Download or read book Fuck this Chronic Illness Too written by Color-Me-Crazy Designz and published by Independently Published. This book was released on 2023-11-29 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Living with a chronic illness can be tough, and sometimes it feels like the world just doesn't get it. Finding ways to relax and have a laugh can be challenging. You deserve more than just sympathy. You need something that understands your unique situation, brings a smile to your face, and lets you escape from all the challenges of daily life with chronic illness. This one-of-a-kind coloring book is packed with understanding, humorous quotes and a healthy dose of adorable cats combined with quirky designs. Enjoy hours of endless entertainment as you color your way through relatable illustrations that perfectly capture the ups and downs of life with a chronic illness. Get ready for some therapeutic laughter! From the creator of Fuck this Chronic Illness. 25 Edgy quotes full of swear words to make those tough days easier Printed single-sided on white paper Perfect gift for anyone with a chronic illness Beautiful designs to take your mind off your illness Get your paws on this coloring book today! CONTAINS ADULT LANGUAGE. NOT INTENDED FOR CHILDREN.
Download or read book Fuck this Chronic Illness Coloring Book written by Color-Me-Crazy Designz and published by Independently Published. This book was released on 2021-02-18 with total page 50 pages. Available in PDF, EPUB and Kindle. Book excerpt: Having a chronic illness is tough. Lighten the load with this encouraging and understanding coloring book for sick chicks ... or anyone with a chronic illness. Swear away your chronic pain. 25 Edgy quotes full of swear words to make those tough days easier Printed single-sided on white paper Perfect gift for anyone with a chronic illness Beautiful designs to take your mind off your illness CONTAINS ADULT LANGUAGE. NOT INTENDED FOR CHILDREN.
Download or read book Sex Interrupted written by Iris Zink and published by . This book was released on 2020-12-15 with total page 172 pages. Available in PDF, EPUB and Kindle. Book excerpt: By the year 2030, as many as 171 million people in the U.S.- more than half of all Americans-will be living with at least one chronic medical condition (data from The Robert Wood Johnson Foundation). Illness or disability can easily derail a person's sex life-but it doesn't have to be that way. Using kindness, honesty, and humor, Iris Zink, BSN, MSN, ANP, RN-BC, explores the ways illness or disability can affect a sexual relationship and offers suggestions on how to regain intimacy. She also describes existing myths about sex and debunks them with real-life examples. Most importantly, you'll learn that, no matter how a person's body changes, no-one should have to give up sex. Ms. Zink has 20 years of experience in treating sexual health complications related to chronic illness, and in writing and lecturing to healthcare providers on sexual health subjects. She has enabled thousands of people to experience fulfilling sex and meaningful intimacy-she can help you, too!
Download or read book Surviving and Thriving with an Invisible Chronic Illness written by Ilana Jacqueline and published by New Harbinger Publications. This book was released on 2018-03-01 with total page 178 pages. Available in PDF, EPUB and Kindle. Book excerpt: “An important antidote to the dogmatic ‘kale and vitamins’ tone of most ‘self-help’ literature.” —Alexa Tsoulis-Reay, senior writer, New York magazine Popular blogger Ilana Jacqueline offers smart and savvy advice, humor, and practical tips for living with an invisible chronic illness. Do you live with a chronic, debilitating, yet invisible condition? You may feel isolated, out of step, judged, lonely, or misunderstood—and that’s on top of dealing with the symptoms of your actual illness. Take heart. You are not alone, although sometimes it can feel that way. Written by a blogger who suffers from an invisible chronic illness, Surviving and Thriving with an Invisible Chronic Illness offers peer-to-peer support to help you stay sane, be your own advocate, and get back to living your life. This compelling guide is written for anyone suffering with an illness no one can see—such as postural orthostatic tachycardia syndrome (POTS), chronic fatigue syndrome (CFS), fibromyalgia, multiple chemical sensitivity (MCS), Lyme disease, lupus, dysautonomia, or even multiple sclerosis (MP). This book will tell you everything you need to know about living with a complicated, invisible condition—from how to balance sex, dating, and relationships to handling work and school with unavoidable absences. You’ll also learn to navigate judg-y or skeptical relatives and strangers and—most importantly—manage your medical care. Suffering from a chronic illness doesn’t mean you can’t live an active, engaged life. This book will show you how.
