This book, with text on the left and drawings on the right, clearly and more thoroughly explains the life of a USHER, from childhood to adulthood. The importance of putting words to your difficulties as soon as possible. How, at each age, does she have to adapt? There is always an adaptation possible. Different means of communication are also presented. This book contains several international testimonials from DeafBlind and USHERS, on their experience and the adaptations they have made with the help of their relatives or professionals. This book shows us what USHERS are capable of accomplishing. Their experience is a hope for each of us. Thanks for their testimonials. sandrine.dangleterre01@gmail.com
Deep down I was glad I got to see what it was! It is important that a guide explains well by giving precise information or clues etc ... for me to see, imagine or guess. " I was born deaf with Type 1 Usher Syndrome, but I didn't know it. This is how I gradually discovered that I did not see like everyone else, but without knowing that my eyes had a problem. I have always liked to travel. This book is an account of my travels; I tell you all the little tips you need to use to cope with your disability, with the help of others as well. But Usher's syndrome remains unrecognized ...
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