About The Foundation

The Parkinson Association of the Rockies connects and empowers people with Parkinson’s to thrive. Through support groups, exercise classes and in-home consults with a Licensed Clinical Social Worker, the Association connects people to the community and critical resources. Exercise classes, education, newsletters, and equipment loan services further empower people with Parkinson’s to thrive. Advocacy efforts empower, engage and connect people with Parkinson’s to use their voice and passion to enhance the care and services available for all people living with this disease. The Association celebrates people with Parkinson’s defining their disease rather than letting the disease define their lives.

Written by an expert team of health-care professionals-including a neurologist, a social worker, a nurse practitioner, a physical therapist, and an attorney/financial planner-this guide takes every aspect of living with chronic degenerative illness into consideration. (Fireside, 1993)

Author David Cram, both a physician and patient himself for ten years, knows firsthand the questions that accompany the diagnosis of Parkinson’s. He understands how vital education and effective treatment are in coping with PD and maintaining the best quality perspectives to enlighten and encourage readers about PD. (Paperback published 1999 by LPC)

The Parkinson Alliance is the umbrella organization for the Parkinson’s Unity Walk, the largest single-day community fundraising event, and Team Parkinson. We are dedicated to raising funds for research to end Parkinson’s disease, support the development of new therapies and improve the quality of life for those living with the disease. The Parkinson Alliance also directly funds and conducts patient-centered outcomes research in its own right, focusing on both motor and non-motor symptoms, and other aspects of well-being such as resilience and coping skills. Together with the Parkinson’s Unity Walk and Team Parkinson, The Alliance has funded more than $30 million in research to date.

Whether you are newly diagnosed or a Parkinson’s disease veteran, whether young onset or late onset, or if you are a care partner for someone with Parkinson’s, you are likely to find something new and interesting in this book.

This book covers symptoms, side effects of medication, support networks, and surgery options, and explores the physical, emotional, and social struggles that face young people with Parkinson's. Resources, advocacy ideas, and an index are also included. (Paperback published 2001 by Hunter House)

The Center is founded on the philosophy that integrated, interdisciplinary care is the most effective approach for patients with movement disorders and disorders involving a group of circuits in the brain called the basal ganglia. The Center delivers motor, cognitive and behavioral diagnoses as well as various treatments all in one centralized location. Care is coordinated and provided by leading specialists from many advanced medical and surgical services.

Team Fox member Robert Silver chronicles his personal experiences and anecdotes of living with Parkinson's disease. A portion of proceeds from book sales will be donated to Team Fox, 100 percent of which will go directly to MJFF's high-impact programs to speed a cure for Parkinson's.

I have Parkinson's Disease and a sense of humor! This is a collection of 100 funny stories about my life with Young Onset Parkinson's Disease. I also share some helpful advice for surviving this disease. Come learn and laugh with me! Laughter is the best medicine. Have a Happy Parkie Day! All profits from this book will be donated to Parkinson's.

Linda Williams served as the first major gifts fundraiser at The Michael J. Fox Foundation (MJFF). While working at MJFF, Linda was diagnosed with primary progressive aphasia, a rare form of dementia. Her daughter, actress Kimberly Williams-Paisley, chronicles her family's journey with her mother's disease in "Where the Light Gets In". With a foreword by Michael J. Fox, Linda and Kimberly's story is an intimate portrait of a family coping with the ripple effects of diagnosis.