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.
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
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.