Book Review 1:
A candid guide for people living with multiple sclerosis. In 1980, at the age of 25, Petrina began showing symptoms of MS, but it wasn't until four years later that she was officially diagnosed and decided to become an advocate for others with the disease. This second edition of her book, first published in 2011, offers fresh perspectives provided by an additional, harrowing decade of experience with MS. Petrina's own story is a key focus, of course, but her main objective is to offer guidance and hope to others. Her background, which she discusses in Part I, tells of her experiences as a National Multiple Sclerosis Society peer counselor and MS blogger (some of her blog posts appear in the back of the book). The second part provides a helpful overview of MS symptoms and treatments as well as other basic information. In Part III, Petrina lays out unvarnished truths about the effects of the disease on the body and the brain; here, with great candor, she explores such topics as the digestive system, sexual dysfunction, spasticity, and what she calls "The Elephants in the Room" mental and behavioral health, substance abuse, addiction, and suicide. Petrina's description of her pregnancy and subsequent MS flare-up is particularly poignant. Part IV includes helpful guidance regarding employment, long-term disability, and relationships with other people in addition to an uplifting section titled "Positives to Having MS," which notes, for example, that "You take nothing for granted." Petrina writes with a relentless optimism, but she's unafraid to reveal the toll that the disease has taken on herself and her family. The author's truth-telling makes her advice all the more affecting. These words from the book's opening chapter are sure to linger: "I didn't have a choice about getting [MS], but I did have a choice about whether I was going to let it control me or manage my life."
A bravely told and brutally honest self-help work. -- KIRKUS INDIE
Book Review 2:
"This is an empowering book that makes the endless details manageable - from her 41years of experience. I felt like I was learning from an old friend over a cup of tea. This should be required reading for doctors, health professionals, MS patients and their families." -- Sharon Baldacci, MSer, Author of A Sundog Moment
Book Review 3:
"I learned so much about MS and also about the human spirit that allows us to cope with whatever we are presented with. Debbie writes in a style that is not only easy to read, but also educates & offers inspiring ways to think about and face life's challenges successfully & gracefully! She doesn't hype management strategies, nor does she make claims about unproven treatments or therapies." -- Barbara Lambing - former Registered Dietitian(retired), Glendale AZ
Book Review 4:
"Debbie Petrina has managed to improve her no-nonsense, been-there-done-that guide to navigating the often choppy waters of multiple sclerosis. For personal advice without the unnecessary puffery, it's just what the doc ordered." -- Dave Bexfield, founder of www.ActiveMSers.org
2021-11-15
A candid guide for people living with multiple sclerosis.
In 1980, at the age of 25, Petrina began showing symptoms of MS, but it wasn’t until four years later that she was officially diagnosed and decided to become an advocate for others with the disease. This second edition of her book, first published in 2011, offers fresh perspectives provided by an additional, harrowing decade of experience with MS. Petrina’s own story is a key focus, of course, but her main objective is to offer guidance and hope to others. Her background, which she discusses in Part I, tells of her experiences as a National Multiple Sclerosis Society peer counselor and MS blogger (some of her blog posts appear in the back of the book). The second part provides a helpful overview of MS symptoms and treatments as well as other basic information. In Part III, Petrina lays out unvarnished truths about the effects of the disease on the body and the brain; here, with great candor, she explores such topics as the digestive system, sexual dysfunction, spasticity, and what she calls “The Elephants in the Room”: mental and behavioral health, substance abuse, addiction, and suicide. Petrina’s description of her pregnancy and subsequent MS flare-up is particularly poignant. Part IV includes helpful guidance regarding employment, long-term disability, and relationships with other people in addition to an uplifting section titled “Positives to Having MS,” which notes, for example, that “You take nothing for granted.” Petrina writes with a relentless optimism, but she’s unafraid to reveal the toll that the disease has taken on herself and her family. The author’s truth-telling makes her advice all the more affecting. These words from the book’s opening chapter are sure to linger: “I didn’t have a choice about getting [MS], but I did have a choice about whether I was going to let it control me or manage my life.”
A bravely told and brutally honest self-help work.
