Hi everyone! So happy this place exists!! I was diagnosed Feb 2011, started Avonex in April 2011, I have been great and feeling fantastic (minus the flu side effects), how I am a nurse and I am around many ill, contagious patients. I recently got a raging flu (yes I took the flu shot) and ended up getting a new lesion on my C3. YIPPEEE!! So because it is new, I am transitioning to Rebif. I am really nervous about the side effects, can anyone tell me if their flu like symptoms were worse? Just more frequent because you dose 3 x/week rather than once a week with Avonex....
Has anyone gone from avonex to rebif? Uggg this sucks sometimes, but we all only get one lap on earth and I will do anything to stay healthy and mobile Hope everyone is well....
Has anyone gone from avonex to rebif? Uggg this sucks sometimes, but we all only get one lap on earth and I will do anything to stay healthy and mobile Hope everyone is well....
Comment