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.

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

My PD Story

Julio Gonzalez
People with PD

Julio Gonzalez

I was diagnosed in 2017 with Parkinson’s disease (PD) after relocating to Gilbert, AZ with my family from South Brunswick, NJ. I suspect that balance issues I have had for a longer period was actually attributed to PD.  My challenges with PD have been primarily with balance and walking, low blood pressure and leg pain. 

For approximately a five-year period I relied on Rock Steady Boxing classes to provide the exercise my body needed to offset my physical challenges.

During the past four years I have served as a member of the Parkinson's Foundation Southwest Chapter board. This provided me with the opportunity to contribute time following my retirement in 2019 from JPMorgan Chase to help with fundraising, community outreach and board development activities. 

Parkinson’s Foundation Chapters provide local resources, support groups, classes and educational programs.

My role includes participation at Moving Day and webinar events. I also tap into the very comprehensive Parkinson's Foundation library to further educate me on various PD related topics.

I leverage the love and support of my family to stay positive and strong, as I continue to face my PD challenges. Continuing with a regular exercise routine should always be part of my health maintenance program. Also, I have always found keeping a good sense of humor as a strong defense against stress and mental health challenges.

My advice to a PD "newbie" is to utilize the vast amount of information available on Parkinson.org to educate yourself and remain informed on PD overall. 

I would encourage them to be part of a PD community or support group, for there is strength in numbers and value in shared knowledge and experiences.

Join the Parkinson’s Foundation volunteer community to support people with Parkinson’s through local events and educational programs. Find your local Parkinson’s Foundation chapter. 

My PD Story

Chris Kustanbauter
People with PD

Chris Kustanbauter

A Walk That Changed Everything

While on vacation in August 2010, my wife Mary and I had just finished a walk when my left hand began shaking. Mary insisted I go to the emergency room (ER), and after an examination, the ER physician attributed it to stress.

Yet back home, the tremor in my left hand persisted. I also began dragging my left leg when I walked, and my left arm didn’t swing when walking. I managed to secure an appointment with a neurologist about two months later. 

After several rounds of tests, he told me, “I think you have Parkinson’s.” He referred me to a Movement Disorders Specialist at the University of Maryland, who confirmed that I had Young-Onset Parkinson’s Disease (YOPD) at age 46.

Taking Control: My Four Pillars

After the initial shock, I decided I was going to take control of my Parkinson’s journey. Drawing on my background in science and clinical research, I spent two months reviewing clinical studies on Parkinson’s and exploring the resources available on the Parkinson’s Foundation website.

From that research, I distilled four key pillars I would focus on to live my best life with Parkinson’s:

  • ExerciseDaily aerobic activity, strength training, flexibility and stretching, and balance training—all grounded in Parkinson’s Foundation recommendations.
  • NutritionA consistent, healthy eating plan to support overall well-being.
  • Optimism & Mindfulness: Maintaining a positive attitude and practicing mindfulness to navigate daily challenges.
  • Social Interaction: Staying connected, joining a Parkinson’s exercise group at my local community center and building new friendships.

Giving Back: Teaching, Research, and Advocacy

Living an exceptional life with Parkinson’s, I felt compelled to help others and share what I had learned. I began presenting to support groups but still felt I could contribute more. 

When I came across the Research Advocate role on the Parkinson’s Foundation website, I knew it was the right fit. I completed the training and became a Parkinson’s Foundation Research Advocate in September 2024.

In 2024, I learned that three of my former neighbors had developed Parkinson’s. For 20 years, I lived in a neighborhood just one-quarter of a mile from a golf course that had been built and opened during that time. Nearby farm fields grew corn and soybeans. Strikingly, four households within a small, concentrated radius—mine included—all had someone develop Parkinson’s.

This felt like far more than coincidence. After researching possible causes, I found that people living near a golf course are twice as likely to develop Parkinson’s as those who do not likely due to the pesticides and herbicides used to control weeds and insects 

I learned that one of those herbicides called paraquat is linked to an increased risk of developing Parkinson's. Paraquat is banned in more than 70 countries, including the European Union and China, yet it remains in use in the U.S.

This information drew me into public policy advocacy. In February 2026, I joined the Parkinson’s Foundation and other advocacy organizations at the Pennsylvania State Capitol to share our stories and urge them to support a bill to ban paraquat in the state. Most were receptive to our concerns — with one lawmaker agreeing to sign on as a co-sponsor. 

My Parkinson’s journey has taught me to fight back with exercise and social interaction, advocate for others, and a Parkinson’s diagnosis is not an ending but an opportunity to live your best life. 

Learn more about how Policy work can impact the lives of people with Parkinson’s. Visit our Advocacy Center to take action in your state now.

My PD Story

Chris Anthony and his wife
People with PD

Chris Anthony

In 2025, I was diagnosed with Parkinson’s disease (PD).

Like many people, I did not arrive at that diagnosis in one clean, dramatic moment. Looking back, I can see signs that were probably there earlier — changes I explained away as age, stress, old injuries or just the normal wear and tear of life.

I spent 24 years in the United States Air Force, retiring as a Senior Master Sergeant, and then continued serving in federal government and consulting roles. I was used to solving problems, pushing through challenges and figuring things out. Parkinson’s, however, was not something I could simply outwork.

