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Items tagged 'VWD'

  • National Haemophilia Journal

Living with type 1 VWD

  • Susie -
  • 11 December 2023

Susie’s story Susie shared her personal story of living with type 1 VWD at the 21st Australian Conference on haemophilia,…

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  • National Haemophilia Journal

Von Willebrand disease

  • Suzanne O'Callaghan -
  • 11 December 2023

SUZANNE O’CALLAGHAN Suzanne O’Callaghan is HFA Policy Research and Education Manager VWDChair ~ Dr Chee Wee TanPersonal story ~Adam Personal story…

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  • National Haemophilia Journal

The challenges of living with VWD

  • Shauna -
  • 11 December 2023

Shauna’s story Shauna shared her personal story of managing quality of life issues while living with Type 3 VWD at…

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  • National Haemophilia Journal

Conference 2023

  • 26 June 2023

The 21st Australian Conference on haemophilia, VWD & rare bleeding disorders will be held face-to-face at the Pullman on the…

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  • National Haemophilia Journal

2023 Conference

  • 20 March 2023

The 21st Australian Conference on haemophilia, VWD & rare bleeding disorders will be held face to face at the Pullman…

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  • National Haemophilia Journal

Living life actively with VWD

  • 20 March 2023

Adam is in his late 40s and has Type 3 von Willebrand disease (VWD), which is a severe form. He…

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  • National Haemophilia Journal

VWD down the generations

  • Fiona -
  • 12 December 2022

Fiona is in her early 50s and found out she had von Willebrand disease (VWD) when she was 6 years…

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  • National Haemophilia Journal

What is VWD?

  • 12 December 2022

 

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  • National Haemophilia Journal

Von Willebrand disease

  • Suzanne O'Callaghan and Robyn Shoemark -
  • 13 September 2022

SUZANNE O'CALLAGHAN Suzanne O'Callaghan is HFA Policy Research and Education Manager Plenary (Arosenius Lecture) – Towards novel treatment options in…

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  • National Haemophilia Journal

Rare Disease Day 2022

  • 14 March 2022

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

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