APELA is a Non-Governmental Organization of People with Disabilities (ONGPD), operating on a non-profit basis. Founded in 1997, APELA’s mission is to raise awareness of Amyotrophic Lateral Sclerosis (ALS), represent the interests of those living with motor neuron diseases, and provide support to both patients and their care networks — including family members, formal caregivers, healthcare, and social care professionals — with the ultimate goal of enhancing well-being.
About
With a strong focus on promoting excellence in ALS care, dignity, and quality of life, APELA adopts a multidisciplinary approach reflected in its technical structure, which includes a multidisciplinary rehabilitation team as well as palliative and supportive care specialists. The Association also provides guidance that facilitates access to information on social rights and other support mechanisms, ensuring faster, well-structured, and compassionate responses.
Terms of support
Each year, more than 700 people living with ALS (PALS) engage with APELA’s services. Learn more at https://apela.pt/.