One of the most difficult aspects of people connected to CdLS is learning that a child with CdLS has died. While it is a sensitive issue to face and discuss with families privately, we feel that it is important to bring the subject to a public forum.
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
vereniging@cdlsworld.org
