This report published by Marie Curie Cancer Care highlights
that the end of life care needs of Black, Asian and Minority
Ethnic communities are varied, growing, and despite examples
of good practice, overall not adequately met.
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This document sets out how local areas can use existing
structures like Health and Wellbeing Boards to bring together
local partners to make further steps towards integration.
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This exercise devised by Dr Paul Russell aims to support GPs
to identify problems in coding, which are contributing to low
rates of dementia diagnosis on practice registers.
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The Dementia Prevalence Calculator presents an opportunity for
all health communities to gain a better understanding of their
local estimated prevalence of dementia in the community, and
among people living in local care homes.
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This report, published Alzheimer’s Society, reveals that
nearly two thirds (62%) of more than 250,000 people with
dementia who live on their own are lonely. This compares to
just 24 per cent of over 55 year olds.
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This resource supports commissioners, clinicians and managers
to commission high-quality evidence-based care for people with
dementia and their carers.
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This quality standard, published by the National Institute for
Health and Care Excellence (NICE), covers the care and support
of people with dementia.
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Building on the Gloucestershire ‘Living Well
Handbook’, this project aims to develop a user-designed
and owned handbook that will serve as a companion to the
dementia journey for people in West Berkshire .
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This report published by the Alzheimer’s Society stresses the
need to lift expectations and to strengthen existing minimum
standards to boost quality of life for people with dementia in
care homes.
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This narrative is based on the statements that patients and
service users could make if the care they experienced was
person centred and coordinated.
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