How do I know that the government’s response to COVID has absolutely nothing to do with caring about our health?
Oh, let me count the ways.
1/ They would have seriously explored treatments and would be encouraging the use of those proven to be effective.
2/ They would have accelerated the development of vaccine technologies with a longer track record of health impact data.
3/ They would have focused efforts on a sterilizing vaccine that prevents infection/transmission, and that doesn’t create conditions that promote vaccine resistant variants to emerge and spread.
4/ They would have produced human bio-distribution and kinetic data on Spike protein expression.
5/ They would have investigated cellular toxicity of the Spike protein.
6/ They would be taking vaccine adverse event data seriously instead of sweeping it under the rug and making excuses to explain away the obvious correlations.
7/ There would be a clear chain of liability.
8/ They would be communicating to the public on a perpetual basis on how to lower the risk of severe COVID (lowering BMI, Vit D, etc)
9/ They wouldn’t mandate a vaccine, especially in light of the issues mentioned above.
10/ They would be expending proportional efforts and deploying resources on other diseases and health conditions that plague mankind.
11/ They wouldn’t be pushing the use of the experimental technology on children who will gain nothing but short term and long term health risk.
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1/ In vitro experiments show antibodies are 41 times less potent against Omicron than ancestral D614G strain. Virtually a total escape for the vaccinated. Red is people who were only vaccinated. Green is people who had a natural infection first (1 year ago), and then vaccinated.
2/ Those with a previous natural infection from a year ago (and then vaccinated) have ~50 times more neutralization potential than those who are only vaccinated. (I estimated the #’s shown in the solid colored boxes because the authors didn’t include the raw data)
3/ Curiously, the study did not investigate antibodies from naturally infected people who were not subsequently vaccinated. Why not? Would this data essentially show there’s no real benefit to vaccination against omicron, and only naturally immunity matters?
Cover story much?
“Up to 300,000 people in the UK are facing heart-related illnesses due to post-pandemic stress disorder (PPSD), two London physicians have warned.
This could result in a 4.5 per cent rise in cardiovascular cases nationally…with those aged between 30 to 45”
1/ “errors were found in their analysis and a follow-up re-analysis of the data revealed a cumulative incidence of spontaneous abortion of 7–8 times higher than the original author’s calculations, which was statistically higher than the typical average for pregnancy loss….”
2/ “Concerns were raised years ago regarding the safety of LNPs due to their biodistribution. For example, they were found to disperse to the ovaries in experimental mice [18].”
3/ “Pfizer’s own pharmacokinetic studies of a surrogate vaccine containing ALC0315 and ALC0159 LNPs demonstrated that they dispersed over a 48 hours period to many rat endocrine and immune organs including the ovaries, adrenals, bone marrow, liver and spleen [19].”
1/ The current mRNA vaccines use an abnormal substitution for uridine; every U is replaced with m1Ψ (N1-methylpseudouridine). This synthetic substitution was made to increase mRNA stability, reduce immunogenicity, and increase expression. But what are the health effects of m1Ψ?
2/As an example, the human protein EMG1 is a pseudouridine N(1)-methyltransferase that methylates pseudouridine at position 1248 in 18S rRNA. It’s also involved in 40S ribosomal subunit biogenesis. Will m1Ψ from the vaccine inactivate this enzyme? genecards.org/cgi-bin/carddi…
3/ If so, what cell types will this inactivation take place, and for how long? What are the implications for ribosomal assembly and protein synthesis in these cells?
1/One of the most concerning things about the constellation of mutations found in Nu is the abnormal combination of deletions and insertions in the N-Terminal Domain (NTD) of Spike. The NTD region is considered the hot spot for enhancing antibodies, which is connected to ADE.
1/ The authors make a strong case that AXL (UFO) is a primary receptor for viral entry, perhaps even more so than ACE2, especially in certain tissue types. Could some of the side effects associated with Spike-expressing vaccines be due to Spike interacting with AXL? Fertility?
2/ Uniprot entry describing the function of AXL in signal transduction. Pay attention to modulation of thrombotic and platelet activity, and endothelial survivability. uniprot.org/uniprot/P30530
3/ Also, AXL is involved in neuronal development and survivability of GnRH neurons, which are responsible for the release of Gonadotropin-releasing hormone (GnRH). GnRH controls reproductive cycle in the female and spermatogenesis in the male.