Showing titles in People with Disabilities

No one would ever guess that simply hanging curtains could be life-changing! In the blink of an eye, Paula's world turned upside down as a broken leg morphed into life threatening events that pushed her reality into a darkness we only see in movies. Legless tells the story of Paula's fight to triumph over heartbreaking trauma while depression and suffering snapped at her desire to live. Unwilling to surrender for the sake of her family, she dug deep into the meaning of life at every setback and found herself changed, transformed and seeing herself through the eyes of a new normal.

Desde muito cedo, Louis aprendeu a lutar. Lutou pela vida desde o nascimento. Com determinação e persistência, enfrentou e venceu, um a um, os obstáculos que o destino lhe impôs. Contra a previsão de vários especialistas, andou, falou, leu, escreveu, chegou à universidade. Aos 20 anos, nos presenteia com este audiolivro em que narra com otimismo, apesar de tudo, sua entrega ao jogo da vida, no qual cada minuto é importante para a vitória.

Russell Joyce was born with a rare craniofacial disorder called Goldenhar syndrome, where the left side of his face was not formed. Years of patchwork surgeries made him more outwardly presentable, but not without deep pain and physical and emotional scars. But a life-changing encounter broke through to him with a power he never thought possible, in the very place he never thought to look—his broken face. This set Russell on a journey to understand what was hindering him and others from experiencing the power of God's grace and being truly set free.

I matti ci incuriosiscono, ci costringono a riflettere, ci cambiano lo sguardo, ci mettono davanti ai nostri fantasmi, non ci lasciano mai indifferenti. La storia dell’uomo è costellata di individui eccentrici, bizzarri, anticonformisti, visionari, in molti casi con disturbi psichici gravi, ma altamente creativi in campo letterario, artistico, scientifico. Partendo da queste considerazioni, è nata l’idea di una sorta di calendario che racconti, al posto del santo del giorno, il matto del giorno.

Alle hören auf "Daffy", nur Daffy nicht: Abenteuer Blindenführhündin - von Jennifer Mai, gesprochen von der Autorin. Alle hören auf "Daffy", nur Daffy nicht. Vor allem wenn die ansonsten so zuverlässige Blindenführhündin gerade etwas Schmackhaftes im Freilauf entdeckt hat, kostet dies Jenny, ihrer Arbeitgeberin, viel Geduld. Die hohen Erwartungen der Passanten sind bald noch schlimmer als Daffys Dickkopf. Denn die Leute vergessen eines nur allzu gern: Ein Blindenführhund macht einen verantwortungsvollen Job, allerdings ist und bleibt er immer noch ein Tier.

Jennifer Cañaveral es mucho más que una historia de superación personal. A pesar de perder su audición a los nueve meses debido a una meningitis, ha destacado a nivel nacional e internacional en áreas académicas, deportivas y profesionales. Su método de lectura de labios y escucha consciente en múltiples idiomas, junto con su narrativa autobiográfica y la técnica del journaling, ofrece una visión única y positiva de sus experiencias en Cali y el eje cafetero.

In this fascinating historical adventure, broadcaster and author Selina Mills takes us on a journey through the history of blindness in Western Culture to discover that blindness is not so dark after all. Inspired by her own experience of losing her sight as she forged a successful journalistic career, Life Unseen takes us through a personal and unsentimental historical quest through the lives, stories and achievements of blind people—as well as those sighted people who sought to patronize, demonize and fix them.

With aspirations of being a successful lawyer, Jonathan embarks on a path to make his dreams come true, but is ultimately, unable to do so due to his schizoaffective disorder. In this candid and unflinching memoir, Jonathan reveals his story in all its rawness: the ups, the downs, the wins, the losses, the highs and the darkest of lows.

Der Wunsch, den Jakobsweg zu wandern und einfach mal rauszukommen, ist für viele Menschen ein Traum - egal, ob man gesund, stark und ausdauernd ist. Auch Menschen mit Behinderung gehen diesen Weg, um ihre Grenzen auszutesten, um auf ein Wunder zu hoffen oder vielleicht, um mal etwas anderes zu erleben. Genau das will ich auch. Etwas Neues sehen und hören - auch als Nichtsehender und Nichthörender, denn ich bin taubblind. Ich möchte dich auf meine Reise mitnehmen. Hier in meinem Buch kannst du mich begleiten.

