Showing titles in People with Disabilities

Living in the Belgian Congo with her husband in the 1960s, Fran’s mother became pregnant with a daughter. However, right after she gave birth in the hospital, she felt strange. Unbeknownst to anyone, another daughter was on the way, but before anybody responded, an hour had passed. Because of the delay, Fran was born with cerebral palsy. Growing up with her siblings in Africa, Fran always felt different. When everyone else was playing and having fun, she would watch and wish she could join in.

The modern world is built for neurotypicals. Needless noise, bright flashing lights, small talk, implication and ‘unwritten rules’; it can be a nightmarish dystopia as far as the autistic population is concerned. In Untypical, Pete Wharmby lays bare the experience of being ‘different’, explaining with wit and warmth just how exhausting it is to fit into a world not designed for you.

Our aim with this narrative is to share our journey through the labyrinth of cancer treatment—the decisions we faced, the paths we chose, and, most importantly, the lessons we learned. We hope to offer guidance, support, and perhaps a sense of solidarity to others who find themselves on a similar journey. This is not your typical medical guide; it is a well-researched companion for every aspect of your cancer journey and a deeply personal account of battling cancer from the perspective of a spouse.

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.

How do you build a life when all that you know is changing? How do you conceive of love when you can no longer recognise those who mean the most to you? A phenomenal memoir, Somebody I Used to Know is both a heart-rending tribute to the woman Wendy Mitchell once was, and a brave affirmation of the woman dementia has seen her become.

At the age of sixty, and having lived with Parkinson’s disease for over ten years, Guy Deacon CBE set out on one last adventure: to drive solo from his home in the UK 18,000 miles and through twenty-five countries to Cape Town on the southern tip of Africa. This incredible journey, across Europe and down the full length of Africa, took the former British Army officer over twelve months. Along the way, he broke down five times, underwent one emergency evacuation, and took 3,650 prescription pills.

As Harry Potter's stunt double, David Holmes's amazing gymnastic skills saw him earn onscreen immortality. He was the first-ever person to play Quidditch on a broomstick; he dodged dragon's fire and dove deep into the Great Lake, without any gillyweed to protect him. Life on set was an adventure. He and Daniel Radcliffe became like brothers, and the cast and crew a second family. Then tragedy struck. During the making of Deathly Hallows Part 1 a stunt went badly wrong and David's spinal cord snapped. He was only 25 and would never walk again.

In Morant's "Letters to My Son, Rōman," an authentic real-time journal, the author of the #1 release, "The Happy Has Been," shares his personal love letters to his son, Rōman, begun while still occupying Mom's belly. It was later, before Rōman's second year, that he was diagnosed with "severe autism," non-verbal in nature.

Der Wunsch, den Jakobsweg zu wandern und einfach mal rauszukommen, ist für viele Menschen ein Traum - egal, ob man gesund, stark und ausdauernd ist. Auch Menschen mit Behinderung gehen diesen Weg, um ihre Grenzen auszutesten, um auf ein Wunder zu hoffen oder vielleicht, um mal etwas anderes zu erleben. Genau das will ich auch. Etwas Neues sehen und hören - auch als Nichtsehender und Nichthörender, denn ich bin taubblind. Ich möchte dich auf meine Reise mitnehmen. Hier in meinem Buch kannst du mich begleiten.

This Autistic Girl Went to Japan is the inspiring story of a young woman who moved halfway around the world in pursuit of happiness. With humor and remarkable candor, Bianca describes the challenges of applying for a visa during a time of terrifying uncertainty, slogging through endless red tape, and the loneliness that comes with being a stranger in a strange land. Oh, and how she wound up evicting a bat from her new apartment, attending a Pokémon GO event with a bunch of middle-aged women, and discovering the best thrift store in all of Tokyo.

Jennifer Cañaveral es mucho más que una historia de superación personal. A pesar de perder su audición a los nueve meses debido a una meningitis, ha destacado a nivel nacional e internacional en áreas académicas, deportivas y profesionales. Su método de lectura de labios y escucha consciente en múltiples idiomas, junto con su narrativa autobiográfica y la técnica del journaling, ofrece una visión única y positiva de sus experiencias en Cali y el eje cafetero.

In The Future Is Disabled, Leah Laksmi Piepzna-Samarasinha asks some provocative questions: What if, in the near future, the majority of people will be disabled—and what if that's not a bad thing? And what if disability justice and disabled wisdom are crucial to creating a future in which it's possible to survive fascism, climate change, and pandemics and to bring about liberation?

Ido in Autismland opens a window into non-verbal autism through dozens of short, autobiographical essays each offering new insights into autism symptoms, effective and ineffective treatments, and the inner emotional life of a severely autistic boy. In his pithy essays, author Ido Kedar, a brilliant 16-year-old with autism, challenges what he believes are misconceptions in many theories that dominate autism treatment today while he simultaneously chronicles his personal growth in his struggles to overcome his limitations.

This is the remarkable and inspirational story of Oksana Masters, who was born with radiation-induced birth defects and suffered appalling abuse as an orphan, before being adopted and moving to the US, where she went on to triumph over her challenges to win ten Paralympic medals in four different sports.

Martin Hibbert was left paralysed from the waist down by the Manchester Arena bombing which killed twenty-two people on 22 May 2017. Martin’s teenage daughter Eve was one of the 940 injured, in Eve’s case, gravely. The dad from Bolton has since become a leading campaigner both for victims of the atrocity and those with spinal cord injuries. Determined to make a difference he took on the ultimate challenge, scaling Kilimanjaro in a wheelchair, becoming the second paraplegic to do so, and raising a million pounds for charity.

An inspiring and unforgettable memoir that provides hope to others who are experiencing depression, mania, or psychosis, RESILIENT is a deeply personal account about life with mental illness, hearing loss and resiliency. Liz's journey provides encouragement for patients, families, friends, and healthcare workers by showing that recovery is possible.

On a hot July afternoon, Joni Eareckson Tada's life was dramatically altered in a split second. A reckless dive into shallow water took an athletic young woman from health and success to life as a quadriplegic in a wheelchair. In the 45 years since the release of this book - which has more than five million copies in print in over 40 languages - Joni's earnest struggle to find hope has resonated with millions of listeners around the world.

On Good Friday 2010, Melanie Reid fell from her horse, breaking her neck and fracturing her lower back. She was 52. Paralysed from the top of her chest down, she was to spend almost a full year in hospital, determinedly working towards gaining as much movement in her limbs as possible and learning to navigate her way through a world that had previously been invisible to her.

On Boxing Day 2022, in Rome, Hanif Kureishi had a fall. When he came to, in a pool of blood, he was horrified to realise he had lost the use of his limbs. He could no longer walk, write or wash himself. He could do nothing without the help of others, and required constant care in a hospital. So began an odyssey of a year through the medical systems of Rome and Italy, with the hope of somehow being able to return home, to his house in London.

In 2011, three years after leaving the NFL, Steve Gleason was diagnosed with ALS, a terminal disease that paralyzes the entire body. Doctors gave him three years to live. He was thirty-four years old. As Steve says, he is now ten years past his expiration date. His memoir is the chronicle of a remarkable life, one filled with optimism and joy, despite the trauma and pain and despair he has experienced.