Wednesday, March 29, 2023

Ivermectin clears out those insta-senescent cells!

From NCBI: 

defective apoptosis [cell death] contributes to both tumorigenesis [tumor generating] and chemoresistance [13].

EFFECTS OF AUTOPHAGY ON CELL GROWTH ABILITY 

To confirm the anticancer effects of autophagy on glioma cells, MTT assay and colony formation analyses were conducted to assess the growth viability of glioma cells. We evaluated the combined effects of IVM and CQ on cell proliferation using U251 and C6 cells. As shown in Figure 4A, IVM co-treatment with CQ decreased the cell growth ability in U251 and C6 cell cells, and notably CQ exhibited a lesser effect on glioma cells. As shown in Figure 4B, we found that IVM co-treatment with CQ significantly inhibited colony formation and induced significant decrease in the colony formation ratio. These results indicated that autophagy increased cell growth ability in U251 and C6 cells.

Autophagy is the destruction of damaged or redundant cellular components occurring in vacuoles within the cell

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Both the CDC and Drosten PCR tests determined WATER was positive for “SARS-COV-2.”

The depth and extent of lies surrounding everything COVID-19 is astounding . . ly evil. 

Here is the direct link to Viroliegy's "20 Undeniable Facts About PCR Tests," August 8, 2021.

Thank you to Lew Rockwell. 

5. None of the PCR tests are FDA-approved and are only out on EUA which forgoes many quality controls:


“The FDA granted the first Emergency Use Authorization (EUA) for a SARS-CoV-2 rRT-PCR diagnostic test on February 4, 2020. Consequently, hundreds of tests for SARS-CoV-2, among them rRT-PCRs, other types of nucleic acid amplification tests (NAATs), and automated and/or multiplex methods based on proprietary platforms, obtained FDA Emergency Use Authorization (EUA). As of August 4th, 2020, the FDA has granted EUAs to 203 diagnostic tests, including 166 molecular tests, 35 antibody assays, and 2 antigen tests. Although the FDA began requiring the submission of validation methods and results as part of EUA application for SARS-CoV-2 diagnostic tests, these tests were not initially required to undergo the rigorous assessment that would normally be part of the FDA approval process.”

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457918/


“So the agency uses an alternative evaluation process that’s designed to vet things more quickly than the usual FDA approval regimen. If a drug or vaccine passes muster, it’s granted an emergency use authorization, or EUA.”

https://www.google.com/amp/s/www.latimes.com/science/story/2020-12-12/why-fda-didnt-approve-pfizer-covid-19-vaccine-eua%3f_amp=true

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Stage 3 throat cancer . . . oncologist is baffled by the almost complete disappearance of his cancer

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Maryland’s Long-Serving Elections Director Linda Malone Resigns Hours After O'keefe Media Exposes Laundro-mat

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Solution. Don’t go to college

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