I do have a question about flair ups - might be kinda dumb, but i would like some info on this.
I read where people have been good for awhile, and then hjave a relapse. What do you actually mean by this. when you have an attack, what happens. The reason I ask this is...
I was dx with MS in December, I started copaxone right away. I get stiff necks, and neck aches, some headaches from time to time, and some lower back aches. My fingers are numb and tingly sometimes, and sometimes not. this can change back and forth several times in the same day. It is noticeable in the morning and before I go to bed, bt my hands can be symptom free all day ong. It almost seems to be posture related Same with the shock feeling I get when I bend my head forward. Sometimes it is there, and sometimes it is not. It seems to follow about the same pattern as my hands. It seems to be more noticable during the evening than during the day.
I guess what I am saying, is that I stay pretty much the same day after day, with little to no change, except for the changes that happen throughout the day. When I am feeling the symptoms thru the day - is this a flair up. And if not, why would my hands feel good one minute, and not the next.
Aslo I note that I have no problems with my legs at all. It seems to be isolated to my hands, except when I bend my head forward, then my feet tingle, but then again, not all the time.
I have been reading lots of things on Lyme disease, and I sure hope that I have been dx correctly. Note two years ago I had a bulls eye rash, with other rashes over the last two years that have come and gone, etc...mmmmmm?
thanks,
Gary