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Items tagged 'HFA & Foundation news'

  • News & Stories

World Haemophilia Day 2024

Today is World Haemophilia Day. Every year on 17 April, World Haemophilia Day is recognised worldwide to increase awareness of haemophilia, von Willebrand disease and other inherited bleeding disorders. This is a critical effort since with increased awareness comes better diagnosis and access to care for the millions who remain without treatment.
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  • News & Stories

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 Day, Rare Disease Day, Glanzmann thrombasthenia, women and peer support, FIFO workers, and mental health.
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  • National Haemophilia Journal

Changes at HFA

  • 19 March 2024
The team has changed recently at HFA. Natashia Coco has taken on the role of Executive Director (Acting) and we welcome Pauline Hill as our Digital Communications Manager.
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  • National Haemophilia Journal

From the President

  • Gavin Finkelstein -
  • 19 March 2024
Another exciting year ahead and the HFA staff have hit the ground running in 2024.
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  • National Haemophilia Journal

HFA has a new website

  • 19 March 2024
Over the past year the HFA team, together with our website developer, Heartburst, have been designing and building a new website for haemophilia.org.au. Check it out - and let us know if you find anything broken!
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  • News & Stories

DCMEF Awards now open

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

International Women’s Day 2024

Today we celebrate the women in the bleeding disorders community – whether they’re women with bleeding disorders or mums, partners, daughters, sisters, nurses, doctors, social workers or counsellors, physios, researchers, or carers. Thank you for being part of our community and advocating for us!
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  • News & Stories

Rare Disease Day 2024

Today is Rare Disease Day – a rare leap year day and very fitting for a worldwide event to raise awareness and generate change for people with rare diseases.
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  • News & Stories

PROBE Australia Study Update

We are building evidence about the needs of men and women affected by haemophilia in Australia.
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  • News & Stories

Welcome to our new website

HFA has a new website! You'll find all of the same great content and information, but in brand new packaging. Over the past 12 months we've been working hard with the team at Heartburst to modernise the HFA website. We have great plans for new features to be added in 2024, so please be patient with us while we're in the process of developing them.
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© 2024
Haemophilia Foundation Australia

Created with Heartburst

Haemophilia Foundation Australia 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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