Since being diagnosed this past December with MG, I’ve done copious amounts of reading and research on Myasthenia Gravis and have found no mention of muscle weakness pertaining to bladder control and sphincter control.

I did want to bring this to the Forum but do not want to appear indelicate. It seems that both of these matters have become troublesome for me in that when I have to pee, I have to pee NOW, and also there are bits of poo that release themselves involuntarily - no matter the time of day or what level of activity I’m experiencing.

I think that for me, this might be part of the generalized muscle weakness that presents with MG.

Does anyone have similar experiences or ideas they might be willing to share?

Thank you.