1/ 🧵💉Adverse Events: All of the threads combined on RNA/DNA/LNP.
People have been asking for easier to comprehend posts.
I am not one to drink, but consider this thread
"science in a shot glass"
All of the threads have study links to back what is stated, and explanations.
2/ The LNP has a charge. It can have a neutral charge, positive charge (+) or negative charge (-).
The RNA and DNA have a negative charge (-). The ionizable lipids have a positive charge (+).
Charge determines where in the body it goes and what it does.
4/Negatively charged LNPs can enter the cardiomyocyte (10:1 ratio (+) LNP to (-) RNA/DNA) and cause MYOCARDITIS.
The DNA contamination changed the charge on the LNP. The DNA is very negatively charged. The scientists involved should have known this.
5/ Highly negatively charged LNP can cause clots. This will drive clot formation thousands of times more aggressively than human body normally would. It makes clots form more quickly, with more fibrin (thick and spindly), and are more difficult to treat.
6/ The LNP can cross the placenta, and "transfect" it--meaning it can enter the cells there, and growing baby.
There is a 100 study 124 tweet thread I made on this. 100+ studies exist on it. This is not a hypothesis.
7/ The plasmid DNA contamination, can cause the body to attack itself, temporarily or indefinitely.
The body sees it as foreign, but also, it could see it as "self", causing the body to attack the tissues the LNP enters and create auto immune situation.
8/ The DNA plasmid contamination may disrupt the normal growth of a baby, causing an auto immune response in the baby, issues with pregnancy, delivery, defects, and other concerns.
9/ Sperm cells can spontaneously "take up" pieces of DNA. Plasmid DNA exists as contamination inside the LNP. If this enters the testes, and reaches the sperm, the sperm can absorb the DNA plasmid, altering it.
11/ The freezing and thawing process is braking the LNPs. it is causing some to leak out. It is also causing some to stick together, expand, and cluster, which can cause blockages. It can cause the RNA inside to break, which can be oncogenic.
12/ Impurities in Positively Charged Lipids in the LNP, can MUTATE mRNA in LNP (Packer et al., 2021); potentially mutating other nucleic acids (RNA,DNA) that may cause: -mutation -Aberrant Protein (toxic) -Noncoding (can be oncogenic) -Misfold/aggregation
13/ When the LNP is made, with the RNA inside of it, not all of it is whole. Some of the RNA is in pieces when it is first made. Some of the whole pieces also break when it is frozen. Pieces of RNA can cause cancer or turn cancer off.
14/ "Over 100 different ionizable lipid chemistries were examined, all of which produced measurable levels of mRNA-lipid adducts. This indicates that the formation of these adducts is not limited to a specific type of ionizable lipid but is a broad class effect." ALL MUTATE.
15/ Positively charged lipids DAMAGE BACTERIA. Bacteria exists in humans in a ratio of 2:1 --bacteria to human cells. Lipid Nanoparticles used in modRNA "vaccines", contain positively charged lipids. The LNPs are going everywhere, including the gut
16/ Liver Cancer: dsDNA is implicated in Hepatocellular Carcinoma.
dsDNA is part of DNA plasmid contamination discovered in💉.
dsDNA is activated by the STING pathway, causing an immune system cascade, which can cause inflammation, injury, and cancer.
19/ How the DNA plasmid contamination is causing the LNP to bind with proteins and cause other harms in the human body. Speicher and friends found the higher the DNA plasmid contamination, the worse the SAE on record.
20/ Could the LNPs alter/impair the mononuclear phagocyte system (MPS), leading to toxicity, reduced pathogen clearance, impaired immune function, and tumor/cancer progression?
Studies show a negative impact after repeated injections of lipids.
21/ Spike protein is known to misfold and aggregate.
When you make a recombinant protein in a lab, in cells, under very controlled conditions (this is when you introduce RNA inside and LNP in a cell even, no human--it can misfold).
22/ Some LNP could not have formed properly in ways that may not have been explained, due to the DNA plasmid contamination. This just makes things far worse, and adds to the buffet of existing bad. LNPs weren't the only thing forming in the mix.
24/ How Zeta Changes in the Human Body (layman's), and Why Pharma Companies are Incorrect Stating their Calculation of Zeta Potential (surface charge) is Accurate, much less, that it will not do harm. Zeta is the starting point for most adverse events.
