Fact Sheets

Veterans and Parkinson’s

More than 110,000 veterans with Parkinson’s disease (PD) receive care through the U.S. Department of Veterans Affairs (VA). The Parkinson’s Foundation is here to help veterans and their loved ones live well with PD. To find resources tailored to the veteran community, visit Parkinson.org/Veterans or call the Parkinson’s Foundation Helpline at 1-800-4PD-INFO (1-800-473-4636).

What is Parkinson’s disease?

Parkinson’s disease is a progressive, neurological disorder that occurs when the cells in the brain that make dopamine start to die. The rate of progression and symptoms are different for everyone. Movement symptoms can include tremors, slowness of movement, stiffness and problems with balance. Non-movement symptoms can include fatigue, depression, anxiety and problems with sleep.

There are nearly one million people in the U.S. living with PD and an additional 90,000 people are newly diagnosed each year. There is no cure for Parkinson’s, but treatment can improve quality of life. Treatment options include medication, exercise, rehabilitation therapies (physical, occupational and speech therapies), surgical options and a healthy diet.

Medical Care and Treatment

Many U.S. veterans with Parkinson’s can access specialized medical care and financial assistance through the VA. The VA provides Parkinson’s treatment at Parkinson’s Disease Research, Education & Clinical Centers (PADRECCs) and their Associated Sites. To learn more, visit www.parkinsons.va.gov or call 1-800-949-1001 x205769. To apply for VA healthcare, visit www.va.gov/health-care/how-to-apply or call 1-877-222-8387.

Agent Orange and Toxic Exposures

In some cases, developing Parkinson's can be associated with exposure to Agent Orange or other herbicides during military service. Agent Orange was a powerful herbicide used in Vietnam from 1962 to 1975, but was also used and stored in other locations. Veterans may be eligible for a free environmental health registry evaluation, disability compensation and other VA benefits. To learn more, visit Parkinson.org/Veterans or call the Veteran Benefits Administration at 1-800-827-1000.

Veterans Benefits

Veterans living with Parkinson’s may qualify for financial benefit programs to help cope with financial challenges. Service members, veterans and families can apply for various VA benefits by:

  • Applying online at www.eBenefits.va.gov.

  • Working with an accredited representative or VSO. Federal law prohibits attorneys and others from charging a fee to assist with the VA application.

  • Calling the VA’s toll-free hotline at 1-800-827-1000, Monday-Friday 9 a.m. to 9 p.m. ET.

Caring for a Veteran with Parkinson’s

The care partner experience is unique to every individual. The Parkinson’s Foundation and VA have resources specially designed for those caring for a veteran with Parkinson’s. Regardless of whether you are early in the journey, caring from afar or supporting a loved one in the advanced stages of Parkinson’s, we have the resources to help. Learn more at Parkinson.org/Veterans.

Hospital Safety

Every person living with Parkinson’s should be prepared for a possible hospitalization including veterans and their care partners. Visit Parkinson.org/HospitalSafety to learn more and order or download your free Hospital Safety Guide.

Mental Health

Mental health concerns like depression and anxiety are common in people with PD. They can be the result of living with a chronic condition, but they can also be a symptom of the disease itself and changes in the brain. Be aware of these symptoms and do not hesitate to talk to your doctor. Keep the Veterans Crisis Line number nearby, just in case: dial 988, then press 1 or text 838255.

Fundraising Events

2026 Big Sur International Marathon Weekend

6:45 am to 1:00 pm PDT
Participant running in Big Sur race

The Parkinson's Foundation is an official charity partner for the 2026 Big Sur International Marathon Weekend. By signing up to run as a Parkinson's Champion you commit to raising funds and awareness for the Parkinson's Foundation, and in return you get access to a free entry (bib) to the race in addition to tons of other fun benefits and perks. Click here to register to run. 

Fundraising Commitments:

  • Marathon - $2,000
  • 11-miler - $1,500

**If you already purchased a bib and want to join us as an Honorary Athlete please email us at Run4PD@Parkinson.org

 

The Big Sur International Marathon is a destination race like no other. Whether you are running 26.2 or the 11 miler up the California coast you will see what makes this tiny community so unique. Towering redwoods, crashing waves, coastal mountains and verdant pastures are featured on this bucket list course. 

