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Cut: The True Story of an Abandoned, Abused Little Girl Who Was Desperate to Be Part of a Family
by Cathy GlassDawn was the first girl Cathy Glass ever fostered. A sweet and seemingly well balanced girl, Dawn's outward appearance masked a traumatic childhood so awful, that even she could not remember it. During the first night, Cathy awoke to see Dawn looming above Cathy's baby's cot, her eyes staring and blank. She sleepwalks--which Cathy learns is often a manifestation in disturbed children. It becomes a regular and frightening occurrence, and Cathy is horrified to find Dawn lighting a match whilst mumbling "It's not my fault" in her sleep one night. Cathy discovers Dawn is playing truant from school, and struggling to make friends. More worryingly she finds her room empty one night, and her pillow covered in blood. Dawn has been self-harming in order to release the pain of her past. When Dawn attempts suicide, Cathy realises that she needs more help than she can give. Dawn's mother eventually confides in her that Dawn was sent away to relatives in Ireland between the ages of 5 and 9, and came back very disturbed. She also sheds light on the reason for Dawn's fascination with matches and Cathy's baby. *SPOILER ALERT*SPOILER INFO FOLLOWS* Eventually Dawn is placed in a psychiatric home for children, and five years later she gets in touch with Cathy. She has been reconciled with her mother and is now training to become a teacher.
Cutting-Edge Therapies for Autism 2010-2011
by Tony Lyons Teri Arranga Mark Freilich Ken SiriFor parents of children with autism, research is a full-time job. For parents with limited time, ability, or resources to do this, Ken Siri and Tony Lyons have compiled the latest in autism theory, research, and treatment. Cutting-Edge Therapies for Autism contains contributions from more than eighty experts on a variety of therapies, models, and multifaceted evaluation and treatment centers. Each contributor gives the reader a basic description of the topic, including its scientific rationale, development, risks, and benefits. Siri and Lyons include the therapies of the future, focusing on current clinical trials, ongoing research, and the researchers striving to better understand autism and find new treatments.
Cutting-Edge Therapies for Autism 2011-2012 (Cutting-edge Therapies For Autism Ser.)
by Tony Lyons Teri Arranga Ken Siri Rita ShrefflerThe parents of children with autism know that research is a full-time job. For parents with limited time, ability, or resources to do this, Ken Siri and Tony Lyons have compiled the latest in autism research and treatment. Cutting-Edge Therapies for Autism contains contributions from more than eighty experts on a variety of therapies, models, and multifaceted evaluation and treatment centers. Each contributor provides readers with an easy-to-understand description of the topic, including its scientific rationale, development, risks, and benefits. Siri and Lyons include the therapies of the future, focusing on current clinical trials, ongoing research, and the researchers who are striving to better understand autism and find new treatments. Revised and updated to reflect the new developments in the last year, the 2011-2012 edition explains possible causes of autism, including food allergies and gastrointestinal diseases in children. An extensive variety of therapies is discussed, from dietary interventions that reduce sugars and remove gluten to animal assisted therapies that place a dog or cat in the care of the autistic individual to help enhance social and developmental skills. Filled with numerous case studies and more than seventy distinct subjects, Cutting-Edge Therapies for Autism is a detailed and informative guide for anyone affected by autism.
Cutting-Edge Therapies for Autism, Fourth Edition
by Tony Lyons Teri Arranga Ken SiriThe parents of children with autism know that learning about treatments is a full-time job. For parents with limited time, ability, or resources, Ken Siri and Tony Lyons have compiled the latest in autism research and treatment. Exploring the possible causes of autism and presenting novel therapies, medications, and interventions, Cutting-Edge Therapies for Autism contains contributions from more than ninety experts on a wide variety of research findings, therapies, models, and multifaceted evaluation and treatment centers.Revised and fully updated to include the latest developments, this fourth edition includes up-to-date information on mitochondrial, antifungal, and physical therapy treatments; about speech, art, music, and sound therapies; and how diets, HANDLE, indigenous healing, and other exciting new treatments can be used to help your child. It also addresses developing technologies, like the iPad, which provides hundreds of apps that help kids with autism communicate and organize their day, and helps parents keep track of therapy schedules. Filled with case studies and research, Cutting-Edge Therapies for Autism is a detailed and informative guide for anyone affected by autism.
