The CdLS Foundation is excited to reveal its new awareness flier! Be sure to check out the fresh new look and timely message designed to raise public awareness of Cornelia de Lange Syndrome (CdLS). We hope this flier helps others recognize signs and symptoms of the syndrome and help more children get diagnosed.
Click here to view and print the PDF version of this flier. Please feel free to distribute it among your family, friends and throughout your community. The more people that know about CdLS, the more children living without a diagnosis have the chance to receive the support and medical attention they need.
For more information about how you can raise awareness for CdLS, please contact Marie at outreach@cdlsusa.org or call 800-753-2357. Already raise awareness for CdLS? Share your stories and encourage others to join your efforts! – JS
CdLS Foundation: The Water Cooler 
I dont usually reply to posts but I will in this case. WOW!!
I love it! Straight and to the point with beautiful photos!
I am a teacher with a student with CdLS, I want to reach out to other educators or professionals who could give me insight to this unique syndrome. I work very close with this child’s parents and we have many questions that we would like to find some answers to. If anyone is willing to link us to doctors, teachers, or other parents for support that would be appreciated. Anyone feel free to call me
Thanks–Jill Knuffman
jknuffman@hotmail.com