Sorry to hear stuff's been wonky.

It is a personal choice for the DMD's. I was on Copax and now rebif due to IPIRs. For the two years on copax, I was "stable". Crossing fingers that the rebif will also be good to me. So far so good.

I too am not sure if they really help since this is a wacky disease to begin with, but I have something my other family members with MS didn't have. So that is why I'm on a treatment of some kind.

From a needle phobe, shots do become routine. The autoinjects help a lot when fine motor skills are blah. LOL, I can give myself one but still cringe and want to run from anyone else coming near me with a needle.

Know that no matter what you decide to do, we're hear for ya.