Chronic Fatigue Syndrome/ME
240 pages, 5 1/2 x 8 1/2
Paperback
Release Date:01 Apr 2011
ISBN:9781849051415
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Chronic Fatigue Syndrome/ME

Support for Family and Friends

Jessica Kingsley Publishers

People with Chronic Fatigue Syndrome (CFS)/ME experience extreme tiredness and a range of other symptoms, including pain, headaches, impaired concentration and memory, anxiety, sleep problems, and palpitations. The condition can affect all areas of a sufferer's life and, in turn, the lives of those who are close to them.

This book provides the families and friends of people with CFS/ME with an accessible introduction to the condition, and explains what can be done to support those who have it. It offers useful advice on how to help a loved one cope with the illness, and suggests ways to help them with everyday issues such as personal hygiene, nutrition, finances, and relationships. Recognizing that coping with the impact of CFS/ME can be just as difficult for the relatives and friends of those with the condition, it addresses the emotional, social, and practical aspects of having a loved one with CFS/ME, explains how to understand the changes in their relationship with the sufferer, how to manage stress, and where to go for further help and support. The book also includes detailed case studies and practical advice from a wide range of people with mild, moderate, and severe CFS/ME, and their loved ones.

This book offers much-needed information and support to the friends, families, and caregivers of people with CFS/ME.

It will also be a useful resource for health professionals who wish to deepen their understanding of CFS/ME, including home healthcare providers, care staff, counselors, therapists, doctors, and nurses.

People with CFS/ME are very much affected by what ‘other people’ think, say or do. If things don't go well, it is usually because those others don't know or understand, or just don't ‘get it’, perhaps feeling frightened, threatened or useless. Here is a straightforward and practical resource to fill those knowledge gaps, drawn from both personal experiences and professional insights. Professor Tony Pinching, Associate Dean, University of Plymouth, UK
Elizabeth Turp is an integrative counselor working in UK National Health Service primary care and private practice. She became ill with CFS/ME in 2005 and, having recovered some of her health, is now writing to pass on what she learned about the condition.
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