On Time: A Parkinson's Podcast
On Time is a podcast about living with Parkinson's disease (PD). People in the Parkinson's community share their candid stories of daily living with the disease. The podcast is a program of the Brian Grant Foundation. Learn more about the Brian Grant Foundation at briangrant.org.
Episodes
Life After a Parkinson's Diagnosis
Episode 1: Permission to Play
Guests: Kevin Kwok, Bill Buckalew, Yvonne Jackson, Dr. Anne Cohn Donnelly, Margaret Burns-Kohn, Allie Signorelli, Jimmy Choi, Michael Fitts, Kuhan Pushparatnam, Dan Dumsha
Creativity often blooms in unexpected soil. In this episode, Larry talks with a wide range of people who discovered (or rediscovered) their creative side after a Parkinson’s diagnosis. From painti...
Life After a Parkinson's Diagnosis
Episode 2: Permission to Fly
Guests: Kevin Kwok, Bill Buckalew, Yvonne Jackson, Allie Signorelli, Jimmy Choi, Michael Fitts, Richard & Angela Huckabee, Dr. Anne Cohn Donnelly, Margaret Burns-Kohn
Parkinson’s might slow you down — but it doesn’t have to keep you grounded. In this episode, Larry shares tips, tricks, and hilarious travel tales from seasoned globetrotters with Parkinson’s. From ...
Life After a Parkinson's Diagnosis
Episode 3: Permission to Pivot
Guests: Kevin Kwok, Bill Buckalew, Yvonne Jackson, Jimmy Choi, Allie Signorelli, Michael Fitts, Dr. Michael Okun, Deena Grinnell, Margaret Burns-Kohn, Richard Huckabee
Living with Parkinson’s is a masterclass in adaptation. In this episode, Larry and his guests share the big and small pivots that make everyday life a little easier—from mobility hacks to medication ...
Life After a Parkinson's Diagnosis
Episode 4: Permission to Laugh
Guests: Matt Eagles, Margaret Burns-Kohn, Dr. Anne Cohn Donnelly, Richard & Angela Huckabee, Kevin Kwok, Bill Buckalew, Yvonne Jackson, Jimmy Choi, Allie Signorelli, Michael Fitts
Laughter won’t cure Parkinson’s — but it might just help you live with it. In this heartfelt and hilarious finale, Larry explores the power of humor with people who’ve learned to laug...
Brian and Max, Brian’s two youngest children, are still in grade school. In this episode we sit down with them and with their mom, Allison, for an intimate conversation about how children process and navigate life with a parent who has Parkinson’s. We discover what they know about Parkinson’s, how they’ve seen it impact their dad, and how their family approaches conversations about the disease.
Jonavan and Maliah, Brian’s middle children, were just grade schoolers when their father was diagnosed with Parkinson’s disease. In this episode, they share their heartfelt reflections on the emotions they experienced upon learning of his diagnosis and how it has influenced their lives and shaped them into the adults they are today.
Anaya and Jaydon were just in grade school when their father received a Parkinson’s disease diagnosis. In this episode, we sit down with them to reflect on how the initial diagnosis shaped their childhood and discuss the strategies, support, and lessons that helped them navigate life alongside their dad's journey with Parkinson's.
Amani and Elijah, Brian's two eldest children, live in the same city as their dad and play a vital role in supporting him as he navigates life with Parkinson's disease. In this episode, we sit down with Amani and Elijah to explore their unique perspectives and experiences as the eldest siblings in the family.
In this final episode of season 6, Brian Grant and his mother, Dorella Grant talk about their time at Camp Lejeune, a U.S. Marine Corps base. And the ongoing battle for accountability and justice for those affected by military environmental exposures. Then, Ted Thompson with the Michael J. Fox Foundation discusses major policy advancements and the role of advocacy in driving legislative change.
In this episode we hear from Dr. Sara Whittingham, a USAF Veteran, physician, Ironman triathlete, wife and mother. In 2020, she was diagnosed with Parkinson's disease. She has become a vocal advocate for Veterans who have been denied benefits despite known exposure to chemicals linked to Parkinson's disease.
About Dr. Sara Whittingham
Sara Whittingham is a USAF Veteran, physician, Ironman triathlete, wife and mo...
In this episode we get the historical context and regulatory challenges surrounding pesticide use with researcher Dr. Caroline Tanner, Director of the Parkinson’s Disease Research, Education and Clinical Center. Then, retired lawyer, Dan Kinel, shares his journey with Parkinson’s, his story of Trichloroethylene (TCE) exposure working for years in downtown New York, and his work in patient advocacy.
About Dr. Caroline Tann...
In season 6 of On-Time: A Parkinson's Podcast, host Larry Gifford explores the environmental toxins linked to Parkinson's disease in a four-part series.
In this opening episode, guest Dr. Ray Dorsey, Neurologist and Author of "Ending Parkinson’s Disease," explores how chemicals in our daily environment, from pesticides in food to industrial pollutants in the air, may be linked to the rise of Parkinson&a...
Special Bonus Episode: Conversation with CND Life Sciences
In this special bonus episode, BGF Executive Director Katrina Kahl talks with CND Life Science's Chief Medical Officer and Co-Founder Todd Levine, MD about the benefits of the company's evidence-based test to help diagnose synucleinopathies, which includes Parkinson's disease.
More about Dr. Levine:
Dr. Todd Levine is one of the three founders of CND Life Scie...
Host Larry Gifford closes our four-part series on stigma and Parkinson's with a conversation with Brian Grant about his personal experiences with stigma and his thoughts on the stereotypes of people with Parkinson's disease.
More about Brian Grant:
Brian Grant was an NBA idol, known for tenacious rebounding and a fearless attitude on the court. During his 12‐year career, he played for five teams and became a stron...
Stigma for people with Parkinson's disease is a global issue, and its manifestations can vary across different countries and cultures. In this episode, host Larry Gifford speaks with Nduta M'mbogori about her experience being diagnosed and living with Parkinson's in Nairobi, Kenya.
Societal expectations and assumptions about how Parkinson’s presents for women can lead to women being overlooked in terms of their own needs and experiences. In this episode, host Larry Gifford talks to Sree Sripathy and Richelle Flanagan, co-founders of the Women's Parkinson's Project, about Parkinson’s Stigma for Women.
More about our guests:
Richelle Flanagan
Richelle is a CORU state registered d...
Host Larry Gifford opens our four-part series defining stigma and exploring what stigma looks like for people with PD with his first guest, Kimball Magoni, PhD.
Dr. Magoni is a licensed psychologist in private practice for more than 35 years. His perspective as a person with Parkinson's makes for a conversation filled with understanding and thoughtful strategies for anyone experiencing internal or external stigma.
More...
People living with Parkinson’s have different comfort levels when talking to others about symptoms they experience. In this episode, Amber wraps up our series with founder Brian Grant covering topics from cringe-worthy social moments to declines in abilities that are tough to face.
Even the most sensitive people can say insensitive things to people living with Parkinson’s disease. In this episode, Amber speaks with Kamal Julka about the comments they have encountered from the most unexpected sources - from strangers at the store to family and friends.
Women with Parkinson’s experience the disease differently than men, and we know so little about why that is. What we do know is there are societal expectations for women, and they are even more complex for women who have PD. In this episode, Amber talks to friend and Parkinson’s advocate, Esther Labib-Kiyarash, about the emotional, social, and physical experience for women with PD.
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