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Spastic Quadriplegia–Bilateral Cerebral Palsy
Understanding and managing the condition across the lifespan: A practical guide for families
Ways to buy
Paperback edition (complete book)
£45.00
Buy ebook edition (Amazon)
Buy ebook edition (Apple Books)
Spastic Quadriplegia breaks down the medical complexity of the condition into a clear, lifelong roadmap, combining world-class clinical expertise with lived experiences to empower all those involved from diagnosis to adulthood.
Whether you are an individual navigating your own care, a parent or family member supporting a loved one, or a healthcare professional looking for a broader perspective, this practical guide offers the expert-backed clarity needed to manage spina bifida with confidence.
“A comprehensive guide for families, health care professionals, and individuals living with this condition.”
—HANK CHAMBERS, MD, PARENT
“Easy to read and understand … knowledge accessible to all.”
—CAROL SHRADER, PARENT
“This book is more than informative; it’s transformative.”
—RACHEL BYRNE, BPT, BS
“A compelling must-read.”
—IONA NOVAK, AM
Key features:
- Clinical excellence: Delivers detailed medical insights and best-practice evidence-based treatment options.
- Holistic perspective: Explores how spina bifida impacts development, participation, and overall quality of life.
- Lifelong focus: Provides tailored guidance that evolves alongside the needs of children, adolescents, and adults.
- Empowered outcomes: Equips families with the tools and confidence to partner effectively with healthcare teams for optimal long-term health.
The Gillette Children’s Healthcare Series distills medical complexity into clear, actionable roadmaps for childhood-acquired physical and neurological conditions. By bridging the gap between clinical research and daily reality, this definitive collection provides a vital guide for those living with a lifelong condition.
Whether you are an individual navigating your own health journey, a parent or family member supporting a loved one, or a healthcare professional seeking a broader multidisciplinary perspective, this series provides the expert-backed clarity needed to manage the condition with confidence.
Co-published by Mac Keith Press and Gillette Children’s Healthcare Press, the series is built on a foundation of collaborative expertise. Every book combines evidence-based, best-practice treatments led by medical specialists with the invaluable lived experiences of individuals and families.
You can now purchase the complete Gillette Children’s Healthcare Series bundle at a 30% discount via this link.
Other titles in the series include:
- Craniosynostosis
- Idiopathic Scoliosis
- Spastic Hemiplegia–Unilateral Cerebral Palsy
- Spastic Diplegia–Bilateral Cerebral Palsy, second edition
- Epilepsy
- Spina Bifida
- Osteogenesis Imperfecta
- Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Causes
Authors and Editors
Series Foreword
Series Introduction
- Cerebral palsy
- Introduction
1.2. The nervous system
1.3. Causes, risk factors, and prevalence
1.4. Diagnosis
1.5. Function
1.6. Classification based on predominant motor type and topography
1.7. Classification based on functional ability
1.8. The International Classification of Functioning, Disability and Health
Key points Chapter 1
- Spastic Quadriplegia
2.1. Introduction
2.2. What does best practice look like?
2.3. Overall management philosophy
2.4. The brain injury
2.5. Musculoskeletal system
Key points Chapter 2
- General health
3.1. Introduction
3.2. Respiratory system
3.3. Feeding, swallowing, and nutrition
3.4. Digestive system
3.5. Urinary system
3.6. Epilepsy
3.7. Sleep
3.8. Pain
3.9. Sensory system
Key points Chapter 3
- Developmental progress and maximizing function
4.1. Introduction
4.2. Therapies
With Susan Ellerbusch Toavs, Candice Johnson and Amy Schulz
4.3. The home program
With Candice Johnson, Amy Schulz and Annabelle Vaage
4.4. Assistive technology
With Susan Ellerbusch Toavs, Candice Johnson, Kaitlin Lewis, Kathryn Pimentel and Amy Schulz
Key points Chapter 4
- Managing musculoskeletal health – Orthopedic care
5.1. Introduction
5.2. Tone reduction
5.3. Musculoskeletal surveillance
With Tom F. Novacheck, Ann Van Heest
5.4. Orthopedic surgery
With Tom F. Novacheck, Ann Van Heest
Key points Chapter 5
- Increasing participation
6.1. Introduction
6.2. Cognition and intelligence
With Richard DiPrima and Susan Ellerbusch Toavs
6.3. Mental and behavioral health
6.4. Puberty
With Candice Johnson
6.5. Community integration
Key points Chapter 6
- Alternative and complementary treatments
- Transition to adulthood
With Tori Bahr
- Adulthood
- Introduction
- Aging in the typical population
- Aging with spastic quadriplegia
- Management and treatment of spastic quadriplegia in adulthood
With Jill Gettings
Key points Chapter 9
- Living with spastic quadriplegia
- Further reading and research
With Elizabeth R. Boyer
Acknowledgments
Appendices (online)
Appendix 1. Measurement tools
Appendix 2. Bones, joints, muscles, and movements
Appendix 3. Epilepsy management
Appendix 4. Scoliosis management
Glossary
References
Index
To grow up with cerebral palsy (CP) is to grow up in a different world, the dimensions of which only you truly know. No two brain injuries have identical effects. Each of us has an injury with unique effects.
I'm a little emotional as I write this review because this book is what I needed as an adolescent. My childhood was stolen from me by teachers who were too blinded by their stereotypes of disability to include me in their classes, so I found redemption in sport. But in the early 2000s the world was very different and we were just ‘spastics’ to be pitied, without much explanation of why this was.
Long live the science that helps us understand ourselves and the phenomena that govern us.
Spastic Quadriplegia–Bilateral Cerebral Palsy is a guide that starts from the essential explanation of the International Classification of Functioning, Disability and Health: the most important thing that my CP has taught me is that there are no ‘incapable’ people in an absolute sense; there are people who are capable of doing some things in a different way. This is an important principle, first of all for parents and all family members, for those who take care of the individual with CP, but also for children and young people who are trying to understand the ‘why’ of life. And these are important principles to live by and questions to answer.
Throughout the 11 chapters, we delve into the lives of individuals with CP, not only through a guide to what CP is and how it affects daily life, but to physiotherapy and assistive technologies, and treatments for children.
I really appreciated the authors' focus on the complexity of CP and the nuances of the lesions, starting from the common motor problems, to analyse every detail and examine the associated problems. This is very useful in understanding that it is not a question of if there are collateral problems, but what they are. Returning to my particular case, for example, until the age of 22, I was convinced that my spastic diplegia only affected the movement of my four limbs. Instead, my field of vision is narrower and presbyopia (the inability to focus on nearby objects) has set in much earlier than average.
These studies are essential to dismantle some of the social prejudices that individuals with CP have to live with and that can be disturbing; for example, for parents who have to face an unusual diagnosis. Parents of children with CP often focus on the immediate and daily problems that will take up most of their time. But advancing age raises specific issues, from puberty to early adulthood to maturity, which this book addresses wisely.
To conclude, the testimonies at the end of the book are enlightening in terms of understanding the challenges that individuals with CP, their families, and carers have to face on a daily basis, but also the prospects and successes that can be achieved.
Laura Coccia for DMCN: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16369




