Memoirs Special Needs

The author of the best-selling phenomenon The Reason I Jump returns with a unique memoir about life as a young adult with severe autism. With an introduction by David Mitchell, who translated this book with his wife, KA Yoshida, this extraordinary new work explores education, identity, family, society, and personal growth, opening a window into the mind of its nonverbal author and providing remarkable insights into autism in general.

Special Heart is a deeply touching personal story told through the eyes of a journalist as he faces the most daunting challenge in life - far more frightening than reporting from battlefields, infinitely more momentous than interviewing newsmakers of the day: caring for his critically ill newborn son. Baier reflects on past challenges as he looks forward with hope, chronicling the steps on his path to national prominence as a television anchor, as well as his unexpected journey into the world of pediatric cardiac disease.

Like many women of her generation, Heather Lanier did everything by the book when she was expecting her first child. But her daughter, Fiona, challenged all of Lanier's preconceptions. Born with an ultra-rare syndrome known as Wolf-Hirschhorn, Fiona received a daunting prognosis: She would experience significant developmental delays and might not reach her second birthday. Award-winning writer Heather Lanier's memoir about raising a child with a rare syndrome, defying the tyranny of normal, and embracing parenthood as a spiritual practice that breaks us open in the best of ways.

On the morning of November 14, 1992, Annette Herfkens, a top Dutch banker, packed her luggage for a romantic getaway with her longtime fiancé, Willem. At 6:25 that morning, Annette and Willem boarded a plane out of Ho Chi Minh City, with 23 other passengers and six crew members, excited to finally have a vacation together. Six minutes before landing, flying at speed of 300 miles per hour, the plane lost altitude and crashed along a mountain ridge in the jungle of Vietnam.

In Love Fiercely, a Catholic father offers prayerful insight into the experience of raising and loving his eldest daughter. Elizabeth Bodoh is nearly blind, nonverbal, suffers from epilepsy and cerebral palsy, and loves music. She enjoys cuddles and eating. A shunt manages the fluid on her brain, and a wheelchair helps her family move her.

I Have Been Buried Under Years of Dust is a remarkable memoir by a mother and her autistic daughter who’d long been unable to communicate - until a miraculous breakthrough revealed a young woman with a rich and creative interior life, a poet, who’d been trapped inside for more than two decades.

Despite being a winner of the Pulitzer Prize for Poetry in 2008, Philip Schultz could never shake the feeling of being exiled to the “dummy class” in school, where he was largely ignored by his teachers and peers and not expected to succeed. Not until many years later, when his oldest son was diagnosed with dyslexia, did Schultz realize that he suffered from the same condition.

In August of 2023, on the day that my Cousin Vinny retired after forty-three years of combating corruption and conducting criminal investigations for the City of New York, I had the pleasure of having lunch with him at a restaurant called the Crab Shack in Queens, New York. This particular event was a long time coming. In fact, cousin Vinny had been promising that the event would take place as long as I could remember. It was in fact, 40 years in the making and then it finally took place. All I can say is, good things come to those who wait, and wait and wait. During my conversation with ...

Now raising their four-year-old daughter, Indiana, alone, after Joey’s passing, Rory Feek digs deeper into the soil of his life and the unusual choices he and his wife, Joey, made together and the ones he’s making now to lead his family into the future. When Feek and his older daughters moved into a run-down farmhouse almost 20 years ago, he had no idea of the almost fairy-tale love story that was going to unfold on that small piece of Tennessee land. He takes listeners on his incredible journey from heartbreak to hope and, ultimately, the kind of healing that comes only through faith.

Clem Bastow grew up feeling like she’d missed a key memo on human behaviour. She found the unspoken rules of social engagement confusing, arbitrary and often stressful. Friendships were hard, relationships harder and the office was a fluorescent-lit nightmare of anxiety. It wasn’t until Clem was diagnosed as autistic, at age 36, that things clicked into focus. Clem reflects as an autistic adult on her formative experiences as an undiagnosed young person, from the asphalt playground of St Joseph's Primary School in Melbourne to working as an entertainment journalist in Hollywood.

