What I'm asking is...did anyone here ever have a negative MRI report(s) before their official MS diagnosis? Just wondering b/c as I've mentioned, mine just recently came back negative. My C-spine had a shadow on it, but was said to probably be "artifactual". Radiologist said if my symptoms persists, that he would like to re-screen me in 4-6 months. My neuro agreed to that last month, but when I saw her this week, she said that she didn't think I had MS and that she would just run another MRI in another year. WHAT!!?? After I had just told her that my symptoms were still continuing and that I was concerned about this "Topamax" that she has me on....& I didn't know if..."my feet/legs and hands/arms going numb with extremely PAINFULL!!! pins-&-needles...ON FIRE!!" was due to the drug's side effects or just the continuing "MS-type" symptoms that I'd been having (along with all the other MS-type symptoms). Maybe she wasn't even listening!! She soooo contradicted herself. She had just told me last month that she thought I definately had an autoimmune disease other than Fibro, but that she couldn't say what just yet. I'm glad my husband decided to go with me this week to be a witness. He wants me to find a new neurologist. Maybe I don't have MS, but I must have something! These horrible symptoms aren't for nothing...and I don't think they are ALL caused by Fibromyalgia! Any ideas/opinions??? HELP!!??
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