Download or read book In Sickness and in Health written by Lucille Carlton and published by Dell. This book was released on 1997 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Married for almost fifty years, Lucille Carlton and her husband Bob had a very good marriage, maintaining sexual intimacy through two chronic illnesses--he cared for her when she was debilitated for many years by a rare skin disease, and she cared for him through sixteen years of Parkinson's Disease. "In Sickness and in Health: Sex, Love and Chronic Illness was originally published by the National Parkinson Foundation and is Lucille's active loving tribute to Bob. In it, she shares their mutual discoveries and what she has learned as a speaker and as a columnist for the National Parkinson Foundation. There are no rules for sex and intimacy. Partners should delight in whatever is mutually acceptable and which brings pleasure to each of them. "In Sickness and in Health gives frank information about sexual practices including non-stressful positions and alternatives to intercourse such as oral sex and masturbation. In the book Lucille Carlton also confronts the issues of women's post-menopausal physical changes, impotence, and depression. She advocates open communication between partners and between couples and their doctors--since it's essential to understand the limitations of an infirmity and the potential side effects of medicine. She addresses the needs of both partners, the afflicted and their caregivers, and has a special chapter about being a senior single and survivorship. The strengths that hold a marriage together in later years are those practiced earlier when both spouses are young and healthy--patience, honesty, humor, giving more than 50% and just not giving up. These are vital ingredients for lasting sexual intimacy. Both partners in a couple also need to understandthat their ever-present need for touching, caring and love may be a crucial factor in coping with the challenge of chronic illness.
Download or read book The Ultimate Guide to Sex and Disability written by Cory Silverberg and published by Cleis Press. This book was released on 2016-09-06 with total page 411 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Ultimate Guide to Sex and Disability is the first complete sex guide for people who live with disabilities, pain, illness, or chronic conditions. Useful for absolutely everyone, regardless of age, gender, or sexual orientation, the book addresses a wide range of disabilities — from chronic fatigue, back pain, and asthma to spinal cord injury, hearing and visual impairment, multiple sclerosis, and more. Expertly written by a medical doctor, a sex educator, and a disability activist, The Ultimate Guide provides readers with encouragement, support, and all the information they need to create a sex life that works for them. The authors cover all aspects of sex and disability, including building a positive sexual self-image; positions to minimize stress and maximize pleasure; dealing with fatigue or pain during sex; finding partners and talking with partners about sex and disability; adapting sex toys; and more.
Download or read book Sexuality and Chronic Illness written by Leslie R. Schover and published by Guilford Press. This book was released on 1988-06-10 with total page 380 pages. Available in PDF, EPUB and Kindle. Book excerpt: This much-needed work presents a clear, sensitive, and practical guide for clinicians who treat sexual problems among chronically ill men and women. Providing a comprehensive analysis of the difficulties faced by these individuals in their attempts to live full lives, the volume teaches clinicians basic skills needed to comfortably discuss sexuality with patients, assess sexual problems using both psychological and medical approaches, and create a systematic treatment plan. Authors Schover and Jensen's consistent emphasis on integrative assessment and therapeutic techniques goes a long way toward rectifying the imbalance often created by a strictly medical or psychological techniques.
Download or read book The Things We Don t Say written by Julie Morgenlender and published by . This book was released on 2020-03-15 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Chronically ill people don't always talk about it. Until now.Spanning different ages, ethnicities, genders, sexual orientations, and diagnoses, forty-two authors from around the world open up in fifty true stories about their chronic illnesses and their search for answers, poor treatment by doctors, strained relationships with loved ones, self-doubt, and more. They share the warmth of support from family and friends, the triumph of learning coping mechanisms, and finding ways to live their dreams. These stories are honest, raw, and real, and if you have chronic illness, you will find comfort and companionship in these pages. For everyone else, if you have ever wanted to know more about your loved one's experience with chronic illness but didn't want to ask the wrong questions, this book will have some answers, and more importantly lead you to a new-found understanding.
Download or read book Love in the Time of Chronic Illness written by Barbara Kivowitz and published by . This book was released on 2018-06-12 with total page 224 pages. Available in PDF, EPUB and Kindle. Book excerpt: Having made an emotional commitment, with or without marriage vows, most people expect their partners to care for them when a devastating diagnosis is made or an accident occurs. But amid the medical, financial, and logistical concerns, a couple's emotional relationship is often an unforeseen casualty when illness and injury occur. For most, a health crisis means both partners need to recalibrate their roles in the new reality of their relationship. Love in the Time of Chronic Illness examines what happens when illness becomes part of a relationship, and includes dozens of real couples' frank stories about navigating the medical and relational mazes. These stories, along with practical and thoughtful guidance from a variety of experts in the medical, spiritual, and legal realms, help partners not just get through a crisis, but grow stronger as a couple.
