Sasha
Senior Member (Voting Rights)
Almost there! Still working on it, $3.5 million ME/CFS mechanistic study with cryotherapy as a way in.
That's interesting - is there a thread on that cryotherapy study?
Almost there! Still working on it, $3.5 million ME/CFS mechanistic study with cryotherapy as a way in.
It seems to have a dodgy rationale, although that doesn't mean it might not work for other reasons.Not sure if this is related.
Research: Cold Exposure and Cryotherapy in ME/CFS, Fibromyalgia and Long Covid
Then again I have problems when I get too cold too. It’s just either less bad or more likely a lot easier to avoid/control than heat.
Understanding why his happens to so many of us, and our bodies react so oddly, particularly for those who are severe it seems, would I think tell us a lot about ME.