The Newborns Are Not Alright: Billions Of Babies Will Inherit Spike Protein Genes

Many people that have tragically subjected themselves to the DEATHVAX™ often claim that they feel “fine” and falsely believe that they are “protected” and that “it could have been worse” when they all invariably do acquire COVID, more at VAIDS symptoms.

These claims are akin to getting exposed to deadly radiation or walking around with undiagnosed late stage cancer and having little reason to believe that life is anything but normal.

As per a recent Swedish research paper on reverse transcriptas showed that in liver cells the RNA is transcribed into DNA and integrated into the human genome, we can now sadly confirm that billions of babies born to those parents that have been exposed to the slow kill bioweapon injections have inherited the spike protein genes.

The showed that the Modified mRNa tends to concentrate in the ovaries and spleen. Reverse transriptase is found in these organs. This means that billions of the new generation will die extremely cruel deaths.

"Abstract Preclinical studies of COVID-19 mRNA vaccine BNT162b2, developed by Pfizer and BioNTech, showed reversible hepatic effects in animals that received the BNT162b2 injection. Furthermore, a recent study showed that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of human cells. In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro. Huh7 cells were exposed to BNT162b2, and quantitative PCR was performed on RNA extracted from the cells. We detected high levels of BNT162b2 in Huh7 cells and changes in gene expression of long interspersed nuclear element-1 (LINE-1), which is an endogenous reverse transcriptase. Immunohistochemistry using antibody binding to LINE-1 open reading frame-1 RNA-binding protein (ORFp1) on Huh7 cells treated with BNT162b2 indicated increased nucleus distribution of LINE-1. PCR on genomic DNA of Huh7 cells exposed to BNT162b2 amplified the DNA sequence unique to BNT162b2. Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure."

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