Welcome to the new CriDuChat.org website! We hope that this website can be a source of credible information regarding Cri du Chat Syndrome (5P- or Lejune's Syndrome).
CriDuChat.org is tool for parents, families, teachers and health professionals to learn more about Cri du Chat (CdCS). It is our mission to be the centerpoint of useful and credible information that is not readily available to all because the syndrome is so rare.
Please have a look as we continue to add more information, contacts of worldwide advocates and other useful information regarding CdCS. Feel free to contact us at any time with any concerns, information or any other content regarding Cri du Chat Syndrome.
CriduChat.org Gets a website facelift
CriduChat.org recieved a major facelift just in time for 2013 Cri du Chat Awareness Week. We are lucky to have so many wonderful professionals, who are also parents, who donate their time and expertise for the benefit of other kiddos and families worldwide.
CdCS Awareness Week 2013
CdCS Awareness Week is May 5-11, 2013. Show your support by contacting your local media and spread the word!
New CdCS Video "I Can" is Now LIVE!
5P- Society and parents from around the world have submitted videos of their children to support the knowledge that CdCS kids CAN do amazing things. Watch the video here
