Sue, I totally missed your post. Duh.

Thanks for your kind words. Many others on the forum have said the exact same thing in the past. I guess I just said it at the right time for you.

I always feel uncomfortable with anyone taking a layman's advice on MG. I always think it's best to have the conversation with your neurologist.

I'm glad it helped. Some people do need that higher or extra dose later in the day to feel better.

Twitching isn't always a symptom of MG. But when you know you have MG, it tends to be one. Though it can be a side effect of certain medications or of electrolyte or fluid imbalances too!

Thanks, Sue. You really are the most sweet and considerate person!

Annie