As this Substack has been diligently reporting every since the Modified mRNA slow kill bioweapon “vaccine” rollout, the world has been in the midst of a turbo cancer epidemic across all demographics…
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 …
Under new MAHA leadership, the criminally corrupt FDA is finally looking into their Emergency Use Authorization (EUA) “vaccine” fraud, and how these murderous depopulation injections are impacting children, long after much of the gene altering damage has been done (by the very same FDA, and their BigPharma and Intelligence-Industrial Complex partners-in-crime):
Cancer. Child deaths. DNA contamination.
FDA leadership is now investigating reports of children dying after COVID shots, while case reports show cancers emerging shortly after vaccination.
Meanwhile, scientists uncovered DNA fragments in the vaccines—levels regulators never flagged.
And with safety questions mounting, CDC advisers admit the shots don’t even behave the way the public was told.
🧵 THREAD
The Food and Drug Administration is mulling over conducting its own evaluation of the levels of DNA in COVID-19 vaccines, an FDA official has disclosed.
“I’ll say that that is something that’s being discussed,” Dr. Tracy Hoeg, a senior adviser to the FDA’s commissioner, told members of the Centers for Disease Control and Prevention’s vaccine advisory panel on Sept. 19.
Before the panel’s members unanimously recommended during the meeting that the CDC roll back COVID-19 vaccine recommendations, a number expressed concerns about growing evidence of higher-than-allowed levels of DNA in the vaccines, the spread of the vaccine beyond the injection site, and the long-term persistence of messenger ribonucleic acid (mRNA)—a key part of the Pfizer-BioNTech and Moderna shots.
The CDC has described mRNA as the entity teaching cells how to make copies of the spike protein to enable protection when the real virus, with its own spike protein, attacks the body.
“After the mRNA delivers the instructions, your cells break it down and get rid of it,” a CDC graphic states.
Retsef Levi, chair of the advisory panel’s COVID-19 immunization workgroup, showed the graphic during the meeting.
“We have a range of things on the mRNA platforms that really suggests that it doesn’t work as intended,” Levi said, citing issues such as the spread of spike protein and mRNA into various parts of the body and “DNA contamination.”
Some scientists, including former Johnson & Johnson scientist David Wiseman, said they were concerned about the impact of residual DNA left behind by the sequence, which had been used in the past for manufacturing other drugs.
That DNA could integrate into the human genome and create autoimmunity problems, Kevin McKernan, who has confirmed the presence of residual DNA in COVID-19 vaccine vials, told The Epoch Times.
“With over a billion doses of the mRNA vaccines administered, no safety concerns related to the sequence of, or amount of, residual DNA have been identified,” a spokesperson said at the time.
“With regard to the FDA-approved mRNA vaccines, available scientific evidence supports the conclusion that they are safe and effective.”
While the sequence has not been detected in Moderna’s vaccine, other testing has found DNA in both the Pfizer and Moderna shots.
McKernan and other researchers in a paper published on Sept. 6 said they found levels of residual DNA in vaccines from the companies that were higher than the regulatory limit set by the FDA.
Why Not Withdrawn?
Dr. Kirk Milhoan, another member of the CDC vaccine advisory panel, said during the meeting that he was “shocked at the lack of pharmacological rigor in dosing,” including dose accumulation, as well as the evidence that the vaccines were contaminated.
“Why is this not pulled off [the market] like any other biologic or medicine that is found to have contamination?” he stated.
Hoeg, the FDA official, told him that some of the relevant information is proprietary.
“I will say the information that we have been provided by Pfizer and Moderna, and what was shared with me, is what they provided to the FDA; it was within the regulatory limits,” she said.
“I will also acknowledge that this is something we take very seriously, and I want to sincerely thank the independent researchers, many of whom I know, who have brought this issue to the public’s attention.
“And at the FDA, we take the public’s safety and the safety of these products incredibly seriously. And I just want to give you all that message that this is not something that is being ignored.”
That’s when Milhoan asked whether the FDA planned an independent evaluation of the products.
“I’ll say that that is something that’s being discussed,” Hoeg said.
“Again, we want to communicate that we take this issue very seriously and thank everyone who has brought this to our attention.”
The new FDA leadership withdrew the emergency authorization for the COVID-19 vaccines but approved them for limited groups, citing a need for the companies to run trials proving effectiveness in younger, healthier populations.
The FDA’s commissioner also announced recently that the agency is investigating reported child deaths following COVID-19 vaccination.
“The shift in focus and openness to investigation of these issues is new,” Dr. Robert Malone, another CDC adviser, told The Epoch Times.
“Previously, the FDA was unwilling to look at issues such as lot consistency and adulteration in these products, and that’s just not consistent with established regulatory norms,” he added later.