Cyborg Detective (American Poets Continuum #174)
by Jillian WeiseIn her third collection of poems, Jillian Weise delivers a reckoning to the ableism of the Western Canon. These poems investigate and challenge the ways that nondisabled writers have appropriated disabled bodies, from calling out William Carlos Williams to biohacking Raymond Carver’s “Cathedral” to chronicling the ongoing headlines of violence against disabled women. Part invective, part love poem, Cyborg Detective holds a magnifying glass to the marginalization and fetishization of disabled people while claiming space and pride for the people who already use technology and cybernetic implants every day.
Cómo Encontré Mi Voz
by Damian Quinn"...las palabras siempre conservarán su poder. Las palabras ofrecen los medios para encontrar el significado y, para aquellos que escuchan, el enunciado de la verdad". - V, 2005 El poder de la comunicación es fundamental; algunos dirían que una necesidad. Todos tenemos ese poder: humanos, insectos, aves, gatos, perros, etc. No importa a cual especie pertenezcamos, todos nos comunicamos. Lamentablemente, a algunas personas se les dificulta, y Damian fue una de ellas. El Trastorno del Desarrollo del Lenguaje, una discapacidad del habla y del lenguaje que padece Damian desde su nacimiento, hace que las frases sean confusas y lentas, incluso si las ideas de Damian son claras. Aquí Damian habla acerca de cómo el TDL ha impactado su vida, y como la organización benéfica Afasic ha estado ahí para ayudarle durante todo el trayecto. Damian tropezó con muchas dificultades a lo largo de su vida para lograr hablar. Cómo encontré mi voz relata el viaje de Damian, desde sus primeros años, sus dificultades para encontrar un diagnóstico y que la enfermedad fuera reconocida, hasta ser escuchado como vicepresidente de Afasic.
D/deaf And D/dumb: A Portrait Of A Deaf Kid As A Young Superhero (Disability Studies In Education Ser. #10)
by Joseph Valented/Deaf and d/Dumb chronicles the author's dumb, 'deaf kid' origins in Bayport, New York to his current life as a «young superhero» writer. Portraying the conflicting cultural worlds of hearing and Deaf, it describes his life in an in-between underworld and his identity as it alternates between being oppressed and empowered. These feelings are inescapably and forever the reality of those who live on the margins of our larger society.
DEC Recommended Practices In Early Intervention/Early Childhood Special Education
by Patricia Miller Susan Sandall Mary E. McleanOffers guidance to parents and professionals who work with children who are differently-abled and developmental delays.
DK Readers L3: Helen Keller (DK Readers Level 3)
by Leslie GarrettIn this new Level 3 Reader, the captivating story of Helen Keller unfolds. Children able to read on their own will be eager to delve in, learning more about Helen's life, from her early days as a deaf and mute infant, to those as an adult who achieved great academic success in spite of her challenges.
DK Readers L3: Helen Keller (DK Readers Level 3)
by Leslie GarrettIn this new Level 3 Reader, the captivating story of Helen Keller unfolds. Children able to read on their own will be eager to delve in, learning more about Helen's life, from her early days as a deaf and mute infant, to those as an adult who achieved great academic success in spite of her challenges.
Dad, Jackie, and Me
by Myron UhlbergJackie Robinson is the new first baseman for the Brooklyn Dodgers--and the first black player in Major League Baseball. A young boy shares the excitement of Robinson's rookie season with his deaf father. <P><P> Winner of the Schneider Family Book Award
Daily Living with a Handicapped Child (Routledge Library Editions: Children and Disability #11)
by Diana M. MillardFirst published in 1984, this book focuses on the support and reassurance needed by parents of children with handicaps. It provides a practical guide in relation to daily care and is equally as relevant to professionals, therapists, teachers, doctors and psychologists who must advise parents. Written by an Occupational Therapist, the book highlights the need to make such children as independent as possible and gives advice on care of a special baby, modifications to the home environment, the needs of a child with a physical handicap, problems of educational handicap, and the place of a child in the family and community.
