Rare diseases affect millions of people across Europe, often leaving them isolated and without access to the specialised care they need. The European Reference Networks for Rare Diseases (ERNs), however, continue to have a significant impact on the lives of up to 36 million people living with rare diseases across Europe.
The European Commission has published the latest edition of the official information brochure on European Reference Networks, highlighting their key role in changing the landscape of rare disease care and impact on the lives of rare disease patients across the continent.
Access the ERN brochure, available in various EU languages, here.