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.
These Pfizer genetic sequences will be passed on forever in not just the “vaccinated,” but, also, in the offspring of unvaccinated individuals procreating with those that have been genetically modified.
And now, for the first time ever, it has been irrefutably proven that DNA contamination from these “vaccines” is not some accidental “contamination” or benign artifact, but, rather, a ticking time bomb that will permanently alter the genetic fabric of humanity.
We have evidence that the SV40 promotor sequences that were deliberately added to Pfizer’s deadly “vaccine” are aggressively replicating inside the very tumors that they are causing, thus accelerating the metastization of VAIDS-induced turbo cancers; to wit:
Pfizer’s vaccine sequence has turned up in biopsies – biopsies from vaccinated individuals who later developed tumors.There were identified SV40 sequences from Pfizer’s vaccine in those tumors. And it’s not diluted. It’s at a copy number so high it looks like it’s replicating inside these tumors. This isn’t just DNA lingering; it’s integrating and growing.
We’re seeing disturbing trends. Increased cancers, immunosuppression, lymphocytopenia – our immune systems are being degraded. And yet, our health agencies refuse to face the obvious. They pretend this is all perfectly normal. They don’t want you to question anything. But the signs are there, and they’re terrifying.
Regulators, from the EMA to Health Canada, claim these contaminants don’t matter, aren’t functional, aren’t an issue. But they know. Internal emails reveal their panic, their requests for Pfizer to clean up its DNA, only to be met with excuses. Pfizer doesn’t even have a proper test to measure DNA length in these vials. They’re giving us half-truths and lies.
The science is unequivocal: DNA fragments, in lipid nanoparticles, can integrate into human genomes. Chronic exposure to foreign DNA, floating in the cytosol, triggers a cascade of immune responses that can lead to cancer. This isn’t just my opinion; it’s backed by literature, and it’s blatantly ignored by regulatory agencies.
We’ve heard excuse after excuse from regulators. “It’s too little to matter,” “It won’t enter cells,” “It won’t reach the nucleus.” Each claim has fallen apart. They retreat at every challenge, changing the story to suit their agenda. The fact is, they know the truth, but they won’t admit it. It’s a deliberate cover-up on a scale we’ve never seen before.
This is no longer about health. This is about power, control, and deceit. The regulators are defending their sponsors, rewriting guidelines, hiding behind blacked-out documents. They’ve crossed a line. This isn’t just a scandal. This is RICO territory. This is collusion, manipulation, a violation of our basic rights and trust.
To everyone reading this: our health agencies have abandoned us. They’re complicit in the greatest violation of medical ethics in modern history. Do not trust their lies. Demand transparency. Refuse to be silenced. We must hold every single one of these actors accountable. This isn’t just a mistake; it’s a crime against humanity.
The video transcript:
So here is the shocker, is that we recently were given cancer biopsies to look at this, because our thinking— if you look through the previous literature on this — if you look in all the wrong tissues you won’t find this.
You have to think about where are you most likely to find such events, and in my opinion that’s probably in a tumor, because tumors tend to grow aggressively. And if it happens to be an immunogenisis event it will overwhelm the tissue in terms of copy number, so you’re more likely to find this in tumors; let’s go looking under the lamp post here.
So we got a colon biopsy from a group in Germany that we’ve been working with, and we were quite shocked by the results. This is a person vaccinated four times by Pfizer. One year since vaccination: tumors emerge. Person dead within a month.
We got three biopsies out of them. One postmortem. All of them have SV40 in the origin of replication from the Pfizer vaccine. We performed some sequencing which we’re going deeper on right now, but even at preliminary sequencing shows this is in fact Pfizer’s vaccine. There are sequences in there from spike and other places.
Now, what is shocking in this work is we were never expecting to find the DNA at the copy number greater than the human genome; like if you get an insertional mutagenesis event and that is a driver mutation, that means that tumor is taking off — the insertional mutation should be at the same copy number as another human gene.
What we were expecting to find was that maybe 10 or 20% of the tumor was actually mutated; therefore, it would come out later on PCR that our human gene— we’re seeing the opposite here: this has expanded inside the patient, and that if we— we’re getting signals inside the PCR that are so hot that it looks like we actually have amplified the vaccine directly from the vial, and that’s impossible.
