Videos & Webinars

Expert Briefing: Artificial Intelligence & Parkinson’s: Understanding the Promise & Pitfalls

May 13, 2026

Artificial Intelligence (AI) is increasingly shaping how health care information is shared and used—including for people living with Parkinson’s and their care partners. But what exactly is AI, and how does it differ from augmented intelligence, which is designed to support (not replace) human judgment?
 
In this Expert Briefing, our speaker will provide a clear, practical overview of AI’s role in the delivery of care for people with Parkinson’s. The session will explore how AI-enabled tools may influence communication, symptom tracking, and care personalization, and how individuals and care partners can engage with these tools responsibly.
 
The presentation will also address key legal and ethical considerations—such as privacy, accuracy, and over-reliance on technology—while emphasizing the ongoing importance of human connection in care.

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Webinar Summary

Additional Resources

Presenter

Allan D. Wu, MD, FAAN
Parkinson’s Disease and Movement Disorders Center
Northwestern University Feinberg School of Medicine, A Parkinson's Foundation Center of Excellence, Program Director, Northwestern Clinical Informatics Fellowship
Department of Pathology, Feinberg School of Medicine, Faculty Clinical Informatics Consultant
Stanley Manne Children’s Research Institute
Ann & Robert H. Lurie Children’s Hospital of Chicago

My PD Story

George Eckenrode
People with PD

George Eckenrode

Imagine you have recently been diagnosed with a chronic disease and you are attending your first educational conference. You are sitting in a large room with several hundred people listening to a physician with a personal connection to this disease begin his presentation.

I felt a wave of hopelessness; I thought what possible good news could he offer me? I felt like leaving. But I didn’t leave, and I am glad I didn’t. 

My name is George Eckenrode. I am 76 years old, retired, married and have recently moved to Phoenix, AZ from Pennsylvania.  I am a father and a grandfather. I am here in Maricopa County because of these last facts: my wife and I have three grandchildren. And they live here!

Fortunately for me, Maricopa County is a Mecca for people with Parkinson’s disease (PD). It is blessed with the full range of PD services: caring compassionate healthcare providers of all disciplines and state of the art institutions dedicated to all aspects of chronic disease care (diagnosis, treatment, care, education, research and support).

PD Lessons Learned

In school I was taught when the planned lesson activity didn’t go well that all experiences are learning opportunities even if they are not planned. Life is like that too. Here are some things I didn’t expect to learn when I got PD.

  • I sleep funny. One question I was not expecting was: “Do you act out your dreams?” Turns out I do! I have Rapid Eye Movement Behavior Disorder (RBD) — and have since learned sleeping disorders are strongly predictive of PD.
  • I smell badly. Not my state of hygiene but my sense of smell. My wife was not surprised by my diminished sense of smell (discovered through a sniff test at my doctor’s office) as evidenced by her having to remind me to take the trash out.
  • I am very mood-y. I have had dysthymia (a form of depression) for years but I never knew I had anxiety till I learned I had PD. Even the depression took on a more negative flavor—that of apathy.
  • I don’t ever forget a face; it’s everything else I forget. I would like to think I just have “tip of the tongue” memory loss; but it’s a lot more. I have the slowness of recall. It doesn’t matter how recently I heard or even used the word. It just won’t come.
  • Welcome to orthostatic hypotension! Such a lovely expression for lightheadedness, isn’t it? I had noticed this for a while before I was diagnosed but I usually blamed it on other causes. What it really was caused by, is my PD.

There is a new person in my life: my “care partner."

I have known my wife for over 50 years. During that time, she has carried a list of monikers: my friend, my girlfriend, my wife, my financial support during grad school, and the mother of my children.

Now with the advent of my chronic illness, she has added one more title — that of care partner.

While most wedding vows still include the part about “in sickness and in health”, the arrival of a PD diagnosis changes that vow from a possibility to a certainty.  As with all other monikers she has carried, this position is again unpaid.

