Hi - I was diagnosed back in january with ms. I know I have had it for approx. 8 years but was misdiagnosed time and time again.
As far as abc drugs - I am on rebif - it's ok. I had some flu like symptoms in the beginning, I got used to that, the injections site is sore but I guess all the drugs do that. The benefit for me is that I do injections 3 times a week. My sister is on copaxone and that is a daily injection. Yuck.
Some things that I learned (it was hard) was that my body needed this medication. I couldn't get used to the fact that I had to do injections. It was scary, awful but after 6 months of doing it I realized I had to and it's not bad anymore at all. I did suffer from fatigue but learned really quick if I gave into it, it ruled my life. I got myself through it by doing yoga every other day and supplimenting some yoga every morning to get me going.
I do nothing different in my life except the injections. My life is the same. Today I shampooed carpets for 2 1/2 hours, moped wood floors, grocery shopped, did laundry. I had to force myself to remember that I am no different than I was, I just have a diagnosis now.
Good luck to you. Oh by the way once my body got used to the meds, my migraines have completely gone away. That was something to live for....
Good luck to you - shannon :d