Posted on 06/01/2021 3:24:14 AM PDT by Fitzy_888
Video at link.
“…My name is malisa alex ,i am from USA . Its a pleasure for me to write this testimony about how i got my Genital Herpes cured a month ago. i have been reading so many comments of some people who were cured from various diseases by Dr. godwin, but i never believed them. I was hurt and depressed so I was [show more]…”
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A comment from another satisfied customer of Dr Godwin who, in the complete absence of a synopsis, I presume is the presenter.
Will that be followed by a true/false question to serve as a pass/fail IQ test? ;)
Luciferase Immunoprecipitation System (LIPS) assay is a rapid, simple, and sensitive test to detect antibody response to respiratory syncytial virus
https://www.fda.gov/vaccines-blood-biologics/science-research-biologics/luciferase-immunoprecipitation-system-lips-assay-rapid-simple-and-sensitive-test-detect-antibody
The same video is on YouTube, from 2017. It has nothing to do with the covid “vaccines” and it has nothing to do with “Dr. Godwin” in spite of what has been “presumed”.
https://www.youtube.com/watch?v=SIIes052B4E
If, however, this stuff is in the “vaccines”, that might explain the magnets sticking to the injection site as some have claimed.
Interesting.
It’s not in the vaccines unless the companies are lying in their vaccine ingredients lists.
Just talked about this yesterday on another forum. Do they use special single purpose needles just for these vaccines? Or do they use “Any production needle” for them also? If these vaccines require a special needle of their own as a kit, the “extra load” could be already in the needle and mixed with the vaccine when it is injected. A “two part” ingredient system and why it would not be detected in the vaccine it’s self.
Anyone know?
Right; but it was in the mRNA formulation that they used to do the pre clinical bio-distribution study on the rats and mice. “Pfizer did not even use the commercial vaccine (BNT162b2) but instead relied on a “surrogate” mRNA producing the luciferase protein.”
“To obtain independent reviews of these EMA regulatory documents, TrialSite contacted both Dr. Robert W. Malone, MD, MS, and another expert that wished to remain anonymous, and provided them copies of the EMA analysis and the FOIA documents. Dr. Malone was the original inventor of the mRNA vaccine technology back in the late 1980s. He currently advises several companies in regulatory affairs and clinical development.
One of TrialSite’s other sources is a senior regulatory specialist who currently serves as the President of a prestigious European association. When asked to review and comment on the EMA assessment, Dr. Malone noted that normal pharmacokinetic and pharmaco-toxicology studies had not been performed before EUA authorization for the product. “I was particularly surprised that the dossier of regulatory documents indicates allowance for use in humans based on non-GLP PK and Tox studies relying on formulations which are significantly different from the final vaccine.“
“After completing a review, TrialSite’s other source noted the following:
“A quick review the Toxicology Section (2.3.3) of The European Medicines Agency (EMA) Assessment Report on Comirnaty (COVID-19 mRNA vaccine) issued on 19 February 2021, raises concerns about data applicability of preclinical study findings to clinical use:
“To determine the biodistribution of the LNP-formulated modified mRNA (modRNA), the applicant did study distribution of the modRNA in two different non-GLP studies, in mice and rats, and determined the biodistribution of a surrogate luciferase modRNA.”
“Thus, one might question the validity and applicability of non-GLP studies conducted using a variant of the subject mRNA vaccine.”
Right. The people buying fetuses wholesale would never lie to you.
Just for diligence, and with my eyes rolled, I’ve tested with a neodymium magnet, and no effect. I’m convinced it’s just a prank for the gullible.
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