In 2022, ALAN received almost 700 requests for support from people affected by a rare disease, representing around 300 different diseases. The annual report, presented at the recent General Assembly,...
For Rare Disease Day 2023, the national alliance representing people affected by a rare disease in Luxembourg, ALAN – Maladies Rares Luxembourg, has published a position paper with its partners....
Our offices, including the Infoline Maladies Rares Luxembourg, will be closed from the 26th of December 2022 to the 2nd of January 2023. We wish our whole community serene holidays among...
To fight the prejudices that people living with a rare disease have to face, ALAN and its partners have launched a new communication campaign in September 2022. The slightly provocative...
In 2021, ALAN supported 562 patients and families affected by a rare disease, representing 241 different diseases. The activity report, presented at the recent general assembly, shows that the number...
For Rare Disease Day 2022, ALAN - Maladies Rares Luxembourg, the national alliance representing people affected by a rare disease in Luxembourg, in collaboration with photographer, Sophie Margue, presents a...
Through a public letter, ALAN and 9 partner associations are launching a public appeal for vigilance, solidarity and respect, while recalling the essential facts regarding the COVID-19 pandemic....
On Thursday, the 14th of October 2021, the inauguration of ALAN's new offices was celebrated in the presence of the mayor of Roeser, Tom Jungen, and the president of the...
“A true superhero’s power is invisible. Just like many rare diseases.” with this tagline, the non-profit organisations ALAN Maladies Rares Luxembourg and EDS Lëtzebuerg are launching their online awareness campaign...
ALAN wanted to better understand how people with a rare disease view the COVID-19 vaccination as well as the effectiveness of the strategy for vulnerable individuals. To this end, ALAN...