No 232 December 2025

Front cover of National Haemophilia December 2025

With the theme of ‘Teamwork: pushing the boundaries’, both the 2025 Australian Bleeding Disorders Conference and Bleeding Disorders Awareness Month were exciting opportunities to put a spotlight on what’s new and emerging in bleeding disorders and coming together to achieve change. In this issue we have reports on Conference highlights and showcase Awareness Month in pictures.

In this issue

Applications for the Damon Courtenay Memorial Endowment Fund are open until 16 January 2026. Grants are to support people with bleeding disorders.
New HFA President, Alan Dursun, introduces himself and his goals for the Australian bleeding disorders community.
Julia Broadbent has joined the HFA team as HFA Office Administrator.
The HFA Awards Program recognises special service to the Australian bleeding disorders community. Four awards were made in 2025.
An Australian research study reports on the views of people with blood disorders, their carers, and the general public on gene therapy.
We share our photo gallery of celebrating Bleeding Disorders Awareness Month in red during October 2025.
In 2025 the World AIDS Day theme 'no one left behind' asks us to show our support for our community affected by HIV and remember those we have lost.
HFA has published haemophilia treatment fact sheets on clotting factor replacement therapy, bispecific antibody therapy, rebalancing therapies and gene therapy.
In 2025 AHCDO funded three research projects to address key knowledge gaps and urgent needs in bleeding disorders.
The Australian Bleeding Disorders Conference 2025 was held at the VOCO Brisbane from 16 to 18 October 2025.
The new and former HFA Presidents share their highlights and key take-aways from the Australian Bleeding Disorders Conference 2025.
The von Willebrand disease (VWD) session at the 2025 Conference was both educational and uplifting.
Tyler tells his personal story of living with Type 1 von Willebrand disease (VWD). Playing sport with precautions, improved medical awareness.
Sophie tells her personal story of advocating for herself while pregnant and managing childbirth with Type 1 von Willebrand disease (VWD).
The session on women with bleeding disorders at the 2025 Conference explored a female-centric approach to treatment and care over the lifetime.
Professor Cedric Hermans spoke with HFA about new and emerging haemophilia therapies, women and girls, and the importance of diagnosis.
The Lifestyle plenary highlighted connection and teamwork with your Haemophilia Treatment Centre to empower people with bleeding disorders to live well.
The Getting Older session highlighted staying active, cardiovascular health, HIV, hepatitis C and liver health, future needs and comprehensive care.
The 2025 Conference spotlighted women, ageing with haemophilia and communicating before medical procedures.
The 2025 Conference highlighted groundbreaking novel therapies for bleeding disorders and how teamwork can transform lives.
The Youth Program at the 2025 Conference brought together young people with bleeding disorders from around Australia to learn, connect and share experiences.
What's coming up in bleeding disorders?
The HFA Council and staff wish you a happy and safe festive season.

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