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March 2024 National Haemophilia now available

The March 2024 National Haemophilia is now available to read on our website. In this issue we highlight World Haemophilia...
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DCMEF Awards now open

The 2024 funding round for the Damon Courtney Memorial Endowment Fund (DCMEF) is now open....

International Women’s Day 2024

Today we celebrate the women in the bleeding disorders community ‚Äď whether they‚Äôre women with bleeding disorders or mums, partners,...

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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...
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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...

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