Shropshire ME Group

Shropshire M.E. Group is a community organisation supporting people across Shropshire who live with myalgic encephalomyelitis (M.E.) and chronic fatigue syndrome (CFS). It helps people connect with others who understand the experience of the illness, particularly those who are newly diagnosed, and encourages access to peer support and practical information. The group offers membership, self-help peer groups and resources for people seeking support. Its website also provides information about M.E. symptoms, diagnosis, treatment and daily life, alongside links to relevant services and guidance.

Shropshire M.E. Group keeps its community informed through news and updates about research, policy and events affecting people with M.E./CFS. Topics include NICE guidance, COVID-19 information, the DecodeME research study and the Government’s ME/CFS delivery plan. The organisation also promotes local activities and events, including fundraising quizzes and concerts, to support its work and the wider M.E. community. People can learn about the group, find support, follow its updates or make a donation through its website.