At first, I had more questions than answers. What did this mean? How fast would it progress? What should I be doing now? How would this affect my family, my future and the way I saw myself?

One of the first challenges was accepting that Parkinson’s is not just a diagnosis you receive and file away. It becomes part of daily life — medication schedules, exercise, therapy appointments, changing symptoms, fatigue and the uncertainty of what comes next. Some days the challenge is physical. Other days, it is mental: learning not to measure today’s life only against what I used to be able to do.

There was also a more personal reason I wanted to understand Parkinson’s better. My dad had Parkinson’s, too. He was diagnosed later in life, in his 70s, around 2005. At the time, I did not have the resources or understanding I have now. His primary doctor largely explained it away as an old man’s disease that made old men shake, and Dad rarely saw a neurologist.

Looking back, I wish I had known then what I know now. Parkinson’s is a complex neurological disease — not just a tremor, not just something that happens to older people, and not something families should have to figure out on their own.

That is one reason the Parkinson’s Foundation matters to me.

After my diagnosis, I began looking for reliable information. The internet is full of opinions, personal stories, miracle claims and self-proclaimed experts. Some lived experience is valuable — I share my own story, too — but I wanted information grounded in science, education and real expertise.

The Parkinson’s Foundation became one of the places I turned to for trusted resources. Its website, Parkinson.org, has helped me better understand symptoms, treatment options, exercise, care partner issues and the importance of building a knowledgeable care team. 

I also receive care through the Norman Fixel Institute for Neurological Diseases at the University of Florida, a Parkinson’s Foundation Center of Excellence. Thankfully, because of advances in care and organizations like the Parkinson’s Foundation, I am in a much different place than my dad was when he was diagnosed.

My involvement with the Parkinson’s Foundation Community Network has also given me a way to turn my diagnosis into something useful. As a Parkinson’s Foundation Ambassador, I have had opportunities to help raise awareness, share resources, attend community events and connect with people living with Parkinson’s and those who care about them.

Chris Anthony and his wife in Cozumel, Mexico

That work matters to me because people with Parkinson’s and their families already know this disease is real. The larger challenge is helping the broader public understand why Parkinson’s deserves more attention, more research, more support and more voices speaking up.

What keeps me happy, healthy and hopeful is a mix of things: my family, exercise, faith, humor, good medical care and the chance to keep serving in a different way. Through the Parkinson’s Foundation, I also learned about Rock Steady Boxing, an exercise program designed for people with Parkinson’s. Participating in Rock Steady Boxing has helped me stay active, challenged and connected to others who understand the importance of movement.

Parkinson’s has changed my life, but it has also given me a clearer sense of purpose. I cannot control everything about this disease, but I can control how I respond to it. I can keep learning. I can keep moving. I can keep showing up.

I have also started sharing my Parkinson’s journey through writing and advocacy. My platform is called From Where I Sit, because I believe perspective is shaped by where we are now and where we have been. From where I sit, Parkinson’s is not just a diagnosis. It is a daily lesson in adaptation, humility, purpose and continuing to move forward.

What advice would I give someone newly diagnosed?

  1. Do not go through this alone. Find credible information. Build a care team you trust. Connect with others who understand the road you are on.

  2. Exercise. Not someday. Now. Movement is one of the most important things we can do for ourselves.

  3. Give yourself some grace. Parkinson’s changes things, but it does not erase who you are.

Parkinson’s may have changed where I sit, but it has not changed the fact that I am still here — still learning, still serving, still speaking up and still trying to make the road a little easier for the next person who hears the words, “You have Parkinson’s disease.”

Join one of our five Parkinson’s Foundation Community Networks and learn how you can volunteer

Raise Awareness

Descubra cómo 5 líderes comunitarios están conectando con las comunidades hispanas y latinas

🧠 ¿Qué aprenderá en este artículo?

Este artículo destaca los esfuerzos de la Parkinson's Foundation para apoyar a las comunidades hispanas y latinas que conviven con la enfermedad de Parkinson a través de subvenciones comunitarias. Se analiza lo siguiente:

  • Las subvenciones comunitarias de la Parkinson's Foundation tienen como objetivo cerrar las brechas en la atención de Parkinson y los recursos a nivel local en todo Estados Unidos.
  • Cinco programas locales que abordan las barreras en la educación y el apoyo para las personas de habla hispana que conviven con la EP.
  • Programas que van desde talleres educativos y grupos de apoyo hasta clases de ejercicio adaptadas a la EP y recursos para cuidadores, ofrecidos en persona y en línea.
  • Cómo encontrar programas locales.
Amigos hablando en el parque

Los miembros hispanos y latinos de la comunidad de la enfermedad de Parkinson (EP) a menudo enfrentan desafíos distintos para vivir bien con Parkinson, incluidas las barreras del idioma, el acceso limitado a la atención médica y las brechas en los materiales educativos culturalmente alineados.

La Parkinson's Foundation reconoce estas disparidades y trabaja activamente para hacer que la atención médica de calidad sea más accesible para todas las personas con Parkinson, en parte a través de nuestro programa de subvenciones comunitarias.

