I have been on rebif since June. I can't tell if its working or not. I hate needles and have had a mishap which led to anxiety and not being able to administer myself for about a month. I'm back to injecting myself but 3 days out of the week are terrible for me. Those evenings are not my own and dictated by rebif.
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Originally Posted by AynaDee
I am on Rebif. I can say I don't like it. It makes my body feel like crap and i'm not so sure its even working. Plus it hurts like an s.o.b. when injecting. And it has chinese hamster ovary cells in it, that's gross.
I do think im going to talk to my neuro about the LDN, the whole 'stopping/slowing the ms progression in its tracks' really was a seller to me lol
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