There are many others of us out there who create a blog to document what life is like with CFS/ME, The most helpful information can be found from them.
There are many others of us out there who create a blog to document what life is like with CFS/ME, The most helpful information can be found from them.
Laura is a hard working campaigner for CFS/ME and is one of the directors of WAMCARE (see assoc). This is her blog and she updates regulary with how she has been feeling and what she has been up to.
I am not sure who this blog belongs to but it is very interesting reading as you can relate to the person at times and just laugh at yourself which with this condition is always good.
Created by Jodi Bassett in 2005 this is a wonderful complex and very knowledgable guide to CFS/ME and covers everything from Diagnosis to recent news and campaigns.
This is a blog by Paul Winter who developed a neurological condition after having a Flu jab. Once you start reading it you start realising that it might not be ME but his story about trying to get a diagnosis is something we all can relate to.
So is it ME?
A Lady called Barbara has created this fun and lighthearted site full of info, Poems, Tips and a great Car battery theory.
CFS uncensored is a Blog covering the daily activitys of a CFS/ME Sufferer in Australia
CFS Recovery give information about different paths to recovery as used by its author. This website is by Frank Jenner.
Alison Bailey Castellina, ME/CFS "expert patient" for 15 years, ME recoverer and campaigner, member of the UK's Chief Medical Officer's Working Group on Chronic Fatigue Syndrome, co-founder of "Young ME" now "The Tymes Trust" and co-founder of UK patient support groups. This site covers physical, emotional and spiritual roads to recovery.
Bruce Campbell Phd first came down with CFS in 1997, On his pages he details how he got himself back to 100%.
Matthew Benton Passes on some information on excercise and treatments he used to to help himself to recover in the last few years.