Items tagged 'General'

Our new VWD fact sheet is now available. It provides simple information about von Willebrand disease to share with others.
A guide to living well with von Willebrand disease (VWD) - from diagnosis to treatment, how it is passed on and special issues for females.
What is von Willebrand disease (VWD) - often called von Willebrand's? This fact sheet covers what causes it, symptoms, diagnosis and treatment.
Read the latest newsletter for HFA. The HFA Newsletter is delivered once per month to our email subscribers.
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.
If you or your child have haemophilia, please share your view on new treatments in the HaemPref (Haemophilia Treatment Preferences) Survey.
The September 2024 National Haemophilia is now available to read on our website. In this issue we promote Bleeding Disorders Awareness Month, talk about raising teens with bleeding disorders, report on our gene therapy snapshot survey and share Jack's latest travel adventures.
Bleeding Disorders Awareness Month is coming up in October 2024. How can you take part? Order your promotional items now!
Heading to the end of the year, we review our progress. Gene and emerging therapies are on the agenda, and Bleeding Disorders Awareness Month is coming up.
Exciting new haemophilia treatments using a range of innovative technologies were highlighted at ISTH 2024 Congress.

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