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Chronic Fatigue Syndrome: What You Need To Know About Cfs/Me: What You Need To Know About CFS/ME Paperback – 17 July 2014
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- Print length120 pages
- LanguageEnglish
- PublisherSheldon Press
- Publication date17 July 2014
- Dimensions13.79 x 0.71 x 21.59 cm
- ISBN-101847093000
- ISBN-13978-1847093004
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Product details
- Publisher : Sheldon Press (17 July 2014)
- Language : English
- Paperback : 120 pages
- ISBN-10 : 1847093000
- ISBN-13 : 978-1847093004
- Dimensions : 13.79 x 0.71 x 21.59 cm
- Best Sellers Rank: 581,695 in Books (See Top 100 in Books)
- 1,579 in Diseases & Disorders Medicine
- 3,719 in Popular Medicine
- 3,750 in Psychiatry
- Customer reviews:
About the author

Dr Meg Arroll (PhD, CPsychol, CSci, AFBPsS, FHEA, MISCPAccred) is a chartered psychologist, scientist and author specialising in health and wellbeing. Dr Meg’s solution-focused approach gives practical tips and strategies for life’s tricky problems, that are both complex and everyday. Dr Meg has written six books on topics ranging from invisible illness to emotional eating and is a regular contributor to national newspapers and magazines such as The Daily Mail, Metro, Psychologies and Women’s Own, Top Sante and Stylist. She also features regularly on various radio programmes including BBC World News, the Kaye Adams Programme on BBC Radio Scotland, Today Extra, UK Health Radio and is a featured guest on various podcasts such as Dr Max's Mind Clinic podcast. Dr Meg translates complex scientific theories and research for the public, always with practical advice for what readers can do to improve their mental and physical health right now. This is psychology-made-simple. Dr Meg splits her time between the UK and the USA, offering flexible online, traditional face-to-face and ecopsychology walk-and-talk sessions in some of the world’s most beautiful parks and grounds. Follow @drmegarroll
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As a Medical Dr myself, I wish I had read it 4 years ago when I was diagnosed with this complex syndrome, with its multiple causes and often-times long road to recovery.
What you will read here can be trusted, as it is written by somebody who not only has personal experience of this illness, but has also researched the field to PhD level herself.
The author covers both mainstream and CAM approaches, looking at the available research on both. If this sounds a little daunting, be reassured that the friendly, personal style of this book is like having a trusted friend guide you through the maze of information (and mis-information) available in this field.
Without being prescriptive, the chapters are logically set out allowing you to hone in on what you feel is relevant to you. There are helpful cross-references between chapters, and useful anecdotes of other people's experiences as they navigate their recovery.
I recommend buying this book to anyone who wants to read something clear, concise and well-researched, aimed at helping you further understand and recover from this devastating illness.
This book is essential reading for anyone with CFS/ME or their carers, family members or partners or anyone working with people experiencing CFS/ME.
If, as a sufferer, you ever feel the need to persuade a doubting family member or friend that this is a real illness, with a biological and physiological core, then I suggest you hand them a copy of this book.
This book offers an excellent general overview of important patient-centric aspects relating to the condition, delivered in a concise, accessible, pragmatic and upbeat style and including a wealth of grounded, agenda-free advice







