Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
I have noticed that I sweat much more since I have been on treatment, not sure if it is a side effect of the Mestinon or Prednison. perhaps someone that is also experiencing this, but not on either the Prednison or Mestinon will be able to shed a bit more light on this
Rgds
Christo
Be well,
Yesterday, this question was asked at our local MGFA chapter meeting. Our MG expert (who happens to be my Neuro) said that profuse sweating can definitely be a side affect of Mestinon. Only a few group members had ever experienced this side effect.
There may be something your Neuro can do to help you deal with the. Also, we have several outstanding group members from Texas (which I realize is a HUGE place) with whom you might want to connect.
Hugs and best wishes,
Rosie
"Nausea, vomiting, diarrhea, abdominal cramps, increased saliva/mucus, decreased pupil size, increased urination, or increased sweating may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly."
That's from WebMD.
I don't take mestinon now--prednisone has remissed my MG so mestinon doesn't do anything useful anymore.
Good Luck
Yes I sweat profusely. My hair around the hairline gets wet even if I am doing nothing.It is fatal for me to wash and dry my hair before I go out.I also have night sweats and my GP said it was probably the mestinon.
L
Be well,
Yesterday was quite mild here and while I was out having coffee I could feel the sweat running down my back and when i stood up there was a wet patch on the chair which i surreptitiously wiped. most embarrassing.
Lorraine