Founding Member Working for ME in Wales Our vision is for a Wales where adults and children with ME, CFS and PVFS and their carers are taken seriously and treated with respect, where diagnosis, treatment and services are accessible without a battle. The Welsh Association of ME & CFS Support…
Founding Member ACAF (Associació Catalana d'Afectades i Afectats de Fibromiàlgia i d'altres Síndromes de Sensibilització Central) is a mutual help association formed by people affected by Central Sensitization Syndromes (CFS/ME - FM - MCS - EHS) where we can communicate and help each other, with the aim of learning to…
Founding Member We want to help society visualize, understand and comprehend the real situation of affected patients. However, relatives also suffer. They often find themselves alone in the face of the illness of the people they love. We would like to help alleviate this feeling of loneliness. It is common…
Founding Member The ME community in the UK is served by a considerable range of charities, with even the largest being relatively small. Recognising the benefit of being able to speak with a louder voice, Forward-ME was established as a coordinating body to provide a unified and perhaps louder voice…
Founding Member The American ME and CFS Society is dedicated to serving the needs of patients and caregivers through support, advocacy, and education. We seek to channel patient perspectives to government agencies, committees and initiatives, and to unify the ME and CFS community by pursuing the common goals of expanding…
Founding Member The ME CFS Foundation South Africa is the first entity of its kind in South Africa (and Africa) founded in response to ME/CFS. We provide healthcare and counselling services for people with ME/CFS who cannot afford it. We raise awareness of ME/CFS and we advocate for the rights…
Founding Member Our mission is empowering people with M.E. to fulfil their potential and secure the care and support they need, while working towards a greater understanding of the illness and ultimately a cure. Alongside providing targeted information, support and advice to children, young people and adults with M.E., we…
Founding Member The Associated New Zealand Myalgic Encephalomyelitis Society (ANZMES) has been serving New Zealanders with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome since 1980. They provide information, support and practical advice for people, families and carers affected by ME/CFS, as well as funding and supporting research, and offering education and training.