I had an appt with my Neuro Monday and she told me about Ampyra ER since it was now available. She is not pushing but wanted me to know about it. I told her I would check it out on the Internet and NT and see what people were saying.

I have been having the "rare" reactions to meds recently and such a bad experience with Avonex that I really don't want to go on anything again.

She is also concerned about trying anything new since I had the outbreak of skin cancers. We both pretty much agreed to just continue to treat my symptoms as we have done for the last 18 years.

I hope it helps Eddie and those of you that are going to try it. I will keep checking on the thread to see how you all are doing.