Counseling Persons with Parkinson's Disease


Book Description

"Counseling Persons with Parkinson's Disease offers a distinctive, practical, philosophically grounded, and person-centered approach to counseling those living with Parkinson's disease and other chronic illnesses. As a seasoned teacher of professional counselors who also lives with Parkinson's, the author demonstrates that chronic illness requires accepting and living with profound loss, but that this loss may lead to personal transformation and constructive ends, wherein one finds new hope, meaning, purpose, happiness, and passion for living. Equal parts memoir and professional resource, this book guides clinicians who give counsel, educators who teach counseling, and anyone wanting to know more about Parkinson's disease and providing support for those who live with it. Parkinson's disease; bereavement; grief, mourning; illness; counseling; task-centered; happiness"--




Counseling Persons with Parkinson's Disease


Book Description

What is it like to live with a chronic illness? How can counselors support those living with one? Allan Hugh Cole Jr. offers answers to these two questions and so many more in Counseling Persons with Parkinson's Disease. In ten succinct chapters, Cole offers a glimpse into life with Parkinson's and presents an insightful approach to counseling someone living with a chronic illness. Cole was diagnosed with Parkinson's Disease in 2016, and--though it hardly happened overnight--he has since discovered a new passion and drive for life. A teacher of social workers and counselors for many years, Cole has unique insight into chronic illness and the care required to help someone diagnosed with one. He delves into the importance of accepting a chronic illness and how this can create an opportunity for personal transformation, newfound meaning, and rejuvenated purpose. In addition to emphasizing the importance of self-reflection, he also offers evidence-based approaches to counseling. Cole's approaches to counseling draw on task-centered social work practice. Throughout the book, he engages with five purposeful actions tied to principles of constructivism, Aristotelian thought, American pragmatism, and theories of interpretation (hermeneutics). At once informative, realistic, humorous, and hopeful, this is a thoughtful guide for clinicians who give counsel, educators who teach counseling, people supporting someone else, and anyone living with a chronic illness.




Parkinson's Disease and Quality of Life


Book Description

Learn to handle the problems that Parkinson's patients face Through Parkinson's Disease and Quality of Life, you will discover common problem areas seen in patients with Parkinson's disease. This book explores problems that interfere with functional independence of patients and gives examples of occupational therapy intervention and treatment techniques. Parkinson's Disease and Quality of Life boldly deals with many seldom talked about real-life issues facing people with Parkinson's disease, including continued sexual intimacy and urinary incontinence. Although these issues may not be curable, this book provides you with effective treatments through data and case studies. Parkinson's Disease and Quality of Life offers caregivers a step-by-step plan to get organized. It includes a plan to put together a workbook of all relevant information, as well as tips on how to safeguard every room for a Parkinson's disease patient. This book helps remind you that the families of the patient must not be forgotten and that they can get the help they need through support groups, community resources, and from professional staffing such as nurses and aides. Parkinson's Disease and Quality of Life will assist you in helping your patients by: using music therapy to help calm patients realizing the legal impact of Parkinson's disease by discussing living wills, health care proxies, durable power of attorney, and revocable and irrevocable trusts with your clients discovering that cognitive changes, dementia, and depression can complicate the treatment of the disease and be more disabling than the loss of motor function exploring the nursing home as a viable options for clients as well as their families Parkinson's Disease and Quality of Life also brings to light the important subject of knowing the patients insurance policies and working out contingency plans, like living wills, before they are needed. This book gives you much-needed information on accessing benefits for Parkinson's patients, including medicare, social security, Veteran's benefits, and much more. Parkinson's Disease and Quality of Life is full of methods and ideas to improve the lives of the Parkinson's patient as well as their families.




Ending Parkinson's Disease


Book Description

In this "must-read" guide (Lonnie Ali), four leading doctors and advocates offer a bold action plan to prevent, care for, and treat Parkinson's disease-one of the great health challenges of our time. Brain diseases are now the world's leading source of disability. The fastest growing of these is Parkinson's: the number of impacted patients has doubled to more than six million over the last twenty-five years and is projected to double again by 2040. Harmful pesticides that increase the risk of Parkinson's continue to proliferate, many people remain undiagnosed and untreated, research funding stagnates, and the most effective treatment is now a half century old. In Ending Parkinson's Disease, four top experts provide a plan to help prevent Parkinson's, improve care and treatment, and end the silence associated with this devastating disease.




Occupational Therapy for People with Parkinson's Disease


Book Description

These practice guidelines draw upon the widest relevant knowledge and evidence available to describe and inform contemporary best practice occupational therapy for people with Parkinson's disease. They include practical examples of interventions to allow occupational therapists to apply new treatments to their practice.




In the Care of Plenty


Book Description

The poems in this book were written after the author was diagnosed young-onset Parkinson’s disease at the age of forty-eight. Some of the poems include reflections on and accounts of his experiences of sadness, darkness, and struggle, especially during the first year following his diagnosis. More of the poems capture experiences of deep questioning, discovery, acceptance, joy, and hope. This range of reflections and experiences is what we would expect for one who mourns and learns to live in peace after a life-changing loss.




