Experience of women with multiple sclerosis about their sexuality

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Campo DCValorIdioma
dc.contributorPerson-centred Care and Health Outcomes Innovation / Atención centrada en la persona e innovación en resultados de salud (PCC-HOI)es_ES
dc.contributorCalidad de Vida, Bienestar Psicológico y Saludes_ES
dc.contributorSalud y Cuidados en Grupos Vulnerables (SACU)es_ES
dc.contributor.authorEsteve-Ríos, Antonio-
dc.contributor.authorGarcia-Sanjuan, Sofia-
dc.contributor.authorEscribano, Silvia-
dc.contributor.authorMonasor Ortolá, David-
dc.contributor.authorCabañero-Martínez, María José-
dc.contributor.otherUniversidad de Alicante. Departamento de Enfermeríaes_ES
dc.date.accessioned2021-09-07T16:35:26Z-
dc.date.available2021-09-07T16:35:26Z-
dc.date.issued2021-08-05-
dc.identifier.citationDisability and Rehabilitation. 2022, 44(18): 5117-5123. https://doi.org/10.1080/09638288.2021.1925750es_ES
dc.identifier.issn0963-8288 (Print)-
dc.identifier.issn1464-5165 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/117635-
dc.description.abstractPurpose: To understand how women with multiple sclerosis (MS) experience their sexuality. Material and methods: This was a qualitative study in which eight women belonging to MS associations in Elche or Alicante (Spain) completed semi-structured interviews. We subsequently carried out a thematic analysis of this data. Results: Four main themes and multiple sub-themes were identified. The first theme was the ‘influence of stereotypes on sexual expression’, which included social and gender perspectives; the second theme was ‘physical and emotional causes of sexual dysfunction’, which were classified as primary, secondary, and tertiary; the third theme was ‘experiencing sexuality in a personalised way’, which included relationships with a partner, the concept of sexuality, and resources for improving sexual function; and the final theme was ‘external support’, which included sexual assistance, professional care, and peer support. Conclusions: Sexual needs change in women with MS after diagnosis of the disease. However, this is not addressed routinely by health professionals. In their search for resources, women with MS highlighted that support from partners and from associations, could constitute a support network for the expression of their sexuality.es_ES
dc.languageenges_ES
dc.publisherTaylor & Francises_ES
dc.rights© 2021 Informa UK Limited, trading as Taylor & Francis Groupes_ES
dc.subjectMultiple sclerosises_ES
dc.subjectWomenes_ES
dc.subjectSexualityes_ES
dc.subjectFunctional diversityes_ES
dc.subjectProfessional healthcarees_ES
dc.subject.otherEnfermeríaes_ES
dc.titleExperience of women with multiple sclerosis about their sexualityes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1080/09638288.2021.1925750-
dc.relation.publisherversionhttps://doi.org/10.1080/09638288.2021.1925750es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccesses_ES
Aparece en las colecciones:INV - CV, BP Y S - Artículos de Revistas
INV - SACU - Artículos de Revistas
INV - PCC-HOI - Artículos de Revistas

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