Multiple Sclerosis Why Not Me


Multiple Sclerosis Why Not Me
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Multiple Sclerosis Why Not Me


Multiple Sclerosis Why Not Me
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Author : Vincent Spoto
language : en
Publisher: Dorrance Publishing
Release Date : 2016-10-25

Multiple Sclerosis Why Not Me written by Vincent Spoto and has been published by Dorrance Publishing this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-10-25 with Medical categories.


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.



Why Not Me


Why Not Me
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Author : Anna Healey
language : en
Publisher:
Release Date : 2002

Why Not Me written by Anna Healey and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2002 with Multiple sclerosis categories.


Autobiographical account of a young woman who was diagnosed with multiple sclerosis. Confined to a wheelchair with a new baby to care for, it was a nightmare for an independent and fun-loving person. However, after the early dark days Healey began to rebuild her life, learning to drive and becoming involved in the public speaking circuit to promote the MS cause. She also learned to sail, going on to compete at the highest levels of Australian sailing. Includes a list of MS society contacts.



I M Not Crazy I M Just A Tad Ditzy


I M Not Crazy I M Just A Tad Ditzy
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Author : Jeanne Phaneuf Champagne
language : en
Publisher: Covenant Books, Inc.
Release Date : 2018-11-16

I M Not Crazy I M Just A Tad Ditzy written by Jeanne Phaneuf Champagne and has been published by Covenant Books, Inc. this book supported file pdf, txt, epub, kindle and other format this book has been release on 2018-11-16 with Fiction categories.


I never set out to write a book. Initially, writing was my awkward attempt at telling those I love how I was personally, emotionally, physiologically, cognitively, and socially affected by relapsing-remitting multiple sclerosis (RRMS). My MS journey began nearly fifteen years before diagnosis. Following the flu many years prior, I dealt intermittently with a multitude of symptoms including seizures, visual obscurities, cognitive challenges, choking issues, loss of balance, muscle spasms, and a myriad of other symptoms. Specialists scratched their heads unable to identify the cause. My experience of a long, drawn-out diagnosis is common among those with this perplexing and often ambiguous disease. Eventually, neurological tests and an MRI revealed "lesions... demyelination... multiple sclerosis." Finally, "it" had a name. Surprisingly, not knowing what was going on all those years was far more exasperating than hearing the actual diagnosis. At least now, I had an answer. Learning all I could about RRMS empowered me to deal more effectively with its unpredictable and haphazard symptoms. I concluded that if I found it challenging to deal with issues ignited by MS, then others must too. If my experiences could help others navigate their way more smoothly through the complex maze of MS, I felt compelled to share them. As my fingers began flying across the keyboard in an effort to write my story, I discovered how difficult it was to be truly open about my journey and the countless symptoms I'd habitually covered for so long. I needed to share it if for no one else's sake but my own. My struggles were showing, and it was becoming more difficult to hide them than it was to live with them openly. I knew the jig was up. Hiding was no longer an option. That's when the writing of this book began.



Me Myself And Ms


Me Myself And Ms
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Author : Gwendolyn Powell
language : en
Publisher: AuthorHouse
Release Date : 2017-08-09

Me Myself And Ms written by Gwendolyn Powell and has been published by AuthorHouse this book supported file pdf, txt, epub, kindle and other format this book has been release on 2017-08-09 with Biography & Autobiography categories.


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.



Women Living With Multiple Sclerosis


Women Living With Multiple Sclerosis
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Author : Judith Lynn Nichols
language : en
Publisher: Hunter House
Release Date : 1999

Women Living With Multiple Sclerosis written by Judith Lynn Nichols and has been published by Hunter House this book supported file pdf, txt, epub, kindle and other format this book has been release on 1999 with Family & Relationships categories.


Women who are living with multiple sclerosis share their experiences andffer advice for other women battling the diesease.



I Awake To Another Day


I Awake To Another Day
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Author : Frederick L. Keller
language : en
Publisher: CreateSpace
Release Date : 2011-07-18

I Awake To Another Day written by Frederick L. Keller and has been published by CreateSpace this book supported file pdf, txt, epub, kindle and other format this book has been release on 2011-07-18 with Health & Fitness categories.


This book is a first-hand account of my journey with Multiple Sclerosis (MS). As I went through the stages of diagnosis to disease management, it became apparent that while there were numerous books written on the subject of MS, most focused on the medical or clinical aspects of the disease. While these sources were certainly empirically informative, they were coldly lacking in the emotional preparation and guidance that I needed. There is a profoundly personal side to any life changing diagnosis, and this is where the true struggle resided for me. I couldn't turn to anything of a nonclinical substance that would help guide me through the emotional and mental turmoil I was experiencing. There was so much I wanted to know not only from my doctors, but also from other people with MS. As I started navigating my way through things in a bit of a clumsy fashion, I was inspired to write down my thoughts and insight as that new person with MS and what they would likely want to know not only about the disease but also about themselves. This book covers the time I reflected over the year leading up to my diagnosis and the first year after receiving my diagnosis with MS. The book is divided into three distinct parts. Part One looks at a wide variety of personal topics and experiences and the impact Multiple Sclerosis has played on each. There are times of frustration, denial and sorrow. There are topics of extreme support and heroes that have stepped up in my journey. There are character traits that can be of benefit and others that can be detrimental. The intent has been to capture these aspects, feelings and thought provoking situations and how MS has touched it all. In a way, this section is a reflection of my own personal struggle through the initial blow of learning about my MS and coming to accept it as a part of who I now am. Part Two focuses on moving from a position of understanding to truly accepting what MS means in my life. Acceptance doesn't just mean sitting still, but gaining a clear mind on how you are going to choose to live with MS. Acceptance is not just formed from the perspective of being that someone with MS, but it is formed by the people around me as well. Friends, coworkers, and family all will be affected by this disease in some way, and it is vitally important that we prepare to help everyone touched by MS come to a pure sense of acceptance. Part Three is all about capitalizing on the sense of acceptance and beginning to focus on those specific efforts and the needed energy to beat it. Knowing there is no cure today does not mean that I just give up. There are so many things that can be done to maintain a "normal" life, but it takes work and a proactive frame of mind. Like many struggles we can all face in our lives, MS is really no different. There is almost always a way to make a situation like this better, but it does take time, effort, and determination. From a personal perspective, this book intends to do two things...to help others better understand the everyday experiences of a person with MS, to know what the disease takes away, and also what the disease gives. The second, to help me as a person with MS move beyond merely accepting this disease and knowing that regardless of what limitations I may end up with, that I can contribute to a better result, a brighter future for someone, be a better father and husband to my family, and look back and feel good about my life...every minute of it. Life can be so much more if I can find the way to live with MS in my life rather than find a way to fit my life into MS. My wish to the second point is that it will do the same for you.



