It was a planned genocide. It was mass murder. They murdered our friends, family and loved ones and they didn't care. They did it for money. No amnesty. Never ever forget what they have done to the children. Your children. Your grandchildren.
 
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https://pubmed.ncbi.nlm.nih.gov/21568886/

Aluminum vaccine adjuvants: are they safe?​


Abstract:

Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science's understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted.

Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences.

In our opinion, the possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated, has not been rigorously evaluated in the medical and scientific community. We hope that the present paper will provide a framework for a much needed and long overdue assessment of this highly contentious medical issue.
 
Remember when the people who wanted to vaxxecute you said that their mRNA poisons would not alter your DNA? New research debunks that claim.




We were told the mRNA shots couldn’t alter your DNA. Sweden just said otherwise.

A bombshell study from Lund University proves Pfizer’s mRNA reverse transcribes into human DNA in liver cells.

This isn’t a conspiracy theory. It’s peer-reviewed science. The enzyme in your body takes the vaccine’s instructions and installs them into your genetic code.

And yes, the CDC’s website still claims this can’t happen.

So let’s be clear:
This isn’t staying in the arm.
It’s rewriting the code of your body.

And if you’re pregnant?

There’s a terrifying implication: these changes may impact your baby’s DNA too. That’s not fear-mongering. That’s molecular biology.

And it doesn’t stop there…

Because if this alters DNA and genetic changes are now on record then denying medical freedom becomes genetic discrimination.

Which means lawsuits are coming.

But here’s the part no one wants to say out loud:

If the spike protein can now be continuously produced by your own cells, That’s not a short-term exposure, That’s a permanent biological factory running inside your body.

The lipid nanoparticles don’t stay in the arm, They travel to organs, Reproductive cells, Even embryos.

What happens when altered sperm meets altered egg?

And they said it was safe.
They said it was settled.
They said it was science.
 

It was a planned genocide. It was mass murder. They murdered our friends, family and loved ones and they didn't care. They did it for money. No amnesty. Never ever forget what they have done to the children. Your children. Your grandchildren.
My barber got the covid vax and died the night of, he was walking home and collapsed in some guy's yard, they said it was a "cardiac arrest"

dude was in his early 40's.
 

Synthetic mRNA Vaccines and Transcriptomic Dysregulation: Evidence from New-Onset Adverse Events and Cancers Post-Vaccination​

sauce/archive

Using high-resolution RNA sequencing on blood samples, researchers discovered that COVID-19 "vaccines" SEVERELY disrupt expression of THOUSANDS of genes - triggering mitochondrial failure, immune reprogramming, and oncogenic activation that can persist for long years post-injection, potentially permanently up to premature death

Differential gene expression analysis compared mRNA-injured patients (cancer, adverse events) to 803 healthy controls - revealing widespread transcriptomic chaos:

Mitochondrial failure - Complex I breakdown, oxidative stress, energy collapse

Immune reprogramming - chronic inflammation, ACE2 suppression, TLR hyperactivation

Oncogenic activation - MYC up, p53/KRAS down, DNA repair suppression

Cellular stress - ribosome overload, misfolded protein buildup, proteasome activation

Epigenetic remodeling - chromatin shifts, methylation changes, nucleosome displacement

Reverse transcription - patterns consistent with LINE-1 activity and persistent plasmid DNA, raising concern for potential genomic integration or sustained foreign gene expression

The landmark study was conducted by scientists from Neo7Bioscience gen-lab (Dr. John Catanzaro, Dr. Natalia von Ranke, Dr. Wei Zhang, Dr. Philipp Anokin), the University of North Texas (Dr. Danyang Shao, Dr. Ahmad Bereimipour, Minh Vu) and Medicinal Genomics (Kevin McKernan). Funded by the McCullough Foundation
 
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