Disability Memoir

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.

Carly-Jay Metcalfe was born with cystic fibrosis, survived a double-lung transplant at the age of 21 and faced a rare cancer at the age of 30. What she has endured should have killed her, but her humour, courage and optimism became her best survival skills. From her hospitalised childhood to her many friendships, loves and losses, Metcalfe shares the fickle nature of life with candour and warmth. She writes with compelling insight about organ donation, opioid addiction and survivor's guilt, while still managing to find joy amongst the wreckage.

Vision in the Dark is Dr. Andre Watson's story of becoming a blind visionary. He is blind, yet he decided to use his life to develop new ways of seeing himself, others, and the world. Andre braved and overcame countless odds. Today he is a licensed clinical psychologist, a world traveler, an award-winning athlete, and a beloved husband, father, and friend. He offers a challenging and awe-inspiring glimpse of life through the eyes of a blind man.

What would you do if it happened to you? If you awoke one day when you were twelve years old to be informed that your life was suddenly over? Well . . . Here is what I did. If you became the wealthiest person you would ever know just three and a half years later? What would that be like? Well, this is what it was like when it happened to me.

Is it possible to find strength in struggle and purpose in pain? Ask Dr. April Jones, a young mother who battled her two-year-old son’s cancer while getting her doctorate. Her struggle to make the heart-wrenching decisions with her family led to a discovery of God, courage, and a happiness within that helped her transform scary misfortune into a joy-filled life. In No Mess, No Message, Dr. Jones shares her real, raw journey and reveals insight into how powerful thinking and strong faith can lead to inner healing.

Subverting an ableist India’s expectations from a disabled person to be ‘inspirational’ and an ‘underdog who made it’ despite their illness, Abhishek Anicca writes about everyday stories of living with disability and chronic illness in this memoir-in-essays.

Just like fox, Heidi has lived on the outer. The ‘official record’ of her life has been her mental health record: primary diagnosis – schizoaffective; comorbidity – major depression, juvenile autism and not her own memories. This is the living, breathing version of Heidi’s mental health file that psych wards, doctors, mental health staff or rehab workers know little about or worse, use as evidence of diagnoses. This is Heidi’s account of what happened, shadowed by the story of a fox who knows he'll never belong.

Andrea struggles to mourn a man who is still alive as she witnesses her father decline into the depths of Alzheimer's. Denial and devastation color her life when she learns her father, Richard, a recently retired surgeon, is diagnosed with Alzheimer's at the age of 67. Her dream to grow closer to him is crushed as the reality of his disease is fully realized. Andrea, a mother of three young children, learns to balance motherhood with daughterhood as she grapples to accept her father's fate.

Disability is neither strange nor distant. Part autobiography, part reflections of social advocate Cassandra Chiu's experiences as a person living with visual impairment, A Place For Us is the story of the first woman to be a guide dog handler in Singapore and the first Young Global Leader of the World Economic Forum in Southeast Asia who happens to be blind.

This honest, outspoken, and thought-provoking memoir by award-winning writer and appearance activist Carly Findlay will challenge all your assumptions and beliefs about what it is like to have a visibly different appearance. Carly lives with a rare skin condition, Ichthyosis, and what she faces every day, and what she has to live with, will have you cheering for her and her courage and irrepressible spirit. This is both a moving memoir and a proud manifesto on disability and appearance diversity issues.

In October of 2008, I was airlifted to Erlanger Hospital in Chattanooga, TN, after a head-on collision with an SUV while riding a motorcycle. When I woke up, I was told I would never walk again or have full use of my hands. Seventy-eight screws, 13 plates, 25 units of blood, and more than 400 stitches and staples later, I became very familiar with physical pain and haven’t had a pain-free day since. That physical battle was harder than I could even begin to explain, but it doesn’t really come close to the one that I went through inside of myself over the years that followed.

A fourteen-year-old teen’s life takes an unexpected turn. Will she be able to overcome the obstacles that life throws at her time and time again? Will she be able to battle her demons and not lose herself, or her life, due to the life-altering diagnosis and the darkness that seems to be lurking around every corner that she turns and overcome? Will she be able to live a life of brighter days ahead of her?

Af's journey starts from the exhilaration of the Rio 2016 Olympic Games to confronting a tumour diagnosis at 29. An unexpected return to the UK meant trading Olympic thrills for surgeries and chemotherapy. This isn't just a tale of medical battles but family relationships, friendships and positivity. Af shared his journey on social media with an unfiltered look into the world of cancer treatment. Set against the vibrant backdrop of Brazil and the medical corridors of UK hospitals, Af's tale is one of resilience, humour, and hope.

I am in a bar in Brooklyn listening to two men, my friends, discuss whether or not my life was worth living. So begins Chloé Cooper Jones' bold account of moving through the world in a body that looks different than most. Born with a rare congenital condition called sacral agenesis, she must contend not only with her own physical pain but the emotional discomfort of others. It is only when she unexpectedly becomes a mother that she confronts the demand to live life fully, propelling her on a journey across the globe, reclaiming the spaces she'd been denied, and denied herself.

I wanted to write a book to uplift mentally ill people of the harshest variety, schizophrenic or schizoaffective like I have. I wanted to tell the story of my own life, like some people see me. I am not a pitiable sad case. I am a hero who’s gone on adventures. Sometimes I was unstable, but that is not the purpose of my story.

In this candid, humorous, and insightful book, author, political science lecturer, and “Dudeist Priest” Arch Grieve provides listeners with a first-hand account of the many lessons he has learned (often the hard way) as a person living with bipolar disorder. This guidebook is a must-listen for anyone who has recently been diagnosed with bipolar disorder or knows someone who has.

Run To The Fire is the exhilarating true story of the incredible life of Rick Collins. A Vietnam veteran whose body was maimed by battle, Rick returned home to extreme tragedy and loss. An unlikely superhero, he blazed a standard of endurance, faithfulness, and sacrifice to be emulated.

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.

Many people give up on God. It’s easy to trust in his goodness and strength when life is easy. But how do we persevere in our faith when life gets hard? Few people can show us how to do that better than Allan Schwartz.

Born with a rare, incurable genetic disorder that doctors misdiagnosed until her 30s, Amy’s right leg swelled until it was 200 percent bigger than her left leg. Her peers bullied her for having an “elephant leg,” and she learned to hide her disability by wearing skirts. In an attempt to recreate her identity as a teenager, she competed in the Miss Junior American Coed Pageant, and—to her shock—she won, only to become known as “the beauty queen with the big leg”.