I am new to this forum, but have been living with MS since 2011. I consider it a mild case because it doesn't really impact my abilities yet (a lot of numbness and tingling in my left hand and leg, but no real loss of function... I'd say 98% functionality).
Given the unique nature of the disease and how everyone experiences symptoms differently, I haven't had much interest or need to reach out to others for support. I just want to deal with my unique brand of MS as it comes to me.
That being said, I might have a few more questions in the future to bounce of others who might be able to relate. My wife, understandably, can't sympathize with me, and my neurologist is awesome but doesn't have the first hand experience to answer some of these questions.
I've been on Rebif since 2011 and have had no flare-ups since my initial diagnosis. Most of the lesions in that initial MRI have vanished and there have been no activity so far in any of the following MRIs.
Now, I'll go ask my first question in the appropriate sub-forum, if I can find the right spot