Are you looking for a fun way to volunteer for the Parkinson's Foundation & raise your voice while raising awareness? Come out and cheer on our incredible athletes! Learn more and apply at Parkinson.org/ChampionsCheer.

If you have questions, send us an email at Run4PD@Parkinson.org. For more information about the race itself, visit the Big Sur Marathon Homepage.
 

Upcoming Events

Fundraising Events

Community Walk Rockford

10:00 am to 1:00 pm CDT
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

Fundraising Events

Community Walk Piedmont Fayette

8:30 am to 11:00 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

10:00 am to 3:00 pm EST
FREE
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Let's Talk About It: Medications, Research, Memory & Anxiety

Hosted by the Parkinson’s Foundation Mid-Atlantic Chapter & Acts Country House

There are many non-motor challenges associated with Parkinson’s disease that may not always be easy to discuss. With a focus on Medications, Research, Memory & Anxiety, this program will provide strategies for coping and talking about it with healthcare providers or loved ones. Learn comprehensive insights with a focused discussion, presentations, and Q&A panel with our speakers.

Speakers:
Whitley Aamodt, MD, MPH, MSCE 
Assistant Professor of Neurology  
Parkinson’s Disease and Movement Disorders Center 
University of Pennsylvania

Muhaimin Id'Deen, PharmD
Jesus Arriaga, OHI

Clinical Pharmacists, Neurology Specialty Pharmacy - Christiana Care Health System

Roseanne D. Dobkin, PhD
Associate Professor of Psychiatry
Rutgers

Lanny Edelsohn, MD
Retired Neurologist - Christiana Care Health System

Deborah Heald
ACTS Country House Rock Steady Boxing Trainer

Check-in and resource fair starts at 10 a.m.; Program starts 11:00 a.m.
Attendance is free. Parking is available onsite

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.
 

A Collaboration with Acts Country House in Wilmington, DE

Country House - Acts Retirement | Wilmington DE

Gold Sponsor:

Event Sponsors:

Amneal logo
Abbott
Supernus

Upcoming Events

Videos & Webinars

Expert Briefing: Addressing the Challenge of Apathy in Parkinson's

September 11, 2024

Apathy can significantly impact the quality of life for people with Parkinson’s disease (PD). This invisible symptom can make it difficult to maintain interest in daily activities and to effectively manage PD symptoms. Apathy can be frustrating for people with Parkinson’s, care partners and loved ones, but understanding it as a symptom and finding ways to cope with it are key to ensuring a good quality of life.

Download Slides

Presenter

Aaron C. Malina, PhD, ABPP
Clinical Neuropsychology 
Northwestern Medicine-Lake Forest Hospital
A Parkinson's Foundation Center of Excellence

Raise Awareness

How To Start A Support Group

Support Group Image

It is vital for people living with Parkinson's disease (PD) and care partners to make social connections and find support. Whether you have been newly diagnosed with PD, have been living with PD for a while, or are caring for someone with PD, connecting with others can help. 

Challenges associated with PD, including movement symptomscognitive changes and emotional fluctuations, can lead to social withdrawal and isolation. Engaging in social activities can provide a valuable support network, combat feelings of depression and loneliness, maintain cognitive function and emotional well-being.  

Why are support groups important? 

Finding the right support group can help you build your PD community. In these groups, people share their experiences, learn from each other, and get access to resources that suit their needs.  

Through these connections, individuals affected by PD not only find companionship and empathy but also gain a sense of belonging and resilience that can improve their PD journey. With the support provided by groups, people affected by PD can navigate the condition with greater confidence, hope and well-being. 

Types of Support Groups 

There are many kinds of PD support groups available. They include: 

  • People with PD: These groups focus on people living with PD, allowing them to share their experiences, learn from each other and offer support. 

  • Care partners: Care partners know Parkinson’s and its ups and downs. These groups provide a space for care partners to share their challenges, receive support and learn coping strategies. 

