For many years now this Substack has been warning of the burgeoning turbo cancer epidemic as a direct result of the PSYOP-19 gene altering Modified mRNA slow kill bioweapon “vaccines…”
This Substack has been covering the surging rise in DEATHVAX™ induced adverse events and VAIDS, with a particular emphasis on the phenomenon referred to as turbo cancer.
As this Substack has been warning for many years now, the turbo cancer epidemic is only now getting underway as a direct function of the Modified mRNA slow kill bioweapon “vaccine” platform that was foisted on humanity during the PSYOP-19 scamdemic; in other words, cancer rates will continue to explode, and the genetically modified young people will be …
…and now we have even more irrefutable evidence that these depopulation injections are driving this exploding cancer scourge.
Before we get to today’s featured article, let us review some other germane recent developments that are truly horrifying and further establish that not only is this entire PSYOP-19 gene altering “vaccine” program a deliberate crime against humanity, but the entire legacy vaccine industry is too:
🚨🚨🚨 Just one paragraph in this shocking paper exposes the whole vaccine adjuvant industry.
What it means is that adjuvants were used - deliberately - to transport residual DNA into cells to create an immune response using oncogenic pathways.
I’ll say that in more verbose terms.
Every human cell has a DNA sensing mechanism that will activate if foreign DNA gets into the cell, to protect your cells from that foreign DNA. If it is activated if sets off an extreme immune response but that immune response cannot keep getting activated - if it does you risk developing cancer in those cells.
The mechanism is cGAS-STING and it has a sister TLR9-MyD88.
And the vaccine industry KNEW that adjuvants work by activating them. And they KNEW that they are oncogenic. And they didn’t care because they also KNEW that activating this pathway will induce antibodies - and the presences of antibodies (irrespective of whether they provide immunity) is what drives the FDA approvals and thereby the cash.
So if you are asking why cancer rates have been skyrocketing in young people and why this has been happening even before COVID, this provides an explanation that every molecular biologist should have been shouting from the rooftops.
And the worst thing?
That every recombinant vaccine (which by necessity contains unknown amounts of residual DNA) is potentially affected. And they have been in use since Engerix B in 1968.
What has this got to do with adjuvants?
Well, while you were all distracted with Aluminium and its neurotoxic effects, what the vaccine industry didn’t tell you was that Aluminium, Triton, Saponins, polysorbates and LNPs are all “transfection agents” - literally microscopic carriers that carry DNA (that shouldn’t be there) into cells (that shouldn’t be subjected to it).
And that process, described in this paper but happening every day in those injected with residual DNA and a transfection agent, is what this paper shows provides rocket fuel to a cancer.
And THAT is why the pharma industry went crazy when we exposed #plasmidgate.
They didn’t want anybody to know.
Don’t believe me? Grok this tweet and watch Grok squirm.
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.
…and all vaccines were laced with plasmids that integrate via cGAS-STING and TLR9-MyD88 pathways with adjuvants activating them, and thus all of these vaccines are highly oncogenic.
❌❌❌ BOMBSHELL NEW PAPER ❌❌❌ THIS IS WHY IT TAKES 10 YEARS FOR NEW BIOLOGICALS TO GET APPROVAL FOR MARKET USE.
“LNP injection triggered acute neutrophil accumulation in the lungs, driven by the release of mitochondrial DNA (mtDNA) from necrotic muscle cells at the injection site. This mtDNA-mediated signaling activated the TLR9-MyD88 and cGAS-STING pathways ... which facilitated the establishment of a pro-metastatic niche.”
Combining SV40 promotor sequences with adjuvants ensured that the turbo cancer epidemic we are now witnessing would be yet another cash cow for BigPharma all while stealthily reducing the population; to wit:
My God. This is a War Crime.
Dr. Weinstein explains that our world was injected with the SV40 virus, which leads to cancer, in his conversation with Joe Rogan.
There MUST be arrests for this EGREGIOUS Attack on Humanity.
Shame on Bill Gates and Dr. Fauci. Shame on you both.
“Free” vaccines courtesy of the tax slaves paying for their own demises, but, hey, some sociopaths got rich at the expense of large swaths of society getting poisoned and prematurely dying in their mass ritual bio-suicides at the alters of $afe and Effective and Trust the $cience:
Between denial of Covid treatment for US Citizens, as a tactic employed to get the vaccine EUA approved... along with the host of poor decisions that were made on our behalf... and finally the vaccine fatality rate now underway and escalating...
We have killed 1.58 million Americans... not including Covid mortality.
But hey, that bought a lot of BMW's and funded a lot of Globzi social initiatives - so we got that going for us.
The most comprehensive analysis to date examining the link between mRNA “vaccines” and cancer identifies convergent mechanistic, clinical, and population-level evidence of turbo cancer.
Cancer is rising at an increasingly alarming pace. Early-onset malignancies are climbing in younger adults, aggressive cancers are appearing in patients with little warning, and U.S. cancer mortality has departed sharply from its pre-pandemic trajectory. Against this backdrop, one of the most important questions in medicine is whether the unprecedented mass deployment of nucleoside-modified mRNA technology could be contributing to cancer initiation, reactivation, or accelerated progression.
In the most comprehensive analysis to date examining the link between mRNA “vaccines” and cancer, we brought together mechanistic biology, published clinical cases, large population cohorts, U.S. cancer-incidence data, and national mortality records to evaluate whether these gene products could induce, accelerate, or unmask malignancy.
