Representing the Australian
bleeding disorders community

HFA site logo

Sign up for HFA eNews today!

Get the latest news, events and our free National Haemophilia magazine

Dr Michiel Coppens

Have your gene therapy questions answered

Dr Michiel Coppens is coming to Australia and we want your questions for a special 'Ask Me Anything' interview about...
WFH Congress 2024

WFH 2024 World Congress

From 21-24 April, HFA visited Madrid, Spain for the WFH 2024 World Congress. Check out some photos from this huge event....
World Haemophilia Day

World Haemophilia Day 2024

Today is World Haemophilia Day. Every year on 17 April, World Haemophilia Day is recognised worldwide to increase awareness of...

Looking for your state or territory foundation?

Click on the map to navigate to the site of each state's foundation

Personal stories
Jenny - acquired haemophilia

Acquired haemophilia – Jenny’s story

Jenny shares her story of how she discovered she had the acquired haemophilia and how it was able to be...
Claire speaking at the 21st Australian Conference on Haemophilia, VWD and Rare Bleeding Disorders

Hopes for the Future

Claire shared her personal story as a parent of young boys with haemophilia at the 21st Australian Conference on haemophilia,...
Girl playing in garden. Image by Emma Bauso for Pexels.

Growing up with Glanzmann thrombasthenia 

Elizabeth’s teenage daughter Grace has Glanzmann thrombasthenia. Elizabeth spoke with HFA about what it was like to find that your...
Woman looking at camera. Image by Adrienn for Pexels.com

Living with Glanzmann thrombasthenia 

Allison is in her mid-40s and was diagnosed with Glanzmann thrombasthenia at birth. She talked to HFA about her experiences...

Join the HFA community

Sign up for the latest news, events and our free National Haemophilia magazine

Skip to content