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A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers

BACKGROUND: Four fifths of the estimated 150 million children with disability in the world live in resource poor settings where the role of the family is crucial in ensuring that these children survive and thrive. Despite their critical role, evidence is lacking on how to provide optimal support to...

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Autores principales: Zuurmond, Maria, Nyante, Gifty, Baltussen, Marjolein, Seeley, Janet, Abanga, Jedidia, Shakespeare, Tom, Collumbien, Martine, Bernays, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379711/
https://www.ncbi.nlm.nih.gov/pubmed/30259548
http://dx.doi.org/10.1111/cch.12618
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author Zuurmond, Maria
Nyante, Gifty
Baltussen, Marjolein
Seeley, Janet
Abanga, Jedidia
Shakespeare, Tom
Collumbien, Martine
Bernays, Sarah
author_facet Zuurmond, Maria
Nyante, Gifty
Baltussen, Marjolein
Seeley, Janet
Abanga, Jedidia
Shakespeare, Tom
Collumbien, Martine
Bernays, Sarah
author_sort Zuurmond, Maria
collection PubMed
description BACKGROUND: Four fifths of the estimated 150 million children with disability in the world live in resource poor settings where the role of the family is crucial in ensuring that these children survive and thrive. Despite their critical role, evidence is lacking on how to provide optimal support to these families. This study explores the impact of a participatory training programme for caregivers delivered through a local support group, with a focus on understanding caregiver wellbeing. METHODS: A qualitative longitudinal study was conducted to investigate the impact of a training programme, “getting to know cerebral palsy,” with caregivers on their wellbeing. Eighteen caregivers, from four districts, were interviewed up to three times over 14 months, to assess impact and the reasons for any changes. RESULTS: Low levels of knowledge, high levels of stigma, physical and emotional exhaustion, and often difficult family relationships with social exclusion of the child and caregiver were common themes at the outset. Caregivers struggled to combine their caring and economic activities. This was exacerbated by the common absence of the father. Two months after completion of the training, their reported wellbeing had improved. The reasons for this were an improved understanding about their child's condition, positive attitudinal change towards their child, feelings of hope, and through the group support, a profound realisation that they are “not on their own.” While relationships within the family remained complex in many cases, the support group offered an important and alternative social support network. CONCLUSIONS: This study illustrates the many benefits of a relatively simple caregiver intervention, which has the potential to offer a mechanism to provide sustainable social support for caregivers and children with cerebral palsy. Any future programme needs to also address more structural issues, including stigma and discrimination, and strengthen approaches to family engagement.
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spelling pubmed-73797112020-07-27 A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers Zuurmond, Maria Nyante, Gifty Baltussen, Marjolein Seeley, Janet Abanga, Jedidia Shakespeare, Tom Collumbien, Martine Bernays, Sarah Child Care Health Dev Research Articles BACKGROUND: Four fifths of the estimated 150 million children with disability in the world live in resource poor settings where the role of the family is crucial in ensuring that these children survive and thrive. Despite their critical role, evidence is lacking on how to provide optimal support to these families. This study explores the impact of a participatory training programme for caregivers delivered through a local support group, with a focus on understanding caregiver wellbeing. METHODS: A qualitative longitudinal study was conducted to investigate the impact of a training programme, “getting to know cerebral palsy,” with caregivers on their wellbeing. Eighteen caregivers, from four districts, were interviewed up to three times over 14 months, to assess impact and the reasons for any changes. RESULTS: Low levels of knowledge, high levels of stigma, physical and emotional exhaustion, and often difficult family relationships with social exclusion of the child and caregiver were common themes at the outset. Caregivers struggled to combine their caring and economic activities. This was exacerbated by the common absence of the father. Two months after completion of the training, their reported wellbeing had improved. The reasons for this were an improved understanding about their child's condition, positive attitudinal change towards their child, feelings of hope, and through the group support, a profound realisation that they are “not on their own.” While relationships within the family remained complex in many cases, the support group offered an important and alternative social support network. CONCLUSIONS: This study illustrates the many benefits of a relatively simple caregiver intervention, which has the potential to offer a mechanism to provide sustainable social support for caregivers and children with cerebral palsy. Any future programme needs to also address more structural issues, including stigma and discrimination, and strengthen approaches to family engagement. John Wiley and Sons Inc. 2018-09-27 2019-01 /pmc/articles/PMC7379711/ /pubmed/30259548 http://dx.doi.org/10.1111/cch.12618 Text en © 2018 The Authors. Child: Care, Health and Development Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zuurmond, Maria
Nyante, Gifty
Baltussen, Marjolein
Seeley, Janet
Abanga, Jedidia
Shakespeare, Tom
Collumbien, Martine
Bernays, Sarah
A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers
title A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers
title_full A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers
title_fullStr A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers
title_full_unstemmed A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers
title_short A support programme for caregivers of children with disabilities in Ghana: Understanding the impact on the wellbeing of caregivers
title_sort support programme for caregivers of children with disabilities in ghana: understanding the impact on the wellbeing of caregivers
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379711/
https://www.ncbi.nlm.nih.gov/pubmed/30259548
http://dx.doi.org/10.1111/cch.12618
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