New to rebif

Hello, I am new to treatment and the ms society website but after seeing my rebif nurse yesterday she said that I should share my experience with people to show people that this has been the beginning of something new to me. It took me 7 years to realise that I needed treatment after a big relapse in January my life changed and I decided on rebif I have a very active dalmation and the thing I found hardest was not being able to take my dog out as I used too over the last few months I have somewhat recovered and now walk about 4 miles a day with him. I have a full time job and taking rebif is now just part of my life not ever going to cure it but I hold on to it not getting any worse right now. As scary as all this is I am proud that I am back in control of my ms rather than it controlling me for anyone that is scared like I was and still am there is hope out there with a positive outlook everything can be achieved. Rant over just wanted to share this. X