Leg Spasms , MS and FibroAnyone?

thats the way i see it now and when my family can be horrible bout it to i just reminde myself that its there loss and thank you :) i have been having better day emotonal since joning here x

nicole years back when i told my friends i had seizures they visited the home a couple of times and just drifted off and i never had no one after that just my family..where my mom and dad cared for me, my 2 sisters left home as they could'nt tolerate my seizures and ehaviour in the one, then i got married and my god that was the worst thing i ever did, it was one abusive marriage and then i met ste and we've been together 11yrs and married 7 and i could'nt wish for a better bloke who's stud by me, then when i was told about the lupus..the sister at the hospital told me to join a Lupus site for more knowledge on what was going to happen with me and i could'nt have wished for a better recetion when joining and to me they're my 2nd family.

To me the friends on the site are more genuine than people we know in everyday life and you'll find this with the fibro site as well...as you get so close to alot of members. :) xxx

yeh i feel great being able to ask questions and not feel silly for it usaly i would cry every day but i havnt so much since joining this site is so much more than infomation as you said it is starting to feel like a close family already
speshly when i dont have any one who understands round me xxxx :)

Hi nicole,

You have'nt found the need to cry...knowing you have loving people in the same boat who totally understand you besides giving the best possible advice...as people around us don't really know as it's one hard struggle daily.

I just love how your minds gone positive now since joining and never let the disease beat you mentally either. xxxx