My PD Story

Michael Citrin headshot
People with PD

Michael S. Citrin

We honor the loss of Michael, who has passed away since the publishing of his story. We value his commitment to the Parkinson's community and dedication to PD advocacy.

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.

Raise Awareness

From Yoga to Boxing: 10 Fitness Videos to Energize Your At-Home Routine

Research has shown that 2.5 hours of weekly exercise, along with medication, can significantly improve the quality of life for people living with Parkinson's. Our Fitness Friday at-home video series is all about helping people with Parkinson’s disease (PD) and their loved ones try new exercises that can help with strength, balance and symptom management.

From Yoga and Tai Chi to full body classes, Fitness Friday videos let you choose the workout that works for you. Explore our most popular Fitness Friday workouts below:

1.  LSVT BIG Movements

In our all-time most popular Fitness Friday video, follow along with LSVT BIG exercises that focus on making “BIG” movements with your arms, legs and torso in all directions. Learn how to work through the small, slow movements that are common with Parkinson’s.

2.  Posture and Strength

Parkinson’s can impact posture, leading to stooped or rounded shoulders or the forward lean of the head or whole body, making you look hunched over. Learn exercises and tips for maintaining posture. Roll through this great workout designed for everyone — take the class standing, seated or both.

3.  Non-Contact Boxing

This high-intensity boxing class will help you move with strength. Stretch and warm up and learn boxing training techniques. This class concentrates on improvement and maintenance of proper boxing form and technique with a focus on complex combinations, footwork drills and fall recovery.

4.  Tai Chi for PD

In this great introduction to Tai Chi, an internal Chinese martial art, follow along with the slow, rhythmic motions that stretch the muscles and joints. Work on stimulating balance, coordination and mental focus that promotes overall health and well-being.

5.   Move to Improve

This video aims to help you feel stronger and more confident with everyday movement. This class incorporates strength, mobility and balance training. Exercises are first done in a seated position then transition to standing.

6.  Dance for Parkinson's

Dance/movement therapy is a form of psychotherapy that uses movement in all forms. Join a medium intensity, creative dance class that encourages large movements, multi-tasking, dynamic balance, weight shifting and aerobic rhythmic coordination. Grab a sturdy chair for this session.

7.  Full Body Workout with InMotion

Join two instructors through an immersive full-body class as they guide you through cardio, strength, balance, agility, brain exercises and flexibility. This immersive and fun workout brings all fitness components together.

8.  Gentle Yoga for Parkinson’s

This soothing and supportive gentle yoga class is designed with PD in mind. Through a series of accessible yoga poses and guided meditation, this video focuses on gentle movements, mindful breathing techniques and relaxation exercises to promote flexibility, improve balance and reduce muscle stiffness commonly associated with PD.

9.  Strong & Steady

This video focuses on exercises aimed to improve gait mechanics and reduce fall risk. Try standing exercises aimed to help improve posture along with the muscles associated with sound walking mechanics, and gait drills that can help you stand strong and move steadily.

10.  Moving for Better Balance

This fun and effective video offers movements to help you become stronger, steadier and safer. These exercises target the specific components of balance that are often impacted by Parkinson’s.

 

Watch all our Fitness Friday videos on our YouTube channel

Podcasts

Episode 171: Allied Health Spotlight: Physical Therapy Recommendations for Exercising Safely

Allied health professionals are a group of healthcare providers whose role and expertise complement the work of physicians. These include specialists such as physical and occupational therapists, speech-language pathologists, nutritionists, and many more. They are just as important as your Movement Disorders Specialists and Neurologists, and play a vital role in creating a comprehensive, well-rounded Parkinson’s care team that caters to your individual needs and addresses your overall well-being. 

