The Care Act Information Duty in a digital age: What do we need to consider for improving both the information and our practice?

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Background Since the implementation of the Care Act 2014, information has been a statutory duty of Local Authorities. Under the Care Act section 4 of the Care Act, Local Authorities (LAs) have particular responsibilities around providing information to carers and care and support recipients, however how that information is, or should be, provided, as well [read the full story…]

The caring dyad: how patients and their informal carers experience severe mental illness and cardiometabolic disease

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Lydia Poole considers the caring dyad (the relationship experience of the patient and their informal carer) and the realities of living with cardiometabolic risk, metabolic syndrome and severe mental illness.

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Trauma-informed care in mental health: why we need it and what it should look like

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Aneta Zarska blogs about a qualitative research study from Australia that outlines what trauma-informed care should look like, by asking people with experience of mental health difficulties.

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Enhancing primary care support for informal carers

An informal carer refers to someone who, “provides unpaid help and support to a partner, child, relative, friend or neighbour who could not manage without this help” (Beesley, 2006). Comparatively, people who choose to be carers have a higher quality of life than those who provide care as it is expected of them. Though health [read the full story…]

Managing demand for social care among adults with intellectual disabilities

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It is clear that adult social care in the United Kingdom (UK), as in many other countries, faces serious challenges, most simply summarised as rising demand from demographic changes and greater pressure on available resources. The interventions to address this will need to be at all levels (national policy and legislation, managing local systems and in individual [read the full story…]

Voices of people living with dementia and their carers on the closure of support services during COVID-19

Voices of people with dementia and their carers on the closure of support services during COVID-19

Caroline Green discusses a qualitative study which considers the effects of COVID-19 on social support services for people with dementia.

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Carers’ experiences of involuntary admission under mental health legislation

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Juliana Onwumere summarises a recent qualitative review that explores carers’ experiences of involuntary admission of family members or loved ones to mental health inpatient units.

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Effective support from health and social services could improve carer well-being, study suggests

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This paper is particularly pertinent to commissioners of both health and social care, as it addresses the needs of informal carers of people suffering from long-term neurological conditions (LTNCs), such as Parkinson’s disease (PD), Motor Neuron Disease (MND), and Multiple Sclerosis (MS). Implications of long-term neurological conditions LTNCs get progressively worse, with sufferers becoming more and [read the full story…]