Living with Chronic Illness

The Experience of Patients and Their Families

First published in 1988, the book presents a vivid account of the reality of life with chronic illness­–from perspective of patients and their families. It looks at expectations, priorities and problems of those most affected by chronic illness and examines strategies they have developed to cope with their considerable disadvantages.

First published in 1988, Living with Chronic Illness presents a vivid account of the reality of life with chronic illness ­– from the perspective of patients and their families. The authors look at the expectations, priorities, and problems of those most affected by chronic illness, and examine the strategies they have developed to cope with their considerable disadvantages. The experience of carers, the ways in which their problems change over time, are also major themes in the book.

The book looks at the everyday life of people with the following conditions: stroke, renal failure, multiple sclerosis, Parkinson’s disease, arthritis, heart attack, epilepsy, rectal cancer, psoriasis, and diabetes. In each case, an overview of the consequences of a particular illness is presented, before discussion of specific problems in daily life – maintaining family relationships, managing treatment regimes, coping with work and home commitments, and living with bodily change and social stigma.

This volume will be of importance to all those concerned with providing support and planning care for the chronically ill – in the health and social services and in voluntary organizations. Students of medical sociology, policy makers and planners will also find the insights and research presented here valuable in the understanding of the daily life of people with chronic illness. It will also be of use for those in professional training, in nursing, social work, general practice and related areas.

Contributor: Robert Anderson (Edited by), Michael Bury (Edited by)

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