The Cornelia de Lange Syndrome (CdLS) Foundation

The CdLS Foundation is a national non-profit organization that has served individuals with CdLS and their families since 1981. The Foundation’s mission is reflected in its slogan: Reaching Out, Providing Help, and Giving Hope.

The Foundation distributes a number of publications to families and professionals caring for individuals with CdLS, as well as hosts meetings and conferences where researchers and families can meet to exchange information. The Foundation also acts as a facilitator between families and professionals, utilizing a team of professionals who lend their expertise to those caring for an individual with CdLS.

Tax ID Number: 06-1057497

Help us give HOPE

to Vihaan and other kids

affected by CdLS