Can I ask you what kind of specialist your wife saw to find she has CMS? Who would you see at USC.
I have the same symptoms, not that severe. Saw hematologist and Rhematologist, none know what's wrong, except blood tests every six months. I don't know if they do care or not. It's been almost two years and think I should find new good doctors who care. I do have HMO but in Los Angeles the medical group or network are the one who control every thing. I'm now ready to go to outside the insurance and pay my own. I have to control my own health not some medical groups who only care about $$$