Items tagged 'Families'

How to deal with problems at school if your child has a bleeding disorder like haemophilia, von Willebrand disease (VWD) or other rare bleeding disorders.
Claire describes international travel with her sons with severe haemophilia: treatments, packing, luggage and planning.
How your Haemophilia Treatment Centre can support you over your lifetime and ensure your wellbeing and best outcomes from treatment and care.
Find answers to your FAQs about von Willebrand disease (VWD) in our new fact sheet - symptoms, types, inheritance, diagnosis and treatment.
Elizabeth shares her experiences of parenting her teenage daughter Grace who has Glanzmann thrombasthenia, a rare hereditary platelet function disorder.
What mental health support services are available and how do you access them?
The PROBE Australia Study is how HFA is building evidence about the needs of men and women affected by haemophilia in Australia. Here's how you can help.

KARA CORDINER, PENNY MCCARTHY AND MEGAN WALSH Kara Cordiner, Penny McCarthy and Megan Walsh are Clinical Nurse Consultants at the…

The importance of our camps for children and families cannot be underestimated. At these camps, children connect with others going…

To celebrate Bleeding Disorders Awareness Week HFA launched this digital movie to showcase Overcoming Challenges of a Bleeding Disorder. 

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