cell response and switches the antibody system into a tolerant state, essentially converting the body into a condition similar to transplant readiness, where it won't reject a foreign organ and won't reject a cancer. It can integrate into the genome next to oncogenes. The Pfizer vaccine contains SV40, a known oncogene. It interferes with dozens of metabolic and signaling pathways that, when overstimulated, drive cancer and don't switch off.
The mechanism that concerns him most is the vaccine's ability to bind and silence tumor suppressor genes like p53 and BRCA. If someone already carries a natural mutation in one of those genes, their cancer arrives 20 or 30 years earlier than it otherwise would have. Interfere with more than two or three of these pathways simultaneously and you pull it forward even further, and when the cancer does arrive, the brakes are gone.
In nearly 40 years he said he's never seen anything like the presentations he's seeing now.
He said we should ban all mRNA vaccines, because they aren't vaccines, they're gene therapies, and giving them to children can interfere with their genome for the rest of their lives. He called allowing these products to go into young people, when we knew none of them were at risk of dying, criminal medical negligence and the crime of the century.
Oncology is now unsurprisingly the Medical-Industrial Complex and BigPharma’s biggest remaining cash cow.
Let us look at the overall mortality data:
Everyone must remember that we are still experiencing Excess Non-Covid Natural Cause Mortality of ~ 2700 deaths per week as of Week 18 of 2026, and rising into the summer months.
As the astute may notice, TES's models now 6+ years out, are DEAD ON ACCURATE ... The PFE is expressing almost exactly as we predicted. Actuarial agencies rewrote their training based upon TES's Covid analyses over the years.
We are closing in on 1 million Americans killed by an unacknowledged factor.
Something has been killing younger Americans to the excess for 5 years continuous now - since the mRNA vaccine inflection date of Week 14 2021 - and it is not Covid.
Those not dying are now disabled before prematurely dying…
🚨🚨 US Disabilities Hit an All-Time High of 37 Million In July: UP 23% Since Feb 2021!
The Signal No One Wants To See
The latest Bureau of Labor Statistics data is out, and the number of Americans ages 16 and over reporting a disability has hit a new all-time high of roughly 37 million. As of July 2026, the Current Population Survey series sits at 37,029,000. That’s not a rounding error or a seasonal blip. It’s the continuation of a trend that broke higher more than five years ago and has refused to mean-revert.
With a not insignificant amount of those with disabilities succumbing to VAIDS-induced turbo cancers, which brings us to the latest oncology data:
Disturbing US Cancer Diagnosis, Treatment, and Mortality trends continue.
Panel 1: 28.4% elevated PPI-Neoplasm Treatment Index (blue) with SEER-confirmed inflection in diagnoses through 2023 (orange)
Panel 2: 9.8% elevated cancer mortality with post-inflection inertia (exceptional uptick in last 6 weeks)
Panel 3: 25% elevation of mortality in younger ages (mitigated/hidden by LOWER rates in traditional older cancer cohort)
Panel 4: New Cancer Patient social chatter index exhibits alarming novel escalation: "Help Us!"
It is beyond me why authorities and the media cannot see the stark cancer inflection and elevated rates of mortality, treatment expense, and social chatter.
They fear the malicious hand of the coercive liars who run our society.
Tocotrienol and Tocopherol forms (all 8) of Vitamin E (400-800mg per day, 7 days a week). A product called Gamma E by Life Extension or Perfect E are both great.
Bio-Available Curcumin (600mg per day, 2 pills per day 7 days a week). A product called Theracurmin HP by Integrative Therapeutics is bioavailable.
Fenbendazole (450mg, 7 days a week) or in the case of severe turbo cancers up to 1 gram — for MEGADOSE 1,350mg-2,000mg/day — for prophylaxis one 150mg tablet once or twice per week
Ivermectin (24mg, 7 days a week) or in the case of severe turbo cancers up to 1mg/kg/day — for MEGADOSE 120mg-200mg/day — for prophylaxis one 12mg tablet once or twice per week
Hydroxychloroquine (10mg/kg/day 7 days a week) - for prophylaxis one 200mg tablet once or twice per week
ImmunX immune support which also greatly increases the bioavailability of both FenbendazoleandHydroxychloroquine (2 capsules per day) —for prophylaxis 2 capsules per day
Removing sugars and carbohydrates (cancer food) from your diet and replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX
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Fortunately we know that Fenbendazole effectively eradicates many turboCancers. In fact, my mother-in-law, original Case Report on fenbendazole.substack.com, had two Moderna mRNA covid shots in the summer of 2021 and developed metastatic breast cancer (lungs, liver, bones) by Nov 2021. She was cancer-free within 4-6 months on daily 222 mg fenbendazole. What is less well-known is that in 2009 she had a bilateral radical mastectomy. So how did a woman with no breast tissue get metastatic breast cancer in 2021? Cancer cells were likely released into circulation by the surgery, embedded throughout the body and held dormant by her immune system - she took high dose (5000 IU vitD3) post surgery since 2009 - mRNA shots activated, then exhausted, her immune system leading to the release of that immune inhibition causing the catastrophic appearance of multiple histologically-confirmed, hyper-aggressive breast cancer tumors…turboCancer. Again, the story has a happy ending: Fenbendazole cured her cancer, a cancer that appears to have also been covid shot-induced turboCancer.
Fortunately we know that Fenbendazole effectively eradicates many turboCancers. In fact, my mother-in-law, original Case Report on fenbendazole.substack.com, had two Moderna mRNA covid shots in the summer of 2021 and developed metastatic breast cancer (lungs, liver, bones) by Nov 2021. She was cancer-free within 4-6 months on daily 222 mg fenbendazole. What is less well-known is that in 2009 she had a bilateral radical mastectomy. So how did a woman with no breast tissue get metastatic breast cancer in 2021? Cancer cells were likely released into circulation by the surgery, embedded throughout the body and held dormant by her immune system - she took high dose (5000 IU vitD3) post surgery since 2009 - mRNA shots activated, then exhausted, her immune system leading to the release of that immune inhibition causing the catastrophic appearance of multiple histologically-confirmed, hyper-aggressive breast cancer tumors…turboCancer. Again, the story has a happy ending: Fenbendazole cured her cancer, a cancer that appears to have also been covid shot-induced turboCancer.
Great summary 2SG! Of discoveries which many of us suspected regarding dangerous and gene editing, life shortening experimental mRNA injections.
I wonder why Pfizer, Moderna etc, don't sue you (us) for defamation. They can't afford the truth to be aired in a public forum.
Unjabbed Mick. We live longer!