Damage (Series In Microscopy In Materials Science Ser.)
by A. M. JenkinsAs the Pride of the Panthers, football star Austin Reid is a likable guy, good with the ladies. Lately though, he doesn't like his life -- or anything else -- so much. And the worst part is that he can't seem to figure out why.
Damaged Angels: An Adoptive Mother Discovers the Tragic Toll of Alcohol in Pregnancy
by Bonnie BuxtonPart heartfelt memoir, part practical guide, "Damaged Angels" recounts Bonnie Buxton's struggles to raise an adopted daughter whom she didn't realize was afflicted with fetal alcohol disorder. Her book also offers guidance to parents who have children with FASD. By the time BonnieOCOs daughter Colette hit first grade, her parents were coping with her frequent stealing and lying, and the necessity of special education. At fourteen, she discovered drugs and sex; by eighteen, she was a crack addict living on the streets. After many frustrating years consulting numerous therapists, a TV news story gave Bonnie the answer she was looking for ? and sent her on a quest for a diagnosis and help for Colette. "Damaged Angels" can aid and comfort all those affected by FASD ? the most common cause of intellectual impairments in most industrialized nations ? and reduce the number of babies born with this disorder in the future. The most important book on fetal alcohol disorder since Michael DorrisOCOs "The Broken Cord, Damaged Angels" is a book for every parent, practitioner, and teacher working with a child with FASD. "
Damn Bunch of Cripples: My Politically Incorrect Education in Disability Awareness
by Lew ShaverI was sitting in a small upstairs room attempting to write this narrative of my education in disability awareness. For over 30 years I have been involved in working with individuals with disabilities as a coach and administrator on the intercollegiate, national and international levels. When I started this journey, at a small, Midwestern University, I had no idea of what I was getting myself into. Now that I have traveled this educational path I have come to realize that it may have been one of the most important learning experiences of my life, an experience I feel needs to be shared. In putting this narrative together, one very real issue I struggled with was how to deal with the present climate of political correctness. My decision was to tell the stories as I remember them, in the language as I remember. To do differently would change and compromise the actual experience. Thus, this is a sharing of feelings and experiences that a coach and his athletes spent in timeless hours in a gym practicing and competing, of thousands of miles traveled throughout the United States and beyond, and days and nights spent together in laughter and frustration.
Dance, Access and Inclusion: Perspectives on Dance, Young People and Change
by Charlotte Svendler Nielsen Stephanie BurridgeThe arts have a crucial role in empowering young people with special needs through diverse dance initiatives. Inclusive pedagogy that integrates all students in rich, equitable and just dance programmes within education frameworks is occurring alongside enabling projects by community groups and in the professional dance world where many high-profile choreographers actively seek opportunities to work across diversity to inspire creativity. Access and inclusion is increasingly the essence of projects for disenfranchised and traumatised youth who find creative expression, freedom and hope through dance. This volume foregrounds dance for young people with special needs and presents best practice scenarios in schools, communities and the professional sphere. International perspectives come from Australia, Brazil, Cambodia, Canada, Denmark, Fiji, Finland, India, Indonesia, Jamaica, Japan, Malaysia, New Zealand, Norway, Papua New Guinea, Portugal, Singapore, South Africa, Spain, Taiwan, Timor Leste, the UK and the USA. Sections include: inclusive dance pedagogy equality, advocacy and policy changing practice for dance education community dance initiatives professional integrated collaborations
Dancing Daisies
by Sara PyszkaBrynn has cerebral palsy and her relationship with her two best friends is just shattered. Brynn is looking forward more than ever to her summer at Camp Lakewood.
