Hear directly from people with lived experience of viral hepatitis as they share their stories, experiences and journeys.
Amanda & Jack
Amanda Davies and Jack Wallace share their personal experiences of hepatitis C, including being diagnosed, undergoing treatment and living with the impact of stigma. Amanda is Chairperson of the NT AIDS & Hepatitis Council and has worked in peer education and blood-borne virus services, while Jack is a Senior Research Officer at the Burnet Institute and has been involved in the hepatitis C response for many years. They reflect on their experiences of testing and treatment, and the importance of listening to people with lived experience.
Nicky
Nicky shares her lived experience and reflects on the importance of connection, understanding and culturally safe care. Nicky’s story helps bring lived experience to the centre of conversations about hepatitis, health and wellbeing. Her story is a reminder that everyone’s experience is different, and that listening to people and meeting them where they are can make a real difference.
Dave & Grace
David shares his experience of living with hepatitis B and hepatitis C, from diagnosis and years of managing his health through to treatment and a liver transplant. His wife Grace joins him to share her perspective as a carer and the role of support throughout David’s journey. Together, they reflect on the challenges of hepatitis C, the impact of stigma and the importance of support, understanding and not giving up.
Next Steps
Want to know more?
Talk to someone
Our free Infoline is free and confidential. We provide non-judgemental support and information about viral hepatitis for the community and workforce.
Frequently Asked Questions
Have a question about hepatitis? In our FAQs, you’ll find common questions and answers about hepatitis A, B, and C and liver health.
Hepatitis Resource Library
Our free hepatitis resources offer expert information about hepatitis A, B and C. Discover factsheets, flyers, posters and more.
