We have two pandemics running in parallel: Sars-Cov-2 whose genome includes Uracil, and an isomeric version of Sars-Cov-2 used in the cmRNA vaccines, coded with Pseudouridine. All spike proteins created by body (In response to the cmRNA vaccines) will be isomeric. So will the antibodies. ICU cases of Covid-19 are caused by two lethal antibodies: REGN10987 and B38. This, then, is the mechanism of the cmRNA (chemically modified RNA or modRNA) vaccines: a huge quantitiy of isomeric abs are being produced, while the immune system can no longer fabricate the same number of regular (normal) abs as before, including the two lethal abs mentioned above. But now, the vaccinated people have a huge number of isomeric abs (including the lethal isomeric versions) in their bodies, which are awaiting an activation. Spike proteins = T-bacilli discovered by Wilhelm Reich a long time ago. Spike proteins = prions = T-bacilli. These prions can become misfolded (dextrorotatory) during a time of stress, a thermal shock (volcanic eruptions), or using biological scalar weapons. It is now well known that there are neurotoxic misfolded antibodies as well. The T-bacilli cause hypoxia and thus clotting.
I had considered for some time if this was a bio-weapon and what property would you give it.
Imagine if you would a virus that when people are in small groups causes no issues. The moment you add population density, you trigger the ability to infect and kill. The Antarctica event was interesting as based on their methodology they should have carried no virus into that isolated area. Instead, what if the vaccinated can produce "Covid19" by mere proximity to each other?
That'd be one heck of a virus, you'd decimate groups of people.. so cities, military, etc. Any group that gathered would self infect and self destroy itself, in theory. This matters more after the booster, when your immune system is gone.
So vaccinated hospital staff with sick vaccinated patients, if the above is correct, becomes a death sentence.
We have two pandemics running in parallel: Sars-Cov-2 whose genome includes Uracil, and an isomeric version of Sars-Cov-2 used in the cmRNA vaccines, coded with Pseudouridine. All spike proteins created by body (In response to the cmRNA vaccines) will be isomeric. So will the antibodies. ICU cases of Covid-19 are caused by two lethal antibodies: REGN10987 and B38. This, then, is the mechanism of the cmRNA (chemically modified RNA or modRNA) vaccines: a huge quantitiy of isomeric abs are being produced, while the immune system can no longer fabricate the same number of regular (normal) abs as before, including the two lethal abs mentioned above. But now, the vaccinated people have a huge number of isomeric abs (including the lethal isomeric versions) in their bodies, which are awaiting an activation. Spike proteins = T-bacilli discovered by Wilhelm Reich a long time ago. Spike proteins = prions = T-bacilli. These prions can become misfolded (dextrorotatory) during a time of stress, a thermal shock (volcanic eruptions), or using biological scalar weapons. It is now well known that there are neurotoxic misfolded antibodies as well. The T-bacilli cause hypoxia and thus clotting.
I had considered for some time if this was a bio-weapon and what property would you give it.
Imagine if you would a virus that when people are in small groups causes no issues. The moment you add population density, you trigger the ability to infect and kill. The Antarctica event was interesting as based on their methodology they should have carried no virus into that isolated area. Instead, what if the vaccinated can produce "Covid19" by mere proximity to each other?
That'd be one heck of a virus, you'd decimate groups of people.. so cities, military, etc. Any group that gathered would self infect and self destroy itself, in theory. This matters more after the booster, when your immune system is gone.
So vaccinated hospital staff with sick vaccinated patients, if the above is correct, becomes a death sentence.
Interesting.