Fundraising Events

Community Walk Broward

8:30 am to 12:00 pm EST
FREE
Group of people going through the finish line at a Moving Day Walk

Get out and move with your community! Every dollar raised supports the Parkinson’s Foundation mission to make life better for people affected by Parkinson’s disease (PD). At Moving Day Community Walks across the country, we’re fighting Parkinson’s and celebrating movement — proven to help manage Parkinson’s symptoms — and we’re doing it together. The Moving Day Community Walk Program is a complement to the Parkinson’s Foundation Moving Day, A Walk for Parkinson’s. These walks are family-friendly and help the Foundation make life better for people with PD.

The Community Walk program offers volunteers an opportunity to organize a walk in their own community that does not have a Moving Day event. The program leverages the personal experiences and community leadership of passionate volunteers to promote Parkinson’s awareness and raise funds for the Parkinson’s Foundation.

Learn more about bringing an event to your area

Upcoming Events

Educational Events

Let's Talk About It: Diet & Swallowing Challenges

10:00 am to 1:30 pm EST
FREE
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Check-in & Resource Fair* begins at 10:00 a.m. and the program starts at 11:00 a.m. 

There are many non-motor challenges associated with Parkinson’s disease that may not always be easy to discuss. With a focus on diet, choking and swallowing, this program will provide strategies for coping and talking about it with healthcare providers or loved ones.  A discussion will take place addressing diet and swallowing issues associated with Parkinson’s disease.

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

Speakers

Mandy Katz MS, RD, CSP, LDN
Registered Dietitian
Director of Healthy Living – Giant Food

Ianessa A. Humbert, PhD, SLP
"Swallowologist"
CEO – Swallowing Wellness

Lucy Bowen
Founding Artistic Director, Bowen McCauley Dance Company
Director, Dance for PD – Mid-Atlantic

Lunch will be served. 
Free Valet parking available onsite in addition to Dupont Circle Metro Access.

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.

A Collaboration with Inspir - Embassy Row

Inspir Embassy Row

Upcoming Events

Educational Events

Managing Changing Symptoms

1:00 pm to 4:00 pm MST
Free
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After many years of good symptom management, Parkinson’s disease may become more challenging. Learn how Parkinson’s symptoms may change over time and new strategies available for managing them. 

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

Upcoming Events

Educational Events

Let's Talk About It: Mental and Emotional Health

9:00 am to 12:00 pm PDT
Free
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Some non-motor symptoms of Parkinson's disease may not be easy to discuss. With a focus on mental and emotional health, this program will provide an overview of common concerns, how to talk about them with healthcare providers or loved ones, and strategies for coping including music therapy.

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

Upcoming Events

Educational Events

Parkison's Sleep and Me

1:00 pm to 4:00 pm MST
Free
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Parkinson’s disease can create many challenges to getting a good night’s sleep. This program provides information on how Parkinson's disease affects sleep quality and addresses ways you can get a better night's sleep while living with PD.

Speakers

Cynthia S. Reed, MD, Parkinson's Wellness Clinic
Dev Ashish, PhD, Banner Health

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

Upcoming Events

Educational Events

Speech and Swallowing

10:00 am to 2:00 pm EST
FREE
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Check-in & Resource Fair* begins at 10:00 a.m. and the program starts at 11:00 a.m. 

Most people with Parkinson’s disease will experience changes in speech, voice and swallowing at some point during the course of the disease. Learn tools and exercises to help you better understand and manage speech, swallowing and communication problems in PD.

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

Speakers

Meka S. Benson, MCD, CCC-SLP
Speech Language Pathologist
ChristianaCare

Sarah Burton-Romero, MS, CCC-SLP
Speech Language Pathologist
Widener University Speech-Language Pathology Clinic

Mindy Myers, MA, CCC-SLP
Speech Language Pathologist
University of Delaware Speech-Language-Hearing Clinic

On-site parking is available. Lunch will be served.

Upcoming Events

Podcasts

Episode 181: What to Know Before Taking Nutritional Supplements for Parkinson’s

People with Parkinson’s disease (PD) may hear, whether through word of mouth or the internet, about herbs or supplements that claim to ease PD symptoms. It’s important to recognize that nutritional supplements are not federally regulated, and there is limited research supporting their overall effectiveness. You should always speak with your healthcare provider before starting a new medication or supplement.

Nutritional supplements can include herbs, vitamins, or other drugs that are often available without a prescription. Since these products are not formally regulated, there is a high risk for potentially dangerous drug interactions when mixed with other medications, regardless of if they are prescribed by a doctor or available over the counter.

In this episode, we speak with Dr. Angela Hill, a pharmacist and professor at the University of South Florida, to better understand the precautions of taking supplements while living with PD. She discusses the potential side effects and risks of taking drugs without fully knowing what’s in their ingredients, as well as the warning signs to watch for. She shares tips for reading and evaluating labels and offers guidance on the type of questions to ask a pharmacist to help decide whether the supplement may be a good fit based on your specific health condition.