In this first episode of our Allied Health Spotlight series, we explore the benefits of including physical therapy in your care plan. Exercise is a vital component for people with Parkinson’s disease (PD) to maintain balance, mobility, and activities of daily living. It should be part of the standard practice of care for every person with PD. Research has shown that exercise is the only intervention with the potential to slow the progression of the disease. In this episode, Physical Therapist Patricia Brown, PT, DPT, NCS of Chapman University in California, who specializes in neurologic diseases, discusses some considerations for exercising safely, taking into account the particular needs of people with PD. She also talks about how to get and stay motivated to exercise and where to find classes or programs.

Released: August 13, 2024

Raise Awareness

5 Volunteers Making a Difference

Across the country and beyond, Parkinson’s Foundation volunteers are going out and making a difference in the lives of people with Parkinson’s disease (PD) and their loved ones. They help us spread awareness and resources to those who need it most.

Ambassadors By the Numbers infographic

The dedication from our volunteers is what makes the Parkinson’s Foundation what it is today. We are honored to recognize five exceptional volunteers at the national level, who each received a 2024 volunteer award.

Dr. Reversa Joseph headshot

Dr. Reversa Joseph - Great Lakes Chapter

Paul Oreffice Volunteer of the Year

“Volunteering for the Parkinson's Foundation is more than just a commitment; it’s a deeply personal mission. Each effort, whether it’s a presentation, a lecture, or a podcast, is a step towards improving the lives of those affected by Parkinson’s, honoring my father’s struggle, and ensuring that every patient receives the comprehensive, integrative care they deserve.”

Read Reversa’s full story


Esther Labib-Kiyarash headshot

Esther Labib-Kiyarash – Southwest Chapter

Rising Star

“Along the way I have learned that there are many things, tips and tricks that the people who live the best with this disease share: exercise, positive thinking, being around others like themselves and giving back. The Parkinson’s Foundation is a great way to give back.”

Read Esther’s full story


Roland and Shelley Frankel and children

Roland and Shelley Frankel – Midwest Chapter

Top Fundraiser

As the somber saying goes, a parent should never have to bury their child. But in March 2023 Roland and Shelley Frankel had to do just that. Their son Graeme had been fighting Parkinson’s for five years and passed from an asthma-related emergency. To keep Graeme’s memory alive, the family decided to start a DIY fundraiser with the Parkinson’s Foundation.

Read Roland and Shelley’s full story


Debra Flynn headshot

Debra Flynn – Florida Chapter

Community Service Award

“I really enjoy volunteering. I see it as another way to celebrate movement. I move my brain cells around; I motivate my soul to do good things; and volunteering moves forward the search for a cure.”

Read Debra’s full story

There are many powerful ways to get involved and support the Parkinson’s Foundation and our work to make life better for people with Parkinson's. Get started with our How You Can Help page. This page will give you options for volunteering, starting your own DIY Fundraiser, or even just donating to the cause.

You can also fill out a volunteer interest form to chat with our volunteer engagement team about how we can best put your skills to use. Help us bring life-saving information and resources to the hands of those who need them most.

Already a volunteer? Check out our course offerings today!

My PD Story

Debra Flynn headshot
People with PD

Debra Flynn

Once upon a time, I started noticing a slight tremor in my right hand. My husband noticed that I did not move my right arm when jogging. I also suffered from frozen shoulder(s), insomnia, constipation, anxiety and fatigue for years.

Doctors continuously told me it was menopause related. Over time, the tremor became more noticeable, and my doctor suggested I see a neurologist, just to “be safe.”

I met with a movement disorders specialist — a neurologist with specialized training in movement disorders — and on November 11, 2015, she confirmed the diagnosis of Parkinson’s disease (PD). I will never forget that day. I was devastated and frightened.

At the suggestion of the movement disorder specialist, I signed up for the local young-onset Parkinson’s disease (YOPD) support group. I went to the first meeting and cried seeing how PD affects people. I cried every time I had to tell someone about the diagnosis. I cried thinking about how life had changed. I cried all the time. Through all this turmoil, my neurologist promised me that life was not over, but I had to take control, no matter how hard it got.

