7 years ago I was disabled and in a wheel chair. Lately I have symptons again like I did 7 years ago. I went to the Dr and he identified what I had in one visit and an MRI and a spinal tap. I just wish that the Dr 7 years ago would have seen the spot on my brain so I could have been on meds then and not in a wheel chair. I missed alot with my three kids and work. I am glad now I know what it is. I also know now not to lay around in pain, it hurts worse. I need to walk around and stretch those muscles. I have alot of nerve damage that can't be reversed but now I can stop it from getting worse maby. If any one has comments on the meds they have out thier for MS patients please let me in on it. Do they affect the diabetes in any way. Is thier wieght gain with any of them.