Informative, practical and uplifting, this is a book for anyone with Parkinson's and for those who care for and support them. It contains answers to almost any question you might ask about Parkinson's, from symptoms and diagnosis to the latest treatments and therapies, as well as the most recent medical research into stem cells and gene therapy. Drawing on her own experience of Parkinson's as well as that of others, Ann Andrews offers accessible advice on how to cope with the impact of Parkinson's on everything from employment, finance and relationships, to exercise, diet and self-care. The resulting combination of the practical and the personal sets this book apart from others on the same topic. Thoroughly researched and perceptively written, this is an empowering resource for anyone needing to adjust their life to Parkinson's.

A realistic, compassionate, supportive guide to living positively with a disease that is usually portrayed in depressing terms. Drawing on her own experience and that of others with early onset Parkinson's, the author combines clear information about the symptoms and treatments with practical strategies for adapting to the challenges of life with the disease.

An informative, practical, personal guide to living positively with the many challenges of Parkinson's disease.

This book is an easy to read account of how I maintain a positive outlook despite dealing with Parkinson's Disease over the past 19 years. I am hoping it helps others with Parkinson's or some other debilitating disease. If nothing else I hope that those who read it get a few laughs. I think people will find this book enjoyable and finish it with a smile on their face, whether they have Parkinson's or not. I am not a rich or famous person with financial resources to try any treatment I want. I am just a regular guy with an irregular disease. Despite the negative impact this disease has on me, I do my best to find and focus on the positives in my life. This book explains that and provides background information on how I got to where I am today. You can contact me via e-mail at [email protected]

The long-awaited update to the definitive guide to successfully living with Parkinson's disease Known for its upbeat, informative, and inspirational guidance, Living Well with Parkinson's includes a wealth of up-to-date medical information for Parkinson's sufferers, who number over 1 million in the U.S. alone. Combined with the author's poignant personal account of her own struggles with the disease, this new edition features coverage of pallidotomy (a new surgical technique), the dramatic implications of recent genetic research, and new drugs and therapies. The book also includes tips on dealing with social services and elder law, maintaining a positive attitude, handling issues with spouses and children, and finding support groups. Glenna Wotton Atwood, a former home economics teacher from Maine, lived with Parkinson's for over two decades until her death in 1998. Lila Green Hunnewell (Rockaway, NJ) is a freelance writer and editor. Roxanne Moore Saucier (Bangor, ME) is a journalist with the Bangor Daily News.

You may have Parkinson's, but Parkinson's doesn't have to have you. This book is a primer, a 101 course, on living well with PD. With patient and caregiver in mind, the authors deliver a practical guide for everything from understanding medications, to caregiving tips, and coping strategies. This book offers a prescription for hope and proactive self-care.

I have had Parkinson's disease (PD) for twenty-two years. I am told I have a mild case, but it is still my PD and I live with it 24/7. I would be a gross understatement to say my life was changed forever. Interesting, many of these changes have made me a more compassionate, empathetic, and caring person. In part, this book was motivated by the following premise: Many of us will experience a life-changing event that will cause us to pause and reassess where we are, what we do, and why we do it. For some, it might be the death of a loved one or a personal tragedy. Or it might be a re-awakening-that aha moment. For me, it was January 2, 1995, when my neurologist said, "Mr. Spekman, I have some bad news for you-you have Parkinson's." My life as it knew it crumpled around me. I could have wallowed in self-pity, but I am a fighter and chose eventually to manage my PD. I have adopted a number of Eastern non-traditional approached to deal with my PD. I have a yoga practice, meditate daily, and engage in massage, acupuncture, and chiropractic adjustments. All these different approaches complement my medication, and all contribute to my being very healthy, given the length of time I have had Parkinson's. I will take you on a journey, my journey, starting with denial to depression to, finally, acceptance. This book is more than the story of one man's journey with PD; it is a story of hope and personal transformation. If you permit me, I am going to take you on a journey that began over two decades ago. I have years to travel so do not ask where the destination is or ask if we are there yet. During the course of this book, I will share with you aspects of my life that were previously know to only a small number of people. It is through this intimacy that you will come to better understand and hopefully better deal with adversity that might affect your life.

How does one deal with a diagnosis of Parkinson’s disease at the age of forty-three? My Degeneration, by former Anchorage Daily News staff cartoonist Peter Dunlap-Shohl, answers the question with humor and passion, recounting the author’s attempt to come to grips with the “malicious whimsy” of this chronic, progressive, and disabling disease. This graphic novel tracks Dunlap-Shohl’s journey through depression, the worsening symptoms of the disease, the juggling of medications and their side effects, the impact on relations with family and community, and the raft of mental and physical changes wrought by the malady. My Degeneration examines the current state of Parkinson’s care, including doctor/patient relations and the repercussions of a disease that, among other things, impairs movement, can rob patients of their ability to speak or write, degrades sufferers’ ability to deal with complexity, and interferes with the sense of balance. Readers learn what it’s like to undergo a dramatic, demanding, and audacious bit of high-tech brain surgery that can mysteriously restore much of a patient’s control over symptoms. But My Degeneration is more than a Parkinson’s memoir. Dunlap-Shohl gives the person newly diagnosed with Parkinson’s disease the information necessary to cope with it on a day-to-day basis. He chronicles the changes that life with the disease can bring to the way one sees the world and the way one is seen by the wider community. Dunlap-Shohl imparts a realistic basis for hope—hope not only to carry on, but to enjoy a decent quality of life.

It was a student's observation about Dr. Case Boot's small writing on the chalk board that first made him aware of his Parkinson's symptoms. Since being diagnosed, Professor of Linguistics Emeritus at Dordt College Dr. Case Boot has learned to walk the journey of Parkinson's and is now sharing his experiences in his new book, Sharing the Road. "My intent with this book is to help others by sharing the story of God's faithfulness to me, to provide information about Parkinson's and how to live with it positively, and to encourage family and friends and those who have Parkinson's disease. This book is my way of responding to the Lord's call to serve Him and others," said Boot in the book's introduction. The book details the symptoms of the disease and shares several treatment options that are available. Boot also explains some of the unusual behaviors of people with the disease and helps readers think about how they should respond. In addition, Boot is honest about the difficulties of coming to terms with the disease. "Parkinson's is not a death sentence but an invitation and a challenge to a new and unfamiliar lifestyle," he says.