Tag Archives: Pseudo-Autonomous Decision Making

Dying Well With Dementia (Alzheimer’s Society)

[A version of this item features in Dementia: the Latest Evidence Newsletter (Royal Wolverhampton NHS Trust), Volume 3 Issue 4, November 2012]. Summary The Alzheimer’s Society’s “My life until the end: dying well with dementia” report gives an overview of … Continue reading

Posted in Acute Hospitals, Alzheimer's Society, Charitable Bodies, Community Care, End of Life Care, For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), National, Pain, Person-Centred Care, Practical Advice, Quick Insights, Standards, UK, Universal Interest | Tagged , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , | Leave a comment

Multi-Case Study: How Persons with Dementia Participate in Decision Making Relating to Health and Daily Care (BMC Health Services Research)

[A version of this item appears in: Dementia: the Latest Evidence Newsletter (RWHT), Volume 3 Issue 2, September 2012]. Summary People with dementia have the right to participate in decisions about their health and social care. This Norwegian qualitative multi-case … Continue reading

Posted in For Carers (mostly), For Doctors (mostly), For Nurses and Therapists (mostly), For Researchers (mostly), For Social Workers (mostly), International, Management of Condition, Quick Insights, Universal Interest | Tagged , , , , , , , , , , , , , , , , , , , , , | Leave a comment