« First « Previous Comments 2 - 4 of 4 Search these comments
think I tore something in my shoulder last night playing volleyball.I once fell out of a high walled tub, having grabbed what I thought was a fixed shower rod only to find out it wasn't. Fell right onto my shoulder which hurt like a sonofabitch for months. My primary care doc advised me against surgery, saying it would heal on its own. He was absolutely right, although it was gradual, and I had to not re-injure it via exercise which took some learning. Don't ever get surgery unless it is a last resort. The body has remarkable healing abilities.
stereotomy saysThe problem is that the J&J is withdrawn in most markets, so we have to deal with the mRNA toxxine. I narrowly dodged a bullet at work wrt to the death jab.
Purebloods! (ref: Red Dawn)
Yes, I'm scheduled to sell off some more equity next year so if the mRNA is all that's left, and we can't get the Novavax (stateside) or Astra-Zeneca (in Europe) then I'm quitting. There's no way I'm taking the mRNA.
The mRNA is a stealth bomber. It's the only thing I've ever heard of which can by-pass a person's restriction enzymes which are critical to prevent one's food from contaminating oneself.
To fight off the mRNA, one will need to basically finish one 60 cap Quercetin Phytosome bottle, every 5 days. So yeah, I suppose if you buy a war chest of it and keep taking it for 6 months, then you'll probably be 'ok' but as far as I'm concerned, that's basically like taking anti-venom dosage all of the time.
With some of the stuff being pitched to treat something the side effects seem to be worse than just dealing with whatever it is
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. View Full-Text
https://www.mdpi.com/1467-3045/44/3/73