Hello everyone
I'm Karen and have had M.E./CFS for over 3 years now. Still learning to pace and accept!!! I live in Mawgan, near Helston and would be great to talk to others about this illness and the effects on mind, body and spirit. So many of my friends and family still find it hard to comprehend.
Look forward to hearing from you all......
Big gentle hugs
Karen
(21-02-2010 01:05 PM)kasa Wrote: [ -> ]Hello everyone
I'm Karen and have had M.E./CFS for over 3 years now. Still learning to pace and accept!!! I live in Mawgan, near Helston and would be great to talk to others about this illness and the effects on mind, body and spirit. So many of my friends and family still find it hard to comprehend.
Look forward to hearing from you all......
Big gentle hugs
Karen
Hi Karen, thought I would give you a quick message to let you know you are not alone.
Acceptance is one of the hardes things,especially when we appear 'normal', but vitally important, so keep working on it!
I will message you again, a bit tired now, but try to keep your spirits up, I have found a lot of good things from this illness, especially spiritually, and appreciation. Look after yourself well, take care, Liz x
HI KAREN i'm a sufferer now for 5 years, its a lonely illness to its nice to have people who understand it to talk to. Take care sha xx
hi karen, i'm new to this illness, only diagnosed 8 wks ago. have had it some time, but oddly enough didnt know it!? I'm experiencing similar things too, people dont understand coz you look 'normal', there was a good cartoon in the newsletter that depicted it well, woman in an oxygen mask and weights attached to her, you'd have to see it. (better than my description, and funnier). well, i'm going to make my introductions, as forrest gump would say, on the intro's board now. Take care of yourself, darren