Cathcart ME Support Group.
The following links may be useful for additional Information and Support on ME/CFS or Local Health issues:-
The ME Association provide information, support and practical advice for people who are affected by ME/CFS/PVFS (Myalgic Encephalopathy/Chronic Fatigue Syndrome/Post Viral Fatigue Syndrome), their families and carers.
Action for ME is a UK charity working to improve the lives of people with ME We campaign for more research, better services and treatments.
The 25% ME Group is a unique nationwide charitable organisation managed entirely by volunteers (most of whom are severely affected by ME) and was set up to offer support services to those severely affected by ME (Myalgic Encephalomyelitis), and their carers. We provide a wide range of services to people affected by severe ME many of whom are virtually housebound and/or bedbound.
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).
Association of Young People with ME provides help, information and support to those with ME/CFS
ME Research UK Is a national charity funding biomedical research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (also known as ME/CFS).
INVEST in ME are an independent UK charity campaigning for bio-medical research into Myalgic Encephalomyelitis (M.E.), as defined by WHO-ICD-10-G93.3.