Social Disabilities

Macy is a girl who's a lot like you and me, but she's also quite different, which is a great thing to be. With kindness, grace, and bravery, Macy finds her place in the world, bringing beauty and laughter wherever she goes and leading others to find delight in the unique design of every person. Children are naturally aware of the differences they encounter at school, in their neighborhood, and in other everyday relationships.

It sucks being with Grandpa in this new town. It sucks that they left the old place without finding Rosco. Travis doesn’t want to do anything, especially try to get by in his classes, which never seems possible, anyway. He’s a Bluefish - stupid, angry, alone. Then, suddenly, there’s a girl. Velveeta. She’s up in his face and she’s not backing down. She is as loud as he is quiet, as outgoing as he is shut in. She’s pretty, in a funky, scarf-wearing sort of way, and she’s smart - way smart - smart enough to figure out that Travis has a secret.

I sincerely believe it is extremely important for legitimately disabled Americans to be cared for in a country that takes pride in helping those who are less-fortunate - not those who are looking for a free ride or for a chance to scam the system but who are truly and sincerely in need. There are policies practiced or enforced by the social security disability program for example that cause deserving applicants to be denied (the main subject of this audiobook) and in some cases, less-deserving or undeserving applicants to be accepted by the same benefits program.

Disability and Political Representation explores how disabled people experience the various stages and aspects of the representation process, drawing upon extensive empirical research and a variety of qualitative and quantitative data. It discusses why increasing the number of disabled politicians matters, not only as a matter of justice and equality but also to better represent the issues and interests of importance to disabled people.

Public Hostage, Public Ransom starts with the autobiographical story of William Bronston, the activist physician whose early professional California training steels him with a deep moral, professional, and cultural bond to the huge 6,000-person disabled population he encounters incarcerated in Willowbrook State School in Staten Island, NY, on whose behalf he daily battles to humanize and ultimately catalyze a federal class action lawsuit against the state to close the death-making institution.

This book is all about getting disability benefits, written by a retired social worker. It includes all the step-by-step instructions. The way this book is written is funny and entertaining. It's a shorter book, but it's some milk and all meat - to use a Christian term. There is no book fluff or filler here.

Luisa L’Audace wächst als einziges behindertes Kind in ihrem Heimatdorf auf. Warum sie im Sportunterricht immer als Letzte gewählt wird, in der Pause nicht mitspielen soll und ihre Freundinnen plötzlich nicht mehr neben ihr sitzen wollen, versteht sie lange Zeit nicht. Während andere Kinder Freizeitbeschäftigungen nachgehen, verbringt Luisa viel Zeit in Krankenhäusern, bei Therapien und Spezialist*innen. Als sie mit 14 einen Rollstuhl bekommt, fühlt sie sich zum ersten Mal in ihrem Leben frei. Doch mit der neu gewonnenen Mobilität nehmen auch die Anfeindungen zu.

Historically, they have borne the labels "freaks" and "oddities"; they have been collected as pets, displayed as spectacles, and treated as comic relief. Now, for the first time, in this comprehensive volume, the lives of dwarfs are explored in all their fullness and humanity. Spanning the centuries from ancient Egypt to the present, this unique social history chronicles the various ways this population has been exploited, describes their strategies for coping, and notes the persistent influence of mythology upon perceptions of them by others.

Si no es cada cuatro años que se celebran los paralímpicos, si no se acerca el Día Internacional de las pcd, cuando las marcas realizan acciones; si no es que el gobierno da beneficios fiscales para impulsar la inserción laboral de este grupo, el resto del tiempo las personas con discapacidad viven entre las sombras.

Oliver Sacks widmet sich in seinem neuen Werk dem Zusammenhang von visueller Wahrnehmung und Bewusstsein. Es gelingt ihm wieder, komplexe Dinge verständlich zu beschreiben. Das Außergewöhnliche: Sacks schildert, wie er selbst 2005 an einem bösartigen Tumor im Auge erkrankte. Er berichtet vom Leben mit dem Krebs und dem Verlust seiner visuellen Fähigkeiten. Doch er entdeckt auch "positive" Phänomene: milde Illusion, Halluzinationen, Veränderungen in der Wahrnehmung von Farben und Umrissen.

