Annual Report 2019

In 2019, ALAN supported nearly 400 patients and families affected by a rare disease, which represents more than 200 different diseases. The number of psychosocial consultations carried out by the multidisciplinary team in 2019 increased by 40% compared to the previous year. In addition to its consultation services and adapted physical activities, the association has focussed heavily  on raising awareness for rare diseases, on strengthening international partnerships and on the National Plan for Rare Disease, most notably through the launch of the Infoline Maladies Rares Luxembourg.

You can download the full Annual Report (in French) here.