Podcasts

Episodio 23: Crear un plan de autocuidado y por qué es importante para los cuidadores

Ser trabajadora social en una clínica significa ser parte del equipo médico y brindar atención a las personas que viven con Parkinson y a sus familias. 

En este episodio, hablamos con Adriana González, trabajadora social en el Centro para el Parkinson y Otros Trastornos del Movimiento de la University of California, San Diego. Como trabajadora social, Adriana ayuda a las familias y a los cuidadores a identificar recursos comunitarios y los apoya cuando enfrentan situaciones difíciles. 

La meta de Adriana es conocer a las familias desde el inicio de la enfermedad para hablar acerca de los diferentes periodos y crear un plan antes de llegar a un momento de crisis. 

Para Adriana, lo más importante es concientizar a la comunidad de habla hispana acerca de la enfermedad de Parkinson para mejorar el manejo médico de esta enfermedad y apoyar a más familias y cuidadores que están tratando de ayudar a su ser querido con Parkinson.

Como noviembre es el Mes Nacional de Cuidadores Familiares, hablamos con Adriana acerca de la importancia del autocuidado: un plan que garantiza que los cuidadores o aliados de cuidado estén atentos a su propio bienestar.

Publicado: 15 de noviembre de 2022

Agradecemos al patrocinador de este episodio de podcast:

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Podcasts

Episode 136: Traveling with Parkinson’s Disease

Parkinson’s disease (PD) can be an impediment to certain activities, but with proper planning, people can still pursue many of the things they have always enjoyed. One of those things is travel – to see family, visit friends, or explore new sights and cultures. One key to enjoying travel is planning. Pay special attention to issues that are known to affect how you feel and function.

Packing extra medications when traveling has always been a good idea, but with today’s unpredictability of flight schedule changes and cancellations, as well as the possibility of contracting COVID, it makes sense to carry even more than a few days’ supply of extra medication. Anticipate managing any shifts in medication timing if you are visiting a different time zone, interruptions to your exercise and sleep routines, in addition to unforeseeable events and changes.

In this episode, we hear from two people with valuable advice and tips for traveling with PD. Rebecca Miller, PhD is a clinical psychologist and Associate Professor of Psychiatry at Yale University School of Medicine and is a person living with PD. Occupational Therapist Julia Wood, MOT, OTR/L is Director of Professional and Community Education at the Lewy Body Dementia Association. An overriding message from both of them is “planning for the unpredictability of today's world.”

Released: September 6, 2022

Podcasts

Episode 92: Clinical Issues Behind Impulse Control Disorders

Impulse control disorders in Parkinson’s disease (PD) are more common than originally thought, affecting an estimated one in six people with PD taking dopamine agonists. They may appear as unhealthy or compulsive levels of shopping, gambling, eating, sexual activity, or involvement in hobbies. They appear to be related to dopamine replacement therapy, so finding the right level of medications can be a challenge to manage symptoms without incurring impulsivity issues. It is important that people with PD, their care partners, and health care professionals be aware of and recognize these activities so that they can be addressed promptly to avoid, for example, social, emotional, economic, and health issues that may result from these disorders. The harm often goes beyond the person with the disorder and can affect family, friends, and others around them. Once recognized, impulse control disorders can often be managed or eliminated by working with a doctor to change dopamine agonist medications or dosage, or in some cases, even going on to deep brain stimulation.

Dr. Mark Groves, Consultant Psychiatrist at the Parkinson’s Foundation’s Center of Excellence at Mount Sinai Beth Israel in New York City, discusses the problem of impulse control disorders, what forms they may take, approaches to recognizing them, and the need to acknowledge them as a biologic condition and not a character or personality flaw.

Released: November 3, 2020

Podcasts

Episode 139: Community Care Programs for Care Partners

Caregiving can be an intensive endeavor, not to mention the physical, mental, emotional, and even financial aspects of it. Just as people with Parkinson’s disease need support services, so, too, do their care partners. In this episode, Social Worker Cara Iyengar, MSW, LISW, the coordinator of the Parkinson’s Foundation Center of Excellence at the University of Iowa in Iowa City, discusses some of the Foundation’s resources that she shares with care partners, her three-pronged approach to supporting them, some of the challenges she faces in bringing support services to people in a rural state like Iowa, and the kind of feedback that she has received from care partners.  

