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Papers

Othering, blame and shame when working with people living with HIV

Pages 62-78 | Received 31 Mar 2015, Accepted 26 Sep 2015, Published online: 19 Nov 2015
 

Abstract

Significant advances in HIV treatment has meant that for the majority of patients with HIV, they are able to live a normal lifespan. However, HIV remains a highly stigmatizing disease with the potential to significantly impact on one’s social identity and sense of self. This paper draws on data from a qualitative study of interviews with five gay men, to explore the experiences of shame in relation to living with HIV. The paper adopts a psychoanalytic lens to highlight the mechanisms of splitting that may be involved at both a social and individual level, and the experience of shame among the participants. The paper aims to use this research data to supplement our understanding of what may be occurring ‘on the couch’ with patients who are living with HIV.

Acknowledgements

I would like to thank the two peer reviewers on an earlier draft of this paper, particularly one reviewer who gave very generous and thoughtful comments and suggestions. Their encouragement helped me rework and shape the earlier draft to its current form.

Disclosure statement

No potential conflict of interest was reported by the author.

Notes

1. Pseudonyms have been used, and some details have been modified to ensure anonymity.

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