Filled with mischievously wry wit, this semiautobiographical narrative is an inspiring and hugely enjoyable day-by-day account of a year in the life of a myalgic encephalomyelitis, or chronic fatigue syndrome, sufferer. Privy to the notable events, everyday routine, and innermost thoughts of Verity Red, the skepticism and lack of understanding surrounding this recently recognized condition is addressed, as well as the common symptoms boredom, the feeling of low self-worth, exhaustion, and the craving for comfort foods.
An unusual book about dealing with M.E. What's that? I didn't really know until a friend who has it (it's an illness) suggested I read this book. But this is no dry medical tome.
It's a glimpse into the daily life of someone who has M.E. (aka Chronic Fatigue Syndrome, I've since learnt) but while you come to understand the effects of M.E., you do so through the humour of the author, who manages to get her message across without resorting to emotional blackmail. She made me laugh, which I think was her intention.
It's clear to me that she is a writer who has M.E. rather than someone who has M.E. who decided to write a book about it. It's not a story that asks for pity, it's an uplifting story about someone dealing with the difficulties they face, with grace and humour. It's not a book about M.E., it's a book about a person. First class.
This book gives an insider's view on what it is really like to live with M.E. although it does veer into a slightly strange fantasy world towards the end. I would highly recommend this read for everyone, not just those who have/are interested in M.E/C.F.S as the character of Verity Red just makes you smile by the way she thinks and how she just jumps off the page. I was sorry to finish the book as I wanted to read more - always a good (sort of) feeling.