So, it's looking increasingly like the mRNA technology they've been boasting about probably doesn't work as planned; our bodies probably don't become eternal spike-producing factories; and any spike - which has little in common with the "virus" itself - was wrapped up directly inside the LNPs, along with bits of DNA, RNA plus E.coli, SV40 & other tidbits. The question now is whether the LNPs actually enter the cells then the nucleus (according to McKernan, yet to be proven) or remain intact, invading the tissues and clogging up circulatory system, or could they in most cases get gobbled up or disintegrate on their journey then get excreted from the body without doing much damage unless you're allergic to components of LNPs.
A key issue is - the lots/batches were of such variable dose quality, why didn't the regulators AT LEAST sample individual lots/batches?
One could argue that since the doses themselves were experimental. with no proven manufacturing track record, a much higher sampling than say 1/1000 vials should have been a minimum - say 50/1000 vials,
THE PANDORA’s VACCINE on Vimeo, https://vimeo.com/807279310, showed other issues with clumping concentrations with doses taken from multi-dose vials (at different times from the same vial - 5 doses per vial? - once opened and prepared via "shaken not stirred" ten times, notwithstanding clumping in general before vials are even opened) and the massive jump in temperature from freezer to body temperature that completed the actual manufacturing process (plus how unstable mRNA is in general).
There isa huge difference between clinical trial concoctions and manufactured and distributed concoctions.
Pfizer tried to replicate "soon to be" manufactured doses in Process 2 with a 250 a side trial which revealed harms at 3-4 times the rate of the clinical trial (Phase 2 - Process 1) - Process 2 outcomes were available to FDA PRIOR to authorization, but were the results distributed to every other health regulator prior to their authorization?
Assuming yr 1st question rhetorical. Yes - 5 doses per vial. I'm sure all of that played a huge role in variable outcomes but key take-away for me is the LNPs themselves are probably the main problem, due to their composition and now the extra stuff we're discovering they contain. Much simpler to put the poison directly into the LNPs. No way imo this was entirely due to accidental contamination. They perfected the art of bactofection (bacteria-mediated transfer of plasmid DNA into mammalian cells) in early 2000s apparently. Shimon Yanowitz has done a couple of presentations on this. In any case they need to clean up their act before they move any further with mRNA vaccines/therapies. McKernan says it's easy to do but maybe he's talking about small quantities.
I believe they all kew what they were injecting into people and they didn't care, as long as they died and/or had life long healthcare needs so Big Pharma could continue to get rich.
So, it's looking increasingly like the mRNA technology they've been boasting about probably doesn't work as planned; our bodies probably don't become eternal spike-producing factories; and any spike - which has little in common with the "virus" itself - was wrapped up directly inside the LNPs, along with bits of DNA, RNA plus E.coli, SV40 & other tidbits. The question now is whether the LNPs actually enter the cells then the nucleus (according to McKernan, yet to be proven) or remain intact, invading the tissues and clogging up circulatory system, or could they in most cases get gobbled up or disintegrate on their journey then get excreted from the body without doing much damage unless you're allergic to components of LNPs.
Yes.
A key issue is - the lots/batches were of such variable dose quality, why didn't the regulators AT LEAST sample individual lots/batches?
One could argue that since the doses themselves were experimental. with no proven manufacturing track record, a much higher sampling than say 1/1000 vials should have been a minimum - say 50/1000 vials,
THE PANDORA’s VACCINE on Vimeo, https://vimeo.com/807279310, showed other issues with clumping concentrations with doses taken from multi-dose vials (at different times from the same vial - 5 doses per vial? - once opened and prepared via "shaken not stirred" ten times, notwithstanding clumping in general before vials are even opened) and the massive jump in temperature from freezer to body temperature that completed the actual manufacturing process (plus how unstable mRNA is in general).
There isa huge difference between clinical trial concoctions and manufactured and distributed concoctions.
Pfizer tried to replicate "soon to be" manufactured doses in Process 2 with a 250 a side trial which revealed harms at 3-4 times the rate of the clinical trial (Phase 2 - Process 1) - Process 2 outcomes were available to FDA PRIOR to authorization, but were the results distributed to every other health regulator prior to their authorization?
https://twitter.com/Kevin_McKernan/status/1681675541735264257
Hugely variable doses in vials = hugely variable outcomes.
Assuming yr 1st question rhetorical. Yes - 5 doses per vial. I'm sure all of that played a huge role in variable outcomes but key take-away for me is the LNPs themselves are probably the main problem, due to their composition and now the extra stuff we're discovering they contain. Much simpler to put the poison directly into the LNPs. No way imo this was entirely due to accidental contamination. They perfected the art of bactofection (bacteria-mediated transfer of plasmid DNA into mammalian cells) in early 2000s apparently. Shimon Yanowitz has done a couple of presentations on this. In any case they need to clean up their act before they move any further with mRNA vaccines/therapies. McKernan says it's easy to do but maybe he's talking about small quantities.
Agreed. I should have made the point about the LNP's/plasmids and didn't.
Can anyone recommend a good Dr in the Palm Beach County FL area to help with medical issues from shedding & or long Covid. So far the Drs are no help
Have you tried the FLCCC network? Here's a few.
https://icfnn.org/index-22.html
Peter Hibberd, MD, FACEP, FAAP, FAAAEM
Board Certified in Emergency Medicine
Palm Beach, FL
(561) 655-4477
(Monday-Sunday) 8am-11:30pm
Treats both Covid for preventative and active illness.
We take great care in making sure patients get access to medications at a reasonable cost.
We only use HIPPA compliant software. Your privacy is guaranteed.
Thomas A. Gionis, MD JD MPH MBA MHA LLM
Florida Medical USA
North Palm Beach, FL
(561) 331-5838
Dr.TomGionis@UCLA.edu
https://floridamedicalusa.com/
Suresh Rajamanickam, MD
Evolution Hyperbaric Institute
Palm Beach Gardens, FL
(561) 767-0721
suresh@mitoreserve.com
https://mitoreserve.com/
Judith Jensen, MSN, ARNP, FNP-BC
Mobile Urgent Care, LLC
West Palm Beach, FL
(561) 677-9999
jjensenarnp@gmail.com
https://mobile-urgentcare.net
I believe they all kew what they were injecting into people and they didn't care, as long as they died and/or had life long healthcare needs so Big Pharma could continue to get rich.