I Wish My Kids Had Cancer is a fatheras gripping, real glimpse of his familyas struggle to survive with two children with Autism. The book intimately, honestly, and powerfully, addresses the emotional, social, financial, political and medical aspects of a family fighting for their very existence. Learn about the struggle, the epidemic and Help Families In Need! Support Autism Through Song! Download the song aState of Emergencya by world-renowned recording artist Sara Hickman. ALL Proceeds Donated to help Families with Autism! Visit www.iwishmykidshadcancer.com to download or visit www.sarahickman.com to download this powerful, emotionally charged song written in response to this book. Encourage others to listen and download! Help provide hope for those with Autism!

Let's face it, cancer sucks. This book provides real-life advice from real-life teens designed to help teens live with a parent who is fighting cancer. One million American teenagers live with a parent who is fighting cancer. It's a hard blow for those already navigating high school, preparing for college, and becoming increasingly independent. Author Maya Silver was 15 when her mom was diagnosed with breast cancer in 2001. She and her dad, Marc, have combined their family's personal experience with advice from dozens of medical professionals and real stories from 100 teens—all going through the same thing Maya did. The topic of cancer can be difficult to approach, but in a highly designed, engaging style, this book gives practical guidance that includes: How to talk about the diagnosis (and what does diagnosis even mean, anyway?) The best outlets for stress (punching a wall is not a great one, but should it happen, there are instructions for a patch job) How to deal with friends (especially one the ones with 'pity eyes') Whether to tell the teachers and guidance counselors and what they should know (how not to get embarrassed in class) What happens in a therapy session and how to find a support group if you want one A special section for parents also gives tips on strategies for sharing the news and explaining cancer to a child, making sure your child doesn't become the parent, what to do if the outlook is grim, and tips for how to live life after cancer. My Parent Has Cancer and It Really Sucks allows teens to see that they are not alone. That no matter how rough things get, they will get through this difficult time. That everything they're feeling is ok. Essays from Gilda Radner's "Gilda's Club" annual contest are an especially poignant and moving testimony of how other teens dealt with their family's situation. Praise for My Parent Has Cancer and It Really Sucks: "Wisely crafted into a wonderfully warm, engaging and informative book that reads like a chat with a group of friends with helpful advice from the experts." —Paula K. Rauch MD, Director of the Marjorie E. Korff Parenting At a Challenging Time Program "A must read for parents, kids, teachers and medical staff who know anyone with cancer. You will learn something on every page." —Anna Gottlieb, MPA, Founder and CEO Gilda's Club Seattle "This book is a 'must have' for oncologists, cancer treatment centers and families with teenagers." —Kathleen McCue, MA, LSW, CCLS, Director of the Children's Program at The Gathering Place, Cleveland, OH "My Parent Has Cancer and It Really Sucks provides a much-needed toolkit for teens coping with a parent's cancer." —Jane Saccaro, CEO of Camp Kesem, a camp for children who have a parent with cancer

Award-winning author and speaker Lynda Young and hospital chaplain Johnna than Ward offer indispensible help and hope that come from years of experiance and comfort, From the initial diagnosis and throughout the daunting journey, this encouraging and extremely helpful resource offers advice, support, and hope from fellow travelers and professionals Who are experienced With what lies ahead. Book jacket.

In What I Wish I Knew Before Cancer: A Young Man's Memoir, Nicholas Steven Parscale shares his experience with battling cancer. Since his diagnosis of pineoblastoma in 2016 at the age of 10, Nicholas has experienced numerous highs and lows, pain and excitement, and relapses and new treatments. Throughout his journey, he has maintained a positive attitude and has learned a great deal about cancer and resilience. In this book, Nicholas's goal is to share what he has learned over the past several years with other children facing the same disease. His hope is that by reading this book and studying his suggestions and experiences, children with cancer and their families can be just a bit more prepared for the long road ahead of them. Observe Nicholas's cancer journey, and see how cancer is a winding road with ups and downs Discover how adopting a positive mindset and attitude truly transforms a dreadful situation and aids in coping with changes Study answers to common questions that may be asked by children, along with their parents and friends, who are having their first experiences with cancer, and receive support in the form of Nicholas's real-life story Feel inspired by the challenges overcome by Nicholas and his family Take a close look at the different treatments and opportunities available to children with cancer Contents: Chapter 1: Some Birthday Surprise Chapter 2: The Best Medicine of All Chapter 3: What Is Cancer, Anyway? Chapter 4: Going Into Whatever's Up Next Chapter 5: Take Charge of Pain Chapter 6: You're Not Alone Chapter 7: Special Opportunities Chapter 8: Here We Go Again Chapter 9: Living Now and for the Future Afterword Appendix A: Dr. Ginn's Notes Appendix B: My Cancer Treatment Timetable

Making Cancer Fun is the go-to resource for families facing childhood cancer. It offers practical ideas, tools and tips for parents interwoven with a personal story of resiliency and hope.Additionally, each chapter contains interactive workbook pages for parents, designed to meet the individual needs of their child. Get ready for a new cancer conversation!

In Authoring Autism M. Remi Yergeau defines neurodivergence as an identity—neuroqueerness—rather than an impairment. Using a queer theory framework, Yergeau notes the stereotypes that deny autistic people their humanity and the chance to define themselves while also challenging cognitive studies scholarship and its reification of the neurological passivity of autistics. They also critique early intensive behavioral interventions—which have much in common with gay conversion therapy—and questions the ableist privileging of intentionality and diplomacy in rhetorical traditions. Using storying as their method, they present an alternative view of autistic rhetoricity by foregrounding the cunning rhetorical abilities of autistics and by framing autism as a narrative condition wherein autistics are the best-equipped people to define their experience. Contending that autism represents a queer way of being that simultaneously embraces and rejects the rhetorical, Yergeau shows how autistic people queer the lines of rhetoric, humanity, and agency. In so doing, they demonstrate how an autistic rhetoric requires the reconceptualization of rhetoric’s very essence.

One of eight volumes in the cross-disciplinary and issues-based SAGE Reference Series on Disability, this volume explores the arts and humanities within the lives of people with disabilities.