Each countries own family community is invited to send a representative (or two) to our two yearly council meeting.
Together we talk about what's going on in each country, which ideas and plans we have for the future and what we did in the last two years to enhance the quality of life of all involved with CdLS
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
info@cdlsworld.org
