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.

This is an illustrated children’s book about a grandmother with Parkinson’s disease. It is very accessible and aimed at helping kids understand what it means for them when a family member is diagnosed.

People and families with Parkinson’s think about deep brain stimulation (DBS) for different reasons and at different times in their journey. In this illustrative poem book, MJFF community member and person living with Parkinson’s John Foley describes his personal journey with DBS from decision-making to daily life with the device. To learn more about John’s story, click the link to download a free copy.

Challenging Parkinson's is a site created by Team Fox member, Ned Neuhaus, to highlight the physical journey of people with Parkinson's, including himself. Forced movement exercise has been proven many times to be the best thing to help, and this is a site about staying active and continually challenging oneself and one's friends with PD to do everything in their power to slow PD’s control over them, including his personal journey with Deep Brain Stimulation (DBS).

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)

The PD Movers - We Keep Moving storybook is a compilation of narratives of African American and Black individuals and caregivers who are living and thriving with Parkinson’s disease (PD). Supported by Columbia University Irving Institute for Translational Science, the authors hope these stories will educate others by removing the mysteries and misconceptions of PD and provide useful resources regarding diagnosis and treatment to allow others to thrive with the disease.

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