Couple of questions.....
I have just started my Rebif treatment in the last week. While I haven't had any side effects immediately after the treatment, I have noticed that the day after the treatment I have very little appetite and a headache. Has anyone else on Rebif felt this way?
The other question is whether the electrical "zaps" I feel down my spine and in my ankle are considered a "symptom" of MS. After I had my Solumedrol treatments, the zaps had subsided and its now been about 5 weeks since then. I'm noticing they are coming back fast and furious. Do doctors generally give you another treatment to stop this from happening? Or is being on the Rebif supposed to do that?
Thanks for any insight you can provide!