Caregivers' perceptions and experience of caring for persons with Down syndrome in Kuwait: a qualitative study.

Aim and Objective: This study aimed to explore how caregivers of persons with Down syndrome (DS) believe caring had an impact on their own lives. A secondary objective was to understand their experience of seeking educational, social, and health care services for the persons with DS. Methods: This q...

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Publicado en:International Journal of Developmental Disabilities Vol. 67; no. 5; pp. 381 - 391
Autores principales: AlShatti, Amna, AlKandari, Dana, AlMutairi, Hessa, AlEbrahim, Dalal, AlMutairi, Abdullah, AlAnsari, Danah, Abduljaleel, Lulwa, AlEnzi, Hassna, AlFoudari, Latifa, AlShaib, Hamad, AlAzmi, Khalid, Ahmed, Jamil
Formato: research tables/charts Journal Article
Publicado: Taylor & Francis Ltd Oct2021
Acceso en línea:Ver este registro en EBSCOhost
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      jtl: International Journal of Developmental Disabilities
      issn: 20473869
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      dt: Oct2021
      vid: 67
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        10.1080/20473869.2021.1910780
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        atl: Caregivers' perceptions and experience of caring for persons with Down syndrome in Kuwait: a qualitative study.
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        au:
          AlShatti, Amna
          AlKandari, Dana
          AlMutairi, Hessa
          AlEbrahim, Dalal
          AlMutairi, Abdullah
          AlAnsari, Danah
          Abduljaleel, Lulwa
          AlEnzi, Hassna
          AlFoudari, Latifa
          AlShaib, Hamad
          AlAzmi, Khalid
          Ahmed, Jamil
        affil: Department of Family and Community Medicine, College of Medicine and Medical Sciences, Arabian Gulf University, Manama, Bahrain
      sug:
        subj:
          Caregiver Attitudes
          Caregivers
          Down Syndrome Rehabilitation
          Patient Care
          Patient Education
          Health Care Delivery
          Caregiver Support
          Caregiver Burden Psychosocial Factors
          Human
          Kuwait
          Qualitative Studies
          Exploratory Research
          Mothers
          Socioeconomic Factors
          Caregiver Burden
          Counseling
          Coping
      ab: Aim and Objective: This study aimed to explore how caregivers of persons with Down syndrome (DS) believe caring had an impact on their own lives. A secondary objective was to understand their experience of seeking educational, social, and health care services for the persons with DS. Methods: This qualitative exploratory study was conducted with 21 caregivers of persons with DS in Kuwait. Results: Caregivers struggled to accept the diagnosis initially that led them to search for answers to many of their concerns about raising a person with DS. For the caregivers, who mostly comprised of mothers, dealing with health conditions that persons with DS suffered from was initially difficult. Caring for these individuals led to heavy impact upon their caregivers' own lives who took extraordinary efforts to cope with the burden. Seeking quality education for the persons with DS and participation in social activities was also challenging, and the caregivers believed that better services, facilities, and benefits for the families of persons with DS may help them better cope with the socioeconomic and psychological burden. Conclusions: Improving the availability of specialized services, the delivery of guidance and counselling, and social integration may help overcome challenges of raising a person with Down Syndrome.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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