Recruitment : coordinator of the national alliance
Pour renforcer son équipe l’a.s.b.l. ALAN – Maladies Rares Luxembourg recherche un(e) : Chargé de mission affaires publiques/Coordinateur d’alliance (m/f) ...
Pour renforcer son équipe l’a.s.b.l. ALAN – Maladies Rares Luxembourg recherche un(e) : Chargé de mission affaires publiques/Coordinateur d’alliance (m/f) ...
In September 2025, the association and national alliance representing people affected by a rare disease in Luxembourg ALAN – Maladies Rares Luxembourg, launched a new online awareness campaign with the...
ALAN’s recent annual report shows that in 2024, the association's psychosocial consultation service received 699 requests for support – a record for the non-profit organization and national alliance representing people...
On the 28th of February 2025 we celebrate the 18th Rare Disease Day, a day dedicated to raising awareness about rare diseases and their impact on the lives of those...
In early October 2024, ALAN launched a new interactive awareness campaign with the support of its partners.The campaign aims to increase the general public’s awareness for rare diseases, and the...
D’a.s.b.l. ALAN – Maladies Rares Luxembourg sicht, fir ee Congé de maternité/parental ze ersetzen, een diploméierte Psycholog/ Psychotherapeut (m/w) ...
In 2023, ALAN - Maladies Rares Luxembourg, the non-profit organisation and national alliance representing people affected by a rare disease in Luxembourg, celebrated its 25th anniversary. In this historic year...
In February 2024, the consultation service of ALAN Maladies Rares Luxembourg received the “EU-Promising Practice in the field of Mental Health” label in recognition of its holistic approach to psycho-social...
On the 29th of February 2024 we celebrate the 17th Rare Disease Day, a day dedicated to raising awareness about rare diseases and their impact on the lives of those...
D’a.s.b.l. ALAN – Maladies Rares Luxembourg sicht, fir säin Team ze verstäerken, een diploméierte Psycholog/ Psychotherapeut (m/w)...