Abstract

  • Sharing the diagnosis – how do carers feel?

    Most professionals agree that carers should be fully informed of the diagnosis of dementia and its implications, but there is much less agreement on whether sufferers themselves should be told. Hilary Husband reports on a survey to investigate carers’ views and experience. Author/s: Hilary Husband For the full article please see the PDF download linked…...

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  • All things bright and beautiful

    Murals not only brighten up any space but can provide an excellent opportunity to involve people with dementia in creative, co-operative work with a satisfying end product. Two projects are described here, by Deborah Neal, and Christine Ridley and Jane Parker. Author/s: Deborah Neal, Christine Ridley, Jane Parker For the full article please see the…...

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  • Back into the swing of her sociable life

    In sheltered housing there is a danger that tenants with advancing dementia will be excluded from social events by other residents. Tracy Petre describes how discovering the unique personality behind a woman’s “problem behaviour” led to ways of reducing her frustration, which allowed her to join in the fun again. Author/s: Tracy Petre For the…...

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  • Developing flexible, responsive teamwork

    Setting up a new community dementia service brought opportunities and challenges for Bob Barber, Lynne Dormer and Dharmachari Prasadu, who describe how it was planned and evaluated after the first year. Author/s: Bob Barber, Lynne Dormer, Dharmachari Prasadu For the full article please see the PDF download linked to the right. The full JDC archive…...

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  • A gift to research helps carers too

    Penelope Roques and Jill Walton describe their dual role as counsellors and researchers in a programme for brain tissue donation at autopsy. Author/s: Penelope Roques, Jill Walton For the full article please see the PDF download linked to the right. The full JDC archive is available if you subscribe....

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  • Where does dementia fit in?

    Many people with dementia are not covered by the new mental health supervision orders. But do we want such an over-intrusive system anyway? asks Dr Tony Whitehead. Author/s: Dr Tony Whitehead For the full article please see the PDF download linked to the right. The full JDC archive is available if you subscribe....

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  • The deep roots of folklore and superstition

    Esme Moniz-Cook and Alec Gill argue that traditional superstitions – often unknown to young care staff – can sometimes be the root cause of “problem” behaviour in people with dementia. Author/s: Esme Moniz-Cook, Alec Gill For the full article please see the PDF download linked to the right. The full JDC archive is available if…...

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  • How to add insult to carers’ injuries

    Doctors’ reluctance to add “dementia” or “Alzheimer’s disease” to death certificates skews the statistics on incidence and prevalence of the diseases, and is insulting and hurtful to carers, say Geoffrey Bamforth and Bernard Ineichen. Author/s: Geoffrey Bamforth, Bernard Ineichen For the full article please see the PDF download linked to the right. The full JDC…...

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  • A window of insight into quality care

    Dementia care mapping is a valuable tool for evaluating quality of care. But by sharing both mapping and results widely and quickly, the Bath project achieved immediate positive change as well. Elizabeth Barnett explains. Author/s: Elizabeth Barnett For the full article please see the PDF download linked to the right. The full JDC archive is…...

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  • Many a slip ‘twixt dose and lip

    Monitored dosage is a useful time-saving system of drug administration, but it does bring its own limitations and dangers. Sally Kennedy shares some words of warning after using the system for five years. Author/s: Sally Kennedy For the full article please see the PDF download linked to the right. The full JDC archive is available…...

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