04:50
Instagram Remembrance Day Video 2024
04:02
Welcome Message from CdLS Board President, Paul Villani
01:04:03
CdLS Foundation Webinar Series: Speech, Language, And AAC Devices
01:17:04
CdLS Foundation Webinar Series: Navigating Your Health Plan
48:43
Introducing the CdLS Health Care Notebook
04:41
International CdLS Remembrance Day 2023
03:22
Remembrance Day 2022
03:04
Welcome Message from CdLS Board President, Katie Terhune
04:01
CdLS 40th Anniversary
02:07
Stand By Me
30:21
COVID-19 and Individuals with CdLS
02:10
No one left behind
47:32
CdLS Conference Fundraising Tips
01:04:31
Gastrointestinal (GI) Challenges: Critical Care and Treatment Approaches
59:18
Neurodevelopmental Disorders Behavioral Management CdLS
01:01:36
How to Address Challenging Behaviors Webinar
05:33
Spotlight On Cornelia de Lange Syndrome
01:04:41
Genetic Testing and CdLS
44:40
Phenotypic Analysis of Patients with SMC1A Mutations and Epilepsy
02:58
Bonnie Royster Speaks about CdLS at 2018 Rare Disease Day!
03:02
CdLS National Conference - Orlando 2016
01:39
Join the CdLS Registry - A message from Board President Richard Haaland, Ph.D.
00:29
Thank you from the CdLS Foundation
01:51
Cornelia de Lange Syndrome (CdLS) Awareness Video
01:24
Team CdLS Down and Dirty (Philly)
01:11
Team CdLS - Merrell Down and Dirty (Hartford)
07:42
Find One Child - CdLS Foundation (2005)
00:30
Cornelia de Lange Syndrome - PSA
25:09
Rare Disease Day 2013 - Hartford, CT (Part 2)
23:11
Rare Disease Day 2013 - Hartford, CT (Part 1)
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About
The Cornelia de Lange Syndrome (CdLS) Foundation is a family support organization that exists to ensure early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS make informed decisions throughout their lives.
For more information, visit: www.cdlsusa.org/
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