u/Objective-Bug8037

With ME/CFS or Long COVID, what kind of help actually makes daily life easier? It could be something small that someone does regularly.

And is there something you still struggle with because you can’t get the right help?

Has anyone with Long COVID or ME/CFS had GPCR autoantibodies tested? What happened after you got the results?

Did your doctor use them to decide what to do next, or were you left with a result that nobody really knew how to interpret?

If you remember which test or laboratory you used, that would help too.