Yes, I know, gmi. Just the thoughts of the whole process exhaust me -- not to mention the pain. Seems I remember something new about a year ago, having a MRI can take the place of a c. unless they find something at which time they go the regular route. I am planning on calling my neuro tomorrow (Wednesday) with these new symptoms. Of course I'll probably just talk with a nurse. Kind of have to chuckle when various MS articles tell us we have to have a good working relationship with our neuro....well, it's kind of hard to have much of anything when we only see them for about 10 minutes twice a year and even phone calls are intercepted. Funny though, the exhorbitant insurance payout goes to him.

If I get no information from him, I'll try my pcp. Thanks for caring!!