ME/CFS Support Group

Hi

Here is a link, that you may find useful

www.shropshiremegroup.org.uk/hints-for-c...-the-esa-50-form.php

Hope it helps

Hi
You can find a guild on the ME (Action fo Me)
www.actionforme.org.uk

Hope this helps
Pat

I followed the ESA guidelines for members as closely as I could and made absolutely sure Atos were totally aware of how this devastating illness affects me on a day to day basis.
What I can do and how it affects me afterwards, what I can't do and remember that it must be possible for any of the descriptors to be completed reliably, repeatedly.
I added loads of extra sheets of info about how I am affected and was fortunate enough to have the backing of two caring Doctors who wrote great supporting letters.

Very best of luck

Jack

To DF whose post on this thread was no 100008 -

It seems that your username here is your real name. Whilst you have not given your full name, it is possible that you would prefer to use an alias on a public forum such as this. If you decide you would like to change your username, please follow the instructions in this FAQ

My full name is showing, how can I stop it?

Hi

Don't know if this will help, but found this link a while ago - it is the ATOS guidelines for CFS/ME

www.postviralfatigue.me.uk/forum/f8/cfs-...a-assessors-870.html

Good Luck!!