I haven't figured it out either. I've had a relapse but I want to know what exactly a remit is too.

They should get better but they may not go completely away. Most all my symptoms have gone away but a few linger. I still get spasticity in my left leg and what I guess would be called an MS Hug in my stomach once in a while. But everyone is different.

Oh, I knew that. I must have forgot for some reason.

I'm a lucky duck - I have no symptoms when I am in remission except for a temperature thing - I don't feel hot or cold on my left side. That's the only thing that stays.

I think it depends on how much damage has been done to your brain. If the mylin has just been "nibbled" on, then the symptoms could go away completely. If it's gone all the way through the mylin to the nerves and caused actual nerve damage, then it could be permanent.

On good days ...I work-out, on bad days, I work-out, its important to keep muscles healthy.

If you were really tierd of not being used..would you jump so quick if I asked you to...?
Same goes with tierd muscles, remember they only feel tierd..

Its coordination that ms upsets, so causing tierdness and pain.

I have RRMS, too and I still have very limited vision in my right eye although I THINK I'm in remission. As someone else mentioned, I think that's because of nerve damage on my optic nerve. My neurologist told me that if I get a new symptom or a symptom comes back or gets worse and lasts for more than 24 hours, it's an exacerbation, a relapse, and that I should call. I've also been told that a relapse can last several weeks and slowly go away. I hope that's helpful.

I to have come to the realization that even tho I am in remission I do still have symptoms; I call it my "new normal". I am not and have never been the same since my first exacerbation. I have good days and bad days. Fatigue is a big problem, I have really bad balance issues, and L'hermittes sign. I guess these are here to stay! Good luck!

All of the above......it can be bad or really bad it's all depends on how you are taking care of yourself and most of all watch your stress level.

I have rrms also, and with my experience... my symptoms never go completely away, but sometimes they aren't as bad..but ya know, ever one is different... I wish you the best, and good luck with the copaxone..I hope it works for ya... :) take care