Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I've been on Rebif off and on for a year. I had flu symptoms sometimes, a couple of really high fevers/chills after I started and re-started. I had site reactions just redness and bruising but I think it was because the needle wasn't going deep enough.
I got very depressed too. I'm sure it was related to the MS as much as the drug but since I have been off it I have been feeling great. The problem I had was that I was still showing new and active lesions while on it so it wasn't for me. I tried Copaxone for a month but the site reactions with that were un-bearable. I'm not on anything right now because my husband and I want to try to have another baby while things are stable. I hope the Rebif helps you but it just wasn't the one for me.
Good luck and write me anytime if you have questions.
*Hugs* Trish
(((hugs)))
I'm starting my fourth month of Rebif and am happy to say I have had no side effects except for the second month of the 44 shot and than it was just a fever and it could be control'd with Aleve or Ibuprofen. After that I've had no problems.
As far as injection site make sure you rotate like they want, you have 4 different spots on each side of the body. I read where some people use on a couple of sites but for me I don't want to take any chances as it would be to easy to keep injecting into the easy spots on your body.
I just want to wish you good luck and remember to premedicate just make sure there is not that little drip of Rebif on the needle before you inject because if there is it sometimes makes for a bad experience and no one wants that.
Take Care and Good Luck
Dave