The British Parliament Does Not Consult The Office for National Statistics (ONS) on Serious Matters of Iatrogenic Death Associated with COVID-19 Vaccination
Dr. Johnson of UK parliament provides estimates to sway against an inquest into the many deaths associated with COVID-19 vaccines while the relevant facts released by the ONS on July 6, 2022 ignored.
The above is my response to Steve Kirsch’s recent post covering the failed ability of British parliamentarians in October 2022 to call for an inquiry into the vaccine-associated deaths.
https://stevekirsch.substack.com/p/the-british-parliament-has-debated/comments
The ONS of the UK has published the actual data (July 6, 2022 in lots of time for the British debate in October 2022) showing there were 2110 COVID-19 deaths alleviated by vaccination while there was an excess of 423,337 non-COVID-19 deaths associated with the toxicity of the vaccines. The vaccines DID NOT avert an estimated 128,000 deaths as claimed. Why are the British parliamentarians quoting “wishful thinking” or otherwise known as “coercion” estimates in October 2022 when the real data was published on July 6, 2022 ???
The Vaccines By Inducing Antibodies and Neutralizing Antibodies to Spike Protein Would Select for Variants and Cause More Severe Disease in the Vaccinated over the Unvaccinated through ADE.
The late Dr. Luc Montagnier a 2008 Nobel Laureate for the discovery of another pandemic RNA virus, HIV-1; predicted that the vaccinated would be at higher risk of transmission and mortality (implied) once immune escape variants emerged and became dominant.
The data below from the ONS confirms the vaccinated were at higher risk of COVID-19 mortality and also non-COVID-19 mortality due to spike protein toxicity with the mRNA vaccines.
The Vaccines Selected for the Immune Escape Variants Alpha then Delta in Humans.
In total agreement with the Nobel Laureate, the late Dr. Luc Montagnier; data from Canada shows the initial emergence and/or dominance of the alpha then delta variants was directly linked to either:
when the ratio of two dose/one dose exceeded 0.5 (ie., when the spike specific antibodies were induced by vaccination) and/or
when there was a loss of negative excess all-cause mortality (loss of heterologous protection ascribed to trained (innate) immunity, see image below) presumably due to spike triggering immunosenescence.
See details here:
Evidence from Ontario Canada clearly shows the alpha variant was more deadly than the original Wuhan strain and the delta variant more deadly than the alpha variant… just as Dr. Luc Montagnier predicted.
Fisman DN, Tuite AR. Evaluation of the relative virulence of novel SARS-CoV-2 variants: a retrospective cohort study in Ontario, Canada. CMAJ. 2021 Oct 25;193(42):E1619-E1625. doi: 10.1503/cmaj.211248.
In part the immune toxicity by spike protein (vaccine or natural infection) relates to the induction of immunosenescence which causes both immunosuppression and inflammation at the level of the foamy macrophage. Immunosenescence causes the initiation of chronic disease and progression and a loss of protection against infectious disease.
The fact that we know the spike based mRNA vaccines provide very high and persistent expression of the spike protein, and that spike protein activates macrophages putatively those pro-inflammatory foamy macrophages [Cao X et al., bioRxiv, Dec 7, 2020; Theobald SJ et al., EMBO Molecular Medicine June 2021] producing HERV-K102 particles, some say through TLR-2 [Khan S et al., Elife, December 2021], the fact that THE HETEROLOGOUS PROTECTION BECOMES LOST (ie., loss of negative EACM associated with the selection of the variants by the vaccines see above image), means the spike protein in vaccines must be inducing IMMUNOSENESCENCE.
This is important because immunosenescence involves both immunosuppression and paradoxically the release of the proinflammatory factors: IL-1beta, TNF alpha and IL-6 [Laderoute M. Discovery Medicine, 2015, 2020]. The former makes one more susceptible to infections and cancers, while the latter causes the initiation and progression of chronic diseases such as cancers, cardiovascular disease, autoimmune disease, allergies, metabolic diseases, dementias and so on.
The New Immunosenescence Paradigm, 2015. [Laderoute M , 2015].
Note that ivermectin, zinc, vitamin D, 7-keto DHEA (a form of DHEA which cannot be converted to testosterone so safer than using DHEA) and isoflavonoids may reverse immunosenescence and thus are likely useful for treating and/or preventing COVID-19 vaccine induced injuries.
SAY what? The vaccines selected for the immune escape variants and now the vaccinated are at increased risk of death?
Yup. It is time to shut down the vaccination program. We would have told you this in February 2021, if the UK ONS would have provided meaningful data in real time and had we not been censored.
It would be interesting to do a a test negative design measuring VE for RSV respiratory infections to determine if COVID-19 vaccination in children (zero, one, two or also boosted) led to a higher risk of RSV hospitalizations this fall or as is apparently currently playing out in Canada. This may be the real risk now to children more so than chronic disease due to the effects of spike protein on innate immunity.