So I have been doing a little research and No (for those who've read my other previous post) I'm not a hypochondriac. I just want to be informed. After all, if I don't inform myself no one will. So to the question. I was reading up on M.E.(not CFS) and I fit most of the symptoms. Not the more extreme severe symptoms like losing speech but the others fit me. I have also had an MRI done a couple of years ago. One or two, I can't really recall the date. On it, the radiologists noted "white" spots but my neuro wasn't concerned about it. I can't recall the exact language of the report. Seems to be a theme, huh? I can't remember........ I was going to him for numbness and tingling in my feet, legs and hands. For those of you with true M.E. (not CFS), have you had a MRI done? What were the findings? What other tests did you have done to confirm? I am going to my rheumy next week and just want to know what to ask her about.