El programa de subvenciones comunitarias de la Parkinson's Foundation apoya a grupos locales en todo Estados Unidos en la mejora de la salud, el bienestar y la educación para las personas que viven con Parkinson. Desde 2011, la Fundación ha invertido más de $12.7 millones en casi 1,000 programas comunitarios.

Conozca a continuación a cinco de nuestros beneficiarios de subvenciones comunitarias, premiados por sus programas educativos, de ejercicio y para cuidadores adaptados y creados para las comunidades de la EP de habla hispana.

Conozca a Irving Vega, PhD: mejoras en el acceso a la educación y los recursos en español en el oeste de Michigan

Irving Vega, PhD, profesor asociado distinguido Red Cedar en Michigan State University, recibió una subvención comunitaria en 2025 para comprender y abordar mejor las necesidades únicas de las comunidades hispanas y latinas en el oeste de Michigan —poblaciones históricamente subrepresentadas en la educación e investigación de la EP.

Como parte de esta subvención, realizó una encuesta comunitaria para evaluar el conocimiento sobre la EP y encontró las siguientes brechas:

  • Aunque la exposición a pesticidas es un riesgo ambiental bien establecido para la EP, muchos miembros de la comunidad latina no lo identificaron como un factor de riesgo.
  • Solo el 16.9% identificó el sexo masculino como un factor de riesgo, a pesar de que los hombres tienen un mayor riesgo de padecer la EP.
  • La mayoría de los encuestados dependen de los médicos como su fuente principal de información (63.6%), pero el 62% informó no saber qué recursos relacionados con la EP están disponibles localmente.

Estos hallazgos destacaron una necesidad urgente de educación accesible y culturalmente adaptada. En colaboración con SABER (Supportive Alliance for Brain Education and Research), el Dr. Vega trabaja junto con socios comunitarios de confianza —Hispanic Center of West Michigan, Latin Americans United for Progress y Exalta Health— para llevar conocimientos sobre la EP que sean lingüística y culturalmente relevantes directamente a las personas que lo necesitan.

La subvención comunitaria de la Parkinson's Foundation hizo posible que el Dr. Vega implementara un modelo multifásico impulsado por la comunidad que de otro modo no habría sido factible, enfocado en:

  • Escuchar a la comunidad
  • Cocrear educación con organizaciones comunitarias
  • Desarrollar la capacidad comunitaria mediante la capacitación del personal en las organizaciones asociadas
  • Coorganizar eventos de aprendizaje comunitarios que reúnen a familias, cuidadores y adultos mayores en espacios comunitarios de confianza

Conozca a Beatriz Arguezo-González, RN: ampliación de un programa de talleres para aumentar la conciencia sobre la EP en Chicago

Basándose en la necesidad de educación accesible, el equipo de Chicago Hispanic Health Coalition, junto con FUERZA (Familias Unidas: Empoderando y Reforzando contra la Enfermedad de Parkinson), se enfoca en las necesidades únicas de los cuidadores.

Ofrecen talleres para ayudar a los miembros de la comunidad a comprender mejor la EP, navegar recursos en línea confiables y ayudarlos a prepararse para hablar con su médico de atención primaria.

La subvención comunitaria de la Parkinson's Foundation, otorgada en 2025, apoya la expansión de su programa de talleres, Door 2 Door, extendiendo su alcance comunitario con recursos y apoyo sobre la EP.

Al expandirse a una plataforma virtual, el Chicago Health Coalition ha alcanzado a más participantes que pueden unirse desde casa. El Chicago Health Coalition además ofrece talleres presenciales y conecta a los participantes con un trabajador de salud comunitario para apoyo. La Coalition también tiene como objetivo proporcionar a los cuidadores herramientas para abogar por una mejor atención para ellos mismos y sus seres queridos que conviven con la EP.

Conozca a Gemma Moya-Galé, PhD: fortalecimiento de la comunidad mediante grupos de apoyo en español

Conozca a Gemma Moya-Galé
Conozca a Gemma Moya-Galé

Una manera importante en que las personas con Parkinson encuentran comunidad y alivio es mediante grupos de apoyo donde las personas se reúnen y comparten sus experiencias, escuchan a sus pares y expresan emociones que las personas sin la EP pueden no comprender.

Gemma Moya-Galé, PhD, profesora asistente en Columbia University en Nueva York y beneficiaria de una subvención comunitaria en 2025, ofrece grupos de apoyo interdisciplinarios mensuales, llamados Espacios Compartidos.

Estos grupos combinan psicoeducación con salud mental e incluyen talleres que enriquecen cada sesión. Estas sesiones no solo proporcionan a los asistentes información práctica y estrategias para vivir bien con la EP, sino que también sirven como un foro para compartir experiencias personales y mejorar la calidad de vida de las personas que viven con la EP y sus familias.

Con la subvención comunitaria, la Dra. Moya-Galé continuará ofreciendo estos talleres, cubriendo una variedad de temas como mindfulness, movimiento y habla, y apoyo lingüístico a nivel local e internacional.

