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Cornelia de Lange Syndrome Association Australasia

REACHING OUT - PROVIDING HELP - GIVING HOPE TO FAMILIES

Family Conference in Canberra 2020

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.

Who we are

The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA) is a family support organisation. We exist to support you and your family. The organisation is dedicated to the emotional wellbeing for anyone touched by this little-known genetic syndrome by providing a community, events and the latest information. We also work to assist the accurate diagnosis of CdLS and promote research into the cause and manifestations of the syndrome.

More information

Getting a CdLS diagnosis may be stressful & overwhelming. We provide information for you here.

Diagnosed with CdLS? Here is some useful information for you.

Click here
Cornelia de Lange Syndrome information

Be part of us
 

Be a part of our supporting community.

Be a new member or renew your membership here.

Click here
Cornelia de Lange Syndrome Family

Join us at our next event

Keep updated with our activities this year.

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Participate in our next activities.

Click here
CdLS events

Donate
 

We rely on your generosity to help those affected by CdLS. Your donation, no matter the size, gives hope for CdLS families.

Join us in making a meaningful difference.

Click here
CdLS Family

Contact Us

Reach out for support if you or a loved one has been diagnosed with CdLS or you suspect they might have CdLS. Want to connect with other CdLS families? We can help connect families with others in you area. 

0409-633-661

president@cdls.org.au

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