Me And Ms Book in PDF, ePub and Kindle version is available to download in english. Read online anytime anywhere directly from your device. Click on the download button below to get a free pdf file of Me And Ms book. This book definitely worth reading, it is an incredibly well-written.
This book is the story of my life with multiple sclerosis. It chronicles the ups and downs of having this debilitating disease, for which there is no cure. MS is an autoimmune disease that affects predominately Caucasian women. Being an African American man, it is something I never thought I would get. But I have it and am forced to deal with it daily. In this book, I will give you some insight into the world of MS. I talk about the many issue of living with MS. There are no medical experts in this story. However, I will give my expertise as one living with this malady. MS affects people in different ways. Some people dont experience the same symptoms as others with MS.
Me, Myself and MS is a true-to-life, heartwarming, and inspirational memoir that deals with what I went through and go through on a day-to-day, more specifically, a minute-to-minute basis in the battle of living with multiple sclerosis. This book will give a detailed description of my life from the moment of diagnoses to the many symptoms, medications, treatments, and some of the possible side effects. It is also a portrayal of the tears, laughter, triumphs, and tribulations that are a part of living with multiple sclerosis. Me, Myself and MS is not only targeted for people living with multiple sclerosis, but it is also for anyone dealing with lifes challenges and who are in need of a little inspiration. It makes a statement that the choice is yours. You can submit to your illness and hardships, or you can see these challenges as a new chapter in your life and move forward fighting tooth and nail with each new blow that is thrown you way. With two hundred people diagnosed weekly with multiple sclerosis, this inspirational book will help ease some of the fears about what you might go through. It is meant to encourage and guide those that are going through this journey or any challenges in their lives. In my family, there are four of us living with multiple sclerosis, and I was the first to be diagnosed. There was no one that I could turn to for advice as to what to expect. I hadnt even heard the words multiple sclerosis or what this illness was, so I wanted to pass along that although you have been given a new life/way of living, you can/will survive your diagnoses. This is a journeyone that I have been on for twenty-three years and counting.
Institute of Medicine,Board on the Health of Select Populations,Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
Author : Institute of Medicine,Board on the Health of Select Populations,Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Publisher : National Academies Press Page : 304 pages File Size : 40,6 Mb Release : 2015-03-16 Category : Medical ISBN : 9780309316927
Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome by Institute of Medicine,Board on the Health of Select Populations,Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Pdf
Myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) are serious, debilitating conditions that affect millions of people in the United States and around the world. ME/CFS can cause significant impairment and disability. Despite substantial efforts by researchers to better understand ME/CFS, there is no known cause or effective treatment. Diagnosing the disease remains a challenge, and patients often struggle with their illness for years before an identification is made. Some health care providers have been skeptical about the serious physiological - rather than psychological - nature of the illness. Once diagnosed, patients often complain of receiving hostility from their health care provider as well as being subjected to treatment strategies that exacerbate their symptoms. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome proposes new diagnostic clinical criteria for ME/CFS and a new term for the illness - systemic exertion intolerance disease(SEID). According to this report, the term myalgic encephalomyelitis does not accurately describe this illness, and the term chronic fatigue syndrome can result in trivialization and stigmatization for patients afflicted with this illness. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome stresses that SEID is a medical - not a psychiatric or psychological - illness. This report lists the major symptoms of SEID and recommends a diagnostic process.One of the report's most important conclusions is that a thorough history, physical examination, and targeted work-up are necessary and often sufficient for diagnosis. The new criteria will allow a large percentage of undiagnosed patients to receive an accurate diagnosis and appropriate care. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome will be a valuable resource to promote the prompt diagnosis of patients with this complex, multisystem, and often devastating disorder; enhance public understanding; and provide a firm foundation for future improvements in diagnosis and treatment.
Multiple Sclerosis is a devastating, incurable disease that afflicts about one in a thousand North Americans. Striking in the prime of life, it is the most common debilitating neurological disorder of people between the ages of 20 and 40. Eighty percent of patients suffer from cognitive impairments, seventy percent from sexual dysfunction, and fifty percent from depression. Few people are prepared for the emotional impact of this unpredictable, disabling chronic condition. Faced with a life-long progressive illness, patients typically experience fear, anger, sadness, grief, guilt, low self-esteem and sexual dysfunction. Half of all MS patients suffer from clinical depression. Other invisible symptoms, such as cognitive impairments and severe fatigue, often leave patients feeling misunderstood and alone. The emotional affects of MS can be more crippling than the physical challenges, yet little has been written on this topic. MS AND YOUR FEELINGS is the first book to specifically address the emotional pain caused by MS. Psychotherapist and MS patient, Allison Shadday, offers readers effective strategies for coping with the psychological trauma of this disease. Shadday shares real-life MS success stories and offers insightful professional advice derived from years of counseling hundreds of chronically ill patients. Her book offers readers hope, inspiration and validation, and teaches them: ·How to come to terms with an MS diagnosis ·How to recognize and overcome negative emotional responses to MS ·Techniques to identify and manage stress triggers that can impact MS symptoms ·Ways to minimize MS-related fatigue ·Strategies for coping with fear, guilt, anger, loss, depression and isolation ·Steps to enhance intimacy and build support networks ·How to deal with cognitive challenges ·Tips for increasing self-esteem ·How to develop a greater sense of emotional security and stability ·Latest information about new treatment options and promising research In addition, noted neurologist and MS expert Dr. Stanley Cohan, Director of the Pacific Northwest Multiple Sclerosis Center writes about the importance of treating the emotional symptoms of MS and discusses the promising future of MS drug research. Full of immediate, useful solutions, MS AND YOUR FEELINGS is an invaluable guide for patients, their loved ones and MS health care professionals.
MS - Living Symptom Free shares Bryant's daily regimens that have resulted in his symptom-free living. With hard-won insight, practical advice, fitness tips, and recipes, this invaluable guide instructs readers on how to eat properly and live a healthy life while controlling, reducing, and eliminating the symptoms of MS. In each user-friendly chapter, Bryant covers topics including symptoms and complications, the author's own road to MS, the benefits of conventional medication, things doctors don't tell you, popular MS diets, vitamins and supplements, exercise and sleep, staying on track, support systems, and more. The guide also features more than twenty-five easy recipes that adhere to many prevalent MS-friendly diets.
What's a Nice Girl Like Me Doing With Ms? by Lin Logan Pdf
This is the story of one woman's walk through life with MS. (Multiple Sclerosis.) It took her many years to accept this diagnosis but once she did, she came at it full force. She was not going to let this "setback" destroy her very successful life. She was in denial right from the very beginning. However, after many years, she finally accepted this in her life and has fought the battle ever since. You will read of her visits with various doctors and learn how she finally accepted this interference in her life.
Managing Multiple Sclerosis Naturally by Judy Graham Pdf
A totally revised and updated edition of the first book to offer a holistic approach to slowing the progression of MS • Provides guidance on special diets and nutritional supplements, exercise, alternative therapies, and the effects of negative and positive thoughts on MS • Explains how to reduce toxic overload from mercury and chemicals • Includes life wisdom and coping strategies from others who suffer with MS Judy Graham is an inspiration. Diagnosed with multiple sclerosis when she was just 26 years old, 35 years later Judy Graham is still walking, working, and has successfully birthed and raised a son who is now an adult. In this totally revised and updated edition of her groundbreaking Multiple Sclerosis, first published in 1984, she shares the natural treatments that have helped her and many others with MS stabilize or even reverse the condition. Beginning with the effects of diet, she explains that many people with MS have been eating the wrong foods and shows which foods are “good” and “bad,” how to recognize food sensitivities, and how to correct nutritional deficiencies using dietary supplements. She also looks at reducing the body’s toxic overload, whether from mercury amalgam fillings, chemicals, or medications. She presents the exercises with proven benefits for MS she has found most reliable and appropriate, such as yoga, pilates, and t’ai chi, and explores alternative therapies that provide relief and support to the body’s efforts to control MS, including acupuncture, reflexology, shiatsu, reiki, and ayurveda. Most important are the insights she provides on the effects of negative thoughts on MS. She demonstrates how a positive mental attitude can actually slow down or even reverse the progression of this disease. Judy Graham is living proof that, as devastating as a diagnosis of MS is, life can still be lived to its fullest.
Author : Maria Ann Lavar Publisher : Less Is More Press Page : 140 pages File Size : 54,5 Mb Release : 2019-06-04 Category : Electronic ISBN : 1733077405
"MS You Don't Own Me," takes you on one woman's inspiring journey from being a victim of disabling MS, to a vibrant and healthy lifestyle. You will be encouraged in your own journey towards wellness, and gain concrete insights into natural options that can mitigate the ravaging effects of Multiple Sclerosis.
This book is an effort at creating a collaborative platform for experts and key stakeholders to share their expertise and experiences with successful practices at creating inclusive environments. The objective is to give the readers multiple blueprints of success providing a varied range of perspectives and solutions. The underlying thought remains that inclusion can truly happen in one way or another but first starts with the singular belief that it can be done. The contributions have been arranged in the following sections: Section A - Inclusive Education: A Global Perspective Section B - Stories of Resilience: Pre-School to University Section C - Healing Touch: Perspectives from Specialists Section D - Creating Inclusive Communities: A Blueprint At the end of each story the editors have included key takeaways, additional pathways and reflective questions for the reader's reference.
The Lady's Handbook for Her Mysterious Illness by Sarah Ramey Pdf
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.
Marry Me, Ms. Stranger by Srinithya Srinivasan Pdf
“Meeting someone and marrying them are two vastly different things,” I said to him quietly, crossing my arms, “What exactly is your plan?” “I’m planning to get married. To you!” He said, looking straight into my eyes. “That was selective hearing on your part, sir.” I said, “I won’t marry you.” His jaw gritted so hard I thought his teeth might shatter. His voice came out in a growl. “Why are you trying so hard not to like me? It’s a pretty good deal.” “It’s a crappy deal wrapped up in stupidity. I would rather have all my teeth pulled out using pliers without anesthesia than marry a stranger,” I replied. “There is no going back, Ms. Iyengar. The sooner you accept it’s better for everyone,” He snapped back, his voice cutting. “What part of ‘no’ don’t you understand? The ‘n’ or the ‘o’? I don’t want to marry you,” I shouted. “You will accept. You will say ‘Yes’ to this marriage.” He enunciated each word slowly as if he was biting them off with his teeth. Who is this stranger who wants to marry Janani? Will she say yes or no? Or will she finally take control of her life, or is there something much larger at play here? So many questions jam together in her brain; Janani didn’t know which to ask first. But she had to make a decision, quick.
Recovering from Multiple Sclerosis by George Jelinek,Karen Law Pdf
A diagnosis of multiple sclerosis conjures up images of wheelchairs and a shortened life, but in fact it's possible to regain mobility and make a recovery. These deeply moving life stories of twelve people from around the world offer real hope to people with MS everywhere. These determined women and men have been able to halt the progression of the disease and recover mobility by making significant lifestyle changes including diet, sunshine, meditation, exercise, and for some, using drug therapy. Based on extended interviews, these stories offer an insight into the different journeys to recovery. They also highlight the challenges faced by people with different types of MS and at different stages in the progression of the disease.
Multiple Sclerosis: A Mechanistic View provides a unique view of the pathophysiology of multiple sclerosis (MS) and related disorders. As the only book on the market to focus on the mechanisms of MS rather than focusing on the clinical features and treatment of the disease, it describes the role of genetic and environmental factors in the pathogenesis of MS, the role of specific cells in the pathophysiology of the disease, and the pathophysiology of inflammatory and neurodegenerative disorders related to MS. The book provides discussion of neurodegeneration and neuroregeneration, two critical emerging areas of research, as well as detailed discussion of the mechanisms of action of the approved and investigational drugs for treatment of MS and the emerging role of magnetic resonance spectroscopy (MRI) in investigations into MS. It is the only book on the market to offer comprehensive coverage of the known mechanisms of MS and related diseases, and contains contributions from physicians and researchers who are worldwide experts in the field of study. Focuses on the pathophysiologic mechanisms of multiple sclerosis and the mechanisms of action in agents for the treatment of MS Discusses the roles of neurodegeneration and neuroregeneration in MS and related diseases Authored and edited by international leaders in the field of MS research
Ms. Collins - You Can't Tell Them It's Me by Clyde Andre Collins Pdf
Mae Collins graduated from a segregated high school at the age of sixteen. She was very intelligent and a visionary. Ms. Collins met a struggling entertainer; his name was James Brown. Ms. Collins was working at the Plaza Hotel in San Francisco, California. She worked at the main desk. She talked to James about his future and his goals; she even loaned him money. Ms. Collins had a vision that James would be superstar. She would give him a suite every time when he could only afford a room. She told him, aEURoeOne day you will stay in suites,aEUR and he did. This book takes you along their journeyaEUR"together to the end.