On 14 May 2024 we were fortunate to have Dr Michiel Coppens join us at the HFA office for an interview about gene therapy. Watch it now.
The report on the UK Infected Blood Inquiry investigating contaminated blood and blood products was released on 20 May 2024.
The 2024 funding round for the Damon Courtney Memorial Endowment Fund (DCMEF) is now open.
From 21-24 April, HFA visited Madrid, Spain for the WFH 2024 World Congress. Check out some photos from this huge event.
Dr Michiel Coppens is coming to Australia and we want your questions for a special 'Ask Me Anything' interview about gene therapy.
It was spectacular seeing people and landmarks across Australia - and the world - go red in support of bleeding disorders.
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.
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.
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!
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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