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An (un)restricted living

A qualitative exploration of the mental health and well-being of people living with HIV in England

Bibliographic Data

ID4883814
AuthorsVasiliki Papageorgiou (0000-0002-2387-6780, The George Institute for Global Health), Louis Cullen (0000-0003-0881-0211, London School of Hygiene & Tropical Medicine), Lucy Cullen (0000-0001-6539-6710), T Charles Witzel (0000-0003-4262-261X, University College London), Alex Sparrowhawk (Trinity House), Flavien Coukan (0000-0002-2666-0125, Imperial College London), John Sewell (0000-0001-7148-2391, University College London), Janey Sewell, Alec Rodger (0000-0001-8817-4651, Royal Free London NHS Foundation Trust), Alison Rodger (0000-0002-7111-3024), C May (0000-0002-0451-2690, Faculty of Public Health), Fiona Burns (0000-0002-9105-2441, Royal Free London NHS Foundation Trust)
Year2025
Volume377
Pages118109
Publication date2025-07-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueSocial Science & Medicine (JOURNAL)
Journal identifiersISSN: 0277-9536 • E-ISSN: 1873-5347
PublisherElsevier BV (PUBLISHER)
DOI10.1016/j.socscimed.2025.118109
PMID40306195
OpenAlexW4409572280
LanguageEN
Citations received4
References cited38

People living with HIV, who have access to treatment, now have normal life expectancy. However, stigma and discrimination continue to affect health and well-being. We conducted focus groups with people living with HIV (n = 37), and key informant interviews (n = 20) with clinical and non-clinical workers who support people with HIV between May and November 2023. We aimed to explore the ongoing challenges and concerns faced by people living with HIV in England to inform a new model of person-centred HIV care. Participants discussed living well in relation to: 1) an unrestricted living; 2) emotional sexual health and intimacy well-being; and 3) autonomy of health and healthcare. Aspirations for an unrestricted living revolved around experiencing life in the same way as others, rather than having to compromise a sense of self or negotiate experiences differently due to their HIV status. Participants also shared a desire to live fulfilled sex lives without fear of being stigmatised due to living with HIV, and of feeling deserving of a satisfying sex life and sexual intimacy. There was also a particular anxiety about sharing an HIV status with new sexual partners. Conversations around sex and intimacy needed to be opened up to cover topics including pleasure and sexual wellness. A compromised autonomy of health referred to physical health; for example, the need for daily medication. Autonomy of healthcare referred to the challenges of negotiating an often fragmented and fractured healthcare service. Some shared experiences of discrimination by non-HIV healthcare workers and a requirement to advocate for their needs which is a specific challenge for marginalised groups. Person-centred care, which uses an intersectional approach to delivering HIV care, would respond to the needs and aspirations of people with HIV and their whole self. This offers the potential to address HIV-related stigma which continues to hinder progress

Family medicine · Human immunodeficiency virus (HIV · Mental health · Psychiatry · Psychotherapist · Qualitative research · Social science · Sociology · Well-being · Gender Studies · Healthcare innovation and challenges · Homelessness and Social Issues · Medicine · Psychology · Social Policy and Reform Studies · Gerontology

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    Open Access•Robert H Remien, Michael J Stirratt et al.•AIDS•2019

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    Open Access•Anne Stangl, Valerie A Earnshaw et al.•BMC Medicine•2019

  • From Conceptualizing to Measuring HIV Stigma

    Open Access•Valerie A Earnshaw, Stephenie R Chaudoir•AIDS and Behavior•2009

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    Open Access•Carmen H Logie, LLana James et al.•PLoS Medicine•2011

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    Open Access•Nicola Gale, Nicola K Gale et al.•BMC Medical Research Methodology•2013

  • Consolidated criteria for reporting qualitative research (Coreq)

    A Jaure, A Tong et al.•International Journal for Quality…•2007

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    Erving Goffman•Stigma•2009

  • HIV Health literacy beyond the biomedical model

    Olivia Hollingdrake, Chris Howard et al.•AIDS Care•2022

  • Shame among people living with HIV

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    Kimberlé Crenshaw, Kimberlé W Crenshaw•Stanford Law Review•1991

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    Open Access•Donald R Thomas, David R Thomas•American Journal of Evaluation•2006

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    Open Access•Kate Gibson, Tessa M Pollard et al.•Social Science & Medicine•2021

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    Open Access•Chadwick K Campbell•Social Science & Medicine•2021

  • Conceptualizing Stigma

    Bruce G Link, Lexi Harari et al.•Annual Review of Sociology•2001

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    Open Access•Michael Bury•Sociology of Health & Illness•1982

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    Open Access•Simon J Williams, Simon Williams•Sociology of Health & Illness•2000

Unique citing works4
Citations per year4
Citation span2026 - 2026 (1)
Citation velocitycurrent
Highly citedNo
Citation typesNeutral: 3

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