Zeigt Titel in Menschen mit Behinderung

In the fall of 1961, a young girl eagerly anticipates the arrival of her baby brother, Ricky. But when he's born, the joy she expected is overshadowed by the unexpected tension that fills their home. Her mother, once lively and full of warmth, becomes distant, struggling to care for two children-especially a newborn with special needs. Raising Ricky is the poignant story of a family transformed, as a sister steps into a role far beyond her years to protect and care for her brother.

Amit Patel is working as a trauma doctor when a rare condition causes him to lose his sight within 36 hours. Totally dependent on others and terrified of stepping outside with a white cane after he's assaulted, he hits rock bottom. He refuses to leave home on his own for three months. With the support of his wife, Seema, he slowly adapts to his new situation, but how could life ever be the way it was? Then his guide dog, Kika, comes along....

We are all born with a series of gifts and curses. It is my experience, that some of those form your self-identity, and dictate much of your life. Attention Deficit Disorder was mine. Growing up I felt hindered by the inability to focus; therefore self-identified as a failure. Yet here I am, 40 years old, professionally and financially successful, artistically trained and skilled, and most importantly happy. In this book, I reflect on why I failed so much at certain elements of my life. I forgive my former self for how I erred as a son, brother, partner and friend.

At age 24, Janet Buttenwieser moved to Seattle with a résumé devoted to public service and fantasies of single-handedly ending poverty. But within a year she’d developed an intestinal illness so rare she wound up in a medical journal. Janet navigated misdiagnosis, multiple surgeries, and life with a permanent colostomy. Like many female patients her concerns were glossed over by doctors. She was young and insecure, major liabilities in her life as a patient. How would she advocate for low-income people when she couldn’t even advocate for herself?

When Joni was paralyzed in a diving accident at the age of seventeen, she quickly understood her life would never be the same. But what she didn't know was how God would use her story to affect the lives of millions of people from across the globe. This little book is full of biblical truths and important lessons Joni has learned along the way. No matter your situation, you'll be encouraged as you discover Jesus' faithfulness in the midst of life's challenges.

Il tempo ha un suono diverso quando sai che sta per finire. Una mamma lo sa, lo sente. Gli ultimi mesi sono volati, scanditi da visite mediche, nuove sfide e momenti preziosi: Cesare ascolta in loop le sue canzoni preferite, esprime desideri. Vuole andare al parco, fare un giro in moto, poi in barca a vela. E mentre Valentina cerca un modo per restare aggrappata all’amore, ai ricordi di ogni risata, il suo Cece si sta spegnendo.

A “raw, vulnerable, and utterly hilarious” (Harper’s Bazaar) memoir about one woman’s experience living with a deformity, and her quest to find freedom and joy in her body “Sosenko’s experience with body shame and judgment, from herself and others, is universal. She shows us her...

For the Love of Stephen: The Story of a Boy Who Was Never Broken is the intimate, heartfelt memoir of a brother who witnessed firsthand the struggles and triumphs of a life lived on the margins of society. Through vivid storytelling, Dr. Stuart D. Jones traces Steve’s journey: his battles with exclusion, his breakthroughs in education, his humor and resilience, his friendships and love, and the tragedy that ended his life too soon.

Ever since he was small, John Robison had longed to connect with other people, but by the time he was a teenager, his odd habits—an inclination to blurt out non sequiturs, avoid eye contact, dismantle radios, and dig five-foot holes (and stick his younger brother in them)—had earned him the...

Le 3 avril 2015, on diagnostique à Marine, jeune étudiante dynamique de 21 ans, une sclérose en plaques, appelée plus communément SEP. L'urgence de la situation, le besoin de prendre une décision quant à la prise d'un traitement ou non et le manque d'informations, l'amène à s'interroger. "La maladie c'est toi qui l'as, il faut donc chercher la solution en toi." Son traitement ? Réaliser un projet rêvé : le voyage.

