Coronavirus pandemic 2019-20 #5

So the Russian adenovirus vax has not produced the mass of heart attack, stroke and other deaths that the precious, superior Pfizer and Moderna
mRNA concoctions have produced. This points to the N1-methylpseudouridine ribosome glitching as being the key factor. So mRNA victims
have a whole spectrum of proteins (antigens) and not just the template spike. The risk of autoimmune and protein folding pathologies is vastly
greater.

Retroviruses exist in nature and the mechanism evolved over millions of years. The Russians basically modify an existing virus to deliver the mRNA payload. Lipid capsule technology originally was forbidden from common use, you could only use it in terminal patients like people with cancer, because the lipids caused clogging of small blood vessels. It could cause sterility in women, and some people got heart attacks. Nanolipid capsule technology supposedly doesn't cause those issues, if you believe them, but it wasn't tested and approved for mass market use until they shoved it through with the clod shot.

And the thing is, you could have made the vaccine just fine with other technologies. For example the Chinese Sinovac didn't use mRNA technology. It is an inactivate vaccine. It used the same technology that has been used to make the hepatitis and influenza vaccines for many years. But of course that couldn't be patented by Big Pharma so they didn't want anything to do with it.

No way the coof is a natural disease.   This is basically a biowarfare agent.    The protein "clots" found in deceased coof vax victims is consistent with this analysis.
That the engineered spike protein produces protein folding pathologies is an established fact even in the published literature (news reports; if I find the paper I will post
it but the video refers to one already: Nystrom and Hammarstrom [2022]: https://doi.org/10.1021/jacs.2c03925).

Given the ribosome glitching the virulence of the spike is even worse.   We do not have a single protein type but a whole family produced by random glitching during
construction in cells form the mRNA template.   The mRNA itself can be altered by thermal damage after being injected into the body.   It does not matter that it was kept
in a portable refrigerator at -80C.   The body temperature is over 37C and it warms up really fast.   The reason we have DNA is that it is more thermally stable than RNA.
RNA viruses experience a lot of antigenic drift.   It is hard to have higher life forms with an unstable genetic template.

Given all the options, the Chinese vaccine is the best option.   Feed the immune system virus pieces.   Don't introduce freaking prion-like randomly varying toxins.

https://www.researchgate.net/publication/363525360_COVID-19_Energy_Protein_Folding_Prion_Disease

COVID-19: Energy, Protein Folding & Prion Disease

The recent recognition of intravascular amyloid formation with deposition of insoluble microthrombi throughout the circulatory system in primary COVID-19 infection or following administration of mRNA vaccines is a pivotal discovery that alters conventional notions about the nature of the underlying pathologic process at play in SARS-CoV-2 infection.

Anyone who claims that gummy worm clots are a conspiracy theory needs to be shot.

The clot shot is producing clots made from amyloid never seen in history.

Safe and effective is newspeak for criminal injury.

Origin...



(Note the relevant bit ends at about 6 minutes... the rest is no worth watching....)

Regarding the vaccination procedure relative to disease onset. For the rabies virus there is a window after infection (animal bite) where a
vaccine can save your life. The virus migrates up the nervous system by hitching a ride on a transport system to the brain over a period
of time determined by the proximity of the bite the the brain. Our immune systems cannot handle the rabies virus at all. It prevents the
apoptosis of infected cells while at the same time triggering it in T4 cells trying to deal with the infection. Attacking brain neurons also is
bad because the immune system does not act the same way as in other tissues on account of the fact that brain tissue does not regenerate.
So the immune system cannot cause collateral damage (which it does in other tissues) without causing irreversible damage.

By contrast, respiratory viruses such as the coof progress instantaneously after infection. There is no latency window lasting weeks and our
immune systems do develop antibodies to such viruses. If you had the coof, you get no (negative) benefit from the vax.

Next time some regime bootlick tries to argue that giving vaxxes after infection with a live virus is perfectly OK, you can tell him to f*ck off and
die since everything depends on the virus.