The Shropshire M.E. Group
People: Improving people’s mental wellbeing
We partner with every GP practice in Shropshire to ensure all those diagnosed with M.E. or Long Covid-19 receive an automatic referral to our charity for support, advice and improved quality of life.
About this cause
Since 1987, we have helped thousands of people, of all ages, in Shropshire diagnosed with M.E./Chronic Fatigue Syndrome. Symptoms include muscle pain, extreme fatigue, nausea, poor balance and memory. Our goal is to reach more people, including the young and from varied ethnic origins. We help sufferers cope with their symptoms by providing monthly Peer Support Groups held in the County. M.E. sufferers can become very isolated and spiral into depression as their symptoms sometimes make it difficult to socialise or gain employment. We aim to help their recovery. We also provide a free library and information service, regular newsletters, a helpful website, a private Facebook page, and information on up to date research on M.E. We aim to also help Long Covid-19 sufferers.
How this cause brings people in the community together
M.E. (Myalgic Encephalomyelitis) is a very debilitating illness affecting physical and mental health. Work and social activities are very difficult for sufferers to maintain. People become isolated and spiral into depression. Our project to partner with GP practices aims to reach all those diagnosed and their carers by routine referral to our charity, thus increasing the diversity and age range of members. Our free monthly peer support group meetings with a skilled counsellor share advice, information and new research. People meet fellow sufferers in a safe place without judgement. For some people this is their only opportunity to meet people and learn how to live better with the illness. Those too ill to leave their home can join an online meeting. We believe no one should suffer alone.