Showing titles in People with Disabilities

Dive headfirst into the urban symphony of "Smelling the Taste of Sound", a riveting memoir of a newly diagnosed, neurodivergent trainee lawyer. Her sensory issues are compounded by the sirens that punctuate the daily grind of a tough, inner-city law firm. Amidst encounters with eccentric characters and surreal personalities, our protagonist navigates the chaos and unorthodox office dynamics with comical observations and resilience.

This compelling memoir traces an extraordinary journey through mental illness and neurodiversity—one of hard-won insight, resilience, and wisdom. Living with bipolar disorder, depression, addiction, and dyslexia, the author’s path weaves through punk rock rebellion, police work, and entrepreneurship—revealing the complex reality of managing mental health and neurodiversity. Another deep depressive episode became the catalyst for a medical diagnosis, professional help, and true healing.

A Short History of Falling – like The Diving Bell and the Butterfly, and When Breath Becomes Air – is a searingly beautiful, profound and unforgettable memoir that finds light and even humour in the darkest of places. We keep an old shoebox, Gill and I, nestled in a drawer in our room...

Die Autorin ist Mutter eines Jungen im Autismus-Spektrum. Seit einigen Jahren lebt sie mit ihrer Familie in Deutschland, wo sie jeden Tag das Leben aus einer anderen Perspektive kennenlernt – durch das Prisma der Mutterschaft, der Auswanderung und der einzigartigen Welt ihres Sohnes.

Theirs was an unlikely life together. Sheila gave birth to Josephine on 11th May 1993 and for twenty-three years they co-existed in a loving mother-daughter relationship, but one with a difference. Josephine suffered catastrophic brain injury at birth, never spoke to Sheila, rarely smiled and was barely able to see the faces of the people who loved her.

In the blink of an eye, life can take an unexpected turn. One moment you're a loving mother of four, cherishing the simple joys of the playground, and the next, you find yourself confined to a 12x12 room in a psychiatric hospital. How does one bridge the gap between the mundane and the unimaginable? How does a perfectly healthy pregnancy spiral into a journey through the depths of the human psyche? In "From Playgrounds to Psych Wards," Amanda Taylor takes you on an extraordinary odyssey through the corridors of her mind, from health through a sudden descent into the abyss of psychosis.

This audiobook provides insight into the life of a neurodiverse Black girl from the Midlands as she embarks on her journey through the UK school system. This book unveils and highlights the unique experiences of neurodiverse people of color and the many challenges they face. In this book, 24-year-old British-Nigerian Oluseyitan Ojedokun gives an account of her struggles through school. She shares the many dreams and goals she had, despite the feeling of constant dismay.

Seahawks star running back Curt Warner and his wife, Ana, were prominent figures in Seattle in the early 1990s. When they dropped from the public eye after Curt’s retirement, everyone assumed it was for a simpler life. But the reality behind their seclusion was a secret they hid from even their closest friends: their twins, Austin and Christian, had been diagnosed with severe autism. What followed was a painful struggle to hold their family and their marriage together in a home filled with chaos, emotional exhaustion, and constant fear for the safety of their unpredictable but beloved boys.

Greg Marshall's early years were pretty bizarre. Rewind the VHS tapes (this is the nineties) and you'll see a lopsided teenager limping across a high school stage, or in a wheelchair after leg surgeries, pondering why he's crushing on half of the Utah Jazz. Add to this home video footage a mom clacking away at her newspaper column between chemos, a dad with ALS, and a cast of foulmouthed siblings. 

When twenty-nine-year-old Christine Schrader was diagnosed with stage four colorectal cancer, she refused to let fear or statistics define her. Instead, she opened her heart—and her journal—sharing the raw reality of treatment, the strength of family, and the stubborn joy she found in small, everyday moments. How Cancer Improved My Life is Christine’s story in her own words: candid, faith-filled, and often laced with the humor that carried her through more than sixty rounds of chemotherapy.

Cosa significa vivere con un cervello che corre più veloce del mondo intorno? In questo libro, Luca Donato racconta con ironia e sincerità la sua vita con il disturbo da deficit di attenzione e iperattività, l'ADHD: un continuo equilibrio tra entusiasmo e fatica, creatività e disordine, energia incontenibile e sensi di colpa. Dall'infanzia irrequieta agli imprevisti quotidiani, dalle sfide sul lavoro alle relazioni affettive, l'autore ci accompagna in un viaggio fatto di inciampi e scoperte, mostrando come la diagnosi non sia un punto d'arrivo, ma l'inizio di una nuova comprensione di sé.

In Your Superpower, Tasha will describe how she overcame hurdles growing up to feeling confident in embracing who she is now. She will interview people from all walks of life to detail disabilities and differences of all kinds, such as blindness, alopecia, acne, mental health, and will show how you can use your difference to make a difference.

Brought to you by Penguin. Meet Lionel, Caroline’s older brother. Born in the 1950s, when little was known about autism, Lionel was considered a peculiarity. From the beginning, he was a silent child, oblivious to the people around him and intent only on playing with his toy trucks. By the...

Trente-deux ans, c'est le nombre d'années qu'il m'a fallu pour mettre un nom sur ma différence. Comment ai-je pu "passer au travers des mailles du filet" durant tout ce temps ? Je vous révèle, au travers de ce récit parsemé d'anecdotes, comment j'ai grandi dans l'ignorance de mon syndrome. Plongez dans mon quotidien et découvrez chacune des étapes clés de mon évolution ainsi que les moyens mis en œuvre pour survivre dans ce monde parfois difficile à appréhender.

Every dyslexic person has their own story. This is my story; my story of discovery. My story of taking ownership and realising that my so-called disability is my greatest gift This is not a conventional audiobook about dyslexia. This is an audiobook about you! You truly conquering your dyslexia, and not being totally reliant on a school, your parents, or other people, but being reliant on yourself. Not letting dyslexia hold you back but push you to become the best version of yourself.

In I'll Pray for You and Other Outrageous Things Said to Disabled People, Hannah Setzer volunteers to go first and say the things that we all think, but rarely say. Hannah has lived her whole life as a disabled woman and is here to share her story, though don't think for a second that this is inspiration porn. In fact, Hannah's disability is the least interesting thing about her!

An upcoming book to be published by Penguin Random House...

The stories in this book are about women who are married to, or were once partnered with, men on the mild end of the autism spectrum, formerly known as Asperger’s syndrome. These women are not autistic, so their relationships are considered neurodiverse (meaning there’s a neurotypical person in a relationship with a neurodivergent person). The focus within the stories is Cassandra Syndrome. A very life-altering phenomenon that often occurs—and usually remains unaddressed—within these relationships.

Devenir aveugle : pour Marie-Christine comme pour quiconque, cette idée est inconcevable et terrifiante. C’est pourtant la sentence que la jeune femme de 30 ans reçoit au printemps 2018 : elle ne verra plus. Jamais. Les couchers de soleil, son visage dans le miroir ou la frimousse de son fils : désormais, tout n’existera que dans sa mémoire, jusqu’au jour où ces images disparaîtront comme peau de chagrin.

Just like fox, Heidi has lived on the outer. The ‘official record’ of her life has been her mental health record: primary diagnosis – schizoaffective; comorbidity – major depression, juvenile autism and not her own memories. This is the living, breathing version of Heidi’s mental health file that psych wards, doctors, mental health staff or rehab workers know little about or worse, use as evidence of diagnoses. This is Heidi’s account of what happened, shadowed by the story of a fox who knows he'll never belong.