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Representing the Victorian
bleeding disorders community

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LATEST NEWS

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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...

HFV Autumn 2024 News

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

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...

Support Groups

Find local support groups in your area

Info for me...

Getting Older Hub

Youth walking

Youth – Factored In

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...

Looking for another 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...
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