Membership » Welcome, please tell us more

Welcome, please tell us more

Last modified by Gerritjan Koekkoek on 2012/03/27 18:05
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Thank you for your interest in the Cornelia de Lange syndrome (CdLS). The Website you have just registered on is meant to help and inform about this rare syndrome.

We would like that this website helps you well and to serve you best we would like to, kindly, ask you the following;

  1. If you would like to ask questions to one of the CdLS Experts some more information about the person with CdLS (if appropiate) is needed by the experts,
  2. If you would like to join one of the associations of the world federation some more detailed contact information is required,
  3. If you would like us to contact you more personally (this email is generated by the website) please mark this in your personal settings, likewise if you like to be contacted by others so you can share stories and experiences.

If you want you can fill in this information by clicking on "Tell us more...";
           
      

This page contains 4 sections (tabs); Profile, Preferences, CdLS Info and CdLS Person. (We continuously try to improve the website, so let us know if something is not clear or if you have an idea for improvement!!)

(This email is generated by the website, it might well be that you have already contacted a CdLS organization, still we would greatly appreciate if you would complete some details, other wise our apologies for asking twice!)

For each section we will show you a screenshot of what and how you can complete that section.

Tags:
Created by Gerritjan Koekkoek on 2011/12/04 08:04

CdLS impressions

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World associations

CdLS is worldwide present, all information is available in English
but if you want to change the language click on a flag of one of the supportgroups in CdLS World
Number of associations: 15
Australia
Canada
Deutschland
CdLS Espagnol
France
Italia
Vereniging CdLS
Polska
Portugal
United Kingdom
United States
Danmark
日本
Schweiz, Suisse
CdLS World

Disclaimer - All of the information contained within these questions and answers 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: umugler@aol.com
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