My PD Story

Jessica R. headshot
People with PD

Jessica R.

I’m 36 years old and live in New York City. Twelve years ago, at just 24 years old, I was diagnosed with Parkinson’s disease (PD). It was completely unexpected, especially since no one in my family has Parkinson’s. At the time, it was hard to imagine what the future would look like. Looking back now, I can honestly say that while Parkinson’s has changed my life, it hasn’t stopped me from living it. In many ways, it has given me a new sense of purpose and a chance to help others.

For many years, I relied on levodopa every two to three hours to manage my symptoms. Finding the right balance was challenging. Some days I experienced dyskinesia, while other days my tremors were more noticeable. I worked closely with my doctors, adjusting doses and trying different approaches, but it often felt like I was chasing the right combination.

In the summer of 2021, while spending more time at home during the pandemic, I realized my symptoms were becoming more difficult to manage. Around that time, I attended a webinar about deep brain stimulation (DBS), and it gave me hope that there might be another option. I talked with my neurologist who felt I was a good candidate. Six weeks later, I had the surgery. After several weeks of programming appointments, we found the settings that worked best for me, and now I only return once a year for adjustments.

For me, DBS was truly life-changing. Since my surgery, I have not needed to take levodopa, and I feel incredibly grateful for the difference it has made in my daily life.

Today, I focus on what I can do. I stay active with Pilates, boxing, and physical therapy. Exercise has become one of the most important tools in managing my Parkinson’s, and it helps me feel strong, both physically and mentally. I also make time for the things that bring me joy. I always have a trip planned or something to look forward to, and that excitement keeps me moving forward. Every summer, I travel to Europe, and Parkinson’s has never stopped me from exploring the world.

Over the past 12 years, I’ve learned that living well with Parkinson’s is about building the right support system and finding what works for you. I’m fortunate to have an incredible team of doctors, and together we’ve found ways to help me continue living the life I want. If sharing my experiences can make someone else’s journey a little easier, then every conversation is worthwhile.

One of the greatest sources of support has been the Parkinson’s Foundation. My doctor introduced me to the Foundation, and it has become a place where I can find trusted resources, connect with others, share my story, and advocate for people living with Parkinson’s — especially those with young-onset Parkinson’s disease.

One thing I’ve learned is that everyone’s Parkinson’s journey is unique. No two people have the same symptoms, treatment plan or experience, and that’s OK. Try not to compare your path to anyone else’s. Focus on taking one step at a time and finding the approach that helps you be the best version of yourself.

When I was first diagnosed, I was encouraged to keep it private, so I only shared my diagnosis with my closest family and friends. For a while, I let Parkinson’s define me. Over time, though, I realized that Parkinson’s is only one part of who I am — it is not my whole story. With the right support, resources and mindset, it’s possible to continue pursuing your goals, making memories and finding joy.

That’s why I choose to share my story. I hope it reminds others that there is hope after a Parkinson’s diagnosis. Be curious, ask questions, advocate for yourself and don’t be afraid to lean on your support system. 

Every year, advances in research, technology and medicine are creating new possibilities for people living with Parkinson’s. Your life may look different than you expected, but it can still be full, meaningful and joyful. Parkinson’s is part of my story, but it is far from the whole story.

Learn more about young-onset Parkinson’s disease.

Educational Events

Mind, Mood and Motion

10:00 am to 1:30 pm EST
FREE
MMM-Banner-940x510_Yoga

Check-in & Resource Fair* begins at 10:00 a.m. and the program starts at 10:30 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. 

Lunch will be served. Parking is 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. 

Upcoming Events

Educational Events

Mindfulness Mondays - Minding the Mind

In this session, we will learn how to notice common difficult habits of the mind, to pause, and then to mindfully return to a better place.  As we do so, we give ourselves the best chance of choosing a better next step.

Virtual
Educational Events

2026 Georgia Chapter Ambassador Retreat

Georgia Chapter Ambassador Retreat | July 31–August 1, Atlanta, GA. Join fellow Parkinson’s Foundation ambassadors for a weekend of connection, learning, collaboration, and planning as we celebrate our impact and prepare for the year ahead.

