ALAN – Maladies Rares Luxembourg is a non-profit association (association sans but lucratif – a.s.b.l) founded in 1998 and declared of public utility in 2000.
Fostering an environment for people living with a rare disease to realize their full potential through recognition, equal opportunities and improved quality of life.
ALAN’s social objective is to support and defend the interests of people affected by a rare disease and to enable and empower them to improve their quality of life.
ALAN’s main missions are:
At ALAN, we stress three core values that guide our professional and personal behaviour: