The Parkinson's Podcast
This podcast is for people with Parkinson's, Parkinson's care partners and Parkinson's providers. You'll hear from movement disorder specialists, neurologists, psychiatrists, physical and occupational therapists, complementary therapists, people with Parkinson's and Parkinson's care partners on how to live well with Parkinson's today.
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Is there a right time for DBS? Neurosurgeons, Neurologists, and People With DBS Weigh In
10/15/2026
Is there a right time for DBS? Neurosurgeons, Neurologists, and People With DBS Weigh In
Deep brain stimulation, or DBS, raises a lot of questions, including what it is, who it's for, when the best time for it is, and what living with it is actually like. This episode brings the best of six Davis Phinney Foundation conversations on DBS into one twenty-minute walk through the whole journey, from the basics to what life is like years after surgery. You’ll hear from two neurosurgeons, two movement disorder specialists, and three people who have lived with DBS for years. Dr. Kara Beasley, DO, is a fellowship-trained functional and restorative neurosurgeon who has practiced in Boulder, CO since in 2012. Dr. Beasely also holds a master's degree in biomedical ethics. Dr. Chengyuan Wu, MD, is Professor of Neurological Surgery and Radiology at Thomas Jefferson University in Philadelphia, where he is Division Chief of Epilepsy and Neuromodulation Neurosurgery and directs the fellowship programin stereotactic and functional neurosurgery. Dr. Delaram Safarpour, MD, is Associate Professor of Neurology at Oregon Health & Science University and medical director of the deep brain stimulation program at the OHSU Brain Institute. Dr. Joohi Jimenez-Shahed, MD, is Medical Director of Movement Disorders Neuromodulation and Brain Circuit Therapeutics at the Icahn School of Medicine at Mount Sinai, and former chair of the Davis Phinney Foundation’s Science Advisory Board. Jill Ater was diagnosed with Parkinson’s at 42, in 2005, and had DBS surgery in 2013 and 2015, one side at a time. Marty Acevedo had DBS surgery in 2016 and has been active in the Parkinson’s Association of San Diego. Kevin Kwok, PharmD, is a retired biopharmaceutical executive who was diagnosed with young-onset Parkinson’s in his late forties and chose DBS in 2013. He has served on the Davis Phinney Foundation’s Board of Directors since 2015. For more on DBS and living well with Parkinson’s, visit dpf.org.
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Disease Modification in Parkinson's: What It Means and What's Coming Next
09/30/2026
Disease Modification in Parkinson's: What It Means and What's Coming Next
Learn more about Parkinson's and find support: Researchers are exploring a growing number of potential disease-modifying therapies for Parkinson's. But what does "disease-modifying" actually mean, and what progress is being made? In this podcast, Chris Krueger of the Davis Phinney Foundation talks with Dr. Lorraine Kalia, a neurologist and Parkinson's researcher, about the science behind disease modification and why finding therapies that change the course of Parkinson's is so challenging. Topics discussed include research targeting alpha-synuclein, inflammation, genetics, mitochondria, gene therapy, and stem cells, while also addressing common questions about experimental and unproven treatments. Dr. Kalia closes with a hopeful message: while researchers continue working toward tomorrow's breakthroughs, there are meaningful steps people with Parkinson's can take today to support their health, well-being, and quality of life. This episode was produced with support from AskBio. Speaker Bio: Lorraine Kalia, MD, PhD, FRCPC is a scientist at the Toronto Western Research Institute and Tanz Centre for Research in Neurodegenerative Diseases. She is also a neurologist specializing in Parkinson’s disease and related movement disorders at the Toronto Western Hospital. She is an assistant professor in the Division of Neurology, Department of Medicine at the University of Toronto. Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter-signup
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A Dietitian with Parkinson's On Gut Health, Dairy, and Eating Without Guilt
09/21/2026
A Dietitian with Parkinson's On Gut Health, Dairy, and Eating Without Guilt
