Scroll To Top

Cornelia de Lange Syndrome Association (Australasia) Inc

Reaching Out - Providing Help - Giving Hope to Families

The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA) is a family support organisation. We exist to support you and your family, with emotional support, a community, and quality information so you can make informed decisions. We also work to assist the accurate diagnosis of CdLS and promote research into the cause and manifestations of the syndrome.

2018 Conference - Brisbane

Our 2018 CdLS Conference and AGM will be held on Saturday 8th and Sunday 9th December at the Park Regis Hotel in Brisbane. Three extremely knowledgeable doctors with a lot of experience in CdLS will be attending: Dr Jane Law (GP specialising in adults with disabilities from Sydney), Dr Barry Lipschitz (Paediatric Gastroenterologist from Melbourne) and Prof Chris Oliver (Psychologist and expert on behaviours in people with intellectual disability, CdLS International SAC, from Great Britain).

full details
NEWS
Research Participation Opportunity - June 2018. Australian and New Zealand CdLS Families are invited to ...
view
WHAT IS CdLS?
We've compiled the most commonly asked questions about CdLS. Start here to understand this condition ...
view
MEDICAL
We keep up-to-date with the latest information from a range of quality organisations and medical sources ...
view
RESOURCES
National, International, and by State. Links to sites, pdfs, audio and video, relevant to our members ...
view
GALLERY
Community events, get-togethers and meetings. Sharing experiences, information and friendship ...
view
FACEBOOK
Join us on facebook. We have an active community there and keep it up-to-date with community news ...
connect
ARTICLES
Articles on CdLS from reputable sources, covering characteristics, behaviours, genetic information ...
view
CdLS IN THE MEDIA
Articles, information and editorials in the Australian Media we've found that touch on CdLS ...
view

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, New Zealand, Malaysia, Philippines, Singapore and other Pacific Nations. We do not receive any regular Government funding, and rely on membership fees for information dissemination via our newsletter 'Keeping in Touch' (KIT). We also produce topic specific information packages, provide counselling, and host awareness activities.

your donation helps us support the CdLS community
© 2018 CdLS Australia
Site by Loqium