Items tagged 'Families'

Haemophilia Foundation Australia is convening the 2025 Australian Bleeding Disorders Conference in Brisbane on 16-18 October 2025.
Adam, Bel and Tayla share their experiences of growing up with a very rare bleeding disorder and what they learned along the way.
HFA is still recruiting people to complete the PROBE Australia Study.
Exciting advancements in gene therapy and other emerging treatments for haemophilia were presented at the Blood 2024 conference.
Rare Disease Day was celebrated on 28 February 2025 to raise awareness and generate change for people with rare diseases, including rare bleeding disorders.
World Haemophilia Day 2025 is a worldwide call to action to close the gaps in care for women and girls with bleeding disorders.

(HaemPref Survey) How do individuals make decisions about treatment? What factors encourage or discourage patients from treatments? What are individuals’…

How to deal with problems at school if your child has a bleeding disorder like haemophilia, von Willebrand disease (VWD) or other rare bleeding disorders.
Claire describes international travel with her sons with severe haemophilia: treatments, packing, luggage and planning.
How your Haemophilia Treatment Centre can support you over your lifetime and ensure your wellbeing and best outcomes from treatment and care.

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