Search
Close this search box.

Items tagged 'pauline'

Bleeding Disorders Awareness Month starts today! For all of October, individuals, families, Haemophilia Foundations and other organisations will come together to raise awareness about haemophilia, von Willebrand disease and other rare bleeding disorders around Australia.
Sunday, 28 July 2024 is World Hepatitis Day. This is a day when we come together worldwide to share the message, 'It’s time for action'.
If you were born male with haemophilia, will your children have haemophilia too?
International Men’s Health Week runs each year in the middle of June. It is an important opportunity to highlight the importance of men’s health, and to promote and support the health and wellbeing of men and boys in our communities.
Paul shares his experience working as an apprentice shipwright and boat builder, a FIFO WHS manager, and today supporting his brother in a business with over 60 employees and a growing client base.
HFA would like to understand what our community members want from their haemophilia treatments and your perspectives on gene therapy in particular.
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.
Jenny shares her story of how she discovered she had acquired haemophilia and how it was able to be successfully treated with the support of her hospital and Haemophilia Treatment Centre.
Claire shared her personal story as a parent of young boys with haemophilia at the 21st Australian Conference on haemophilia, VWD and rare bleeding disorders. This is a transcript of her presentation.
Elizabeth’s teenage daughter Grace has Glanzmann thrombasthenia. Elizabeth spoke with HFA about what it was like to find that your child has a very rare bleeding disorder and their family experiences as Grace grows up.
Skip to content