Educational Events

Social Engagement: Improv for Parkinson's Taster

Virtual ( Zoom )
1:00 pm to 2:00 pm EST
FREE
Couple sitting on the couch on a tablet

Wellness Wednesday: Social Engagement Series

Tightrope Impro Theatre's Improv for Wellness team is excited to rejoin PD Health @ Home to offer another Improv for Parkinson's Taster!

Are you a person with Parkinson's Disease or a Parkinson's-like condition? Are you curious about the benefits of Improv for Parkinson's? Join our taster session to try out some improv games, learn about the research and benefits, and see what programs we have to offer!

Speakers

Megan Dunlop, Facilitator of Improv for Parkinson's

Rosemary Morrison, Wellness Coordinator of Improv for Work and Wellness

There is no charge to attend, but registration is required.

Due to the nature of our social engagement programs and to protect the privacy of participants, we will not be recording or archiving these programs. By not recording, it's our hope that the program provides a comfortable environment that encourages meaningful participation.

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

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

Light of Day

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
Advancing Research

Partnering with Morehouse School of Medicine to Diversify Genetic Data

Dr. Branson, Movement Disorders Specialist

Chantale Branson, MD, is the first-ever movement disorders specialist — a neurologist with specialized training — to work at Morehouse School of Medicine in Atlanta, GA. In addition to treating and helping people with Parkinson’s disease (PD), she is committed to improving the health disparities that Black and African American individuals face in the PD community.

Under Dr. Branson’s direction, Morehouse is the first historically Black institution of medicine to become a PD GENEration: Mapping the Future of Parkinson’s Disease research site. Every research site works alongside the Parkinson’s Foundation to offer genetic testing and counseling to people with PD, in English or Spanish, at no cost.

“We have a very diverse group of people who are participating,” Dr. Branson said. “We want to encourage more community members to take part in the study so they can improve their disease management, learn more about potential implications for their family, be connected with relevant PD trials and impact the future development of improved treatments — for themselves and future generations.”

Pioneering Change

To date, Morehouse has enrolled the most Black and African American participants for PD GENEration, which is on its way to reaching its 1,000 participant goal for this demographic.

The international genetics initiative is designed to be inclusive and accessible to populations of focus, which are groups of people in need of increased access to care, resources and research efforts. A common misconception surrounding Parkinson’s is that it only impacts older white men. Black and African American people with Parkinson’s are often:

  • Diagnosed at a lower rate than white people with the disease.
  • Diagnosed later in disease progression, once symptoms considerably impact day-to-day living.

Dr. Branson has dedicated her career to helping improve these statistics for the Black community over time. “At Morehouse, we work to provide that missing connection between having a provider or physician who represents you, who looks like you, to participate and be involved in your care,” she said.

Before Morehouse, Dr. Branson tirelessly worked to develop the first movement disorders clinic at Grady Hospital — the largest public hospital in Georgia and the tenth largest in the U.S. that provides care to all, including those without healthcare insurance and those with incomes below the federal poverty level.

Acknowledging History to Create Change

Today there are numerous regulations in place set to ensure clinical trials follow ethical practices, but this was not always the case. “Due to the historical issues and in regard to race in the United States, research has not been very common within the community, particularly within different diseases such as the Parkinson’s disease and neurological disorders,” said Dr. Branson.

The notorious Tuskegee study that was reported nearly 50 years ago, where researchers withheld detrimental treatments from hundreds of Black men in Alabama for decades, is still top of mind when it comes to distrust in medicine and research among Black and African Americans.

Dr. Branson also references the story of Henrietta Lacks, a Black woman who died of cervical cancer in 1951. Tissue samples of her cancerous cells were given to a researcher and shared with others without Henrietta’s knowledge or informed consent — a historical lesson that is now a staple of medical ethics. Known today as HeLa cells, these cells remain a vital tool in disease research due to their ability to endure and replicate in the laboratory.

Openly discussing these and the other historical wrongs of medical and research communities, as well as reminding patients of the safeguards in place that help protect them in research studies are cornerstones for how Dr. Branson practices medicine. “Sometimes patients may have preconceived notions or ideas about the clinical research history within the Black community. Having that conversation about understanding the past in order to discuss the present is very important,” said Dr. Branson.

Diversity is Essential to Finding a Cure

Chantale at a Morehouse event
Dr. Branson (left) and a student at a Morehouse event.

No two people with Parkinson’s are identical, which is why ensuring diversity and inclusivity in Parkinson’s research is critical to accelerating breakthroughs towards a cure. Diversity in research accelerates the rate that researchers can better understand PD and drives better outcomes for the entire PD community.

