"A great leap forward for the social and cultural condition of dwarfism." -- Andrew Solomon, Newsday This landmark volume is the first to trace the exciting developments in the field of dwarfism research and treatment over the past century -- particularly during the past fifty years. Dr. Betty M. Adelson, a psychologist, has unearthed and synthesized the most significant information about dwarfing conditions, from articles written a century ago to current books and specialized databases.

This book provides an in-depth analysis of the social and spatial experiences of people with dwarfism, an impairment that results in a person being no taller than 4' 10". This book engages with the concept that dwarfism's most prominent feature - body size and shape - can form the basis of social discrimination and disadvantages within society. By ignoring body size as a disability, it is hard to see the resulting disabling consequences of the built environment. Using a mixed-methods approach and drawing on the work undertaken by human geographers and disability studies academics, this book analyses how the relationship between harmful cultural stereotypes and space shapes everyday experiences of people with dwarfism and works to socially exclude them in diverse ways. Showing how spatial and social barriers are not mutually exclusive but can influence one another, this book responds to the limited academic work on the subject of dwarfism, whilst also contributing to the study of geographies of body size. It will be of interest to all scholars and students of disability studies, human geography, the built environment, sociology and medical humanities.

Strong and Mighty Max was written by a mother of a child who was born with achondroplasia. Achondroplasia is a rare condition affecting 1 in 25.000 births. Children born with the condition have shorter limbs and slightly larger head than their peers, and have normal intelligence. This beautifully illustrated book encourages children to celebrate that each one of us in unique and different in some way. The revised edition has guided educational activities for primary aged children. To discuss differences, disabilities and the importance of kindness. The new character Katy challenges the reader to think about the importance of education to understand differences.

“It's okay with me if you picked up this book because you're curious about what it's like to live with dwarfism. But I hope that you'll take away much more—about adapting to the world when it won't adapt to you.”—from Dwarf A memoir of grit and transformation for anyone who has been told something was impossible and then went on to do it anyway. Tiffanie DiDonato was born with dwarfism. Her limbs were so short that she was not able to reach her own ears. She was also born with a serious case of optimism. She decided to undergo a series of painful bone-lengthening surgeries that gave her an unprecedented 14 inches of height—and the independence she never thought she’d have. After her surgeries, Tiffanie was able to learn to drive, to live in the dorms during college, and to lead a normal life. She even made time to volunteer, writing to troops stationed abroad, and one of those Marine pen pals ultimately became her husband. Dwarf is a moving and, at times, funny testament to the power of sheer determination, and has been compared to Andrew Solomon's Far From the Tree. Watch her Good Morning America segment: https://abcnews.go.com/Nightline/dwarf-womans-story-undergoing-controversial-lengthening-surgeries/story?id=17841466

Money (medical psychology and emeritus pediatrics, Johns Hopkins U. Hospital) gathers together a century's worth of information on the physical, social, and mental effects of child abuse and neglect. The work concludes with a review by Joshua Kendall of the Kaspar Hauser figure in 19th- and 20th-century prose, poetry, and drama. Contentious and fascinating. Annotation copyright by Book News, Inc., Portland, OR

From the acclaimed author of Floating in My Mother’s Palm and Children and Fire, a stunning story about ordinary people living in extraordinary times—“epic, daring, magnificent, the product of a defining and mesmerizing vision” (Los Angeles Times). Trudi Montag is a Zwerg—a dwarf—short, undesirable, different, the voice of anyone who has ever tried to fit in. Eventually she learns that being different is a secret that all humans share—from her mother who flees into madness, to her friend Georg whose parents pretend he’s a girl, to the Jews Trudi harbors in her cellar. Ursula Hegi brings us a timeless and unforgettable story in Trudi and a small town, weaving together a profound tapestry of emotional power, humanity, and truth.

MANAGEMENT OF GENETIC SYNDROMES THE MOST RECENT UPDATE TO ONE OF THE MOST ESSENTIAL REFERENCES ON MEDICAL GENETICS Cassidy and Allanson’s Management of Genetic Syndromes, Fourth Edition is the latest version of a classic text in medical genetics. With newly covered disorders and cutting-edge, up-to-date information, this resource remains the most crucial reference on the management of genetic syndromes in the field of medical genetics for students, clinicians, caregivers, and researchers. The fourth edition includes current information on the identification of genetic syndromes (including newly developed diagnostic criteria), the genetic basis (including diagnostic testing), and the routine care and management for more than 60 genetic disorders. Written by experts, each chapter includes sections on: Incidence Diagnostic criteria Etiology, pathogenesis and genetics Diagnostic testing Differential diagnosis Manifestations and Management (by system) The book focuses on genetic syndromes, primarily those involving developmental disabilities and congenital defects. The chapter sections dealing with Manifestations and Management represents the centerpiece of each entry and is unmatched by other genetic syndrome references. Management of Genetic Syndromes is perfect for medical geneticists, genetic counselors, primary care physicians and all healthcare professionals seeking to stay current on the routine care and management of individuals with genetic disorders.

Becky Kennedy was more than her parents had bargained for. Born a dwarf, her early medical problems nearly overwhelmed the family's resources. But as surely as she recovered and grew into a healthy little girl, Becky became more than Dan and Barbara Kennedy could have hoped for: not merely a miniature likeness of themselves, but a little person with such a unique perspective that she opened their eyes to a whole other world.In "Little People," Dan Kennedy confronts the deepest of parental fears: What if my child is different? His search for an answer provides a penetrating look at how our culture of diversity clashes with the reality of dis-ability and the belief that we have a right to the so-called perfect child.

If you're skeptical about changing society's discriminatory treatment of people with dwarfism and other disabilities, Van Etten offers hope with these words: "Advocacy makes change possible when people call out what is wrong, care enough to stand up for what is right, commit to the cause for as long as it takes, and have confidence in God's power to change hearts." Van Etten repeatedly demonstrates the power of advocacy in this book. Titans of industry are now required to lower ATMs, gas pumps, and elevator buttons to be within reach of people previously ignored. Public transportation must be accessible. Cheering crowds applauding dwarf tossing contests are silenced. Many homeowners, school children, and volunteer leaders enjoy equal access, respect, and civility. Read this book and be inspired to advocate for the changes you-and others-need. It can be done. "This is a terrific book. When a righteous voice needs to be amplified, Angela rose to the challenge time and time again. Her seemingly endless supply of energy comes from her faith in God and her love of the underdog." ~ Bill Klein, Co-author of Life is Short and Co-Star of TLC's Little Couple." Be inspired and encouraged by Angela's determination to take on all challenges, and eventually overcome and master them with an ample dose of faith and humor." ~ Genevieve Cousminer, Esq., former Director of the Coalition for Independent Living Options, Inc." You will learn a lot about the challenges that dwarfs face in their everyday lives - and about the life and activism of this remarkable woman." ~ Dan Kennedy, Author of Little People: Learning to See the World Through My Daughter's Eyes." Angela Van Etten contributed in countless ways to the advancement of the dwarfism community, the disability community, and the broader community." ~ Gary Arnold, Little People of America Past President. "This book offers the reader a grand tour of local, state, and federal opportunities for advocacy. The only requirement is passion, dedication, a thick skin, patience, and a sense of humor." ~ Jim Kay, LPA Historian