I would be curious to know more about the rare diseases these patients were determined to have.
I wonder what kinds of things they looked for aside from the common things that may be ruled out before an ME/CFS diagnosis is made at the doctor's office (and not just in a clinical study).
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.