Literature DB >> 25190331

Transitioning to adulthood with a progressive condition: best practice assumptions and individual experiences of young men with Duchenne muscular dystrophy.

Yani Hamdani1, Bhavnita Mistry, Barbara E Gibson.   

Abstract

PURPOSE: Youth with progressive conditions are living longer, and there is increased health care focus on assisting them with "transitioning" to adult services and adult life. The purpose of this investigation was to examine key discourses and normative assumptions underpinning transitions best practices and how they are reflected in the experiences of young men with Duchenne muscular dystrophy (DMD).
METHODS: Using a critical perspective, we qualitatively analyzed influential transitions best practice documents to identify their underpinning discursive assumptions. We compared these to the analysis of qualitative interviews and diary data from a study of 11 young men with DMD.
RESULTS: Transitions best practices are underpinned by discourses of developmental progression. They reproduce notions that associate successful transitions with becoming as independent as possible, approximating normal life trajectories, and planning for future adulthood. The accounts of youth with DMD both reflected and resisted these future-oriented discourses in creative ways that maintained positive personal identities.
CONCLUSIONS: Normal developmental progression towards typical adult roles constitutes the generally accepted aims of transitions practices. Such aims may not be appropriate for all youth with disabilities. We suggest that alternative understandings of the life course and approaches to care need to be considered alongside dominant practices. Implications for Rehabilitation Children and youth with progressive conditions, such as DMD, are living longer and there is increased interest in designing programs that will assist them with "transitioning" to adulthood. Transitions best practices reflect dominant social values and assumptions about what constitutes a successful adulthood, embedded in goals such as independent living, self-management and obtaining work. Rehabilitation professionals should be aware of both positive (e.g. feelings of achievement) and negative (e.g. anxiety about the future) consequences of transitions practices that emphasize normal social developmental trajectories and milestones. Discussions with youth should offer multiple possibilities for living a good life in the present and provide support to address negative feelings and the progressive effects of DMD.

Entities:  

Keywords:  Development; Duchenne muscular dystrophy; life course perspective; transitions; young men

Mesh:

Year:  2014        PMID: 25190331     DOI: 10.3109/09638288.2014.956187

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  11 in total

1.  Achieving Life Milestones in Duchenne/Becker Muscular Dystrophy: A Retrospective Analysis.

Authors:  Andrew Donaldson; Debra Guntrum; Emma Ciafaloni; Jeffrey Statland
Journal:  Neurol Clin Pract       Date:  2021-08

Review 2.  Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Susan D Apkon; Angela Blackwell; Mary K Colvin; Linda Cripe; Adrienne R Herron; Annie Kennedy; Kathi Kinnett; James Naprawa; Garey Noritz; James Poysky; Natalie Street; Christina J Trout; David R Weber; Leanne M Ward
Journal:  Lancet Neurol       Date:  2018-02-02       Impact factor: 44.182

3.  Health Care Transition Experiences of Males with Childhood-onset Duchenne and Becker Muscular Dystrophy: Findings from the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet) Health Care Transitions and Other Life Experiences Survey.

Authors:  Pangaja Paramsothy; Adrienne R Herron; Molly M Lamb; Kathi Kinnett; Jodi Wolff; Michele L Yang; Joyce Oleszek; Shree Pandya; Annie Kennedy; Darryl Cooney; Deborah Fox; Daniel Sheehan
Journal:  PLoS Curr       Date:  2018-08-21

4.  Needs management in families affected by childhood-onset dystrophinopathies.

Authors:  Kristin M Conway; Katy Eichinger; Christina Trout; Paul A Romitti; Katherine D Mathews; Shree K Pandya
Journal:  SAGE Open Med       Date:  2019-03-02

5.  Measuring Duchenne muscular dystrophy impact: development of a proxy-reported measure derived from PROMIS item banks.

Authors:  Carolyn E Schwartz; Roland B Stark; David Cella; Katrina Borowiec; Katherine L Gooch; Ivana F Audhya
Journal:  Orphanet J Rare Dis       Date:  2021-11-22       Impact factor: 4.123

6.  Interplay of disability, caregiver impact, and out-of-pocket expenditures in Duchenne muscular dystrophy: a cohort study.

Authors:  Carolyn E Schwartz; Roland B Stark; Katrina Borowiec; Ivana F Audhya; Katherine L Gooch
Journal:  J Patient Rep Outcomes       Date:  2022-03-10

7.  Siblings' life aspirations in the context of Duchenne muscular dystrophy: a mixed-methods case-control study.

Authors:  Carolyn E Schwartz; Elijah Biletch; Richard B B Stuart; Bruce D Rapkin
Journal:  J Patient Rep Outcomes       Date:  2022-09-10

Review 8.  Current Trends and Challenges in Pediatric Access to Sensorless and Sensor-Based Upper Limb Exoskeletons.

Authors:  Guillaume Gaudet; Maxime Raison; Sofiane Achiche
Journal:  Sensors (Basel)       Date:  2021-05-20       Impact factor: 3.576

Review 9.  Duchenne and Becker muscular dystrophy in adolescents: current perspectives.

Authors:  Jennifer G Andrews; Richard A Wahl
Journal:  Adolesc Health Med Ther       Date:  2018-03-15

10.  Palliative care for young adults with life-limiting conditions: public health recommendations.

Authors:  Karen A Cook; Kim Bergeron
Journal:  BMJ Support Palliat Care       Date:  2020-06-19       Impact factor: 4.633

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