The Data Is In! It is Well Past Time to Truly "Follow the Science"
Think it's a good idea to keep getting injected with mRNA, clearly it is not
The current CDC definition of “up-to-date” on COVID-19 vaccination provides a meaningless classification of risk of COVID-19 in the adult population.
The latest Cleveland Clinic preprint study reveals those receiving bivalent vaccination are at higher risk of developing COVID.
Vaccination status was “up-to-date” or “not up-to-date” based on whether or not a person had received at least one dose of a COVID-19 bivalent vaccine.
Source: https://www.medrxiv.org/content/10.1101/2023.06.09.23290893v1
Among 48,344 working-aged Cleveland Clinic employees, those not “up-to-date” on COVID-19 vaccination had a lower risk of COVID-19 than those “up-to-date”.
COVID-19 occurred in 1475 (3%) of 48,344 employees during the 100-day study period. The cumulative incidence of COVID-19 was lower in the “not up-to-date” than in the “up-to-date” state. On multivariable analysis, not being “up-to-date” with COVID-19 vaccination was associated with lower risk of COVID-19.
What was even more interesting was when stratified by most recent prior SARS-CoV-2 infection, there was no difference in risk of COVID-19 between the “up-to-date” and “not up-to-date” states within each most recent prior infection group, except for those not previously known to be infected.
Among those not previously known to have been infected and recovered the “up-to-date” state was associated with a higher risk of COVID-19 than the “not up-to-date” state. This may suggest pathogenic priming, also known as antibody dependent enhancement, induced by the injections.
There is a dose response to the COVID genetic vaccines
This study comes on the heels of another study out of Cleveland Clinic that concluded the risk of COVID-19 increased with time since the most recent prior COVID-19 episode and with the number of vaccine doses previously received.
Source: https://academic.oup.com/ofid/article/10/6/ofad209/7131292?login=false
In essence there is a dose response with these genetic vaccines, the higher the number of genetic vaccines previously received, the higher the risk of contracting COVID-19.
This study also found that the current bivalent vaccines were only about 29% effective overall in protecting against infection with SARS-CoV-2 when the Omicron BA.4/5 lineages were the predominant circulating strains, and effectiveness was lower when the circulating strains were no longer represented in the vaccine.
Both of these studies concluded natural immunity works and lowers your risk of repeat infection with SARS-CoV-2.
Pfizer clinical trial document shows adverse events after receiving the genetic vaccines
Not that we needed more evidence of this but Pfizer knew that the genetic vaccines was causing harm. This document shows the company observed nearly 1.6 million adverse events covering nearly every organ system.
The 393-page confidential Pfizer document, dated Aug. 19, 2022, shows that Pfizer observed over 10,000 categories of diagnosis, many of them very severe and very rare.
Source: https://www.globalresearch.ca/wp-content/uploads/2023/05/pfizer-report.pdf
Then came the disturbing revelation of DNA contamination in the genetic vaccines
Contamination was found in the form of dsDNA in both the Pfizer and Moderna products. These expression vectors do not belong in the injections.
Source: Figure 3: Adapted from Figure 2 in ‘Mixing’ section from https://www.caymanchem.com/news/intro-to-lipid-nanoparticle-formulation
The left-over expression vectors used to manufacture the mRNAs are at contamination levels 100-fold higher than originally proposed and imply trillions of DNA molecules per dose. This has implications for integration into our genome.
The DNA contamination issue is explained in more detail here and here.
Informed consent cannot be obtained with poorly characterized therapeutics.
Surely the regulatory body will follow the science
Information on the DNA contamination was presented to the VRBPAC committee during the 182nd meeting on June 15, 2023.
One would think that after hearing all this data that the regulators would halt the injections until further review of the science. Instead the VRBPAC committee voted unanimously to recommend that the COVID-19 vaccine be updated to target emerging subvariants of omicron. The FDA panel also recommended that drug makers abandon the bivalent design and instead move to a "monovalent" vaccine that only targets omicron subvariants. FDA told regulators to prepare fall COVID-19 injections to target Omicron XBB1.5.
Photo shared from The Matt Walsh Show https://www.imdb.com/title/tt13455662/
We need new leadership that is not blind to the science.