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All I ever wanted was to be normal. But when I was diagnosed with a horrible disease, my life became filled with insurmountable challenges far from normal. Terrified I wouldn’t have a life worth living, I went to an academy where everything changed for me. I was exhilarated to discover my life was just beginning. Living without my parents and dealing with my disease alone scared me. But after making friends, my temporary home was better than I could have imagined

Author Eiren Caffall is the inheritor of a family legacy of two hundred years of genetic kidney disease and the mother of a child who may inherit that legacy. A literary memoir on loss, chronic illness, and generational healing, Caffall’s The Mourner’s Bestiary is also a meditation on grief and survival told through the stories of animals in two collapsing marine ecosystems—the Gulf of Maine and the Long Island Sound—and the lives of a family facing a life-threatening illness on their shores.

Schon als Teenager wusste Fern Brady, dass sie anders war. Als sie zufällig über Autismus las, wusste sie instinktiv, warum. Hier war die Erklärung für ihre Wahrnehmungsstörungen, ihre Meltdowns, ihre Unfähigkeit, soziale Signale zu deuten. Doch erst mit 34 folgte endlich die befreiende Diagnose. In dieser schonungslos ehrlichen Autobiografie erzählt sie ohne Rücksicht und mit dem ihr eigenen Witz von Neurodiversität zwischen Sexismus und Ableismus und ihrem offenen Umgang damit.

When Jade unexpectedly suffered from a rare condition which left her paralysed and in a wheelchair at the age of twelve, she never imagined that she'd one day meet her husband John and that together they would take to social media to dispel the stigma surrounding disability, one story at a time. From questions about suffering and sex to family and faith, Jade and John speak honestly and humorously about life as an inter-able couple.

Wie können wir Inklusion endlich umsetzen? Eine so persönliche wie politische Geschichte. 2016 wird Hadija Haruna-Oelker Mutter eines behinderten Kindes. Immer wieder trifft sie auf Barrieren und trennende Systeme, die seit Jahrzehnten bekannt sind: Bürokratie, pseudoinklusive Schulen oder unhinterfragte Diskriminierungen und Abwertungen im Alltag.

Nadeem's journey is a story told by a mother about her son—it’s not just about a mothers love, it also shows his compassion towards her, his siblings, family and friends. It shows us how he never let his illness define who he was even when the doctors were curt and less kind with their delivery of information. This book tells us the story about a fight to survive, a story about a mother’s love for a child and a story about how a community comes together to support each other.

During an ordinary Fall afternoon, Kimber Hanchey-Ogden was delivered devastating news: Seth, her 17-year-old son, had been hit by a car and airlifted to a hospital! Having sustained a traumatic brain injury, doctors told her that if Seth made it, he would never be able to walk or talk; he would not remember his past or understand humor. And that was just for starters.

¿Sientes que nadie te escucha y nadie sabe el dolor que sientes dentro de ti? Pues, empieza esa búsqueda de un entendimiento verdadero sobre tu persona y cuán importante tú eres. ¿Cómo puedes cambiar algunas cosas que no están bien en tu vida y a quien debes escuchar cuando la sociedad te dice que no encajas con ella? Qué si puedes tornar ese pensar de la sociedad y decirles yo soy lo que soy porque mi aporte es invaluable para aquellos a mi alrededor.

The Sound of Her Voice: My Blind Parents’ Story is the inspiring chronicle of a remarkable couple (both blind since childhood) who—against all odds—lived full and productive lives. Mario became the first blind graduate of the University of Notre Dame Law School and was later elected Judge of two different county courts in Muncie, Indiana. Jane, who was fiercely independent from a young age, ran the household and raised four sighted children without outside assistance.

Carla Sosenko was born with Klippel-Trenaunay Syndrome, a rare vascular disorder that resulted in legs of different sizes, a mass of flesh on her back,­­ a hunched posture, and other idiosyncrasies big and small. She spent years trying to hide under layers of clothing, and then experimented with the opposite: wearing tiny dresses and short shorts, daring people to stare so she could make them regret it. No matter what she did, she was worried that she didn’t measure up.

Ellen Keane spent most of her teens uncomfortable with her limb difference and battling to hide her insecurities. It was only when she embraced her difference that she found her superpower. She started to believe in her unique abilities and gradually find the success that she had never dreamed possible. Perfectly Imperfect is for anyone struggling to accept who they are. With anecdotes from her own life, practical advice and good-natured humour, Keane challenges you to let go of waiting until everything is perfect and instead embrace your imperfections and accept who you are, flaws and all.

Blind Vision is a fascinating account of a unique and inspiring career in open-water swimming. But more than that, it is a story for anyone that’s ever been told they can’t. James Pittar is living proof that no matter what the odds, with dedication, passion, and the right people around you, you can.

Born with severe brain defects, Suzy was sentenced to a life of “nevers.” With the unwavering support of her mother, Jane, and extended family, Suzy’s miraculous journey has given many experts reason to question the medical textbooks that have been written. From predictions that she would never walk, talk, or function in society, Suzy overcame all these obstacles with determination and perseverance—not even allowing final-stage renal failure at the age of twenty-four to deter her.

At the age of 30, Jake found himself hospitalized, grappling with the weight of anxiety, depression, and paranoia. Soon, he received the life-altering diagnosis of schizophrenia. In this intimate and illuminating book, you are invited into Jake's world, a world he shares with his mother, Laurette, through alternating chapters.

In 2019, Greta Morgan was on the rise. She had toured with Vampire Weekend, collaborated with Jenny Lewis, and garnered critical acclaim with her own musical projects. But in March 2020, after contracting COVID-19, she was diagnosed with spasmodic dysphonia, a neurological disorder with no known cure that left her unable to sing. Her once crystalline voice now reduced to a hush, she saw her career come to an abrupt standstill.

Growing Up With Asperger's provides advice, stories, and anecdotes for autistic listeners both young and old, and parents of autistic children. Funny and down-to-earth with an honest look at life from an autistic perspective.

In The Anti-Ableist Manifesto, founder of Diversability and creator of the viral TikTok Anti-Ableism series Tiffany Yu takes listeners on a revelatory examination of disability. Yu celebrates the power of stories and lived experiences to foster the proximity, intimacy, and humanity of disability identities that have too often been 'othered' and rendered invisible

Have you ever felt like there was no light at the end of the tunnel? Or do you struggle why bad things are always happening to you? Do you feel like no one hears you and no one knows the pain and suffering inside of you? Then begin to search for a real understanding of your life and how important you are.

The year is 1950. A child is born in Louisiana. She takes her first breath emerging from a pisspot, unaware of the challenges that await her. Sandra Jean Cole, a blind Black woman who was raised by sharecroppers, introduces us to the people and events that impacted her life as she became the first totally blind public school teacher in East Baton Rouge Parish. Her story is a classic tale of starting from where you are in life and making the most of it.

This book is about one mom's journey in raising a child with special needs. Her daughter Lydia has Down syndrome. This is the story of their life together. Kerry Lynn Patton shares the blessings, trials, and what their family has learned by having Lydia in their lives. This is not meant to be a “How To” book for raising a child with special needs, but rather a book to encourage moms, dads, family, and friends. This delightful book is written in whimsical and heartfelt “snippets" for the listener to enjoy a little at a time or easily in one sitting.