Atlanta, GA
Raise Awareness

Celebrating Our 2026 National Volunteer Award Recipients

🧠 What will you learn in this article?

This article celebrates 2026 Parkinson’s Foundation National Volunteer Award recipients, recognizing the dedicated volunteers whose leadership, service, fundraising and community-building efforts help advance our mission. It highlights:

  • How each honoree supports and impacts the PD community.
  • Their PD story.
  • How volunteers help us strengthen connections and move research forward.

Volunteers are at the heart of the Parkinson's Foundation mission. Across the country, they raise awareness, build community, support programs, advocate for change and help connect people living with Parkinson's disease (PD) and their families to the resources they need.

Each year, the Parkinson's Foundation recognizes exceptional volunteers through our national volunteer awards. These awards celebrate key people whose service, leadership and dedication have made a lasting impact on the Parkinson's community.

We are proud to introduce our 2026 National Volunteer Award recipients. Meet John, Dale, Jordan, Jen, Rocky and Cindy below — and let their stories inspire you as they have us. 


John with family at a Moving Day event

Paul Oreffice Volunteer of the Year: John Poma 

John embodies the spirit of service. His leadership spans community, state and national levels — from chairing Moving Day Richmond and the Volunteer Leadership Summit to representing Virginia at the Parkinson’s Policy Forum. Through the People with Parkinson's Advisory Council, he has advised on PD GENEration: Powered by the Parkinson’s Foundation, reviewed community grants and encouraged young investigators at the research grantee summit, demonstrating his commitment to advancing science and care.

Beyond his formal roles, John consistently uses his voice to raise awareness of REM sleep behavior disorder and the lived experience of Parkinson's through local and national media. He partners with healthcare providers at Virginia Commonwealth University, a Parkinson’s Foundation Center of Excellence and beyond — including researchers at Mass General and Harvard — to advance the Foundation's mission. John believes in empowering others through education and has spoken at major events, including the Planning for Prevention of Parkinson's conference.

“One of the guiding principles of my longtime professional career in and around healthcare is that helping one person may not change the world, but it may change the world for that one person.”- John Poma

Read John's full story


Dale Picciano waving a flag at a Moving Day event

Rising Star Award: Dale Picciano

Dale’s impact has been extraordinary in a short amount of time. His authenticity, leadership and willingness to openly share his diagnosis have helped break down barriers and create meaningful awareness around PD within the first responder and firefighter communities. By leveraging his lifelong connections, he not only raised significant funds for the Parkinson’s Foundation but also expanded our reach into a passionate and service-oriented network of supporters.

What makes Dale especially deserving of the Rising Star Volunteer Award is the way he channels his own experience into action for others. Rather than stepping back after his diagnosis, he stepped forward — becoming a fighter, advocate, fundraiser and source of inspiration. His dedication perfectly reflects the spirit of courage, community and perseverance that this award represents.

“I am honored and privileged to walk amongst many heroes that are fighters, that won't quit and are fighting back.” – Dale Picciano

Read Dale's full story


Top Fundraiser Award: Jordan Levin, Jen & Rocky Pontikes

Jen and Rocky Pontikes, along with Jordan Levin, transformed one idea into an inspiring movement that united hundreds of people during Parkinson's Awareness Month. Through the Million Meter Challenge, participants rowed, walked, biked and ran together to demonstrate the power of movement while raising critical funds to advance Parkinson's research and improve care.

Jen and Rocky enjoying a glass of wine

What began with Jen's passion for rowing as a way to manage her Parkinson's symptoms grew into a multi-state community effort that inspired more than 300 participants to move more than 24 million meters and raise more than $185,000 for the Parkinson's Foundation. Their creativity, leadership and ability to bring people together exemplify the spirit of this award.

