My Special Eye

There are many things that make Bruno special. He loves riding his bike and playing soccer, he is a great brother and is passionate about animals. He also has a prosthetic eye and in this book he tells you all about it. You will discover why Bruno got his special eye, how does he take care of it, how to protect eyes from accidents and what is a visit to the ocularist like. Having such a special eye is just one of the many things that make Bruno unique. This positive book will be a great resource for any child with vision in one eye, with or without a prosthetic eye, scleral shell or cosmetic lens. My Special Eye is also available in Spanish (Mi ojo especial: Un libro para niños sobre prótesis oculares) and Italian (Il mio occhio speciale: Un libro per bambini sulle protesi oculari). For more information, visit facebook.com/MySpecialEye/ From the Author: The story behind My Special Eye book My Special Eye was created a few years after my son lost vision in his left eye when he was 2 years old. One year later he had surgery to replace his eye with a prosthetic eye. It is an understatement to say that this affected our family deeply. Apart from the shock and pain for the suffering of our child and the anxiety for his future, we found ourselves dealing with something completely unexpected that we knew nothing about. Ocular prosthesis, scleral shell, hydroxyapatite implant, uveitis, phthisis bulbi, band keratopathy, evisceration, enucleation... suddenly all these terms became part of our day-to-day vocabulary. My Special Eye is the children's book we would have liked to have at that time. It will be a useful resource for any child with vision in one eye, a prosthetic eye or a scleral shell. Explaining a child that he or she needs an ocular prosthesis is not easy. However when the time came we found that our son and his sibling were way ahead of us in terms of acceptance, resilience and positivity. Also we soon realised that losing vision in one eye didn't limit our child in any way. For him his prosthesis meant that now he had a special eye that could be taken in and out. Nothing more and nothing less. I hope My Special Eye book will help monocular children and their families to realise that having a prosthetic eye is just one of the many things that make them so special and unique.

Jenny Sue's eyes are not the same as other people's eyes. Her right eye looks in one direction, while her left eye sometimes wanders. Jenny Sue has a travelin', lazy eye. Although it makes her different, it also helps her see the world in a special way. Here is a charming story about one very inspiring little girl who overcomes her disability and offers inspiration to others. My Travelin' Eye is a 2009 Bank Street - Best Children's Book of the Year.

A family's journey of how an incredible young boy's cancer diagnosis leads to bravery, self discovery, and a new extraordinary eye! An illustrated children's story written to aid patients, and help their siblings understand retinoblastoma from diagnosis, to enucleation, to living with an ocular prosthesis. Join this family as they learn of a child's cancer diagnosis at the doctors office, treatment at the hospital, and acceptance of a new prosthesis at home. Meet all the wonderful doctors, ophthalmologists, nurses and ocularists that help out along the way. About the author Taline Dorna is an elementary teacher (grade one), by profession; and a mother to 3 children under the age of 6. When her youngest was 5 months old, he was diagnosed with retinoblastoma (a very rare eye cancer). She searched high and low for story books that feature a child with a prosthetic eye and they were few and far between. As a result, she decided to write a children's story book that could be used in a classroom setting as a social story; or for newly diagnosed patients, as well as a way to spread general awareness about retinoblastoma.

Can you imagine not being able to speak or communicate? The silence, the loneliness, the pain. But, inside you disappear to magical places, and even meet your best friend there. However, most of the time you remain imprisoned within the isolation. Waiting, longing, hoping. Until someone realises your potential and discovers your key, so your unlocking can begin. Now you are free, flying like a wild bird in the open sky. A voice for the voiceless. Jonathan Bryan has severe cerebral palsy, a condition that makes him incapable of voluntary movement or speech. He was locked inside his own mind, aware of the outside world but unable to fully communicate with it until he found a way by using his eyes to laboriously choose individual letters, and through this make his thoughts known. In Eye can Write, we read of his intense passion for life, his mischievous sense of fun, his hopes, his fears and what it's like to be him. This is a powerful book from an incredible young writer whose writing ability defies age or physical disability - a truly inspirational figure. Foreword by Sir Michael Morpurgo A portion of the proceeds from the sale of this book will be donated to Jonathan Bryan's charity, Teach Us Too. http://www.teachustoo.org.uk/

NEW YORK TIMES BESTSELLER “As sweet and funny and sad and true and heartfelt a memoir as one could find.” —from the foreword by Augusten Burroughs Ever since he was young, John Robison longed to connect with other people, but by the time he was a teenager, his odd habits—an inclination to blurt out non sequiturs, avoid eye contact, dismantle radios, and dig five-foot holes (and stick his younger brother, Augusten Burroughs, in them)—had earned him the label “social deviant.” It was not until he was forty that he was diagnosed with a form of autism called Asperger’s syndrome. That understanding transformed the way he saw himself—and the world. A born storyteller, Robison has written a moving, darkly funny memoir about a life that has taken him from developing exploding guitars for KISS to building a family of his own. It’s a strange, sly, indelible account—sometimes alien yet always deeply human.

"This is the second edition of an encyclopedic reference work of consumer health about the adult human eye. It covers common eye complaints such as dry eye, ocular migraine, device-related eyestrain, and conjunctivitis, along with newer forms of laser eye therapy and lens implants. The second edition features a new chapter on cosmetics and the eye, along with updated content about diagnostic testing, new forms of eyeglass materials, colored contacts, and therapies for medical conditions for all areas of the eye"--

Ms. Ringgold's personal account of sudden vision loss and her subsequent adjustment is full of practical advice and cheerful encouragement. It's told by the 87-year-old retired college teacher who maintained her independence and zest for life. Readers will get an enlightening perspective into her initial reactions, the ongoing accommodations one must make to loss of vision, and ways to continue one's activities both indoors and out. This newly reissued version brings the information up to date, and an extensive resource section and listing of available services complete this essential guide.

This book was created for our daughter Maya. Maya was born with microphthalmia. We found there was not a lot of information out there about the condition. This book is our journey through Maya's first two years. It show her progress and how her prosthetic eye was made.