Any one with FMS?

crutches

hello fellow fibro survivors!i know how much effort posting takes so ive thanked you all.

debbiedolittle_2

hi i also have fms ,after years of not knowing what was wrong i finaly know, i must say everyone on this site are really nice and have been brill to me and have given me some great advice and support, i am waiting to hear from the dla to see if my claim has gone through , they are waitnig for a report of my doctor, i think the support of everyone on this forum is a brill thing, so hang on in there:beer:

emilyt

Hi there Debbie,
I was wondering how you were getting on. At least you now know what is wrong. ie. you have a name for your illness. I used to think it was all in my head and i was going crazy.
Good luck with the DLA decision.
I am here if you ever want to PM me feel free
Emilyx

donnalove

hiya
i have fms had it for 10-12 years slowly progressed over the years, last year i lost my ib and lost my tribunal, so i am now having to find the energy to find a part time job, the one thing i have found to help with the exhaustion side is plain old luccazade lol.:)
it doesn't help the pain but it makes me feel a bit more energetic for a while, although i will say the pain slightly increases at the end of the day, i take a paracetamol which helps me sleep. i also get dla but only low rate.

donna