Literature DB >> 15948875

Parents' perspectives on coping with Duchenne muscular dystrophy.

C L Webb1.   

Abstract

BACKGROUND: The author, who has a grown son with Duchenne Muscular Dystrophy (DMD), has personally experienced a lack of available information for parents about coping with DMD. Therefore, as a longtime personal goal, she developed this study to address that lack of information.
METHODS: Fifteen semi-structured interviews were conducted with 23 parents (n = 7 with both parents; n = 1 with two sisters; n = 6 with mothers only; n = 1 with father only). The purpose of the interviews was to examine the strategies parents use to cope when their sons have DMD. The interviews were conducted in 12 states, taped and transcribed.
RESULTS: Grounded theory analysis of the interview data indicated the willingness of these parents to share information to empower others like themselves.
CONCLUSIONS: Parents want to be heard and valued as experts on DMD by medical and other professionals who interact with their sons. In addition, they want to proactively participate in their sons' lives and to encourage other parents to do the same.

Entities:  

Mesh:

Year:  2005        PMID: 15948875     DOI: 10.1111/j.1365-2214.2005.00518.x

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  7 in total

1.  Psychosocial Needs and Facilitators of Mothers Caring for Children with Duchenne/Becker Muscular Dystrophy.

Authors:  Holly L Peay; Bettina Meiser; Kathleen Kinnett; Aad Tibben
Journal:  J Genet Couns       Date:  2017-08-12       Impact factor: 2.537

2.  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

3.  A Nationwide, Population-Based Prevalence Study of Genetic Muscle Disorders.

Authors:  Alice Theadom; Miriam Rodrigues; Gemma Poke; Gina O'Grady; Donald Love; Graeme Hammond-Tooke; Priya Parmar; Ronelle Baker; Valery Feigin; Kelly Jones; Braden Te Ao; Anna Ranta; Richard Roxburgh
Journal:  Neuroepidemiology       Date:  2019-01-18       Impact factor: 3.282

4.  Participation and quality of life in children with Duchenne muscular dystrophy using the International Classification of Functioning, Disability, and Health.

Authors:  Roxanna M Bendixen; Claudia Senesac; Donovan J Lott; Krista Vandenborne
Journal:  Health Qual Life Outcomes       Date:  2012-05-22       Impact factor: 3.186

5.  Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports.

Authors:  Karen T Nozoe; Ricardo T Akamine; Diego R Mazzotti; Daniel N Polesel; Luís F Grossklauss; Sergio Tufik; Monica L Andersen; Gustavo A Moreira
Journal:  Sleep Sci       Date:  2016-08-18

6.  Prednisone and Deflazacort in Duchenne Muscular Dystrophy: Do They Play a Different Role in Child Behavior and Perceived Quality of Life?

Authors:  Susan Sienko; Cathleen Buckon; Eileen Fowler; Anita Bagley; Loretta Staudt; Mitell Sison-Williamson; Kathy Zebracki; Craig M McDonald; Michael Sussman
Journal:  PLoS Curr       Date:  2016-06-17

7.  Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.

Authors:  Lotte Krabbenborg; L E L M Vissers; J Schieving; T Kleefstra; E J Kamsteeg; J A Veltman; M A Willemsen; S Van der Burg
Journal:  J Genet Couns       Date:  2016-04-20       Impact factor: 2.537

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.