קהילה

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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mission

לוח האירועים שלנו   

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.
Supports
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Contact information

Gwilym Conran

President

Email: president@cdls.org.au

Phone: +61 409 633 661

PO Box 151, Darwin, NT 0801

Read more about our community...

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אחרת פנה למרכז המומחיות הלאומי שלך

Network of experts for The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA)


הקהילות שלנו

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Dansk

Cornelia de Lange foreningen

דנמרקנורווגיהשוודיהפינלנד
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English

CdLS Foundation UK and Ireland

הממלכה המאוחדתאירלנד
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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

ספרד
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English

Canadian CdLS Foundation

קנדה
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עברית

(CdLS) האגודה הישראלית תסמונת קורנליה דה לנגה

ישראל
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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

גרמניהאוסטריהשוויץ
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Español

Comunidad Argentina del Sindrome Cornelia de Lange

ארגנטינה
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Português

Associação Brasileira Síndrome Cornélia de Lange

ברזיל
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Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

איטליה
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Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

פורטוגל
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Nederlands

Vereniging Cornelia de Lange syndroom

הולנדבלגיה
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Français

ASSOCIATION FRANÇAISE DU SYNDROME DE CORNELIA DE LANGE

צרפתשוויץבלגיהאלג'יריה
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Polski

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

פלין
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English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

ארצות הברית
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English

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

אוסטרליהניו זילנדמלזיההפיליפיניםסינגפור
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Español

Fundación CdLS COLOMBIA

קולומביה

About the website contents

All of the information on this WebSite 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: 

Send a email: info@cdlsWorld.org