How do we include people’s real experiences of depression, anxiety and psychosis in research? The SUNRISE project explores why subjective experiences remain undervalued, how we might integrate them more fully, and what this means for mental health science. Join the conversation and complete the survey.
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Laura Hemming summarises a recent paper exploring how best to involve patients and the public in doctoral research, its impact and the resources needed.
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Catherine Needham reviews a study by Chapman (2019) which considers older people’s knowledge and understanding of the social care system in Northern Ireland.
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The National Health Service is aiming to provide a patient-centred health service, and this involves all staff and all departments. NHS England has produced four “bite-size guides to patient and public participation”. The guides, in particular the first one, are aimed at clinical commissioning groups, to help them involve the public, especially patients and carers, [read the full story…]
