I myself am on Copaxone 3X weekly. Shots. I have been using it for 7 1/2 years. At yr 7 I had an MRI as it was a new neurologist. ( My last neurologist only did a MRI once every two years. ) I had for 6 years no new lesions. Yes everyone is different. I myself had no new problems so why change. As much as I hate needle. I did not and would not change to a pill. The old saying " If it isn't broken don't fix it" I think applies in your case. Good luck dear.

And hows that working for you?

I did Copaxone for 4 years...and when a pill came out, I grabbed that option. I did Aubagio for about 3 years. Hair came out, as expected, but WOW! It came back...HUGE. My fine, straight hair is now curly and thick. Unrecognizable! BUT...I think it did something to my intestines, too. Diarrhea for too long. When I was down to 101 lbs, the neuro took me off. Now, I’m on Tecfidera. The flushing is more than I can handle...and will check this site for advice. Good luck to you!

Yes my specialist did tell me that would be a side effect of aubagio ... Thank you for that! I am looking for some feedback on the aubagio and this helped :)

I used to take Copxone 3x a week now I have been taking Aubago for about 2 years and it’s doing what it’s dupposed to do I feel the same as I did on the shots just no pain when swallowing the pill I hated taking shots all Aubago has caused hair loss at first now it’s doesnt ....