Items tagged 'VWD'

Suzanne O'Callaghan reports on a Congress session on VWD diagnosis and treatment, including emerging therapies.

Sam, mother to 7-year-old TJ, shares her story about raising a young son with type 2A VWD

Simoni and Javonte caught up to talk about growing up with a bleeding disorder, treatment, playing sport and why it's important to share your story.

An overview of new and emerging VWD therapies currently being studied. Most are experimental but show promising directions for future care.

The session on women with bleeding disorders at the 2025 Conference explored a female-centric approach to treatment and care over the lifetime.

Sophie tells her personal story of advocating for herself while pregnant and managing childbirth with Type 1 von Willebrand disease (VWD).

Tyler tells his personal story of living with Type 1 von Willebrand disease (VWD). Playing sport with precautions, improved medical awareness.

The von Willebrand disease (VWD) session at the 2025 Conference was both educational and uplifting.

At ISTH 2025 researchers shared advances in emerging therapies for haemophilia and von Willebrand disease (VWD).

What’s it like to grow up with a very rare bleeding disorder? Some of our community members talk about their experiences.

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