Jeanne Carlin explores a study on decision making in male carers of people with dementia and reflects on her own experiences in interpreting the findings.
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Sarah Carr looks at a literature review assessing how choice is working for family carers in the context of social care personalisation.
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Jeanne Carlin discusses a review about influences on adult children carers’ well-being and thinks about what the evidence means for Care Act implementation.
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Caroline Struthers is frustrated by the lack of high quality research identified by this recent review, which looks at interventions to improve the experience and well-being of those caring for people with severe mental illness.
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What are the experiences of families who are supporting their adult sons and daughters with learning disabilities to move on to their own homes?
Here, Mandy Johnson looks at a study, which sets out to answer that question.
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Mary Larkin finds out if a US carer support programme is effective for black and minority ethnic carers of people living with Alzhemier’s disease.
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Lack of sleep for parents has been associated with depression, stress and anxiety and sleep problems for parents of children with learning disabilities are common.
Here, Rachel Allen looks at an evaluation of the effectiveness of a sleep management intervention that was delivered through support to groups of parents.
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In this blog, Ermintrude looks at secondary analysis of carer surveys and discusses the findings on hours of unpaid care in the context of obligations under the Care Act.
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Clarissa Giebel analyses an Australian qualitative study into family carer feelings and responses, when their loved one with dementia is admitted to hospital.
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Martin Stevens discusses research on gender inequality and intergenerational patterns of care in Europe and reveals possible potential implications for current social care reform.
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