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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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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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…]
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…]
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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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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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…]
