The European Commission has recently released a special ERN booklet to raise awareness about European Reference Networks. This publication offers an overview of the 24 networks and highlights their contributions to the field of rare diseases.
To compile this booklet, each ERN was invited to share three success stories, demonstrating the tangible and meaningful impact of these networks on patient care.
The key message that emerges from this publication is the significant added value that the EU brings in supporting patients with rare diseases and their families, as well as the Commission’s commitment to increasing awareness of the European Reference Networks’ activities.
You can read the booklet HERE