Fighting Ms


Fighting Ms
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Author : Erin Morrow Still
language : en
Publisher: iUniverse
Release Date : 2009-11

Fighting Ms written by Erin Morrow Still and has been published by iUniverse this book supported file pdf, txt, epub, kindle and other format this book has been release on 2009-11 with Health & Fitness categories.


In the spring 1999, at eighteen years old, I was diagnosed with Multiple Sclerosis. The idea of a newly diagnosed book that focused on wellness began once I finally got my MS under control. It took four long years of understanding what my body needed to be healthy, while experiencing life as a college student at Appalachian State University. I found myself searching for a wellness summary of multiple sclerosis. Why couldn't I find everything I needed in one place? This idea seemed like something most newly diagnosed individuals would have already asked for, but it was nowhere to be found. I didn't want too much information at once, only what I needed to start out healthy and stay positive. In addition to needing a wellness summary, I sought to find other young people who were just beginning life with multiple sclerosis. I needed to know people who were positive and could laugh this off with me. In 2003, I established my role as an MS patients' advocate by founding with the help of the MS Society a young men's and women's group in middle Tennessee. Then in 2005, I was awarded the Betaseron Champion of Courage grant to write the book we have all been waiting for--a wellness guide to MS for the newly diagnosed. Lance Armstrong says it best when he explains why children cope with cancer so much better than adults. He says, It's a fact that children with cancer have higher cure rates than adults with cancer, and I wonder if the reason is their natural, unthinking bravery. Sometimes little kids seem better equipped to deal with cancer than adults. They're very determined little characters, and you don't have to give them big pep talks. Adults know too much about failure; they're more cynical and resigned and fearful. Kids say, I want to play. Hurry up and make me better.' That's all they want. This quote helps me each day and will continue to be my approach to life. I will never forget the news of my diagnosis and thinking about how I couldn't wait to get back to school to feel normal again. The MS could come along if it wanted to, but I was going to get back to life no matter what it took. When I was younger, I used to love reading Young and Modern, or YM to most teenagers. There are stories in this magazine under a section called Say Anything, and they always made me laugh out loud. Of course these were juvenile stories of walking out of the bathroom with your skirt tucked in your tights or something of that nature. I realized that there where others out there who had it worse than I did, and sadly, that always seemed to make me feel better. This is why telling our MS stories will help to enable other newly diagnosed individuals not only to begin this journey in a positive state, but also to find the strength they need from someone who might have it worse. I love my health-conscious lifestyle and feeling good about my body, so I needed health tips and recipes, too. Plus, I found friends and resources along the way that helped to make this book complete. This book is designed to help us join together and find the positive in all we have to face. I would like each individual who has been diagnosed with MS to be able to relate to some of the experiences he or she reads in this book and know that we still enjoy wonderful lives, even with this heinous disease. Reaching out to others and finding a positive network will help make us all stronger. My dream for this manuscript is to be passed along to someone newly diagnosed, and let them know that we can beat this disease together! I will leave you with a final quote by Lance Armstrong. If children have the ability to ignore odds and percentages, then maybe we can all learn from them. When you think about it, what other choice is there but to hope? We have two options, medically and emotionally: give up, or fight like hell.



Self Inflicted Destruction


Self Inflicted Destruction
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Author : Nora Aloraini
language : en
Publisher: Xlibris Corporation
Release Date : 2015-06-20

Self Inflicted Destruction written by Nora Aloraini and has been published by Xlibris Corporation this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-06-20 with Biography & Autobiography categories.


For a Saudi teenage girl it took me a lot of courage to do this but In this book I will share with you my story with multiple sclerosis in details. And I have contacted multiple sclerosis patients and let them write down what are their most hated symptoms and how does it feel to them and how they overcome it when it strikes them and gathered it all in this book. I hope that this book will be the guide that I needed for myself when I was first diagnosed, the guide that will help you overcome this disease and prove to you that you’re strong.



Living With Multiple Sclerosis


Living With Multiple Sclerosis
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Author : John Morris Fenley
language : en
Publisher: iUniverse
Release Date : 2003-10

Living With Multiple Sclerosis written by John Morris Fenley and has been published by iUniverse this book supported file pdf, txt, epub, kindle and other format this book has been release on 2003-10 with Biography & Autobiography categories.


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!



Me And Ms


Me And Ms
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Author : Tim Carr
language : en
Publisher: Xlibris Corporation
Release Date : 2016-05-18

Me And Ms written by Tim Carr and has been published by Xlibris Corporation this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-05-18 with Biography & Autobiography categories.


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.