Released: November 1, 2022

Thank you to this episode’s podcast sponsor:

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Podcasts

Episode 141: How Social Workers Can Help Ease Anxiety about the Unknown

The news of a Parkinson’s diagnosis can be overwhelming. So many questions arise, including how it will change the person’s life, what lies ahead, and what to do first. Social workers can be a vital resource in helping a newly diagnosed person, care partner, and family navigate the road ahead, as well as provide ongoing support through the course of the disease. They are the health professionals who know and can coordinate many of the most helpful resources. Or as social worker Lance Wilson, LSW, C-SWHC, ASW-G, the education outreach coordinator for the Jefferson Health Comprehensive Parkinson’s Disease and Movement Disorder Center in Philadelphia, a Parkinson’s Foundation Center of Excellence, puts it, social workers are the Yellow Pages for health care, tying people into the resources they need. He says social workers can help put people’s minds at ease by assessing their needs and lining up professionals who can provide medical, mental health, spiritual services, and more.

Released: December 13, 2022

Podcasts

Episodio 22: Cambios cognitivos

Cuando uno piensa en la enfermedad de Parkinson (EP), es fácil asociarla más con los síntomas motores, como la rigidez o el temblor; pero también existen síntomas no motores, como los cambios de estado de ánimo, la ansiedad o la depresión.

En este episodio, hablamos con la doctora Elsa Baena, neuropsicóloga clínica en el Barrow Neurological Institute, Centro de Excelencia de la Parkinson’s Foundation, acerca de estos cambios cognitivos asociados con el Parkinson.

La doctora Baena explica la conexión entre el Parkinson y la cognición y cómo pueden prepararse las personas con Parkinson para estos cambios (no sólo las maneras farmacológicas, sino también las terapéuticas).

Asimismo aprenderemos acerca de los miembros del equipo de atención médica que pueden apoyar a una persona con Parkinson y a sus familiares con estos cambios cognitivos.

Lanzado: 18 de octubre de 2022

Raise Awareness

How 5 Community Leaders Are Reaching Hispanic and Latino Communities

🧠 What will you learn in this article?

This article highlights Parkinson’s Foundation efforts to support Hispanic and Latino communities living with Parkinson’s disease through community grants. It discusses:

  • Parkinson’s Foundation Community Grants aim to close gaps in Parkinson’s care and resources locally across the U.S.
  • Five local programs that are addressing barriers in education and support for Spanish-speakers living with PD. 
  • Programs that range from education workshops and support groups to PD-tailored exercise classes and care partner resources, offered in person and online.
  • How to find local programs.
Group of senior friends laughing together outside

Hispanic and Latino members of the Parkinson’s disease (PD) community often face distinct challenges to living well with Parkinson’s, including language barriers, limited healthcare access and gaps in culturally aligned educational materials. 

The Parkinson’s Foundation acknowledges these disparities and actively works to make quality healthcare more accessible to everyone with Parkinson's, in part through our Community Grants program.

The Parkinson’s Foundation Community Grants program supports local groups across the U.S. in enhancing health, wellness and education for people living with Parkinson’s. Since 2011, the Foundation has invested more than $12.7 million in nearly 1,000 community-based programs.

Meet five of our community grantees below, awarded for their tailored educational, exercise and care partner programs created for the Spanish-speaking PD communities.

Meet Irving Vega, PhD: Improving Access to Education and Spanish Resources in West Michigan

Irving Vega, PhD, Red Cedar Distinguished Associate Professor at Michigan State University, received a 2025 Community Grant to better understand and address the unique needs of the Hispanic and Latino communities in West Michigan — populations historically underrepresented in PD education and research.

As part of this grant, he conducted a community survey to assess awareness of PD and found the following gaps:

  • While pesticide exposure is well-established environmental risk to PD, many Latino community members did not identify it as a risk factor. 
  • Only 16.9% identified male sex as a risk factor, despite men being at higher risk for PD. 
  • Most respondents rely on doctors as their primary source of information (63.6%), but 62% reported not knowing what PD-related resources are available locally. 

These findings highlighted an urgent need for culturally tailored, accessible education. In collaboration with SABER (Supportive Alliance for Brain Education and Research), Dr. Vega works alongside trusted community partners — Hispanic Center of West Michigan, Latin Americans United for Progress and Exalta Health — to bring linguistically and culturally relevant PD knowledge directly to the people who need it.

