Showing titles in People with Disabilities

This is a very real and bloody look at the journey I made from 19 to 29. I will walk you through the icy halls of drug addiction and dealing, college in Santa Barbara (specifically Isla Vista), depression, suicide, and overdoses. The second part of the book I could only write just recently, as I was, by the Grace of God, able to live the life I knew I always should. Please come with me through the very real and honest look at what it was like to be a young man in the 2010s and how through a million close calls, I finally found life.

When Jeremy and Emily Freeman’s teenage son Caleb was in a devastating car accident, doctors gave him a 10 percent chance of survival. Fear of losing a child was all too fresh for the Freemans—their seven-year-old son, Trey, had died just four years earlier from a genetic immunodeficiency. But God. In #butGod Jeremy shares the incredible story of Caleb’s recovery, the darkness that nearly overtook their family in the waiting, and the #butGod movement that captured the prayers of Christians around the world.

Have you ever wondered how a blind person pours a cup of coffee? Or how they and their guide dog know when it's safe to cross a busy road? When Lois Strachan lost her sight at the age of 21 years, she had to learn the answers to these and countless other questions of how to live as a blind person in a sighted world. In this delightfully quirky and entertaining book, Lois shares some of the secrets she discovered about how to live an “ordinary” life in an extraordinary way despite her disability.

You'll relate, you'll cry, and you'll want to learn more. A story of triumph over tragedy, again. In this moving tale, you'll follow Cristi Bundukamara's life as a blissful newlywed who hopes to give back to the world. Her family grows quickly in the form of both biological and adopted children. Cristi has all that she hoped for and more when a senseless drowning rocks her family. While struggling to pick up the pieces, more tragedy ensues and Cristi has to dig deep to keep moving forward.

先天性疾患を持って生まれ、「生まれた時から歩けなくなることは分かっていた。」という彼が、１２歳で車いすユーザーになり、車いすバスケに出会い、銀メダルを獲るまでをまとめたヒューマンエッセイ。

私たちは本当に「見て」いるのか?触れて、聴いて、初めてわかる、この社会のかたち。時に鋭く、そしてあたたかく。ユーモアに満ちた随想集。

A late bloomer’s coming-of-age memoir asks how does one accept and free themselves from visible and invisible disabilities and still retain their sense of connection and humor? Nothing Special is a disarmingly candid tale of two sisters growing up in the 1970s in rural Connecticut. Older sister Chris, who has Down syndrome, is an extrovert, while the author, her younger, typically developing sister, shoulders the burdens and grief of her parents.

Kicking ASSpergers is the triumphant memoir of one man’s journey with autism and his quest for happiness and self-empowerment despite the many challenges life throws at him. Detailing his struggles with acute anxiety, depression, OCD, psychosis, and suicidal ideation, as well as social stigma and medical bias, Jeremy Tolmie moves through his childhood and into adulthood. Over time, Jeremy starts to alienate the people in his life with his erratic and dangerous behavior. When he meets Dave Ray, a home share provider, Jeremy starts to learn how not to let autism rule his life.

Just when life seemed rosy and the sun was shining, Dr. Bhaskar Bora sustained a severe spinal cord injury in July 2019 following an operation, which left him with paralysis of both legs, a nonfunctioning right hand, and a long stay in the hospital, eventually leading to a forced medical retirement from his medical career and a wheelchair in place of a sports car. Poorer financially but richer in experiences of life, he is now a voice for the disabled and has written the book The Second Chance in Life as an honest reflection of his life experiences.

Negli ultimi decenni si è verificata una profonda rivoluzione nella cura della sclerosi multipla, una disfunzione del sistema immunitario che colpisce 122.000 italiani e 2,5 milioni di persone nel mondo. Grazie allo sviluppo di nuovi farmaci sempre più efficaci e a fondamentali scoperte, dai fattori di rischio genetici e ambientali al ruolo rigenerativo delle cellule staminali nel cervello, ora, finalmente, la vita delle persone che soffrono di questa malattia è sempre più vicina alla normalità.

