| dr says ms but lets wait n c
my official dx is demylenating disease, unspecified, spastic paraparesis, neuropathy, & basil artery migraines (BAMS). I had a LP done a little over 2yrs. ago that showed elevated basic mylen protien levels but not Obands. This was done a week after my first episode of numbness in entire rt. side of body. I read that these levels can be elevated in a ms patient just after a relapse. My neuro. (a ms specialist) said it was nothing to worry about. Then I had 2 bouts of ON dx by a neuro. opthomologist. She alos stated that I had no periferial vison & had colorblindness. My neuro. did a vept & again said it was a little abnormal, but nothing to worry about. He has been doing MRI's every 3mts. finding only 1 lesion on my spine & degerative disc disease. Did I mention that I also see a uro. & have toself-cath4x a day dueto myneurogenic bladder. Now I am taking baclofen, neurontin, marinal, topamax. restoril, flomax(bladder), klonopin, loratab, paxil, & iv solu-medral 2days monthly. My neuro. says he isn't ruling out ms yet( they have ruled out everything else). What else could there be. I have all the symptoms, which he is treating, i have to use a walker alot of the time. He is discussing a muscle biopsy???? He wanted to start me on IvIG, but insurance denied it without a dx. What is he waiting on fora dx? He keeps saying that it takes some people longer than others to get a dx. Is he waiting on me to meet the McDonald Crieteria? I thought that you could get a dx without going by that if you had enough clinical findings, documented relapses, etc.. I guess I'm just confussed as to what my dr. is thinking & how he's treating me. it seems as if he's trying to treat me as if I have ms, but is affraid to give me the official dx & start treating me with the real ms drugs so that I don't progress, hopefully.
Please someone respond.
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