It must be so frustrating to not receive more guidance from your neuro with this kind of big decision. I have never taken Rebif, and am a relative newbie to both MS and Copaxone, so am by no means an expert. However, I’d be happy to talk to you about my experience on Copaxone (started last November, all is still fresh in my mind, lol). I don’t know if that would help you at all in this decision, but just let me know…..
There are people on this board who are indeed on Rebif, so hopefully someone can provide you with some additional information.
By the way, I only live a few hours away from Sacramento. Maybe I need to come get one of those cookies you mentioned. I am a sucker for a good cookie. J