Born without arms or legs below his elbows and knees, Kyle Maynard excels as a champion athlete, inspirational speaker, college student, and male model. No Excuses is his inspirational autobiography that shows how a positive, can-do attitude gives someone we might see as disadvantaged the advantage over life.

Ido in Autismland opens a window into non-verbal autism through dozens of short, autobiographical essays each offering new insights into autism symptoms, effective and ineffective treatments, and the inner emotional life of a severely autistic boy. In his pithy essays, author Ido Kedar, a brilliant 16-year-old with autism, challenges what he believes are misconceptions in many theories that dominate autism treatment today while he simultaneously chronicles his personal growth in his struggles to overcome his limitations.

Brought to you by Penguin. From the remarkable man whose life inspired the heartstopping film, ‘I Swear’, a book that offers extraordinary insight into what it’s like to live with a severe form of Tourette’s Syndrome: a fascinating, complex condition that’s more common than most of us...

Ce parcours c'est avant tout une belle histoire d'amour. Une histoire à deux qui malheureusement se termine mais accroît le désir inconditionnel de devenir père, le combat d'un homme pour connaître la paternité, y compris seul. À travers ce témoignage, Mathieu Ceschin se livre sans filtre sur ce combat, celui d'une vie, pour toucher à la paternité.

Mit drei Jahren erlitt Ingrid Mundschin-Bohn eine Hirnhautentzündung, an der sie fast gestorben wäre. In Deutschland, wo sie als Tochter eines deutschen Vaters und einer Schweizer Mutter aufwuchs, war gerade der Krieg zu Ende gegangen, die Medikamente waren immer noch knapp, und die Ärzte wollten keine Antibiotika verschwenden an einem Kind, das in ihren Augen bereits abgeschrieben war. Aber Ingrid Mundschin ließ sich nicht abschreiben, sondern wuchs zu einer lebensfrohen und selbstbewussten Frau heran.

A journey through rare disease, a dream of flying, and the gratitude found in acceptance. When Jonathan first threw his parachute—in that instant—the rushing air was still, the falling stopped, and a dream of flying began to take shape: soaring, free from the burdens he carried, held in the sky by a fabric wing. But a cancer diagnosis began a cascade—surgeries, treatments, recurrences, and life-altering side effects. Learning to fly felt impossible.

Lissa Bachner was born with a passion for horses and won her first blue ribbon at age five. Other awards would follow as a young rider, and for years Lissa trained with jumpers, tackling more difficult leaps, and working to perfect her ride. When blindness struck in her teens, it appeared her passion for riding would come to an end. How could she jump hurdles when she could barely navigate through her own home? But success, trust, and love came to Lissa when her trainer convinced her to buy a "diamond in the rough" from Germany.

Almost 10 years after learning that her son is autistic, Julie Green was also diagnosed, shedding light on a lifetime of feeling othered and misunderstood. Motherness traces Julie's journey from childhood to early motherhood, when she must advocate for her son while navigating her own struggles. With more girls and women being diagnosed in the last decade—many of them later in life—the face of autism is changing. Motherness provides a rich, intensely personal account of what it is like to be autistic through the lens of both a mother and child.

A Father, His Son, and an Unrelenting Quest for a Cure At the age of twenty-seven, Whitney Dafoe was forced to give up his life as a photographer who traveled the world. Bit by bit a mysterious illness stole away the pieces of his life: First, it took the strength of his legs, then his voice...

Chronically Awkward is not a story told for sympathy — it’s a story told for truth. It is a raw, unfiltered account of one person’s lifelong attempt to exist in a world that keeps insisting on rules he never agreed to play by. Jason takes listeners through the tangled intersections of autism, ADHD, trauma, and chronic illness — through the systems that failed him, the people who shaped him, and the quiet victories that kept him here. It’s both memoir and mirror; a reminder that surviving isn’t the same as living, and that sometimes we only find who we are after everything else falls apart.