Populations of focus — including Black and African Americans, Latinos, women and others — are adversely affected by health disparities, underrepresented in, and historically excluded from, research. These populations also receive less care. Because of this, the full impact of the disease within these communities is still unknown. The shared value of helping populations of focus find quality Parkinson’s care is shared by the Parkinson’s Foundation and Morehouse — and presented itself through PD GENEration.

“The partnership aims to make each unit testing and counseling more accessible for Black and African American people with Parkinson’s disease and by doing so we hope to have a significant impact on improving clinical outcomes and increasing research participation,” said Dr. Branson.

Together, the Parkinson’s Foundation and Morehouse formed a two-way partnership. “Working alongside Morehouse has allowed us to tailor and elevate our reach on a local level and ultimately, help us utilize these successes to further our reach on a national scale,” said Amasi Kumeh Director, Research Partnerships at the Parkinson’s Foundation.

PD GENEration at Work

PD GENEration: Powered by the Parkinson's Foundation

All PD GENEration participants are provided a genetic test and counseling at no cost. Afterward, participants are encouraged to review their results with their PD doctor.

“Everyone has been very excited to participate in this particular study,” said Dr. Branson. “I want to encourage community members to take part in PD GENEration, so they can improve their disease management, learn more about their family’s risk of Parkinson’s disease potentially be connected to clinical trials and impact the development of improved treatments and medication for generations to come.”

In the coming year, the Parkinson’s Foundation will work alongside Morehouse to create new tools for the Black PD community, and host in-person events for the greater Atlanta area and beyond. “Working with Morehouse allows us to better learn how to reach the black and African American community and help make life better for everyone with Parkinson’s and their family members. We hope to utilize everything we learn through this partnership to make inclusivity and diversity a cornerstone to all Foundation research initiatives,” said Amasi.

Learn More

Educational Events

La enfermedad de Parkinson y la cognición

Virtual ( Zoom )
1:00 pm to 2:00 pm EST
Gratis
Woman on the couch looking at an ipad

EP Salud: Miércoles de Bienestar - La enfermedad de Parkinson (EP) y la cognición (o los procesos cognitivos): comprendiendo y mejorando la salud de su cerebro

Regístrese Aquí

El propósito de esta charla es educar a las personas con Parkinson y sus cuidadores acerca del impacto de la EP en los procesos cognitivos, discutir los rasgos más comunes y relevantes acerca de los aspectos cognitivos y la EP y cómo éstos también pueden afectar otras áreas como el bienestar emocional. Se hablará de la importancia de mantenerse conectados y los recursos de apoyo disponibles.

Presentadora

Annelly Buré-Reyes, PhD
Assistant Professor, División de neuropsicología
Departmento de neurología
University of Miami Miller School of Medicine

Este programa es gratuito y está disponible para cualquier persona interesada, incluyendo a las personas con Parkinson y sus familiares, amigos, personas de apoyo y promotores de salud.

¿En busca de algo más? Podrá encontrar todos nuestros videos de EP Salud en Casa- PD Health @ Home en YouTube.

La conferencia se transmitirá en vivo utilizando la aplicación de videollamadas Zoom.

Educational Events

Young-Onset Parkinson’s Disease: Caring for Others

Virtual ( Zoom )
4:00 pm to 6:00 pm CDT
FREE
Young family

Young-Onset Parkinson's Disease Webinar Series

How do you find harmony in juggling it all? Caring for your parent or family member or your children, plus all the things going on in your life. Join us to discuss how to talk about caring for yourself while living with PD,  as well as caring for others, setting boundaries, and how to find resources.

Join us for an educational presentation, followed by a Q&A session with our speaker. We will then have the opportunity to connect with others in the Young Onset community via Zoom breakout rooms to continue the discussion.

Speaker

Joan Hlas, MD
Struthers Parkinson’s Center, A Parkinson's Foundation Center of Excellence

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

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

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
Educational Events

Young-Onset Parkinson’s Disease: Planning and Your Rights

Virtual ( Zoom )
4:00 pm to 6:00 pm CDT
FREE
Young family

Young-Onset Parkinson's Disease Webinar Series

Join us for an overview on laws governing the rights of individuals in the workplace, including reasonable accommodations and medical leaves.  Daniel Olson will present this interactive session, which will allow you to learn about disability laws and have your questions answered.  Mr. Olson is the Co-Chair of the Employment Law Practice Group at Bassford Remele, P.A., in Minneapolis, and an Adjunct Professor of Employment Law at the University of St. Thomas School of Law.

Join us for an educational presentation, followed by a Q&A session with our speaker. We will then have the opportunity to connect with others in the Young Onset community via Zoom breakout rooms to continue the discussion.