One afternoon, Emma Nadler gets a call from her daughter's doctor that changes her life forever. Faced with the realities of raising a child with a rare genetic condition, Nadler must confront her preconceptions of motherhood and her perfectionistic beliefs. Nadler—who also happens to be a psychotherapist—offers a rare window into the unconventional ways she and her family adapt to their improbable path. Every relationship in her life—with herself, her husband, children, friends, and even clients—is reimagined as she navigates the heartbreak and hilarity of her daily life.

Told through an experimental mix of intimate anecdotes and interactive visuals, this book immerses listeners in Emmy Award-winning documentary filmmaker James Robinson's point of view, allowing them to see the world through his disabling eye conditions.

When Schuyler Rummel-Hudson was 18 months old, a question about her lack of speech by her pediatrician set in motion a journey that continues today. When she was diagnosed with bilateral perisylvian polymicrogyria (an extremely rare neurological disorder), her parents were given a name for the monster that had been stalking them from doctor to doctor, and from despair to hope, and back again.

One morning, Jenny McCarthy sensed something was wrong and ran into her two-year-old son Evan's room to discover he was having a seizure. In that moment, Jenny was thrust into the midst of a medical odyssey. After numerous misdiagnoses and many harrowing, life-threatening episodes, Evan was finally diagnosed with autism. Jenny didn't know what to do next and found herself alone, without any resources except for her determination to help her son.

Named president and CEO of NBC at the age of 43, he faced a two-headed dragon: on one hand, distrust from the network people deeply skeptical of the "suit" from GE, their new corporate parent; and on the other, fiscal oversight demands from a cautious, conservative institution reluctant to invest heavily in a media business they didn't understand. For the next 20 years, he managed to navigate the fine line between the two and in the process completely reinvent - and save - the network.

In the pursuit of possible links between childhood vaccines, intestinal inflammation, and neurologic injury in children, Wakefield lost his job in London’s Royal Free Hospital, his country of birth, his career, and his medical license. A recent General Medical Council ruling stated that he was “dishonest, irresponsible and showed callous disregard for the distress and pain of children.” Maligned by the medical establishment and mainstream media, Wakefield endeavors to set the record straight.

Misfit, truant, delinquent. John Robison was never a model child, and he wasn’t a model dad either. Diagnosed with Asperger’s syndrome at the age of 40, he approached fatherhood as a series of logic puzzles and practical jokes. When his son, Cubby, asked, “Where did I come from?” John said he’d bought him at the Kid Store and that the salesman had cheated him by promising Cubby would “do all chores”. He read electrical engineering manuals to Cubby at bedtime.

Jadie never spoke. She never laughed, or cried, or uttered any sound. Despite efforts to reach her, Jadie remained locked in her own troubled world - until one remarkable teacher persuaded her to break her self-imposed silence. Nothing in all of Torey Hayden's experience could have prepared her for the shock of what Jadie told her - a story too horrendous for Torey's professional colleagues to acknowledge.

Like all mothers, Emily Rapp had ambitious plans for her first and only child, Ronan. He would be smart, loyal, physically fearless, and level-headed, but fun. He would be good at crossword puzzles like his father. He would be an avid skier like his mother. Rapp would speak to him in foreign languages and give him the best education. But all of these plans changed when Ronan was diagnosed at nine months old with Tay-Sachs disease, a rare and always-fatal degenerative disorder. Ronan was not expected to live beyond the age of three....

A dramatic and remarkable narrative of an extraordinary teacher's determination, from the author of the Sunday Times bestsellers The Tiger's Child and One Child. Torey Hayden faced six emotionally troubled kids no other teacher could handle - three recent arrivals from battle-torn Northern Ireland, badly traumatized by the horrors of war; an eleven-year-old boy, who only knew life inside an institution; an excitable girl, aggressive and sexually precocious at the age of eight; and seven-year-old Leslie, perhaps the most hopeless of all, unresponsive and unable to speak.