Click here for a map of the local and world-wide FA community

Individuals with Fanconi anaemia and their family members can actively participate in our research through non-invasive donation of samples such as a mouth swab. If you would like to help progress the research into treatments for Fanconi anaemia please write to

For FAmilies please visit Fanconi Anaemia Support Australasia and sign up for updates about what is happening in family support, standard of care and research in our region.

To learn more about Fanconi anaemia check out the excellent resources at the Fanconi Anemia Research Foundation (FARF) website at

The 3rd Fanconi anaemia Family Meeting is tentatively scheduled to be at the Royal Children's Hospital in Melbourne, Australia, October 30th and 31st, 2020.

To be added to the mailing list for the meeting, please register your interest here.

See the website for past meetings.