Learn more about Parkinson's and find support: https://dpf.org In part two of this conversation from our Live Well Today webinar series, Davis Phinney Foundation's Chris Krueger and Richelle Flanagan, a registered dietitian living with young onset Parkinson's, cover gut motility, including constipation, an under-recognized pelvic floor problem, and gastroparesis, address the dairy question, and explain why the Mediterranean diet has the strongest research support for people with Parkinson's. The conversation also covers sugar and insulin resistance, probiotics, alcohol, and how to eat well without guilt when things don't go to plan. Richelle Flanagan is a registered dietitian with over 20 years' experience. She was diagnosed with Parkinson's in 2017, when she was 46, after noticing symptoms while 3 months pregnant with her daughter. In addition to her interest in diet and nutrition, she is passionate about the unmet needs of women with Parkinson's. She is a co-founder of the Women's Parkinson's Project and My Moves Matter, a digital health app to meet the specific needs of women living with Parkinson's. Learn more about Richelle's work at https://www.mymovesmatter.com Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter-signup
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A Dietitian with Parkinson's On Meds, Meals, and Vitamin Levels to Check
09/17/2026
A Dietitian with Parkinson's On Meds, Meals, and Vitamin Levels to Check
Learn more about Parkinson's and find support: https://dpf.org In part one of this two-part conversation from our Live Well Today webinar series, Davis Phinney Foundation's Chris Krueger sits down with Richelle Flanagan, a registered dietitian living with young onset Parkinson's, to discuss how protein interacts with levodopa and why meal timing affects how well your medication works, which key nutrients people with Parkinson's are most commonly deficient in, and why getting your levels checked matters. The conversation also covers iron and magnesium timing, protein redistribution, intermittent fasting, and fueling for exercise and fatigue. Richelle Flanagan is a registered dietitian with over 20 years' experience. She was diagnosed with Parkinson's in 2017, when she was 46, after noticing symptoms while 3 months pregnant with her daughter. In addition to her interest in diet and nutrition, she is passionate about the unmet needs of women with Parkinson's. She is a co-founder of the Women's Parkinson's Project and My Moves Matter, a digital health app to meet the specific needs of women living with Parkinson's. Learn more about Richelle's work at https://www.mymovesmatter.com Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter-signup
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Is It Parkinson's? Early Signs, Diagnosis, and What Can Help
09/11/2026
Is It Parkinson's? Early Signs, Diagnosis, and What Can Help
Learn more about Parkinson's and find support: https://dpf.org Although a tremor is the most well-known symptom of Parkinson's, a tremor may not be the earliest symptom. Symptoms like loss of smell, constipation, acting out dreams, anxiety, and changes in handwriting can show up years before a diagnosis. Cognitive neurologist Dr. Jeffrey Maneval joins Chris Krueger to walk through the most common early signs, why Parkinson's is so often confused with conditions that mimic it, and the tests that can bring clarity, from sleep studies and DaTscans to skin biopsy and genetic testing. You don't have to wait for a formal diagnosis to start treating symptoms. Dr. Maneval discusses how early interventions, including physical therapy, Parkinson's boxing, voice therapy, and mental health support, can help you live well today, even before you have a diagnosis. Dr. Jeffrey Maneval is a board-certified neurologist at MaineHealth specializing in cognitive disorders, including dementia, Alzheimer's disease, and Parkinson's disease. As Director of Cognitive and Behavioral Neurology, he is dedicated to advancing patient care, education, and research to improve the lives of people living with neurological conditions. Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter-signup This episode is sponsored by CND Life Sciences, the developer and provider of the Syn-One skin biopsy test.
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Parkinson’s Treatment Gaps: How Emerging Therapies May Help
09/02/2026
Parkinson’s Treatment Gaps: How Emerging Therapies May Help
Learn more about Parkinson's and find support: In this episode of the Parkinson’s Podcast, we welcome Dr. Abhi Mahajan and two retired physicians living with Parkinson’s, Doug Redosh and Stan Livingston, for a discussion about what’s missing in current Parkinson’s treatments, how the next generation of treatments may help, and how people with Parkinson’s might approach emerging treatments as they become available. This episode is sponsored by AskBio. Sign up for updates on webinars, events, and resources for the Parkinson's community:
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Parkinson’s: When Desire Shifts, Touch Feels Different, and Bodies Change
08/20/2026
Parkinson’s: When Desire Shifts, Touch Feels Different, and Bodies Change
