The World Federation of CdLS Support
The World Federation of National CdLS Support Organizations (CDLS World) is a not for profit voluntary HUB of world-wide organisations and communities united by Cornelia de Lange syndrome with one common mission to reach out, provide help and give hope.
mission
Our mission
"We are determined to contribute to an early and accurate diagnosis of the Cornelia de Lange syndrome (CdLS), to support research into aspects of the syndrome, to help people with CdLS and to parents, brothers and sisters, grandparents, families help carers and doctors to make decisions based on good information. ""
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The World Federation of CdLS Support
The World Federation of CdLS Support
The World Federation of CdLS Support
The World Federation of CdLS Support
The World Federation of CdLS Support
The International Federation of National CdLS Support Organizations (CDLS World)
The World Federation of National CdLS Support Organizations (CDLS World) is a not for profit voluntary HUB of world-wide organisations and communities united by Cornelia de Lange syndrome with one common mission to reach out, provide help and give hope.
Supports multiple communities
Supports
Read more about our community... Calendar of our events Onderzoek Themakamers
Our Volunteers and Supporters...
Latin America Liaison
Council member
Gerritjan Koekkoek
Treasurer
Clare Crawford
Volunteer Spanish-speaking Communities
Andrea Morales
Chairman
David Axtell
Chair of the Care Council
Bernadette Dalingwater
Network of experts for The World Federation of CdLS Support
The dream for our community
With the Cornelia de Lange World federation we have a dream. To share our dream with you in order to convince you to join us we made this video to show you what seeing, talking, learning and sharing is about.
