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dc.contributor.authorTabassum, Kinza
dc.contributor.authorFox, Jackie
dc.contributor.authorFuller, Sara
dc.contributor.authorHynes, Sinéad M.
dc.date.accessioned2021-06-03T13:29:59Z
dc.date.available2021-06-03T13:29:59Z
dc.date.issued2021-05-26
dc.identifier.citationTabassum, Kinza, Fox, Jackie, Fuller, Sara, & Hynes, Sinéad M. (2021). Dating with a Diagnosis: The Lived Experience of People with Multiple Sclerosis. Sexuality and Disability. doi:10.1007/s11195-021-09698-9en_IE
dc.identifier.issn1573-6717
dc.identifier.urihttp://hdl.handle.net/10379/16797
dc.description.abstractMultiple Sclerosis (MS) is a neurological condition which usually manifests between the ages of 20 40 years. This is a critical period for developing relationships, particularly romantic relationships. People with MS can experience sexual dysfunction, limb weakness, fatigue, pain, reduced mood and bladder/bowel dysfunction; potentially affecting their ability to participate in many meaningful activities, including those associated with romantic relationships, dating or engaging in sexual intercourse. Dating or starting romantic relationships can be difficult for people with physical disabilities as they can experience stigma, negative societal attitudes and the fear of requiring care from potential partners. Dating experiences of people with progressive conditions like MS have not been explored in detail. The aim of this study was to develop a rich understanding of how living with MS interacts with/influences dating and developing romantic relationships. The study used a descriptive phenomenological design and a purposive sampling strategy. Colaizzi s descriptive phenomenological method was used to analyze the data (Colaizzi, 1978). Five females and two males, aged 23 51, participated in two online focus groups. Dating with a diagnosis of MS is a highly personal phenomenon, characterized by individual differences in values and experiences. Core to the phenomenon was personal decision-making about disclosure of the diagnosis and ongoing adaptation to the fluctuating nature of the condition with partners in new/developing relationships. The findings will help health professionals working with adults with MS understand this important aspect of their lives.en_IE
dc.description.sponsorshipOpen Access funding provided by the IReL Consortium. This research is supported by Health Research Board Summer Student Scholarship 2020 (Ref: 2020SS-2020–060).en_IE
dc.formatapplication/pdfen_IE
dc.language.isoenen_IE
dc.publisherSpringeren_IE
dc.relation.ispartofSexuality and Disabilityen
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectMultiple sclerosisen_IE
dc.subjectDatingen_IE
dc.subjectRomantic relationshipsen_IE
dc.subjectDiagnosisen_IE
dc.subjectIrelanden_IE
dc.titleDating with a diagnosis: The lived experience of people with multiple sclerosisen_IE
dc.date.updated2021-06-01T15:57:50Z
dc.identifier.doi10.1007/s11195-021-09698-9
dc.local.publishedsourcehttps://doi.org/10.1007/s11195-021-09698-9en_IE
dc.description.peer-reviewedpeer-reviewed
dc.contributor.funderHealth Research Board Summer Student Scholarship
dc.contributor.funderHealth Research Board
dc.internal.rssid26067413
dc.local.contactSinéad Hynes. Email: sinead.hynes@nuigalway.ie
dc.local.copyrightcheckedYes
dc.local.versionPUBLISHED
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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland