Ms And Your Feelings Handling The Ups And Downs Of Multiple Sclerosis

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.

Collects the best advice from the nonprofit organization Can Do Multiple Sclerosis, including information on managing daily activities, getting more active, finding social support, changing one's diet and much more. Original.

The National Multiple Sclerosis Society estimates that 400,000 people in the United States have been diagnosed with MS. Because MS is a chronic disease, people with this diagnosis will live with the disease for years. MS sufferer Margot Russell and Dr. Allen C. Bowling, a nationally known MS expert, team up to help you: Recognize signs and symptoms Understand the types of MS Decide on treatment and find the right doctor Explore alternative therapies Take charge by creating a management plan Develop strength and avoid relapse And more! Filled with tips for daily living (like staying cool) and the latest information on new treatments, this reassuring book offers more than medical advice. It gives readers with MS the strength, knowledge, and resources they need so they can live a full, active life!

Your trusted, compassionate guide to living with MS Being diagnosed with multiple sclerosis (MS) doesn't mean your life is over. Everyone's MS is different and no one can predict exactly what yours will be like. The fact is, lots of people live their lives with MS without making a full-time job of it. Multiple Sclerosis For Dummies gives you accessible, easy-to-understand information about what happens with MS—what kinds of symptoms it can cause, how it can affect your life at home and at work, what you can do to feel and function better, and how you can protect yourself and your family against the long-term unpredictability of the disease. You'll learn how to make treatment and lifestyle choices that work for you, what qualities to look for in a neurologist and the rest of your healthcare team, how to manage fatigue, the pros and cons of alternative medicine, why and how to talk to your kids about MS, stress management strategies, your rights under the Americans with Disabilities act, and so much more. Covers major medical breakthroughs that slow the progression of the disease and improve quality of life for those living with MS Helps those affected by MS and their family members understand the disease and the latest treatment options Helpful and trusted advice on coping with physical, mental, emotional, and financial aspects of MS Complete with listings of valuable resources such as other books, websites, and community agencies and organizations that you can tap for information or assistance, Multiple Sclerosis For Dummies gives you everything you need to make educated choices and comfortable decisions about living with MS.

Describes multiple sclerosis, including its symptoms, possible causes, treatments, and controversial research in the future of treating and possibly curing the disease.

My caregiver training started early in life, extended through the 44 years after Eileen was diagnosed as having multiple sclerosis, and did not end until her death in 2001. At home, I provided full care to her, planned and thought ahead, but always was willing to sacrifice my personal freedom, and to suffer frequent heartbreak. As a caregiver I received a lifetime of gratitude from Eileen, to give me satisfaction of having successfully met her daily MS demands. The early training I received in childhood coincided with the years of the Great Depression, from the late 1920's, through the 1930's, and the first years of the 1940's. During that time I had the least possible financial assistance from anybody, yet I became an unpaid electrician, plumber, carpenter, auto repairer a Mr. Fixit for the entire Fenley family. The four years I served in the US Army were very pleasant, advancing from private to major, in an endless procession of challenging but interesting extra duties, in addition to my regular ones. These I describe as my lucky Army breaks. I have bared my soul. Happy reading!

Discussing everything from diet and exercise to stress and emotion management, Live Your Life, Not Your Diagnosis provides tools readers can use immediately to help them feel better while living with a diagnosis. Written by a master certified mindset coach who was diagnosed with multiple sclerosis in 2000, readers won’t find negative, scary stories about how a diagnosis will hurt them. Instead, they will find stories of bravery, wellness, support, and detailed steps on how they too can live their life—not their diagnosis.

An empowering guide for increasing your quality of life, navigating challenges, and embracing opportunities Julie Stachowiak, PhD is the About.com Guide to Multiple Sclerosis. As an epidemiologist who is also a person living with MS, Julie has an in-depthunderstanding about the scientific developments around MS and the personal side of living with a chronic illness. In the Multiple Sclerosis Manifesto, Julie shows you how to create your own personal MS manifesto and provides practical tools and reassurance to help you ìget betterî in your life, from optimizing medical care and managing symptoms, to strengthening relationships, dealing with emotions, and embracing activism. Committed to making the hard parts easier and the good parts last longer, Julie show you how to figure out what you need, identify opportunities, understand challenges, and get your needs met. With the Multiple Sclerosis Manifesto, youíll know how to: Create your personal mission statement Protect yourself by learning more about medications you are currently taking or considering to take Determine what you want in a doctor and how to evaluate the doctor you have Celebrate your successesóand why itís essential that you do Make disclosing your MS status to friends, family and others easier Find a support group

Everything You Need To Know About Multiple Sclerosis: For MS Warriors, their Family, Friends and Care Givers If you are newly diagnosed with MS, know someone who is, or if you are a partner or caregiver of someone with MS, no doubt you have questions about MS. Everything You Need to Know About Multiple Sclerosis has answers. It may not actually have everything but it answers questions about what is and why is MS, different types of MS, various MS symptoms and medications. It looks at MS and diet, exercise, smoking (cigarettes and marijuana), drinking, relationships, sex, pregnancy... In addition, several partners of MS Warriors chime in about their experiences. View the table of contents (So what's in the book) below.... In short while this book may not have everything you need to know about MS, this is a comprehensive book about MS.

