community

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.
Neemt deel in de CdLS World federation
ondersteuning
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contact informatie

Gwilym Conran

President

Email: president@cdls.org.au

Phone: +61 409 633 661

PO Box 151, Darwin, NT 0801

Uitgebreide informatie over ons

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onze communities

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Dansk

Cornelia de Lange foreningen

denemarkennoorwegenzwedenfinland
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English

CdLS Foundation UK & Ireland

verenigd koninkrijkierland
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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

spanje
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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

duitslandoostenrijkswitzerland
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Español

Asociación Argentina del Sindrome Cornelia de Lange

argentina
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Português

Associação Brasileira Síndrome Cornélia de Lange

brazil
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Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

italië
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Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

portugal
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Nederlands

Vereniging Cornelia de Lange syndroom

nederlandbelgië
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Français

ASSOCIATION FRANCAISE DU SYNDROME DE CORNELIA DE LANGE

frankrijkswitzerlandbelgiëalgerije
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Polski

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

polen
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English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

verenigde staten
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English

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

australiënieuw-caledoniëmalaysiëphilippijnensingapore
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Español

Fundación CdLS COLOMBIA

colombia

Over de website-inhoud

Alle informatie die u hier vindt is ter informatie, geen medisch advies! De plaats voor het vinden van specifieke medische adviezen, diagnoses en de behandeling is uw arts. Gebruik van deze site is strikt op eigen risico. Als u vind dat iets onjuist is, verduidelijking behoeft, verbeterd kan worden, laat het ons dan weten.

Stuur een email: vereniging@cdlsworld.org