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Women’s experiences of living with lipedema
Luleå University of Technology, Department of Health, Learning and Technology, Nursing and Medical Technology.ORCID iD: 0000-0003-0313-6002
Luleå University of Technology, Department of Health, Learning and Technology, Nursing and Medical Technology.ORCID iD: 0000-0002-7388-069x
Luleå University of Technology, Department of Health, Learning and Technology, Nursing and Medical Technology. Department of Caring Sience, Ersta Sköndal Bräcke University College, Sweden.
2022 (English)In: Health Care for Women International, ISSN 0739-9332, E-ISSN 1096-4665, Vol. 43, no 1-3, p. 54-69Article in journal (Refereed) Published
Abstract [en]

Lipedema is a chronic, progressive disease that almost exclusively affects women and often misdiagnosed as obesity or primary lymphedema. Research concerning lipedema is sparse, and there is a lack of studies focusing on women’s experiences of living with the illness. We interviewed fourteen women with lipedema with the aim of describing their experiences of living with lipedema. Our results show that women felt controlled by their body, and were fat-shamed and viewed by others as a person who lacked character. They received unsupportive advice on how to manage from healthcare, and blamed themselves while striving to take responsibility.

Place, publisher, year, edition, pages
Taylor & Francis, 2022. Vol. 43, no 1-3, p. 54-69
National Category
Nursing
Research subject
Nursing
Identifiers
URN: urn:nbn:se:ltu:diva-86454DOI: 10.1080/07399332.2021.1932894ISI: 000672216900001PubMedID: 34252343Scopus ID: 2-s2.0-85110483954OAI: oai:DiVA.org:ltu-86454DiVA, id: diva2:1581834
Note

Validerad;2022;Nivå 2;2022-03-08 (joosat)

Available from: 2021-07-26 Created: 2021-07-26 Last updated: 2022-07-04Bibliographically approved

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Melander, CatharinaJuuso, PäiviOlsson, Malin

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CiteExportLink to record
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