Like many, I am sick & tired of being sick & tired! I've been ill since 2001 after contracting mononucleosis and have been treated mainly with medications, which their side effects have caused more problems, and yes you guess it, more prescriptions. I would be very happy to feel even the slightest bit better than currently. I have an appointment to see my new GP doctor this 7/20/12. So far, she's very compassionate and takes the time to go over things with me, but she has not suggested any new or treatment protocols. My question is: What are some (affordable, as I'm on SSDI) test/treatments and/or prescriptions that have shown some positive effects on CFS/ME patients. Thanks in advance.