Hi everyone. So here's the update: Well, my MS specialist Neuro called me in response to my worsening symptoms and pain. He told me that I do not have MS but that I do have NMO (Devics). My test for the NMO igG was positive and my brain lesions arent MS lesions, theyre from NMO. So the ms symptoms I've been having are really transverse myelitis. Wow! I'm not sure what to think now. MS was bad enough!
So now they're getting me in to go over treatment, and pain management...
Anyone have experience with NMO treatment?
Thanks!
So now they're getting me in to go over treatment, and pain management...
Anyone have experience with NMO treatment?
Thanks!
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