CdLS World Federation

CdLS World Federation

All over the world people; Parents, Sisters, Brothers, Family, Doctors, Caretakers, Educators and others, get together in small groups. These small groups are about Cornelia de Lange Syndrome, that's what unites them. Many of these groups have united in the federation; CdLSWorld. This is what we are: a federation of support groups from all over the world!

Support... Support

You’re told a person you care for has CdLS. It is very rare, so it's hard to find the support you need. We can link you with nearby support groups.

PanelL2.png Meet

Globally, there are others in the same situation as you. If they connect to us we can help you find them. Maybe you want to meet someone nearby with similar experiences.

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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