Learn more about Parkinson's and find support: https://dpf.org Intimacy, in all its forms, doesn't disappear with a Parkinson's diagnosis, but it does change. In this episode, Dr. Kelly Rees joins Chris Krueger for a candid conversation about staying close when Parkinson's changes your body, your self-image, and your relationship. They talk through what to do when touch becomes unpleasant, how to navigate mismatched desire without pressuring each other, impulse control changes related to dopamine agonists, and how couples stay connected when symptoms mean sleeping in separate beds. Whether you live with Parkinson's or care for someone who does, Dr. Rees's closing advice holds the whole conversation: don't give up on yourself. Kelly Rees, PhD is a board-certified therapist who specializes in intimacy, relationships, and sexual wellbeing in the context of Parkinson's. Dr. Rees has 15 years of clinical experience working with adults and couples, and she co-developed a program offering free intimacy and relationship classes to the Parkinson's community. Her work focuses on how Parkinson's symptoms, medications, body changes, and shifting roles can affect desire, connection, and communication, and on helping individuals and care partners adapt in ways that support quality of life and emotional closeness. This conversation comes from the Davis Phinney Foundation's June 2026 Live Well Today webinar. Watch the full webinar video here: https://youtu.be/G6c7SQnHrLs Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter
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A Pocketful of Hope: The Harmonica Parkinson's Project
07/16/2026
A Pocketful of Hope: The Harmonica Parkinson's Project
Learn more about Parkinson's and find support: https://dpf.org For many people with Parkinson’s, speech and swallowing issues are among the more difficult symptoms of Parkinson’s. Having speech and swallowing challenges can be isolating and lead to complications like aspiration. In this episode of The Parkinson’s Podcast, listen in as Kevin Lockette, Neal Tomita, and Cheryl Lippman describe their experience with the Harmonica Parkinson’s Project and how playing the harmonica can help people with Parkinson's improve their speech and swallowing while also connecting with their community. For more about the Harmonica Parkinson’s Project visit https://www.harmonicaparkinsonsproject.com/ Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter-signup
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What Makes Gravel Cycling Different—and Why It Matters for Parkinson's
07/08/2026
What Makes Gravel Cycling Different—and Why It Matters for Parkinson's
Learn more about Parkinson's and find support: https://dpf.org In this episode of the Parkinson’s Podcast, Chris Krueger talks with Linda English, David Dietz, and Rachel Ritter about cycling on gravel roads while living with Parkinson’s. This podcast was produced in Partnership with Dirty Free Hub, a non-profit organization that provides information about gravel cycling routes in 10 states, British Columbia, and Tasmania. Learn more about Dirty Free Hub at . The following is a list of equipment our guests recommended: for ease of stopping and starting for safety when sharing roads with cars A can be placed on the handlebars or helmet can help riders stay more upright Sign up for updates on webinars, events, and resources for the Parkinson's community: https://dpf.org/newsletter-signup Learn more about Parkinson's and find support: Sign up for updates on webinars, events, and resources for the Parkinson's community:
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Walking Soccer for Parkinson's: Building Community and Confidence
06/30/2026
Walking Soccer for Parkinson's: Building Community and Confidence
Soccer and Parkinson’s may not seem like an obvious connection—but for a growing number of people around the world, the beautiful game offers far more than exercise. In this episode of the Parkinson’s Podcast, Chris Krueger talks with Keith Sides about his experience participating in a Walking Soccer for Parkinson’s program. Together, they discuss balance, coordination, confidence, community, and the value of trying something new after a Parkinson’s diagnosis. Whether you’re a lifelong soccer fan or have never kicked a ball before, this conversation explores how finding enjoyable ways to move can support living well with Parkinson’s. Read the blog post about the Walking Soccer for Parkinson's program and find links to other resources about walking soccer: Learn more about Parkinson's and find support: Sign up for updates on webinars, events, and resources for the Parkinson's community: Davis Phinney Foundation, Copyright 2026
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Urinary Urgency, Vertigo, and Vision Changes: Parkinson's and the Senses (Part 3)
05/27/2026
Urinary Urgency, Vertigo, and Vision Changes: Parkinson's and the Senses (Part 3)
