Our biennial national family conference provides education and support to families of individuals with CdLS.
Attendees receive free head-to-toe consultations with experts from a range of medical and educational fields; attend workshops on legal concerns, educational issues and medical/behaviors challenges; and have opportunities to meet other families facing similar challenges.
Join us for the Cornelia de Lange Syndrome (CdLS) Foundation National Family Conference, June 23-26, 2016, in Orlando, FL. Attendees have an opportunity to gain knowledge on how to best care for their child and meet other families facing similar challenges. Individuals with CdLS receive free head-to-toe consultations with experts from a range of health and educational fields.
Not only will attendees be better equipped to face challenges throughout their children’s lives, but also they will leave with a sense of belonging. Events that help connect families include a gathering for grandparents, separate get-togethers for moms and dads, and a social hour for siblings ages eight and over.
Registration for conference is scheduled to open February 15, 2016. Information will be found on this page at that time.