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Representing the Victorian
bleeding disorders community

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HFV Autumn 2024 News

The latest issue of The Missing Factor is now available to read online....
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HFV AGM 2023

We are pleased to invite HFV members to our Annual General Meeting to be held on Sunday 10th December 2023 at Healesville Sanctuary, Robert Eadie...
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HFV Spring 2023 News

Spring has arrived! Catch up on the latest news with HFV here....
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Youth walking

Youth – Factored In

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Women with bleeding disorders

Find information for women and girls with bleeding disorders, including carrying the gene, haemophilia testing, VWD in females, self-advocacy and...
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Personal StoRies...
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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...
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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,...
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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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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...
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© 2024
Haemophilia Foundation VIC

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Haemophilia Foundation Victoria acknowledges the Traditional Owners and Custodians of Country throughout Australia, the land, waters and community where we walk, live, meet and work. We pay our respects to Elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples.​

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