I like support groups — who knew?

Support groups have been a vital part of healthcare for decades now. My first neurologist in Phoenix recommended beginning an exercise program and mentioned a specific one in particular. Attending that exercise program opened the door to a world of PD support including joining a support group. It became clear to me after attending my first Parkinson’s support group that this group would play an important role in my life going forward.

It was a place to ask questions, questions no doctor could answer, unless, of course, he too had Parkinson’s. It was also a place to hear and tell stories and to hear and share information. And as its name indicates, a place to receive and offer support.

Things are changing but is it PD?

For those of us, like me, diagnosed in our seventh or eighth decade of life, we are often already experiencing some changes in our body’s functioning. The question then becomes: is this change (in hearing, bladder control, memory) PD-related or is it aging or something entirely different? 

Questioning is good, both at our doctor’s office as well as with our care partner and our support group. Questioning means we are paying attention, something we may not have been doing before the tip of the PD iceberg broke the surface.

Closing Thoughts

My wife is fond of making the following sound statement: “When you have met one person with PD, you have met one person with PD.” And now you have met one person with PD and what he has learned and continues to learn.

From exercise classes to support groups, find Parkinson’s resources near you.

My PD Story

Gary Gosselin
People with PD

Gary Gosselin

INTENT. Perseverance. You’re not alone.

I was diagnosed with Parkinson’s disease (PD) in May 2020, right in the middle of the COVID-19 pandemic. Like a lot of people, I don’t remember much of what the doctor actually said. I do remember walking out of there thinking, “OK, now what?”

Because I was adopted, I don’t have any family medical history to rely on. My mind went straight to my two sons and four grandchildren — what does this mean for them? I remember thinking I need to understand this, for them as much as for me.

Those first months were a bit of a blur. A lot of appointments, a lot of questions, and a lot of just trying to make sense of it.

Some mornings just took a little more to get going. Nothing dramatic — I’d sit for a minute before starting. Just taking a moment before the day began. Some days it was fatigue or just feeling a step behind — the kind of things people don’t really see.

That’s where one word started to matter: Perseverance. I had it written on a card on my file cabinet and I saw it every day. It wasn’t anything fancy, but it reminded me to keep moving forward, even when I didn’t have it all figured out.

A few years later, through the Parkinson Voice Project, I was introduced to another word: INTENT — living and speaking with purpose.

Those two words just clicked for me.

So, in 2024, I made a simple wristband — partly for myself, and partly to thank the people who had helped me along the way. I ordered just 10. INTENT on one side, Perseverance on the other.

That was it. No plan, no idea it would go anywhere. I put it on every morning. I started sharing them—and then people began to ask about them.

Then something happened that changed everything.

I was on a Parkinson’s Zoom call with a group from Boston, telling the story of the Resolve Band, when someone held one up. They had gotten it the day before through Parkinson Voice Project — one of the ones I had sent to Dallas to thank them for their project.

That’s when it hit me — this thing had taken on a life of its own. And the message was pretty simple: You’re not alone.

Since then, hundreds of bands have been made available to people with Parkinson’s disease, care partners and clinicians at no charge. It’s also led me into some advocacy work, which has been another way to stay connected and give something back.

For me, though, it still comes back to something simple. Focus on what you can control. Stay engaged. Keep moving forward. I’ve been lucky. I’ve got a great family who’s been with me every step of the way.

I’ve also had the chance to participate in research studies and clinical trials, including PD GENEration: Powered by the Parkinson's Foundation.

Participating in PD GENEration helped me understand what my diagnosis really meant — not just for me, but for my family. When I got the results back, I sat down and wrote an email to my two sons, my wife and other family members to walk them through it. That’s how important it felt to me. The process itself was straightforward, but more than anything, it felt like I was doing something that mattered — for them and for others down the road.

What I didn’t expect was how much that experience would carry forward. A few months later, I was in Washington, DC, at the Parkinson’s Policy Forum, meeting and advocating with my senators and congressman.

