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naraburns  nihil supernum  1yr ago (text post)   33352 thread views

Culture War Roundup for the week of February 27, 2023

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It's the binding site of the virus. The ACE2 receptor, its more common in muscles and the heart is loaded with it. The reason the vaccine fucks your shit up is micro clots and autoimmune shenanigans, the reason the virus fucks your shit is damage to muscles and also auto immune shenanigans.

There is no "long covid" all of the symptoms of it are consistent with clot/hypoxia damage to nerves and fine veins.

I don’t know the science specifically but this explanation makes sense to me.

It seems to me vaxxes and virus fuck up your heart. Which if the vaccine is only working 4 months at a strong effect raises big questions to me on how much we should be vaxxing. And could explain continual excess deaths.

This is not the right take.

You should be much more concerned about the size, shape, and ability to move through your body compartments with a Vaccine, than with a virus entering your mucosa.

The virus, if anything, is very limited by ACE2 receptors, whereas the lipid nature of the mRNA droplet allows it to merge into literally any cell and make it into an antigen producing cell. Much more than ACE2

The virus, if anything, is very limited by ACE2 receptors, whereas the lipid nature of the mRNA droplet allows it to merge into literally any cell and make it into an antigen producing cell. Much more than ACE2

This is sort of like saying "the antibiotic, which can get into every cell" or "the air conditioner, which can change the room temperature in a way that affects every cell". You're writing as though you think it's significant that it affects every cell, but you give no reason why that's actually significant.

Now I think I'll go eat a hamentash. The carbohydrates in it, entering my body, will affect the synthesis of ATP in every cell in my body.

Well, the carbohydrates will not fold into a protein. Carbohydrates mainly going to enter the blood stream as glucose, simple principle of digestion and metabolism in human physiuology.

Using your muscle cells, vs. using one of your cardiac muscle cells, is why you do not want mRNA droplets in your blood stream interacting non-specifically with your organs

My understanding of the way the mRNA vaccine works, is that it induces cells to generate proteins that match the one of the virus, so your immune system can attack, and train on it. If the virus' structure limits what kind of cells it can attack, and the vaccine has no such limits, and thus can trigger an immune response against any type of cell, that would mean it can cause greater damage.

There can of course be other factors that could turn all that around, and still have damage done by the virus be worse than the damage done by the vaccine, but the argument cannot be dismissed by sheer snark.

Yes. Imagine someone saying "Let's try injecting the antigens into their heart!"

Well, we know the mRNA enters the bloodstream, so it could transfect any cell...

This is not all proven - the vaccine entering body tissues because there's no known characterization of nanolipid particle pharmacokinetics is the main issue her. There's no concentrated ACE2 receptor in testicles, but the nanolipid particle will be exposed to the testicles via the blood stream (at the testicle blood barrier, which the vaccine can cross).

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