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Muscular Dystrophy
Third Edition
Alan E.H. Emery
160 pages
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12 Black and white photos and 13 line drawings
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196x129mm
978-0-19-954216-1
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Paperback
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06 March 2008
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- An informative and compassionate guide for sufferers and their families
- Addresses both the physical and psychological challenges faced by sufferers of muscular dystrophy (MD)
- Provides new advice on genetic counselling for families at risk
- Accesibly written, with no medical jargon
- A truly authoritative book, written by someone with over 40 years' experience of treating patients with MD
The muscular dystrophies are a group of genetic diseases that severely affect children and adults. For sufferers and their family, the illness presents enormous physical and psychological challenges. Written specifically for people with muscular dystrophy and their families, this book answers many of the questions asked about how and why muscular dystrophy occurs, and how it will affect the life of a recently diagnosed child.
As well as presenting the reader with advice and an explanation of muscular dystrophy, the book also guides the reader towards further information on societies and
support groups around the world, and reliable internet resources. It also contains a full glossary to aid the reader in their understanding of the disease.
The different types of muscular dystrophy are described throughout with a minimum of technical jargon. Questions relating to exercise, physiotherapy, surgery, and the emotional effects of the diseases are answered, and advice is given on the problems of schooling and choice of career.
Since publication of the first edition in 1994, the genes for almost all the different types of dystrophy have been identified, enabling prevention through genetic counselling, therefore relieving some of the worry for affected families. Drawn from his many years of experience treating patients, Professor
Emery provides authoritative, yet compassionate advice for people living with this illness.Readership: Written specifically for people with muscular dystrophy and their families.
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Alan E.H. Emery, Honorary Fellow, Green College, University of Oxford, UK
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Review(s) from previous edition
"For the 2nd Edition: "No family (with a member who has any form of muscular dystrophy (MD)) should be without a copy of Alan Emery's book nor should any PCT or medical training unit fail to have easy access to the copy... Apart from the easy 'accessibility' of [the book], the chapter layout makes it eminently usable as a reference, a really useful handbook for anyone with an interest in MD". - Stephen Gazzard, Muscular Dystrophy Campaign, Oxford (Published in 'Neuromuscular Disorders', 14 (2004) 83-84
"For the 2nd Edition: "This book, like the first edition, will be valuable to patients, families, counsellors, clinicians and researchers... Alan Emery is one of the father figures of muscular dystrophy research."" - 'The Quokka', Magazine for the Muscular Dystrophy Association of Australia, October 2000
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1: What is muscular dystrophy?
2: Confirming the diagnosis
3: Different types of muscular dystrophy
4: Treatment
5: Living with muscular dystrophy
6: Education and employment
7: Inheritance and genetic counselling
8: Professional and voluntary support
9: The future
10: Further reading and useful contacts
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Martin Butler
Conductor's score and parts on hire
Available on Hire
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£42.00
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These are the AS and A2 components for the OCR specifications
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The specification in this catalogue, including without limitation price, format, extent, number of illustrations, and month of publication, was as accurate as possible at the time the catalogue was compiled. Occasionally, due to the nature of some contractual restrictions, we are unable to ship a specific product to a particular territory. Jacket images are provisional and liable to change before publication.
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