I shared this story — how PD GENEration gave my family clarity and relief — and how programs like it only exist because of the broader research infrastructure supported by non-profits like the Parkinson’s Foundation and the NIH.

For me, it wasn’t just participating in a study. It became something I could speak to —real experience, real impact — and use to advocate for continued investment in Parkinson’s research so more families can have that same clarity.

Participating in research and advocacy work has given me another way to stay engaged and give something back. What gives me hope is the community and the fact that things are moving in the right direction.

Gary Gosselin at the World Parkinson Congress 2026

I just returned two days ago from Phoenix, where I attended the World Parkinson Congress, where I gave out many English and Spanish wristbands and presented a poster abstract related to the Resolve Band and advocacy work.

If I had one thing to say to someone newly diagnosed, it would be this: Take a breath. You don’t have to solve this all at once. Just take the next step. That’s what I do.

Every day starts the same way—

With INTENT.

And with Perseverance.

Some days it’s just for me. Other days, it starts a conversation.

By joining PD GENEration study, participants can discover new knowledge about their genetics, understand their family’s risks and help benefit generations to come. Learn more and enroll today.

Professional Education

Moving through Parkinson's: Does Intensity and Dose Matter?

Virtual ( Zoom )
1:00 pm to 2:00 pm EST
Free
Parkinson's Professional Exchange banner

Exercise is now clearly recognized as a key part of the Parkinson's treatment plan. It is a core component of comprehensive Parkinson's care and a potential disease-modifying intervention. Learn about new exercise research focusing on high vs moderate intensity, domains of exercise, and implementation strategies for people with Parkinson's.

Featuring special guests: Jimmy Choi and Daniel Corcos, PhD with moderator, Sneha Mantri, MD, MS, FAAN.

Upcoming Events

Educational Events

Mind, Mood and Motion

11:00 am to 2:30 pm EST
FREE
Mind Mood & Motion (man running)

Check-in & Resource Fair* begins at 11:00 a.m. and the program starts at 11:30 a.m. 

Exercise is a powerful tool for managing Parkinson’s disease symptoms at every stage. This program explains how staying active supports movement, mood, and thinking- and may even slow disease progression. Participants will learn practical ways to build exercise into daily life for better mobility and overall well-being. 

*The Resource Fair will feature local Community Partners that provide services and support for the Parkinson’s Community.

Speakers

Sara Hooshmand, MD 
Tonya Bernard, DPT
Amanda Mower, OT

Lunch will be served. Parking available on site.

There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends and the community. 

Sponsor

Upcoming Events

Educational Events

Parkinson's Basics: What You Need to Know

Virtual ( Zoom )
1:00 pm to 2:00 pm EST
Free
Husband and wife lookin at a tablet while on their porch

This program offers an introduction and basic overview of Parkinson’s disease (PD). PD varies from person to person and changes over time. Discover its causes, common symptoms, available treatments and effective strategies for managing them. Learn practical daily living tips to empower you to take charge of your health and to navigate the challenges of living with PD.

Speaker

Rozena Davis, APRN-CNP
The Ohio State University Wexner Medical Center
A Parkinson's Foundation Center of Excellence

There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.

PD Health @ Home is presented by the Light of Day Foundation, whose generosity has made this programming possible.

Light of Day

This is a virtual program, taking place live, using the online Zoom platform. Instructions on joining the webinar are provided after registering.

Upcoming Events

Raise Awareness

Insights from our 2026 State of the Community Survey

🧠 What will you learn in this article?

  • Key takeaways from the Parkinson’s Foundation 2026 State of the Community Survey.
  • How the Foundation will use survey results to help shape programs and resources.
  • Real-world insights about care, research participation, and more for the Parkinson’s disease (PD) community.  
Couple filling out survey together

Each year, the Parkinson’s Foundation surveys the Parkinson’s disease community to learn what topics matter most and what support people need.

