In autumn 2026 ALAN launches a new online awareness campaign: “Well Meant”. Through a series of 9 short videos and a thought-provoking approach, the campaign aims to foster understanding...
ALAN’s 2025 Annual Report highlights the scale of support needs among individuals and families affected by a rare disease. Last year, the association’s psycho-social consultation service received a new record...
On the 28th of February 2026 we celebrate the 19th Rare Disease Day, a day dedicated to raising awareness about rare diseases and their impact on the lives of those...
Our offices, including the Infoline Maladies Rares Luxembourg, will be closed from the 20th of December 2025 to the4th of January 2025. We wish our whole community serene holidays among their...
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...
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...