There is a reason majority of PhDs in biology and immunology refused the RNA injections
SARS-CoV-2 Spike is a highly pathogenic protein on its own.
SARS-CoV-2 is an endothelial disease.
The injections were not sterilizing and do not prevent infection or transmission.
They are “leaky” injections. This means they remove the evolutionary pressure on the virus to become less lethal. It also means that the injected are perfect carriers. In other words, those who get injected are a threat to the unvaccinated, not the other way around.
All of the injections underwent minimal testing, with highly accelerated clinical trials.
SARS-CoV-2 Spike was GOF'd to bind to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part of the renin-angiotensin-aldosterone system, or RAAS. Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that are basically like little dotted lines that say “cut here”, which attract a living organism’s own proteases (essentially, molecular scissors) to cut them. There is a possibility that S1 may be proteolytically cleaved from S2, causing active S1 to float away into the bloodstream while leaving the S2 “stalk” embedded in the membrane of the cell that expressed the protein.
SARS-CoV-2 Spike has a Superantigenic region (SAg), which promotes extreme inflammation.
Anti-Spike antibodies were found in one study to attack the body’s own cells. Those who have been injected with SARS-CoV-2 Spike have developed blood clots, myocarditis, Guillain-Barre Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the SARS-CoV-2 injections promotes autoimmune reactions against healthy tissue.
SARS-CoV-2 S Protein injections do not only bind to ACE2. It it suspected to have regions that bind to basigin, integrins, neuropilin-1, and bacterial lipopolysaccharides as well.
Manufacturers claim that SARS-CoV-2 mRNA injections cannot be integrated into the human genome, because messenger RNA cannot be turned back into DNA. This is false. There are elements in human cells called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by endogenous reverse transcription. Because the mRNA used in the vax is stabilized, it hangs around in cells longer, increasing the chances for this to happen. If the gene for SARS-CoV-2 Spike is integrated into a portion of the genome that is not silent and actually expresses a protein, it is possible that people who take these S protein injections may continuously express SARS-CoV-2 Spike from their somatic cells for the rest of their lives.
By injecting healthy people with a protein that causes their bodies to produce Spike in-situ, they are being inoculated with a pathogenic protein. A toxin that may cause long-term inflammation, heart problems, and a raised risk of cancers. In the long-term, it may also potentially lead to premature neurodegenerative disease.
Absolutely nobody should have been compelled to take these rushed injections with unknown long term data under any circumstances.
An hour and a half of only one side of the hydroxychloroquine discussion.
No mention of the research that showed early use of it to be ineffective: "Conclusion:
Hydroxychloroquine did not substantially reduce symptom severity in outpatients with early, mild COVID-19." https://www.acpjournals.org/doi/10.7326/m20-4207
"the largest outpatient therapeutic trial of hydroxychloroquine published to date. Like dozens of smaller trials published before, it failed to demonstrate any benefit to hydroxychloroquine in preventing progression of COVID-19 among outpatients with initially mild COVID-19" https://www.thelancet.com/journals/lanam/article/PIIS2667-193X(22)00085-0/fulltext
An hour and a half of only one side of the hydroxychloroquine discussion.
No mention of the research that showed early use of it to be ineffective: "Conclusion:
Hydroxychloroquine did not substantially reduce symptom severity in outpatients with early, mild COVID-19." https://www.acpjournals.org/doi/10.7326/m20-4207
"the largest outpatient therapeutic trial of hydroxychloroquine published to date. Like dozens of smaller trials published before, it failed to demonstrate any benefit to hydroxychloroquine in preventing progression of COVID-19 among outpatients with initially mild COVID-19" https://www.thelancet.com/journals/lanam/article/PIIS2667-193X(22)00085-0/fulltext
There is a reason majority of PhDs in biology and immunology refused the RNA injections
SARS-CoV-2 Spike is a highly pathogenic protein on its own.
SARS-CoV-2 is an endothelial disease.
The injections were not sterilizing and do not prevent infection or transmission.