That means after you inject someone with 300 microliters — this person got 4 (Pfizer doses), so 1.2mL’s — you should have a 64,000 fold dilution into their body. So we should see 6CT shift, and where this PCR signal comes out from dilution alone. We don’t see that. We see something where it’s coming in at the same concentration as the original vial, or higher.
That tells us the DNA is replicating.
That tells us the mammalian origin of replication that is in Pfizer’s vaccine is active in human tumors.
So, this filed up. It’s not peer-reviewed. We doing deeper sequencing now, but this may explain shedding…
It is important to appreciate that while shedding may sicken an unvaccinated person with the spike proteins (SP2), it will, unlike the source of the shedding, in no way genetically alter their DNA. So while an unvaccinated person being shed upon is certainly not a particularly optimal situation, they still remain '“pure-blooded.”
The implications are staggering:
Turbo Cancer Epidemic: Aggressive cancers are appearing in vaccinated individuals at an alarming rate, fueled by the DNA integration and the spike protein's suppression of tumor-suppressor pathways.
Generational Impact: Once integrated into the genome, this DNA is heritable, meaning the genetic modifications will persist in offspring.
Immune System Degradation: Alongside the cancer risks, we are seeing immune suppression, lymphocytopenia, and a cascade of immunological dysfunctions that leave individuals vulnerable to diseases they could once fend off.
Anyone who received even a single dose of Pfizer’s C19 “vaccine” is irreparably genetically harmed, as are their progeny.
While the Pfizer genetic mutations can never be reversed, the associated lifelong VAIDS symptoms may be effectively managed and kept at bay with a synergistic treatment approach that to readers of this Substack is well known.
In the face of this unprecedented global eugenics bioterrorism escalation, Ivermectin and Fenbendazole emerge as lifesaving interventions. Their mechanisms are proven, affordable, and safe.
Why Ivermectin and Fenbendazole Work
Ivermectin, initially developed as an antiparasitic, is a masterclass in cellular warfare
Targeting Cancer’s Command Center
Ivermectin interrupts the WNT/β-catenin signaling pathway, a crucial mechanism that cancer cells exploit for growth and invasion.
Imagine cancer as a rogue army. Ivermectin destroys their communication lines, leaving them isolated and vulnerable.
Triggering Cancer Cell Suicide
Through apoptosis (programmed cell death), Ivermectin forces cancer cells to self-destruct.
It’s like hitting the “eject” button on a self-destructive machine.
Starving Cancer Cells
By disrupting glucose transporters, Ivermectin cuts off the energy supply to cancer cells, which are notoriously sugar-hungry.
Cancer cells are like gas-guzzling SUVs; Ivermectin shuts down their fuel pumps.
Fenbendazole - The Cellular Scaffolding Destroyer
Known as a veterinary antiparasitic, Fenbendazole has emerged as a potent cancer-fighting agent
Dismantling Cancer’s Skeleton
Fenbendazole binds to beta-tubulin, collapsing the microtubule scaffolding that cancer cells need in order to divide.
It’s like removing the support beams from a collapsing building.
Cutting Off Cancer’s Sugar Addiction
Fenbendazole interferes with glycolysis, the sugar-metabolism process cancer cells rely on to thrive. Cancer cells are reckless sugar addicts; Fenbendazole shuts down the candy store.
Fenbendazole reactivates p53 - the tumor suppressor disabled by spike proteins - giving the body its natural defense mechanism back. p53 works like a security system. When a cell becomes damaged or abnormal, p53 steps in, assesses the situation, and decides whether to repair the cell or shut it down permanently.
The revelations from two bombshell studies highlight the catastrophic failures of mRNA vaccines
Spike Protein Sabotages p53
Known as the “guardian of the genome,” p53 repairs DNA damage and prevents precancerous cells from becoming malignant. The spike protein not only suppresses p53 but also blunts chemotherapy’s effectiveness.
Unchecked, this leads to explosive cancer growth.