The Parkinson’s Foundation Community Grant made it possible for Dr. Vega to implement a multi-phase, community-driven model that would not have been feasible otherwise, focused on:

  • Listening to the community
  • Co-creating education with community organizations
  • Building community capacity through training staff at partner organizations 
  • Cohosting community-based learning events that bring together families, caregivers and older adults in trusted community spaces 

Meet Beatriz Arguezo-González, RN​: Expanding A Workshop Program to Raise PD Awareness in Chicago 

Building on the need for accessible education, the Chicago Hispanic Health Coalition team, alongside FUERZA (Familias Unidas: Empoderando y Reforzando contra la Enfermedad de Parkinson), focuses on the unique needs of care partners. 

They offer workshops to help community members better understand PD, navigate reliable online resources and help prepare them speaking with their primary care doctor. 

Their 2025 Parkinson’s Foundation Community Grant supports the expansion of their workshop program, Door 2 Door, extending its community reach with PD resources and support.

By expanding to a virtual platform, The Chicago Health Coalition has reached more participants who can join from home. The Chicago Health Coalition additionally offers in-person workshops and connects participants a community health worker for support. The Coalition also aims to provide care partners with tools to advocate for better care for themselves and their loved ones living with PD.

Meet Gemma Moya-Galé, PhD: Strengthening Community Through Spanish-Language Support Groups

Gemma with friends
A group of people at a conference table

One important way people with Parkinosn’s find community and relief is through support groups where people come together and share their experiences, hear from their peers and express emotions that people without PD may not understand. 

Gemma Moya-Galé, PhD, Assistant Professor at Columbia University in New York and a 2025 Community Grant recipient, provides monthly interdisciplinary support groups, called Espacios Compartidos

These groups combine psychoeducation with mental health and include workshops that enrich each session. Not only do these sessions provide attendees with practical information and strategies to live well with PD, but they also serve as a forum to share personal experiences and improve the quality of life for people living with PD and their families.

With the Community Grant, Dr. Moya-Galé will continue to offer these workshops, covering a variety of topics such as mindfulness, movement and speech, and language support locally and internationally.

“Thanks to this Community Grant, we are achieving the work we are passionate about and we hope to continue for a long time. Our groups welcome Hispanic/Latiné people living with PD and their families and our goal is to empower this wonderful community.” - Dr. Moya-Galé

Her goal is to continue raising PD awareness, create resources for participants based on the Espacios Compartidos experience and share these with organizations interested in creating similar programs.

Meet Sara Correal: Expanding Access to Exercise from Austin to Abroad

Sara leading exercise classes

A 2023 study in rural California found worse movement and non-movement symptoms in Latino communities. Since exercise can boost cognitive function and improve some PD symptoms, establishing an exercise routine soon after diagnosis is essential.In Austin, TX, Power for Parkinson’s en Español, helps address this gap by providing free, symptom-directed exercise programs both in-person and online. 

Sara Correal, Director of Programming and Innovation at Power for Parkinson’s, found this Community Grant to be instrumental in helping her expand and strengthen its Spanish-language program. 

  • Locally, the grant supported the delivery of in-person classes that provide a safe, culturally responsive space for movement, education and community connection.
  • Internationally, they expanded their Spanish-language YouTube channel, making high-quality Parkinson’s-specific exercise resources accessible to people and families beyond their Austin community. 

“This Community Grant funding ensures classes could be offered on a regular basis, providing reliability and continuity. This stability is essential for building trust and long-term engagement,” said Sara. 

As a result, the program has reached thousands of people around the world who would not have otherwise had access to Spanish-language, PD-specific exercise routines

By intentionally focusing resources on a specific, underserved community, Sara and her team aligned their programming with participants’ cultural and linguistic needs, removing language barriers that often limit access to evidence-based PD care. This approach allows content to be available, accessible and relevant.

Meet Dr. Jose Cabassa: Providing Free Community Boxing Programs in NYC

People exercising at a boxing gym

In New York, Jose Cabassa, MD, founder of the Moving Brains Foundation, provides a free, weekly in-person exercise class at a professional boxing gym to help those living with PD incorporate exercise as part of their treatment plan.  

“Parkinson’s Foundation Community Grant funding helps us reach the Latino community and provide resources in English and Spanish, making information more accessible. This is especially important in complex family structure, where the older generation with PD may understand better in Spanish, while the same information may be more accessible to their children in English,” said Dr. Cabassa.

The Community Grant funding allowed for promoting these classes across Harlem, Washington Heights and the Bronx in NY — where more than 1 million Latinos live. The grant also fostered collaborations with fellow grant recipients with the goal of improving the lives of people in their community.

