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Rebif v Copaxone

Hi all, I've come for some advice. I recently had an appointment with my ms nurse to discuss treatment options. There's so much to take in. I initially went in there think I don't want any pills and not keen on self injecting. Which only left infusions. I wanted Lemtrada until she told me about the side effects and I'm not keen on having to have blood tests every month for 5 yrs. So now I'm deciding on Rebif or Copaxone. Can anyone give any info on how the treatment worked for them and their experiences. Really appreciate the advice. Dukes