Doing Great…..except for my feet!
I was diagnosed in 2021 just about a month after my first covid vaccination. My Neurologist is managing the illness very well with mestinon and cellcept. I feel very fortunate that the disease is as controlled as well as it is.
BUT……
I am dealing with what I understand is called nocturnal cramping in my calves and feet. Not a major issue, but what a pain in my butt.
Are others dealing with this, and how are you managing it? Just curious…….I’d be glad to share my more of my thoughts if anyone is interested
Hey there, it is great to hear from you! We greatly appreciate you sharing your experience. It’s great to hear that your neurologist is effectively managing your condition with mestinon and cellcept. Here is an article I recommend with tips for coping with those nightly cramps: https://myasthenia-gravis.com/living/leg-cramps-night. Jodi, Team Member
