Asociación Galega de Lupus (AGAL)

We give voice to an invisible disease and walk alongside those who live with it, because no one should face lupus alone. We are AGAL, a non-profit organization founded in 1997 to support people with lupus in Galicia. Declared a public benefit organization, we work every day to improve their quality of life by offering information, support, and hope.

What is the aid used for?

Galician Lupus Association (AGAL)

In Galicia, between 2,500 and 3,500 people live with lupus, a chronic, autoimmune disease that is often invisible, but which transforms our lives and forces us to learn to live differently. Although there is no cure, we know that support, information, and comprehensive care make a huge difference in our daily lives. This project was born to offer more than just medical treatment: spaces where we can care for ourselves inside and out, share experiences, and strengthen our physical and emotional well-being. Here we find understanding, strength, and community. With your support, we can continue to support each other, build a network, and give hope to those of us living with lupus. Because even though lupus isn't always visible, together we make it more bearable. Join us, collaborate, and walk with us!