I probably have never had a flare. At least not like what I've read here. Mostly when something happens to me, it does not go away. (Numbness in feet and legs, tingling, etc) I don't walk at all really, but am waiting to go back on Ampyra. I had to stop it for insurance reason as. I walked while taking it, slowly, but I walked. Soon after stopping it, I stopped being able to walk at all. I am now as scooter girl!

I was diagnosed in 2011 with RRMS. I seem to have taken the same path as you. My Dr now thinks it's SPMS. I am still on Copaxone. I am supposed to repeat two MRI s in November. We will decide on any changes when the results are in. I will either stay on Copaxone or switch to another DMD. He still wants me on one.

My mobility, basically walking and balance.

It does help a lot of people. I know that they will help you get it for free if your insurance doesn't pay for it. I tried it when we were without insurance for three months. They said that we made too much money the year before. But it's definitely worth a try.

My Dr wants me to try Amprya for my walking. I've had the prescription on my coffee table for about a week. I'm a little reluctant to take it. Number one my insurance doesn't pay for it and I found out that I don't qualify for Medicaid. So I was dropped on the new year. I really don't know if I qualify to get the second prescription or not. So I don't ant to start it if I can't continue it. I'm applying on the healthcare . Gov but I don't know if this ins pays for it yet. I'm going crazy mad with my Ins. Does Amprya really help you. Right now I'm not so steady on my feet. I have balance issues.