Parkinson's Disease


Book Description

Parkinson's Disease: Improving Patient Care is a clinically-focused text for healthcare professionals involved in everyday management of Parkinson's disease patients. Concise chapters and abundant tables make it easy to read or use as a handy reference.




Counseling Individuals with Communication Disorders


Book Description

*A complete overview of the psychology of a wide variety of communication disorders * Presents optimal strategies to help patients and their families cope with the emotional issues accompanying communication disorders * Offers case studies drawn from Dr. Rollin's 40 years of clinical experience * Discusses ethical principles and delineates counseling boundaries




My Toughest Faceoff


Book Description

After being a first-round draft pick of the Detroit Red Wings in 1974, Brent Peterson embarked on a successful National Hockey League playing career that lasted 11 seasons. During his career, he played for Detroit, the Buffalo Sabres, Vancouver Canucks, and Hartford Whalers. When he retired as a player, Brent immediately became an assistant coach with the Whalers before moving back to Portland, Oregon to become the head coach of the Portland Winter Hawks of the Western Hockey League. After leading Portland to the Memorial Cup championship in 1998, Brent wanted to pursue his dream of becoming a head coach in the NHL, so he left Portland and took an assistant coaching position with the expansion Nashville Predators. Brent was later promoted to the position of associate head coach. Soon after that promotion, things took a turn when Brent was diagnosed with Parkinson's disease, a degenerative neurological disorder for which there is no known cure. For a year Brent and his wife Tami kept Brent's diagnosis a secret, even going so far as to borrow the money needed for medications so that they did not have to use Brent's insurance out of fear that the Predators would find out about his condition. When Brent's symptoms became more obvious to the people who were around him every day, he and Tami made the decision to go public with the information that would likely end any chances of a team hiring him to be their head coach. Brent made the news public first by telling the Predators following their elimination from the playoffs in 2004. The team rallied around the affable coach they call Petey. In addition to keeping his position as Nashville's associate head coach, Brent established the Peterson for Parkinson's Foundation in hopes of raising awareness and funding for research. Away from the ice, Brent received some counseling from Michael J. Fox, one of Parkinson's most visible faces. It was that same advice that Brent turned around and gave to former NBA star Brian Grant after he too was diagnosed with the same disease. Like Brent, Grant struggled with the emotional trauma of having been diagnosed with Parkinson's at such a young age. At Brent's urging, Grant established a foundation of his own. Early in the 2010-11 NHL season, Brent's symptoms became more and more difficult to manage. His balance was affected, making it dangerous for both him and the players to be out on the ice together. Following Nashville's elimination from the 2011 playoffs, Poile announced that the team had made the decision that Brent would no longer be a coach. The Predators kept Brent on staff though, creating the position of hockey operations advisor to tap into Brent's years of experience in working with the players. Those same symptoms that made Brent step away from behind the bench were also affecting his quality of life, and the decision was made to undergo the radical medical procedure called Deep Brain Stimulation. DBS is a series of four medical procedures that involve wires being surgically implanted into the brain and then connected to a device inside of the patient's chest. That device sends signals to the brain, and those signals mimic the effects of the chemical dopamine. The results were nearly instantaneous. The morning prior to the system being turned on, Brent needed assistance getting his shoes and socks on before traveling to the hospital. The next day, he was running on a treadmill at the Predators' practice facility. DBS is not a cure for Parkinson's, but it does replicate the effects that medication has on a patient. Brent still has Parkinson's and probably always will. The symptoms will reappear at some point and his condition will likely worsen again, but now he has a renewed outlook on life and a renewed ability to do the things that drive him; being a good husband, father, hockey man, and advocate for Parkinson's patients everywhere.




Non-Motor Symptoms of Parkinson's Disease


Book Description

Patients with Parkinson's disease (PD) are known to suffer from motor symptoms of the disease, but they also experience non-motor symptoms (NMS) that are often present before diagnosis or that inevitably emerge with disease progression. The motor symptoms of Parkinson's disease have been extensively researched, and effective clinical tools for their assessment and treatment have been developed and are readily available. In contrast, researchers have only recently begun to focus on the NMS of Parkinson's Disease, which are poorly recognized and inadequately treated by clinicians. The NMS of PD have a significant impact on patient quality of life and mortality and include neuropsychiatric, sleep-related, autonomic, gastrointestinal, and sensory symptoms. While some NMS can be improved with currently available treatments, others may be more refractory and will require research into novel (non-dopaminergic) drug therapies for the future. Edited by members of the UK Parkinson's Disease Non-Motor Group (PD-NMG) and with contributions from international experts, this new edition summarizes the current understanding of NMS symptoms in Parkinson's disease and points the way towards future research.