Thanks everyone

I am not sure I am much the wiser - sounds like a gradual slide - no fireworks to mark the 'new status'. No telegram from the Queen to say 'Congratulations' and no 'ticker tape' parades.

I have had so much residual stuff that has stayed with me since my original diagnosis - double vision, foot drop, issues with coordination and some with bladder control. It just makes me wonder these days, since I haven't had a relapse in years, but I fall more, and generally feel weaker on my left side, I am much more emotional (and unable to control it), and not coping near as well.

Thanks for the insight.

Hugs

That's one of the many things that stinks about this disease--nothing is for sure.

I don't understand how neurologists determine this either...

Ann, your emotional reactions could be pseudobulbar affect...there's a new med for it called Nudexta. It helps me somewhat...I saw an actual commercial about the disorder on TV last week.