Mostrando títulos en Personas con Discapacidades

Si no es cada cuatro años que se celebran los paralímpicos, si no se acerca el Día Internacional de las pcd, cuando las marcas realizan acciones; si no es que el gobierno da beneficios fiscales para impulsar la inserción laboral de este grupo, el resto del tiempo las personas con discapacidad viven entre las sombras.

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.

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.

At the age of thirty-one, Dave Kelly lost his eyesight to a rare disease called retinitis pigmentosa (RP). Up until then, he had lived a life like any other young man, albeit one blessed to be growing up in Liverpool during the heyday of The Beatles and Liverpool FCs win against Leeds in the 1965 FA Cup. But then, one day everything changed. Dave was faced with a choice. He could either let blindness defeat him or he could face it head-on and live as fulfilling a life as he possibly could.

Quentin Kenihan is living proof that superheroes don't need capes, just the right attitude. When he was a kid, Quentin loved Superman. Ironic, really. Quentin didn't need kryptonite to reveal his weakness - born with a rare bone disorder, osteogenesis imperfecta, his bones broke all on their own. When Quentin was seven, Mike Willesee made a documentary about him. Australians fell in love with his wit and never-say-die attitude. Over the years he grew up before our eyes. But there was a dark side to his life. The true story was never told...until now.

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?

Eddie Ndopu was born in 1990 with Spinal Muscular Atrophy (SMA), a rare degenerative motor-neuron disease, and told that he wouldn't live beyond age five. Now, thirty-one years old and stronger than ever, he continues to celebrate each turn around the sun as an existential defiance of the odds. Gay, Black and a wheelchair user, he is now an eminent thought-leader and holds positions at two of the most important organizations on the planet. Sipping Dom Pérignon Through a Straw is Eddie's odds-obliterating story that illustrates what true leadership can look like.

Rheumatoid arthritis was taking over my life. I could barely walk, dress myself, and perform simple daily tasks. I did everything I could to find healing. I tried all of the special diets; I was on all of the medications. Something wasn't right, and I was just getting sicker. This audiobook is about healing from the inside out. Your body is your greatest gift, dearest friend. The only difference between having a body that is your enemy and a body that is your friend is learning to speak its language. You can overcome chronic pain! You are worthy of a great life full of health and happiness!

What do you do when your reality slips away? If you're Sky Yardley and Jane Dwinell, you accept each new challenge, reshape your life, and write. When Sky was diagnosed with "probable early stage Alzheimer's" at age 66, he was determined to live as fully as possible. He researched dementia, talked about dementia, connected with other people with the disease, and wrote about it.

As a stroke survivor who has seen every obstacle imaginable, giving up would have been easy, but "where there's a Bill, there's a way." Along with the support of his family, stroke buddies, countless friends, faith, hope and perseverance he has beaten all odds. Born and raised in South Texas, an athlete his entire life, with a root in faith and family, Bill was well on his way to writing a book about coaching and basketball when a severe stroke stopped him in his tracks.

As a neurodivergent child in a hundred-year-old house, Zaji Cox collects grammar books, second-hand toys, and sightings of feral cats. She dances and cartwheels through self-discovery and doubt, guided by her big sister and their devoted single mother. Through short essays that evoke the abundant imagination of childhood, Plums for Months explores the challenges of growing up mixed race and low-income on the outskirts of Portland, Oregon.

This book is based on a true story about a young lady who really never had a chance and the cycle changed in a way like no other. Her daughter grew up and did her best of making things better for the next generations to come. In this honest and stunning novel, Latoyi Jackson has given her audience a moving story of child neglect along with abuse of an adult with mental illness. Along with secrets which has damaged several individuals during the process.

At the age of 16, Marc Hoberman moved from Yonkers, New York, to Hollywood, Florida. Moving away from his friends was hard enough, but being diagnosed with epilepsy shortly thereafter was even harder. Marc’s story follows him from high school up to his present-day life as an author, teacher, husband, and father. His struggles with seizures, toxic medications, and loneliness were a certain recipe for disaster. Marc’s sense of humor, support network, and successful search for a doctor who would save his life prompted him to make his private story public.

Le 3 avril 2015, on diagnostique à Marine, jeune étudiante dynamique de 21 ans, une sclérose en plaques, appelée plus communément SEP. L'urgence de la situation, le besoin de prendre une décision quant à la prise d'un traitement ou non et le manque d'informations, l'amène à s'interroger. "La maladie c'est toi qui l'as, il faut donc chercher la solution en toi." Son traitement ? Réaliser un projet rêvé : le voyage.

In August 2007 Dianne Woodford woke up to find that she had lost her sight overnight at the age of 38. A type one diabetic since the age of 13 and a single mother of three, Dianne was determined not just to accept it and let people care for her. Instead she set up her own charity to help others in a similar situation and began her own journey to independence with a little help from Hattie, her guide dog.

Kimberly Crowe, a highly esteemed figure in her field, made a triumphant return for the third consecutive year with an event of unparalleled magnitude, leaving an indelible mark on International Women's Day. This annual celebration, known as IWD 2023, served as a resounding tribute to the awe-inspiring endeavors of women and girls worldwide, who have tirelessly worked to shape the future.

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.

Our Life Our Way: A Memoir of Active Faith, Profound Love and Courageous Disability Rights explores an extraordinary love story grown out of engagement with both disability rights advocacy and christian faith communities. This memoir contains thoughtful, often entertaining, and sometimes heart-wrenching anecdotes of a couple’s journey to create their profound relationship and Christian marriage, in a world not yet ready for them.

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.

Essere una donna disabile in un mondo in cui l'immagine femminile appare sempre patinata e perfetta non è facile, ma Antonella Ferrari, attrice e ballerina, malata di sclerosi multipla, non si è mai arresa tanto da diventare un punto di riferimento, una fonte di ispirazione per tante persone meno fortunate. "Mi sono beccata tantissime porte in faccia, tantissime delusioni ma dovevo andare avanti anche per tutti quelli che vivono bloccati per colpa di una malattia."