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‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum
Lupus is a multi-system autoimmune rheumatic disease with increased morbidity and mortality. Some manifestations are life-threatening with many aspects of living with the disease, difficulties in diagnosis and accessing appropriate medical care, having an impact on quality of life. The disease itsel...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952333/ https://www.ncbi.nlm.nih.gov/pubmed/33104839 http://dx.doi.org/10.1007/s00296-020-04726-x |
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author | Sloan, Melanie Bosley, Michael Blane, Moira Holloway, Lynn Barrere, Colette D’Cruz, David Walia, Chanpreet Naughton, Felix Howard, Paul Sutton, Stephen Gordon, Caroline |
author_facet | Sloan, Melanie Bosley, Michael Blane, Moira Holloway, Lynn Barrere, Colette D’Cruz, David Walia, Chanpreet Naughton, Felix Howard, Paul Sutton, Stephen Gordon, Caroline |
author_sort | Sloan, Melanie |
collection | PubMed |
description | Lupus is a multi-system autoimmune rheumatic disease with increased morbidity and mortality. Some manifestations are life-threatening with many aspects of living with the disease, difficulties in diagnosis and accessing appropriate medical care, having an impact on quality of life. The disease itself, and these patients’ perspectives, are currently poorly understood and under-researched. The LUPUS UK forum of conversations between over 25,000 members provides a rich environment to explore the views of these patients. Conversations on the LUPUS UK online forum were qualitatively explored using virtual ethnography and thematic analysis. The forum itself and positive medical relationships were widely considered to provide a means of support, understanding and validation. Forum members expressed difficulties in diagnosis, disease management, and the psychological and physical impact of living with an unpredictable, poorly understood disease, often with life-changing symptoms. Invalidating personal, social and medical environments were perceived as exacerbating these difficulties. Delays in diagnosis and misdiagnoses were frequently discussed as causing significant damage, especially when symptoms were disbelieved or dismissed. Invalidation was the key theme with further themes of: Uncertainty, Medical (mis)communications and misunderstandings, Navigating health systems and Resilience and support. Although effective care and support was reported by some members, the negative impact of living with an incurable, life-changing disease was often exacerbated by perceived invalidation, uncertainty, and difficulties in multiple areas of members’ lives. Improved knowledge of the disease and greater support at all stages of the diagnostic journey could improve outcomes and quality of life for these patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00296-020-04726-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7952333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-79523332021-03-28 ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum Sloan, Melanie Bosley, Michael Blane, Moira Holloway, Lynn Barrere, Colette D’Cruz, David Walia, Chanpreet Naughton, Felix Howard, Paul Sutton, Stephen Gordon, Caroline Rheumatol Int Observational Research Lupus is a multi-system autoimmune rheumatic disease with increased morbidity and mortality. Some manifestations are life-threatening with many aspects of living with the disease, difficulties in diagnosis and accessing appropriate medical care, having an impact on quality of life. The disease itself, and these patients’ perspectives, are currently poorly understood and under-researched. The LUPUS UK forum of conversations between over 25,000 members provides a rich environment to explore the views of these patients. Conversations on the LUPUS UK online forum were qualitatively explored using virtual ethnography and thematic analysis. The forum itself and positive medical relationships were widely considered to provide a means of support, understanding and validation. Forum members expressed difficulties in diagnosis, disease management, and the psychological and physical impact of living with an unpredictable, poorly understood disease, often with life-changing symptoms. Invalidating personal, social and medical environments were perceived as exacerbating these difficulties. Delays in diagnosis and misdiagnoses were frequently discussed as causing significant damage, especially when symptoms were disbelieved or dismissed. Invalidation was the key theme with further themes of: Uncertainty, Medical (mis)communications and misunderstandings, Navigating health systems and Resilience and support. Although effective care and support was reported by some members, the negative impact of living with an incurable, life-changing disease was often exacerbated by perceived invalidation, uncertainty, and difficulties in multiple areas of members’ lives. Improved knowledge of the disease and greater support at all stages of the diagnostic journey could improve outcomes and quality of life for these patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00296-020-04726-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-10-26 2021 /pmc/articles/PMC7952333/ /pubmed/33104839 http://dx.doi.org/10.1007/s00296-020-04726-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Observational Research Sloan, Melanie Bosley, Michael Blane, Moira Holloway, Lynn Barrere, Colette D’Cruz, David Walia, Chanpreet Naughton, Felix Howard, Paul Sutton, Stephen Gordon, Caroline ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum |
title | ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum |
title_full | ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum |
title_fullStr | ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum |
title_full_unstemmed | ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum |
title_short | ‘But you don’t look sick’: a qualitative analysis of the LUPUS UK online forum |
title_sort | ‘but you don’t look sick’: a qualitative analysis of the lupus uk online forum |
topic | Observational Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952333/ https://www.ncbi.nlm.nih.gov/pubmed/33104839 http://dx.doi.org/10.1007/s00296-020-04726-x |
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