Books & Resources

In his fourth memoir published in 2020, Michael uses his trademark sense of humor to share personal stories and observations about illness and health, aging, the strength of family and friends, and how our perceptions about time affect the way we approach mortality.

There are many words to describe Michael J. Fox. Actor. Husband. Father. Activist. But readers of Always Looking Up will soon add another to the list: Optimist. Michael writes about the hard-won perspective that helped him see challenges as opportunities.

Michael draws on his own life experiences to make a case that real learning happens when life goes skidding sideways.

Combining his trademark ironic sensibility and keen sense of the absurd, he recounts his life -- from his childhood in a small town in western Canada to his meteoric rise in film and television which made him a worldwide celebrity.

Whether the diagnosis is yours or that of a loved one, Parkinson's Disease for Dummies contains everything you need to know about living with this disease. This book is an easy-to-understand, straightforward, and sometimes humorous guide that offers proven techniques for coping with daily issues, finding the right doctors, and providing care as the disease progresses.

(John Wiley & Sons, 2022)

MJFF founding Patient Council member Dave Iverson is a retired broadcast journalist, filmmaker, and the author of "Winter Stars: An Elderly Mother, an Aging Son and Life's Final Journey." Iverson’s memoir offers an intimate, unvarnished portrait of navigating life’s obstacles and caring for our loved ones.

From a world-renowned and beloved doctor, an accessible guide with 100 delicious tried-and-tested recipes for healthy living — to eat well, live well, and stay well. Tapping this holistic approach, The Wellness Principles also touches on healthy living beyond the plate through physical exercise, stress management, better sleep, and complementary therapies.

The PD Avengers are a global alliance of people living with Parkinson’s, partners and friends, standing together demanding change in how the disease is seen and treated. As a patient led organization, the PD Avengers add urgency to research, wellness and advocacy by uniting people and organizations to the cause of ending Parkinson’s disease. Learn more at www.pdavengers.com

After receiving a Parkinson’s diagnosis, Torrance York focused her camera on the goal to integrate this life-altering information into her sense of self. In Semaphore, her response to this personal challenge, York presents a visual journey of poetic images that articulate the shift in her perspective post-diagnosis. York’s quiet, generous and luminous photographs bare human vulnerability, while inspiring optimism and connection. Semaphore includes 67 photographs and texts by York and Rebecca Senf, PhD. 

Interested readers may preorder Semaphore and learn more about the artist at  www.torranceyork.com

Gloria Gottesman was diagnosed with Parkinson’s in 2012. Wishing she’d had a positive way to explain Parkinson’s disease to her own grandchildren, she wrote a book, Pilot to Co-Pilot, for families to share with their children to take the scare out of Parkinson’s disease. The book is illustrated by her granddaughter, Ellie.