Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I am fairly sure that the rebif makes a significant difference. My last mri showed that my brain lesions were inactive.
I have been on it nearly 6 years and have no complaints. My advice would be to give it more of a chance, but talk to your neuro.
But Rebif worked for me as far as keeping my MS at bay. I have not progressed much in since 2002 when I first started taking it. But I am really tired of it and ready for a change. If Tecfidera doesn't work, I'll probably go back on it. Best of luck with it.
I hate the new auto injector and that is what caused me to want to change meds. I like the old hand manual injection method.