Items tagged 'Newly diagnosed'

Joanna McCosker reports on the Congress workshop to improve diagnosis and care for women and girls with bleeding disorders.

Monique Manzanera reports on a Congress session on resilience and recovery with practical coping strategies for mental wellbeing.

Alan Dursun shares his reflections on the World Federation of Hemophilia 2026 World Congress and Global Youth Leadership Training.

Complete our national survey and let us know how HFA can best provide services and be relevant to the bleeding disorders community!

The HFA Women Bleed Too survey explored the experiences of Australian women and girls with bleeding disorders in health care settings.

The 2026 version of the HFA red folder - Haemophilia: a guide for parents of a newly diagnosed child is now completed!

In May 2026 HFA hosted a family day for the South Australian bleeding disorders community for a day of learning and fun.

Haemophilia Foundation Australia joined the global bleeding disorders community to mark World Haemophilia Day on 17 April 2026. See the photos!

Australia was well-represented at the World Federation of Hemophilia 2026 World Congress as speakers, poster presenters and delegates.

Alan Dursun, HFA President, reflects on the WFH World Congress, women and girls with bleeding disorders and other relevant news.

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