I was on C from 2006 until 2010. I did get new lesions and had a series of flares. This was within the first 2 years. After that, my brain MRIs have stayed the same. I haven't had an MRI in a little over a year so I don't know.

Also, I still got flares even on C. They just weren't as intense and didn't last as long. That was the only difference I noticed.

Getting a 2nd opinion may be worth it. It doesn't sound like this neuro is willing to work with you. In other words, he sounds like a "It's my way or hit the highway" kind of neuro.

Let us know how things work out for you guys.

I was on C for 4 years and DID have flare ups while on it. In the end I simply couldnt take it anymore, as it made me feel miserable.

DMDs cause you to have FEWER relapses, and fewer lesions to come on, but it wont prevent them all. It will just make them less severe.

Its a tricky spot to be in. I hope you are able to talk WITH your MD instead of having him talk at you. I hate when they do that.

Thank you very much for your replies. As we've thought and talked about it for the last few days it seems that a switch from Copaxone may be the best thing to do to see if he can find something more effective. I am going to post another thread soon to ask about the other options we have.