5 S.T.E.P.S. to Being Your Own Patient Advocate--Enhanced Edition

My Health. My Body. My Voice

Nonfiction, Health & Well Being, Health, Ailments & Diseases, Immune System
Cover of the book 5 S.T.E.P.S. to Being Your Own Patient Advocate--Enhanced Edition by Cristy L. Kessler, EdD, Sharon K. Miller, Buckskin Books
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Author: Cristy L. Kessler, EdD, Sharon K. Miller ISBN: 9780989998727
Publisher: Buckskin Books Publication: December 2, 2013
Imprint: Language: English
Author: Cristy L. Kessler, EdD, Sharon K. Miller
ISBN: 9780989998727
Publisher: Buckskin Books
Publication: December 2, 2013
Imprint:
Language: English
Cristy Kessler should be dead. The fact that she’s not is because she took charge of her own medical care. When she took it upon herself to find out why she had spent her lifetime battling pain and illness, Kessler embarked upon a journey of discovery in which she endured multiple treatments and procedures that resolved some, but not all, of her issues. Finally, armed with a diagnosis of multiple autoimmune diseases, she took charge and, with the help of a powerful team of doctors, Kessler identified the treatment that could save her life, a treatment denied by her insurance company and prohibited in the United States by the FDA. As Michael Seres, author of the blog, “Being a Patient Isn’t Easy,” and a transplant survivor himself, says in the Foreword, “With her book, she has been able to articulate in a very simple way the critical steps that every patient living with a long-term condition should abide by. She writes with complete honesty and lovely touches of humour….this is a book every single patient should read at least once. And, if you are a clinician, then this should be on your bookshelf or on your laptop as a constant reminder of the paths and decisions…patients have to take.” Throughout her medical journey, Kessler developed the skills and strategies necessary to act as her own patient advocate, which, in the end, saved her life. Speaking directly to her readers, Kessler describes the five STEPS toward taking control of your health care with the assistance and support of a network of medical experts, family, and friends. Sensibility. Kessler urges you to pay attention to what your body is telling you and to record and describe symptoms carefully so that the doctor knows everything necessary for appropriate care. Most importantly, she says you must refuse to let anyone—even a doctor—dismiss your symptoms. Teamwork. Kessler urges you to take full responsibility for leading your team of doctors to make certain they are all working together, not at cross purposes. Don’t be afraid to change doctors if you need to. Put together a support network of family, friends, colleagues who can do for you what you cannot do for yourself. Education. This is a critical aspect in directing your medical team. Kessler advises you to do research and to use the Internet wisely to investigate symptoms and treatment and to share information collaboratively and respectfully with your doctors. Educate your support network; don’t keep secrets about your condition from the people who mean the most to you. Let them walk with you on your journey. Patience and Perseverance. Kessler acknowledges that being a “patient patient” is not always easy, but she urges you to find a balance between waiting calmly and recognizing when to act on something urgent in your life and circumstances. Ask questions you need answers to, be patient when you need to, and always persevere toward your objective of getting the best possible treatment available – no matter where it might be. Sustainability. Finally, Kessler insists that you are responsible for sustaining your body, mind, and spirit. Sustainability takes many forms. Whether it is through your faith or through personal and social networks, it is important to meet the needs of your whole self. Find a reason to get out of bed every day and find ways to pay it forward. Find one thing you can make time for each day that provides you with joy. In this genuinely compelling, honestly scripted, and engaging chronicle of her medical and personal journey, Kessler shares those strategies for others to use when faced with difficult medical situations. This enhanced ebook contains all of the pictures that appeared in the print version of the book, including additional ones, most of which are in color. There are also video links that help to illustrate Cristy's journey.
View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart
Cristy Kessler should be dead. The fact that she’s not is because she took charge of her own medical care. When she took it upon herself to find out why she had spent her lifetime battling pain and illness, Kessler embarked upon a journey of discovery in which she endured multiple treatments and procedures that resolved some, but not all, of her issues. Finally, armed with a diagnosis of multiple autoimmune diseases, she took charge and, with the help of a powerful team of doctors, Kessler identified the treatment that could save her life, a treatment denied by her insurance company and prohibited in the United States by the FDA. As Michael Seres, author of the blog, “Being a Patient Isn’t Easy,” and a transplant survivor himself, says in the Foreword, “With her book, she has been able to articulate in a very simple way the critical steps that every patient living with a long-term condition should abide by. She writes with complete honesty and lovely touches of humour….this is a book every single patient should read at least once. And, if you are a clinician, then this should be on your bookshelf or on your laptop as a constant reminder of the paths and decisions…patients have to take.” Throughout her medical journey, Kessler developed the skills and strategies necessary to act as her own patient advocate, which, in the end, saved her life. Speaking directly to her readers, Kessler describes the five STEPS toward taking control of your health care with the assistance and support of a network of medical experts, family, and friends. Sensibility. Kessler urges you to pay attention to what your body is telling you and to record and describe symptoms carefully so that the doctor knows everything necessary for appropriate care. Most importantly, she says you must refuse to let anyone—even a doctor—dismiss your symptoms. Teamwork. Kessler urges you to take full responsibility for leading your team of doctors to make certain they are all working together, not at cross purposes. Don’t be afraid to change doctors if you need to. Put together a support network of family, friends, colleagues who can do for you what you cannot do for yourself. Education. This is a critical aspect in directing your medical team. Kessler advises you to do research and to use the Internet wisely to investigate symptoms and treatment and to share information collaboratively and respectfully with your doctors. Educate your support network; don’t keep secrets about your condition from the people who mean the most to you. Let them walk with you on your journey. Patience and Perseverance. Kessler acknowledges that being a “patient patient” is not always easy, but she urges you to find a balance between waiting calmly and recognizing when to act on something urgent in your life and circumstances. Ask questions you need answers to, be patient when you need to, and always persevere toward your objective of getting the best possible treatment available – no matter where it might be. Sustainability. Finally, Kessler insists that you are responsible for sustaining your body, mind, and spirit. Sustainability takes many forms. Whether it is through your faith or through personal and social networks, it is important to meet the needs of your whole self. Find a reason to get out of bed every day and find ways to pay it forward. Find one thing you can make time for each day that provides you with joy. In this genuinely compelling, honestly scripted, and engaging chronicle of her medical and personal journey, Kessler shares those strategies for others to use when faced with difficult medical situations. This enhanced ebook contains all of the pictures that appeared in the print version of the book, including additional ones, most of which are in color. There are also video links that help to illustrate Cristy's journey.

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