I talked to my neurologist this morning. He said the MRI was about the same as the one last year. there was a slight area in the white matter but he said it is something that shows up commonly in people who have migraines so he thinks that is all it is from, but it wasnt there last year on the MRI. He is taking the wait and see approach, as he did last year when he didnt know what was wrong with me. He admits to not knowing what is causing me to feel bad. I see my regular doctor tomorrow and hope she has more advice to offer other than to suffer and wait it out. He said he does not think it’s MS, so that’s good. but the bad is not knowing what is causes me to feel so bad. I’ve been through this before and it’s even more frustrating now that it’s been a year and it’s the same load of crap from the doctors, and I feel worse now than I did then. reading back though to this time last year I may have been just as fatigued as I am now I just dont remember it. the other big problems that are worse now are really bad dizziness and of course tingling all over, used to just be my face but now it’s everywhere. my legs and arms are weak, I keep getting bad muscle spasms, they are like the bad leg cramps you get when pregnant and wake up screaming, ok that’s how I was when pregnant at least, but now it’s in my back and arms and sometimes thighs. my body is so out of whack it’s driving me nuts! and the drs arent helping either…we’ll see what my favorite dr says tomorrow, hoping she’s still on her “i’m willing to find out what it is no matter what” kick….