@oxidativestate@noahparker305 That study is mice and their bmr is significantly different over 48 hrs than humans. That would be a very extended fast in humans not forty eight hours. This does not translate well at all. Did you not read your own study?
@Sin_Nombre89241@TCW_CAP@NoLimitGains Bro it’s an ai slop account don’t give it attention. You can tell by the way it writes. It’s just copy pasted chatgpt
@MaryBowdenMD Wrote a case study on using nicotine patches to treat an acute covid associated cholinergic crisis with rapid resolution of symptoms. Likely saved the patient. My current place of employment doesn’t seem interested
I’m glad. That’s great for your n=2 but that’s what you can call anecdotal. Evidence and real world translation states otherwise. Even mild infection can cause chronic issues hence why we saw elevated TMA levels in children, who seem to be hit the least initially. Now long COVID has hit that group despite them not having the same vaccination rate as adults. Even with it being underdiagnosed or excused away.
Seroprevalence also doesn’t make a ton of room for zero infection individuals. Not saying there aren’t hence my reference to hla/mhc1 aggressive expressors. But chances are there wasn’t a ton of testing going on on an individual level like that.
@EthicalSkeptic@Cryptogal3 lol yeah I can say this. People get reinfected whether they took the shot or not. And each subsequent reinfections is not benign. That being said there is some evidence of people who have aggressive hla/mhc1 responses that may not get reinfected as easily.
@EthicalSkeptic Hadn’t heard this hypothesis. Would make more sense than delta -> omicron I suppose. Especially with the whole “it was just immune pressure” excuse, that being said, genomic sequencing and surveillance isn’t really my specialty. Will have to look into what you said
Could be. I think QC was trash because there was a lack of incentive associated with legal indemnity. However I am seeing a lot of increase in ANA positivity and chronic inflammation with recent symptom onset. Some without getting a shot at all. Post infection, maybe lingering low grade infection like a flame that doesn’t go out. Maybe there’s the issue with original antigenic sin too. Could make a case for exosomal shed I suppose. Why antibodies instead of tcells was the focus doesn’t make sense to me with a virus that mutates so quickly. Also the mutations we’ve seen make me suspect a bit of fuckery. Most of them made sense. Omicron straight up fucking did not.