Faked Disability


Book Description

250 color photos 8.1/2 x 11 * Monster shark fishing, tackle, techniques, boats, destinations, safety, tournaments, stories, equipment information, photos and illustrations. * Beautifully illustrated in full color In this book you will find everything you need to know on how to find, catch and release big sharks. The nine action packed stories in this book will intrigue you enough to go out after one of these beasts. If the stories don't grab you, the 250+ color pictures and graphs will get your attention. Purchasing this book will save you tons of money on gas, gear, and chum by obtaining knowledge on how to find the right sharking grounds and by sight fishing. Shark Fishing, is not a one-time read, you will want to keep this one "on board". "Capt. Mike Schmidt assisted Gurney Productions in obtaining top side and underwater footage for Shark Hunter Series'. He was able to attract, catch, and release large Makos for exhilarating, invaluable footage for the show." Scott Gurney, Producer, Shark Hunters Series. "I have been fishing seriously for sharks in Southern California and around the world for over a decade and this book is the most complete, up to date resourc




Faked Disability


Book Description

Faked Disability, A Shame of America! A textbook to recognize the problem. A Warning to America! "You cannot bring prosperity by discouraging thrift; you cannot strengthen the weak by weakening the strong; you cannot help the wage earner by pulling down the wage payer; you cannot help the poor by destroying the rich; you cannot build character and courage by taking away a man's initiative and independence; and you cannot help men permanently by doing for them what they could and should do for themselves." Abraham Lincoln Society becomes strained and inefficient when there are large numbers of people not working for the common good. The psychological effects of malingering can be horrible. It destroys an individual as a person. He has fallen into a trap and has been enslaved by a generous system, which is quite easy to defraud. It is a rare person who under proper conditions will not accept a hand out from the government or big business. There are also people who will starve to death before they will accept charity. It should be made very clear that every American I know believes in giving all the aid possible to people with real disability and even more than is available. Many people have the mentality of believing that they are entitled to welfare from the big government if they decide they want it. The question must be asked, "Is it fair to society and to the patient in particular to provide him with 'eating bread' of idleness when it has been obtained by fraud?" Eating the bread of society by lying is sinning against God and society. Doctors and lawyers, are you also sinning against God and society when you knowingly, falsely or ignorantly help a person get undeserved money from the government or big business?




Faked Disability: A Shame of America


Book Description

Faked Disability, A Shame of America! A textbook to recognize the problem. A Warning to America! “You cannot bring prosperity by discouraging thrift; you cannot strengthen the weak by weakening the strong; you cannot help the wage earner by pulling down the wage payer; you cannot help the poor by destroying the rich; you cannot build character and courage by taking away a man’s initiative and independence; and you cannot help men permanently by doing for them what they could and should do for themselves.” Abraham Lincoln Society becomes strained and inefficient when there are large numbers of people not working for the common good. The psychological effects of malingering can be horrible. It destroys an individual as a person. He has fallen into a trap and has been enslaved by a generous system, which is quite easy to defraud. It is a rare person who under proper conditions will not accept a hand out from the government or big business. There are also people who will starve to death before they will accept charity. It should be made very clear that every American I know believes in giving all the aid possible to people with real disability and even more than is available. Many people have the mentality of believing that they are entitled to welfare from the big government if they decide they want it. The question must be asked, “Is it fair to society and to the patient in particular to provide him with ‘eating bread’ of idleness when it has been obtained by fraud?” Eating the bread of society by lying is sinning against God and society. Doctors and lawyers, are you also sinning against God and society when you knowingly, falsely or ignorantly help a person get undeserved money from the government or big business?




Fake Disability


Book Description

Sad as it may sound, but yes most of our veterans today are claiming some kind of fake disability. Why are they doing this? Simply because they know they could easily get away with it. They can receive a pension for life ranging from $129 to $3,225 per month. The Veterans Affair (VA) system is old and very flawed. It is not designed to detect most of these fake disabilities. I'll show you exactly how our veterans are able to get away with this dishonorable act. My hope in this book is it will serve as a wake-up call for VA to finally upgrade their whole processing system on disability. This will eliminate the temptation for our beloved veterans to commit fraud. This book is also for those who truly have a legitimate claim and how to get the benefits. I will guide you from start to finish on how to file your claim. If you were in the military or a member of your family, served or are currently serving from one year or twenty years on active duty, reserve, or guard, It doesn't matter whether you got out of the service fifty years ago or just getting out today, it doesn't matter whether you finished your enlistment contract or not, then this book is for you. If you have a legitimate claim then this book will help you get what you truly deserve.




Disability Visibility


Book Description

“Disability rights activist Alice Wong brings tough conversations to the forefront of society with this anthology. It sheds light on the experience of life as an individual with disabilities, as told by none other than authors with these life experiences. It's an eye-opening collection that readers will revisit time and time again.” —Chicago Tribune One in five people in the United States lives with a disability. Some disabilities are visible, others less apparent—but all are underrepresented in media and popular culture. Activist Alice Wong brings together this urgent, galvanizing collection of contemporary essays by disabled people, just in time for the thirtieth anniversary of the Americans with Disabilities Act, From Harriet McBryde Johnson’s account of her debate with Peter Singer over her own personhood to original pieces by authors like Keah Brown and Haben Girma; from blog posts, manifestos, and eulogies to Congressional testimonies, and beyond: this anthology gives a glimpse into the rich complexity of the disabled experience, highlighting the passions, talents, and everyday lives of this community. It invites readers to question their own understandings. It celebrates and documents disability culture in the now. It looks to the future and the past with hope and love.