SV40 Promoter and DNA Integration
The SV40 promoter, a known oncogene activator, was found contaminating vaccine lots at levels far exceeding regulatory safety limits. This sequence facilitates genetic integration and cellular dysfunction. In lay terms, this contamination acts as a cancer trigger embedded in every dose.
Together, these findings explain the global surge in turbo cancers: aggressive, treatment-resistant malignancies appearing post-vaccination. This is not just a public health crisis; it’s a betrayal of humanity.
The Synergistic Power of Ivermectin and Fenbendazole
When combined, Ivermectin and Fenbendazole deliver a one-two punch to cancer:
It’s like Special Ops in action - Ivermectin disrupts the bad guys’ operations, and Fenbendazole demolishes their hideouts.
The enhanced protocol developed by Dr. Makis demonstrates the potential of aggressive dosing for severe cases
Ivermectin: 1–2 mg/kg/day, gradually increasing for maximum effectiveness.
Fenbendazole: 888 mg/day, a significant increase over the New and Improved Tippens Protocol.
A man in his 60s diagnosed with early-stage prostate cancer (Gleason 7, 3+4 and 4+3), with bilateral disease involving the prostate apex and base. Major U.S. cancer centers offered him two grim options: invasive prostatectomy or radiation treatment. Both promised debilitating side effects and no guarantees of a cure.
After the patient followed the Joe Tippens Protocol (222 mg/day Fenbendazole), Dr. Makis introduced an enhanced protocol:
Ivermectin - Starting at 1 mg/kg/day and increasing to 2 mg/kg/day.
Fenbendazole - Increased to 888 mg/day, or 1 gram.
Liver and kidney function tests remained normal, with only a slight bilirubin elevation, showing the protocol’s safety.
In just 35 days
PSA levels dropped from 4.4 to 2.46—the lowest in two years.
This 44% reduction occurred without invasive procedures or chemotherapy.
The patient’s bilateral prostate disease showed significant regression.
Dr. Makis’ findings are not isolated. They reveal the suppressed potential of affordable, off-patent drugs that could revolutionize oncology. Yet, oncologists either deny knowledge of these treatments or outright lie about their risks—a damning indictment of a profit-driven healthcare system.
This approach has shown unparalleled success in even aggressive cancers, providing a template for future treatment guidelines.
Big Pharma’s Stranglehold and Why The Simple Solutions Are Suppressed
The success of Ivermectin and Fenbendazole against cancer—and their potential to combat vaccine-induced harm—poses an existential threat to Big Pharma. These drugs are cheap, off-patent, and widely available. They represent the very antithesis of the pharmaceutical industry’s profit-driven model, which thrives on chronic conditions, expensive treatments, and lifelong dependency.
While there is no possible way to reverse the genetic modifications caused by the Pfizer “vaccine,” the following protocol will attenuate the relentlessly persistent VAIDS fallout from this horrific condition, and it will also protect those that have remained genetically pure and unaltered:
The incoming administration under RFK Jr. represents a once-in-a-lifetime chance to tear down the corrupt Medical Industrial Complex systems that have enabled this public health catastrophe.
Championing Affordable Treatments
By endorsing and funding research into Ivermectin, Fenbendazole, and similar therapies, the administration can expose the pharmaceutical industry’s lies and offer genuine hope to millions.
Accountability for Vaccine Manufacturers
The SV40 promoter contamination and spike protein revelations demand a full investigation and legal action against those responsible. This is not just a public health issue; it’s a matter of justice for the countless lives harmed or lost.
Restoring Trust in Healthcare
Transparency, accountability, and a commitment to evidence-based medicine can rebuild the public’s trust in healthcare—a trust shattered by the vaccine scandal.
A complete and outright ban of the entire Modified mRNA platform is long overdue. Mass arrests of not just the BigPharma C-Suites, Fauci, Gates, GAVI, the various “nonprofits,” WHO, UN, NIH, UN, CFR, the MSM quislings, but also the Intelligence Industrial Complex as a whole given their C19 patents, total complicity and direct involvement in the PSYOP-19 scamdemic and associated DEATHVAX™ democide project.
But the first step in achieving justice is to become as healthy and as hard to kill as possible.
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They want you dead.
Do NOT comply.
