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Missing Factor Magazine, Winter, 2024
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Missing Factor Magazine, Winter 2024
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Representing the Victorian
bleeding disorders community

Haemophilia Foundation Victoria Logo
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Haemophilia inheritance in males video

New video: Haemophilia inheritance in males

If you were born male with haemophilia, will your children have haemophilia too?...
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Person on edge of cliff looking over ocean

Tips to Alleviate Anxiety

Monique from Beautiful Minds, spoke with us at the HFA conference about anxiety, and how we can overcome it....
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Bleeding disorders family

HFV WINTER 2024 MAGAZINE

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Getting Older Hub

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Factored In for Youth

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Getting Older Hub

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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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Bleeding Disorders Awareness Month
This October help us raise awareness for haemophilia, von Willebrand disease and other bleeding disorders.
Find out more

Calendar

Jul
28

World Hepatitis Day 2024

NATIONAL

Oct
1

Bleeding Disorders Awareness Month 2024

NATIONAL

Oct
16

22nd Australian Conference on Haemophilia, VWD and Rare Bleeding Disorders

NATIONAL

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

Alternatively, click here to visit Haemophilia Foundation Australia.

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Personal StoRies...
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Paul

Paul talks about his career

Paul shares his experience working as an apprentice shipwright and boat builder, a FIFO WHS manager, and today supporting his...
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Jenny - acquired haemophilia

Acquired haemophilia – Jenny’s story

Jenny shares her story of how she discovered she had acquired haemophilia and how it was able to be successfully...
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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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© 2024
Haemophilia Foundation VIC

Created with Heartburst

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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