Get connected

Get connected

Last modified by Gerritjan Koekkoek on 2011/10/10 07:14

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You never have to feel alone, the CdLS World Federation can connect you with other CdLS families in your country or beyond.

We have multiple options for you to get involved;

  • Connect to one of our member-supportgroups who are active in many countries. You can find contact data for each of our members on this website
  • If you have questions and would like to consult a expert; you can register and post your questions...
  • Just register on this website, tell us more about yourself. We will help you from there to find your best option; select one of our support groups and you will have the opportunity to connect to families of that supportgroup

Find below the list of our supportgroup members

(please select the country below to see the contact information) 

  
Australia (Malaysia/ New Zealand)Portugal
CanadaSpain
DenmarkUnited Kingdom Ireland
France (Switzerland)United States of America
Germany
Chili
ItalySouthKorea 
JapanCentral America
NetherlandsArgentina
Poland..

If you reside outside a country supported by our members; we can help to connect you with families from your country (please click here) 

Tags:
Created by Gerritjan Koekkoek on 2011/05/17 19:18

About you..

Only when registerd...

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: 19
Australia
Australia
Australia
Canada
Deutschland
España
France
Italia
vereniging CdLS
vereniging CdLS
Polska
Portugal
CdLS Foundation UK & Ireland
CdLS Foundation UK & Ireland
CdLS Foundation USA
Danmark
日本
Schweiz, Suisse
CdLS World
Chile
South Korea
Central America
Central America
Central America
Central America
Central America
Argentina

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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