Títulos em Pessoas com Deficiências

Gracie wrote Comfort in Darkness after being diagnosed with Parkinson’s Disease, a terminal sentence which he views as the greatest fight of his life, one he knows he will eventually lose. This is Gracie’s defining life statement about his spiritual and technical practice. For the first time, he reveals his time-tested theories and techniques of invisible Jiu Jitsu, a combat system anyone can use to awaken their power and apply it to their everyday lives. An indispensable tool for any fighter or seeker, Comfort in Darkness teaches how to balance and align the mind, body, and spirit.

After years of unexplained health problems, Polly Atkin's perception of her body was rendered fluid and disjointed. When she was finally diagnosed with two chronic conditions in her thirties, she began to piece together what had been happening to her - all the misdiagnoses, the fractures, the dislocations, the bone-crushing exhaustion, the not being believed. Some of Us Just Fall combines memoir, pathography and nature writing to trace a fascinating journey through illness, a journey which led Polly to her current home in the Lake District.

Blind War by Tamer Zaid is a compelling autobiography that recounts the author's journey through adversity as a blind Palestinian navigating life in America. It chronicles his battles with internal and external conflicts, from health challenges like leukemia and blindness to cultural identity struggles and societal expectations. Tamer's story is one of resilience, self-discovery, and finding strength amidst chaos. It highlights the unwavering support of family, the resilience of the human spirit, and the power of faith and determination to overcome life's most daunting obstacles.

Born with Epidermolysis Bullosa (EB), a rare and excruciatingly painful condition that makes her skin as fragile as butterfly wings, Emma Fogarty was not expected to survive infancy. Today, at 41 years of age, she is the oldest living Irish person with the condition, continuing to defy the odds with extraordinary strength, resilience and remarkable achievements. However, every accomplishment Emma makes comes with its own set of obstacles.

For years, renowned ethics scholar Deni Elliott lived with her own moral dilemma: though severely visually impaired since birth, she spent decades attempting to "pass" as sighted, often finding ingenious but problematic workarounds in the process. Everything changed in her 40s when an ophthalmologist diagnosed her as legally blind and she could no longer hide her impairment. To maintain her independence, she would need to use a guide dog and openly present as disabled–a label she had rejected for decades.

Almost 10 years after learning that her son is autistic, Julie Green was also diagnosed, shedding light on a lifetime of feeling othered and misunderstood. Motherness traces Julie's journey from childhood to early motherhood, when she must advocate for her son while navigating her own struggles. With more girls and women being diagnosed in the last decade—many of them later in life—the face of autism is changing. Motherness provides a rich, intensely personal account of what it is like to be autistic through the lens of both a mother and child.

As two siblings, we were walking toward the light. In our mind's eye, it shined brightly, that green light of hope, as multiple sclerosis greatly impacted our lives. We accepted help along the way but not as a sign of defeat. A disabled person is seen as a burden and unfortunately is treated as such. The world doesn't have the patience or understanding of the tremendous struggle one bears living in a world not meant for frailty. This has been a journey of many decades. MS can lead to other health challenges that are formidable in and of themselves, like JC virus or PML.

According to the Center for Diseases Control, 133 million Americans—one out of every two adults—have at least one chronic illness, and half of these are women. While many of these individuals finally have a diagnosis, and are no longer “sick”, they’re still not “well.” They’ve gone through the treatments, taken the medications, and yet still find themselves suffering. So, what do you do after you’ve discovered the root of your condition, and you’re still not healed?

Phyll Zone spent a lifetime feeling lost. Labeled “lazy,” “spacey,” and “careless,” he struggled in a world that refused to speak his language. The constant storm of ADHD and the silent sabotage of dyslexia weren't just academic challenges; they were emotional earthquakes that shattered his self-worth. Lost in Translation is more than a memoir—it’s a revelation. It’s the story of a late diagnosis that finally provided the map to a bewildering mind, transforming a lifetime of shame into a powerful new identity.

