Clefting is a common birth defect, and it is one of the most fixable. This guide helps alleviate parents' fears by explaining what a cleft is and what can be done about it. Illustrations.

"This book was written for brothers and sisters of a new baby with cleft lip/palate. It is also intended for children born with a cleft to help them learn about themselves. Children may not understand why they, or the new baby in their family, have a cleft. This book is meant to provide some answers to questions children may not know how to ask"--Introduction.

Beth and Her Cleft is an illustrated children's book designed to help children, their siblings, and their families understand all about cleft lip and palate. It is written through the eyes of an older sibling who was first confused about why her baby sister looked and spoke differently. She observes her sisters progression through the necessary surgeries and supportive steps taken to treat Beth's cleft lip and palate. Her families love and support for Beth help her become confident and strong. Beth and Her Cleft is written in rhyming verses and is easy for children to follow. It is written to be humorous and casual. The author, Dr. Bastidas, is a pediatric plastic and craniofacial surgeon based in New York. He wrote this book to help families speak openly about clefts and to comprehend the timeline and events required to treat cleft lip and palate. 100% of the proceeds are used to fund the Saving Faces Foundation (a 501c3 organization dedicated to treating children with visible birth anomalies). You purchasing this book is essentially a donation to our charity and will be used to help other children.

Comprehensive Cleft Care: A Family Edition For parents, learning that their newest family member may bring some unexpected challenges along with the blessing of his or her arrival can take a bit of adjustment. They have questions and need a trusted source of information to allay their fears. You are that source. However, most of the time, parents receive almost too much information to take in all at once, and questions arise as they digest the information. The parents of your patients may wonder: Did I hear that right? What does that term mean? What should I do next? What is in store for my family? From diagnosis to treatment options, Comprehensive Cleft Care: A Family Edition provides families with important information to help them fully understand their child's condition and its treatment. Authored by parents and professionals, this unique work was written with real-life challenges in mind. Two of the book's editors have raised cleft-affected children. As a result, the information provided is not only informative and helpful, but also personal, readily accessible, and relevant from a parent's perspective. This book enables parents and families to play a central role in navigating their child's care while working alongside the rest of the care team. Written in easy-to-read language, it contains over two dozen short chapters that mirror topics discussed in the corresponding text written for health care professionals, Comprehensive Cleft Care, Second Edition. Topics covered include the fundamentals of care, psychosocial and educational aspects, cleft lip and palate repair, speech and hearing, airway and breathing issues, dental and orthodontic principles, and more. By providing up-to-date information in a clear and concise format, this book can help to educate parents and to alleviate much of the anxiety they have regarding their child's condition and its treatment. Published with a complimentary eBook, this guide is an invaluable resource for families seeking to help their cleft-affected child reach his or her full potential.

Brave Blake By: Paige L. Starr Looking different can be scary, but it does not mean it is bad. This book was inspired by the author's younger brother who was born with a cleft lip-a birth defect that originates from Van der Woude Syndrome. This book is a nod to him and what he has gone through as a child. Brave Blake tells the story of Blake who is hoping to win the 2nd grade's "Best Smile" competition, but fears that his birth defect will hinder what his classmates think of him. On the first day of school, he faces the known bully who questions him about his scar. Nervous, Blake fabricates a story to deflect from the truth. The bully finds Blake in a fib and calls him out in front of the class and Blake is left feeling defeated, but his brothers console him and help him regain his confidence. Simultaneously, the bully realizes why Blake told the story instead of telling the truth. When announcement day approaches, the kids come to terms with the results and find friendship. The author hopes people who read Blake's story embrace their difference and wear it as a permanent accessory.