I have been on avonex for about 6 months and still have mild bad days, not major bad days just very tired and legs hurting and mild dizzy spells I guess I was expecting to be a whole new person, and I do have more good days then bad was just thinking it would be all good. Anyone else still have symptons
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avonex how do you feel
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my new normal
I don't feel as good as I did before MS, but rarely do I feel really bad. Most of the time I just have aches and some fatigue and some numbness/tingling.
It has been explained to me that this is my "new normal". With the damage on the brain and to the spine I will never return to normal, so I just have to accept that this is my new normal and drive on.
Tough to accept? Sure. But since I have lived with it for 18 months as my new normal it is now my normal. Is that about clear as mud?
After the shot I usually have an extra fatigued day and a few more aches and pains but nothing I can't deal with.
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Boy can I relate!
I've been self-injecting Avonex for 15 years. My first six months were just horrible adjusting to the meds, but, slowly the side-effects lessened. Mostly good days (from little or no Avonex side-effects).
I did start on an anti-depressant as Avonex seemed to escalate my anxieties/depression. I still continue with both the Avonex and the AD.
But, now more bad days than good. I was dx a few years before any of the DMD's were available. Avonex has been my silver lining in the MS cloud.
Nothing stops MS progression, but remember: a positive anything is better than a negative nothing.
Stick with it! (pun intended)Life isn't about waiting for the storm to pass; it's learning to dance in the rain!
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