Items tagged 'VWD'

Rare Disease Day is celebrated worldwide on 28 February to raise awareness about the experiences of people with rare diseases. The…

Simoni tells her personal story of growing up with the challenges of type 3 (severe) VWD.

SUZANNE O'CALLAGHAN Suzanne O'Callaghan is HFA Policy Research and Education Manager Von Willebrand disease   Chair ~ Susie Couper VWD…

The 20th Australian Conference on Haemophilia, VWD and Rare Bleeding Disorders was held 8-9 October 2021. The event was a…

Simoni’s story   This is a transcript of Simoni’s presentation at the 20th Australian Conference on Haemophilia, VWD and Rare…

Perry’s story   Perry spoke about his personal story of living with von Willebrand disease (VWD) at the 20th Australian…

The virtual 20th Australian Conference on Haemophilia, VWD and Rare Bleeding Disorders, 8-9 October 2021 is shaping up well, with a…

Mary Jane's story Mary Jane* is an Australian community member with von Willebrand disease (VWD). She spoke to HFA about…

The 20th Australian Conference on Haemophilia, VWD and Rare Bleeding Disorders will take place this year from 8-9 October 2021…

You may have noticed in your social media and e-news that we have been releasing lots of new videos recently!…

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