Well, it was easier for me. We had a very difficult times when my symptoms hit. We just had our first child. Her typically hard working husband stated sleeping 12 hours a days and providing very little baby help. I knew something was wring. I sought answers but didn't share alot with her, which made things worse. It took almost 15month before MG got on my radar. Before that, I was thinking strokes, brain tumors, Narcolepsy.. So once we figured out MG we were just glad it is something I can live with.
My concern now is maybe she doesn't understand how bad it may get. She doesn't do research herself. I'm not sure how to tell here all the different possibilities of this disease.

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