Results from our 2026 State of the Community Survey guide Parkinson’s Foundation programs and resources, ensuring we stay focused on what matters most to people affected by PD.

This year, more than 9,000 people (people with PD, care partners, family members, friends and health professionals) took the survey in English and Spanish —up 30% from 2025. Responses came from all 50 states and from people outside the U.S., giving us valuable insight into the experiences and needs of our global Parkinson’s community.

2026 State of the Community Survey Findings

Below are key findings from this year’s survey.

1. Understanding symptoms, medications, and treatments remain top priorities.

Survey participants continue to mention movement symptoms, non-movement symptoms ,and knowledge about medications and treatment options as top concerns. More than half identified movement symptoms (61%) and non-movement symptoms (52%) as most concerning, especially tremor, gait and balance, sleep, mood and cognition.

Participants expressed strong interest in learning more about symptom management and treatment options. Similarly, Spanish-speaking community members were most interested in research updates and treatments options.

Key takeaway

People want clear, trusted information about symptoms, treatment options and research. We will use these findings to guide future education and programs.

Visit our PD Library to explore topics that matter most to you.

2. Uncertainty about what to discuss during medical appointments and barriers to care continue to impact the community.

A big challenge during appointments is knowing which symptoms and questions to ask the PD doctor, and many find it hard to talk about mental and emotional health. Similar to last year, most people said they spend 15–30 minutes with their provider.

“I believe in narrative medicine, where I encourage patients to share their Parkinson’s story — focusing on the symptoms affect them the most and working together to create a personalized care plan that empowers them to take an active role.”

— Sneha Mantri, MD, Parkinson’s Foundation Chief Medical Officer

About 25% of respondents went to the emergency room or stayed in the hospital in the past year, and only 38% knew about the Parkinson’s Foundation Hospital Safety Guide.

Although most reported not having barriers to care, others said it can be hard to get services and support. In the English survey, the most common barriers were:

  • Not knowing what services are available or how to get them
  • Trouble getting appointments
  • Having to travel far to get care

For Spanish-speaking participants, the cost of services was the top barrier, while other challenges included language, transportation and not having enough services available.

Key takeaways

Medical appointments can feel overwhelming, especially as symptoms change over time. These findings show a need for tools and resources that help people feel ready and more confident during healthcare visits. Learn how to make the most of your care.

Getting Parkinson’s care looks different for everyone. Understanding barriers of accessing quality care helps us see where more education, support and outreach are needed.

3. Awareness of PD GENEration is growing, but research participation gaps remain.

In the English survey, half of participants had heard of PD GENEration: Powered by the Parkinson’s Foundation, compared to only 33% among Spanish-speaking community members. But hearing about it doesn’t always mean participating in the study. About 60% of people who were aware and eligible took part in PD GENEration, with substantially fewer Spanish speakers taking part (32%).

Outside of PD GENEration, most respondents said they have not participated in clinical research studies.

Key takeaway

These findings show we can do more to explain clinical research and help people understand how to take part in research studies, including in PD GENEration.

PD Trial Navigator is a new program that helps connect PD GENEration participants to relevant studies, while providing personalized support throughout the process.

4. People are seeking trusted information, support and community resources.

Participants shared that the Parkinson’s Foundation website, Parkinson.org, was the most-used resource. Spanish-speaking community members also highlighted online education programs, including webinars and Expert Briefings, as most helpful.

Reflecting on the resources that have been most helpful, participants also pointed out areas that were missing, or underrepresented, in their community, particularly around exercise programs and emotional health resources.

When asked about the policy issues that matter most, participants identified increasing research funding and improving the review and approval process for new treatments as top priorities.

Digital tools may help with learning, tracking symptoms and managing care, yet many participants (60–70%) said they do not know about these tools or do not use them.

Key takeaway

These findings show why it’s important to have trusted, easy-to-use resources that support learning, emotional health, connection and confidence throughout the Parkinson’s journey. Explore our blog for the latest information.

