Listed below are some of the bloggers and support groups on the world wide web who go the extra mile, often despite the handicap of their illness.
One of the prerequisites for my support is that the group or blogger supports the biological model of ME and CFS, rather than the biopsychosocial model which advocates CBT and GET as the main form of treatment for the illness.
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).