The FDA did not respond to a request for comment by the time of publication.
Levi wrote on X that the discussions during the meeting were the first time the advisory panel went over “critical risks and uncertainties like immune response to repeated boosting, biodistribution, pharmacokinetics, and potential impurities.”
Levi and Milhoan, before they were appointed to the panel, called for the Pfizer and Moderna vaccines to be withdrawn. Malone in 2023 said that regulators should withdraw the Pfizer vaccine due to the presence of the DNA sequence, which he said made the product adulterated.
What the Companies Said
Darin Edwards, a Moderna executive, told advisers during the meeting that outside testing of the vaccines has been flawed.
“Part of our release testing is [the] detection of DNA in each lot,” he said. “We use industry-standard methods to perform these assessments. That is specific to DNA and does not detect RNA, which is a flaw and a problem with some of the other methods cited.”
A Pfizer official added: “We did measure residual DNA within our product, and our assay was validated to be specific for residual DNA and not RNA within the product.”
Dr. Wafik El-Deiry, director of the Legorreta Cancer Center at Brown University, said in a presentation to the panel that the FDA limits for DNA were for “naked DNA,” or unencapsulated DNA. The COVID-19 vaccines are encapsulated by lipid nanoparticles to help prolong the mRNA so it can teach the body.
Malone asked the companies during the meeting: “The thresholds that were used to establish that you were within allowed parameters, are those that the FDA determined as acceptable for naked DNA?”
“The thresholds were developed for our product,” a Pfizer representative said.
“The product thresholds are for our specific product,” Edwards said.
Dr. El-Deiry’s Response
El-Deiry told The Epoch Times in an email that he interpreted the comments as the companies using certain quality control assays that suggested to them that the DNA impurities were within FDA limits.
“The sensitivity of their assays has been questioned and clearly multiple others have identified DNA impurities that exceed the 10 ng FDA limit, and such DNA was present after they eliminated RNA by using powerful ribonucleases,” or enzymes, El-Deiry said.
While the exact impact of the impurities remains unclear, a number of case reports and case series have described cancer developing in vaccinated individuals shortly after vaccination, El-Deiry told the panel.
A Moderna representative told the committee: “We note that one of today’s presentations includes assertions not aligned with the broader scientific evidence. Some conclusions extend beyond what referenced studies support or are contradicted by careful reading.
“Others appear based on isolated case reports that are presented without relevant clinical context, or omit a larger body of evidence to the contrary.”
The panel later voted to recommend that people should only receive COVID-19 vaccines after consulting with health care providers and considering individual factors, such as whether they have an underlying condition, such as obesity.
Members also said the CDC should add more information about the vaccines to information statements, including that “prolonged and persistent exposure to spike, mRNA and nano-lipids particles is associated with post-vaccine syndrome (PVS) injuries as well as potentially other side effects that are currently only partially understood,” and that doctors should discuss such risks, as well as benefits, before proceeding with vaccination.
Not a single vaccine is safe, effective or necessary, but the “free” PSYOP-19 EUA Modified mRNA injections are particularly destructive, and are driving the highly profitable turbo cancer epidemic — this is irrefutable now.
The CDC and FDA are criminal agencies that must be shut down, and their respective “leadership” need to be indicted, arrested and prosecuted to the full extent of the law, except that in a two-tiered Banana Republic judicial system, it is exceedingly improbably that justice will ever be served; in fact, these depopulation injections have still not been pulled from the market.
And yet there is hope nonetheless, because turbo cancers as well as Alzheimer’s, mood disorders, Parkinson’s and the various other “vaccine” adverse events may be attenuated and cured using the following treatment strategy:
New & Improved Joe Tippens Protocol
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 (300mg, 6 days a week) or in the case of severe turbo cancers up to 1 gram — 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 prophylaxis one 12mg tablet once or twice per week
VIR-X immune support (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 FLAV-X
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When will WE put a stop to this murderous, genocidal and democidal enterprise by the ***shylocks***.?? All means are fine with these monsters to decimate and eliminate us Christians first followed by the rest of the world. - All four poison factories - moderna - pfizer - johnson & johnson - astra zeneca - are the creation of these outcasts and managed by them. Arrest them, accuse them of mass murder, convict and condemn to meet Mr Guillotine, in Public Place, good riddance for the whole world.
When will WE put a stop to this murderous, genocidal and democidal enterprise by the ***shylocks***.?? All means are fine with these monsters to decimate and eliminate us Christians first followed by the rest of the world. - All four poison factories - moderna - pfizer - johnson & johnson - astra zeneca - are the creation of these outcasts and managed by them. Arrest them, accuse them of mass murder, convict and condemn to meet Mr Guillotine, in Public Place, good riddance for the whole world.
Trillion dollar question. When will the sheep catch on to this?