Dancing in the Storm
by Amie Darnell Specht Shannon HitchcockIn the tradition of Out of My Mind and Rules, and inspired by the co-author&’s own life, this is a heartfelt, candid, and illuminating story of a girl learning to live fully with a rare genetic disorder.Kate&’s life in Baton Rouge, full of friends and family, gymnastics and Girl Scouts, is just plain great. But then, at the age of twelve, she suddenly develops a mysterious shoulder pain that won&’t go away . . . and that will change her life forever. It turns out that Kate has one of the rarest genetic disorders in the world, Fibrodysplasia Ossificans Progressiva. FOP causes bone to form in places in the body where it shouldn&’t, and there&’s no cure yet. Kate will need to learn how to live with this difficult new reality, helped by those close to her and by a new pen pal named Amie, who has been living with FOP for years.Drawing upon much of Amie Specht&’s own experiences with FOP, she and esteemed novelist Shannon Hitchcock have created a poignant, eye-opening, and uplifting story of finding courage and joy in the face of adversity.
Dancing with Max: A Mother and Son Who Broke Free
by Emily Colson Charles W. ColsonMeet a remarkable young man. Max doesn't communicate like we do. But he communicates better than we do about the most important things. Max doesn't think like we do. But his actions reflect deep spiritual truths. With candor and wit, Emily Colson shares about her personal battles and heartbreak when, as a suddenly single mother, she discovers her only child has autism. Emily illuminates the page with imagery making you laugh, making you cry, inspiring you to face your own challenges. Chuck Colson, in his most personal writing since Born Again, speaks as a father and grandfather. It is a tender side Max brings out of his grandfather, a side some haven't seen. As Emily recalls her experiences, we discover that Max's disability does not so much define who he is, but reveals who we are. Dancing with Max is not a fairy tale with a magical ending. It's a real life story of grace and second chances and fresh starts in spite of life's hardest problems. And Max? Max will make you fall in love with life all over again, leaving you dancing with joy.
Dancing with Max: A Mother and Son Who Broke Free
by Emily Colson Charles W. ColsonMeet a remarkable young man. Max doesn’t communicate like we do. But he communicates better than we do about the most important things. Max doesn’t think like we do. But his actions reflect deep spiritual truths. With candor and wit, Emily Colson shares about her personal battles and heartbreak when, as a suddenly single mother, she discovers her only child has autism. Emily illuminates the page with imagery—making you laugh, making you cry, inspiring you to face your own challenges. Chuck Colson, in his most personal writing since Born Again, speaks as a father and grandfather. It is a tender side Max brings out of his grandfather, a side some haven’t seen. As Emily recalls her experiences, we discover that Max’s disability does not so much define who he is, but reveals who we are. Dancing with Max is not a fairy tale with a magical ending. It’s a real life story of grace and second chances and fresh starts in spite of life’s hardest problems. And Max? Max will make you fall in love with life all over again, leaving you dancing with joy.
Dangerous Medicine: The Story behind Human Experiments with Hepatitis
by Sydney A. HalpernThe untold history of America&’s mid-twentieth-century program of hepatitis infection research, its scientists&’ aspirations, and the damage the project caused human subjects &“Sydney Halpern has written a compelling, if unsettling, history of hepatitis research during World War II and the Cold War. It will become a must-read for anyone interested in bioethics and medical history.&”—Susan E. Lederer, author of Subjected to Science and Flesh and Blood From 1942 through 1972, American biomedical researchers deliberately infected people with hepatitis. Government-sponsored researchers were attempting to discover the basic features of the disease and the viruses causing it, and to develop interventions that would quell recurring outbreaks. Drawing from extensive archival research and in-person interviews, Sydney Halpern traces the hepatitis program from its origins in World War II through its expansion during the initial Cold War years, to its demise in the early 1970s amid an outcry over research abuse. The subjects in hepatitis studies were members of stigmatized groups—conscientious objectors, prison inmates, the mentally ill, and developmentally disabled adults and children. The book reveals how researchers invoked military and scientific imperatives and the rhetoric of a common good to win support for the experiments and access to recruits. Halpern examines the participants&’ long-term health consequences and raises troubling questions about hazardous human experiments aimed at controlling today&’s epidemic diseases.
