To Those Newly Diagnosed With ME/CFS: Four Things I Learned the Hard Way

I hit a nerve with my “Nothing” post about what I did (and mostly what I didn’t do) after I was diagnosed. And many of the reactions I heard from others touched on the number one, most important, know-this-if-nothing-else piece of advice I wish every doctor would give to every person diagnosed with ME/CFS.

More @ No Poster Girl

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