Introduction for the federation


CdlS World has been founded in 2001 in occasion of the first International CdLS Conference and currently it's members support families in alemania , algeria , argentina , australia , austria , brasil , bélgica , colombia , dinamarca , españa , estados unidos , filipinas , finlandia , francia , irlanda , israel , italia , lblflagcanada , malasia , noruega , nueva zelanda , países bajos , polonia , portugal , reino unido , singapur , suecia , suiza ,  and is maintaining contact with single  families in many more countries. We welcome groups that would like to join the federation. 

CdLS World; what do we do?

  1. From all over the world the Experts who know most about CdLS and a specific topic have formed a international Scientific Advise Committee (SAC). We make sure the SAC is informed about needs of the families and caretakers, so they can publish relevant news, present on conferences and answer questions in our Ask the Expert service;
  2. To act as a forum of best practice for support group services for people with CdLS, including organizing an International Conference every two years;
  3. to act as a resource base for the wider families of people affected by CdLS throughout the world for both research and for families.  

Sobre el contenido del sitio web

Toda la información contenida en este sitio web tiene únicamente fines educativos. El lugar para obtener consejos médicos específicos, diagnósticos y tratamientos es su médico. El uso de este sitio es estrictamente bajo su propio riesgo. Si encuentra algo que cree que necesita ser corregido o aclarado, por favor háganoslo saber en: 

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