Disability Memoir

Annie and Rolf Lulloff were entering an exciting stage of life in 1976 when the first signs of health issues that lie ahead for Annie began to emerge. A sudden loss of sense of smell, severe anxiety attacks, vision issues, and other neurological challenges piled up, eventually culminating in a diagnosis of Parkinson’s disease on New Year’s Eve, 1989. But the Lulloffs were not about to let Parkinson’s get the best of them.

My journey with mental illness, specifically bipolar disorder, has woven itself throughout my life for 40 years. Whether it was active, or dormant, it has always lurked in the shadows. But, this illness, like any illness, can be managed and maintained.This story is particularly relevant for today's society. It is our charge to know a segment of our society who, for the most part, is misunderstood. When the Brakes Fail provides a forum for understanding the myths, the injustices, and the stigma of mental illness.

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. 

When Markisha was pregnant, the doctors found out her baby has anencephaly and told her the best option she has was to get an abortion. She refused and kept going with the pregnancy. The doctors gave the baby a short time after birth to live, but she lived up to two and a half years old. Her name was Miracle.

Arriving in the UK from Jamaica at the tender age of 14, Keisha shares her empowering lived experiences growing up with undiagnosed Dyslexia and Dyspraxia, while facing several intersectional challenges that include culture, race, and the UK education system.

“Canal dói?” “O que é que eles fazem no Japão?” “Os Menudos são legais?” Stella Estrela não se dedica a responder nenhum desses questionamentos, mas a apresentar a autora dessa lista tão peculiar de perguntas. Stella nasceu com a síndrome de Williams-Beuren, uma desordem genética rara que impôs, de saída, enormes desafios a ela e a seus pais.

Escrito quando Naoki Higashida tinha apenas 13 anos, o conjunto de ensaios reunidos neste audiolivro conta, do ponto de vista do próprio Higashida, a experiência de ser autista. Preso em seu mundo individual, muitas vezes ele exibe comportamentos vistos como estranhos, peculiares, “inadequados”. Seja repetindo palavras e frases aparentemente sem sentido ou evitando contato visual com outras pessoas, Naoki tem uma enorme dificuldade de se comunicar e de socializar.

Theresa Marafito, daughter of Irish immigrant parents, was born in 1933 in New York City, blind in one eye with partial vision in the other. She was a precocious child who wanted to appear “normal” to her peers and family, regardless of her disability. Her game was to be independent, not dependent, and would rarely ask for help. At 19, she graduated magna cum laude with two master’s degrees. Theresa and her husband, Jerry, who was also visually impaired, would build a house on a shoestring budget and had two daughters; one who was also born visually impaired.

Sam always knew he was starting life on the back foot. When his parents split, Sam, his mother and his brother had to learn to survive in a world not built for single-parent families. Add to that Sam's diagnosis with a form of dwarfism and the odds seemed stacked against them. As surgeons kept breaking and resetting Sam's legs in attempts to keep him walking, disability and poverty collided, and it took all the family's strength not to crumple in the impact. In Broke, lawyer and disability advocate Sam Drummond weaves a poignant, stirring and deeply compassionate tale of life on the fringes.

«Sono Rachele e ho 29 anni. A un mese dalla nascita, è stato detto ai miei genitori che avevo la fibrosi cistica, una malattia genetica degenerativa da cui non si può guarire. La malattia non si vede perché colpisce principalmente gli organi interni; tutte le secrezioni sono alterate e molto dense, il muco ristagna ed è difficile respirare. Quando sono stata invitata a un evento della Fondazione per la Ricerca sulla Fibrosi Cistica, mi sono chiesta: come faccio a unire la mia passione per i motori con quello che mi sta più a cuore?»

Robert was a young man struggling to make it on his own when in 1990, he suffered a violent and traumatic experience when someone put a bullet through his brain. Robert tells the amazing story of survival during a time when life shriveled to dark emptiness and his future seemed hopeless.

A story about a dead man walking. A journey through depression, happiness, divorce, death, survival, and so much more. Stories about life as a chef and life with a traumatic brain injury (TBI). These are the real stories about the difficult process of recovery from a motorcycle accident and how life continues afterward.

When I found out I had cancer, I only knew one person who had beat it, and she did not come to mind. Finding out the president had beat it without chemo or radiation gave me hope. I feel my assistance was critical to my beating cancer. Your own research and knowledge, along with your gut feelings, will help guide you. This book is my belief, and I feel cancer is beatable because I was able to beat it. I believe thinking out of the box is sometimes the solution.

Sent blind soon after birth, David Hume stubbornly refused to live the limited life well-meaning elders and social norms expected. To date, that encompasses years in a blind institute, two marriages, grieving for two outstanding wives, founding recruiting firms, devising marketing techniques, facing business collapse, sailing ocean races, and through much of it, being the lead singer in popular bands. If you enjoy a short biography that inspires, saddens, cheers, and sticks in your memory, then don't put aside Blind Without Barriers.

Riding the Rollercoaster invites listeners to embark on an emotional and enlightening journey. By sharing her story, the author gives a voice to countless individuals who grapple with this condition, offering a beacon of hope for a brighter future.

Cancer is cancer. Chemo is chemo. Right? That's what Mel thought before she received her diagnosis. But she quickly found out she had a lot to learn! From bird poo to shingles, Aunt Sally to burnt boob, and too many other "special joys" to mention: Who knew?

When my wife Cheryl saw what I was doing, she asked me to chronicle our almost 30-year journey through Alzheimer's. As I began to write and post blogs of the trip, it became apparent that I had a love of writing and an audience for our story. I soon developed a large following, and the blog almost took on a life of its own. The blog has morphed into much more than I ever dreamed. From the comments and feedback I received on many posts, it became apparent that I needed to try and turn this into a book. Many people battling this disease and being caregivers need to know they are not alone.

Johann König verliert als Kind durch einen Unfall fast vollständig seine Sehkraft. Wie kann man sich Kunst erschließen, wenn man sich auf seine Augen nicht verlassen kann? Was ist Sehen überhaupt, wenn die Welt um einen herum verschwimmt? In seinem Buch "Blinder Galerist" beschreibt Johann König, wie es ihm gelang, die Welt und die Kunst neu wahrzunehmen. "Die Bilder, die im Kopf entstehen, sind genauso wichtig wie die Bilder an der Wand".

I have always had difficulty seeing. It started as a child with difficulty seeing at night. Never in my wildest dreams did I think I would one day be diagnosed with a rare condition that could eventually take my vision completely. This book touches on some of the struggles I, and others suffering with visual difficulties, go through. It is my hope this will give an understanding to others and help those dealing with their own issues to find peace knowing they are not suffering alone.

Imagine waking up and everything you knew was suddenly unrecognizable. No memory of your friends, family, or even your children remains. This is the story of one brave woman beginning her new life after a traumatic brain injury. Join her on this journey of discovering faith, love, adversity, and victory through the unforeseen events of life.