Learn more about our policy and advocacy priorities here.

What These Results Mean for Our Community

In both the English and Spanish surveys, we saw common themes:

  • People want education about symptoms and treatment options.
  • Many people need more help getting care and talking with their doctor.
  • More people are hearing about research, but few are joining studies.
  • People want trusted information and support.

These results remind us that living with Parkinson’s, caring for someone with Parkinson’s and connecting with the PD community look different for each person. Hearing directly from the community helps us keep improving our programs, education and resources.

Next Steps

The Parkinson’s Foundation will keep listening and responding to the community’s needs and priorities. We will keep working to advance our mission and make life better for everyone affected by PD.

While no single survey can capture the full range of experiences within the Parkinson’s community, the insights shared through surveys like the State of the Community Survey help guide our programs, resources, research, and advocacy efforts. That is why we continue to seek feedback in multiple ways and encourage people with Parkinson’s, care partners, and family members to join our survey initiative and participate in future surveys.

To help shape future Parkinson’s Foundation initiatives and ensure your voice is heard, consider joining our survey initiative. Learn more about our Surveys here.

Raise Awareness

Resultados de nuestra Encuesta Acerca del Estado de la Comunidad 2026

🧠 ¿Qué aprenderá en este artículo?

  • Conclusiones clave de la Encuesta Acerca del Estado de la Comunidad 2026 de la Parkinson's Foundation.
  • Cómo la Fundación utilizará los resultados de la encuesta para ayudar a dar forma a los programas y recursos.
  • Perspectivas del mundo real sobre atención, participación en investigaciones y más para la comunidad de la enfermedad de Parkinson (EP).
Pareja completando una encuesta

Cada año, la Parkinson's Foundation encuesta a la comunidad de la enfermedad de Parkinson para conocer qué temas son más importantes y qué apoyo necesitan las personas.

Los resultados de nuestra Encuesta del Estado Acerca del Estado de la Comunidad 2026 orientan los programas y recursos de la Parkinson's Foundation, asegurando que nos mantengamos enfocados en lo que más importa a las personas afectadas por la EP.

Este año, más de 9.000 personas (personas con la EP, cuidadores, familiares, amigos y profesionales de la salud) respondieron la encuesta en inglés y español, un aumento del 30 % con respecto a 2025. Las respuestas provinieron de los 50 estados y de personas fuera de los EE. UU., lo que nos brinda información valiosa sobre las experiencias y necesidades de nuestra comunidad global del Parkinson.

Resultados de nuestra Encuesta Acerca del Estado de la Comunidad 2026

A continuación se presentan los hallazgos clave de la encuesta de este año.

1. Comprender los síntomas, medicamentos y tratamientos sigue siendo una prioridad principal.

Los participantes de la encuesta continúan mencionando los síntomas motores, los síntomas no motores y el conocimiento sobre medicamentos y opciones de tratamiento como principales preocupaciones. Más de la mitad identificó los síntomas motores (61 %) y los síntomas no motores (52 %) como los más preocupantes, especialmente temblor, marcha y equilibrio, sueño, estado de ánimo y cognición.

Los participantes expresaron un gran interés en aprender más sobre el manejo de síntomas y las opciones de tratamiento. De manera similar, los miembros de la comunidad de habla hispana estaban más interesados en actualizaciones de investigación y opciones de tratamiento.

Conclusión clave

Las personas desean información clara y confiable sobre síntomas, opciones de tratamiento e investigación. Utilizaremos estos hallazgos para guiar la educación y los programas futuros.

Visite nuestra Biblioteca de la EP para explorar los temas que más le importan.

2. La incertidumbre sobre qué discutir durante las citas médicas y las barreras para la atención continúan afectando a la comunidad.

Un gran desafío durante las citas es saber qué síntomas y preguntas hacerle al médico de la EP, y muchos encuentran difícil hablar sobre la salud mental y emocional. Similar al año pasado, la mayoría de las personas dijeron que pasan de 15 a 30 minutos con su proveedor.

