Seizures and Epilepsy in Children is the go-to resource for caregivers and families with children who have epilepsy and seizures.

For the parent of a child with epilepsy, an easy-to-read guide to understanding and managing the disorder while helping your child achieve and maintain a high quality of life. From a leading neurologist, experienced nurse practitioner, and registered dietician comes the complete guide to managing your childís life with epilepsy. Epilepsy in Children offers the practical advice and information you need to manage your childís seizures safely and effectively, understand the latest treatment options, and find hope for a seizure-free future. Key Features: Get the right diagnosis for your child and the correct treatment to reduce the frequency of seizures faster Learn the benefits and risks of pharmaceutical, surgical, and alternative therapies including the ketogenic diet Help your child maintain a normal life at school, with friends, and in sports and other activities Navigate the transitions from infancy and childhood, to puberty, to becoming a young adult

Epilepsy book for kids is the perfect way to explain Epilepsy to young children whether they have a family member with Epilepsy or friends with Epilepsy. It helps raise epilepsy awareness and hidden disabilities awareness and raises money for epilepsy charities at the same time with a donation from every copy sold of this book. It was qn honour meeting the royal family at the patrons lunch due to her book as well as being short listed for the young epilepsy charities champion awards in 2012 and getting an award from the Bristol Post in2013 too.

Uses a simple story about a young girl at school to present information about epilepsy.

A question and answer reference book for parents whose children have epilepsy.

This book provides the tools you need to raise a child with epilepsy, to support his/her social development, provide effective discipline, and negotiate the educational system. Each stage in your child's life presents unique issues and problems, ranging from finding day care to school programming to driving. This book is organized so that you can go to the information that you need when you need it, returning for updates as your child grows and new issues emerge. In her 20 years of working with children with epilepsy, Dr. Blackburn has been continually impressed by the fact that no two children with epilepsy are the same. Each child and each family has unique needs. Because of this, she works with a team. The unique talents of each team member let the group meet the unique needs of each patient. This book will help you build the resource team for your child. In addition to providing you with basic tools, the book identifies resources, places you can contact, additional materials you can read, and the kinds of professionals that may be in your community to help you and your child. Every parent is busy, and parents of children with epilepsy may be evenbusier than most. This book has been organized with the busy parent in mind. The first four chapters are a "must read" for every parent. Theyprovide the basic tools for understanding epilepsy, behavior management and school programming. The final chapter summarizes parenting of a child with epilepsy, providing an easy to remember checklist. Issues for parenting a toddler with epilepsy are far different than issuesfor parenting an adolescent. You can go to the information that you need,when you need it, returning to the book for an update as your child grows and new issues emerge. You can select the section that is important to you in understanding your child, reading the other chapters when you have time and/or want to know more about the brain in general. Childhood epilepsy may provide speed-bumps in the road to adulthood, but it does not have to be a barricade. For 20 years, Dr. Blackburn has helped parents negotiate the speed bumps, creating an owner's manual for their child. Now, she helps you make this journey.

Nearly three million people in the United States live with epilepsy every day and another 180,000 Americans develop epilepsy every year. Around the world, more than 60 million people have epilepsy. Epilepsy impacts everyone in different ways, as well as their families, friends and professional caregivers. This enlightening book presents the firsthand personal accounts of children with seizure disorders and their parents. In their own words, these children and parents vividly describe the experiences of handling the crisis of the initial seizure, adjusting to the diagnosis of epilepsy, coping with seizures, managing medications and side effects, and dealing with health care providers, teachers, schoolmates, siblings, and friends. Their stories reveal the terror, uncertainty, and frustration felt by children an dparents after an initial seizure or a diagnosis of epilepsy and document the ongoing trials, tribulations, and triumphs of coping with seizures, medication schedules and side effects, health care providers and hospitals, schoolmates, siblings, relatives and friends. These accounts provide realistic insights into the myriad issues encountered in living with childhood epilepsy. The book also includes a straightforward medical discussion of childhood seizures, written in layperson's terms; a glossary of medical terms; and a guide for schoolteachers and parents.