families – Haemophilia Foundation ACT

Kathryn Body, our counsellor since 2016, has taken long service leave from 27th November 2023. Kathryn has advised HFACT that…

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.

“Lyn” (not her real name) is mother to several children with von Willebrand disorder. She was interviewed by Suzanne O’Callaghan,…

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

I keep learning new things in my journey with a bleeding disorder and I’ve come to the opinion that this…

Haemophilia treatment has changed over the years. The story of ‘Poppa’ Erl, grandfather, and grandson Roman, shows just how much….

Amanda (Mindi) Palm is an Australian community member and blogger who moved to Sweden for a few years. She explains…

Ben and Kylie have a son, Ryder aged 4 with severe haemophilia A. Being the father of a small boy with…

What does access to the latest evolution of haemophilia treatments mean for a family? Leah shares her experience about new…

Items tagged 'families'