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Family caregiver identity a literature review

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Lowry, Samantha Exploring the social context of dementia caregiving : emotions and identities. DClinPsych thesis, University of Warwick. Request Changes to record. Family caregivers are significant in the care of people with dementia, whilst the changes that occur as a result of dementia impact on both the person with dementia and family caregivers.
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A caregiver is a paid or unpaid member of a person's social network who helps them with activities of daily living. Since they have no specific professional training, they are often described as informal caregivers. Typical duties of a caregiver might include taking care of someone who has a chronic illness or disease; managing medications or talking to doctors and nurses on someone's behalf; helping to bathe or dress someone who is frail or disabled; or taking care of household chores, meals, or processes both formal and informal documentation related to health for someone who cannot do these things alone. With an aging population in all developed societies, the role of caregiver has been increasingly recognized as an important one, both functionally and economically. Many organizations that provide support for persons with disabilities have developed various forms of support for carers as well.
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Spillover Effects on Caregivers’ and Family Members’ Utility: A Systematic Review of the Literature

Deborah Cristina de Oliveira oliveiradc. Catherine D. Vass catherine. Background: Despite the increasing older population providing care for family members with dementia at home, there is no consensus in the literature in terms of how caring impacts on their quality of life QoL and the association of the family carer's age with QoL outcomes.
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Skip to search form Skip to main content You are currently offline. Some features of the site may not work correctly. DOI: Adams and W. Dudley and M.
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