«Gracias a esta subvención comunitaria, estamos logrando el trabajo que nos apasiona y esperamos continuar por mucho tiempo. Nuestros grupos dan la bienvenida a personas hispanas/latinas que viven con la EP y sus familias y nuestro objetivo es empoderar a esta maravillosa comunidad». - Dra. Moya-Galé

Su objetivo es continuar aumentando la conciencia sobre la EP, crear recursos para los participantes basados en la experiencia de Espacios Compartidos y compartirlos con organizaciones interesadas en crear programas similares.

Conozca a Sara Correal: ampliando el acceso al ejercicio desde Austin hacia el extranjero

Conozca a Sara Correal

Un estudio de 2023 en California rural encontró peores síntomas motoresno motores en comunidades latinas. Dado que el ejercicio puede mejorar la función cognitiva y mejorar algunos síntomas de la EP, establecer una rutina de ejercicio poco después del diagnóstico es esencial. En Austin, TX, Power for Parkinson's en Español, ayuda a abordar esta brecha al proporcionar programas de ejercicio gratuitos dirigidos a los síntomas tanto presenciales como en línea.

Sara Correal, directora de Programación e Innovación en Power for Parkinson's, encontró que esta subvención comunitaria fue fundamental para ayudarla a expandir y fortalecer su programa en español.

  • A nivel local, la subvención apoyó la entrega de clases presenciales que proporcionan un espacio seguro y culturalmente receptivo para el movimiento, la educación y la conexión comunitaria.
  • A nivel internacional, expandieron su canal de YouTube en español, haciendo que recursos de ejercicio de alta calidad específicos para Parkinson sean accesibles para personas y familias más allá de su comunidad de Austin.

«Este financiamiento de la subvención comunitaria asegura que las clases puedan ofrecerse de manera regular, proporcionando confiabilidad y continuidad. Esta estabilidad es esencial para construir confianza y compromiso a largo plazo», dijo Sara.

Como resultado, el programa ha alcanzado a miles de personas alrededor del mundo que de otra manera no habrían tenido acceso a rutinas de ejercicio específicas para la EP en español.

Al enfocar intencionalmente los recursos en una comunidad específica y desatendida, Sara y su equipo alinearon su programación con las necesidades culturales y lingüísticas de los participantes, eliminando las barreras del idioma que a menudo limitan el acceso a la atención basada en evidencia para la EP. Este enfoque permite que el contenido esté disponible, sea accesible y relevante.

Conozca al Dr. Jose Cabassa: proporcionando programas comunitarios gratuitos de boxeo en NYC

Conozca al Dr. Jose Cabassa

En Nueva York, el Dr. Jose Cabassa, fundador de Moving Brains Foundation, ofrece una clase de ejercicio presencial gratuita semanal en un gimnasio de boxeo profesional para ayudar a quienes conviven con la EP a incorporar el ejercicio como parte de su plan de tratamiento.

«El financiamiento de la subvención comunitaria de la Parkinson's Foundation nos ayuda a alcanzar a la comunidad latina y proporcionar recursos en inglés y español, haciendo que la información sea más accesible. Esto es especialmente importante en estructuras familiares complejas, donde la generación mayor con la EP puede comprender mejor en español, mientras que la misma información puede ser más accesible para sus hijos en inglés», dijo el Dr. Cabassa.

El financiamiento de la subvención comunitaria permitió promover estas clases en Harlem, Washington Heights y el Bronx en NY, donde viven más de 1 millón de latinos. La subvención también fomentó colaboraciones con otros beneficiarios de subvenciones con el objetivo de mejorar las vidas de las personas en su comunidad.

«¡No espere para comenzar! ¡Hágalo! Aunque los programas de ejercicio pueden ofrecer una variedad de enfoques, el primer obstáculo para incorporar el ejercicio como tratamiento es la constancia», dijo el Dr. Cabassa, alentando a las personas a unirse a un programa local de la EP.

Cómo encontrar un programa comunitario

Gracias a la dedicación de los participantes de la subvención comunitaria, las comunidades de habla hispana con la EP en todo el país están obteniendo mejor acceso a educación, ejercicio y apoyo.

Estos cinco beneficiarios de la subvención comunitaria están derribando barreras, construyendo conexiones y empoderando a las personas y sus familias para vivir bien con el Parkinson.

Ya sea que usted conviva con la EP o esté apoyando a un ser querido, hay programas disponibles para satisfacer sus necesidades.

Para obtener ayuda para encontrar un programa cerca de usted, llame a nuestra Línea de Ayuda al 1-800-473-4636, opción 3 para español. 

Raise Awareness

Temblores, estremecimientos y todo lo demás: enfrentando los síntomas motores del Parkinson

🧠 ¿Qué aprenderá en este artículo?

  • Los síntomas motores (movimiento) pueden afectar casi todos los aspectos de la vida de las personas con Parkinson.

  • Descubra cómo el ejercicio, los medicamentos y las terapias pueden ayudar a las personas con la enfermedad de Parkinson a moverse con mayor facilidad en cada etapa.

  • Los síntomas —incluyendo el temblor, la rigidez (agarrotamiento), la bradicinesia, la distonía, los problemas de marcha y equilibrio, y los cambios en el habla— se deben a la pérdida progresiva de las neuronas que producen ‑dopamina.

