Founding Member The Solve ME/CFS Initiative (Solve M.E.) is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid and other post-infection diseases. Our work with the scientific, medical, and pharmaceutical communities, advocacy with government agencies,…
Founding Member Our mission is to promote awareness and recognition of myalgic encephalomyelitis (a disease also known as chronic fatigue syndrome), to help those affected and to help promote research. AQEM is a group of volunteers united around a common project, through which each of our personal victories is added…
Founding Member #MEAction is an international network of patients fighting for health equality for ME by building community and mobilizing patients, families, and allies. We were founded with the belief that while we may find it difficult to advocate for ourselves in the physical world, by making our activism accessible,…
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…