1/ 🚨"35-year-old woman contracted Lou Gehrig's disease after her first Pfizer dose."
ACTIVATION of DORMANT GENES in BOTH ADENOVIRUS AND RNA BASED.
These "products" like adenovirus and RNA/DNA can be DORMANT (see linked thread) and then become ACTIVE. Not just cancer :(
READ👇
1/ 🚨 THEY KNEW.
"REACTIVATION" potential of ADENOVIRUS VECTORS used for "gene therapy", including the use of DNA PLASMID with LATENT and REACTIVATED STATES for BOTH and why this is important for SHEDDING and DISEASE.
🚨DATE of ISSUE: JANUARY 2020. COINCIDENCE?
2/ Pierre Kory and others have talked a lot about shedding--they are correct. The studies are on viral vectors--these are viral vectors. There are studies I have and so do others on this, but to drive it home--right here:
3/ back to the first document: this was released 01/2020, right before the world was about to go into forced measures against the people, demanding they get injected with something that needs FIFTEEN YEARS of testing. The US had the gene sequence form CHINA in this moment.
💉i have a guess!!! Part of my time on my educational path, I was spending in the clinic in Neuro opthalmology. We had a lot of patients that had age-related macular degeneration or diabetes related. They would go for the eye injections of things like alflibercept. I'm not a neurophthalmologist however I worked with them and I learned things.
Im just typing on my phone so you're going to have to bear with me.
"significantly increases the risk of developing a condition called non-arteritic anterior ischemic optic neuropathy, or NAION, more than doubling the likelihood.
NAION is a rare condition that causes a lack of blood flow to part of the optic nerve, which connects the eye to the brain. Without blood flow, the affected areas swell up, stop working correctly and start to die, resulting in severe vision loss or blindness, according to the Cleveland Clinic. "
All right. Ozempic mimics naturally occurring hormone called glucagon-like peptide-1 . That's GLP-1. It signals to the brain that you are full, suppressing appetite and reducing food intake.
But this is acting like a ligand. And a ligand attaches itself to a receptor. It's like a lock and key.
GLP-1 (glucagon-like peptide-1) is a ligand, specifically acting as the natural ligand for the glucagon-like peptide-1 receptor (GLP-1R). The ligand matches the lock and then it signals the body to do things and in this case it signals not to be hungry.
And the ligand can have different shapes but also have charge. And some of these receptors also respond to a charge. We're talking about positive and negative charges.
And below chief nerd is being awesome and posting that there's an eye condition occurring as a result of ozempic.
Well, one might have the thought that the ligand that is made synthetically for ozempic has a chance of connecting with other receptors in the human body.
And the eye, has receptors, and one receptor is called Endothelin-1 (ET-1)
ET-1 is a ligand that binds to endothelin receptors (EDNRA and EDNRB) to cause vasoconstriction, which can cause decreased blood flow to the retina and optic nerve head.
And this condition might be treated by endothelin receptor antagonist. That means it increases blood flow by interacting with that receptor and it gives it a different signal.
But here's the thing: this has already been studied.
"Glucagon-like peptide-1 receptor agonist liraglutide inhibits endothelin-1 in endothelial cell by repressing nuclear factor-kappa B activation".
So they already knew. Because this research happened over 10 years ago.
They already knew it there was a link.
I don't have the full mechanism figured out and it's a Saturday night at 9:00 p.m. and this lady should be doing something else but here we are.
1/ 🦠🧬 New publication on cGAS STING and IRF7. Might want to investigate spike protein and plasmid DNA contamination with neurodegenerative disease like Parkinson's, Epstein Barr Virus, autoimmune, and cancer. Just dropping the articles for anyone to read in this thread.
1/ 🚨💉Lipid Impurities in mRNA! This is a MAJOR concern for the RNA and LIPID NANOPARTICLE platform! It is not being addressed!
08/2023: I presented this and more at the COVID Conference and below.
Please read all of the implications--it is for ALL RNA, not just spike and Ψ.
3/ This study was done in vitro, meaning in a lab--not in an animal. Researchers used human saliva as a medium to test the survival and transformation potential of plasmid DNA.
🦠Transformation= bacteria takes up DNA outside of it, and it becomes a part of its own genome.