Learn more about Parkinson's and find support: In part three of this three-part series on Parkinson's and the senses, the panel covers vision changes like difficulty driving at night, light sensitivity, depth perception, and how DBS adjustments can affect focus. They also discuss vertigo, dizziness, and the urinary urgency that many people with Parkinson's experience but rarely talk about, including practical strategies like pre-boarding flights and planning bathroom access. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Season 7 Episode 8 Davis Phinney Foundation, Copyright 2026
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Sensory Overload, Proprioception, and Touch: Parkinson's and the Senses (Part 2)
05/20/2026
Sensory Overload, Proprioception, and Touch: Parkinson's and the Senses (Part 2)
Learn more about Parkinson's and find support: In part two of this three-part series on Parkinson's and the senses, the panel discusses how Parkinson's affects hearing, touch, and the ability to handle busy environments. They cover brain processing sound slower, overstimulation in noisy and crowded places, proprioception and not knowing where your body is in space, the challenge of touchscreens and keypads, and how loss of dexterity has directly impacted their careers. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Season 7 Episode 7 Davis Phinney Foundation, Copyright 2026
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Phantosmia, Lost Flavors, and More: Parkinson's and the Senses (Part 1):
05/14/2026
Phantosmia, Lost Flavors, and More: Parkinson's and the Senses (Part 1):
Learn more about Parkinson's and find support: In part one of this three part series on Parkinson's and the senses, Amber, Chris, Sree, Kat, Stan, Larry, and Kristi talk about how Parkinson's affects the senses we don't always think about. The panel digs into smell and taste, from olfactory hallucinations and not knowing if you smell to craving stronger flavors, safety concerns around spoiled food and gas leaks, and digestive changes that come along for the ride. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Season 7 Episode 6 Davis Phinney Foundation, Copyright 2026
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Freezing in Crosswalks, Gratitude, and Saying Goodbye: The Parkinson's Podcast Unfiltered Finale
04/15/2026
Freezing in Crosswalks, Gratitude, and Saying Goodbye: The Parkinson's Podcast Unfiltered Finale
Learn more about Parkinson's and find support: https://dpf.org In the series finale of the Parkinson's Podcast Unfiltered, hosts Heather Kennedy, Kat Hill, and Chris Krueger answer audience questions, including how to handle well-meaning strangers who grab you when you're frozen or struggling to walk. The conversation turns to what they're each grateful for after years of living with Parkinson's, from the people they've met to the deeper lessons in patience, self-compassion, and acceptance. They also open up about why the podcast has become harder to sustain as their own symptoms progress. It's an honest, heartfelt farewell that captures everything this show has been about. Sign up for updates on webinars, events, and resources for the Parkinson’s community: https://dpf.org/newsletter-signup Season 7 Episode 5 Davis Phinney Foundation, Copyright 2026
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Parkinson's, Love, and Making Room for the Hard Stuff
03/16/2026
Parkinson's, Love, and Making Room for the Hard Stuff
Learn more about Parkinson's and find support: In this episode, Kat's husband Ken joins the panel to talk through the realities of planning ahead, from living trusts and hard family conversations to knowing when your plan needs to change. The conversation also takes on the language of "fighting" Parkinson's, and why both Kat and Ken have moved toward something more like partnership with the disease than battle. Along the way, the panel gets into the tension between independence and asking for help, and what honest communication actually looks like in a relationship shaped by chronic illness. Sign up for updates on webinars, events, and resources for the Parkinson’s community: https://dpf.org/newsletter-signup Learn more about the Davis Phinney Foundation for Parkinsons's: https://dpf.org Season 7 Episode 4
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Sexual Health, Levodopa Myths, Hypoxia Research, and More with Dr. Bas Bloem, Pt 2
02/15/2026
Sexual Health, Levodopa Myths, Hypoxia Research, and More with Dr. Bas Bloem, Pt 2
Learn more about Parkinson's and find support: In part two, Dr. Bas Bloem and Polly Dawkins tackle some of the most pressing topics in the Parkinson's community. They address sexual health, levodopa phobia head-on, share breakthrough research on intermittent hypoxia, and discuss the overlooked connection between gut health and medication effectiveness. This episode offers both cutting-edge science and practical guidance for living well with Parkinson's. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Podcast Produced by Sia Urroz, Davis Phinney Foundation