The success of food allergy activism in highlighting the dangers of foodborne allergens shows how illness communities can effectively advocate for the needs of their members. In Food Allergy Advocacy, Danya Glabau follows parents and activists as they fight for allergen-free environments, accurate labeling, the fair application of disability law, and access to life-saving medications for food-allergic children in the United States.

Nate Trainor, born with Joubert syndrome, could not communicate with words until he was 21. Stuck in a system that prematurely labeled him "profoundly retarded", Nate shares his battles with the public school system to be included, his incredible efforts to prove his intelligence, and the breakthroughs that finally gifted him with words and a voice. His journey proves how one man at a vast disadvantage can prevail in a world that seems hostile or indifferent to him.

Da Rosa bliver født i en lille provinsby i slutningen af 1800-tallet, er hendes muligheder i livet allerede yderst begrænsede. Hun er pige i et mandsdomineret samfund, men ydermere har hun et medfødt handicap - hun er med datidens sprogbrug vanfør. Vi følger først Rosas tilværelse som barn i provinsen, hvor hun møder stor fordømmelse fra omgivelserne, fordi hun er anderledes. Siden hører vi om hendes ophold på et vanførehjem i København. Romanen beretter både om de dårlige vilkår, mennesker med handicap havde i slutningen af det 19.

While finishing off her degree in Gerontology at Umass Boston, Yvonne Decelis started writing about her life in the hope of showing others with similar conditions that they are not alone in the trials they face. Yvonne goes over her upbringing and life prior to, during, and after diagnosis covering things like medications, “healthful living”, work, SSDI disability benefits, friendships, and relationships, etc. This was also written for people seeking information on how to interact with others who have "invisible illnesses" like MS, Fibro, Post-traumatic Stress injury, etc.

Fifteen million working age Americans have a disability. Only four million have jobs. Learn the seven steps to create a workplace where people with disabilities can thrive. Jade was asked by her new boss to spearhead her organization's disability inclusion initiative. On her way home that evening, she was in a horrific accident. While unconscious, she met seven people who taught her how to create a disability inclusive organization. Behind Gold Doors is a great resource to create a disability-inclusive organization.

Meg Zucker was born with one finger on each hand, shortened forearms, and one toe on each misshapen foot, caused by a genetic condition called ectrodactyly. She would eventually pass this condition on to her two sons, and, along with her husband, raise them and their adopted daughter, who has her own invisible differences. Born of the family’s hard-won experiences, this book offers invaluable advice on raising confident, empathetic, and resilient children who succeed, not despite but because of their differences.

Do you have a special needs child or know someone who is? Room at the Table: Encouraging Stories from Special Needs Families is rooted in the 2 Samuel 9 account of King David, who extended kindness to Jonathon's disabled son, Mephibosheth, and granted him a seat at the king's table.

Connected at the chest by a band of flesh, Chang and Eng Bunker toured the United States and the world from the 1820s to the 1870s, placing themselves and their extraordinary bodies on exhibit as "freaks of nature". More famously known as the Siamese twins, they eventually settled in rural North Carolina, married two white sisters, became slave owners, and fathered 21 children between them. More than a biography of the twins, this is a study of 19th-century American culture and society that reveals how Americans projected onto the twins their own hopes and fears.

For more than 40 years, professionals in the field of disability studies have engaged in debates over the use of aversive interventions (such as electric shock) like the ones used at the Judge Rotenberg Center. This book is a historical case study of the Judge Rotenberg Center, named after the judge who ruled in favor of keeping its doors open to use aversive interventions.

One story in this audiobook - How to Get Social Security Disability Benefits - is all about getting disability benefits, written by a retired social worker. It includes step-by-step advice and more. The way this book was written is funny and entertaining. It's a shorter book, but it is some milk, and all meat, to use a Christian term. There is no fluff or filler in this audiobook. The other story in this audiobook - My Mom Is Dying Should I Be Sad? - is about the dilemma of forgiveness I had to face when my 86-year-old mom lay on death bed.