Start with the basics...why dna mutations lead to cancer and how the healthy immune system corrects it.
https://youtu.be/c34f6lYJ690?si=P8LMrBV2Lwr39AuN
Then...proof there are dna fragments in the covid shots...
Proof the fragments translated into dna mutations.
Proof the immune system is altered by the covid vaccines, making it harder for the immune system to prevent the mutation from becoming cancerous.
Here is this to get started.
https://gettr.com/comment/c275f476081
Under-oath Senate testimony https://youtu.be/IEWHhrHiiTY?si=Kuh8NJcM0705sT6s
Start at 3:30. He says he sequenced it himself and found the DNA fragments
Then at 5:08 he said it is likely that the dna fragments permanently integrate into the vaccinated person's dna.
6 min. Possibly causes cancer
He said rare but possible.
Dna is permanent, maybe a lifetime. RNA is temporal.
The more pieces of dna in the vaccine, the more opportunities the dna has to modify the genome of the vaccinated person.
At 10:20 Shows the dna plasmid that Pfizer used to clone spike proteins.
Problem is, they didn't remove the dna fragments they had used to replicate the RNA. That is how the contamination happened.
Modifying genomes using DNA grown in bacteria increased production speed of the RNA and reduced cost (versus using synthetic DNA being used to grow RNA).
They didn't seem to care that this practice is hazardous.
Pfizer did know this was unsafe, because they deliberately broke up the DNA into euqal-sized fragments and did not report it to the FDA.
More under-oath testimony on the dna fragments
https://gettr.com/post/p2vr5zu9601
Here is the part about the boosted IgG4 antibody immune cell getting hyper busy shutting off the immune system. When this antibody is overdeveloped, turbo cancers result because the immune system doesn't do its daily clean-up of mutations.
https://www.igor-chudov.com/p/booster-caused-immune-tolerance-explains?utm_campaign=post_embed
UK cancer stats
https://makismd.substack.com/p/turbo-cancer-data-pfizer-and-moderna
https://www.bitchute.com/video/tc41BOL241ir/
Good at 11:18.
Particularly 14:18 where he discusses how it translates into the genome.
Wow. This is startling. Thanks for posting it.
Sustained presence of nms-mRNA in the cytoplasm deregulates endogenous transposable elements (TEs), leading to reverse transcription of the vaccine-mRNA. Intracellular accumulation of the nms-mRNA and the reverse transcribed cDNA molecules triggers intrinsic cytosolic RNA and DNA sensory pathways. Simultaneous activation of these pathways initiates a coordinated innate response against both types of non-self nucleic acids, prompting type-I interferon and pro-inflammatory cytokine production which if unregulated, leads to autoinflammatory and autoimmune conditions. Activated TEs increase the risk of insertional mutagenesis of the retrotranscribed vaccine mRNA, which can disrupt coding regions, enhance the risk of mutations in tumour suppressor genes, and lead to sustained DNA damage.