Thanks for the info, good to know I shouldn't be getting a change in dx just yet 😊, which also means hopefully they won't take me off the copaxone, not that I particularly like the bee stinging welts that it leaves, but given the potential side-effects of the alternatives, I think I'd prefer to stick with the known evil. Cuz if the hospital neuros were wrong about possible change in my dx, I'll keep the hope that they were equally wrong in the possibility of changing meds.