The struggle to belong: a qualitative exploration of challenges in social spaces faced by children with Duchenne muscular dystrophy attending neuromuscular disorders clinic.

Duchenne muscular dystrophy children exploration qualitative study social challenges

Journal

Disability and rehabilitation
ISSN: 1464-5165
Titre abrégé: Disabil Rehabil
Pays: England
ID NLM: 9207179

Informations de publication

Date de publication:
24 Aug 2024
Historique:
medline: 24 8 2024
pubmed: 24 8 2024
entrez: 24 8 2024
Statut: aheadofprint

Résumé

Duchenne muscular dystrophy (DMD), a genetically linked muscle disease, is one of the most devastating diseases with currently no cure. Developing essential social skills as a child moves into adolescence is particularly problematic in DMD. The present study is an exploration of the social challenges faced by children with DMD. A qualitative study was conducted among ten children diagnosed with DMD receiving treatment in a neuromuscular disorder clinic of a tertiary referral care center in Southern India. Participants were recruited purposively and were interviewed face-to-face and through telephone. The recorded interviews were transcribed and analyzed using reflexive thematic analysis. Mean age of the children was 13.9 (range: 13-15) at the time of the interviews, and six children had stopped schooling. The overarching theme generated from the interviews was The study highlighted the struggles of children that become a complex social problem for them. Efforts need to be made to be child-centric and encourage inclusion by improving accessibility and social support through sensitization programs. This is an addition to the existing body of literature from the Indian context and points toward the need for creating awareness about social inclusion in the healthcare professionals, general public and in schools.Strengthening the social support system with referrals to and liaising with other relevant internal and external services and resources, home support services is important.This can prepare the children with Duchenne muscular dystrophy with adequate information about social connections and prepare them emotionally.Mainstreaming of children with the necessary support of various stakeholders in the society will go a long way to ensure quality of life of the children.

Autres résumés

Type: plain-language-summary (eng)
This is an addition to the existing body of literature from the Indian context and points toward the need for creating awareness about social inclusion in the healthcare professionals, general public and in schools.Strengthening the social support system with referrals to and liaising with other relevant internal and external services and resources, home support services is important.This can prepare the children with Duchenne muscular dystrophy with adequate information about social connections and prepare them emotionally.Mainstreaming of children with the necessary support of various stakeholders in the society will go a long way to ensure quality of life of the children.

Identifiants

pubmed: 39180333
doi: 10.1080/09638288.2024.2394642
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-8

Auteurs

Dinesh Kumar (D)

Neuropalliative and Supportive Care Project, NIMHANS, Bangalore, India.

Priya Treesa Thomas (PT)

Department of Psychiatric Social Work, NIMHANS, Bangalore, India.

Gargi S Kumar (GS)

Neuropalliative and Supportive Care Project, NIMHANS, Bangalore, India.

Arun M (A)

Department of Psychiatric Social Work, NIMHANS, Bangalore, India.

Sidhanta Kumar Sahoo (SK)

Department of Psychiatric Social Work, NIMHANS, Bangalore, India.

Arun Sadasivan (A)

Department of Counselling Psychology, Montfort College, Bangalore, India.

Seena Vengalil (S)

Department of Neurology, NIMHANS, Bangalore, India.

Atchayaram Nalini (A)

Department of Neurology, NIMHANS, Bangalore, India.

Classifications MeSH