ALAN - Maladies Rares Luxembourg City: Bascharage Phone : +3522661121
Welcome to the ALAN association
The Luxembourg association for people living with a rare disease - ALAN - is a non-profit organisation (NPO). From its start, it has been supporting people and their families affected by neuromuscular diseases and, since January 2005, it offers help to people living with rare diseases.
Founded in 1998 by individuals with neuromuscular diseases and their families, ALAN's objective is to improve the quality of life of those affected. The Association has been a Registered Charity since 29 April 2000.
During the past years, in order to support and improve the quality of life of those diagnosed with a rare disease, ALAN has created a permanent team of professionals and volunteers.
For more information about Rare Diseases in Luxembourg: please consult the website: www.alan.lu