Bringing together people & families affected by FA

Fanconi Anaemia Support Australasia (FASA) is a membership-driven volunteer organisation which aims to unite and inform the FA community in Australia, New Zealand and beyond.

Fanconi Anaemia (FA) is a rare, life-limiting genetic disorder causing bone marrow failure in children and a predisposition to gynaecological, head and neck cancers, together with other complications both in childhood and in later life.

FA Support Australasia

Online Family Meeting

2022

Annual FA Family Meetings

Online via Zoom

An annual event that allows families to hear from researchers and clinical experts in the research and treatment of Fanconi anaemia (FA).

Early detection of mouth cancer

Join a research project

Join Us

Fanconi Anaemia Support Australasia is a membership based organisation. Please sign up now – it’s free – so we can keep in touch from time to time and strengthen the network of FA family and friends.

Join the conversation

Got a question? Looking for advice? Need to vent?

The FA Australia/New Zealand Facebook group has been chatting and supporting each other for many years. Now they’ve adopted FASA and have become our first social media meeting place. All FASA members are invited to stop by, join up and say hi. We’ll post information on upcoming events to that Facebook page as well as to our home website.

Donations & Fundraising

Support FASA

FASA is a work in progress. We will need to raise some funds to cover expenses and support new activities for our FA community. Donations of $2.00 or more are tax-deductible in Australia. If you would like to leave a gift you can do so here

FA Research

If you would like to make a tax deductible donation towards research into Fanconi Anaemia you can do so through the St Vincent’s Institute, where FA research in Australasia is based.

FASA acknowledges the generous support of the Fanconi Anemia Research Fund (FARF) in the United States.

© Copyright 2020 Fanconi Anaemia Support Australasia Inc.

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