Cornelia de Lange Syndrome Foundation, Inc.
302 West Main St. #100
Avon, CT USA 06001
Phone: 860-676-8166
Phone: 800-223-8355
Fax: 860-676-8337
email: info@cdlsusa.org

Connect With The Foundation


Who are our Members?

  • the loving parent whose child is diagnosed with the syndrome...
  • the pediatrician who ensures a child with CdLS receives the best treatment possible...
  • the caring grandparent whose concern extends to the well-being of their children and their children's children...
  • the family friend who wants to learn more about what CdLS is and how they can help...
  • the big brother or little sister who would not trade their sibling with CdLS for anything...
  • the newborn whose diagnosis of CdLS was just confirmed...
  • YOU?

We invite you to be a part of our CdLS community.
Simply fill out the form on this page and click Submit.



CdLS FOUNDATION MEMBERSHIP FORM

Fields marked with an asterisk (*) are required.

TELL US ABOUT YOU

Name *

Street Address *

City *

State/Province *

Postal Code *

Country *

(If you reside outside the United States and there is a National Association in your country,
we will forward your information to them.)

Telephone *

E-mail *

Have you contacted the CdLS-USA Foundation before? *    Yes     No

TELL US ABOUT THE PERSON WITH CdLS IN YOUR LIFE

Name *

Gender: *
Male Female 

Age *

Date of Birth *

Your Relationship to this Person *

Has a diagnosis of CdLS been confirmed?     Yes     No

RELEASE INFORMATION

I wish to receive mailings from the CdLS-USA Foundation,
including the bimonthly newsletter, Reaching Out
I give permission to the CdLS-USA Foundation to release my name
for the purpose of mutual support.


ADDITIONAL COMMENTS (500 character maximum)


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Last Updated 4/17/06
© CdLS-USA Foundation, Inc., 2006.