9798346476856 - the apert syndrome sourcebook: a comprehensive guide for families di white mat, cheryl (9 risultati)

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Da: PBShop.store UK, Fairford, GLOS, Regno UnitoPBShop.store UK
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Da: Ria Christie Collections, Uxbridge, Regno UnitoRia Christie Collections
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Da: GreatBookPricesUK, Woodford Green, Regno UnitoGreatBookPricesUK
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Da: GreatBookPricesUK, Woodford Green, Regno UnitoGreatBookPricesUK
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
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Taschenbuch. Condizione: Neu. Neuware - For families affected by Apert syndrome, the journey often begins with unexpected questions and challenges, but it also opens doors to a life filled with resilience, growth, and love. The Apert Syndrome Sourcebook is here to guide you through each step, offering compassionate insight, prac…tical advice, and the latest medical knowledge to empower parents, caregivers, and individuals affected by this rare genetic condition.Inside, you'll find in-depth explanations of Apert syndrome's genetic basis and physical characteristics, presented in a way that's clear and accessible. Explore the science behind the FGFR2 mutation, discover the importance of genetic counseling, and learn about the surgical and therapeutic options that can enhance quality of life. Real stories, like Emily's journey of strength and adaptation, show how families can rise to meet challenges, finding support, community, and joy along the way.This book also addresses the emotional side of Apert syndrome, with guidance on navigating family dynamics, building a support network, and celebrating every unique milestone. It encourages families to look beyond the diagnosis, seeing each child's individual strengths and possibilities. From early medical care to empowering young adults with Apert syndrome to live fulfilling lives, The Apert Syndrome Sourcebook provides a roadmap of resilience, hope, and meaningful connections.>ABOUT THE AUTHOR.

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- Print on Demand
Da: CitiRetail, Stevenage, Regno UnitoCitiRetail
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Paperback. Condizione: new. Paperback. For families affected by Apert syndrome, the journey often begins with unexpected questions and challenges, but it also opens doors to a life filled with resilience, growth, and love. The Apert Syndrome Sourcebook is here to guide you through each step, offering compassionate insight, pract…ical advice, and the latest medical knowledge to empower parents, caregivers, and individuals affected by this rare genetic condition.Inside, you'll find in-depth explanations of Apert syndrome's genetic basis and physical characteristics, presented in a way that's clear and accessible. Explore the science behind the FGFR2 mutation, discover the importance of genetic counseling, and learn about the surgical and therapeutic options that can enhance quality of life. Real stories, like Emily's journey of strength and adaptation, show how families can rise to meet challenges, finding support, community, and joy along the way.This book also addresses the emotional side of Apert syndrome, with guidance on navigating family dynamics, building a support network, and celebrating every unique milestone. It encourages families to look beyond the diagnosis, seeing each child's individual strengths and possibilities. From early medical care to empowering young adults with Apert syndrome to live fulfilling lives, The Apert Syndrome Sourcebook provides a roadmap of resilience, hope, and meaningful connections.Whether you're a parent, relative, friend, or individual with Apert syndrome, this book will help you understand and embrace the journey ahead-one filled with purpose, support, and an unbreakable bond of love. ABOUT THE AUTHOR Cheryl White has been a dedicated health science writer for more than 30 years. With an undergraduate degree in Health Sciences and two master's degrees, Cheryl's passion for helping people live healthier lives comes through in her writing, making complex health issues understandable and accessible for all readers. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.