Títulos em Pessoas com Deficiências

Alex Oberholzer verbrachte seine ersten zwölf Lebensjahre im Kinderspital. Affoltern am Albis bei Zürich, in einer hermetisch abgeschlossenen Welte und ohne Kontakt zu den Eltern. In knappen, berührenden Episoden erzählt der Autor vom Leben mit Behinderung, von Kusiosem und den prägenden Erlebnissen seiner ganz besonderen Kindheit und Jugend. "Erinnere ich mich zurück, so tauche ich ein in ein gigantisches Wechselbad der Gefühle. Von Schmerz, Qual und Ungerechtigkeit über Gleichgültigkeit und Langeweile bis hin zu grenzenlosem Glück, Euphorie und Triumph.

My name is Joseph A. Peragine. I am a paranoid schizophrenic. On October 22, 2000, I tried to kill myself in a severely hallucinogenic state due to undiagnosed paranoid schizophrenia. I was suffering from this illness for many years leading up to that day. Every October since I started my recovery in 2000, I reflect on my life and am extremely thankful that I was fortunate enough to have been given a second chance.

In "Not Now Please: Living through Racism, Ableism, and Grief," Elizabeth takes you on an intimate journey through the intersecting worlds of adversity, resilience, and transformation. This compelling narrative is a candid exploration of personal experiences that touch upon the deep-rooted issues of racism, ableism, and the complexities of grief.

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.

An Unexpected Story of Hope & Perserverance: As a young child, something was wrong with Michael. He lacked basic motor skills and was unable to follow simple instructions or answer questions. Testing revealed a diagnosis of autism with a low IQ. Experts insisted that leading an independent life would be impossible for him...and school was not an option.

I am not trying to be a role model, just a possibility. There are obstacles, and people may not always treat you properly, but there is progress. My story is one of many that doesn't choose death over paralysis. It's just a story that doesn't get told often enough.

A touching and deeply personal memoir, Our Brother Jim recounts the author’s experience growing up with a brother with disabilities. Through his parents’ constant care and his family’s loving encouragement, Jim exceeded every doctor’s expectations, learning to do those “everyday” things that proved so difficult for him—like walking, counting, and communicating with others. With a radiant smile and a delightful sense of humor, Jim left a beautiful mark on the world around him. This book is to remember him.

Kimberly Crowe, a highly esteemed figure in her field, made a triumphant return for the third consecutive year with an event of unparalleled magnitude, leaving an indelible mark on International Women's Day. This annual celebration, known as IWD 2023, served as a resounding tribute to the awe-inspiring endeavors of women and girls worldwide, who have tirelessly worked to shape the future.

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.

In her most revealing memoir yet, Carrie is candid about the challenges of marriage, motherhood, and keeping one’s identity in the midst of raising a family. She gives the listener a glimpse into life with a diagnosed child. She shares their experience with puberty, social media, high school, and steps toward independent living. Composed as a series of powerful letters, her writing is gritty yet tender. In prose that is nearly poetic, Carrie makes you feel as though you are old friends, sitting down for a cup of coffee and a heartfelt conversation.

Founder of advocacy organization Diversability and creator of the viral Anti-Ableism Series on TikTok, Tiffany Yu takes readers on a revelatory examination of disability—how to unpack your biases and build a disability-inclusive and accessible world. As the Asian American daughter of...

The Umbrella Picker tells the true story of a woman who was lost for 45 years until she learned that she is Autistic. After a long and relentless journey of searching for answers, the hand of fate finally revealed to her what she had waited a lifetime for. Learning she was Autistic was life changing. She is no longer lost, and having found her own, unique way, Jane has written the (brutally honest!) book she wished was available to her years earlier.

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!

Amanda Harris presents her inspiring autobiography. Travel with her as she shares her life experiences from diagnosis of a visual impairment, at only a few weeks old, to becoming a successful business owner and motivational speaker. An honest, moving and funny story highlighting transformation from the only disabled child in the playground to a strong independent woman.

This is a philosophical and observational book based on the challenges and the triumphs of Paddy Slattery's life which include a severe spinal cord injury leaving him paralyzed, two near-death experiences, and his debut film hitting the cinema and Netflix just as Covid was beginning to make headlines.

This English professor grew up spacey and overweight. Drowning in the unrealistic demands of motherhood, Livingston steals her son's ADHD medication and watches it transform her life—for good and bad. She grows weary of subjective diagnoses and chemical treatments from traditional psychology experts, and experiments with functional medicine—brain mapping and nutritional supplements—as a way to understand her brain's potential, bio-hacking her way to a healthy body and mind.

Un salto facile, provato mille volte in allenamento, qualcosa che va storto: un dolore insopportabile, il corpo che sembra finire all'ombelico, il terrore negli occhi del padre. A soli 16 anni Giulia Ghiretti passa dal preparare i Mondiali di trampolino elastico a un reparto di neurochirurgia. Il verdetto è crudele: non potrà più saltare, e nemmeno camminare. Ma niente può fermare Giulia, che scopre il nuoto, il suo nuovo sport.

After a shocking diagnosis for a rare pituitary disease, and with her eighteen-year marriage in shambles, Risa's life has fallen far from picture-perfect. Recovering from brain surgery and desperate to get back to her former self, she signs up for the bike tour of a lifetime-six weeks from Canada to Mexico on the Pacific Coast Highway. The old Risa could have done the ride in her sleep, but for the new Risa, trapped in a body that no longer feels like her own and stuck in the company of her brain tumor, Bubba, the ride becomes a challenge unlike anything she's ever faced.

Weeks after giving birth, Holly Frances went from being a healthy 26-year-old new mom to paralyzed and on life support—in less than 72 hours. Diagnosed with a rare autoimmune disorder called Guillain-Barre Syndrome, Holly was trapped in her body, unable to move, speak, or hold her newborn daughter. Life Support tells the story of how Holly struggled to overcome the despair, hopelessness and physical pain, to regain her health and get back to being a mother to her daughter.

The yard was a huge piece of property with a forest out back (or at least a few dozen trees). We had a barn and a horse (really a very small pony, but I didn’t know that then) named Romeo, because he liked to roam—often ending up out of the fenced pasture and out on the street. We had chickens, as well, in a coop by the barn up at the edge of the forest.