Asociación ELA Andalucía

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease of unknown origin, without a cure and with a short life expectancy. In 90% of the patients it courses randomly, with no family history. ELA Andalucía is an association that was born in 2005, Declared of Public Utility, and that works day by day so that affected people and families have access to different aid and local social health services, which improve their well-being in the short and medium term.

What is the aid used for?

Colectivo de familias con ELA en casa

Las familias son nuestra prioridad, con ellas mantenemos un proceso de escucha activa para conocer sus necesidades y poder satisfacerlas con servicios personalizados: atención psicológica, agilización de recursos sociales públicos, visitas domiciliarias, fisioterapia en casa, préstamos de productos para la autonomía y la comunicación (sillas duchas, grúa de traslados, lectores oculares, avisadores adaptados, camas articuladas…), talleres formativos online, servicio de información general ELA.