Health Charities That specialise in Chronic fatigue syndrome

Action for M.E. was established for the relief of people suffering from the disease MyalgicEncephalomyelitis, (commonly known as M.E., or CFS/ME), and to provide information, advice and support, and to promote public education, campaigning and research into the disease. On a day to day basis we provide telephone support to people with M.E., manage Online M.E Centre and publish 'InterAction'.

To provide information and support for people with ME/CFS/PVFS

TO PROMOTE AND PROTECT THE PHYSICAL AND MENTAL HEALTH OF SUFFERERS OF, AND ADVANCE THE EDUCATION OF THE GENERAL PUBLIC IN ALL AREAS RELATING TO , MYALGIC ENCEPHALOMYELITIS (ME) , MULTIPLE SCLEROSIS (MS) , DEPRESSION AND STRESS RELATED CONDITIONS IN ENGLAND AND WALES THROUGH THE PROVISION OF FINANCIAL ASSISTANCE , SUPPORT , EDUCATION AND PRACTICAL ADVICE.

To support people living with from ME/CFS and to raise awareness of the illnesses.

IIMER PROMOTES BIOMEDICAL RESEARCH/EDUCATION/AWARENESS OF MYALGIC ENCEPHALOMYELITIS (ME). WE ORGANISE ANNUAL INTERNATIONAL ME CONFERENCES/RESEARCH COLLOQUIUMS; MARKET & PUBLISH EDUCATIONAL MATERIAL ON ME (DVDS, BROCHURES, GUIDELINES & JOURNALS); PUBLISH A FREE NEWSLETTER; INITIATED NATIONAL/INTERNATIONAL CAMPAIGNS FOR CROWDFUNDING/AWARENESS FOR ME; FUND BIOMEDICAL RESEARCH INTO ME.

By providing a fully dedicated Self-Care Co-ordinator, who organises a range of gentle activitiesthat promote a healthy lifestyle. The Co-ordinator also provides practical guidance and support tomembers who face the challenge of managing, or recovering from ME/CFS. Other support includes monthly meetings across Dorset, twice year newsletters, updates on latest research, helpful events.

The charity is engaged in activities or providing facilities or equipment which support Cobham Free School (CFS). Activities include fundraising events such as summer fairs, Christmas fairs, movie nights and school discos held on school premises as well as events for parents and staff such as barn dances, race nights and summer balls held at various local venues. All funds raised are for to CFS.

To relieve the suffering of people living in Sheffield and surrounding districts who are affected by Myalgic Encephalomyelitis [ME] or Chronic Fatigue Syndrome [CFS] through the provision of special adapted remedial yoga classes, related information and social contact.

Raising funds for the Lanchester Primary School.

Run by user-volunteers, mainly ME/CFS sufferers, this charity aims to provide information, support and assistance to help fellow members understand, manage and recover from ME. We offer:- monthly meetings, quarterly newsletter, lending library, social events, therapeutic activities, informal support networks.

Shropshire ME Group is a self-help group supporting patients of CFS/ME to understand and cope with their symptoms. This is achieved by: establishing a number of county-wide Peer Support Groups, held monthly; providing a free library of ME related publications; issuing a regular newsletter, running a website and holding an annual conference to update members on medical advances in treating ME.

The Association champions clinically effective practice in treating ME/CFS and other primary fatigue conditions by supporting UK clinical professionals working in the field. It achieves this through the delivery of education and training, provision of information on clinically effective treatments and recent research, and networking opportunities. Activitities can be accessed on line -BACME.info

We inform, support and represent those affected by the Chronic Fatigue Syndrome - ME across Sussex and Kent.

To promote, for the benefit of the public, research into the principles & practice of osteopathy in the treatment of Myalgic Encephalomyelitis (M.E.), otherwise known as Chronic Fatigue Syndrome, & to disseminate the useful results of such research.

Relief of poverty by providing training and development for female ex-offenders, ethnic minority women/refugees and other disadvantaged women to gain skills to improve their chances to gain employment. To sign post to other services that may help them. Supporting underpriveleged families by providing books and other related educational material for their school going children.

WAMES activities in Wales: campaign for recognition of ME as a neurological illnesscampaign for appropriate health, education, social care services, benefits and researchraise awareness of MEoffer support to young people with MEprovide information in Welsh and English for people with ME, their families & professionalsaid local support groups

The role of our charity is to relieve sickness, poor health and disability and to promote optimal healing and physical wellbeing through the provision, study and research of integrative medicine, initially for sufferers of Myalgic Encephalomyelitis and Chronic Fatigue Syndrome (ME/CFS) and later for sufferers of other serious and chronic illnesses.

Meetings and Socials;Newsletter;Weekly free, adapted yogaBenefit and Work informationAwareness leaflets publication and distributionEquipment to borrowComprehensive book and CD libraryPhone line enquiry/info linePrivate Facebook groupRepresentation at steering groups at local level, NHS and government.

Raising Awareness May 12th International Fibromyalgia/ME/CFS Light up the Night event. Annual fundraising event, Accrington.