Cornelia de Lange Syndrome Association (Australasia) Inc
Reaching Out - Providing Help - Giving Hope to Families
Notice of Cornelia de Lange Syndrome Association Australasia Incorporated (ABN 97 070 990 653) Annual General Meeting
To be held via Zoom on Saturday November 27th at 1330 ACST. Please click here for corresponding time zones and a printable pdf.
Voting rights will only be afforded to financial members. Nominations for committee members will only be available to financial members.
Please click the PayPal Button below to make payment for this years fees: $25 AUD per family per year.
Alternatively, a transfer can be made to: BSB 062245 - Account 10091486. Please add a payment reference of *Family Name* Fees 21.
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.
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.
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