We provide a range of services and activities dedicated to improving the quality of life of those affected by ME/CFS and for their carers, family and friends:
 
• Telephone: Our team of volunteers provide readily accessible support and advice even to the most severely affected via our Telephone Helpline. We are working hard to have this service professionally resourced and funded.
 
• Internet: Our website provides easy access to the latest ME/CFS news, information and services and we endeavour to respond in a timely manner to e-mail enquiries.
 
• Member Forums: Our members enjoy access to and can participate in our online community and discussion Forums airing and sharing views and opinions on a variety of ME/CFS related topics.
 
• Newsletter and e-Bulletin: Members and interested health professionals receive a quarterly printed newsletter and periodic e-Bulletins alerting them to the latest developments in the world of ME/CFS.
 
• Publications and Events for Patients and Health Professionals: Through a variety of media including workshops, seminars and publications we provide easy access to information regarding diagnosis, treatment and management of ME/CFS for Patients and Health Professionals, including the very best Clinical Guidelines available globally.
 
• Support Groups and Useful Links: We maintain a wide ranging list of other useful organisations and links relevant to ME/CFS.
 
• Media Liaison: We maintain working relationships with interested journalists providing them with information and commentary on issues and developments in the field of ME/CFS.