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   <dc:title>The impact of a peer social support network from the perspective of women with fibromyalgia: A qualitative study</dc:title>
   <dc:creator>Mantas Jiménez, Susana</dc:creator>
   <dc:creator>Reig Garcia, Glòria</dc:creator>
   <dc:creator>Bosch Farré, Cristina</dc:creator>
   <dc:creator>Suñer Soler, Rosa</dc:creator>
   <dc:creator>Juvinyà Canal, Dolors</dc:creator>
   <dc:creator>Pla-Vila, Núria</dc:creator>
   <dc:creator>Noell Boix, Rosa</dc:creator>
   <dc:creator>Boix Roqueta, Esther</dc:creator>
   <dc:creator>Mantas Jiménez, Susana</dc:creator>
   <dc:subject>Fibromiàlgia</dc:subject>
   <dc:subject>Fibromyalgia</dc:subject>
   <dc:subject>Malalties cròniques</dc:subject>
   <dc:subject>Chronic diseases</dc:subject>
   <dcterms:abstract>Background: Fibromyalgia is a chronic and complex disease whose management by patients requires a high level of commitment. Patient empowerment therefore represents an important milestone in chronic disease treatment and control. We explored the impact of a peer social support network from the perspective of women with fibromyalgia. Methods: A generic qualitative design was proposed for the study, for which women who had been diagnosed with fibromyalgia were purposefully selected. Six semi-structured interviews were conducted, and the collected data were thematically analysed. Results: Three key themes emerged regarding the peer social support network: (1) empowerment (facilitating acceptance of the diagnosis and acting as a source of information); (2) effects on well-being and quality of life (attenuated the stigma, improved physical well-being, provided emotional support and was a socialization medium); and (3), valuable aspects (transmitted feelings of being understood and listened to and increased personal feelings of satisfaction). Conclusions: A peer social support network for women with fibromyalgia exerts positive effects on their physical, mental, and social well-being and empowers them to better manage their disease. Healthcare for women with fibromyalgia should include strategies that connect them through peer social support networks</dcterms:abstract>
   <dcterms:issued>2021-12-04</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:type>peer-reviewed</dc:type>
   <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/ijerph182312801</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/1660-4601</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>MDPI (Multidisciplinary Digital Publishing Institute)</dc:publisher>
   <dc:source>International Journal of Environmental Research and Public Health, 2021, vol. 18, núm. 23, p. 12801</dc:source>
   <dc:source>Articles publicats (D-I)</dc:source>
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