@SafaeEl 

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SafaeEl

Rebif

Hello everyone, My neurologist prescribed Rebif for me, does anyone here has informations about it or is having it as his treatment. Please, What should i know about it before i start it? Also I'm from Morocco(Marrakech), if there anyone here who is from Morocco and who had MS too so that i learn about the procedure in here. Thank you all.
@potter

I was on Rebif for 5 years they should have a nurse teach you where, when and how to do your shots. If not I can try to direct you, it is easier if you have someone to give them to you. I took my shots Sunday night, Tuesday night and Thursday night. That way I would feel my best on the weekend. I always felt sluggish the next day after my shot. I don't have a job so I didn't need to be at my best on Monday mornings like people who work. I am taking Tecfidera now a pill at breakfast and a pill with dinner is much easier. I had to stop taking Rebif because of skin rejection. Everyone reacts differently to the same drug, you may not have any problems at all. Potter

@SafaeEl

My neurologist told me just that i have to take it subcutaneous 3 days a week ( i think i'm gonna take them monday wednesday friday ) and she gave me informations about the dosage i need that's all what she told me. Besides my mom is gonna give them to me. I would prefer to take pills but my neurologist told me that pills are for those who are in an advanced stad of the disease and that i can't take them in my situation. Thank you so much @potter, most of times doctors don't tell us all what we need to know that's why i want to hear advice from people who already experienced what i'm going to experience because they give some very interesting details that could avoid us lot of trouble.