“The Parkinson's Foundation introduced me to an extraordinary community of people living with Parkinson's, care partners, advocates, researchers and healthcare professionals. Through those connections, I found my voice. What began as one of the most difficult moments of my life became my purpose.” - Jen Pontikes                                        

Read Jen and Rocky’s full story

Jordan lifting weights at an event

“My hope is simple: to support the research and education that may one day cure or ease these brutal diseases, and to ensure that caregivers are never left without the information, resources and support they need on their own journey.”- Jordan Levin

Read Jordan's full story


Cindy Finestone

Community Service Award: Cindy Finestone

Cindy leads by example through extraordinary service to the Parkinson's community. As President of the Parkinson’s Foundation New York Chapter Board, facilitator of the Women with Parkinson's Community Network, Research Advocate and dedicated Moving Day volunteer, she consistently gives her time, leadership and compassion to support others living with Parkinson's.

When Cindy logged her volunteer hours for the year, she wasn't seeking recognition — she simply wanted to ensure the impact of her chapter was reflected. Only then did she realize she had contributed an incredible 339 volunteer hours, a testament to the countless ways she strengthens her local Parkinson's community.

“Being involved in the Parkinson’s Foundation makes me feel like I’m doing something that’s helping. Everything I do is somehow related to the Foundation. I attend a PD support group of 60 women, some of whom have become my closest friends — and I found this group through the Foundation. I call the Helpline for referrals. I go on Parkinson.org every time I feel a new symptom coming."- Cindy Finestone 

Read Cindy's full story


Congratulations to our 2026 award recipients! As we celebrate these six outstanding people, we are grateful for every volunteer who gives their time, talents and passion to help us make life better for people living with Parkinson's.

Explore the many ways you can volunteer with us today

Educational Events

Building Your Parkinson’s Toolbox

Virtual ( Zoom )
12:30 pm to 4:00 pm CDT
FREE
Froedtert banner

Check-in starts at 11:30 am and the program starts at 12:30 pm. A complimentary boxed lunch will be provided.

Please join the Parkinson's Foundation Midwest Chapter in partnership with the Froedtert & the Medical College of Wisconsin Movement Disorders Team, a Parkinson’s Foundation Center of Excellence, for our Parkinson's Disease Symposium: Building Your Parkinson’s Toolbox. 

This educational program will offer practical information and strategies to support everyday health and well-being, for those affected by Parkinson’s. Attendees will hear from experts on topics including sleep and fatigue, preparing for medical appointments, fall prevention/home safety, nutrition, and self-care for care partners. Throughout the day, participants can also connect with local vendors and community resources that provide valuable information. Whether you are navigating Parkinson's yourself or caring for a loved one, this program offers tools, education, and encouragement.

Speakers:

Karen Blindauer, MD
Froedtert & MCW health network

Sheila Rane Eichenseer, MD, MS
Froedtert & MCW health network

Molly Sievers, DPT, NCS
Froedtert & MCW health network

Devri Lybeck, DPT
Froedtert & MCW health network

Katherin Kraiss, MS, RN, CD, CNSC
Froedtert & MCW health network

Charlene Thomas, RN 
Froedtert & MCW health network

Erika Stadter, RN
Froedtert & MCW health network

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.

This program is a partnership with the Parkinson's Foundation Midwest Chapter and the Froedtert & the Medical College of Wisconsin Movement Disorders Team- a Parkinson's Foundation Center of Excellence.

froedtert

Upcoming Events

Educational Events

Mindfulness Mondays - Minding the Mind

In this session, we will learn how to notice common difficult habits of the mind, to pause, and then to mindfully return to a better place.  As we do so, we give ourselves the best chance of choosing a better next step.

Virtual
Educational Events

2026 Georgia Chapter Ambassador Retreat

Georgia Chapter Ambassador Retreat | July 31–August 1, Atlanta, GA. Join fellow Parkinson’s Foundation ambassadors for a weekend of connection, learning, collaboration, and planning as we celebrate our impact and prepare for the year ahead.