"Don’t wait to start! Do it! Although exercise programs may offer a variety of approaches, the first hurdle in incorporating exercise as treatment in consistency,” said Dr. Cabassa, encouraging people to join a local PD program. 

Finding a Community Program

Thanks to the dedication of Community Grant participants, PD Spanish-speaking communities across the country are gaining better access to education, exercise and support. 

These five Community Grant recipients are breaking down barriers, building connections and empowering people and their families to live well with Parkinson’s. 

Whether you are living with PD or supporting a loved one, there are programs available to meet your needs. 

For help finding a program near you, call our Helpline at 1-800-473-4636, option 3 for Spanish.

My PD Story

Gary Krajewski headshot
People with PD

Gary Krajewski

My Parkinsonism Story

In late 2018, an ear, nose and throat (ENT) physician noticed a resting tremor in my left hand, reduced left arm swing and a pill-rolling movement. After an MRI, I was initially diagnosed with Parkinson’s disease (PD), but the diagnosis was later revised to Parkinsonism/atypical Parkinsonian syndrome

My symptoms have included a mild left-hand tremor, reduced arm swing, lightheadedness, balance issues and some urinary symptoms, while remaining relatively stable over time. 

Parkinsonism is a set of movement symptoms associated with Parkinson’s and other disorders. It describes symptoms rather than a specific disorder.

Atypical Parkinsonism is a group of progressive brain disorders with some of the symptoms seen in PD. Symptoms are often more serious early on.

What has helped me!

After my diagnosis, I decided to focus on what I could do rather than what I had lost.

In 2024, I became a Parkinson’s Ambassador and helped launch a local PD Art & Music Night with support from Duke Health Movement Disorders Center, a Parkinson’s Foundation Center of Excellence. The event has grown successfully over multiple years. I am also involved with Moving Day and Parkinson’s Revolution fundraising efforts and began serving as a Board Member for the Parkinson’s Foundation Carolinas chapter in 2026. 

Managing Parkinsonism has centered on four daily priorities: exercise, speech, sleep and nutrition. I also maintain a daily art practice that helps me express my experiences living with Parkinsonism and supports others in the PD community. 

Advice

My advice for those newly diagnosed is to shift the question from “Why?” to “What?” Instead of asking why this happened, ask: 

What can I still do? 
What resources are available? 
What steps can I take today to live well? 

Focusing on those questions has helped me move forward with purpose and hope.

For me, it has been helpful to arrange Parkinson’s Foundation resources into a daily life survival kit. I believe that gives me a better perspective on WHAT I need every day.

Explore Parkinson’s Foundation resources today. 

My PD Story

Melinda Young headshot
People with PD

Melinda Young

I was diagnosed with Parkinson’s disease (PD) in March 2023, just a couple weeks before my 43rd birthday. I went to the appointment alone after a long drive. I did a series of tests and was told matter-of-factly that I had Parkinson’s. 

I didn’t really react... no big emotional response. I was just like “Okay… what do I need to do?” I left with information, medication options and a plan for more testing.

That’s just how I handle big things. I’ve had a lot of those moments in life, and I go into “figure it out” mode. I told my son and my parents right away, then my sister, my closest friends and my supervisor. I also posted on social media about it pretty quickly because I didn’t want people to make assumptions about why I’m shaking.

After my diagnosis I discovered the Parkinson’s Foundation and the People with Parkinson’s Advisory Council while researching online. When I saw the announcement for the council I immediately applied — I was eager to learn more about Parkinson’s and contribute in a meaningful way to a community that understands the journey.

Being a member of the People with Parkinson’s Advisory Council is incredibly rewarding. It feels empowering to have a voice and to be part of shaping resources and support for others living with Parkinson’s. 

At times, I wish I could contribute even more. Balancing a demanding full-time leadership role, family responsibilities and living in a rural community can be challenging, but I remain deeply committed to the work and the impact the council makes.

After diagnosis, my emotions took a while to catch up. It was almost a year later when I first felt real frustration. During an OT (occupational therapy) appointment I realized how much my movement had changed.

Another year passes and the grief really showed up. 

One quiet morning, I was lying in bed next to my partner and I could feel my left arm tremoring. I put my hand on it, gently held it for a moment, and said, “I’m so sorry you’re broken.” It sounds kind of ridiculous, but it felt real. I needed to apologize to my own body. 

