Looking for some simple information about von Willebrand disease (VWD) to share with others?
Our new Von Willebrand disease (VWD) fact sheet has answers to a range of FAQs with the very latest information:
Share it with your family – or keep it on hand for new doctors or school or other situations where you want to give a quick explanation.
And don’t forget to talk to your Haemophilia Treatment Centre (HTC) to keep up-to-date with treatment options for VWD.
Download the fact sheet from the HFA website.
Or contact HFA for print copies:
E: hfaust@haemophilia.org.au
T: 03 9885 7800
Our thanks to the health professional experts and the HFA VWD consumer focus group for their contributions and advice.
Haemophilia Foundation Australia acknowledges the Traditional Owners and Custodians of Country throughout Australia, the land, waters and community where we walk, live, meet and work. We pay our respects to Elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples.
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