u/LegitimatePart497

Let me start by saying I have MS - diagnosed 9 months ago.

Around 3 months ago I developed lid ptosis. It was triggered by fatigue and sunlight. That lead to lab work for Mysthenia Gravis, which was negative. Now my MS specialist wants to send me to Mayo to be evaluated. Is this normal? It seems like a leap to travel for an evaluation. My weakness has spread to my arms and hands, to the point I can barely carry a drink, hold my phone, or brush my hair.