  • Combined Groups: Many support groups welcome people with PD and care partners, fostering a supportive environment where both groups can share experiences, offer mutual support and learn from each other's perspectives. 

  • Young-Onset PD (YOPD): These groups cater to those diagnosed with PD at a younger age, addressing unique challenges and concerns relevant to them. 

  • Virtual: Online communities that allow members to share experiences from the comfort of their own home. 

  • In-person: Face-to-face gatherings where people can meet to discuss their experiences. 

Tips for Starting A Support Group 

If you have not found a support group that is the right fit for you, consider starting your own. Explore our Support Group Guide for a step-by-step planning process. The most important part of any support group is to ensure members feel accepted, respected and comfortable when attending the group.  

Building and launching a support group requires planning, organization and attention to detail. The “let’s get started” phase can be overwhelming, but breaking down a big task into smaller tasks can make planning more manageable. Consider these key aspects before launching a support group: 

  1. Who will attend this group? 

This step is crucial for building the foundation of your support group. Make sure you know your audience before you figure out any specific details about the group. You can choose from the types of support groups above to get started.  

  1. Where will the group take place? 

If you decide to start an in-person support group, start looking for a potential meeting space. The location can make or break your group. Rule out locations that are not easily accessible.  

These locations are generally open to hosting support groups: 

  • Public libraries 

  • Hospitals 

  • Community living centers 

  • Places of worship (remember accessibility requirements for older buildings) 

  • Town halls 

  • Senior centers 

  • Senior living facilities or nursing homes 

Each community is unique, so consider what other possibilities could exist in yours. Talk to people and let them know what you are looking for. Let others spread the word to help you secure a solid, consistent location. 

  1. How often will your group meet? 

Many PD support groups meet monthly. Find the frequency that works for your group. Consider that the more often you meet, the faster members can become fatigued, and more planning will be required. Meeting less than once a month can limit the group’s ability to build relationships.  

Having a consistent day of the month (for instance, the second Tuesday of each month) helps people to remember when the group meets. 

An even bigger consideration is time of day — will you meet in the morning, afternoon, or evening? Make the decision that works best for you as a leader and ask potential participants for feedback. Establishing a regular time and place will help your group expand as more people become aware of its existence. 

  1. What is the support group’s format? 

There are many formats you may choose to use for your group. The best advice is to stay flexible. You may start out with a formal meeting agenda and decide that you want to change things up and go less formal. Listen to what your group members tell you!  

To help “break the ice” at the start of each meeting, particularly for new members in attendance, introductions are a great technique. Not only does everyone get a chance to say something, but it also helps members remember names and relationships. 

  1. How long are meetings? 

Support groups usually meet for no more than 90 minutes. It also may be helpful to design a break halfway through for refreshments and a rest room break. Find what works best for the group. 

Parkinson’s Education and Finding Guest Speakers 

Besides planning the basics, it is also important to consider things like topics for each meeting and if you plan to have a guest speaker. One common need for the Parkinson’s community is disease education.  

Guest speakers can include:  

  • Local PD experts you or group members know. 

  • Parkinson’s Foundation volunteer. Email us at Volunteer@Parkinson.org and we can help connect you to someone in your area. 

If you are not sure where to start, ask your group members for suggestions and topic recommendations. 

Promoting Your Group 

Promotion is essential for a successful support group. Word of mouth can help but it is typically not enough. Consider creating a flyer or letter announcing the group, starting date, location and contact person. If you have a speaker scheduled, be sure to include that information and the topic they will be discussing. 

Social media can also be helpful in raising awareness of your new group. It can be especially helpful for reaching younger people with PD and their care partners. Managing a social media page could be a great volunteer role for a group member to take on. 

How To Find A Support Group 

Here are two ways to find a local PD support group: 

  1. Visit our Parkinson’s Foundation Chapter page to search for one in your area. 

  1. Call our Helpline at 1-800-4PD-INFO (1-800-473-4636) or email Helpline@Parkinson.org

For more information on starting a support group, check out our Support Group Guide

My PD Story

Michael Citrin headshot
People with PD

Michael S. Citrin

After living with Parkinson’s disease (PD) for more than 30 years, I know how it impacts a person’s life and their loved ones.  