This is a story in Victorian England of how in 1884 Frederick Treves, Surgeon and Lecturer in Anatomy at the London Hospital arranged for the "Elephant Man" (whose distorted grotesque face and deformed body made him a "freak") to visit the medical college next to the hospital for the purpose of a lecture. They would later become friends and Treves the savior of the man named John Merrick. This is Treves' memoir.

I Kept Walking opens in 1940s Tehran when a misguided prank leaves three- year-old Minou frozen in fear. Days later, a doctor breaks the news to her mother: "Your daughter has polio." To understand why nothing is as it seems-the cause of her polio or why her dutiful Jewish mother, who was married off at 13, thwarted her dream of marriage, Minou must flee Iran and confront the psychological toll of her polio. I Kept Walking is the audacious account of a bold young woman who was unwilling to be crushed by polio or the prohibitions of a conservative society.

Jessica Knight grew up on a dairy farm in rural Victoria, her crib next door to where all the cows were milked. It's a loving Mormon household, a god-fearing home. While they don't have very much, it's their values and good humor that allows them to laugh at what scares them. All young Jessica wants is to be good and make her parents and her Heavenly Father happy. She cleans the house and helps out with her siblings; all the while being subjected to intensive medical tests and major surgeries. Doctors consider her a puzzle and a medical mystery.

You are more than your limits. Choosing to see herself as more than a person with a disability and wheelchair user, Lolo chooses to live a bold and courageous life now because representation matters. She created this intersectional guide to provide tools for people with disabilities to thrive in personal growth, independence, and community building. Add this guide to your list of inclusion books!

Carly-Jay Metcalfe was born with cystic fibrosis, survived a double-lung transplant at the age of 21 and faced a rare cancer at the age of 30. What she has endured should have killed her, but her humour, courage and optimism became her best survival skills. From her hospitalised childhood to her many friendships, loves and losses, Metcalfe shares the fickle nature of life with candour and warmth. She writes with compelling insight about organ donation, opioid addiction and survivor's guilt, while still managing to find joy amongst the wreckage.

私たちは本当に「見て」いるのか?触れて、聴いて、初めてわかる、この社会のかたち。時に鋭く、そしてあたたかく。ユーモアに満ちた随想集。

Negli ultimi decenni si è verificata una profonda rivoluzione nella cura della sclerosi multipla, una disfunzione del sistema immunitario che colpisce 122.000 italiani e 2,5 milioni di persone nel mondo. Grazie allo sviluppo di nuovi farmaci sempre più efficaci e a fondamentali scoperte, dai fattori di rischio genetici e ambientali al ruolo rigenerativo delle cellule staminali nel cervello, ora, finalmente, la vita delle persone che soffrono di questa malattia è sempre più vicina alla normalità.

Lorenzo Amurri non nasce come scrittore, lo diventa in seguito a un tragico incidente di sci che, a soli 26 anni, frantuma la strada artistica sulla quale viaggiava sin da giovanissimo: chitarrista rock, produttore musicale. Un ragazzo dinamico e trasgressivo senza mezze misure. Dall'incidente e dalla sua nuova condizione segnata dalla tetraplegia e dall'impossibilità di stringere ancora tra le braccia la sua chitarra, Lorenzo rinasce. Nel 2008 decide di affidare al suo blog Tracce di ruote "riflessioni, denunce e cronaca della sua seconda vita".

A late bloomer’s coming-of-age memoir asks how does one accept and free themselves from visible and invisible disabilities and still retain their sense of connection and humor? Nothing Special is a disarmingly candid tale of two sisters growing up in the 1970s in rural Connecticut. Older sister Chris, who has Down syndrome, is an extrovert, while the author, her younger, typically developing sister, shoulders the burdens and grief of her parents.

Bill Rush lived with a significant disability of quadriplegic cerebral palsy. He did not have use of his arms, hands, or voice. Society’s prejudices proved to be a greater obstacle than his disability in attaining his first life goal of completing college. Rush chronicled his extraordinary life from childhood until graduation from the University of Nebraska - Lincoln in Journey Out of Silence, first published in 1986. This second edition brings back into print Bill's original chronicle. It also contains an introduction to Our Life Our Way, the sequel.

A Michele La Pusata, dodici anni fa, è stata diagnosticata la Sclerosi laterale amiotrofica, meglio conosciuta come SLA. Prima, la sua era una vita più che normale, tra figli, lavoro e piccole incombenze, poi non lo è stata più. Non si mette mai in conto di affrontare una malattia lenta e invalidante come questa e infatti nessuno è preparato.