Post Viral Fatigue Chat & Forum

My recovery story from Post Viral Fatigue / Myalgic Encephalomyelitis / Chronic Fatigue Syndrome / ME / CFS

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  1. #1
    Senior Member
    Join Date
    Nov 2010
    Posts
    260

    Helen, This is brilliant. Thanks! My Team Leader is supposed to be coming out to do a home visit as he's new to the team and just wanting to learn more about my illness so this will be a fantastic printout to give him.

    Ang
    x


    --
    I won't let ME/CFS and Fibromyalgia rule my life, I'll just adjust it accordingly!


  2. #2
    Senior Member
    Join Date
    Jul 2009
    Posts
    590

    Great stuff, nice find Helen!



  3. #3
    Senior Member
    Join Date
    Feb 2010
    Posts
    812

    I was very very impressed with this booklet written by Action For ME, "An Employers Guide To ME" which is to be given to employers of anyone with CFS/ME.
    I truly recommend printing it out and giving a copy to your boss if you are in work!

    <a href="http://www.actionforme.org.uk/Resources/Action%20for%20ME/Documents/get-informed/Employers%20Guide%20A5%20booklet.pdf" target="_blank" rel="nofollow">http://www.actionforme.org.uk/Resources/Action%20for%20ME/Documents/get-informed/Employers%20Guide%20A5%20booklet.pdf</a>

    Action for ME do loads of other brilliant booklets

    <a href="http://www.actionforme.org.uk/get-informed/publications" target="_blank" rel="nofollow">http://www.actionforme.org.uk/get-informed/publications</a>
    <em>edited by Helen82 on 7/14/2011</em>



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