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Holistic Approach to Parkinson's: Exercise, Supplements, and More With Dr. Bas Bloem, Pt. 1
02/11/2026
Holistic Approach to Parkinson's: Exercise, Supplements, and More With Dr. Bas Bloem, Pt. 1
Learn more about Parkinson's and find support: In this first part of our two-part conversation, Dr. Bas Bloem and Polly Dawkins discuss why a holistic approach to Parkinson's care matters. They explore the latest evidence on exercise as a disease-modifying treatment, the critical role of supplements and nutrition, and how optimizing every aspect of your life—from sleep to stress management—can transform your quality of life. Whether you're newly diagnosed or living with Parkinson's for years, this conversation offers practical, evidence-based strategies for taking control of your care. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Podcast Produced by Sia Urroz, Davis Phinney Foundation
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How Our Approach to Living With Parkinson’s Changes as It Gets Harder
01/09/2026
How Our Approach to Living With Parkinson’s Changes as It Gets Harder
In this episode of the Parkinson's Podcast Unfiltered, the group is joined by a special guest to respond to a listener’s question about how their relationship with Parkinson’s has changed over time. Together, they talk through the different ways they have named and understood Parkinson’s since diagnosis, including ideas of fighting, endurance, acceptance, and daily negotiation. The conversation moves between personal stories, practical coping strategies, and reflections on how identity, energy, and priorities shift as symptoms progress. Rather than settling on one way of framing Parkinson’s, the episode explores how those frames evolve. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Learn more about the Davis Phinney Foundation for Parkinsons's:
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Parkinson’s Clinical Trials: Red Flags, Safety, and What to Consider
12/23/2025
Parkinson’s Clinical Trials: Red Flags, Safety, and What to Consider
In this episode of the Parkinson’s Podcast, Chris Krueger talks with a clinical research team from University of Toronto about how the clinical trial process works, how participants can have the best experience in a trial, and why a team approach to trials is necessary and good. In this episode, you’ll hear from Dr. Alfonso Fasano, Dr. Arturo Abundes Corona, Sara Naghdlou, a clinical research coordinator with a background in biomedical engineering; and Yu-Yan Poon, a registered nurse who supports trials at the University of Toronto. This episode is sponsored by BlueRock Therapeutics. Sign up for updates on webinars, events, and resources for the Parkinson’s community: Learn more about the Davis Phinney Foundation for Parkinsons's:
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Home Independence and Safety in Parkinson’s: What to Plan for at Each Stage
12/10/2025
Home Independence and Safety in Parkinson’s: What to Plan for at Each Stage
Occupational therapist and aging-in-place expert Carol Chiang joins us to discuss her new book, Age in Place or Find a New Space. Carol explains why meaningful interactions—not just safety—belong at the center of planning for life with Parkinson’s, and how “the choices you make today become the consequences you live with tomorrow.” In this podcast episode, Carol discusses the importance of early-stage steps like decluttering and fall-prevention basics, practical visual cueing for freezing, how to break home updates into manageable pieces, and honest caregiver conversations. Carol also shares how to think about modifying a home versus considering a move, and why planning early protects both independence and connection. A grounded, hopeful conversation about creating a home that supports who you are and how you want to live. Learn more about Carol and her work, and find her book at: Explore the OT-curated home-modification resource she mentioned: Ask Samie: Sign up for updates on webinars, events, and resources for the Parkinson’s community: Learn more about the Davis Phinney Foundation for Parkinsons's: GUEST BIO Carol Chiang is an Occupational Therapist and founder of Evolving Homes®, specializing in aging-in-place, age tech, and smart home solutions. With 25 years of experience, she helps individuals and families decide whether to “Age in Place” or “Find a New Space®,” and supports them through the home changes required at each stage of Parkinson’s. A Certified Parkinson’s Wellness Recovery therapist and former Olympic-caliber athlete, Carol teaches the importance of planning ahead, using exercise as medicine, and building habits that protect long-term independence. She consults with organizations, startups, and universities worldwide, and has contributed to AARP, the Davis Phinney Foundation, the National Kitchen & Bath Association, and international aging conferences.
