Experiences of diagnosis, care and treatment among Aboriginal people living with hepatitis C
Abstract Objective: Aboriginal Australians are disproportionately affected by hepatitis C (HCV). There are a range of barriers to HCV care, often beginning with poor diagnosis experiences. Little research exists on the experiences of Aboriginal Australians living with HCV. This study aimed to descri...
Main Authors: | Loren Brener, Hannah Wilson, L. Clair Jackson, Priscilla Johnson, Veronica Saunders, Carla Treloar |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2016-04-01
|
Series: | Australian and New Zealand Journal of Public Health |
Subjects: | |
Online Access: | https://doi.org/10.1111/1753-6405.12402 |
Similar Items
-
Health workers’ perspectives of hepatitis B-related stigma among Aboriginal and Torres Strait Islander people in New South Wales, Australia
by: Elena Cama, et al.
Published: (2023-08-01) -
Using One’s Right of Inspection: Australia, the United Nations, Human Rights and Aboriginal People
by: Ludivine Royer -
Globalisation and the Australian Aborigines: gain or strain?
by: Ludivine Royer
Published: (2007-01-01) -
Young Aboriginal people’s engagement with STI testing in the Northern Territory, Australia
by: Stephen Bell, et al.
Published: (2020-04-01) -
Evaluation of the Deadly Liver Mob program: insights for roll-out and scale-up of a pilot program to engage Aboriginal Australians in hepatitis C and sexual health education, screening, and care
by: Carla Treloar, et al.
Published: (2018-02-01)