What medication, therapy, or alt. treatment that helped the most?

I am taking Copaxone. I had also taken rituximab for RMS.

I have minimal side effects from the treatment... lots of fatigue and shortness of breath. But the doctor says it is working in slowing the progression. So I am hopeful it continues to do so.

I am also on Copaxone and have not had shortness of breath as a side effect but definitely fatigue. I'm hopeful for the same@msslady 

Has anyone taken Ocrevus or Gilenya? I am currently on Tysabri but I tested positive for the JC Virus so I have to switch meds. 

@Cgonlag I do take ocrevus and it does work. but it tends to wear off at the end of 6 months. Plus when u start it fatigue is a side affect. Just makes most people sleepy

Thank you! Had you tried any of the pill options? (If you dont mind me asking). 

I'm currently taking Ocrevus, but I've had difficulty walking for a year now. What helps with that?

I am an MS fighter of 30 years now. I have been on:

Copaxone - did fine, hated the injections

Once oral meds became available, I jumped on that opportunity

Tecfidera - had a severe allergic reaction. My face swelled up - I looked like Will Smith in the movie Hitch

Aubagio - I have been on Aubagio for about 5 years now. I love it. MRI's are showing no new lesions and RRMS has been stable.

I've had difficulty walking for a year now. I was diagnosed 2 years ago, and a pretty good, and established pool player. I'd just like to walk better again. Suggestions?

@DCircular I have a friend from my MS group who takes Ampyra which I think is meant for walking. I'll have to ask her more about it. I don't have any experience with it myself but maybe you can ask your doctor about if it'd be a good option for you?

I've taken Ampyra for some time. It initially helped me with balance, but nothing more. Walking is still a difficulty.