«Creo en la medicina narrativa, donde aliento a los pacientes a compartir su historia de Parkinson —enfocándose en los síntomas que más les afectan y trabajando juntos para crear un plan de atención personalizado que les permita asumir un papel activo». 

— Dra. Sneha Mantri,  directora médica en jefe de la Parkinson's Foundation

Aproximadamente el 25 % de los encuestados acudió a la sala de emergencias o permaneció en el hospital en el último año, y solo el 38 % conocía la Guía de seguridad hospitalaria de la Parkinson's Foundation.

Aunque la mayoría informó no tener barreras para la atención, otros dijeron que puede ser difícil obtener servicios y apoyo. En la encuesta en inglés, las barreras más comunes fueron:

  • No saber qué servicios están disponibles o cómo obtenerlos
  • Dificultad para obtener citas
  • Tener que viajar lejos para recibir atención

Para los participantes de habla hispana, el costo de los servicios fue la principal barrera, mientras que otros desafíos incluyeron el idioma, el transporte y no tener suficientes servicios disponibles.

Conclusiones clave

Las citas médicas pueden resultar abrumadoras, especialmente a medida que los síntomas cambian con el tiempo. Estos hallazgos muestran la necesidad de herramientas y recursos que ayuden a las personas a sentirse preparadas y más seguras durante las visitas de atención médica. Aprenda cómo optimizar su atención médica para el Parkinson.

Recibir atención para el Parkinson es diferente para cada persona. Comprender las barreras para acceder a atención de calidad nos ayuda a ver dónde se necesita más educación, apoyo y divulgación.

3. El conocimiento de PD GENEration está creciendo, pero persisten las brechas en la participación en investigación.

En la encuesta en inglés, la mitad de los participantes había oído hablar de PD GENEration: Impulsado por la Parkinson's Foundation, en comparación con solo el 33 % entre los miembros de la comunidad de habla hispana. Pero oír hablar de ello no siempre significa participar en el estudio. Aproximadamente el 60 % de las personas que conocían el estudio y eran elegibles participaron en PD GENEration, con una participación sustancialmente menor de hispanohablantes (32 %).

Fuera de PD GENEration, la mayoría de los encuestados dijeron que no han participado en estudios de investigación clínica.

Conclusión clave

Estos hallazgos muestran que podemos hacer más para explicar la investigación clínica y ayudar a las personas a comprender cómo participar en estudios de investigación, incluido PD GENEration.

PD Trial Navigator es un nuevo programa que ayuda a conectar a los participantes de PD GENEration con estudios relevantes, al mismo tiempo que proporciona apoyo personalizado durante todo el proceso.

4. Las personas buscan información confiable, apoyo y recursos comunitarios.

Los participantes compartieron que el sitio web de la Parkinson's Foundation, Parkinson.org, fue el recurso más utilizado. Los miembros de la comunidad de habla hispana también destacaron los programas de educación en línea, incluidos los webinars y los Expert Briefings, como los más útiles.

Al reflexionar sobre los recursos que han sido más útiles, los participantes también señalaron áreas que faltaban o estaban subrepresentadas en su comunidad, particularmente en torno a programas de ejercicio y recursos de salud emocional.

Cuando se les preguntó sobre los temas de política que más importan, los participantes identificaron el aumento de la financiación para la investigación y la mejora del proceso de revisión y aprobación de nuevos tratamientos como principales prioridades.

Las herramientas digitales pueden ayudar con el aprendizaje, el seguimiento de los síntomas y la gestión de la atención, sin embargo, muchos participantes (60–70 %) dijeron que no conocen estas herramientas o no las usan.

Conclusión clave

Estos hallazgos muestran por qué es importante contar con recursos confiables y fáciles de usar que apoyen el aprendizaje, la salud emocional, la conexión y la confianza a lo largo del recorrido con el Parkinson. Explore nuestro blog para obtener la información más reciente.