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Parkinson's Related Exhaustion, Personal Care Challenges, and Why Exercise Helps
12/02/2025
Parkinson's Related Exhaustion, Personal Care Challenges, and Why Exercise Helps
In this episode of the Parkinson's Podcast Unfiltered, hosts Heather Kennedy and Kat Hill, along with Chris Krueger, honor their late friend Wayne Gilbert and explore the challenging distinction between fatigue and apathy. They offer practical advice for managing energy levels, including the counterintuitive insight that more movement can actually reduce tiredness, and share tips for grandparents navigating visits with multiple grandchildren. The conversation also tackles personal grooming struggles, with candid solutions like wash-and-go haircuts, dry shampoo, and simplified self-care routines that make daily life more manageable. Sign up for updates on webinars, events, and resources for the Parkinson’s community: https://dpf.org/newsletter-signup
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Gene Therapy for Parkinson’s: Myths vs. Facts
11/17/2025
Gene Therapy for Parkinson’s: Myths vs. Facts
In this episode of the Parkinson’s Podcast, learn about gene therapy for Parkinson’s, including common misunderstandings and ongoing research about it. This episode contains some technical terms and abbreviations. For your convenience, here is a short list of definitions that might be helpful. AADC – Aromatic L-Amino Acid Decarboxylase: An enzyme that helps make dopamine (not a rock and roll band) AAV – Adeno-Associated Virus: A harmless virus used to deliver gene therapy CDNF – Cerebral Dopamine Neurotrophic Factor: A protein that helps keep dopamine-producing cells healthy DBS – Deep Brain Stimulation: A surgical treatment that uses electrical signals to help control symptoms GAD – Glutamic Acid Decarboxylase: An enzyme that helps rebalance brain circuits. GBA – A gene linked to Parkinson’s risk GCH1 – GTP Cyclohydrolase 1: An enzyme that supports dopamine production. GDNF – Glial Cell Line-Derived Neurotrophic Factor: A protein that helps protect brain cells LRRK2 – A gene linked to Parkinson’s risk PARK2 – A gene linked to Parkinson’s risk PET – Positron Emission Tomography: A brain scan that shows chemical activity PINK1 – A gene linked to Parkinson’s risk SNCA – A gene linked to Parkinson’s risk More information about Gene Therapy for Parkinson’s is available here: Sign up for updates on webinars, events, and resources for the Parkinson’s community:
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Pickleball and Parkinson’s: Building Dexterity, Balance, and Community
11/12/2025
Pickleball and Parkinson’s: Building Dexterity, Balance, and Community
In this episode of The Parkinson’s Podcast, Foundation Program Manager Beau Boughamer talks with neurologist Vanessa Hinson and Helen Power, a person living with Parkinson’s, about the sport that’s sweeping the country—and transforming life with Parkinson’s. Dr. Hinson, a movement disorder specialist at the Medical University of South Carolina, shares how pickleball supports balance, coordination, confidence, and connection through her eight-week program for people with Parkinson’s. Helen describes how the game brought her movement, joy, and community, proving that staying active can also mean having fun. Sign up for updates on webinars, events, and resources for the Parkinson’s community—delivered to your inbox.
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ON-OFF Fluctuations in Parkinson’s: Why They Happen and What You Can Do
11/06/2025
ON-OFF Fluctuations in Parkinson’s: Why They Happen and What You Can Do
In this episode, we talk with Dr. Aaron Haug about what the terms ON and OFF mean in the context of Parkinson’s, what ON-OFF fluctuations are, and how to work with your doctor to help manage them. Dr. Haug is a movement disorder specialist based in Englewood, Colorado. Sign up for updates on webinars, events, and resources for the Parkinson’s community—delivered to your inbox. https://dpf.org/newsletter-signup Watch Aaron Haug's video about Tremors and Dyskinesias here: https://youtube.com/shorts/jcjNOnaA0as?feature=share This episode is sponsored by BlueRock Therapeutics. Learn more here: https://www.bluerocktx.com Aaron Haug, MD, is a neurologist and movement disorder specialist in Colorado. He earned his bachelor’s degree at Creighton University and his medical degree at the University of Kansas. He completed a neurology residency and a fellowship in movement disorders at the University of Colorado, including a year as chief resident.
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Confronting Cognitive and Emotional Challenges: The Neuropsychology of Parkinson's - Part 3
10/08/2025
Confronting Cognitive and Emotional Challenges: The Neuropsychology of Parkinson's - Part 3
