Brian Grant Foundation

On Time: A Parkinson's Podcast

Health EN ↓ 38 episodes

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.

Author

Brian Grant Foundation

Category

Health

Podcast website

briangrant.org

Latest episode

Oct 6, 2025

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Episodes

Permission to Play 06.10.2025

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 afte...

Permission to Fly 06.10.2025

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...

Permission to Pivot 06.10.2025

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 eas...

Permission to Laugh 06.10.2025

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 hu...

Brian and Max Grant 22.04.2025

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 Grant 15.04.2025

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 Grant 08.04.2025

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 Grant 01.04.2025

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.

Advocating for a Safer Future 28.10.2024

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.

A Champion for Veterans 21.10.2024

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, Iron...

The TCE and Pesticide Connection 14.10.2024

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 advocac...

Environmental Toxins and Parkinson’s 07.10.2024

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...

Conversation with CND Life Sciences 29.04.2024

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 on...

Brian’s Perspective on Stigma 22.04.2024

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 fi...

Parkinson’s Stigma Internationally 15.04.2024

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.

Parkinson’s Stigma for Women 08.04.2024

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...

What Does Stigma Look Like for People with Parkinson’s? 01.04.2024

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 intern...

Things We Don't Often Talk About 24.11.2023

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. 

Things That People Say 17.11.2023

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. 

Things that Women Deal With 10.11.2023

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.

Things That Affect Eating 03.11.2023

From tremors and slowness to changes in sense of smell and taste, those living with Parkinson's face several hurdles when it comes eating. In this episode, Amber speaks with founder Brian Grant about eating - from fears about swallowing to awkward social situations.  

India 22.06.2023

This year India’s population surpassed the population of China. In this episode, Dr. Soania Mathur speaks with Dr. Maria Barretto about the experiences of people with Parkinson's in the world’s most populous country. 

Spain 15.06.2023

As we get ready to arrive in Barcelona for the World Parkinson Congress, we wanted to learn more about the experience of people living with Parkinson’s in Spain. In this episode, Dr. Soania Mathur is joined by Paqui Ruiz who lives in Spain.

Uganda 08.06.2023

For some people in our global Parkinson’s community, the misconceptions about the disease and its causes can lead to complete isolation. In this episode, Dr. Soania Mathur speaks with Hannington Kabugo about his experience with Parkinson's in Uganda.

Peru 01.06.2023

This year the World Parkinson Congress is coming to Barcelona. As the WPC approaches, Dr. Soania Mathur is talking with people impacted by Parkinson’s around the world to hear about their experiences living with the disease. In this episode, she's joined by Ana Maria and Ray who are living in Peru.

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