Kawasaki Disease Europe was created with the aim of becoming a point of reference for families and professionals involved in Kawasaki disease, a rare condition that primarily affects children.
We are a European network bringing together parents, physicians, and researchers to share experiences, information, and best practices.
Our goal is to raise public awareness of Kawasaki disease by making its reality more visible, promoting understanding, and providing concrete support.
We believe in the strength of networks, in cross-country collaboration, and in the value of mutual listening to help build a more informed and supportive future.