In your own words, describe a "Relapse"

tt89 · Family Member Joined: Aug 13, 2008 Posts: 49 Location: USA

Thanks in advance to everyone that reponds here.

Trying to get a better understanding of how to tell if you have a relapse or flare up and what is the difference in your opinion.

Thank you so much.... Wink

VodooDoll · Posted: Wed Aug 20, 2008 11:15 am Post subject:

tt89

Keep in mind that each person's reaction to MS is unique. Not everyone's relapes or flares will act in a certian way.

Relapes, exacerbations or flare ups are when you have a worsening of existing symptoms and/or the appearence of new symptoms that don't resolve by themselves.

What works best for me is the wait and see game.

cheerleader · Posted: Wed Aug 20, 2008 1:45 pm Post subject:

hey tt89-
My husband had one monster exacerbation...his first "attack" in 2/07. He had pins and needles, trouble walking, bad pain, fatigue and spasms. It took about six weeks before getting diagnosed, since at first he thought it was a pinched nerve. After dx and steroids, he was left with fatigue, pain and spasms, but the pins and needles were gone and he could walk again.

No new MS symptoms since then, but the remaining symptoms are not the same every day. Some days the spasms are bad, some days the pain, and the fatigue is a constant. I don't think this is an "exacerbation" but is just from the damage done during his initial flare.

Some people recover completely after a flare, some are left with damage and continuing symptoms. I think the red flag is a new symptom...that usually signals an exacerbation.

hope this helps-
AC
_________________
Husband diagnosed RRMS March 2007
pursuing endothelial healing
Copaxone, Swank, supplements, laughter

tt89 · Family Member Joined: Aug 13, 2008 Posts: 49 Location: USA

Thanks so much for these explanations...
Im wondering if I'm having a flare up too because I notice new things but I was not sure if its Copaxone related ( switched to Copaxone from Betaseron)....UGH

Im seeing a new Neuro Doc ( Duke) because the group Im in is too big and too many patients and I think Im falling through the cracks...and they told me the first few years of your Dx are critical yet Im pawned off on my PCP and I think they just have to many docs and patients in that clinic. Im the least bothersome patient...if and when I call, its serious..but they just leave me hanging to many times and I truly trusted their words that they'd be there every step of the way....well they were on the first appt, after that....GONE like the wind..

Thanks....

cheerleader · Posted: Wed Aug 20, 2008 8:01 pm Post subject:

DIM · Posted: Fri Aug 22, 2008 2:16 am Post subject:

I asked many times the same and the most common answer is "new symptoms"!

tt89 · Family Member Joined: Aug 13, 2008 Posts: 49 Location: USA

Thank you to all the wonderful people that take the time to reply to my postings...
I wish you all a peaceful weekend.
Sincerely
T Very Happy

catfreak · Posted: Sat Aug 23, 2008 9:11 pm Post subject:

I too have been told "new symptoms".

But, when I went back to neuro on the 11th for my checkup after starting Rebif and everything was out of whack, he put me on steroids which I assume was because I was having an exacerbation or relapse.

It's so hard for me to separate daily MS problems and new problems. I think if something new happens to me then it must be related to something old so I overlook the problem. I it so confusing for me.

I think stress brings mine on.

CF
_________________
Seriously..Do I really have to get up and go to work today? Do you know how tired I am?