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.
3/ There is net charge (positive and negative charges added up--similar to if you add 3 + -5 = -2 ).
That is it's net charge.
Zeta potential is the kinetic charge (a potential of interaction)
Positively charged LNPs cause MASSIVE clots in the lungs.
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.
The LNP crosses the placenta.
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.
10/ DNA plasmid contamination in modRNA "vaccines" DO NOT HAVE TO ENTER THE NUCLEUS to impact GENE EXPRESSION, and be implicated in CANCER RISK!
The DNA plasmid interacts with different areas i the body, and can impact what genes do.
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.
17/ Thyroid damage and auto immune disorders are linked to dsDNA. dsDNA is found in the current plasmid DNA contamination.
This is slightly different in the thyroid ( histone H2B)
Study + cases on 💉injury.
18/ MYOCARDITIS
(DNA plasmid contamination was recently found in c@vid modRNA "vaccines")
in ANIMAL STUDIES CAUSES: MYOCARDIAL INFLAMMATION IN MURINE HEARTS after exposure and damages the CARDIOMYOCYTE
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.
23/ RAPID AAD-Aortic Aneurysm and Dissection (tearing/rupture) is lethal.
Plasmid DNA is dsDNA.
dsDNA can enter cells from the body's own sources, or a contamination event (💉)
dsDNA is shown to cause AAD
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.
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