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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.

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.

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.

An ambulance rushed her away to the emergency room at a local hospital. Her life was forever changed in that moment. In this powerful memoir and inspirational self-help book, Kimberly Muka Powers shares her triumphant story of living with bipolar type one disorder with psychotic features. Humbled by this life-altering mental health diagnosis, she learns to rise above the setbacks of her illness and empowers others to do the same.

¿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.

"La situazione di Cesare è molto grave. È giusto che te lo dica. Fate tutto quello che potete con lui, non rimandate." La storia di Valentina, Federico, Ale, Terry e Cece si è interrotta qui, tra le mura di un ospedale e la paura di non avere più tempo. Loro, però, si erano Fatti una promessa: anche nei momenti più bui, tra le ombre, avrebbero cercato la felicità. Così, tra feste di compleanno e gite in canoa, la loro storia continua, e con l’estate ormai alle porte il loro viaggio diventa molto di più.

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.

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.

My name is Tzemah Yoreh, and I am a congregational rabbi on the autism spectrum. How is that possible? How can I thrive in a profession that is pastoral, that rewards extroversion, that seems mostly for those who intuitively grasp social dynamics? In So Compassionate it Hurts: My Life as a Rabbi on the Spectrum, I share my personal journey of being a religious leader on the spectrum, how I've used my gifts to positively impact my congregation (and, in turn, myself), and stories that I hope can inspire those with similar challenges to keep pushing and pursue their passions.

Embark on a powerful and inspirational journey with Dawn Green as she battles against the odds in a 35-year-long quest to uncover the truth behind her mysterious and life-threatening health issues. This gripping memoir takes listeners through the highs and lows of an extraordinary life marked by persistence, resilience, and unwavering hope. The book opens with the author's early years, when she first realized that her health was beginning to decline. In succession, a series of perplexing symptoms began to plague her.

Raymond Antrobus was first diagnosed as deaf at the age of six. He discovered he had missing sounds—bird calls, whistles, kettles, alarms. Teachers thought he was slow and disruptive, some didn’t believe he was deaf at all. The Quiet Ear tells the story of Antrobus’s upbringing at the intersection of race and disability. Growing up in East London to an English mother and Jamaican father, educated in both mainstream and deaf schooling systems, Antrobus explores the shame of miscommunication, the joy of finding community, and shines a light on deaf education.