  • El ejercicio y los medicamentos (especialmente la levodopa) son los tratamientos más eficaces.

Pareja de personas mayores estirando al aire libre

La enfermedad de Parkinson (EP) puede dificultar moverse cuando quiera, de la manera en que quiera y puede ser igual de difícil mantenerse quieto. Desde el temblor y la rigidez hasta los calambres musculares y la dificultad para caminar, los problemas motores pueden afectar todos los aspectos de la vida diaria en la enfermedad de Parkinson. Descubra cómo el ejercicio, los medicamentos y otras estrategias pueden ayudarle a moverse con mayor facilidad.

El siguiente artículo se basa en una de las Charlas con Expertos - Expert Briefings de la Parkinson's Foundation, que explora los síntomas motores en la EP, presentada por el especialista en trastornos del movimiento, el Dr. Pablo Coss, de la residencia de Neurología y la subespecialidad en trastornos del movimiento del University of Texas Health Science Center at San Antonio, parte de la Red Global de Atención de la Parkinson’s Foundation.

Puntos clave para el Parkinson

La enfermedad de Parkinson se denomina un trastorno del movimiento porque afecta la forma en que la persona se mueve. Aunque los síntomas suelen desarrollarse lentamente con el tiempo, el Parkinson es progresivo; las necesidades pueden cambiar a medida que la EP avanza a través de sus etapas. La historia de una persona, sus síntomas y el examen físico se utilizan para hacer el diagnóstico.

Para considerar un diagnóstico de la enfermedad de Parkinson, debe estar presente la lentitud de movimiento (bradicinesia) junto con alguno de los siguientes:

  • Temblor en reposo: movimiento rítmico e involuntario que tiende a ocurrir cuando la parte del cuerpo afectada está en reposo. Esto tiende a afectar un lado del cuerpo en las etapas tempranas de la EP.

  • Rigidez (agarrotamiento): resistencia al movimiento causada por la activación involuntaria de los músculos en reposo.

  • Problemas de equilibrio (inestabilidad postural) que provocan tropiezos y caídas. 

Dopamina y movimiento

Aunque los científicos aún trabajan para comprender las causas del Parkinson, sabemos que se trata de un trastorno cerebral progresivo que daña las neuronas productoras de dopamina. La dopamina es un mensajero químico que regula el estado de ánimo y ayuda al cuerpo a moverse con fluidez.

Cambios motores en la EP

La pérdida de dopamina en una zona del cerebro llamada sustancia negra y otros cambios químicos en la enfermedad de Parkinson interfieren con las señales cerebrales, lo que provoca muchos síntomas no motores —incluidos cambios emocionales, problemas gastrointestinales y fatiga— y afecta el movimiento de distintas maneras, entre ellas:

  • Bradicinesia: lentitud de movimiento que puede afectar a todo el cuerpo, causando fatiga y dificultad para caminar o realizar actividades cotidianas. También puede causar: 

    • Enmascaramiento facial: rigidez en los músculos del rostro que dificulta expresar emociones.

    • Desafíos con movimientos de las manos, lo que dificulta más hacer cosas como abrir una bolsa, abrir un envase o escribir. La micrografía, escritura pequeña y amontonada que se ve frecuentemente a principios de la EP, suele estar conectada con la lentitud de movimiento.

    • Dificultad para ponerse de pie después de estar sentado.

  • Temblor. Las personas con Parkinson suelen tener temblor en reposo en una mano, pero también puede afectar las piernas, la mandíbula o la cara. El temblor de la mano suele describirse como “pill-rolling”, como si la persona estuviera haciendo rodar una pastilla entre el pulgar y el índice.

Alrededor de un 70% de las personas con Parkinson experimentan temblores. Para algunos, los temblores son leves, pero para otros pueden causar inseguridad e interferir con el sueño y las tareas diarias.

El temblor de acción, otro síntoma de la EP, sucede cuando la parte del cuerpo afectada está moviéndose o tratando de hacer una tarea como escribir o tomar de un vaso. Muchas personas con Parkinson experimentan una combinación de temblor de acción y de reposo.

  • La rigidez, que a veces se describe como “rigidez en tubo de plomo”: la resistencia del cuerpo al movimiento durante un examen físico (cuando está relajado) puede ser tan fuerte que puede sentirse como si el examinador intentara doblar un tubo de metal pesado. La rigidez puede conducir a:

    • Molestias dolorosas y dificultad para dormir

    • Menor movimiento de brazos y piernas al caminar

    • Rigidez facial

  • Distonía; calambres y retorcimientos musculares dolorosos y repetitivos, frecuentes en Parkinson, pueden:

    • hacer que los dedos se engarroten o mantengan una posición anormal

    • provoquen que el tobillo se gire hacia adentro naturalmente y que los dedos se giren

    • impactar la cara y los ojos, dificultando para algunos abrir los ojos de manera voluntaria

    • ir acompañado de un movimiento que puede sobreponerse con otras formas de temblor de la EP

  • Hipofonía (problemas del habla) puede incluir un habla suave o arrastrada, dificultades con la articulación, menor volumen o monotonía al hablar lo que, — a la par de la rigidez facial—, puede ser que la expresión emocional sea un desafío. Hipofonía también puede provocar respiraciones poco profundas, vacilantes, acelerada.

