Find support, or help research
People near you who know what living with ALS (motor neurone disease) is like, and ways you can help find better treatments.
Support groups in Spain
- Asociación ELA/EMNPatient association in Spain for people with ALS/MND and their families; member of International Alliance of ALS/MND Associations.All of Spain
- Asociación Española de Esclerosis Lateral Amiotrófica (ADELA)Patient association in Spain for people with ALS/MND and their families; member of International Alliance of ALS/MND Associations.All of Spain
- Fundación Española para el Fomento de la Investigación de la Esclerosis Lateral Amiotrófica (FUNDELA)Spanish foundation promoting ALS research and supporting people with ALS; member of the International Alliance of ALS/MND Associations.All of Spain
- Fundación LuzónFoundation in Spain for people with ALS/MND and their families; member of International Alliance of ALS/MND Associations.All of Spain
Contact details come from each group's own page and are checked every 3 months.
Help research
You do not need to join a trial to help. Below are the programmes we found in Spain and how to reach them. You contact them yourself: Frontlight does not collect or pass on your details.
Give blood or tissue for researchResearchers use stored samples to find what causes ALS (motor neurone disease).
Share your health dataA registry collects health data, without your name, so research teams can study many people at once.
Take part as a healthy volunteerStudies need people without ALS (motor neurone disease) to compare with. Family and friends can help.