‘You can have a dog put to sleep but my mother had to go through hell.’ End of life issues are especially difficult for people with dementia and their family carers, as the person themself is often unable to make and communicate their views in a way that would be respected by our autonomy-centred healthcare decision-making frameworks. Drawing on empirical data from a socio-legal study funded by the British Academy, Professor Rosie Harding of the University of Birmingham explores the social, ethical and legal challenges of maximising dignity for those dying with, and of, dementia.