Sign up for updates on webinars, events, and resources for the Parkinson’s community—delivered to your inbox. https://dpf.org/newsletter-signup In the final episode of this three-part series, Connie Carpenter Phinney and Dr. Mark Mapstone explore the emotional and cognitive changes that can occur as Parkinson’s progresses. They talk openly about issues like apathy, anxiety, executive function decline, and how these changes can affect relationships, communication, safety, and daily life—including decisions around driving and independence. While the conversation acknowledges grief, frustration, and loss, it also offers insight, practical advice, and strategies for living well through change. This episode is for anyone facing or seeking to understand the emotional and cognitive realities of Parkinson’s—people diagnosed, care partners, and clinicians alike. Connie Carpenter Phinney is a co-founder of the Davis Phinney Foundation and has been her husband’s care partner for over 25 years. Her background in science combined with her lived experience and curiosity helped shape this conversation with neuropsychologist Dr. Mark Mapstone. Connie is the host of the Foundation’s Care Partner Meetup, a monthly virtual meetup for Parkinson’s care partners held the first Tuesday of each month. To attend the meetup, sign up here: https://davisphinneyfoundation.org/events/parkinsons-care-partner-meetup/ Dr. Mark Mapstone is Professor of Neurology at the University of California, Irvine School of Medicine. He is a member of the UCI Institute for Memory Impairments and Neurological Disorders and a Fellow of the UCI Center for Neurobiology of Learning and Memory. His research focuses on pre-clinical detection of neurological disease using cognitive tests and biomarkers obtained from blood. He has a special interest in developing strategies to maintain successful cognitive aging. In the clinic, he specializes in cognitive assessment of older adults with suspected brain disease. Dr. Mapstone earned a PhD in Clinical Psychology at Northwestern University and completed fellowship training in Neuropsychology and Experimental Therapeutics at the University of Rochester. He received a Career Development Award from the National Institute on Aging and his research has been funded by the National Institutes of Health, the Michael J. Fox Foundation, and the Department of Defense. This content is possible thanks to the generosity of our listeners. Every day more people are diagnosed with Parkinson’s, and this means our work is more important than ever. Please support our work by visiting https://dpf.org/donate. Interested in our Living with Parkinson's Meetup, Care Partner Meetup, or Live Well Today Webinars? Learn how to join. https://dpf.org/webinars
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The Neuropsychology of Parkinson's - Part 2: What to Expect from a Neuropsych Evaluation
10/01/2025
The Neuropsychology of Parkinson's - Part 2: What to Expect from a Neuropsych Evaluation
Sign up for updates on webinars, events, and resources for the Parkinson’s community—delivered to your inbox. In this episode, Connie and Dr. Mapstone dive into the role of neuropsychology in Parkinson’s care. They explain what a neuropsychological evaluation is, what to expect during an office or virtual visit, and how results can help guide treatment, daily planning, and care strategies. This episode also discusses why someone might be referred, how testing works, and what insights it can offer for both individuals and families. **This content is possible thanks to the generosity of our listeners. Every day more people are diagnosed with Parkinson’s, and this means our work is more important than ever. Please support our work by visiting Connie Carpenter Phinney Connie Carpenter Phinney is a co-founder of the Davis Phinney Foundation and has been her husband’s care partner for over 25 years. Her background in science combined with her lived experience and curiosity helped shape this conversation with neuropsychologist Dr. Mark Mapstone. Connie is the host of the Foundation’s Care Partner Meetup, a monthly virtual meetup for Parkinson’s care partners held the first Tuesday of each month. To attend the meetup, sign up here: https://davisphinneyfoundation.org/events/parkinsons-care-partner-meetup/ Dr. Mark Mapstone Mark Mapstone is Professor of Neurology at the University of California, Irvine School of Medicine. He is a member of the UCI Institute for Memory Impairments and Neurological Disorders and a Fellow of the UCI Center for Neurobiology of Learning and Memory. His research focuses on pre-clinical detection of neurological disease using cognitive tests and biomarkers obtained from blood. He has a special interest in developing strategies to maintain successful cognitive aging. In the clinic, he specializes in cognitive assessment of older adults with suspected brain disease. Dr. Mapstone earned a PhD in Clinical Psychology at Northwestern University and completed fellowship training in Neuropsychology and Experimental Therapeutics at the University of Rochester. He received a Career Development Award from the National Institute on Aging and his research has been funded by the National Institutes of Health, the Michael J. Fox Foundation, and the Department of Defense. Interested in our Living with Parkinson's Meetup, Care Partner Meetup, or Live Well Today Webinars? Learn how to join. https://dpf.org/webinars
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The Neuropsychology of Parkinson's - Part 1: Brain Changes and Impact
09/26/2025
The Neuropsychology of Parkinson's - Part 1: Brain Changes and Impact
