Disability Memoir

Lionheart is an inspiring story of love, forgiveness, and the power of music. On April 27, 2016, while riding his bicycle in Nashville, Tennessee, David was hit by a distracted driver. Doctors told him he would never walk again. His life had changed forever. Lionheart is the richly detailed and intimate account of David's crash, recovery, and return to music: From thinking he lost everything, to appearing on national television (twice), to marrying his soulmate, Kristi - to finding a life and purpose beyond his wildest imagination.

Not that anyone wishes to be paralyzed in a motorcycle accident, but tragedy set the stage for triumph and the making of a real life fairy tale. When the harsh reality of paralysis turned the dream of having a family together into a nightmare for Erik and Jennifer, they had to face their deepest fears and live courageously, because sometimes fairy tales are just stories of love's perseverance.

In Everything Is Going to be K.O. Kaiya Stone writes about her own experiences of living with specific learning difficulties: from struggling at school to being diagnosed with dyslexia and dyspraxia while at university, to performing her own one-woman stand up show inspired by her journey. Always funny and unfailingly honest, Kaiya outlines the frustrations of having SPLDS but also the ways in which they have fuelled her creativity.

Bárbara Anderson narra con brutal franqueza el día a día de tener un hijo con discapacidad: los retos dentro y fuera de casa, las complicaciones de salud y de vida; los cambios de prioridades; el Everest de cada día al tener un hijo con - hasta ahora - un diagnóstico irreversible como es la parálisis cerebral infantil.

Find Another Dream, written and performed by Maysoon Zayid, is the true story of how a Muslim Jersey girl with cerebral palsy creates her own path to stardom. The daughter of Palestinian immigrants, as a child she dreamed of one day dancing on Broadway. As a teen, a bubble-bursting choreographer told her to “find another dream”, so she set her sights on becoming a soap star, undeterred by the fact that the odds were against her.

Diagnosed with cerebral palsy as a child, Kyle Pease had grown up supporting his athlete brothers Brent and Evan from the sidelines. While his condition limited his ability to play sports, it didn't dampen Kyle's passion for them, nor did it stop the Pease family from including Kyle in various excursions. From rolling his wheelchair up Bridal Veil Falls in Yosemite National Park to zipping down Colorado snow slopes, there was never a dull moment with the Pease brothers. Where there was a wheel, there was a way to adventure.

Waking one morning to find he has little to no motor control, Jamieson only wants the world to return to how it had been before. After a diagnosis of multiple sclerosis, he thinks his life is over. What he doesn’t know is that it’s only just begun. Trying to navigate through the world in a body he no longer understands, Jamieson must travel through the dark forest of depression while waging a constant battle against himself. Over time, he learns what he’s truly capable of and what it actually means to be courageous.

Untether is the story of JT Mestdagh, a young man born with a death sentence and who is now an entrepreneur and adventurer on a mission to empower people to untether from limiting beliefs and to soar to their highest dreams...Untether tells a story of courage, determination, and overcoming. Young or not-so-young, you will come away with a renewed sense of hope and possibility. Learn that you are not a mistake; you are created for something amazing.

Emily Owen was a highly intelligent teenager who was also athletic and a skilled musician. Tragically, in her late teens she was diagnosed as suffering from Neurofibromatosis Type 2 (NF2). Since then, Emily has survived many complicated surgical procedures, been close to death, and seen the gradual erosion of all the abilities that defined her personality including the total loss of her hearing. Despite this, she has a remarkable sense of humor and has coped with everything she has been through due to her strong Christian faith, her supportive family, and indomitable personality.

Raising Will is a heartfelt, humbling memoir written by a Texan-turned-Minnesotan mother and child psychologist. Her heart breaks for Will when he is repeatedly banned from Fun Friday in first grade shortly after he is diagnosed with ADHD. The family zigzags through an obstacle course of therapy, medication side effects, tutoring, and sleepless nights, while shining a light on Will's inherent strength - blues guitar. Listeners will surely recognize themselves in this story and find solace, laughter, and hope as they celebrate the surprising blessings ADHD can bring.

In 2018, Joe Hammond, wrote a piece for the Guardian about the 33 birthday cards he was writing for his two sons. It was shared by thousands. In A Short History of Falling he tells the story behind that piece, about the experience of living with - and dying of - motor neurone disease (ALS). A Short History of Falling is not a lament. It is a deeply imaginative meditation on what it feels like to confront the fact that your family will persist through time without you.

In 1991, at the height of the Somali civil war, 12-year-old Abdi Warsame ran for his life through the streets of Mogadishu. In a flash, his legs were paralyzed and his cousin killed. With his country literally falling apart around him, Abdi had little hope for recovery. But, with his faith, his family, and his indomitable spirit, Abdi pursued every available route for a better life.

Debie Monax loved math - its consistency and predictability. In math, all one had to do was follow the proper process and apply appropriate principles to produce a guaranteed result. She applied the same mindset to her life, believing that if she understood the rules and applied the proper principles to all her decisions, she would have the life she dreamed of.

By the time native Sicilian Mariagrazia Buttitta turned 26, she’d planned out the perfect life. After finishing her residency in Buongiorno Medical School, she’d be primed for a job at the prestigious Roma Hospital, the first step toward becoming an Italian Dr. Oz. Instead, she wakes up to discover a medical diagnosis that leaves her almost completely blind. Her family, frustrated and desperate, seeks medical aid in the US, but it comes with a steep price.

I am a woman living with cerebral palsy (CP) since birth. When I was prepping for graduation and finishing my final honors essay for school, I had a realization that based on experience, most of the world does not think or experience life the way I do. Despite my CP, the world still didn't seem to process experiences, feelings, or ideas the same way I've learned to be my normal way of functioning.

Life moves fast. Too fast for some people. This is the true story of what it's like to live in a world where you can't keep up. Bobby was ten months old when my mom and dad rescued him from birth parents who were slowly killing him. He was adopted into our family after a lengthy custody battle. Instead of that settling him, it set off a lifelong struggle to find a place to belong, a place to call home. Like an old-fashioned merry-go-round, the world moved at a speed that was just too fast for Bobby. He couldn't keep up, which prevented him from keeping a job.

On June 10, 2008, Carol Decker walked through the hospital doors a healthy woman with flu-like symptoms and early labor contractions. Three months later, she returned home a blind triple-amputee struggling to bond with a daughter she would never see. Unshattered recounts Carol's fight for survival against sepsis and its life-shattering complications. From excruciating skin grafts to learning how to function in daily life without lower legs, a left hand, and her sight, Carol takes us on a personal and raw, yet inspiring journey.

Award-winning author Mark Richard delivers a fascinating and unique memoir. Born in the South with deformed hips, Richard was tagged a “special” child. Nothing was expected of him. But as a young man, he decided to strike out and experience as much of our strange world as he possibly could.

"My name is Linda Buchan, and when I was 18 years old I died. It was Saturday, June 27, 1998, when my young life ended and my new life began. A life that was to be so completely different to the one that I had envisaged, the one that I had expected...." In Linda Buchan's raw and powerful memoir, she shares her journey from the terrible night when the life and future she thought lay ahead of her was shattered.

La réalité quotidienne d'un non-voyant est un pays étranger. Quel est son rapport au monde ? À la ville et à la nature, à la nécessité de se déplacer, d'utiliser des écrans tactiles, de traverser les rues, de reconnaître les gens ? Invité à donner des cours au Québec, l'historien Jacques Semelin nous propose un récit de voyage d'un genre nouveau. À la fois le sien, dans une ville dont il découvre tout, et le nôtre, dans la tête et le corps d'un non-voyant.