A roadmap to advance dementia research and care by 2025

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Clarissa Giebel unfolds and reviews a new roadmap to advance dementia research in prevention, diagnosis, intervention and care by 2025.

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One psychosis fits all? What do families and clients say about caregiver interventions?

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Laoise Renwick writes her debut elf blog on a recent systematic review of barriers and facilitators to implementing family support and education in early psychosis intervention programmes.

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NICE guidelines: mental health problems in people with learning disabilities

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Rachel Allan and Tom Crossland present the recent NICE guidance on mental health problems in people with learning disabilities, and comment on how useful these new recommendations are for people with learning disabilities and their care givers.

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Mental health support for children with learning disabilities

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In her debut blog, Christine Burke from the Mental Health Foundation considers what good mental health support should look like for children and young people with learning disabilities.

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Reminiscence groups for people with dementia and their family carers: REMCARE trial

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Elizabeth Collier writes her debut blog on the REMCARE randomised controlled trial of reminiscence groups for people with dementia and their family carers.

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Impact of functional alterations on quality of life in Alzheimer disease

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Clarissa Giebel analyses a qualitative study of how functional alterations impact quality of life in Alzheimer disease.

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Carers’ experiences of involvement in care planning

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Mike Clark summarised a recent qualitative study of carer involvement in care planning, and reflects on what has changed for mental health carers in the last 20 years.

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Challenging behaviours in adults with intellectual disabilities linked to injury in their carers?

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Genevieve Young Southward takes a look at a recent study on the incidence, types and causes of injury in family and paid carers of adults with intellectual disabilities in Scotland.

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Decision making among male carers of people with dementia

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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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