Mostrando títulos en Personas con Discapacidades

Voices of Women 2025, Vol. 4 is more than a book, it's a movement. Compiled by international speaker and community builder Kimberly Crowe and published by Woodhouse Publishing, this powerful anthology gathers the stories of women from across the globe who dared to rise, reclaim their voices, and create change in their lives, their communities, and the world.

Jean-Baptiste Dethieux est le père d'une enfant porteuse d'un handicap qui la rend à certains moments toute petite et démunie et à d'autres, grande et forte, si forte qu'elle semble embrasser le monde dans son entier, s'en amuser ou s'en réjouir dans une innocence désarmante. Elle est alors, non seulement cette enfant souffrant d'un handicap, mais aussi l'incarnation d'une joie simple et d'une force de vie irradiante.

Anna grew up in a house that was loving, even if her mum was ‘a little eccentric’. They knew to keep things clean, to stay quiet, and to look the other way when things started to get ‘a bit much for your mum’. It’s only when her mother reaches her 70s and Anna has a family of her own, that the cracks really start to appear. More manic. More irrational. More detached from the world. And when her father, the man who has calmed and cajoled her mother through her entire life is diagnosed with cancer, the whole world turns upside down.

“Old World Blues, New World Nazis” by Ana Franko is a haunting political allegory reflecting the rise of extremism in modern America. Set in a near-future where MAGA forces rule through fear and division, this fictional diary captures the voice of a young Mexican girl hiding from political persecution. Blending historical echoes of fascism with current debates on immigration, nationalism, and human rights, it paints a chilling picture of what happens when democracy crumbles under hate. A must-read for those following U.S. politics, the 2024 election aftermath, and the global rise of ...

Embark on a powerful and inspirational journey with Dawn Green as she battles against the odds in a 35-year-long quest to uncover the truth behind her mysterious and life-threatening health issues. This gripping memoir takes listeners through the highs and lows of an extraordinary life marked by persistence, resilience, and unwavering hope. The book opens with the author's early years, when she first realized that her health was beginning to decline. In succession, a series of perplexing symptoms began to plague her.

Hallo, ich bin eine Autistin im "Spektrum" und erfuhr es erst mit 30 Jahren! Natürlich war ich bei einem Spezialisten, denn zu Anfang konnte ich mir nicht vorstellen, tatsächlich eine Autistin zu sein. Denn ich hatte keine Ahnung von Autismus. Das was ich las, gefiel mir nicht. Um es kurz zu machen, ich wollte keine Autistin sein, bin es aber und es war ein heftiger Schock, behindert zu sein, ohne es gewusst zu haben. Neben dem Schock, fühlte ich mich schrecklich alleine und irgendwie von mir selbst im Stich gelassen. Denn ich lebte ein Leben, womit ich nicht klar gekommen bin.

Fred Rutman was certainly up against it. It being the Grim Reaper. The Reaper unleashed its full arsenal, pitting Fred against much of the medical system he trusted with his life. Even if Fred won the initial battles, could he win the war? The Summer I Died Twenty Times is a medical trauma memoir unlike any other. In one package, Fred Rutman provides all the overcoming adversity, resilience and beating the odds a listener expects. With a side of sarcasm and humor. He may not be the hero you expected. He just might be the hero you need.

David Paterson overcame severe disability and racial prejudice to become a state senator, lieutenant governor, and - unexpectedly - governor of New York. Paterson was the first and only blind governor - other than a man who held the title for 11 days in 1975 - and the fourth person of African descent to hold the office of governor in American history. Paterson may also be the only governor in history to have been arrested outside the governor's office prior to his service.

For many years, Jeffrey Demitrack searched for a meaningful and fulfilling relationship and, most of all, hoped that one day he would find a significant other who understood and unconditionally accepted his struggles with epilepsy. People have their insecurities, and relationships already are hard without throwing seizures into the mix, so his search has been a challenging one.

Emily Owen was a highly intelligent teenager who was also athletic and a skilled musician. Tragically, in her late teens she was diagnosed as suffering from Neurofibromatosis Type 2 (NF2). Since then, Emily has survived many complicated surgical procedures, been close to death, and seen the gradual erosion of all the abilities that defined her personality including the total loss of her hearing. Despite this, she has a remarkable sense of humor and has coped with everything she has been through due to her strong Christian faith, her supportive family, and indomitable personality.