Speaker

Daniel Olson, Co-Chair
Employment Law Practice Group, Bassford Remele
Adjunct Professor of Employment Law, University of St. Thomas School of Law

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

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
Educational Events

Young-Onset Parkinson’s Disease: Intimacy and Incontinence

Virtual ( Zoom )
4:00 pm to 6:00 pm CDT
FREE
Young family

Young-Onset Parkinson's Disease Webinar Series

Many people living with Parkinson’s disease experience non-motor symptoms that can impact urinary and sexual functioning. Although these topics can be uncomfortable to discuss, learning more about what can be done could positively impact quality of life.

Join us for an educational presentation, followed by a Q&A session with our speaker. We will then have the opportunity to connect with others in the Young Onset community via Zoom breakout rooms to continue the discussion.

Speaker

Dr. Matthew Ziegelmann, Mayo Clinic Rochester

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

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
Raise Awareness

8 Questions You’ve Always Wanted to Ask a Physical Therapist

Jenny Wilhelm and group at walk

Did you know that physical therapy can help delay the progression of Parkinson’s disease (PD) symptoms? Jenny Wilhelm, PT, DPT, NCS, is a physical therapist at Oregon Health and Science University, a Parkinson’s Foundation Center of Excellence. We asked Jenny the most frequently asked questions about Parkinson’s disease and physical therapy.

What is the difference between physical therapy and exercise?

Exercise is a tool that physical therapists use to treat people with Parkinson's disease. Exercise can take several different forms such as aerobics, strengthening, stretching and balance.

Physical therapy can help you design an exercise program that will benefit you personally. In addition to the movement symptoms addressed by exercise, physical therapy can also improve your non-movement symptoms such as pain, low blood pressure and bladder or bowel problems. We teach people with Parkinson’s life strategies so they can stay safe at home, and we also train care partners to help support their loved one with PD.

How can physical therapy benefit people with Parkinson’s disease?

I would give my hats off to occupational therapists first, for teaching people with PD how to adapt their behavior and how to move. Physical therapists are next in line in helping with activities of daily living: getting on and off the toilet, sitting down and standing up from the couch and getting in and out of bed.

Physical therapy can help people with Parkinson's throughout the stages of the disease. Early on, we educate clients about the types of exercises that might be most effective for them. Later in PD, the physical therapist can help problem solve and make modifications to address new or changing symptoms. We help people with Parkinson’s adapt to everyday life scenarios in a way that is easier, safer and more enjoyable.

Is seeing a physical therapist who specializes in movement disorders more effective than seeing a general physical therapist?

In a perfect world, all people with Parkinson’s disease would be seen at a Center of Excellence by an interdisciplinary team. Research has shown that people with PD do better if they see someone who knows a lot about Parkinson’s.

For people who live in rural areas, however, it may be difficult to find a physical therapist who specializes in Parkinson’s. If you do not have access to a PD specialist, try to see someone who at least knows neurological physical therapy. Or you could try virtually seeing a physical therapist who specializes in Parkinson’s. Even if you only check in with this person a few times per year, their guidance will help with your overall symptom management.

Why did you become a physical therapist?

The story of how I became a physical therapist is a little unique. I've always been interested in research. I started doing research at the University of Nebraska when I was 16. Then I grew into basic neuroscience research but as I was doing that, I really missed people. I ended up in physical therapy for myself for a low back injury, and it seemed like a good fit.

I got into physical therapy school, and my combined interest in physical therapy and neuroscience led me to specialize in neurological conditions.

Can you share a feel-good story about helping people with PD?

Last year, I supported a van full of people who were doing a 130-mile relay race to raise awareness for Parkinson’s. I met with half a dozen people with Parkinson's (most of whom I had never met before) and assessed them on their symptoms and ability to walk two legs of a relay, to help them finish this race successfully.

During the race itself, we encountered some obstacles due to various PD symptoms. I had to get out of the van and massage someone’s foot at 2 a.m. because her dystonia was so bad that she couldn't walk. I had to help someone with gait training because they were pushing themselves and walking fast. I had to help hydrate someone who had low blood pressure. Despite these setbacks, however, everyone was determined to complete the race.

The important thing is that we were able to successfully support this team and get them across the finish line. I think the experience was empowering for this small group of individuals. The hope is that their success can inspire other people to step up to the challenge and raise awareness for Parkinson’s.

What do you do to manage the stress of your job?

I'm a part of a huge team, which is super helpful. In clinic, I work primarily with people with Parkinson's, but I see patients who are living with all neurological diseases. With PD, I have such a functional team that it makes a huge difference in being able to treat patients effectively. When there are issues, I can lean on other people to help me through problems that I might be having.

I am also a big fan of vitamin N: nature. My family and I do a lot of outdoor activities — being outside is my biggest stress management tool.

