Bere Miesen – författare

Dementia in Close-Up is a clear and practical guide to dementia and the world of the dementia sufferer.Bere Miesen assumes no medical or specialist knowledge and uses first hand accounts and real-life examples to examiners on patterns of behaviour and responses of sufferers and their carers. He focuses on the complex and varied relationships between the sufferer, their family and professional carers, and explores the conflict that can sometimes be engendered by dependency, fear and sustained closeness.Going beyond the purely medical descriptions of dementia, Dementia in Close-Up strives to give families and health professionals the means to form caring and rewarding relationships and to help everyone involved.

Care-giving in dementia is a new speciality with its own rapidly growing body of knowledge. This second volume of contributions from leading practitioners and researchers around the world is a handbook for all those involved in hands on caring, or in planning care, for persons with dementia. Volume 2 of Care-Giving in Dementia provides a rich source of information on most recent thinking about individualised long-term care of both dementia sufferers and their families. Key themes in Volume 2 are: the subjective experience of dementia the provision of care for family carers differing cultural perspectives of dementia the crucial importance of life-history information for understanding a person's reaction to their illness. Chapters on the search for an ethical framework and the best environment within which to provide care are particularly timely.

Care-giving in dementia is a new speciality with its own rapidly growing body of knowledge. This second volume of contributions from leading practitioners and researchers around the world is a handbook for all those involved in hands on caring, or in planning care, for persons with dementia. Volume 2 of Care-Giving in Dementia provides a rich source of information on most recent thinking about individualised long-term care of both dementia sufferers and their families. Key themes in Volume 2 are: the subjective experience of dementia the provision of care for family carers differing cultural perspectives of dementia the crucial importance of life-history information for understanding a person's reaction to their illness. Chapters on the search for an ethical framework and the best environment within which to provide care are particularly timely.