“This is one of the most comprehensive and educational books on the subject of craniosynostosis. I congratulate Dr. Barta and the team at Gillette Children’s for putting together a thorough, detailed, and well-written book. It covers all aspects of craniosynostosis and plagiocephaly, and it is a valuable resource for providers and patients and their families. The educational material that is elegantly presented provides patients and their families with the information they need to make an informed decision, and it highlights the unique and holistic treatment approach followed by the experts at Gillette Children’s.”
WALEED GIBREEL
Pediatric Plastic and Craniofacial Surgeon, Mayo Clinic, Rochester, Minnesota
“I had the pleasure of reading Craniosynostosis, authored by health care providers Ruth Barta, MD, and Cheryl Tveit, RN, with parent Heather Comstock. This is a remarkably comprehensive review of all things related to craniosynostosis and is a terrific source of information for parents and families of infants and children affected by this rare and complex condition. It leaves no stone unturned. I hope it brings some level of comfort to parents and patients dealing with the challenges of craniosynostosis.”
CHRISTOPHER R. FORREST
Medical Director, SickKids Craniofacial Program, Toronto; Professor, Division of Plastic, Reconstructive and Aesthetic Surgery, University of Toronto
“This is an excellent and informative book that is both clear and factual. It serves as a valuable resource for families, providing them with essential knowledge about craniosynostosis and empowering them to engage confidently with medical and health professionals. The personal stories included offer hope and reassurance, reminding families that they are not alone in their journey. This is the book I wish I had when my son was diagnosed with sagittal craniosynostosis in 2019.”
ELAINE KINSELLA
Parent; Chartered Psychologist and Associate Professor in Psychology, University of Limerick, Ireland
“This book provides an insightful exploration into the complexities of craniosynostosis, a condition where the bones in an infant’s skull fuse prematurely. Through a blend of personal narrative and scientific research, it offers a comprehensive understanding of the condition’s causes, symptoms, and treatment options. What sets this book apart is its compassionate portrayal of families affected by craniosynostosis. By sharing their stories, the authors shed light on the emotional challenges they face, from diagnosis to treatment decisions. Additionally, the book delves into the latest medical advancements, offering hope to families navigating this complex problem. It serves as an informative resource for those seeking knowledge about the condition; its real strength lies in its ability to inspire empathy and solidarity among readers.”
EMMA CORDES
Assistant Professor, Indiana University Department of Surgery, Division of Plastic Surgery; Director of Cleft and Craniofacial Program; Director of Global Surgery Program
“Craniosynostosis will be a valuable resource, especially for parents who are just learning of their child’s diagnosis. The detailed explanation of the condition, the pronunciation of words, and the definitions are all beneficial to the reader in providing information all in one place—my favorite aspect. Incorporating personal stories gives a sense of reality, as well as comfort and reassurance often sought by those affected by craniosynostosis. I firmly believe this book will help educate and bring further awareness to the condition.”
LINDSAY WALKER
Chief of Staff, Shriners Children’s Southern California, Pediatric Orthopedic Surgeon, Pediatric Spine Surgeon, UCLA Clinical Assistant Professor, US
“This is a great reference book for all things craniosynostosis. It is appropriate for medical professionals as well as parents and caregivers who want to dig deeper into what they might anticipate for their child—not only in the early period of surgery but also beyond. The book is well designed and organized in such a way that the reader can more specifically find what they need. The personal stories and photographs so graciously shared by the families speak to how those having a child with craniosynostosis are affected in a way that we as providers are unable to fully comprehend. We know how to take care of these kids; families know what it is like to live it.”
CHERYL HOLIHAN
Pediatric Nurse Practitioner Otolaryngology, University of Texas Southwestern, Dallas; Volunteer, Children’s Surgery International