  • Marcha parkinsoniana—Cambios en la forma en que camina una persona debido a la EP, provocando pasos pequeños arrastrados, hombros encorvados, menor balanceo de los brazos o dificultad para levantar los pies.

Estos problemas de equilibrio y de la marcha, —junto con pasos cortos y rápidos que tienden a acelerarse (festinación), inclinación hacia atrás y falta de equilibrio—, aumentan el riesgo de caídas y lesiones, al igual que la congelación de la marcha: una sensación temporal pero peligrosa de que los pies están pegados al suelo. Las áreas concurridas, las puertas y los umbrales pueden desencadenar el congelamiento de la marcha.

Aumentar la dopamina: ejercicio y medicamentos

Woman taking medication

Debido a que la pérdida de dopamina impulsa los síntomas motores del Parkinson, aumentar la dopamina es la forma más eficaz de manejarlos y el ejercicio es una de las maneras más simples de ayudar a incrementarla y ralentizar la progresión de la enfermedad.

El ejercicio puede aliviar los síntomas motores del Parkinson y mejorar la fuerza y el equilibrio. Encontrar un ejercicio que disfrute puede darle la motivación para mantenerse activo. Nuestros ejercicios Viernes de Ejercicio de EP Salud en Casa, una colección de videos de ejercicio adaptados para personas con Parkinson, pueden ayudar a mantenerlo activo en casa.

La levodopa es el tratamiento más eficaz para la enfermedad de Parkinson. Las células cerebrales metabolizan la levodopa para convertirla en dopamina. Se suele combinar con carbidopa; esto permite que una mayor cantidad de levodopa llegue al cerebro sin ser metabolizada primero en el intestino (donde puede causar náuseas).

Para mantener los niveles necesarios de dopamina que ayuden al cuerpo a funcionar de manera óptima, es fundamental tomar los medicamentos exactamente como se prescriben. Es común que el médico ajuste la dosis a medida que la enfermedad de Parkinson progresa, para manejar los cambios en los síntomas.

Existen muchas formulaciones de levodopa, entre ellas:

  • Liberación inmediata (Sinemet IR), a menudo recetada en tres o más dosis al día.

  • Liberación controlada (Sinemet CR), a menudo recetada en tres o más dosis al día. 

  • Las formulaciones más recientes de liberación prolongada (Rytary o Crexont) pueden ofrecer efectos más rápidos y de mayor duración. Estas pueden recetarse de dos a cuatro veces al día.

  • Las terapias con bomba administran un suministro continuo de medicamento:

    • Vyalev administra foscarbidopa/foslevodopa mediante una bomba portátil y una aguja insertada debajo de la piel.

    • Duopa proporciona un gel continuo de carbidopa/levodopa a través de una sonda colocada quirúrgicamente.

  • La levodopa inhalada (Inbrija) se utiliza según sea necesario para tratar la reaparición de los síntomas entre las dosis regulares de carbidopa/levodopa, de cuatro a cinco veces al día.

Los efectos secundarios de la levodopa pueden incluir: nausea, estreñimiento, mareo, baja presión arterial, somnolencia, alucinaciones, o cambios en el comportamiento, como la hipersexualidad (trastorno de control de impulsos.)

Con el tiempo, algunos medicamentos para el Parkinson también pueden causar movimientos irregulares (discinesia), incluidos retorcimiento, balanceo, contorsiones y movimientos tipo “baile”. Esto puede ocurrir con frecuencia después de tomar una dosis, cuando la levodopa alcanza su máxima eficacia en el cuerpo.

Progresión del Parkinson, fluctuaciones motoras y tratamientos avanzados

Aunque la enfermedad de Parkinson afecta a cada persona de manera diferente, a medida que avanza, en muchas personas la reaparición o el empeoramiento de los síntomas (fluctuaciones motoras o periodos en “off”) entre las dosis de los medicamentos puede ocurrir con mayor frecuencia. Esto puede provocar un aumento de la discinesia, el desequilibrio o las caídas, o la necesidad de dispositivos de asistencia — herramientas diseñadas para mejorar la vida diaria.

Hable con su médico acerca de sus inquietudes. Él o ella puede trabajar con usted para ajustar su medicación o explorar tratamientos avanzados.

Los medicamentos utilizados para mejorar el efecto y la duración de la levodopa incluyen:

Estos medicamentos pueden causar diversos efectos secundarios, incluyendo náuseas, discinesia, dolor de cabeza, presión arterial baja, mareo, retención urinaria o decoloración de la orina, problemas de sueño o insomnio.

La cirugía puede ser una opción para los síntomas motores en el Parkinson avanzado. Las opciones pueden incluir:

Aprenda más

Para aprender más acerca de cómo manejar los síntomas motores de la enfermedad de Parkinson, explore los recursos a continuación o llame a nuestra Línea de Ayuda gratuita al 1-800-4PD-INFO (1-800-473-4636), opción 3 para español:

My PD Story

Steve and Lisa Fischlin
People with PD

Steve and Lisa Fischlin

Steve Fischlin’s journey with Parkinson’s disease (PD) started with a tremor in his foot, followed by his right arm not swinging while he walked. His next symptom was a stoic expression that left his wife, Lisa, asking if he wasn’t having fun — she noticed he wasn’t smiling. Two appointments with different neurologists and a series of tests confirmed Steve had PD and left him and his family with more questions than answers.