Being Heumann


Book Description

A Publishers Weekly Best Book of the Year for Nonfiction "...an essential and engaging look at recent disability history."— Buzzfeed One of the most influential disability rights activists in US history tells her personal story of fighting for the right to receive an education, have a job, and just be human. A story of fighting to belong in a world that wasn’t built for all of us and of one woman’s activism—from the streets of Brooklyn and San Francisco to inside the halls of Washington—Being Heumann recounts Judy Heumann’s lifelong battle to achieve respect, acceptance, and inclusion in society. Paralyzed from polio at eighteen months, Judy’s struggle for equality began early in life. From fighting to attend grade school after being described as a “fire hazard” to later winning a lawsuit against the New York City school system for denying her a teacher’s license because of her paralysis, Judy’s actions set a precedent that fundamentally improved rights for disabled people. As a young woman, Judy rolled her wheelchair through the doors of the US Department of Health, Education, and Welfare in San Francisco as a leader of the Section 504 Sit-In, the longest takeover of a governmental building in US history. Working with a community of over 150 disabled activists and allies, Judy successfully pressured the Carter administration to implement protections for disabled peoples’ rights, sparking a national movement and leading to the creation of the Americans with Disabilities Act. Candid, intimate, and irreverent, Judy Heumann’s memoir about resistance to exclusion invites readers to imagine and make real a world in which we all belong.




The Sexual Politics of Disability


Book Description

While the civil rights movement has put disability issues centre-stage, there has been minimal discussion of disabled people's sexuality. This book, based on first-hand accounts, takes a close look at questions of identity, relationships, sex, love, parenting and abuse and demolishes the taboo around disability and sex. It shows the barriers to disabled people's sexual rights and sexual expression, and also the ways in which these obstacles are being challenged. Variously moving, angry, funny and proud, The Sexual Politics of Disability is about disabled people sharing their stories and claiming their place as sexual beings. It is a pioneering work, and essential reading for anyone interested in disability or sexual politics.




No Pity


Book Description

“A sensitive look at the social and political barriers that deny disabled people their most basic civil rights.”—The Washington Post “The primer for a revolution.”—The Chicago Tribune “Nondisabled Americans do not understand disabled ones. This book attempts to explain, to nondisabled people as well as to many disabled ones, how the world and self-perceptions of disabled people are changing. It looks at the rise of what is called the disability rights movement—the new thinking by disabled people that there is no pity or tragedy in disability and that it is society’s myths, fears, and stereotypes that most make being disabled difficult.”—from the Introduction




About Us: Essays from the Disability Series of the New York Times


Book Description

Based on the pioneering New York Times series, About Us collects the personal essays and reflections that have transformed the national conversation around disability. Boldly claiming a space in which people with disabilities can be seen and heard as they are—not as others perceive them—About Us captures the voices of a community that has for too long been stereotyped and misrepresented. Speaking not only to those with disabilities, but also to their families, coworkers and support networks, the authors in About Us offer intimate stories of how they navigate a world not built for them. Since its 2016 debut, the popular New York Times’ “Disability” column has transformed the national dialogue around disability. Now, echoing the refrain of the disability rights movement, “Nothing about us without us,” this landmark collection gathers the most powerful essays from the series that speak to the fullness of human experience—stories about first romance, childhood shame and isolation, segregation, professional ambition, child-bearing and parenting, aging and beyond. Reflecting on the fraught conversations around disability—from the friend who says “I don’t think of you as disabled,” to the father who scolds his child with attention differences, “Stop it stop it stop it what is wrong with you?”—the stories here reveal the range of responses, and the variety of consequences, to being labeled as “disabled” by the broader public. Here, a writer recounts her path through medical school as a wheelchair user—forging a unique bridge between patients with disabilities and their physicians. An acclaimed artist with spina bifida discusses her art practice as one that invites us to “stretch ourselves toward a world where all bodies are exquisite.” With these notes of triumph, these stories also offer honest portrayals of frustration over access to medical care, the burden of social stigma and the nearly constant need to self-advocate in the public realm. In its final sections, About Us turns to the questions of love, family and joy to show how it is possible to revel in life as a person with disabilities. Subverting the pervasive belief that disability results in relentless suffering and isolation, a quadriplegic writer reveals how she rediscovered intimacy without touch, and a mother with a chronic illness shares what her condition has taught her young children. With a foreword by Andrew Solomon and introductory comments by co-editors Peter Catapano and Rosemarie Garland-Thomson, About Us is a landmark publication of the disability movement for readers of all backgrounds, forms and abilities. Topics Include: Becoming Disabled • Mental Illness is not a Horror Show • Disability and the Right to Choose • Brain Injury and the Civil Right We Don’t Think • The Deaf Body in Public Space • The Everyday Anxiety of the Stutterer • I Use a Wheelchair. And Yes, I’m Your Doctor • A Symbol for “Nobody” That’s Really for Everybody • Flying While Blind • My $1,000 Anxiety Attack • A Girlfriend of My Own • The Three-Legged Dog Who Carried Me • Passing My Disability On to My Children • I Have Diabetes. Am I to Blame? • Learning to Sing Again • A Disabled Life is a Life Worth Living




Why I Burned My Book and Other Essays on Disability


Book Description

'Personal inclination made me a historian. Personal encounter with public policy made me an activist.'