What does the ME Association do?

- We fund medical research into ME/CFS.

- We provide factsheets containing all you need to know about ME/CFS including our ME/CFS/PVFS – An Exploration of the Clinical Issues’ (also known as the ‘Purple Book’). It contains everything that health professionals and patients need to know about this devastating neurological disease.

- - We use our medical education budget to help increase knowledge and understanding among healthcare professionals. This includes sending hard copy of the ME Association's ME/CFS/PVFS Clinical & Research Guide and a quarterly medical magazine (ME Essential Medical). 

- We publish a quarterly magazine 'ME Essential' which our members receive via the post, please visit our website to become a member from £18 a year.

- We campaign and support people with ME/CFS in the UK. 

- We have a helpline called ME Connect which is staffed by a fully trained and supervised team of volunteers and available 365 days a year - 10am-12noon, 2pm-4pm & 7pm-9pm - Please reach out if you need to talk to someone who understands by calling  0808 801 0484.

Please support the ME Association by sharing our posts to help raise awareness of ME/CFS.

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