A diagnosis of MS can feel overwhelming, even terrifying. Though over 400,000 American's have received that diagnosis, succinct answers on the issues surrounding MS can be hard to come by. This guide is the definitive resource for those who need information on this debilitating disease. Organized in an accessible question-and-answer format, it includes information on diagnosis, epidemiology, and the condition's emotional, social, and economic aspects, as well as descriptions of common medications and helpful advice for managing symptoms.

Because most people who are diagnosed with MS are between the ages of 15-55 years, the disease has a significant impact, not only on the individual with the disease, but also on the family members and loved ones whose lives are interwoven with them. Families experiencing multiple sclerosis often find themselves in uncharted territory. Prior patterns of interacting with each other may no longer work; roles often shift with dramatic emotional impact; guilt, anger, sadness, and a sense of burden may create a barrier to intimacy, joy, growth, and family unity. There are ways out of this debilitating situation, and many families have restored their balance, humor, productivity and family solidarity. Multiple Sclerosis: A Guide for Families can lead the way for your family to strengthen its coping skills and to receive targeted information about the disease and its ramifications. This complete yet highly readable guide for families living with multiple sclerosis addresses these issues and more. Families must learn how to strike a reasonable balance between the interests and needs of its members, and to accommodate the limitations imposed by MS without allowing them to impact every aspect of family life. This is easier said than done, and extensive discussions consider how the basic goals of living with this chronic disease can be met.

Multiple Sclerosis…Why Not Me? by Vincent Spoto Upon being formally diagnosed with MS in the summer of 2006, I immediately began interferon treatment. For approximately two years after being diagnosed, there were no visible symptoms. Then in fall 2008 I began to limp. As time went on, my gait became impacted & has since gotten slowly but progressively worse. I currently suffer from secondary progressive MS. Presently, I am fully ambulatory but do utilize a cane. In addition to my gait issues, my balance is off and I do get fatigued often. I am determined not to let MS get the best of me. After falling victim in 2007 to a Reduction in Workforce (RIF) associated with the collapse of the secondary mortgage market on Wall Street, I teamed up with two partners & formed an advisory / consulting business. Today, my business continues to thrive & do well. My determination to deal with my MS & be ready for the cure is founded in four main principals. These are: Remain Engaged in the Marketplace / Workforce. Remaining engaged in the workforce keeps me abreast of current marketplace events, allows me to maintain relationships, network with others & provides me with a sense of accomplishment necessary for overall well-being. Remain Physically and Socially Active. I find exercise to be critical in that it keeps me active. Admittedly, some days are more difficult than others, but I push myself to get out of the house & exercise. Additionally, meeting with & talking to others on a regular basis keeps me engaged and socially relevant. Remain Positive. Dwelling on the negative takes too much energy & only drives one to become depressed. While I am often times frustrated, I remain optimistic about the future & remain confident that a cure is forthcoming. Remain Knowledgeable. Having knowledge is having power; with respect to MS, this is essential. Today, progress towards a cure is being made at a rapid pace. It is critical to always ask questions, stay informed and do your homework. When, not if a cure is identified, I plan to be ready to take full advantage of all those little things that life has to offer. MS … Today it stands for Multiple Sclerosis. Let’s hope tomorrow it stands for Mystery Solved.

This publication is for the person with MS and for your family and friends, to provide you a better understanding of the emotional aspects of living with MS and to help you find ways of dealing with the changes the condition can bring.

The last few years have witnessed a revolution in our understanding of multiple sclerosis (MS). New treatments have transformed the prospects for many who have this chronic disease and MS is increasingly a manageable disease. This book explains the latest medical thinking on MS. It explores how to ease symptoms such as balance and mobility problems, and how to get the best from medical treatments. The book also suggests self-help techniques and lifestyle changes that may help. Topics include: types of MS diagnosis drug treatment managing side effects treating pain and fatigue bladder, bowel, swallowing and other problems coping with the mental and emotional burden diet and MS complementary and alternative remedies

Managing Your Multiple Sclerosis is an invaluable handbook for anyone who has MS or cares for someone who has it. Aimed at people who already have some knowledge or experience of the condition, the book examines the issues of treatment, therapies and rehabilitation in a comprehensive, yet easy-to-read manner.

Multiple sclerosis (MS) - a disease of the central nervous system - is the most common disabling neurological condition affecting young adults today. In her authoritative and inspiring book, Cynthia Benz demystifies the illness, explains its symptoms and patterns and offers a wealth of practical advice on coping with MS on a day-to-day basis. Including information on: - How to cope with stress and remain optimistic - Available therapies - from traditional drugs and physiotherapy to alternative treatments including acupuncture, homeopathy and massage - What help is on offer and where it can be found Revised and updated for the 21st century this is the essential handbook for people with MS, parents and carers alike.

Women who are living with multiple sclerosis share their experiences and offer advice for other women battling the disease