Obtenga más información sobre nuestras prioridades de política y defensa aquí.

Qué significan estos resultados para nuestra comunidad

En las encuestas tanto en inglés como en español, vimos temas comunes:

  • Las personas quieren educación sobre los síntomas y las opciones de tratamiento.
  • Muchas personas necesitan más ayuda para obtener atención y hablar con su médico.
  • Más personas están oyendo hablar de la investigación, pero pocas se unen a los estudios.
  • Las personas quieren información confiable y apoyo.

Estos resultados nos recuerdan que vivir con Parkinson, cuidar a alguien con Parkinson y conectarse con la comunidad de EP es diferente para cada persona. Escuchar directamente de la comunidad nos ayuda a seguir mejorando nuestros programas, educación y recursos.

Próximos pasos

La Parkinson’s Foundation seguirá escuchando y respondiendo a las necesidades y prioridades de la comunidad. Seguiremos trabajando para avanzar en nuestra misión y mejorar la vida de todas las personas afectadas por la EP.

Si bien ninguna encuesta puede capturar toda la gama de experiencias dentro de la comunidad de Parkinson, la información compartida a través de encuestas como la Encuesta Acerca del Estado de la Comunidad ayuda a guiar nuestros programas, recursos, investigación y esfuerzos de defensa. Por eso seguimos buscando comentarios de múltiples maneras y alentamos a las personas con Parkinson, los cuidadores y los familiares a unirse a nuestra iniciativa de encuestas y participar en futuras encuestas.

Para ayudar a dar forma a las futuras iniciativas de la Parkinson’s Foundation y asegurarse de que su voz sea escuchada, considere unirse a nuestra iniciativa de encuestas. Obtenga más información sobre nuestras encuestas aquí.

Fundraising Events

2026 Athens Marathon

6:00 am to 6:00 pm EEST
Parkinson's Champions runners

The Parkinson's Foundation is a charity partner for the 2026 Athens Marathon. By signing up to run as a Parkinson's Champion you commit to raising funds and awareness for the Parkinson's Foundation, and in return you get access to a free entry (bib) to the race in addition to tons of other fun benefits and perks. You can apply to run now through our realbuzz application.

Fundraising Commitments:
•    Marathon - $4,000

History brought to life; the Athens Marathon is the original marathon finishing in the legendary stadium where the first Olympic games of the modern era took place in 1896. The route boasts such famous heritage sites as the Marathon Tomb and attracts runners from all over the world to be part of history. Sold out for general entry in less than 36 hours - secure your spot on the start line with us! Please note, there is a time limit of 8 hours. 

If you have questions, send us an email at Run4PD@Parkinson.org. For more information about the race itself, visit the Authentic Athens Homepage or the realbuzz Athens Landing Page.

Upcoming Events

Fundraising Events

2026 Irish Life Dublin Marathon

6:00 am to 6:00 pm IST
A family smiling at the camera after a Champion's event by the ocean.

The Parkinson's Foundation is a charity partner for the 2026 Irish Life Dublin Marathon. By signing up to run as a Parkinson's Champion you commit to raising funds and awareness for the Parkinson's Foundation, and in return you get access to a free entry (bib) to the race in addition to tons of other fun benefits and perks. You can apply to run now through our realbuzz application.

Fundraising Commitments:
•    Marathon - $4,000

With its iconic route past Dublin’s most famous landmarks, a relatively flat course and optimum running temperatures, the Irish Life Dublin Marathon is unmissable. Known as the friendliest marathon, thousands of spectators take to the streets to cheer you on and show the power of support. It's the only marathon to traverse Dublin city centre - join over 22,000 runners in 2026 and make your miles mean more. Plus, all charity runners get access to the exclusive realbuzz finisher party for free!

If you have questions, send us an email at Run4PD@Parkinson.org. For more information about the race itself, visit the Irish Life Dublin Homepage or the realbuzz Dublin Landing Page.
 

Upcoming Events

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