Sign up for updates on webinars, events, and resources for the Parkinson’s community—delivered to your inbox. https://dpf.org/newsletter-signup In the first episode of our three-part series about neuropsychology and Parkinson’s, Connie Carpenter Phinney and Dr. Mark Mapstone explore how brain chemistry, especially dopamine, relates to thinking, movement, and mood in Parkinson’s. They break down key terms like cognition and executive function and offer insights into how Parkinson’s affects brain systems beyond motor symptoms. This episode lays the groundwork for understanding how the brain works—and what happens when it changes. **This content is possible thanks to the generosity of our listeners. Every day more people are diagnosed with Parkinson’s, and this means our work is more important than ever. Please support our work by visiting https://dpf.org/donate.** Interested in our Living with Parkinson's Meetup, Care Partner Meetup, or Live Well Today Webinars? Learn how to join. https://dpf.org/webinars Visit https://dpf.org to learn more about the Davis Phinney Foundation for Parkinson's. Speaker Bios: Connie Carpenter Phinney Connie Carpenter Phinney is a co-founder of the Davis Phinney Foundation and has been her husband’s care partner for over 25 years. Her background in science combined with her lived experience and curiosity helped shape this conversation with neuropsychologist Dr. Mark Mapstone. Connie is the host of the Foundation’s Care Partner Meetup, a monthly virtual meetup for Parkinson’s care partners held the first Tuesday of each month. To attend the meetup, sign up here: https://davisphinneyfoundation.org/events/parkinsons-care-partner-meetup/ Dr. Mark Mapstone Mark Mapstone is Professor of Neurology at the University of California, Irvine School of Medicine. He is a member of the UCI Institute for Memory Impairments and Neurological Disorders and a Fellow of the UCI Center for Neurobiology of Learning and Memory. His research focuses on pre-clinical detection of neurological disease using cognitive tests and biomarkers obtained from blood. He has a special interest in developing strategies to maintain successful cognitive aging. In the clinic, he specializes in cognitive assessment of older adults with suspected brain disease. Dr. Mapstone earned a PhD in Clinical Psychology at Northwestern University and completed fellowship training in Neuropsychology and Experimental Therapeutics at the University of Rochester. He received a Career Development Award from the National Institute on Aging and his research has been funded by the National Institutes of Health, the Michael J. Fox Foundation, and the Department of Defense.
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Advanced Parkinson's, Feeling Velcroed to the Bed, and More
09/11/2025
Advanced Parkinson's, Feeling Velcroed to the Bed, and More
Sign up for updates on webinars, events, and resources for the Parkinson’s community—delivered to your inbox. https://dpf.org/newsletter In this episode of the Parkinson's Podcast Unfiltered, hosts Heather, Kat, and Chris tackle one of the toughest questions of this season of Unfiltered: how to manage apathy and depression in advanced Parkinson's while also navigating a healthcare desert. This episode also includes discussion of strategies for sleep, including how to turn over and get comfortable when you feel "velcroed to the bed," as well as some ideas about exercise options for people with limited mobility, from chair yoga to simple seated movements that anyone can do. Finally, your Unfiltered hosts explore creative outlets like the Haiku for Parkinson's program and other artistic practices that can provide new opportunities for emotional expression and therapeutic benefits for people living with Parkinson's. Have a question or comment for the hosts of the Parkinson’s Podcast: Unfiltered? Send it here. https://dpf.org/unfiltered Interested in our Living with Parkinson's, Care Partner, or Live Well Today webinars? Learn how to join. https://dpf.org/webinars To subscribe to our podcast and YouTube channel visit: https://www.youtube.com/@davisphinneyfdn/podcasts
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Precision Medicine and Parkinson’s: The NEULARK Study
09/05/2025
Precision Medicine and Parkinson’s: The NEULARK Study
To subscribe to our podcast and YouTube channel visit: https://www.youtube.com/@davisphinneyfdn/podcasts More people with Parkinson's are impacted by the LRRK2 (often pronounced "Lark two") gene than you might expect. The NEULARK study is a phase II clinical trial designed to investigate whether a new treatment being researched, NEU-411, can slow disease progression and improve quality of life for people with Parkinson’s disease. NEU-411 is an oral medication designed to inhibit overactivity of the LRRK2 gene. In this episode of The Parkinson’s Podcast, we talk with Dr. Fatta Nahab about the NEULARK study. This episode is sponsored by Neuron23, who is also sponsoring the NEULARK study. Our guest, Dr. Nahab, is Vice President of Clinical and Digital Development for Neuron23. For more information about the NEULARK trial please visit: https://parkinsonsresearchlrrk2.com/ or https://clinicaltrials.gov/study/NCT06680830 Season: 6 Episode: 19
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Accessibility, Attention (ADD), and More in Parkinson's
08/06/2025
Accessibility, Attention (ADD), and More in Parkinson's
To subscribe to our podcast and YouTube channel visit: https://www.youtube.com/@davisphinneyfdn/podcasts Heather, Kat, and Chris share their experiences with accessibility and travel challenges while living with Parkinson’s. They dive into attention and focus, including what it’s like to live with both Parkinson’s and ADD. The conversation also covers the realities of freezing of gait—from how it starts to how they manage it day to day. Real, personal, and full of lived insight. Visit to learn more about the Davis Phinney Foundation for Parkinson's. Season: 6 Episode: 18
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