'There's Nothing Wrong With You; You Just Need to Lose Weight'—A Qualitative Exploration of Pelvic Floor Dysfunction Among Women With Multiple Sclerosis and Their Interaction in Seeking Pelvic Healthcare.

Introduction: Within 10 years of multiple sclerosis (MS) progression, nearly all women will have experienced symptoms associated with bladder, bowel and/or sexual health. Yet despite the impact these symptoms have on physical, psychological and social well‐being, it remains an underserved area withi...

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Published in:Health Expectations Vol. 27; no. 4; pp. 1 - 12
Main Authors: Addington, Christine, Bradshaw, Andy, Hagen, Suzanne, McClurg, Doreen
Format: research tables/charts Journal Article
Published: Wiley-Blackwell Aug2024
Online Access:View this record in EBSCOhost
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      dt: Aug2024
      vid: 27
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        atl: 'There's Nothing Wrong With You; You Just Need to Lose Weight'—A Qualitative Exploration of Pelvic Floor Dysfunction Among Women With Multiple Sclerosis and Their Interaction in Seeking Pelvic Healthcare.
      aug:
        au:
          Addington, Christine
          Bradshaw, Andy
          Hagen, Suzanne
          McClurg, Doreen
        affil: Department of Physiotherapy and Paramedicine, Glasgow Caledonian University, Glasgow, UK
      sug:
        subj:
          Pelvic Floor Disorders Psychosocial Factors
          Women's Health
          Multiple Sclerosis Complications
          Feminism
          Intersectionality
          Professional-Patient Relations
          Human
          Pelvic Floor Disorders Risk Factors
          Qualitative Studies
          Action Research
          United Kingdom
          Thematic Analysis
          Female
          Stigma
          Patient Attitudes Evaluation
          Health Services Needs and Demand
          Interviews
          Snowball Sample
          Purposive Sample
          Data Analysis Software
          Adult
          Middle Age
          Aged
          Adult: 19-44 years
          Middle Aged: 45-64 years
          Aged: 65+ years
          Female
      ab: Introduction: Within 10 years of multiple sclerosis (MS) progression, nearly all women will have experienced symptoms associated with bladder, bowel and/or sexual health. Yet despite the impact these symptoms have on physical, psychological and social well‐being, it remains an underserved area within the UK healthcare system. Study Aim: This research employs a participatory research approach framed within the principles of intersectional feminism to collaboratively investigate the lived experiences of pelvic floor dysfunction (PFD) and healthcare interactions among UK‐based women with MS. Setting and Participants: Women residing in the United Kingdom with MS were invited to participate in online interviews facilitated by the primary author. Analysis: A thematic framework analysis offering a structured yet adaptable approach to data collection and interpretation. Results: One focus group involving four women with MS and seven individual, one‐to‐one interviews with women with MS provided insights into the challenges associated with navigating both MS and PFD. Four main themes included: Navigating MS and PFD; Cycles of Control; Mind, Mobility and Bladder Embodiment; Silenced Voices: The Impact of Taboos/Stigma/Dismissal on Preventing Access and Resistance through Collective Community. Six subthemes were also identified. Taken together, these themes cumulatively reflect PFD as an unmet healthcare need. Conclusion: Our findings underscore negative healthcare experiences, inadequate information provision and unmet needs related to PFD, emphasising the compounding effects of gender and disability biases. Impact: We hope that these insights can lay the groundwork for developing tailored therapeutic interventions and improved PFD healthcare for women with MS. Potential solutions include using existing MS support communities. Public Contributions: Women with MS were actively involved in co‐producing interview scripts for one‐to‐one interviews. The primary author shared study findings at an MS group event, engaging in discussions with over 30 individuals, including people with MS and their loved ones. MS advocates played a pivotal role in contextualising the study within the broader lived experience of MS.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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