They are “leaky” injections. This means they remove the evolutionary pressure on the virus to become less lethal. It also means that the injected are perfect carriers. In other words, those who get injected are a threat to the unvaccinated, not the other way around.
All of the injections underwent minimal testing, with highly accelerated clinical trials.
SARS-CoV-2 Spike was GOF'd to bind to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part of the renin-angiotensin-aldosterone system, or RAAS. Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that are basically like little dotted lines that say “cut here”, which attract a living organism’s own proteases (essentially, molecular scissors) to cut them. There is a possibility that S1 may be proteolytically cleaved from S2, causing active S1 to float away into the bloodstream while leaving the S2 “stalk” embedded in the membrane of the cell that expressed the protein.
SARS-CoV-2 Spike has a Superantigenic region (SAg), which promotes extreme inflammation.
Anti-Spike antibodies were found in one study to attack the body’s own cells. Those who have been injected with SARS-CoV-2 Spike have developed blood clots, myocarditis, Guillain-Barre Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the SARS-CoV-2 injections promotes autoimmune reactions against healthy tissue.
SARS-CoV-2 S Protein injections do not only bind to ACE2. It it suspected to have regions that bind to basigin, integrins, neuropilin-1, and bacterial lipopolysaccharides as well.
Manufacturers claim that SARS-CoV-2 mRNA injections cannot be integrated into the human genome, because messenger RNA cannot be turned back into DNA. This is false. There are elements in human cells called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by endogenous reverse transcription. Because the mRNA used in the vax is stabilized, it hangs around in cells longer, increasing the chances for this to happen. If the gene for SARS-CoV-2 Spike is integrated into a portion of the genome that is not silent and actually expresses a protein, it is possible that people who take these S protein injections may continuously express SARS-CoV-2 Spike from their somatic cells for the rest of their lives.
By injecting healthy people with a protein that causes their bodies to produce Spike in-situ, they are being inoculated with a pathogenic protein. A toxin that may cause long-term inflammation, heart problems, and a raised risk of cancers. In the long-term, it may also potentially lead to premature neurodegenerative disease.
Absolutely nobody should have been compelled to take these rushed injections with unknown long term data under any circumstances.
My RNA injections sent me to the ICU with severe vaccine injuries.
I am very grateful for my 5 clots and strokes. Very sudden and very effective
I STAND WITH BIG PHARMA!!!!!
Fuck the kids, inject them all with experimental myocarditis.
Completely biased.
An hour and a half of only one side of the hydroxychloroquine discussion.
No mention of the research that showed early use of it to be ineffective: "Conclusion: Hydroxychloroquine did not substantially reduce symptom severity in outpatients with early, mild COVID-19." https://www.acpjournals.org/doi/10.7326/m20-4207
"the largest outpatient therapeutic trial of hydroxychloroquine published to date. Like dozens of smaller trials published before, it failed to demonstrate any benefit to hydroxychloroquine in preventing progression of COVID-19 among outpatients with initially mild COVID-19" https://www.thelancet.com/journals/lanam/article/PIIS2667-193X(22)00085-0/fulltext
Awesome anonymous opinion from a biased fully vaccinated Leftist who admits being injured by the forced medical experiment
More fan fiction from the impostor folks.
It's kinda touching that she spends time thinking up stuff about me.
Completely biased.
An hour and a half of only one side of the hydroxychloroquine discussion.
No mention of the research that showed early use of it to be ineffective: "Conclusion: Hydroxychloroquine did not substantially reduce symptom severity in outpatients with early, mild COVID-19." https://www.acpjournals.org/doi/10.7326/m20-4207
"the largest outpatient therapeutic trial of hydroxychloroquine published to date. Like dozens of smaller trials published before, it failed to demonstrate any benefit to hydroxychloroquine in preventing progression of COVID-19 among outpatients with initially mild COVID-19" https://www.thelancet.com/journals/lanam/article/PIIS2667-193X(22)00085-0/fulltext