Thanks for sharing, Kelly.
I was a bit amused when I read the Q & A section on CIS...it stated in the answer that patients with CIS are in denial and need to get early treatment so as not to have a relapse.

It took me years before the neuros were convinced that I indeed had MS...not the other way around I wonder if I would have been healthier now if the neuros had put me on Copaxone when I first began presenting sxs?