I'm hopeful that it is the cause but it seems like that totally depends on whichever doctor you are talking to! We had discussed having it removed in November of last year but covid delayed everything. I reached out to Mayo at that time and have multiple consultations upcoming. I love living in Montana but definitely feel like I need a tertiary center to help find a solution. I've become so depressed over this it is hard to function. So I will wait to see if the Mayo team agrees this is myasthenia, the pituitary tumor, or something completely different.