I first noticed tremors in my arm while participating in a fox hunt. It took more than eight years and several specialist visits to finally confirm my symptoms were a result of Parkinson’s disease.  

While my journey has not always been smooth, I’ve found happiness in keeping PD at bay by taking control of my treatment and working to overcome the physical and emotional effects of Parkinson’s. I’ve learned that viewing life through Parkinson’s can help you cherish each positive moment and work toward fulfilling your dreams. 

After all I’ve been through with this disease, I want to offer some advice that has worked for me to manage Parkinson’s. I recently wrote “Thirty Years with Parkinson’s Disease The Unscientific Truth” as a free study or self-help guide, using my life experience as an example. If you are interested in reading it, please contact Kelly Austin at kaustin@parkinson.org. Here are some of the thoughts I share in it: 

  • Create an action plan that includes several small steps you can take on gradually. 

  • Be your own advocate. Ask questions and don’t be afraid to question your treatment plan. 

  • Find a quarterback in a doctor, someone who can help you navigate PD. 

  • Determine what matters most to you and those you care about. Use this as a guide for your care plan so that you can achieve your goals and pursue your interests. 

  • Add lots of exercise and mental stimulation into your life to keep your brain and body working. Don’t crawl into a fox hole and never get out. 

I would not have been able to fight this disease for so long if it were not for the support of my late wife, Adrienne, my family and my doctor. For more than 20 years, I drove 100 miles to see Dr. Lucien Côté, at Columbia University Irving Medical Center, a Parkinson’s Foundation Center of Excellence. He was an incredible man and doctor. He spent so much time with each of his patients, asking them questions and taking meticulous notes and forming treatment plans that were tailored to each patient. I am forever grateful to him, and I miss his kindness, comfort and wisdom. 

Explore Parkinson’s Foundation resources for the PD topics and symptoms that matter most to you right now.
I want to learn more >>

I am also grateful for organizations like the Parkinson’s Foundation. Parkinson’s is not episodic, but I’ve found the medical world is set up to treat things in snapshots. That is not how Parkinson’s works, so people are often stuck looking for resources and support themselves. The Parkinson’s Foundation is wonderful because it provides education and helps people navigate the disease to live well. As proof of my gratitude for their educational work, I have made a substantial planned gift to the Parkinson’s Foundation. 

Michael Citrin biking

I firmly believe every person should have a life, even if they are fighting a disease like PD. I’m very protective of “me” and I don’t let the disease control me. I prioritize exercise and singing in my church choir. I’ve traveled and spent many years riding my motorcycle around the country with my wife. Today I ride a tadpole-configured, fat boy recumbent trike. I have never run from PD. I embrace it and the surprises it brings to my life. I hope these tips help others do the same. 

Make a lasting impact with a planned gift to the Parkinson’s Foundation. Learn more at Parkinson.org/PlannedGiving.

Educational Events

Navigating Long-Term Care with Parkinson’s

Virtual ( Zoom )
1:00 pm to 2:00 pm EST
FREE
Navigating Long-Term Care Banner

This webinar highlights the importance of planning for long-term care and the role of elder law in protecting your assets and securing quality care. Participants will learn about different care options, their costs, and payment sources like Medicare and Medicaid. The session will also cover eligibility for these programs, helping attendees make informed decisions about their long-term care and financial security.

Speaker

Lauren L. Fink
Shareholder and Attorney at 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

Expert Briefing: The Latest Advances in Parkinson’s Research and Treatment

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

Wellness Wednesday: Expert Briefing Series

Join us for an in-depth look at the latest advancements in Parkinson’s disease research and the emerging treatments. This webinar will cover the current medication pipeline, highlighting new therapies and their potential impact on symptom management. Participants will also learn how to identify and participate in relevant clinical studies, staying informed on the cutting-edge research that is shaping the future of Parkinson’s care.

Speaker

Kevin McFarthing, PhD
Parkinson's Research Advocate, Oxford, UK

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.

Thanks to our sponsor, BioVie Pharmaceuticals.  For more information on their clinical trial, for which you may be eligible click here.

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

Light of Day

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

Upcoming Events

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