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.

About the website contents

All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at: 

Send a email: info@cdlsWorld.org