Lorenzo Amurri non nasce come scrittore, lo diventa in seguito a un tragico incidente di sci che, a soli 26 anni, frantuma la strada artistica sulla quale viaggiava sin da giovanissimo: chitarrista rock, produttore musicale. Un ragazzo dinamico e trasgressivo senza mezze misure. Dall'incidente e dalla sua nuova condizione segnata dalla tetraplegia e dall'impossibilità di stringere ancora tra le braccia la sua chitarra, Lorenzo rinasce. Nel 2008 decide di affidare al suo blog Tracce di ruote "riflessioni, denunce e cronaca della sua seconda vita".

A little over a year of living with bipolar type one. I ended a year off of medications deeply in love and with a stay in jail for joy-riding and fleeing and eluding. My family suffered, my friends suffered, and I suffered. This is a journal starting after my stay in jail. I respond to the journal entries all the following year, surprised mostly by the degree of my mental illness. This is not a self-help audiobook, and I struggle most of the time, not really coming up with many good solutions to my issues. Nothing about the past couple years has been easy.

This book chronicles the journey of Eritrean-born Joseph Woldu. As a child refugee, he found himself having to adapt to changes of place, language, and customs; then as a man forced to relearn much of the same after involvement in a disastrous accident two days before the 9/11 terrorist attacks. What makes Joseph's story so incredible is not that he survived change and tragedy, but how he continually found the strength to improve himself and his circumstances. His story reflects the importance good relationships play in our lives.

We were walking this journey together, yet alone. Two siblings from a close-knit, boisterous family of six. There is nothing like the camaraderie of family to give you the determination to persevere in spite of any obstacle. We were overwhelmed by the disease of multiple sclerosis as well as other autoimmune diseases. Our outward appearance of healthiness was deceiving. Unbeknownst to us, the disease of multiple sclerosis would eventually consume mobility, sight, memory, fine motor skills, speech, and so much more.

They say if you want to make God smile, tell him you have a plan. Dwight’s plan was to live his dream, teach math, coach football, and build a comfortable life for himself. Fate had other things in store for him. The story of Dwight’s physical and emotional journey from life as an able-bodied young man chasing his dreams only to have his world turned upside down by the thoughtless act of a 71-year-old drunk driver.

It never gets better, but it does get easier. That’s the first thing Roz says to anyone who asks him for advice. Anyone who’s fighting like hell, just hanging on or putting the pieces back together. When you’re broken, fixed becomes an obsession.

Stoney McGurrin, in his debut book, brings us on the adventure of his lifetime. Having spent months in the hospital as a four-year-old, where he almost lost his arm, only to have it saved by a famous French surgeon Dr. Chance, he left Leitrim as a teenager on ship across the Atlantic to New York City. The stories are exciting, sad, happy, and true; from 1941 to the present, from pencil to paper.

Look at It This Way answers questions we all may have been reluctant to ask, it gives us a glimpse into what blind people experience living in a sighted world, and it breaks through barriers that may cause people to think that differences equate to superiority or inferiority.

In 1895, a specialist straps five-year-old Katharine Hathaway, then suffering from spinal tuberculosis, to a board with halters and pulleys in a failed attempt to prevent her from becoming a “hunchback” like the “little locksmith” who does odd jobs at her family’s home. Forced to endure her confinement for ten years, Katharine remains immobile until age fifteen, only to find that none of it has prevented her from developing a deformity of her own.

As a result of complications during the birthing process, Amanda was born with cerebral palsy. This book recounts the trauma she experienced as a child, enduring physical, mental, sexual, and emotional abuse from her family, and having a mother who cannot tolerate her cerebral palsy. Amanda found comfort and solace in her grandmother, her '"Gragwa", throughout her childhood. Amanda exposes the naked truth of life with cerebral palsy as she deals with growing up and various relationship issues, friendship issues, loss, and many other things.