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

Press Room

Welcome to the CdLS Foundation Press Room. Here you can view 2008 CdLS Foundation press releases and CdLS-related news coverage. For specific information about CdLS and the Foundation, please go to About Us. Links to 2006 and 2007 press archives are below.


News Releases

CdLS in the News

  • Living With CdLS (5/13/08)
    KTTC
    May 10 is CDLS Awareness Day. If you've never heard of CDLS, it's a syndrome that effects about one in 10,000 people. And one family from Zumbrota is living with this syndrome every day.
  • Walk-a-thon to Raise Awareness about CdLS (5/9/08)
    Seacoast News
    Mom Marcia Knowles is rallying a "Hoof It 4 Hunter" walk-a-thon to raise awareness. …
  • Hope for Hunter (5/9/08)
    The Daily News
    Tiny, 2-year-old Hunter Knowles is a precious toddler -blond curls and big, blue eyes. …
  • Acceptance Guaranteed (Part 1) (5/7/08)
    The Keene Sentinel
    There's a place Amy N. Haskell can go where no one will ask uncomfortable questions. …
  • Acceptance Guaranteed (Part 2) (5/7/08)
    The Keene Sentinel
  • Living with Cornelia de Lange Syndrome (3/12/08)
    Warwick Beacon
    The parents of 11-year-old Doug Canning consider themselves very lucky. …









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Last Updated 8/19/08
© CdLS-USA Foundation, Inc., 2008.