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AYME (Association of young people with ME) AYME (pronounced 'aim') is a UK-based independent registered charity dedicated to giving help, friendship, support and vital contact to children and young people with Myalgic Encephalopathy (M.E) . AYME's activities, including this web site, are run by the young members themselves, overseen by their Founding Chairman.
Tymes Trust Tymes Trust is the longest established national UK service for children and young people with ME and their families. It is a respected national charity whose entire professional team give their time free of charge. They work constantly with doctors, teachers and other specialists, and played a major role in producing the children’s section of the Dept of Health Report on CFS/ME (2002).
HealingWell.com Community, Information, Resources on Diseases, Disorders and Chronic Illness.
The National ME Centre We provide a unique blend of help, care and support to sufferers and their families: The Centre offers a fully integrated service for the management of this complex illness. This includes, and is dependent upon, the skills of professional clinicians and therapists as well as volunteer support workers, many of whom have themselves experience of ME.
Action For ME Our aim is to heighten understanding of the impact M.E.* has on the lives of those who have it and to improve the quality of services for people who suffer from this debilitating illness.
Sleepydust.net A colourful and inspirational website bursting with information, tips, and advice on dealing with CFS, FMS, and their symptoms. Money worries, work-at-home guidance, benefits information, info on treatments, remedies, support, recommended books and much, much more.
CFS Support This site has been designed for Chronic Fatigue Syndrome / Myalgic Encephalopathy Sufferers, People living with people who have CFS/ME and also people who would like to know a bit more about CFS/ME.
MERGE MERGE is the Myalgic Encephalomyelitis Research Group for Education and Support. The charity's principal aim is to commission and fund scientific investigation into the causes, consequences, and treatment of myalgic encephalomyelitis (ME) and related conditions. On this site you will find research news, educational literature, and information on accessing social care services and support.
Co-Cure The name "Co-Cure" stands for "Co-operate and Communicate for a Cure." The mailing list has been established with the goal of furthering co-operative efforts towards finding the cure for the illness(es) commonly referred to as Chronic Fatigue Syndrome (CFS) and Fibromyalgia (FM).
Gloucester City ME Group The Gloucester City ME Group holds regular meetings and publishes a monthly newsletter so that all members can be kept in touch with the latest information and events.
Satori-5 ME/CFS, MCS/TILT, HRS, Alternative Health, and Networking Resources - Scotland, UK.
ME/CFS Parents A community for parents, parents-to-be and people considering parenthood who suffer from ME/CFS.
M.E. Support M.E. Support is an extensive Website founded by M.E. sufferer Louise Sargent.
M.E. Singles This site is intended to help adult M.E. sufferers who are alone, find a partner.
Rainbow M.E. Group The Rainbow M.E. Group offer support for people with M.E., carers, their family and friends throughout Exeter and surrounding areas.
Aquamarine Aquamarine is nationwide group of people in their twenties and thirties with ME.
Jennie Williams B.ED - Medical Intuitive I am an experienced Intuitive and my passion is to help people experience the full potential of the power of healing. As a result of my own experience of suffering with M.E.for 5 years and working through my recovery, I now have a particular desire to help those suffering with M.E.
Overton Studios Trust Providing worldwide holistic online and offline production and support for sufferers from ME, CFS, PVS, CFIDS and Fibromyalgia.
CFIDS REPORT Cutting edge news and commentary for the CFIDS community.
Christians With M.E. This support group allows Christian sufferers of ME/CFS and/or Fibromyalgia to contact each other via an email list and forum.
Sussex ME/CFS Society The Sussex ME/CFS Society is the registered charity that informs, supports and represents those affected by ME/CFS in East Sussex, West Sussex and Kent.
The Environmental Illness Resource Chronic Fatigue Syndrome/M.E. Information at The Environmental Illness Resource. Includes information, news and research updates, doctor authored articles and forums.
*Short Notes/Useful Info*
Posted By: Daniel Source: http://www.foggyfriends.org Comments: If you are interested in a link exchange, please contact us HERE.