The Family conference

The Family conference

Last modified by Gerritjan Koekkoek on 2009/02/14 14:24
Thursday July 23 (evening) – to Sunday July 26 (Breakfast)

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There is a packed conference programme where families can learn of the latest developments and strategies for working with people affected by CdLS and hear of health treatments and threats long before the information becomes published. Many of the professionals will be on hand to hold individual private consultations with families to help assess issues affecting the person with CdLS.

The event will start with individual meetings for different countries run by their national professional directors and will give a précis of the SAC meeting in their home language. All main sessions will have simultaneous translation for those languages for which there are 10 or more families attending.

The UK is also looking for language volunteers to help with interpretation for doctor consults. Meantime we are planning a series of trips out suitable for all ages for the siblings and young people attending the conference. And in the evenings there is plenty of fun for all the family at our planned social events.

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Created by Gerritjan Koekkoek on 2009/02/14 14:20
Translated into en by Gerritjan Koekkoek on 2009/02/14 14:23

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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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