One thing Steve did know was that exercise is proven to help ease Parkinson’s symptoms, so he got moving.

“That first year he was walking every day,” Lisa said. “Rain or shine, he went out walking. His friends at work made sure he walked during his lunch hour. We walked together, our neighbor walked with him, it was a consistent routine.”

All this walking made Steve and Lisa wonder if there was a race or walk that supported the Parkinson’s community, which led them to Moving Day, A Walk for Parkinson’s.

“We immediately got on the committee and started making connections,” Lisa said. “We were both working at the time and had a fairly large Moving Day team, and we were one of the top fundraising teams for the last four or five years for Sacramento. It was a great way for all of us to come together and support Steve and his diagnosis.”

Steve retired in 2020 to focus on his health, and Lisa joined him when she retired in 2023. They wanted to dive deeper into the Parkinson’s community and became members of the Parkinson’s Foundation California Chapter Board. They continued fundraising for Moving Day, but they wanted to do more.

They created the non-profit, FISCH 4 Parkinson’s, a Steven J. Fischlin Charity, dedicated to raising awareness and supporting people with Parkinson’s. They launched a signature fundraising event through the non-profit, the annual FISCH 4 Parkinson’s Golf Tournament. The first tournament, held in August 2024, raised more than $26,000, which they donated to the Parkinson’s Foundation. The event returned in August 2025, raising $35,000 to support the Foundation.

“In the second year we were able to expand the tournament, get sponsorships and really reach out to the wider Parkinson’s community beyond our family and friends,” Lisa said. “It took some time to explain what we were trying to accomplish, and for Steve to feel comfortable telling his story and making connections.”

This tournament has helped Steve and Lisa support the Parkinson’s Foundation and has helped them create their own support network of people near them in the Parkinson’s community.

Steve and Lisa with friends at the 2025 FISCH 4 Parkinson’s Golf Tournament
Parkinson’s Foundation friends at the 2025 FISCH 4 Parkinson’s Golf Tournament, including Vikas Chinnan, Donna Cline and Jeff Bell.

“Last year we had several golfers at the tournament who had Parkinson’s,” Steve said. “Now we meet up with them and their wives three or four times a year. We get dinner and catch up and talk about how we’re doing and things about Parkinson’s we can all relate to. We’re always trying to find more people to join our group.”

In August 2026, the tournament raised $40,000 for the Parkinson’s Foundation. For Steve, the event is much more than a day on the golf course.

“Supporters come not only to play, but also because they believe in the cause and want to be part of something larger,” Steve said. 

Steve and Lisa are passionate about supporting the Parkinson’s Foundation because of the resources and information they have received.

“When you find out you or a loved one has Parkinson’s, you have to just start digging in and learning about it,” Lisa said. “We use the Parkinson’s Foundation website, attend webinars and Steve participated in PD GENEration because his kids were wondering if this was something they could be passed down.”

“The Foundation doesn’t just support people with Parkinson’s, it supports the whole family and care partners, and that’s so important.” - Lisa

Steve and Lisa have also found a great deal of support through the University of California (UC) Davis Health Center for Movement Disorders & Neurorestoration, a Parkinson’s Foundation Center of Excellence. In 2024, the center opened a multidisciplinary clinic that brings together care providers from several specialties, including neurology, speech therapy, physical therapy, nutrition and more.

“To be able to have one stop and ask all these experts questions and find support is incredible,” Lisa said. “We’ve made really strong connections through UC Davis, and we’re able to talk to them throughout the year. This clinic is possible because of the Parkinson’s Foundation, and it makes us feel like we are never alone.”

In 2026, FISCH 4 Parkinson’s directed half of the funds it raised for the Parkinson’s Foundation to the Parkinson’s Foundation Center of Excellence at UC Davis in Sacramento, where Steve receives care.

“Access to a Parkinson’s Foundation Center of Excellence has shown us how vital specialized Parkinson’s care is,” Steve said. “We want other families to have that same expertise, support and hope.”

“Right now, the multidisciplinary clinic is only open on Tuesdays, and it runs on donation, so we want to make a difference and support it,” Lisa said. “We’re proud to support the Parkinson’s Foundation and everything it does for people with Parkinson’s, while also supporting this resource right in our own community. We want to be loud about this disease, share our story and raise money to find better treatments and a cure.”

“I’ve met other people who have Parkinson’s, and I will always talk to anyone about it,” Steve said. “It’s a small world and we want to meet with people, do whatever we can to help. We want to talk about it, and we want to help find a cure.”

For Lisa, advocacy has become just as important. She and Steve have joined Parkinson’s advocacy efforts at the federal and state levels, meeting with lawmakers and sharing their story to draw greater attention to the Parkinson’s community.

“We’ve learned that our voices matter,” Lisa said. “Whether we’re talking with a golfer at our tournament, a researcher, a healthcare professional or a member of Congress, we can help people better understand what Parkinson’s looks like for patients and caregivers.”

