My last mri, which was January of this year showed no new or active lesions.
I've talked to some people who said they couldn't do a shot everyday. I guess with me, it's mind over matter. I have soreness sometimes depending on where I do the shot; mostly my legs, but overall I just do it.
I will stay on copaxone for as long as it's doing what it is suppose to do. I started ampyra in March of 2010. When first starting it, I danced at an affair at least 5 times, my gait improved and my mobility. Since being on it for a while, it has sort of plateaued, but I still have some improvement since I have been on it. It is taken every 12 hours, and if I don't take it, I know that I haven't. I will continue on it as long as I can.
The other medicine I take is provigil for fatigue. I have never taken it as prescribed because to me it is a bit strong. I only take a half tablet if I want to stay up longer or have things I have to do in my house. For the burning, I take Neurontin occasionally. I take it only when the burning is really bad. I don't take any other medicine for my Multiple Sclerosis.
I take health supplements like vitamin B, omega 3, vitamin d, co-Q10.