I am 76, diagnosed a few months ago. I had realized something was wrong a year before. It took that long to find a referral to a neurologist for treatment. I too wondered if my MG would have stayed occular and not progressed to generalized had I been able to be treated earlier. I have been doing well on Mestinon and progesterone low doses. Sr180 and 10 mg. I walk every day and do 20 minutes of stretching and calisthenics daily. Some days I am stronger but I still move however I can. I have been sleeping well. About 6-8 hrs. I do get up a few times for the bathroom. I am getting out now to play cards. I'll get back to my hobbies when I get there. Looking forward to travel to see my great grand babies in Nova Scotia. We will see this year, 2023, how that turns out.
I have a positive outlook on life. I help wherever I can and have always been a community booster.
I post this story to let you know acceptance and researching and advocacy all work to deal with this disease. I will adjust to my new norm. I won't hike 2 hrs but I can do 20 minutes and shop walk for an hour or two at a time
I can't paint all day but I can 3 hrs at a time.
Now thinking about the thymectomy route should my neurologist talk to me about it.
Will this work for a 76 yr old? Will it be stressful to my body and set me back? Will I take the chance it's possible for remission? Not enough research out there to make a case one way or another.
My story so far.