UK survey on experiences of men with non-cancer-related lymphoedema: part one

Author:

Cooper-Stanton Garry1,Gale Nicola2,Sidhu Manbinder3,Allen Kerry4

Affiliation:

1. Doctoral Researcher, Associate Dean UCLan, Clinical Nurse Specialist Lymphoedema, University of Birmingham, Health Services Management Centre (HSMC), 40 Edgbaston Park Road, Birmingham, B15 2RT

2. Head of School of Social Policy, Professor of Health Policy and Sociology, University of Birmingham, School of Social Policy, Muirhead Tower, Edgbaston, Birmingham, B15 2TT

3. Associate Professor, School of Social Policy, HSMC, Park House, Edgbaston, Birmingham, B15 2RT

4. Associate Professor Head of Education, University of Birmingham, School of Social Policy, HSMC, Park House, Edgbaston, Birmingham, B15 2RT

Abstract

This initial article delves into the methodology, methods and theories, while the subsequent article will centre on the discoveries, discussion and conclusion. The study aimed to address the research question: how do men perceive their engagement in the self-management of non-cancer-related lymphoedema? An interpretivist qualitative methodology was employed, utilising an online survey based on the validated lymphoedema quality of life tool (LYMQoL). The data underwent inductive narrative inquiry. The study incorporated theories such as hegemonic masculinity and the health, illness, men and masculinities (HIMM) framework. The findings will be detailed in the second article in this series. This article has delineated the objective, methodologyand methods, employing a qualitative interpretivist approach through narrative inquiry. The study incorporated masculinity theories, including hegemonic masculinity and HIMM. The second article will present the findings and their significance within the broader literature.

Publisher

Mark Allen Group

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