Atlanta, GA

My PD Story

John with family at a Moving Day event
People with PD

John Poma

Everyone’s journey with Parkinson’s is unique, and mine began with REM Sleep Behavior Disorder or RBD. In 2018, I experienced episodes of acting out my dreams, which led to a diagnosis of RBD at Virginia Commonwealth University (VCU) Health in late 2019. I was later referred to a movement disorders specialist and enrolled in a RBD research study. Although I did not initially have Parkinson’s disease (PD), my symptoms gradually progressed over time. In 2022, I was diagnosed with Parkinson’s. 

John and his wife at an event

From the earliest days in 2020 of learning about RBD and its connection to Parkinson’s and other synucleinopathy, I made a commitment to become engaged in research and volunteer as a study participant. Learning about the science of Parkinson’s has changed how I see the disease. It gives patients like me a way to move from fear towards hope, purpose and contribution. 

I don’t want to be defined by Parkinson’s and how its symptoms impact me. Instead, I want to be defined by what I have done to make a difference and advance understanding of Parkinson’s. So, instead of feeling defined by Parkinson’s, I began to see how I could contribute to progress. 

It is through my participation in a research program at Massachusetts General Hospital in Boston, MA that I also learned of the important work of the Parkinson’s Foundation. In addition to participating in research, I realized my contribution could also come through patient advocacy, mentorship and education. 

John speaking on stage at a Parkinson's Foundation conference

One of the true privileges of my adult life came in July 2023 when was I was invited to join the Parkinson’s Foundation People with Parkinson’s Advisory Council

Living with Parkinson’s and its movement and non-movement symptoms is never easy, and no one day is ever the same. In recent months, living with Parkinson’s has been more difficult for me. However, I have learned that there is something incredibly special about the Parkinson’s community. We are there for each other. We understand what is sometimes difficult for others to understand. And we support each other along the way. 

Friends and family at a Moving Day event

As a member of the advisory council, I learned how our collective voices can change how people understand Parkinson’s; how patients and caregivers are supported; and how research and policy through research programs like PD GENEration (and now also PD GENEration Insights) can accelerate better outcomes. 

I also quickly learned that there is no better way to build community and support the work of the Parkinson’s Foundation than to participate in one of the Parkinson’s Foundation Moving Day events held coast to coast.

Find your nearest Moving Day event now. Ready to do more? Find out how you can get involved!

When you are living with PD, it is not always easy to find the resources that are available to you in the community. Parkinson’s is also a disease that impacts more than just the individual. Instead, it also impacts both your spouse and your family.

When I moved to Richmond in 2022, it was difficult to find the different programs available to people with Parkinson’s in a large urban area. Moving Day changes that and was the reason for my wanting to bring Moving Day to Virginia in 2024. It brings together the many resources available in our community for people with PD and their families. 

John hugging another Moving Day volunteer

We will hold our third Moving Day Richmond, VA, on October 24 at the Richmond Raceway — and I can think of no event that is more meaningful, powerful or uplifting. Moving Day is a celebration of resilience, hope, and the strength of a community determined to change the future of Parkinson’s. 

Moving Day also embraces the power of exercise, which is proven to manage and improve Parkinson’s symptoms. From the earliest days of my diagnosis, I learned that exercise plays a central role in managing Parkinson’s.

The focus of my week is participating as much as my work schedule will allow in a local program called LiftPD. LiftPD is structured around training, therapy and prevention strategies designed to slow progression and maintain function. LiftPD depends heavily on grants and community support, and again, it is my hope that my lived experience with Parkinson’s can help guide and strengthen LiftPD’s efforts to ensure that individuals at every stage of the disease have access to functional exercise programs that enhance mobility, confidence and quality of life.

John with family at a Moving Day event

When I speak, I often say it is an oxymoron to stand here and say I feel lucky. However, I feel incredibly lucky. I am fortunate to have an exceptional care team at VCU Health, and I am grateful for the opportunities I have had to help advance our understanding of Parkinson’s and its future. 

One of the guiding principles of my longtime professional career in and around healthcare is that “Helping one person may not change the world, but it may change the world for that one person.” 

Explore Parkinson’s Foundation volunteer opportunities today.

