Along with your MS, do you also have an ileostomy - maybe due to past Ulcerative Colitis - and have tried or are using Dalfampridine (or its brand name, Ampyra)? If so, I need your feedback because...
That's me! I started Dalfampridine around the first of the month. The trouble, though, is that 4 - 5 times a week, I'm finding a whole tablet visible in my pouch. It follows that tablets must be there other times as well, but remain unseen.
If this is also you, I'd love to her from you.
* Are you still on it? and
* Do you still feel a benefit anyway?
* Or have you and/or your doctor found a workaround?
* If so, please explain.
I hope I'm not the only one ;)