Showing titles in People with Disabilities

This short biographical work describes the experiences of Chimezie Ihekuna, a Nigerian man born with a facial deformity. From one scenario to the next, Chimezie encounters ostracisation and indifference from peers and elders alike. He reflects candidly here on the impact this has had on his life. His story is an invitation to empathy for all those who listen.

In this moving memoir, Joy Clausen Soto vividly brings us into her world. We see her go from her dream job to fighting for her life, and how she is able to come back from it all. You can't avoid falling in love with her quirks, indomitable spirit, and wry sense of humor. Soto takes listeners on a compelling journey as she faces cancer and the challenges she encounters while re-entering "normal" life.

Sometimes, dyslexia can go unnoticed for years, almost half a lifetime in fact. The effects of dyslexia are more than just bad spelling and illegible handwriting. I didn’t realize I was dyslexic until I was 41. By that time, I’d lost my job due to spelling mistakes more times than I can remember. But dyslexia is more than just making mistakes.

Tracey had been told this so often as a child. Yet, two months after the horse-riding accident, Tracey was still not able to fulfil it. In fact, at that stage, she couldn’t do anything for herself. You’d think that after nearly losing her life and her abilities to live life as it was before because of the riding accident, that she’d be nervous about getting back on a horse. But her love for horses and riding was so deeply ingrained within her that she couldn’t imagine a life without it. Getting back on a horse...she was determined that she would.

Randi-Lee’s true story of coming to terms with her depression. Sharing thoughts around suicide and the harsh reality of feeling the need to hide these thoughts, each chapter outlines coping strategies that can help an individual explore their own mental health and lovingly embrace themselves. Worksheets are provided at the end of the book to but the strategies into practice. Stopping the stigma of mental health starts with speaking honestly and openly. Topics discussed include: therapy, medication, coping mechanisms, suicide, negative self-talk, positive self-talk, and self-care.

Tiffani, the author, becomes an intimate friend as you speaks to you about her deepest thoughts, fears, and worries. Her love, strength, honesty, and determination to care for her family at all costs is inspiring.

This book begins with focusing on dealing with the societal ramifications/stigma of mental health disorders, the LGBTQ spectrum, and also looking at the religious stigma of the two. Finally, I will be telling my life story mainly from the years of 2012 to 2018 for the most part. Coming to terms, with my mental health disorder and identifying as a gay male.

A young man with special powers is forced to retire from a life of violent crime and escape from New York City at the age of 18. He gets his life together and becomes a respected physician. Thirty years later, he is afflicted with a mysterious illness silently sweeping across the globe. While desperately struggling to find redemption and a cure, he learns that violent associates from his past and federal law enforcement agents are still relentlessly in pursuit.

When a 200-pound glass partition fell on Donna Fado Ivery's head resulting in brain injury, disability, and chronic pain, she could no longer count on walking, speaking, or thinking. How would she care for her infant, her preschooler, her husband, and herself? How would she continue to serve as pastor? With humor and humility, this inspirational memoir speaks to Donna’s struggle through medical, social, and church prejudice with the abiding support of family and the Holy Spirit.

Kelley Jo Burke embarks on a wild journey to understand many things, including the part where her grandfather sort of murdered her grandmother. Returning to a house filled with her first memories of childhood, she begins to explore the complex origins of her own anxiety. Along the way, she reflects on alienation and immigration, mental health and generational trauma, and the nature of memory itself. A memoir filled with raw honesty, comedy, tragedy, and grace.

This is my true life story growing up with dyslexia. How I almost allowed dyslexia to destroy my life. The education system failed me. I slipped through the cracks. Dyslexia controlled most of my life. I could still have a life without reading and writing. I was able to get married. Raise a family and run my own business. How my whole world changed overnight. For 62 years, I stayed silent.

Pulling back the veil of disability, the family’s journey offers insights and understanding about the inherent complexities of daily life. With a son labelled "disabled", the family is committed to fostering a “good life” for Matthew. Standing against ingrained societal tendencies that patronize and marginalize people with disabilities, they reject segregated approaches.

Shot point-blank in the side of the neck, Michael Kiel was completely paralyzed from the neck down on April 16, 1993. As a 19-year-old sophomore at Penn State - Altoona campus, the world he knew vanished. It was turned upside down and inside out, and the next four months in the hospital and rehab center would test every fiber of his being. This memoir is about his perspective on life - his entire life - before, during, and after a life-altering spinal cord injury.

A displaced person (now called refugee or economic migrant), aged 19, escapes in 1950 from behind the Iron Curtain with his mother's and her friends' help. He maneuvers through minefields and swims across icy waters and past Russian patrols to reach Salzburg and then Switzerland, hoping to catch up with his brother (who by then had migrated to Australia). He makes it back again, falls in love, but then emigrates to Canada to start a new life, gets to University in Toronto, and is then joined by his mother after escaping in 1956 during the Hungarian uprising.

Life is hard. Add in a disability, and it can be even more challenging. Tait knows. In My Name Is Tait, Tait writes about his successes, challenges, and hard times as he faces a world that doesn’t always accept his disability. In this book, you’ll have a front seat as Tait shares his thoughts on disability, family, education, work experience, and much more.

Perhaps, you are one of three girls, or one of five boys that was sexually abused by the time you were 18 years old. Unfortunately, I fell into that nasty category. In preparing to write my first memoir, Identifying and Healing Childhood Sexual Abuse, I came upon a list of approximately 99 different after-effects that come as a result of sexual abuse. Finally, I held in my hands, a list of words that totally and completely described myself! I pray that this audiobook will give you the information that you need for a total and complete healing in your life!

Just before Christmas in 2012, at age 53, John LeMieux lost his left leg to a recurrence of sarcoma. The unique 20-hour rotationplasty surgery - never done on a man his age - was followed by six months of bed rest. It was only the beginning of years of physical, spiritual, and emotional growth. In this memoir, John recounts the lows and highs of a life forever altered.

The book is an exciting true story filled with adventure and humorous anecdotes. The narrative starts by providing a background from earlier ancestors - through four generations. The author gives a unique account, beginning in Chipinge, located in Zimbabwe's eastern highlands. The villagers are confused by the ambiguous nature of how their ancestral land changed ownership.

This collection of poems was written from the day the author was sent to the emergency room through her first phase of radiation and chemotherapy treatment. Christina uses poetry to share her lived experience as a teacher, a patient, a psychologist, and a neurodivergent person. Kiss Your Brain: Diagnosis Diaries shares poems that fit under the categories of “on beautiful brains", “on resilience", and “on renewal".

The world spun and rolled as I collapsed at Macy’s in San Francisco to the voices of Christmas carols being sung and bells ringing. Fresh out of the ICU and a week later, a beige man gave me a beige folder with a dark diagnosis that would color the rest of my life - multiple sclerosis. This set off a tidal wave, a tsunami inside of me that ravaged my body and crushed my lungs. The MS Diaries is a memoir that seeks to impart the journey inside one man’s mind struggling with a severe chronic illness through uncensored personal anecdotes and humorous situations.