Comunauté

The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA)



Who we are

CdLS Australia is a non-profit organisation which is run by volunteers, usually parents, who have a family member with CdLS.

The Australian support group was formed in 1981 in Victoria, when three mothers met, and for the first time in many years were able to compare their experiences.

The group was incorporated in 1995 and countries supported by CdLSA are Australia and New Zealand, with outreach to Malaysia, Philippines, Indonesia Singapore and other Pacific Nations.

We do not receive any regular Government funding, but rely on membership fees and donations to provide support to families.

 

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The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA)

Who we are

CdLS Australia is a non-profit organisation which is run by volunteers, usually parents, who have a family member with CdLS.The Australian support group was formed in 1981 in Victoria, when three mothers met, and for the first time in many years were able to compare their experiences.The group was incorporated in 1995 and countries supported by CdLSA are Australia and New Zealand, with outreach to Malaysia, Philippines, Indonesia Singapore and other Pacific Nations.We do not receive any regular Government funding, but rely on membership fees and donations to provide support to families.
Participe à la campagne The World Federation of CdLS Support
Soutiens
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Informations de contact

Gwilym Conran

President

Email: president@cdls.org.au

Phone: +61 409 633 661

PO Box 151, Darwin, NT 0801

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Nos communautés

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Dansk

Cornelia de Lange foreningen

danemarknorvégesuèdefinlande
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English

CdLS Foundation UK and Ireland

royaume-uniirlande
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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

espagne
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English

Canadian CdLS Foundation

canada
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עברית

(CdLS) האגודה הישראלית תסמונת קורנליה דה לנגה

israël
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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

allemagneautrichesuisse
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Español

Comunidad Argentina del Sindrome Cornelia de Lange

argentine
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Português

Associação Brasileira Síndrome Cornélia de Lange

brésil
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Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

italie
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Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

portugal
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Nederlands

Vereniging Cornelia de Lange syndroom

pays-basbelgique
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Français

ASSOCIATION FRANÇAISE DU SYNDROME DE CORNELIA DE LANGE

francesuissebelgiquealgérie
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Polski

Stowarzyszenie Dzieci i Rodzin Cornelia de Lange Syndrom (CdLS) w Polsce

pologne
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English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

états-unis
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English

The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA)

australienouvelle-zélandemalaisiephilippinessingapour
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Español

Fundación CdLS COLOMBIA

colombie

À propos du contenu du site Web

Toutes les informations contenues dans ce site Web sont uniquement destinées à des fins éducatives. Pour obtenir des conseils, des diagnostics et des traitements médicaux spécifiques, adressez-vous à votre médecin. L'utilisation de ce site est strictement à vos propres risques. Si vous trouvez quelque chose qui, selon vous, nécessite une correction ou une clarification, veuillez nous en faire part à l'adresse suivante : 

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