Download or read book Easy for You to Say written by Miriam Kaufman and published by Firefly Books. This book was released on 2012-11-01 with total page 287 pages. Available in PDF, EPUB and Kindle. Book excerpt: Practical information for teens and their families. Praise for the previous edition: This very unusual book...is loaded with the kind of information disabled teens often need but may be too embarrassed to ask for. --Booklist The teen years are some of the most demanding. Even the most well-adjusted youth struggles with the intense daily challenges of friends, family, school and wider society. But these problems pale in comparison to those faced by teenagers with a handicap or chronic illness such as spina bifida or cystic fibrosis. "Get over it" or "it's just a phase" is idle advice and little more than offensive. "Easy for you to say," is the teenager's often-heard -- and reasonable -- response. Easy for You to Say profiles the lives of uniquely challenged teens as they work hard to make sense of the world and their places in it. The questions they pose are frank and courageous, many include street language that teens can identify with and readily understand. The issues front and center in their lives are addressed, such as family, doctors and medical issues, friends and dating, school and work, alcohol and street drugs, medications and sexuality. Useful charts give reliable information on medication interactions and side effects. Kaufman is straightforward and honest, and provides solid information. Easy for You to Say to Say addresses issues that often are not easy or pretty. It offers solid practical advice, straight talk and honest answers to questions that many would be too embarrassed to ask.
Download or read book Super Sick written by Allison Alexander and published by Phoenix Quill Press. This book was released on 2021-05-31 with total page 252 pages. Available in PDF, EPUB and Kindle. Book excerpt: Superheroes aren't sick. They certainly don't have chronic pain, sexual dysfunction, or diarrhea. After all, spandex suits and sudden bowel movements don't mix. Do they? With raw sincerity and tongue-in-cheek humour, Alexander holds nothing back while discussing how to navigate doctors, dating, sex, friendships, faith, and embarrassing symptoms. Part memoir, part research, part pop culture analysis, Super Sick offers a friendly hand to anyone with chronic illness, a reminder that they aren't alone and have much to offer the world. With a new foreword, updated information, and bonus materials, this second edition is a must-read for anyone who has-or knows someone who has-a chronic illness.
Download or read book The Lady s Handbook for Her Mysterious Illness written by Sarah Ramey and published by Anchor. This book was released on 2021-05-11 with total page 434 pages. Available in PDF, EPUB and Kindle. Book excerpt: The darkly funny memoir of Sarah Ramey’s years-long battle with a mysterious illness that doctors thought was all in her head—but wasn’t. In her harrowing, darkly funny, and unforgettable memoir, Sarah Ramey recounts the decade-long saga of how a seemingly minor illness in her senior year of college turned into a prolonged and elusive condition that destroyed her health but that doctors couldn't diagnose or treat. Worse, as they failed to cure her, they hinted that her devastating symptoms were psychological. The Lady's Handbook for Her Mysterious Illness is a memoir with a mission: to help the millions of (mostly) women who suffer from unnamed or misunderstood conditions—autoimmune illnesses, fibromyalgia and chronic fatigue syndrome, chronic Lyme disease, chronic pain, and many more. Ramey's pursuit of a diagnosis and cure for her own mysterious illness becomes a page-turning medical mystery that reveals a new understanding of today's chronic illnesses as ecological in nature, driven by modern changes to the basic foundations of health, from the quality of our sleep, diet, and social connections to the state of our microbiomes. Her book will open eyes, change lives, and, ultimately, change medicine. The Lady's Handbook for Her Mysterious Illness is a revelation and an inspiration for millions of women whose legitimate health complaints are ignored.
Download or read book Guiding Principles for Developing Dietary Reference Intakes Based on Chronic Disease written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2017-12-21 with total page 335 pages. Available in PDF, EPUB and Kindle. Book excerpt: Since 1938 and 1941, nutrient intake recommendations have been issued to the public in Canada and the United States, respectively. Currently defined as the Dietary Reference Intakes (DRIs), these values are a set of standards established by consensus committees under the National Academies of Sciences, Engineering, and Medicine and used for planning and assessing diets of apparently healthy individuals and groups. In 2015, a multidisciplinary working group sponsored by the Canadian and U.S. government DRI steering committees convened to identify key scientific challenges encountered in the use of chronic disease endpoints to establish DRI values. Their report, Options for Basing Dietary Reference Intakes (DRIs) on Chronic Disease: Report from a Joint US-/Canadian-Sponsored Working Group, outlined and proposed ways to address conceptual and methodological challenges related to the work of future DRI Committees. This report assesses the options presented in the previous report and determines guiding principles for including chronic disease endpoints for food substances that will be used by future National Academies committees in establishing DRIs.