Create your own Parkinson’s fundraiser! Visit Parkinson.org/DIY to get started.

Raise Awareness

People with Parkinson’s Share What’s Helped Them

🧠 What will you learn in this article?

This article shares real experiences from people living with Parkinson’s and highlights what helps them maintain quality of life. It highlights how:

  • Staying physically active and mentally engaged can improve movement, mood and cognitive function.

  • A positive mindset and sense of purpose help people cope with challenges and live more fully.

  • Building community and support systems reduces isolation and provides encouragement.

  • Learning about Parkinson’s empowers individuals to better understand symptoms and manage their care.

We asked out social media community what helps them live well with Parkinson's

Parkinson’s disease (PD) looks different for everyone. Symptoms vary, as do the ways people maintain and improve their quality of life. People with Parkinson’s often discover strategies that work best for them, whether it’s staying physically active, keeping mentally engaged, connecting with others or practicing gratitude.

The Parkinson’s Foundation offers a wide range of resources to help people manage their symptoms. Additionally, some of the most meaningful insights come from those living with Parkinson’s themselves.

We asked our social media community to share what has helped them live well with Parkinson’s. Here’s what they had to say:

Exercise and Movement

Staying physically active was one of the most popular strategies. Research shows that regular exercise can improve mobility, balance, mood and even cognitive function for people living with Parkinson’s. Many described movement not just as therapy, but as empowerment.

“Exercise and staying mentally active have helped me the most. I was diagnosed in 2018. Don’t give up. Sometimes I have to force myself to exercise, but I always feel better when I do.” - Val

“I was diagnosed at age 75 and I plan on being here for a long time. I exercise every day, walk a couple of miles, take my medication and listen to my doctor.” - Frank

“A dance class called Dance Health Alliance has helped me a lot. You can even do it sitting in a chair if you have balance issues. It’s definitely helped improve my walking.” - Christine

Exercise at home with our PD Health@Home Fitness Friday videos. Sign up for our next live Fitness Friday or check out our On-Demand videos right now.

Mental Engagement and Hobbies

Keeping the brain active can be just as important as keeping the body moving. Engaging in hobbies, learning new skills and staying mentally stimulated may support cognitive health and overall well-being.

For many, creative expression and intellectual engagement provide both joy and a sense of purpose.

“Learning new tunes and staying musically active has been a real benefit. I’ve been a professional musician for over 50 years and staying active in my music career — even at age 71 — has helped keep my Parkinson’s under control.” - Joe

“I write short stories, read, belong to a book club and take part in quizzes.” - Val

Mindset, Hope and Perspective

A positive outlook doesn’t erase the challenges of Parkinson’s — but many people shared that mindset plays a powerful role in how they navigate them.

“I was diagnosed 25 years ago, in my 40s and I’m now in my 70s. Focus on what you still have. If you have love, learning and laughter — even a friendly phone call or a good book — you are lucky.” - Fillis

“What truly helped me was hope with purpose. When I stopped seeing Parkinson’s as an ending and started seeing it as a teacher, everything changed. Healing isn’t just about the body — it’s about the mind, heart and spirit working together.” - Ellen

“After my diagnosis, I started learning about Parkinson’s and its treatments. I’ve learned to accept it, appreciate the small blessings, exercise, take my medication as prescribed and live with a positive attitude.” - Daisy

These reflections remind us that resilience can take many forms, including acceptance, gratitude, determination or simply continuing forward one day at a time.

Community and Support

Connecting with others who understand Parkinson’s can reduce isolation and provide encouragement. A strong online or in-person support network often makes a meaningful difference.

“As a woman in my 30s with young-onset Parkinson’s, community has helped me the most. Exercise is second and reading The Parkinson’s Plan has also been incredibly helpful.” - Erin

“Joining the Facebook group Life With Parkinson’s and accessing resources like yours has been extremely helpful. I also participated in an eight-week class for the newly diagnosed through my local hospital.” - Lin 

Many people living with Parkinson’s find that sharing experiences, learning together and supporting one another strengthens both confidence and quality of life.

Explore our Community Network groups that empower key groups within the PD community — including people who are newly diagnosed, women with PD, those with early-onset PD and more! Find your community.

Learning about PD

Learning more about Parkinson’s can bring clarity, reassurance and empowerment. Understanding movement and non-movement symptoms can help people feel more in control of their care.

“Education has helped me so much. I didn’t realize many of my symptoms were part of Parkinson’s. Learning about the disease helped me understand that I’m not crazy. Physical therapy has also made a huge difference.” - Sharon

When people understand what is happening in their brain and bodies, it can ease uncertainty and make it easier to advocate for the care they need.

Explore Parkinson’s resources that address your most concerning symptoms right now.

Living Well with Parkinson’s

Living well with Parkinson’s does not mean symptoms disappear — it means finding tools, support and perspective that help you move forward.

As these shared experiences show, there is no single path. What works for one person may look different for another, and that’s okay.

If you’re looking for support, resources or ways to connect, we are here to help. Explore resources and information at Parkinson.org or contact our Helpline at 1-800-4PD-INFO (1-800-473-4636).

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