My PD Story

Dale Picciano at a Moving Day event
People with PD

Dale Picciano

For most of his life, Dale Picciano has answered the call to serve others.

In 1977, I joined the U.S. Marines, an experience that shaped my commitment to community and service. Reflecting on that chapter of my life, I was honored and privileged to walk amongst many heroes that are warriors. Semper Fi. 

Dale Picciano waving a flag at a Moving Day event

A few years later, in 1981, I began a 32-year career as a firefighter and paramedic with the City of Miami. For more than three decades, I was honored to help others during some of their most difficult moments. I was always surrounded by people who inspired me.

I retired in 2013, looking forward to traveling, spending time with family and friends, and enjoying the next chapter of life. But I had been experiencing a combination of mysterious movement and non-movement symptoms for years, not knowing why. In retirement, I was finally diagnosed with Parkinson's disease (PPD) in 2022, at the age of 65.

Like many people living with Parkinson's, I turned to the Parkinson's Foundation for information and resources — but I found so much more, I found community.

The Parkinson's Foundation became an invaluable resource for me to depend on. I was encouraged to give back and support the Foundation in its continuing efforts in the Parkinson's community. I wanted to make a difference again with my life by volunteering.

Dale Picciano waving a flag at a Moving Day event

I went into action. In my first year participating in Moving Day Miami, my team raised more than $14,850 for the Parkinson's Foundation. Drawing on my career in firefighting, I personally reached out to fellow firefighters through phone calls, face-to-face conversations and community outreach. 

I was happy to connect with my fellow firefighters to help raise awareness about Parkinson's and encourage important discussions within the first responder community.

“Dale’s efforts helped connect the Parkinson's Foundation with an entirely new network of supporters while increasing awareness among a community that may face an increased risk of developing Parkinson's, which is one of the reasons the Foundation named him Rising Star Volunteer Award in 2026,” said Celeste Tennant, Parkinson’s Foundation Director of Volunteer Engagement.

Dale practices boxing with a trainer at an event

Today, I remain active in my PD community, where I am a member of Rock Steady Boxing Miami. I fight alongside others who are resilient and determined to live stronger with this disease. Looking around the gym, I see a familiar spirit in the people beside me.

I am honored and privileged to walk amongst many heroes that are fighters, that won't quit and are fighting back.

From Marine and firefighter, to Parkinson's fighter and volunteer, I believe in service. I bring the same service-driven mindset that got me through my career into my volunteer work with the Parkinson’s Foundation. 

A Parkinson's diagnosis could slow anyone down, but it can also help you step forward, raise awareness and build a new community.

Dale received the Parkinson’s Fondation Rising Star Volunteer Award for demonstrating that even in the face of adversity, there are always new ways to serve. Find out how you can volunteer today.

Educational Events

Integrative Health in Parkinson’s Care

1:00 pm to 3:00 pm EST
FREE
Integrative banner

Check-in & Resource Fair begin at 12 pm and program begins at 1pm.

Managing Parkinson’s disease (PD) symptoms goes beyond traditional medications, with integrative health and holistic approaches offering additional support. This program introduces participants to non-drug options—such as massage, acupuncture, red light therapy, and CBD—that can help relieve symptoms and enhance daily well-being. By exploring integrative health's focus on root causes and whole-body wellness, participants will gain a deeper understanding of how these therapies can address symptoms and improve overall quality of life, providing a more balanced and individualized approach to PD management. 

Speaker: 
Kayla Daniel, MA OSU Wexner & the Movement Disorders Clinic at OSU Wexner

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.

 

Upcoming Events

Educational Events

Mindfulness Mondays - Minding the Mind

In this session, we will learn how to notice common difficult habits of the mind, to pause, and then to mindfully return to a better place.  As we do so, we give ourselves the best chance of choosing a better next step.

Virtual
Educational Events

2026 Georgia Chapter Ambassador Retreat

Georgia Chapter Ambassador Retreat | July 31–August 1, Atlanta, GA. Join fellow Parkinson’s Foundation ambassadors for a weekend of connection, learning, collaboration, and planning as we celebrate our impact and prepare for the year ahead.