So, we took control. We retired early and moved to Florida. It is here that I signed up for Rock Steady Boxing. I am a fighter and have met the most amazing people at Rock Steady Boxing. I also attend spin classes and Pilates as part of my personal goal to keep on moving! It still felt like there was more I could do to change the trajectory of my life. Yep, there sure was. Enter Parkinson’s Foundation.

I connected with the Parkinson’s Foundation through Moving Day Chicago (my hometown). When we moved to Florida, I attended Moving Day Boca Raton and Palm Beach. I signed up for PD GENEration and three other clinical studies. I attended Foundation-sponsored seminars, which is where I met Karen Lopez and became involved in the local chapter.

Today I am a Parkinson’s Foundation Ambassador, a Board Member on the Fund Development team, and I was honored to be the Chair of a successful Moving Day Palm Beach 2024. I have also been part of our Regional Grant Review team for the past two years and I sign up for every relevant clinical trial.

I really enjoy volunteering. I see it as another way to celebrate movement. I move my brain cells around; I motivate my soul to do good things; and volunteering moves forward the search for a cure. Volunteering is really the most effective way to use one’s voice. Being awarded the Parkinson’s Foundation Community Service Award is the ultimate recognition of how important it is to advocate for ourselves and others affected by PD.

PD has changed my life. I am married to a host of medications governed by a time clock, and I deal with nasty and unpredictable symptoms, and it is truly humbling! However, living with Parkinson’s is also a true blessing in that it has given me the gift of friendship, support and has shown me the way to help advocate for others.

Explore the many ways to volunteer with the Parkinson’s Foundation. Fill out our volunteer interest form today.

My PD Story

Photo of Rod Marino speaking into a microphone
People with PD

Rod Marino

Many people with Parkinson’s disease (PD) try speech therapy to combat the changes in voice and speech that are often the earliest signs of Parkinson’s. But Rod Marino went a step further and purchased a karaoke machine so he could start singing on his own, in his basement.

Rod has lived with Parkinson’s for 24 years and has learned to battle the disease with a positive attitude, great sense of humor and a song. He keeps his body strong by staying active and riding a stationary bike every day. He keeps his mind sharp by being active in the community as a board member for the local senior center. He keeps his soul sharp through music. 

Rod found out about the Parkinson's Foundation from one of his doctors when he was first diagnosed, who recommended visiting Parkinson.org for helpful information. Early on, Rod read that voice dysfunction and speech issues are the earliest sign of motor impairment in Parkinson’s — specifically that the voice softens as the disease progresses. 

To combat the issue, he decided to take voice lessons and now sings every day! After setting up his karaoke machine and using it consistently, his voice therapy turned into passion, and he started singing in public. 

Rod finds happiness in making other people happy. He does just that spending time at the local senior center, visiting with members and hosting events, like weekly bingo. He also oversees a singing group that his wife, Diane, conducts. 

In time, he formed a band called the Don-Rod Duo with a friend.  The band performs at the Sheila Ray Center in Elk Grove Village (IL), farmers markets and other locations in the community.  

Diane introduces the duo by telling the story of how music and song have helped Rod maintain his voice. The duo takes the stage and sings a wide range of cover songs that range from Dean Martin and Neil Diamond to Frank Sinatra, adding jokes to entertain the audience. 

Today he shares his music and tells his story to the audience members. Stories about his Parkinson’s sometimes come into the light, helping spread awareness about the disease.   

Rod's biggest piece of advice is to be open about having Parkinson's and allow family members and friends to help whenever possible. People should not be alone on the journey, as he has found that loved ones are eager to help in any way that they can.

Rod's motto is "Don't give up and stay involved." He is a true inspiration to so many members of the community. He wishes to share his story, so that others may learn how music has helped him on his Parkinson’s journey.

Explore local Parkinson’s classes, wellness programs, in-person events and more when you connect with your Parkinson’s Foundation Chapter. Find your chapter now.

Videos & Webinars

Controlando los síntomas de la enfermedad de Parkinson

Hay mucho que saber acerca de la enfermedad de Parkinson. Aprenda cómo se trata y, lo más importante, cómo llevar una vida mejor con Parkinson. 

