Info. for Newbies
Posted , 6 users are following.
Thought it might be useful if we started up a thread for 'newbies'...... as all our info over the last few months appears to have gone AWOL.
We could all add bits of really useful info that we have posted on the forum in the past (if we can remember, that is :lol: ) and gradually build up a quick reference/support thread.
So I'll begin ........
Hi to any newbies
We are a group of folk that have one main thing in common - CFS/ME. We have got to know each other over the past months and have formed a fantastic support group - always here for each other ....... to have a laugh, a moan, share a good idea, or piece of info. ....... or maybe just a shoulder (or five) to cry on.
We all have varying degrees of the illness, some of us fairly mildly who are still able to work and others of us who are really very poorly ...... and those of us inbetween.
We always look forward to others joining us and make them very welcome ....... and help them in any way we can.
So please if you suffer from CFS/ME please do join us.
0 likes, 10 replies
Teedie
Posted
Hi to anyone newly diagnosed or had CFS/ME long term :D
Please feel free to join in the fun or simply ask any question or tell us about your experience.
You can be sure that we will all introduce ourselves at some point 8)
LouLou
Posted
Any questions from anyone feel free to ask.
alicia
Posted
Please feel free to join in and do not run off thinking you have logged into a mad house.
There is a wealth of experience on this forum, unfortunately it has been lost. But we are still here and can guide you through anything you wish to know about fatigue, joint and muscle pain, brain fog, cognitive difficulties, mood swings, sleep problems, IBS, in fact if you have a symptom, please share it for the benefit of others.
Enjoy our forum. alicia x
katie.k.
Posted
M.E. by Dr Anne MacIntyre (who is also a fellow sufferer). It is published by Thorsons Health.
There is also a foreward by the writer Clare Francis, who begins by describing ME 'is to experience hell twice over, firstly through the devastation of the disease itself, and secondly through the lack of diagnosis, information and support that most sufferers are still having to endure'
I think we can all relate to that
Dale
Posted
Bit out of date now but I have been away. I tried to order that book Katie but it was unavailable at Waterstones.
To any newbies, I am Dale. I have, compared to most, mild ME, but it is still c**p!
Been ill all week and now I find the forum has gone! :yikes:
Anyone joining now will not understand our banter or the relationships we have established :shock:
I am gutted :evil:
Dale xxx
Dale xxx
Teedie
Posted
alicia
Posted
James had us sussed before the collapse. :roll:
katie.k.
Posted
Sorry you have been really poorly ........
I've seen the ME book I mentioned, advertised to buy on the net only very recently.
We all felt gutted for a while but that's precisely what was intended :roll:
But bad luck whoever ..... cos it hasn't stopped us and never will :lol:
hilary
Posted
Patient Admin Team
katie.k.
Posted