The findings converge on the same alarming picture: TURBO CANCER IS REAL.
And the implications extend far beyond COVID-19 vaccination, because the same underlying mRNA technology is now being pushed directly into cancer treatment.
Below is a concise breakdown of what we found:
MECHANISTIC EVIDENCE
We identified 35 distinct cancer-promoting mechanisms converging through 4 major routes: (1) protooncogene activation, (2) mutation pressure, (3) protein–protein interaction network interference, and (4) cancer stem-cell clonal acceleration.
Key mechanisms include EGFR/RAS/MAPK and STAT3–MYC activation, p53/BRCA suppression, impaired DNA repair, residual plasmid DNA and SV40 regulatory elements, LINE-1 reverse transcription, m1Ψ-associated frameshifting, chronic LNP inflammation, immune suppression, and cancer stem-cell expansion—pathways capable of promoting genomic instability, uncontrolled growth, immune escape, dormancy reactivation, and metastatic outgrowth. The full inventory of cancer-promoting mechanisms can be found in Table 4 of our study.
Our central concurrent-hit model proposes that these processes do not necessarily operate independently or sequentially. Multiple cancer-promoting hits overlap in the same susceptible host, compressing the time required for dormant, indolent, or microscopic disease to become clinically aggressive.
CLINICAL EVIDENCE
The published clinical literature includes 333 documented turbo cancer cases across 27 countries, involving lymphomas, leukemia, melanoma, breast cancer, lung cancer, glioblastoma and other glial tumors, sarcomas, and pancreatic cancer. The vast majority of these cases occurred following COVID-19 vaccination, with a minority following SARS-CoV-2 infection.
Approximately 86% of the post-vaccination cases occurred after nucleoside-modified mRNA products—about 56% after Pfizer-BioNTech, 25% after Moderna, and another 5% after exposure to both mRNA products across different doses.
Across these cases, recurring patterns include rapid cancer progression, short-latency recurrence, reactivation of previously controlled disease, and tumors involving the injection site or nearby draining lymph nodes.
Lymphoid malignancies represent the largest category in the published case literature, while glioblastoma and pancreatic adenocarcinoma were among the cancers most consistently associated with reports of unusually rapid progression.
POPULATION EVIDENCE
The population-level evidence reinforces these clinical and mechanistic signals.
OUR CDC WONDER ANALYSIS: At least 119,130 EXCESS U.S. CANCER DEATHS, rising to approximately 153,000–197,000 after accounting for mortality displacement.
INDEPENDENT CDC WONDER ANALYSIS: 154,330 excess U.S. cancer deaths, closely matching the lower end of our corrected range.
UNITED STATES (SEER): Early-onset cancer incidence surged 6.4% in just 2 years, from 2021–2023, alongside sharp increases in brain and nervous-system tumors (+19.5%), colorectal cancer (+19.4%), small-intestine cancer (+15.5%), ovarian cancer (+12.8%), stomach cancer (+7.3%), and female breast cancer (+3.6%).
SOUTH KOREA: A nationwide cohort of 8.4 million people found vaccinated individuals had an increased 1-year cancer risk across 6 cancer types: thyroid, gastric, colorectal, lung, breast, and prostate cancer.
ITALY: Vaccinated residents had a 23% higher risk of cancer hospitalization, with an adjusted hazard ratio of 1.23 compared with unvaccinated residents.
These findings come from entirely different data streams and study designs, yet they repeatedly point toward the same concern: accelerated cancer emergence and progression following the era of widespread mRNA exposure.
mRNA ONCOLOGY DANGER
The very mRNA platform now linked in our paper to 35 oncogenic mechanisms is being repurposed to treat cancer itself.
Modern individualized mRNA cancer products encode patient-specific mutated tumor proteins and package them into RNA delivery systems designed to generate a strong immune response against those targets.
But the fundamental safety problem remains: where does that encoded antigen actually get expressed?
The platform can distribute systemically, causing vulnerable tissues including the heart and brain to express tumor-derived antigens—raising the risk of off-target immune attack, cardiac injury, and neurological damage.
Even more concerning, the LNP delivery vehicle itself promoted metastatic outgrowth in mice even without mRNA cargo, suggesting that some oncologic liabilities reside in the platform itself—not only the encoded antigen.
And now the first randomized test of individualized mRNA as monotherapy in residual cancer has FAILED. The Phase 2 BioNTech BNT122-01 trial enrolled 327 patients with molecularly confirmed residual colorectal cancer, crossed its futility boundary, and was terminated due to a mortality imbalance.
This matters enormously because these therapies are being moved into precisely the patients most vulnerable to accelerated disease: people already subjected to multiple mRNA boosters with residual cancer and genomic instability.
OUR CALL
On the combined weight of the mechanistic, clinical, and population evidence, we call for IMMEDIATE MARKET WITHDRAWAL of nucleoside-modified mRNA-LNP products from broad preventive use and a halt to their expansion into adjuvant and neoadjuvant cancer treatment.
35 mechanisms. Hundreds of documented turbo cancer cases across 27 countries. Up to ~197,000 excess U.S. cancer deaths by our analysis. A failed randomized mRNA cancer trial. And the same technology is now being pushed deeper into oncology.
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
Do NOT comply.
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