This Is MS Multiple Sclerosis Knowledge & Support Community

My doctor and I decided Rebif is my best option (I hate long needles, don't want to mix my shots, and can't handle possible IPIRs from Copaxone because of asthma). He prescribed me the Rebidose disposable autoinjectors. Has anyone on here tried them? What do you think?!

I was diagnosed a month ago and only have done one course of IV steroids, 1000mg a day. I could only sleep for two hours at a time, my legs were jittery as hell and I had to take Protonix for heartburn. But they worked, so I can deal with that. I did an oral dose pack afterward, the dose was so much...

I have never had to inject myself with anything before. Now that I am recently diagnosed with RRMS, my neurologist wants me to research Rebif and start me on it next month. Sure hope the Rebidose will make it easy on me, I HATE NEEDLES.

Hi everyone, I'm 25 years old and was diagnosed on 3/15 after a couple years of symptoms that seemed unrelated and didn't make much sense. An episode of Bell's palsy, numbness, mild ataxia. I woke up on 3/14 with a terrible headache, vertigo, and was staggering like I was drunk. Next thing I know, I...