Títulos em Pessoas com Deficiências

Lachi is an award-winning musician and leader who awakens the world to this truth: Disability has long shaped our culture and is an identity worth brazenly celebrating. In this book, Lachi welcomes listeners into the vibrant world of Disability Culture, centering identity, innovation, and unapologetic pride.

I never planned to write about my life with cerebral palsy (CP), but after years of absurd, frustrating, and hilarious experiences, I had to share them. This book is part memoir, part guide to navigating an able-bodied world when your body has its own agenda. From my mom almost being mistaken for a prostitute to a first date disaster in a movie theater, my life is full of bizarre encounters. Doctors talk over me, cops have been afraid of me, and strangers treat me like a sideshow.

You will laugh and cry when you listen to how Patti Smith lovingly and honestly reveals transformative lessons gleaned from forty-plus years of caring for (and being tutored by) her son, Christopher. His diagnosis as a baby with Down Syndrome at first tilted her world off-axis, only to reveal itself to be the thing that actually set her worldview at the exact right angle.

Embark on a poignant journey with "Crimes of Dementia," a heartfelt exploration authored by my beloved Terri Lee Martin. In both “Content and Cover,” this book is a testament to Terri's legacy, a legacy tragically interrupted by the relentless grip of dementia. In this book, my words offer a profound glimpse into the emotional odyssey of caregiving. It unfolds as a touching portrayal of the challenges and triumphs that come with caring for someone gradually slipping away.

This powerful memoir tells the inspiring journey of a blind woman who survived years of abuse, homelessness, and betrayal—only to rise stronger than ever. After enduring physical, emotional, and psychological torment at the hands of those she trusted, she found the strength to escape, rebuild her life, and reclaim her power. Through faith, resilience, and an unbreakable spirit, she transforms from a victim to a survivor, proving that no matter how deep the darkness is, there is always a path to freedom, healing, and hope.

Twenty-three-year-old Ardra Shephard is sleeping with the wrong guy, living in a crappy apartment, and spending money she doesn't have on designer shoes, boozy brunches, and weekends in NYC. Making mistakes while you figure stuff out is what your twenties are all about. Then a doctor tells Ardra she has MS, and those two letters split her life into a Before and After.

The spoiler is that Platinum, the shiny precious metal we may associate with glamour and wealth, was an ingredient in one of the chemo compounds. In this context, it functioned as a poison, carrying out the bizarre miracle of chemotherapy where death and life meet. Tracing through the paradoxical tensions of treatment, healing from treatment, succumbing to medicine and claiming autonomy, Hannah Kate guides us through essential components of the journey. There are material resources that will support you—yet much of what is needed requires connecting with the fundamental elements of life.

What if the very thing that once held you back… became your superpower? In Breaking the Limits, renowned neuromuscular physician Dr. Nivedita Jerath takes you on an unforgettable journey through the lives of extraordinary individuals living with disabilities—people who refused to be defined by their diagnoses and instead, reshaped their futures. From courageous patients to trailblazing athletes, scientists, artists, and entrepreneurs, this powerful audiobook explores how strength can be found in struggle, and how disability can be a launching point for purpose, innovation, and greatness.

Autism is the fastest growing and most common developmental disorder. Imagine the frustration and anxiety over taking your child to a team of medical specialists to be told that they have a lifelong and often debilitating developmental disorder with no cure and limited treatment options? Lauren's parents knew something was different about her from the time she was an infant but as she entered Kindergarten in the fall of 1986 her differences were very obvious to everyone around her as compared to other children her age.

For years, they came in on weekends to plan and practice—nearly sixty surgeons, nurses, and anesthesiologists, preparing to harmonize in a vast medical symphony. For the team at Mayo Clinic, it was their most complex surgery to date: a face transplant. At the heart of this event was Andy Sandness. He grappled with feelings of isolation and shame after a disfiguring suicide attempt but was determined to reclaim his future, to be seen as ordinary, and to belong again.

Time in nature supports our well-being. For people who are neurodivergent, it can also stimulate our senses, feed our curiosity and help us find others who share our deep passions. But why do natural environments have such profound effects? If children with autism, ADHD and other neurodivergences spend more time outdoors, could it improve their educational experiences and outcomes? And if they nurture nature connections into adulthood, could this form the roots of their identities?

In Fractured Realities, Ryder Budden shares a deeply personal and raw account of his life with schizophrenia, offering a rare glimpse into the struggle, resilience, and hope that defines his journey. From vivid hallucinations and delusional paranoia to the gradual path toward healing, this memoir explores the highs and lows of navigating a fractured reality. Ryder's story begins with childhood encounters with the impossible, from seeing extra limbs in reflections to vivid visions of God.

What if the barriers we face aren’t walls but bridges waiting to be built? In Unstoppable: The Ric Nelson Story, disability rights advocate Ric Nelson invites listeners into his extraordinary journey of resilience, advocacy, and empowerment. Born with cerebral palsy, Ric learned early that the world wasn’t designed for someone like him. But instead of retreating, he chose to rewrite the narrative—not just for himself, but for countless others navigating similar challenges.

Living with multiple sclerosis was never going to be easy. The phrase 'I rule it, it doesn't rule me' was to become Lydia's benchmark. She clung fiercely to these words. They would booster her strength in the years ahead when at times, fear of the pain and its affects, especially the horrendous agony of an MS attack, would almost break 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 Raymond'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, Raymond explores the shame of miscommunication, the joy of finding community and shines a light on the decline of deaf education in Britain.

Beyond What You See is the eagerly awaited sequel to Confessions from Disability Limbo. Author Kevin Nuñez guides listeners through an active spiritual journey spanning from January 2022 to spring 2025, expanding from disability awareness to God awareness. Kevin uses a fun conversational style to lift others beyond their circumstances. After feeling lost for several years, Kevin realized there was more to his life than his physical limitations. His physical weaknesses revealed his strengths.

Learning to adapt to life after being diagnosed with chronic pain and illness is extremely difficult. Life as you knew it, along with your hopes and dreams for your life, literally gets turned upside down in an instant. This comes with a lot of deep complicated emotions from grief, sadness, anger, frustration to living in a constant state of uncertainty and stress. Most people assume that if you get sick, a medical professional like Dr. House will work endlessly until they have answers and a cure so you can go back to living the life you used to know.

Athena Stevens has never learned the name of the doctor whose lack of intervention at her birth lead to her cerebral palsy, but she feels the consequences of his actions – and inaction – every day. The factor observed first and foremost in her life will forever be the effects of what other people have done to her, rather than her accomplishments. And yet, she was groomed to believe that she would overcome any force that stood in her way.

Living with AuDHD is like being a unicorn—misunderstood, contradictory, and often invisible to others. You shine with creativity and innovation, but struggle to fit in — always feeling 'too much'. Autism and ADHD pull you in opposite directions, creating a lifetime of contradictions no one else can see. AuDHD isn’t listed in diagnostic manuals because until 2013, you couldn’t be diagnosed with both conditions — despite a co-occurrence rate of approximately 50-70%. These two neurotypes often clash, like opposing magnets in the brain. ADHD craves novelty; autism resists change.

Uma coletânea das melhores crônicas publicadas no projeto Histórias de cego, inicialmente um blog e depois um canal de youtube onde muito além de contar um pouco da sua vivência em uma sociedade tão visual, Marcos Lima nos mostra o mundo por seus olhos.