Power Over Parkinson's Profile Interviews

Join us for a special episode of the POP Profiles Series as we interview scientists from the Nelson Lab at the University of California, San Francisco (UCSF).

Led by Dr. Alexandra Nelson, the lab investigates the neural circuits of the basal ganglia to understand how motor control breaks down in disorders like Parkinson's disease and dystonia, utilizing state-of-the-art approaches in electrophysiology, optogenetics, and behavior. Watch to learn about their latest findings, day-to-day lab life, and the human side of pioneering neuroscience research.

Support the show

In this episode of the POP Profiles Series, we sit down with Donna Parkhurst, the inspiring founder of Moved by Parkinson’s.

Donna shares her deeply personal journey with Parkinson’s disease, a journey that began long before her own diagnosis. Having served as a caregiver for her mother, who also battled the disease, Donna brings a unique and profound perspective to the Parkinson's community.

Tune in as Donna opens up about:

• The Journey to Diagnosis: How her experience as a caregiver shaped her own understanding and acceptance of her diagnosis.
• Choosing Action Over Despair: Her powerful decision to face the disease head-on and share her journey with radical honesty.
• The Reality of Symptoms: Breaking the stigma by showing the raw, unfiltered truth of living with Parkinson's.
• Building a Movement: How her vulnerability has cultivated an incredibly supportive, active, and global community through Moved by Parkinson’s.

Donna’s bravery, resilience, and optimism are a testament to the power of taking control of your story. Whether you are living with Parkinson's, caregiving for a loved one, or looking for inspiration to overcome life's challenges, Donna’s story will move you.

Support the show

In this powerful episode of our POP Profiles Interview Series, Power Over Parkinson’s President and host Margaret Preston sits down with three inspiring women living with young-onset Parkinson’s disease: Allie Signorelli, Reka Janisse, and Esther Labib-Kiyarash.

Together, they share their personal journeys to diagnosis, the realities of living with Parkinson’s at a younger age, and the unique challenges women face—many of which are often overlooked or misunderstood. From navigating careers and family life to addressing symptoms that present differently in women, this conversation sheds light on the true face of Parkinson’s beyond the stereotypes.

This honest and heartfelt discussion aims to raise awareness, foster understanding, and empower others in the Parkinson’s community.

Whether you’re living with Parkinson’s, supporting a loved one, or simply want to learn more, this episode offers insight, connection, and hope.

Support the show

In this episode of POP Profiles, part of the Power Over Parkinson’s series, we sit down with Dr. Jamie Eberling, SVP and Head of Imaging at the Michael J. Fox Foundation, to discuss one of the biggest challenges in Parkinson’s research: developing an alpha-synuclein tracer. Alpha-synuclein is the protein that accumulates in the brains of people with Parkinson’s disease, but scientists still cannot reliably image it in living patients. Dr. Eberling explains why finding this tracer is so complex—and why solving it could be a major breakthrough. We explore how an alpha-synuclein tracer could transform diagnosis, accelerate therapeutic development, improve clinical trials, track disease progression, and ultimately move the field closer to disease-modifying treatments and a cure.

Support the show

In this special Power Over Parkinson’s interview, we sit down with Gary Griffiths—a U.S. military veteran, former firefighter, and a dedicated voice in the Parkinson’s disease (PD) community. Gary shares his powerful story of a life spent in service, from protecting his country to protecting his community, and now advocating for those living with Parkinson’s. Gary opens up about, his decades of work in the military and fire service, his Parkinson’s diagnosis and the challenges that followed, how he transformed adversity into positive purpose, and his ongoing advocacy, awareness efforts, and support for our mission at Power Over Parkinson’s His story is one of resilience, leadership, and unwavering positivity and commitment to helping others.

Support the show

In our latest installment of POP Profiles, Power Over Parkinson’s President, Margaret Preston, sat down with Dr. George Ackerman, founder of Together for Sharon, a grassroots Parkinson’s awareness initiative dedicated to honoring his late mother, Sharon Riff Ackerman. The conversation explored Dr. Ackerman’s deeply personal journey—from his mother’s Parkinson’s diagnosis to his mission to educate, connect, and empower families affected by the disease. He shared insights into how Together for Sharon uses storytelling and community outreach to amplify voices within the Parkinson’s community, while also advocating for greater research support and public understanding of the disease. Throughout the interview, themes of hope, advocacy, and connection emerged. Dr. Ackerman emphasized the importance of uniting organizations like Power Over Parkinson’s and Together for Sharon to strengthen awareness efforts and improve the lives of those living with Parkinson’s.

This inspiring conversation serves as a reminder that through shared stories and collaboration, we can continue to build a stronger, more supportive Parkinson’s community.

Support the show

Dr. Annie Killoran, Clinical Associate Professor of Neurology and Psychiatry and the University of Iowa, joins us as we discuss why understanding Parkinson’s Disease stages is helpful for both clinicians and patients. We cover how staging the disease can better help in identifying and delivering targeted therapies as well as how it can aide in the acceptance of the disease and its many and varied characteristics. Dr. Killoran also takes us through general treatment options, touches on current research, and stresses why exercise is a critical component of disease management. This discussion offers a terrific overview of an array of important Parkinson’s topics.

Support the show

Dr. Rachel Dolhun, Chief Medical Advisor of the Michael J. Fox Foundation, joins us as we breakdown an array of Parkinson’s topics including exercise, disease management and therapeutics, and current research and development. She offers simple strategies and clear takeaways that will equip viewers with an actionable plan as they work with their own neurologists in managing PD. 

Support the show

Dr. Sule Tinaz, Associate Professor of Neurology at the Yale School of Medicine in the Movement Disorders Division and Clinical Neurosciences Imaging Center, joins us to talk, you guessed it, exercise! We can never hear too much information and advocacy on exercise. Why? Because it’s the only known intervention that is known to alleviate the symptoms and slow the progression of the disease. Dr. Tinaz’s research is focused on developing personalized therapies that people can use to cope with their symptoms. She believes we are not passive receivers of our experiences but active agents, as we can actively impact how this disease progresses, particularly through exercise. 

Support the show

Allie Signorelli, Parkinson’s Advocate and person with young onset Parkinson’s (YOPD), shares her journey to diagnosis and how she’s positively impacting the Parkinson’s community at a national level. Allie is lending her voice through advocacy and harnessing her career experience, particularly in fundraising and event management, to serve our community and aid in research that’s related to both therapeutics as well as the cure that we are all hoping for! Allie is an inspiration to us all and our community is lucky to have her finding her “silver linings” as someone with YOPD. 

Support the show