• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of and finding treatments for complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia (FM), long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

    To register, simply click the Register button at the top right.

In need of a doctor, bad!


Senior Member
Ive been on this site for a little while but have been ill for 13 years now.

I have been to Mayo Clinic, Wake Forest, and several other research centers over the years.

I’m in need of a CFS doctor as that’s what these different centers have told me I have. I tried a few POTS doctors but they don’t think I have classic POTS, more likely CFS.

I put my name on the list for Nancy Klimas but that could be 8 months away... I’m not sure I’ll make that considering the scary relapses I’m having that hospitalize me.

Any help?
Last edited: