To support my friends Martyn and Kerrie. In his words:


As most of you know Kerrie (my wife) has had ME / CFS (Chronic Fatigue Syndrome) since January 2012 and while she has improved, she is still a long way from where she was before she was diagnosed.

Action for M.E. takes action to end the ignorance, injustice and neglect faced by people with M.E. We do this by meeting need now to improve the lives of people with M.E. while taking action to secure change for the future.

For more information visit www.actionforme.org.uk