During the episode, Dr. Hill mentions additional resources for evaluating herbal medications and understanding medication timing. Click here to view the articles, along with her contact information for any follow-up questions.

Released: July 15, 2025

About Angela M. Hill, Pharm. D., CRPh

Videos & Webinars

Top Hospital Safety Tips

Already a delicate balance, Parkinson's disease (PD) symptom management can be even trickier in the hospital because:

  • People often do not get enough movement opportunities.

  • Parkinson’s medications may not be given following the at-home schedule.

  • Medications that worsen PD are sometimes prescribed.

  • PD medication doses are often delayed or missed. 

In this video, learn how to advocate for your best care while in the hospital. 

Download or order your free Hospital Safety Guide today. 

Educational Events

Let’s Talk About It: Non-motor Symptoms

12:00 pm to 3:30 pm EST
FREE
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Check-in & Resource Fair* begins at 11:00 a.m. and the program starts at 12:00 p.m. 

There are many non-motor challenges associated with Parkinson’s disease that may not always be easy to discuss. With a focus on mood, sleep disturbances, and fatigue, this program will provide strategies for coping and talking about it with healthcare providers and/or loved ones.

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

Speakers

Kathrin LaFaver, MD
Neurologist
Department of Neurology
Albany Med Health System

Paul Glovinsky, PhD, FAASM
Former Clinical Director
St. Peter’s Sleep Center, Albany, NY
Private Practice, New York, NY

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

Upcoming Events

My PD Story

Cecilia smiling brightly next to a bouquet of flowers at what appears to be a formal event.
People with PD

Cecelia LaValle

Ceceilia LaValle’s family and friends knew her as the life of any party — an entrepreneur, a great artist, a wonderful cook, a devoted sister, wife and mother.

“She was an integral figure in our family and had so much enthusiasm for life,” said Neilia LaValle, one of Ceceilia’s younger sisters.

When Cecelia was diagnosed with Parkinson’s disease (PD) in the early 1990s after noticing rigidity in her left arm, she leaned into her passions and was determined to live life to the fullest as she bravely fought PD.

She had already been diagnosed with PD by the time she met her fourth husband, and ultimate care partner, Jimmie Amox, while they were enrolled as graduate students at Louisiana Tech University. Though she made several careers for herself, art always drew her back in.

“Her art really blossomed during her graduate studies,” said Deanna LaValle High, one of Ceceilia’s younger sisters. “I would say that Cecelia was at the peak of her artistic capability and showing every sign of continuing to grow as an artist, when she was diagnosed with Parkinson's. She continued to make art until the disease finally robbed her of that ability.”

Cecelia’s family rallied around her, researching PD and supporting her as she explored treatment options. Jimmie said she was determined to continue living her life and was invested in finding PD care that allowed her to do so. She consulted with several doctors around the world and tried many treatments to alleviate her symptoms, including the hallucinations.

“I lost my mom long before she passed away, due to the hallucinations,” said Michele Smith, Cecelia’s daughter. “It was difficult for our family to watch her deteriorate.”

Before Cecelia passed away in 2016, Neilia spoke to a friend who had recently started her own non-profit to raise money for breast cancer, which inspired Neilia to do the same and support a cause near to her heart — Parkinson’s disease.

“Seeing what my sister was going through made me want to help find a cure for Parkinson’s,” Neilia said. “I don’t want other people to go through what my family and my sister went through.”

Neilia uses her foundation to support organizations like the Parkinson’s Foundation that are working to find a cure for PD. She’s proud to honor her sister and to continue her fight for a cure.

“It seems like more and more people are directly impacted by Parkinson’s. We need to get more people actively involved in supporting organizations that are looking for a cure, like the Parkinson’s Foundation. There is hope, and that is what we need to use to keep us going.”
- Neilia LaValle

Like Neilia, other members of Cecelia’s family are inspired by the Parkinson’s Foundation and happy to see more resources for people with Parkinson’s, care partners and their families.

“Many of the current treatments and resources available now were not available when Cecelia was diagnosed,” said Jimmie. “Organizations like the Parkinson’s Foundation have changed that. If I could offer advice to those newly diagnosed with Parkinson's disease or people entering the Parkinson's care partner world, I would say that the first thing you need in your toolbox is love for each other. Grow that love every day. Get to truly know each other and constantly question reactions to new experiences with this disease.”

“If you are new to Parkinson’s, take stock of yourself and your priorities,” said Deanna. “And, if you are inclined to live life fully like Cecelia, do it, do it, do it. As best you can.”

With your support, we can invest in research that will help us find new treatments and a cure for Parkinson’s in years, not decades. To make a donation, visit Parkinson.org/Donate.

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