Ralph Baric co-authored: "On the basis of these findings, scientific review panels may deem similar studies building chimeric viruses based on circulating strains too risky to pursue..."
"Coupled with restrictions on mouse-adapted strains and the development of monoclonal...
antibodies using escape variants." 2. "HeLa cells were grown..." [cancer-causing agent] 👀
Uni of N. Carolina at Chapel Hill Institutional Review Board "approved protocols."
"The cultures are also grown on an air-liquid interface..." [Aerosolized] 3. Transfected into Vero E6...
Project & Lab Safety Plan ID: 20145741 GID: 12279
"This paper has been reviewed by the funding agency, the NIH." Continuation of studies requested "and this has been approved by the NIH."
USAID...
"20 NOV 2015 In the version of this article initially published online, the authors omitted a funding source,
USAID - EPT - PREDICT funding from ECOHEALTH ALLIANCE, to ZLS." *Zheng-Li Shi*
Withholding source funding? Scroll
Is this what's being given to those who are receiving the genetic therapies, such as the #COVID19 vax, monoclonal antibodies (mabs), and/or convalescent plasma? Is this what Gates meant by "next time"?!?
Are they saying these aren't contaminated?!
Correction: Hela cells are infectious though cancer.
Alarming: Kevin McCairn states that the fibrin-like structures (clots), being retrieved by embalmers/surgeons, are amyloidogenic and can "seed" misfolding (more clots). Others are verifying his work in more detail.
"This proteinaceous form [...] it's misfolded amyloidogenic fibrin."
"You've made the body produce this toxic peptide that can act as a seed," to cause misfolding.
"Infective peptide," that "once it comes into contact with fresh plasma, it is able to initiate the misfolding..."
I've clipped certain sections to distill the pertinent data:
According to Google, in Sep 20, 2005, the PREP Act was attached to a DOD Appropriation Bill. Review:
"The bill specifies that even if a company knew a product was defective, a plaintiff cannot establish willful misconduct if the manufacturer was operating under the regulatory approval or Emergency Use Authorization
of the FDA:
"(c)(5)(A) EXCLUSION FOR REGULATED ENTITIES.— ...an act or omission by a covered person... shall not constitute 'willful misconduct' if such covered person is regulated by the Secretary [HHS/FDA]... and the Secretary did not choose to take an enforcement action
EXPERIMENTAL monoclonal ANTIbodies showing up on the 0-18 schedule, and AMERICAN kids, AS OF TODAY, are being coerced (not recommended) to take more "vaccines".
The schools and extracurricular programs are providing the pinch against the parents, which causes them to have to bring the children back and forth to the doctor. The doctor finds out the injection
being requested by these non-medical programs, they administer the requested injection and document it to keep the child's routine from being further disrupted. There should be thousands of cases just like these...
NIH VRC expanded partnership w Mod...for full scale research into a pan coronavirus *vaccine platform*;
...only for HHS to approve similar work without P3CO (Pandemic Pathogen Care Oversight Framework) review...
👀
P3CO was designed to allow greater flexibility for
vxc development.
Planned experiments/ collaboration:
WIV - Wuhan
ECNU - East China Normal
UNC - Chapel Hill, NC
NWHC - National Wildlife HC
PARC - Palo Alto Research Center
Link to source video at the end of this thread. I'm going to weave (seemingly unrelated) research throughout.
The subthreads will have additional info.
I welcome all comments, as this I treat information through the lens of
being skeptical, but verifying where I can.
Morgellons
This technology/medical phenomenon is completely new to many.. but most definitely not new to those working w/in the industries.
Keep going. I'm not done.