Atlanta, GA

My PD Story

Jen and Rocky enjoying a glass of wine
People with PD

Jen and Rocky Pontikes

In 2023, I was diagnosed with Parkinson's disease (PD) at the age of 50. To say it was a shock would be an understatement. It was the kind of news that stops you in your tracks and changes everything.

In the beginning, I had a lot of questions and very few answers. My husband, Rocky, and I found ourselves navigating unfamiliar territory while trying to understand what this diagnosis meant for our future and our family. Like so many people living with Parkinson's, I quickly learned that while the diagnosis was life-changing, it did not define us.

While I was still processing my diagnosis, Rocky reached out to the Parkinson's Foundation to learn how he could get involved and support the Parkinson's community. He joined the Parkinson’s Foundation Midwest Chapter early on and became connected to an incredible network of people who understood this journey.

Jen and Rock posing for a picture outside with their sons

For nearly two years, we kept my diagnosis private from our four boys as we worked through it ourselves. Once we finally shared the news, something shifted in me. I decided I was all in. Instead of hiding from Parkinson's, I wanted to learn, connect and help others.

The Parkinson's Foundation introduced me to an extraordinary community of people living with Parkinson's, care partners, advocates, researchers and healthcare professionals. Through those connections, I found my voice. What began as one of the most difficult moments of my life became my purpose.

That purpose inspired Rocky and me to become Parkinson's Champions. We are strong believers in clinical trials, and I have personally participated in two of them. Through these experiences, we developed a deep appreciation for the importance of clinical research and the role it plays in advancing better treatments and outcomes. 

Without these trials, progress stalls. That realization strengthened our commitment to supporting this work in every way we can, including raising awareness and funding for the Parkinson's Foundation.

Jen, Rock, and Jordan

As a planner by nature, I believed that with the right idea and the right team, we could create meaningful impact. We joined forces with fellow Parkinson's Champion and good friend, Jordan Levin, to build a community-wide challenge designed to inspire people to get active while raising awareness and funding for the Parkinson's Foundation.

What began as a competitive rowing challenge quickly evolved into something far more meaningful. We realized the real value wasn't in competition — it was in getting people moving. From there, the challenge expanded beyond rowing to include power walking, running, biking and any form of movement people enjoyed.

In the end, it became less about competition and more about movement, community and coming together in support of a cause that matters deeply to us.

Jen doing yoga

The Million Meter Challenge became something much larger than Parkinson's disease alone. It became a reflection of life itself.

The Million represented connection and community. We didn't have a million people, but it often felt like we did.

The Meters represented movement. Every step, every row, every spin mattered. Nothing was taken for granted.

The Challenge became a reflection of what we can accomplish together through movement, connection and community as the foundation of living well. No one has to endure this disease alone.

Interested in joining the next Million Meter Challenge?

Follow @MillionMeterChallenge on Instagram for updates on future challenges.

Our biggest takeaway was the power of community and the reminder that we are all in this together. We were incredibly proud to watch our Million Meter Challenge movers accomplish things they never thought possible and to see the challenge grow far beyond anything we originally imagined.

Jen and Rock with 3 of their sons

Parkinson's is not a club anyone wants to join. But the Million Meter Challenge showed us that together, anything is possible. It reminded us that health is something we should never take for granted and reinforced one simple but powerful message: Don't wait for disease to knock on your door before you start taking care of your body, your mind and your life.

Through the Parkinson's Foundation, the Million Meter Challenge and the people we've met along the way, I've learned that while Parkinson's changes lives, community changes them too.

Looking back, my diagnosis changed the course of my life in ways I never expected. It also introduced me to a community that helped me find hope, purpose and the confidence to use my voice. 

Jen & Rocky are recipients of the Parkinson’s Foundation Top Fundraisers Award.  Learn how you can become a Parkinson’s Champion today. 

