Naive question, but I’m serious. Can one substance really cause that many maladies?
I spotted this in the long list: “Acute respiratory distress syndrome;Acute respiratory failure”
Rather ironic that they mRNA material is supposed to PREVENT that from happening.
Seems to me if it messes with DNA, which is in every cell in the body, it can impact ANY body process or cascade of body processes.
Seems like it causes every malady. Maybe the list of maladies it doesn't cause is shorter.
The long answer is no, but the short answer is yes.
For example, you like everyone have lots of undesirable things going on in your body.
The immune system is excellent at triage and repair.
Suddenly there is a huge anomalous production of bad spike proteins.
I imagine there is some kind of Red Alert, all hands on deck moment were suddenly your herpes zoster, or some pesky cancer cells, or other undesirables are left completely alone.
the automatic repair systems cannot cope with damage. The mRna transcribes into Dna faster than the auto-repair can fix it.
faster than you can say ‘defund the police’ everything starts going to hell
“Can one substance really cause that many maladies?”
When it’s RNA, yes. It’s basically hacking the complicated computer programs running...human life.
What could go wrong?
‘Naive question, but I’m serious. Can one substance really cause that many maladies?’
[Read this. Unlike natural mRNA, the synthetic “vax” mRNA sticks around, keeps making spike proteins, and travels to organs throughout the body.]
On the Vaccine Frontlines
More safety issues, fraud and lack of efficacy continues to haunt the Feds
Robert W Malone MD, MS
https://rwmalonemd.substack.com/p/on-the-vaccine-frontlines?s=r
Another pre-print paper just published that validates the synthetic mRNA found in the vaccines is not degrading and continues to produce protein.
In vitro Characterization of SARS-CoV-2 Protein Translated from the Moderna mRNA-1273 Vaccine In medRXiv , by Timothy Veenstra, Elisha Injeti, Bradley Pauley doi: https://doi.org/10.1101/2022.03.01.22271618
Of interest is that the authors of this article contacted Moderna and Pfizer-BioNTech and asked about how much protein was expressed and the duration of expression in pre-clinical testing. This is the response they received:
In communications with Moderna and Pfizer-BioNTech regarding the proteins expressed by their synthetic mRNA vaccines, each company’s medical information group disclosed that that they had not examined the protein dynamics more than 48 hours post-transfection in cell culture. Owing to its proprietary status, they would not disclose any information related to the nature of the protein that was expressed.
And there you have it. The FDA never required Moderna and Pfizer-BioNTech to analyze duration or amount of protein expressed in cell culture after 48 hours, prior to injecting into humans. Let alone doing a thorough evaluation in either non-clinical animal models or in humans.
The paper goes on:
Cell lysates and supernatants were analyzed using western blotting to determine the size of protein expressed from the Spikevax vaccine mRNA (which has not been previously reported in the literature). Cell lysates and supernatants collected at 1, 3, 6, 12 and 24 hrs, and 5, 9, and 15 days, were analyzed using an ELISA and western blotting for presence of Spikevax-synthesized protein. Western blotting using a mouse monoclonal antibody from R&D Systems revealed three prominent bands at a molecular weight of approximately 180 kD (Figure 2), which can be seen most prominently in the cell lysates at 24 hours post-infection with the vaccine. The three bands with distinct molecular weights may arise from differential post-translational modifications (most likely glycosylation) that occurs as the proteins expressed from the mRNA vaccine are processed.
SARS-CoV-2 protein expression was detectable in cell lysates within 6 hours of treating the cells with the vaccine (Figure 2). Protein levels peaked at 24 hours and remained detectable over 5 days. No SARS-CoV-2 spike protein was detectable in the NIH 3T3 cell lysates after 12 days. The cell supernatants did not contain any detectable vaccine-induced protein
This paper validates again that the mRNA in these genetic vaccines are not degrading rapidly once inside cells and that the Moderna vaccine continues to produce protein up until 12 days after transfection in this in-vitro model. Of note: only two cell lines were tested.
Remember, natural mRNA degrades usually within 45 minutes and no longer than a few hours. That this synthetic mRNA is not degrading rapidly is extremely worrying. Particularly as we also know that the synthetic mRNA is immunosuppressive.
The cell paper quoted below also confirms that vaccine mRNA is not degrading and spike protein in lymph nodes is much more extensive than in the COVID-19 patent lymph nodes:
“The observed extended presence of vaccine mRNA and spike protein in vaccinee LN GCs (lymph node germinal centers) for up to 2 months after vaccination was in contrast to rare foci of viral spike protein in COVID-19 patient LNs”
The two papers together validate the findings that the synthetic mRNA is not degrading.
Having synthetic mRNA migrate to regions of the body and continue producing protein is not normal.
This new development has to be addressed by the FDA now.
Furthermore, According to the CDC, for as long as to six weeks after vaccination, lymph nodes can be so swollen that this result can be detected via mammogram. Due to this issue, many physicians advise waiting six weeks after taking the jab before getting a mammogram.
Now think about the fact that synthetic mRNA, which is producing spike protein can be found for at least two months after inoculation in lymph node germinal centers.
Coincidence? I think not. I certainly think that lymph node swelling and mRNA that is not degrading and has migrated to other regions, including LNs, needs to be investigated now. It is past time for more studies to be performed on the safety of these vaccines.
At the very least, these vaccines should not be administered to children and should not be mandated until such a time as when we know they are safe.