A great opportunity!


We hope that many families and professionals will take the opportunity to have an extended vacation to discover more of Europe before or after the World Federation Conference.

Most of all we hope that people attending – whether they be parents, grandparents, siblings, doctors, teachers, social workers, community care support staff and the people with CdLS themselves, will have fun. We believe that by meeting together to share common thinking and new ideas we will make the world a better place for people with CdLS.

Om indholdet af hjemmesiden

Alle oplysninger på dette websted er udelukkende til undervisningsformål. Det er din læge, der er det rette sted at få specifik medicinsk rådgivning, diagnoser og behandling. Brug af dette websted sker udelukkende på eget ansvar. Hvis du finder noget, som du mener, der skal rettes eller præciseres, bedes du give os besked på: 

Send en e-mail: info@cdlsWorld.org