Podcasts

Episode 192: What Your Gut Has to Do with Parkinson’s

Interest in the gut microbiome and its potential role in Parkinson’s disease (PD) continues to grow. Before exploring the latest research, it’s helpful to understand what the microbiome is, the role it plays in overall health, and why researchers are studying its connection to Parkinson’s.

In this episode, we speak with Dr. Lisa Deuel from the University of Vermont Medical Center about what researchers currently know, and don’t know, about the relationship between the gut and Parkinson’s. She explains the gut-brain connection and discusses common gastrointestinal issues experienced by people with Parkinson’s, such as constipation and gastroparesis (limited ability to empty the stomach). She wraps up by sharing practical strategies to support gut health.

Key Takeaways:

  • Research is still limited on whether changes in the gut microbiome may contribute to the risk of developing Parkinson’s disease.
  • Gastrointestinal issues, including constipation and gastroparesis, are common non-movement symptoms of Parkinson’s.
  • Practical Strategies for Supporting Gut Health:
    • Stay hydrated and drink water 
    • Eat a high fiber diet in moderation
    • Consider probiotics 
    • Stay active and moving

Released: July 14, 2026

Science News

Two New Studies Show Adaptive Deep Brain Stimulation May Improve Walking in Parkinson’s

🧠 What will you learn in this article?

This article highlights two studies, published in Nature Medicine, that show promise for using new adaptive deep brain stimulation (DBS) methods to treat walking difficulties in Parkinson’s disease (PD). Highlights include:

  • Unlike traditional DBS, adaptive DBS adjusts stimulation in real time based on movement or brain signals. 
  • Both studies identified personalized brain signals (neural biomarkers) to tailor stimulation for specific movement. Both approaches improved walking while preserving traditional DBS benefits for symptoms such as tremors and stiffness.
  • Researchers at Lausanne University Hospital in Switzerland used brain signals to identify and tailor stimulation for different activities. 
  • Researchers the University of California, San Francisco (UCSF) used different brain signals to time and adjust stimulation to participant’s walking rhythm.
Parkinson's Foundation Science News blogs

Deep brain stimulation (DBS) is the most common surgical treatment for Parkinson’s disease (PD). It uses continuous electrical pulses to help control movement symptoms like tremor, stiffness and slowness. For many, DBS can be life changing. Its big shortfall is that it delivers the same stimulation all the time, which does not help with walking difficulties — including unsteady gait, freezing of gait (a sudden inability to move when walking) and falls. These are among the most disabling and dangerous PD symptoms with limited treatment options.

Recently, major advancements have been made in adaptive DBS (aDBS), which is when a DBS device adjusts its stimulation in real time based on a person’s symptoms or behavior. Studies show that aDBS is more helpful for controlling typical “on/off” symptoms (such as tremor and rigidity) compared to traditional DBS treatment. Now, two new studies published in Nature Medicine suggest that aDBS may also hold promise for treating gait impairment in people with Parkinson’s. 

  1. One study, conducted by a team at Lausanne University Hospital in Switzerland, developed a system that uses brain signals to detect which locomotor (the ability to move) activity a person is performing — such as sitting, standing, walking or turning — and selects stimulation settings optimized for that specific activity.
  2. The other study, led by a team at the University of California, San Francisco (UCSF), took a different approach: timing stimulation to specific phases of the walking cycle, footstep by footstep, guided by brain signals unique to each individual participant.

Both studies were small and early-stage but highlight that adaptive DBS could improve walking in ways that traditional DBS cannot. 

Study Results

The primary focus of both studies was whether adaptive DBS settings that target gait are feasible and safe, and whether they could improve walking compared to traditional continuous stimulation. Encouragingly, neither study reported negative events. 

Adaptive DBS was well tolerated in all participants, and both studies found that it still helped manage the movement symptoms — like tremors and stiffness — that traditional DBS provides. Beyond safety, both teams also tracked changes in participants’ walking patterns, including step consistency, symmetry and falls.