Download or read book Fuck Off I m Coloring written by Dare You Stamp Co. and published by Cider Mill Press. This book was released on 2016-09-06 with total page 112 pages. Available in PDF, EPUB and Kindle. Book excerpt: Color the shit out of this new stress-relieving swear word adult coloring book! With daily stresses like annoying coworkers, red-faced bosses, endless traffic, and whatever shit you have going on at home, sometimes all you need to tell everyone to “fuck off.” Now you can say it in color! Relieve some stress with easy and beautiful art—that also happens to feature your favorite profanities. Feel the “zen” wash over you as you color in or outside the lines however you damn well please. Take your defiance up a notch with more complex patterns, or take the easy route when you unwind. Do whatever the fuck you want.
Download or read book Yet Will I Praise Him Living and Parenting with a Chronic Illness written by Hannah Wingert and published by Ambassador International. This book was released on 2020-11-17 with total page 131 pages. Available in PDF, EPUB and Kindle. Book excerpt: Motherhood can often feel overwhelming and isolating, but for moms with a chronic illness, those feelings are often intensified. When your life is a constant battle with pain, fatigue, and isolation, it's easy to lose sight of any joy in your life. Wife and mother Hannah Wingert knows this all too well. After finally being diagnosed with a chronic illness following the birth of her fourth child, Hannah has had to come to terms with her diagnosis and to learn to be a wife and mother in the midst of her invisible illness. In her inspirational book, Yet Will I Praise Him, Hannah opens up candidly about her own struggles of living and parenting with a chronic illness. She will help you understand: -how to use your chronic illness to grow in your faith, -how to balance your marriage and parenting, and -how to live each day with hope so you can not only survive the challenges you face, but also thrive. Hannah covers everything from the tough questions such as "Why doesn't God heal me?" to "Why doesn't my husband 'get it?'" She also provides savvy advice and practical tips she's learned along her journey. Though Yet Will I Praise Him is written by a mom for moms, it also covers information such as how the five stages of grief work when you have a chronic illness and what not to say to a parent with a chronic illness, making it beneficial for anyone who has a loved one who lives with a chronic illness.
Download or read book Changing Health Care Systems and Rheumatic Disease written by Institute of Medicine and published by National Academies Press. This book was released on 1997-02-09 with total page 253 pages. Available in PDF, EPUB and Kindle. Book excerpt: Market forces are driving a radical restructuring of health care delivery in the United States. At the same time, more and more people are living comparatively long lives with a variety of severe chronic health conditions. Many such people are concerned about the trend toward the creation of managed care systems because their need for frequent, often complex, medical services conflicts with managed care's desires to contain costs. The fear is that people with serious chronic disorders will be excluded from or underserved by the integrated health care delivery networks now emerging. Responding to a request from the National Institute of Arthritis and Musculoskeletal and Skin Diseases, this book reflects the results of a workshop that focused on the following questions: Does the model of managed care or an integrated delivery system influence the types of interventions provided to patients with chronic conditions and the clinical and health status outcomes resulting from those interventions? If so, are these effects quantitatively and clinically significant, as compared to the effects that other variables (e.g., income, education, ethnicity) have on patient outcomes? If the type of health care delivery system appears to be related to patient care and outcomes, can specific organizational, financial, or other variables be identified that account for the relationships? If not, what type of research should be pursued to provide the information needed about the relationship between types of health care systems and the processes and outcomes of care provided to people with serious chronic conditions?
Download or read book Unseen written by Jacinta Parsons and published by Affirm Press. This book was released on 2020-09-29 with total page 252 pages. Available in PDF, EPUB and Kindle. Book excerpt: Jacinta Parsons was in her twenties when she first began to feel unwell - the kind of unwell that didn't go away. Doctors couldn't explain why, and Jacinta wondered if it might be in her head. But she could barely function, was frequently unable to eat or get out of bed for days, and gradually turned into a shadow of herself. Eventually she got a diagnosis, but knowing she had Crohn's disease wouldn't stop her life from spiralling into a big mess of doctors, hospitals and medical disasters. With chronic illness her constant companion, she had to learn how to function in a world set up for the well. What's most extraordinary about Jacinta's story is how common it is. Nearly half of Australians live with a chronic illness, but most of these conditions are not obvious, often endured in secrecy and little understood. They are unseen. With compelling candour, Jacinta trains a microscope on the unique challenges of living with an invisible condition. She lays bare the struggles with shame, loss of identity, the threat of mortality, and the profoundly complex relationships between the chronically ill and their own bodies, as well as with those around them. It's a story of trying to fix an unfixable illness, getting beaten down then clawing back up, and how that experience can shape a life.
