Crowdfunding: Trial By Error: Reporting on ME, CFS, ME/CFS, "Medically Unexplained Symptoms," and now Long Covid, April 2022

As I've said many times, this crowdfunding is among my least favorite things to do. I wish I could figure out another method of funding my work, but I haven't come up with one. Unfortunately, it's not the kind of project that gets funded by major donors and foundations.
I should stop worrying about it David, no one else does ... except for the BPS folks, which is as good a reason as any for you to stop worrying ;).
 
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Conversely we don't yet have solid evidence it is the same. Strong indications suggest there is a strong overlap, but it would be very presumptuous to insist at this stage they are exactly the same. We just don't know yet.


Except that MECFS is diagnosed based on symptoms—if you meet the diagnostic criteria, then you have the disease. Otherwise we would have different diseases based on what your trigger was, which doesn’t make sense.
 
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