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Recent News

ALAN receives European award for its commitment

12 August 2020
ALAN’s 25th anniversary: academic session, children’s book & advocacy campaign

21 September 2023
Annual Report 2019

17 August 2020

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Recent News

ALAN’s 25th anniversary: academic session, children’s book & advocacy campaign

21 September 2023
Results from the Rare Barometer survey on the diagnostic odyssey

8 June 2023
General Assembly: annual report & new president

4 May 2023

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About Us

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.
It is ALAN’s mission to improve the quality of life of individuals who are affected by a rare disease.

ALAN is supported by the Ministry of Health, AFM-Téléthon and generous donors.

Reconnue d’utilité publique par arrêté grand-ducal du 29 avril 2000Registre de commerce : F 22 42Agréments : SANTE 2021/19 et 2020/02

(+352) 266 112 - 1info@alan.lu

Parc Luxite
13, rue de l'Innovation
L-1896 Kockelscheuer

CCPL LU95 1111 0004 2638 0000
BCEE LU89 0019 1300 5184 5000
BLUX LU30 0080 3239 1490 2001

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