2 new adaptive DBS studies graphic

The Swiss study enrolled six people with Parkinson’s who had DBS implants in the subthalamic nucleus. The team used recordings from the implanted DBS device, combined with detailed motion tracking, to develop algorithms that could detect which activity a person was performing — walking on flat ground, avoiding obstacles, turning, etc. — and automatically adjust stimulation settings to match.

  • This approach improved movement across multiple daily activities while preserving the benefits of traditional DBS for other movement symptoms.
  • This system successfully decoded and adjusted to locomotor activities in real time, even as participants’ symptoms changed or took levodopa medication throughout the day — a key challenge for adaptive approaches.

The UCSF study enrolled five people with Parkinson’s who received DBS implants in the globus pallidus region, along with additional recording devices in other brain regions. Using those recordings, they found that the brain produces distinct electrical patterns during specific phases of walking — for example, when the leg swings forward. 

These patterns were unique to each participant, appearing at different frequencies and brain locations. By identifying each person’s individual ‘gait signature,’ the researchers were able to program the neurostimulator to deliver brief boosts of stimulation timed to match each step.

  • During in-clinic testing, this adaptive DBS strategy improved step variability and step symmetry compared to traditional DBS stimulation.
  • Three participants completed a multi-day trial in their own homes, where neither the participants nor the researchers knew which type of stimulation was being used. In this real-world setting, adaptive DBS maintained general movement symptom control and reduced falls.

While these are early results need to be confirmed in larger studies, they offer a promising glimpse into a fundamentally new way to address one of the most challenging aspects of Parkinson’s: walking difficulties.

Highlights

  • Two studies, both published in Nature Medicine, tested adaptive DBS systems designed to target movement symptoms that automatically adjust to what a person is doing in real time.
  • Both studies used personalized brain signals, unique to each participant, that specifically indicated different types of movement or activity. 
  • The Swiss study used activity states— for example, recognizing whether a person was sitting, walking, or turning — to switch between optimized stimulation settings.
  • The UCSF study used step-level precision — synchronizing stimulation pulses to the exact rhythm of each individual step – to make adjustments.
  • Both approaches improved walking measures while maintaining the benefits of traditional DBS for other movement symptoms like tremor and stiffness.
  • Neither study reported negative events and showed that these aDBS techniques were well tolerated.
  • Both studies were small (six and five participants). Larger trials are needed to confirm these findings.

What Does This Mean?

Falls are a leading cause of injury and hospitalization for people with Parkinson’s. Since walking is a highly complex activity that requires precise coordination, traditional DBS with consistent stimulation often does not address balance and walking issues. Instead of delivering the same stimulation all the time, adaptive DBS devices adjust in real-time based on the brain’s activity. These studies leveraged this concept to specifically target gait impairment, indicating an important shift in how DBS could help walking symptoms. 

If larger studies confirm these findings, adaptive DBS could offer a meaningful improvement in daily life for people living with Parkinson’s — especially those experiencing gait and balance challenges.

These studies worked by identifying unique, personalized brain signals that were specific to each participant. The algorithms for adaptive DBS were then optimized based on this brain activity — a form of individualized, precision medicine. In addition, the physical location of the participants’ DBS implant varied between studies; the success of both platforms indicates that these treatments can be effective regardless of the DBS implant location, offering hope for more people with Parkinson’s.  

What Does This Mean for People with Parkinson’s?

These studies are in the early stages and have only been tested on a very small number of people. Neither paradigm is ready for widespread clinical use. However, hope lies in the fact that these studies have already moved beyond the lab and are being tested in people living with Parkinson’s. Additionally, the Swiss study used a commercially available DBS neurostimulation device, removing an important barrier to access and suggesting that widespread implementation in the near future may be feasible. 

Next, larger trials will need to confirm the findings to improve features for long-term use and to better understand who would benefit most. People experiencing walking difficulties and falls related to Parkinson’s should talk to their doctor about current treatments and keep an eye out for future adaptive DBS clinical trials. 

Learn More

The Parkinson’s Foundation Helpline (1-800-4PD-INFO) provides answers to questions about PD symptoms and management. Learn more about this topic with the below resources: 

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