Literature DB >> 19474233

The lived experience of hope among parents of a child with Duchenne muscular dystrophy: perceiving the human being beyond the illness.

André Samson1, E Tomiak, J Dimillo, R Lavigne, S Miles, M Choquette, P Chakraborty, P Jacob.   

Abstract

OBJECTIVES: Duchenne muscular dystrophy (DMD) is genetically determined, progressive and incurable. Our study's primary objective was to describe the lived experience of hope among parents of a child with DMD.
METHODS: Semi-structured interviews were conducted with 12 parents having a child with DMD. A qualitative/ phenomenological approach was utilized to analyse the essential aspects of this experience.
RESULTS: We show that the experience of parental hope emerges from the cognitive appraisal of DMD. The child's illness can be perceived in three ways: as a severe loss, a call to adapt or a way to rediscover the child. Each of these appraisals leads to different ways of hoping. Parents can hope for a cure, the child's well-being or to see their child becoming a whole person. Hope can help parents absorb the initial crisis, sustain their adaptation or prepare for the fatal outcome. DISCUSSION: Previous research has demonstrated that cognitive appraisal plays a central role in psychosocial adaptation to illness. Our research indicates that perception can also shape the nature of hope and suggests that health professionals should pay particular attention to the nature of parental hope. The fabric of parental hope can give an indication of how parents are coping and adjusting.

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Year:  2009        PMID: 19474233     DOI: 10.1177/1742395309104343

Source DB:  PubMed          Journal:  Chronic Illn        ISSN: 1742-3953


  12 in total

1.  Uncertainty, hope, and coping efficacy among mothers of children with Duchenne/Becker muscular dystrophy.

Authors:  Megan Bell; Barbara B Biesecker; Joann Bodurtha; Holly L Peay
Journal:  Clin Genet       Date:  2019-04-03       Impact factor: 4.438

Review 2.  Therapeutic misconception: hope, trust and misconception in paediatric research.

Authors:  Simon Woods; Lynn E Hagger; Pauline McCormack
Journal:  Health Care Anal       Date:  2014-03

3.  Mothers' psychological adaptation to Duchenne/Becker muscular dystrophy.

Authors:  Holly L Peay; Bettina Meiser; Kathleen Kinnett; Pat Furlong; Kathryn Porter; Aad Tibben
Journal:  Eur J Hum Genet       Date:  2015-08-26       Impact factor: 4.246

4.  Communication regarding breathing support options for youth with Duchenne muscular dystrophy.

Authors:  Eric Ferguson; Marilyn Wright; Teresa Carter; Cindy Van Halderen; Renata Vaughan; Margaret Otter
Journal:  Paediatr Child Health       Date:  2011-08       Impact factor: 2.253

5.  "Suddenly we have hope that there is a future": two families' narratives when a child with spinal muscular atrophy receives a new drug.

Authors:  Elin Hjorth; Malin Lövgren; Ulrika Kreicbergs; Thomas Sejersen; Eric Asaba
Journal:  Int J Qual Stud Health Well-being       Date:  2021-12

6.  "I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophy.

Authors:  Lorenza Magliano; Melania Patalano; Alessandra Sagliocchi; Marianna Scutifero; Antonella Zaccaro; Maria Grazia D'Angelo; Federica Civati; Erika Brighina; Giuseppe Vita; Gian Luca Vita; Sonia Messina; Maria Sframeli; Marika Pane; Maria Elena Lombardo; Roberta Scalise; Adele D'Amico; Giulia Colia; Michela Catteruccia; Umberto Balottin; Angela Berardinelli; Maria Chiara Motta; Corrado Angelini; Alessandra Gaiani; Claudio Semplicini; Luca Bello; Roberta Battini; Guja Astrea; Giulia Ricci; Luisa Politano
Journal:  J Neurol       Date:  2013-11-08       Impact factor: 4.849

7.  Quantifying the burden of caregiving in Duchenne muscular dystrophy.

Authors:  Erik Landfeldt; Peter Lindgren; Christopher F Bell; Michela Guglieri; Volker Straub; Hanns Lochmüller; Katharine Bushby
Journal:  J Neurol       Date:  2016-03-10       Impact factor: 4.849

8.  Family context in muscular dystrophies: psychosocial aspects and social integration.

Authors:  Lorenza Magliano; Luisa Politano
Journal:  Acta Myol       Date:  2016-10

Review 9.  Current and emerging treatment strategies for Duchenne muscular dystrophy.

Authors:  Jean K Mah
Journal:  Neuropsychiatr Dis Treat       Date:  2016-07-22       Impact factor: 2.570

Review 10.  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
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