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All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at:

Send a email: info@cdlsWorld.org

The World Federation of CdLS Support

info@cdlsworld.org

Latest news

Join Us for International CdLS Remembrance Day
Resolution for People Living with a Rare Disease adopted by the United Nations
2021 CdLS-Day Latino Challenge
the Rare 2030 young citizens ask...
An Open Letter to the Special Needs Sibling
Promotion of Paul Mulder

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