Daniel Isn't Talking
by Marti LeimbachMelanie Marsh is an American living in London with her British husband, Stephen, and their two young children. The Marshes' orderly home life is shattered when their son Daniel is given a devastating diagnosis. Resourceful and determined not to acceptt what others, including her husband, say is inevitable, Melanie finds an ally in the idealistic Andy, whose unorthodox ideas may just prove that Daniel is far more "normal" than anyone imagined. Daniel Isn't Talking is a moving story of a family in crisis, told with warmth, compassion, and humor.From the Trade Paperback edition.tephen's ex-fiancée, a woman apparently intent on restaking her claim on Stephen. Melanie does have one strong ally in Andy, a talented and off-the-wall play therapist who specializes in teaching autistic children. Andy proves that Daniel is far more capable than anyone imagined, and Melanie finds herself drawn to him even as she staggers toward resolving her marriage.Daniel Isn't Talking is a moving, deeply absorbing story of a family in crisis. What sets it apart from most fiction about difficult subjects is the author's ability to write about a sad and frightening situation with a seamless blend of warmth, compassion and humor.
Daniel Kish: A Different Way to See (Fountas & Pinnell Classroom, Guided Reading)
by Julius SmithersonNIMAC-sourced textbook. CHANGING IDEAS ABOUT BLIND PEOPLE. Daniel Kish is blind, but he learned how to see things around him. Now he's teaching blind children how to see too.
Daniel's Music: One Family's Journey from Tragedy to Empowerment Through Faith, Medicine, and the Healing Power of Music
by Jerome Preisler The Trush FamilyIn 1997, Daniel Trush, a bright, active, outgoing twelve-year-old, collapsed on the basketball court and fell into a deep coma. Rushed to the hospital, he was found to have five previously undetected aneurysms in his brain. One had burst, causing a massive cerebral hemorrhage.While Daniel remained comatose, the uncontrolled pressure inside his skull caused him to suffer multiple strokes. Tests showed that his brain functions had flat-lined, and doctors would soon tell his parents his chances of survival were slim to none--or that he'd likely remain in a vegetative state if he awakened.But the doctors were wrong.Daniel's traumatic injury did not bring his life to a premature end. Thirty days after lapsing into a coma, he would return to consciousness, barely able to blink or smile. Two years later, he took his first extraordinary steps out of a wheelchair. A decade after being sped to the emergency room, Daniel Trush completed the New York Marathon.But his incredible journey into the future had just begun. With music having played a crucial role in his recovery, Danny and his family launched Daniel's Music Foundation, a groundbreaking nonprofit organization for people with disabilities. In time DMF would be honored on a Broadway stage by the New York Yankees, gaining notoriety and admiration across America.Daniel's Music is the gripping story of Daniel's recovery against odds experts said were insurmountable; of medical science, faith, and perseverance combining for a miracle; and of an average family turning their personal trials into a force that brings joy, inspiration, and a powerful sense of belonging to all those whose lives they touch.
Danny's People: A Memoir and Manifesto About Autism
by Virginia BovellSociety disables us more than autism ever could &‘My brain&’s still fizzing, my heart&’s still sore and I&’m already re-reading&’ Sally Phillips Virginia&’s son Danny has a way of lighting up a room. He&’s warm, personable and has an infectious laugh. He forms lasting relationships and has known his best friend since they were little. He is also nonverbal and autistic, and requires round-the-clock care and a liquid diet. And for this reason, there are many who would rather not encounter Danny. Challenging the view that autism is something that needs to be &‘cured&’, Virginia Bovell testifies to the extraordinary care Danny has received for over 30 years and the everyday kindness and decency of the people – &‘the band of angels&’ – that surround him. She asks us to consider what makes a thriving individual versus an inadequate one; what it means to be ill versus what it means to not to conform; what roles society values and rewards; and how humans might flourish outside of failing political and economic systems. 'An inspiring testament and a celebration of neurodiversity.' Manni Coe, author of Brother. Do. You. Love. Me