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RESEARCH ARTICLE (Open Access)

Stigma, support, and messaging for people recently diagnosed with HIV: a qualitative study

Loretta M. Healey https://orcid.org/0000-0002-5718-861X A , Shirin R. Markham A , David J. Templeton A B C D , Lionel Rabie E and Anthony K. J. Smith https://orcid.org/0000-0002-0005-9542 F G *
+ Author Affiliations
- Author Affiliations

A Department of Sexual Health Medicine, Community Health, Sydney Local Health District, Sydney, NSW 2050, Australia.

B Sexual Assault Medical Service, Royal Prince Alfred Hospital, Sydney Local Health District, Sydney, NSW 2050, Australia.

C The Kirby Institute, UNSW Sydney, Sydney, NSW 2052, Australia.

D Central Clinical School, The Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.

E ACON, Sydney, NSW 2010, Australia.

F Centre for Social Research in Health, UNSW Sydney, Sydney, NSW 2052, Australia.

G Australian Human Rights Institute, UNSW Sydney, Sydney, NSW 2052, Australia.

* Correspondence to: anthony.smith@unsw.edu.au

Handling Editor: Tiffany Renee Phillips

Sexual Health 21, SH24045 https://doi.org/10.1071/SH24045
Submitted: 27 February 2024  Accepted: 3 October 2024  Published: 17 October 2024

© 2024 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC)

Abstract

Background

Despite advances in antiretroviral treatment and the message of undetectable equals untransmittable (U=U), there remain challenges related to stigma and quality of life for people living with HIV. This study aimed to understand the experiences of people recently diagnosed with HIV at a clinical service, to guide insights into how to improve care and support in the contemporary treatment era.

Methods

This qualitative study involved semi-structured interviews with individuals diagnosed with HIV between 2016 and 2021 at RPA Sexual Health service (a sexual health clinic in Sydney, Australia), or who were referred to the clinic directly after diagnosis. Participants were recruited through a short survey questionnaire between May 2022 and May 2023, and interviews were transcribed and analysed thematically.

Results

Fourteen participants were interviewed for the study, eight of whom were born outside of Australian or Aotearoa New Zealand. We found that diagnosis was still a shocking event requiring careful support; that there was ongoing stigma, shame, and reduced sexual confidence following diagnosis; and that beyond initial diagnosis, some people would benefit from ongoing support and education about key concepts regarding HIV treatment.

Conclusion

Our study suggests that HIV diagnosis remains disruptive, and sexual stigma is a key issue negatively impacting quality of life. Health providers can mitigate these issues by supporting the ongoing psychosocial needs of people with HIV in the early period of adjusting to HIV diagnosis, and referring to peer-based and other services. Initiating conversations about sex and dating and checking understandings of key health messages over time may promote improved care.

Keywords: Australia, diagnosis, healthcare workers, HIV, men, sexual behaviour, sexual confidence, stigma, treatment.

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