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.
cloudsintheysky
Hi all,
I just started on Rebif recently and I'm now up to my full dose which I've had a few times. I have quite a lot of Achiness and I've also been feeling a little depressed. Maybe it's just a bad week in general. Has anyone had depression on rebif and what did you do? Is it something that passes with time?
Thanks for your help.
I just started on Rebif recently and I'm now up to my full dose which I've had a few times. I have quite a lot of Achiness and I've also been feeling a little depressed. Maybe it's just a bad week in general. Has anyone had depression on rebif and what did you do? Is it something that passes with time?
Thanks for your help.
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I was on Rebif for just over a year and a half, became totally suicidal due to the depression associated with the Rebif, the meds also did not agree with me on the MS side, had a few relapses during my time on Rebif, was actually looking at being medically boarded, my neuro moved me onto Copaxone, I have now been on it for about a year, still working, have not had a relapse and on mood stabilizers for depression and anxiety, but all in all, coping better with the fatigue etc.
Good Luck
Best of luck to you!
I'm going to be in touch with my doc next week. I don't mind taking the shot, but I usually wake up feeling tired and not very excited about things. If it helps prevent relapses that would be great - maybe I need other medication to help with the side effects.
i feel reallly depressed for the first few months on rebif (since i have a tendency to stop taking it, i know it happens every time), ive thought about an antidepressant, but just take turmeric & nothing else, the depression does pass for me
Speak to your doctor about what is going on to find out if taking Wellbutrin and/or switching meds might be right for you.
Best wishes to you,
EP
Anyway, yes Rebif can cause a lot of things but the fatigue problem is still a problem for me after all these years. Sometimes it is bad and other days it is not noticeable. But lately, the day after a shot, I tend to fall and I don't want to go out.
Makes me want to change drugs. Am thinking seriously about changing to Tecfidera. Won't miss the fatigue problems at all. But wondering if I am just changing from one problem to another.
I do not think that any of the side effects go away, just are better some weeks. Perhaps for you they might go away but for me they haven't. The anxiety is still just as bad and when I don't take Rebif, it goes away.
MS is such an unpredictable disease. I know of friends that have done just the diet and exercise, and friends who are on a list of meds. For me, I think the decision to stay on meds and changing my lifestyle has been helpful to hit MS from both directions.
(((HUGS)))