“You Take This Day by Day, Come What May”: A Qualitative Study of the Psychosocial Impacts of Living with Duchenne Muscular Dystrophy
Open Access
- 6 May 2024
- journal article
- research article
- Published by Springer Nature in Advances in Therapy
- Vol. 41 (6) , 2460-2476
Abstract
Introduction Studies have reported health-related quality-of-life impacts of Duchenne muscular dystrophy (DMD); however, further research is needed to understand how those with DMD experience their condition and how psychosocial impacts evolve over time in response to disease progression. This qualitative study explores the social and emotional implications of key transitions, challenges and adaptations throughout the disease course from the perspective of patients and family caregivers. Methods Semi-structured interviews were conducted with men and boys with DMD, and/or their caregivers, in the USA. Thematic analysis was used to examine patterns in data collected across the interviews. Results Nineteen participants were included. Three major themes were identified: (1) barriers to participation are multifaceted; (2) an emotional journey shaped by ‘inevitable progression;' (3) family provides critical tangible and emotional support. This study illustrates that psychosocial impacts of DMD are shaped by knowledge of the condition’s natural history alongside other factors including the extent of social barriers, personal growth and adaptation, and family support. Conclusions Findings provide insight into the strength and resilience with which individuals and their families respond to daily challenges and major clinical milestones and highlight the relative importance of loss of upper limb function as a transition in DMD affecting health-related quality-of-life.Keywords
Funding Information
- Sarepta Therapeutics
This publication has 53 references indexed in Scilit:
- PCR176 Time Trade-Off Utility Values for Health States Characterizing Progressive Muscular Degeneration in Duchenne Muscular Dystrophy (DMD)Value in Health, 2022
- PCR105 The Impact of Key Health State Transitions on Health-Related Quality of Life (HRQOL) in Duchenne Muscular Dystrophy (DMD): A Qualitative StudyValue in Health, 2022
- Feasibility and Efficacy of Online Strategies to Recruit Parents of Children With Rheumatic Diseases for ResearchACR Open Rheumatology, 2022
- A worked example of Braun and Clarke’s approach to reflexive thematic analysisQuality & Quantity, 2021
- Characterizing health state utilities associated with Duchenne muscular dystrophy: a systematic reviewQuality of Life Research, 2019
- Reconstructing normality following the diagnosis of a childhood chronic disease: does “rare” make a difference?European Journal of Pediatrics, 2018
- Enablers and barriers of men with Duchenne muscular dystrophy transitioning from an adult clinic within a pediatric hospitalDisability and Health Journal, 2017
- Men with Duchenne muscular dystrophy and end of life planningNeuromuscular Disorders, 2017
- The level of agreement between child self-reports and parent proxy-reports of health-related quality of life in boys with Duchenne muscular dystrophyQuality of Life Research, 2014
- Neuropsychological and neurobehavioral functioning in Duchenne muscular dystrophy: A reviewNeuroscience & Biobehavioral Reviews, 2013