In this author's second book, she details her personal "Roadmap to Healing" that she discovered in order to overcome chronic depression, PTSD, agoraphobia, anxiety, night terrors, obsessive worrying, fibromyalgia, TMJ, plus more! So much devastation was heaped on her as a child due to the selfish act of sexual abuse, but her life has been transformed - and she wants to share what she has learned to help you heal.

In Get in the Boat, Darlene Fuchs shares the powerful and poignant story of her father Richard's experience as a caregiver to his wife Gail during her decline into dementia. This memoir, based on the journals of Richard Sonnichsen, is a heart-wrenching yet inspiring exploration of the enduring power of love, faith, and resilience in the face of life's most difficult challenges.

This is my personal story of battling leukemia as I entered my so-called “golden years.” Turning 65 marked the beginning of a series of profound changes, brought on by both family struggles and personal health challenges. Eventually, I was diagnosed with a rare form of leukemia. I endured grueling chemotherapy, fought through debilitating side effects, and then faced yet another blow — new heart complications and the looming possibility of a second, entirely different cancer.

Blue Water. Nearly two decades after a young-onset Parkinson’s disease diagnosis, Peter Hunt discovers more to smile about every day as he searches for meaning in life’s daily routine. According to Hunt, happiness is a choice, a coping tool to help humankind deal with pain and discomfort. He contends that when considered with an open heart and leveraged with the genuine kindness of helping others, even partial meaning can unlock a divine joy of presence that overshadows most human suffering. Using this recipe for living, Hunt uncovers fragments of meaning in the most unusual—and often...

In 1989, at the tender age of 12 years old, Ms. Meadows awoke from a coma to find herself suddenly struck blind and severely brain injured. This greatly complicated her young life. When she was yet a minor child, her mother sued the doctor who caused this tragedy. This ultimately made Ms. Meadows' situation more desperate than ever. After the settlement; Ms. Meadows' parents continued to deny her treatment for her injuries. As a result, her life went off the rails in a huge way.

A witty and honest account about Lorraine Ansell’s journey with chronic pain due to Hypermobile Ehlers Danlos Syndrome. This genetic life long condition cannot be cured, only managed. Lorraine talks about her life in constant pain and how that has created her personality and even clothes choices. Lorraine’s life is a continual compromise of activities and choices. This book explores her journey as well as the issues with tissues which she now realises were actually a thing and how much pain she has been in. Listen to how she comes to face up to pain and learns to accept and work with pain.

This is book about a man with MS who must learn to make light of his life to bring light to life. Josh got MS at the age of 28 and at that moment he was almost 400 lbs married, straight, and was in a dark place where he tried to commit suicide multiple times. But then he turned his life around and lost 200lbs, got a divorce, came out of the closet, and began stand-up comedy. This brought the light back into his life, gave him a platform to share his story and spread awareness about MS.

For fans of rags-to-riches stories, Be There When I Return is not just about overcoming epilepsy and finding success—it is also for those who are looking for a celebration of love in its purest form. When thirty-one-year-old Michael starts to act out of character, it gets the attention of his roommate and a woman he has started dating. After denying anything is wrong with him, Michael finally decides to visit a neurologist. His life takes an unexpected turn when he receives a life-altering diagnosis of epilepsy.

An insider history of the Blind Boys of Alabama, the longest running group in American music, and the untold story of their world, written with band members and key musical colleagues. The Blind Boys of Alabama are the quintessential Gospel vocal group, and the longest-running musical...

Oliver Mol was a successful, clever, healthy twenty-five-year old. Then one day the migraine started. For ten months, the pain was constant, exacerbated by writing, reading, using computers, looking at phones or anything with a screen. Slowly he became a writer who no longer wrote, and a person who could no longer could communicate with the modern world. In literature, and life, Oliver began to disappear. His doctors can't figure out how to fix him. He suffers a breakdown. One evening, high on pain killers, Oliver Googles the only thing he can think of.