Guest guest Posted January 11, 2000 Report Share Posted January 11, 2000 Your story sounds just like mine! Symptoms for the last 4 years. Diagnosed as possible MS in May of '96. My current neuro didn't feel that I had MS. She kept searching and testing and re-testing until Oct. '99 when I was diagnosed with ACM1. I don't know if I should have the surgery or not since I have survived the last 4 years. At least now I know what I have. I am just afraid I may develop a syrnix or something. Good Luck, Tina ACM1 5mm herniation tmfuller@... Quote Link to comment Share on other sites More sharing options...
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