Is it ever too late to start physical therapy?

It is never too late to start physical therapy. People with PD may want to see a physical therapist for numerous issues throughout the course of the disease. I see a lot of people who have back pain or shoulder pain. They may not be coming to me directly because of Parkinson's, but I can help address their pain issues so they can continue to exercise.

Ideally, you would begin seeing a physical therapist shortly after diagnosis. But even if you are in the late stages of PD, there are still ways that physical therapists can help you move better and improve your quality of life.

If you have not yet seen a physical therapist, talk to your movement disorders specialist or neurologist to get a referral.

What is one takeaway the PD community should know about physical therapy?

I have never seen someone living with Parkinson's with an issue that physical therapy can't address. No matter what stage of PD you are currently in, there is a role for physical therapy to make your life a little bit easier.

For help finding a physical therapist near you, contact our Helpline at 1-800-4PD-INFO (1-800-473-4636).

Educational Events

Parkinson's 101: What You and Your Family Should Know

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

Wellness Wednesdays

This program will provide a basic overview of Parkinson’s disease.  Learn what Parkinson’s is, what causes it, common symptoms, treatments, and strategies for managing symptoms.

Speaker

Pravin Khemani, MD, FAAN
Medical Director, Movement Disorders
Department of Neurology, Swedish Neuroscience Institute
Seattle, WA

There is no charge to attend, but registration is required.

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

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
Educational Events

Parkinson’s Research and Care

1:00 pm to 5:00 pm EST
FREE
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Check-In starts 12:30pm

Participants will learn how research helps shape treatments and identify new care strategies for managing Parkinson's symptoms. This program will also provide information on current research in Parkinson's.

*This program may include moderately scientific terms and concepts.*

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.

Speakers

Stephen L. Lee, MD, PhD

Dr. Lee is a Movement Disorders Specialist in the Department of Neurology at Dartmouth-Hitchcock Medical Center. He completed his PhD and MD at Washington University School of Medicine and his Neurology Residency in St. Louis.

Dr. Lee joined DHMC after completing his Movement Disorders Fellowship at Vanderbilt University Medical Center in 2004. He is a co-founder and director of the Parkinson’s and Movement Disorders Center at DHMC, and Assistant Professor at Geisel School of Medicine at Dartmouth. Dr. Lee is a member of the Parkinson’s Study Group, which is a non-profit group of physicians and other healthcare providers experienced in the care of people with Parkinson’s and dedicated to clinical research of Parkinson's disease.

Matthew C. Havrda, PhD

Dr. Havrda is an Assistant Professor of Research in Molecular and System Biology at the Geisel School of Medicine at Dartmouth College. He completed his PhD in Biochemistry and Molecular Biology at the University of Maine and has served on multiple study panels including Neurotoxin Exposure and Treatment of Parkinson’s with the Department of Defense, Parkinson’s Foundation Review Committee, the Target Validation Program with the Michael J. Fox Foundation and the Impact of Aging on Chronic Conditions with the National Institutes of Health.

He has lectured extensively on inflammasomes in Parkinson’s research, served on numerous steering committees and consultations regarding Parkinson’s Disease, and holds an inventor patent in Method and agent for treating and preventing neurodegenerative diseases. He is currently an ad hoc reviewer for several scientific journals, including the Journal of Neuroinflammation and Toxicological Sciences.

COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
Educational Events

Social & Emotional Wellness

12:30 pm to 4:00 pm EST
FREE
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Check-In begins at 12:00 pm

Emotional and social health is an important part of living well with Parkinson’s disease. Many symptoms of Parkinson’s can affect emotional and social wellness. Learn how various clinical and creative therapies can support not only symptom management but the overall well-being of the person living with PD.  

Speaker

Dr. Gregory Pontone, MD
Johns Hopkins

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

PARKING: The parking garage adjacent to Hotel is owned and managed by the Dulaney Center (not Sheraton Baltimore North). Hotel guests are permitted to access and use the garage at all times. There is a Hotel preferred rate of $6.00 per car for up to 3 hours and $15.00 per car per day (up to 24 hours).

COVID SAFETY: The health and safety of our participants, sponsors, volunteers and staff are our top priority. We continue to monitor CDC recommendations and will adhere to state and local COVID guidelines in place on the event day. Adjustments will be made if necessary.

Upcoming Events

Educational Events

Mindfulness Mondays - Mental Well-being

Each month, Dr. Rush invites you to slow down, breathe, and reconnect with yourself and your Parkinson’s community through a guided mindfulness practice. Together, we’ll explore simple ways to ground the body, calm the mind, and cultivate compassion and clarity that you can carry into your week.

Virtual
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