That moment stuck with me all day, I was constantly on the verge of tears. I ended up finally crying that night when he asked me what was wrong. I told him. I couldn’t hold it in anymore. I avoided sharing my thoughts and feelings about what's going on because I don't want anyone to worry... Not my parents, my son, my love... No one.

Parkinson’s doesn’t feel inspiring to me. It feels like loss, frustration, anger and being tired all the time. “Hope” for me isn’t about being positive. It’s just getting up and dealing with it anyway.

And today… today was one of those days.

Recently I was at a work event, and the expo center is about a half mile from my hotel. I walked back and forth a few times. At first, I was kind of proud of myself. But by the end of the night, I was hurting and struggling just to get back. I had to stop multiple times.

I can’t fully explain how much that sucks.

Before all of this, I walked a few miles every day without thinking about it. Now a half mile felt like too much. 

I’m frustrated with my body. Today, I hate Parkinson’s.

I’ve been trying to act unbothered... trying to be strong, to accept it, to not let it define me. But the truth is, some days I’m not okay. Some days I’m scared, sad, angry, insecure, in pain, tired, lonely… and at times, hopeless.

Through the lows and dim highs, the Parkinson’s Foundation remains an invaluable resource for me. I regularly turn to Parkinson.org as my first source when I have questions or need support. 

Resources that have been especially helpful include the Substantial Matters podcast, virtual PD Health @ Home educational programs like Mindfulness Mondays, the Women with Parkinson’s Community Network and the Hospital Safety Guide. These tools have provided practical guidance and a sense of connection, which is so important when navigating life with Parkinson’s.

Many days it feels like too much work to try to slow progression through movement and exercise when I already have so little time and energy. And when I do try, my body doesn’t always cooperate. Some days, it feels easier to just give up.

But this is the part people don’t always see. This is Parkinson’s too.

I can hate it today… and still show up again tomorrow. I’m not giving up just yet.

Find the resources that work for you. Explore our resources today.

My PD Story

Jordan and his dad
Care Partners

Jordan Levin

My Parkinson’s story is told from the perspective of a caregiver — and, in a sense, from two of them. 

Stephen and Judy Levin

I help care for my father, Stephen Levin, who was diagnosed with Parkinson’s disease (PD) more than 10 years ago and, more recently, with dementia. At the same time, I support my mother, Judy Levin, who is his primary caregiver. In other words, I am both a caregiver and a “caregiver to the caregiver.” That distinction matters, because the people we so easily overlook are often the caregivers themselves — frequently long-standing spouses — who quietly need and deserve support of their own.

My father’s condition had been declining gradually, with mild dementia emerging around 2023. But nothing prepared us for the sudden sea change in early 2025, triggered by a viral illness we later learned can wreak havoc on people with PD. Almost overnight, our lives were thrown into a tailspin: hospitalization, a stay in a rehabilitation facility, and ultimately full-time in-home caregivers, along with two separate moves to accommodate his needs. 

We were unprepared and uneducated about what to expect, forced to move quickly and make weighty decisions with imperfect information.

Jordan and his mom

As much as this care was about improving my father’s quality of life, it was equally about my mother — her mental well-being, her sense of balance, and her access to support groups and community. We managed through sheer grit, relentless networking, and the pooled time and love of a close-knit family and an extended circle of friends.

The stress on a caregiver is real and deep, and the physical and mental toll cannot be underestimated. 

Jordan with his family

Caregivers absorb a flood of information — some of it conflicting — while consulting doctors and specialists, taking on responsibilities a partner once handled (including bills, household finances and more), welcoming new people into their lives, and often juggling jobs and other family obligations at the same time. This is exactly where more resources, and more recognition, are so badly needed.

This cause is personal. There is a history of neurological conditions on my father’s side of the family, including both Parkinson’s and various forms of dementia, and several friends and their loved ones are walking this same road. I believe deeply in medical research — and just as deeply in the power of daily movement and a healthy lifestyle to help prevent or blunt the onset of neurological disease.

Jen, Rock, and Jordan

That belief led my friends Jen and Rocky Pontikes and me to create the Million Meter Challenge, a month-long rowing event we completed as Parkinson’s Campions, with the Parkinson’s Foundation. The event was about teamwork, movement and showing up — and together we raised awareness and funds for Parkinson’s. 

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 is a recipient of the Parkinson’s Foundation Top Fundraisers Award. Learn how you can become a Parkinson’s Champion today. 

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