After a failed spinal surgery left him broken, Dr. Bhaskar Bora found himself facing a death-in-life: stripped of his identity, his independence, his ego. But in the ashes of collapse, a new truth emerged — one revealed in both the Bhagavad Gita and the paradoxes of quantum science: that consciousness cannot be destroyed, that suffering can be a teacher, and that brokenness itself can become the doorway to wholeness.

Fetal alcohol spectrum disorder (FASD) affects up to 1 in 20 people, and is particularly prevalent among young people in the adoption and fostering system. As a hidden brain injury, FASD can manifest in ways that often lead to challenging behaviors, which can feel overwhelming for caregivers relying on traditional parenting strategies. In this supportive guide, Barb Clark shares her experiences raising a child with FASD - what she got wrong, what she got right, and what you can do to support your own family.

Mike grew up on a tree farm in Missouri and spent his childhood on horseback with dreams of becoming a cowboy. The connection he formed with horses shaped his earliest understanding of freedom and purpose. But as adulthood beckoned, he traded his saddle for a suit, building a thriving career and raising a family while his childhood aspirations faded into memory. When a devastating diagnosis of a rare genetic neurological disease struck in his mid-thirties, everything changed.

This is the biography of a young man with some neurological differences, written in the first person. Through his eyes, we see how he perceives his life and negotiates his reality. His world and his understandings of life may be different from the norm, but we learn to appreciate a special type of soul that should be acknowledged and celebrated as part of human diversity. This book demonstrates the love and nurturance of his mother and the dynamics of his relationship with her. We also enjoy hearing about the comfortable lifestyle that Marcelo has been given, including his worldwide travels.

In this emotionally rich first memoir, the New York Times bestselling author of True Biz retraces her path out of the hearing world and into the deaf community—and seeks to understand the journeys her own children must take. Sara Nović’s early years were filled with music, Bible study, and a strong desire to fit in. But when she failed her school’s mandated hearing test, her worldview was thrown into chaos. Desperate not to be marked as different, she told no one, staying in the hearing world for as long as she could by brute force.

When Bryan Silman was diagnosed with terminal liver cancer, hospice gave him two weeks to live. What followed defied every medical prediction—and became a story no one saw coming. I Am Warrior is the true account of one man’s refusal to die. Written in collaboration with Misty McConnel and Maryam Farooq, this powerful narrative blends raw memoir, emotional psychology, and lived philosophy.

This isn’t your typical recovery memoir. In Not Another Recovery Success Story (Or Is It?), Mike Allen offers a raw, unfiltered look at his decades-long battle with alcoholism, mental illness, and the crushing weight of an identity crisis. With brutal honesty and dark humor, Allen explores how his addiction wasn’t just about alcohol—it was about trying to fill the void of not knowing who he really was.

Jarred McGinnis was born into a Southern US clan where masculinity, capability, and physical violence were all closely intertwined. He was also the victim of violence outside the family: a car crash that has left him in a wheelchair since his early 20s. Two decades later, he is the father of two small girls, living first in East London and now in Marseille. In this ground-breaking memoir, Jarred writes about the family that formed him, and of breaking the chain of intergenerational harm.

Kristy Sheridan survived a deadly plane crash and a sixty-foot plummet off a cliff before she learned to seek God’s will over her own desires. The crash of American Airlines Flight 1420 broke Kristy’s neck and stripped away the identity she found in her prized career. A decade later, she broke her neck again when she fell more than sixty feet down a canyon in Germany. Still, Kristy’s faith remained stagnant.

Driven by the pursuit of perfection and the desire to truly be loved and accepted, Cynthia battled an eating disorder for thirteen long years. “Starving, Bingeing, Purging” is her raw, authentic story, told firsthand; a story not just of suffering, but of resilience, victory, and hope against all odds. In this book, Cynthia openly explores the complex issues of anorexia, bulimia, purging, and food addiction, and shares the intimate details of her journey to reclaim her life.

After losing both legs from the pelvis down at the age of five, Spencer West tackled challenge after challenge, learning to navigate a world set against those with disabilities. In this deeply personal and transformative guide, he reveals how he stopped living by the expectations of others and instead embraced his true identity, passions, and purpose.