FDA “Future Framework” Democide-Decision
FDA has a historic- decision to make on June 28 2022 – one that could affect everyone’s lives. If approved, all reformulated future mRNA Covid shots will skip clinical trials… just in time for the kids…
If the FDA authorizes Covid-19 shots for kids on June 14 and 15 and then approves the “Future Framework” on June 28th, the shots that will be given to kids in the future will be the reformulated shots that skipped clinical trials.
How you know the world is run by evil reason — what number are we up to now? Unbelievable – the FDA could skip clinical trials in future to save the mRNA industry from the utter failures – where are the good guys… where is the sanity… where are the people protecting the children and humanity from this pharma-takeover, this mass-democide, WHERE?
Their decision to skip clinical trials for mRNA could extend to democide like we have never seen – you can see exactly what they want and how they intend to get-around their failures – they know their future clinical trials will make the public lose faith because there’s so many more of us watching them now – calling out their corruption, their deception, their failure to protect our loved ones. We need to make people aware of their “safe & effective” marketing campaign and global deception, and what they are planning because everyone who has been blindly-trusting these criminals will blindly-trust again and again and again and again unless they are aware of the nefarious crap that is going on at FDA/CDC/WHO etc.
We are really in an inverse world where insanity and greed and the soulless have the reigns.
FDA timeline:
The FDA’s “expert advisory committee” (VRBPAC) met on April 6, 2022 to discuss the “Future Framework” for the first time. All of the committee members agreed:
- that Covid-19 shots are not working
- that boosting multiple times a year was not feasible
- and that the shots need to be reformulated.
- They also unanimously agreed that there are no “correlates of protection” that one can use to predict what antibody levels would be sufficient to prevent SARS-CoV-2 infection.
On June 28 the VRBPAC will meet once again to discuss the “Future Framework” and it will be presented as a done deal because manufacturers want a decision on vaccine strain selection by June in order to deliver shots for September vaccination appointments.
So if the FDA authorizes Covid-19 shots for kids on June 14 and 15 and then approves the “Future Framework” on June 28th, the shots that will be given to kids in the fall will be the reformulated shots that skipped clinical trials.
It gets worse…
V. Monovalent Covid-19 shots failed, so maybe throwing two, three, or four variants into a single shot will make it better?
When it comes to the flu shot, the FDA tries to hedge their bets by putting four strains of the virus into a single shot (so called “quadrivalent” vaccines). This strategy does not work. But these people are not very clever so that’s exactly what they are planning to do with future Covid-19 shots.
- (If you haven’t seen my post on the NZ Labs – they found nanotechnology and other nefarious details with the Quad Flu vaccine too that the world needs to know about!)
The Future Framework is 100% guaranteed to fail. If the “Future Framework” is approved, effectiveness of these shots will decrease, adverse events will increase, these shots will fuel the evolution of variants that evade the vaccines, and there will be no clinical trial data before these reformulated Covid-19 shots are unleashed on the unsuspecting public.
The “Future Framework” is a plan to rig the Covid-19 vaccine regulatory process in perpetuity.
The “Future Framework” would take the “flu strain selection process” that fails every year and apply it to future (reformulated) Covid-19 shots. Federal bureaucrats, many of whom have financial conflicts of interests, would choose which SARS-CoV-2 variants to include in a yearly (or twice yearly) Covid-19 shot. In the process, all future Covid-19 shots will be deemed automatically “safe and effective” without further clinical trials because they are considered “biologically similar” to existing Covid-19 shots.
We must stop the “Future Framework” before June 28.
- Full details on Dr Toby Rogers substack: The FDA’s proposed “Future Framework” is the worst idea in the history of public health
Watch the Full Interview: Defend the Rights of the Poor – An Interview with Dr Toby Rogers (1 hr 20 mins)
- Dr Toby Rogers Links
- Studies mentioned in Full Interview Video:
- Mawson, A. and colleagues (2017a) “Pilot comparative study on the health of vaccinated and unvaccinated 6-to 12-year-old US children.” Journal of Translational Science
https://doi.org/10.15761/JTS.1000186 - Mawson, A. and colleagues (2017b) “Preterm birth, vaccination and neurodevelopmental disorders: a cross-sectional study of 6-to 12-year-old vaccinated and unvaccinated children.” Journal of Translational Science
https://doi.org/10.15761/JTS.1000187
- Mawson, A. and colleagues (2017a) “Pilot comparative study on the health of vaccinated and unvaccinated 6-to 12-year-old US children.” Journal of Translational Science
- FDA Links
- Vaccines and Related Biological Products Advisory Committee June 28, 2022 Meeting Announcement JUNE 28, 2022 https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-june-28-2022-meeting-announcement
- Vaccines and Related Biological Products Advisory Committee June 14-15, 2022 Meeting Announcement JUNE 14 – 15, 2022 https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-june-14-15-2022-meeting-announcement
- FDA Livestream (9 hours) VRBPAC – APRIL 6 2022 https://youtu.be/x8rq247E80I “Vaccines and Related Biological Products Advisory Committee (VRBPAC) to discuss considerations for future COVID-19 vaccine booster doses and the process for selecting specific strains of the SARS-CoV-2 virus for COVID-19 vaccines to address current and emerging variants.”
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