Welcome to ALAN – RARE DISEASES LUXEMBOURG –
The Luxemburgish association for people living with a rare disease - in short called ALAN - is a non-profit organisation (NPO). From it's start, it has been supporting people and their families affected by neuromuscular diseases, and since January 2005, it is offering 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.
You can find on our website : www.alan.lu, information on rare diseases, useful links as well as a list of the association's objectives. Please do not hesitate to contact us. Your suggestions and comments are welcome.
Please find here the video "Endlech Vakanz" by Yann Tonnar showing Christiane and Chris Romitelli on their voyage during the "Päischtcroisière 2015".