The development and implementation of a National Plan for Rare Diseases is a must to guarantee equal access to diagnostics, therapy, care and research for all individuals living with a rare disease.

On the 7th of May 2018 the first National Plan for Rare Diseases was presented by Luxembourg's Minister of Health, Lydia Mutsch.

To learn more about the plan, read the Minister's speech (in French) or take a look at the complete National Plan for Rare Diseases (in French).