El Parkinson es una enfermedad individualizada. Si bien la experiencia de cada persona con el Parkinson es única, cuanto más sepa, más empoderado estará para desempeñar un papel activo en su autocuidado y manejar su vida con Parkinson.

My PD Story

Troy Cook headshot
People with PD

Troy Cook

At 48 years old, I heard the words "Troy, you have Young-Onset Parkinson's Disease." It took me some time, but as a public speaker who invites audiences to define success and fulfillment on their own terms, I knew I had to figure out a way to start wrapping my personal stories of Parkinson’s into each presentation. And I did.

On July 12, 2017, I had the opportunity to look into my own life to find strength and inspiration. After more than 18 months of chronic and debilitating pain, fatigue, tremors and other symptoms, I finally had an answer: Parkinson’s. This life-altering diagnosis put my lifelong beliefs to the ultimate test.

Over the next few years, I began finding ways to get involved and build my Parkinson’s community. I became active in organizations that support those dealing with chronic and life altering health conditions, which has helped me gain perspective on my own situation. My recent activity as a Parkinson’s Foundation Heartland Chapter board member is an extension of that work.

Continuing to be a public speaker has inspired me as I am able to incorporate the learnings from my own journey and the stories of other's journeys to provide inspiration to audiences.

I’ve had time to think of advice I’d give to others who are new to Parkinson’s, including:

  • First, there is not one path in navigating this journey. Each of us must make decisions that are best for ourselves and those who are present to support us.

  • Learn as much as possible about your symptoms and characteristics that have led to your diagnosis. Because PD manifests itself in unique paths to each person, gathering as much information and perspectives is key to making wise decisions on treatment.

  • Find a care team that best aligns with your needs. Don't be scared to change that team as time evolves. Your disease will evolve, and sometimes that means changing the team members is needed.

  • Turn to the Parkinson’s Foundation. The vast amount of information, data and research findings pushed out through emails, Parkinson.org and events has been significant in keeping me informed and hopeful.

Troy Cook public speaking

My expertise in public speaking has been acquired through years of studying, asking questions of, presenting to and consulting with audiences and groups from Fortune 500 firms to leadership conferences. These principles and traits include hitting control+alt+delete to redefine societal defaults for success; establishing and measuring goals with specific strategies; finding wisdom to overcome adversity and inevitable change.

Now, especially after releasing my first book, Change Is Inevitable, Growth is Optional, I continue to be inspired by the tremendous stories of others who have faced adverse change and find a pathway to growth. This inspiration has led me to me to participate in such experiences as running in masters track meets, fundraising for worthy causes, and speaking before audiences to share my experiences.

Everything so far has led me to my newest way to advocate for people with Parkinson’s: becoming a Parkinson’s Champion and hosting my first fundraiser. On June 8, I will be competing as a Parkinson’s Champion in the 6 in 6 Challenge. I will compete in six track and field running events on the same day in approximately six hours.

I chose the number six because every six minutes someone is diagnosed with Parkinson’s disease. In the roughly six hours it takes me to complete the 6 in 6 Challenge, 60 people will learn of their new Parkinson's diagnosis.

Long before public speaking, running was always my passion. I have been active as a runner since my teenage years. I ran track, coached high school and middle school track, and ran a triathlon (which may be the next challenge.)

In my Parkinson’s experience, I challenge my body each day to get stronger and maintain strength so that I can delay the disease. But for many people with Parkinson's, simple physical activities are an extreme challenge. For those who can't challenge themselves to the level I still can, I am honored to take on a new physical challenge in their honor.

Support Troy’s Parkinson’s Champion event, 6 in 6 Challenge, or learn more about becoming a Parkinson’s Champion.

My PD Story

Michael Sierchio and his wife
People with PD

Michael Sierchio

Finding My Balance: A Personal Journey with Parkinson’s

When I look back, my journey with Parkinson’s disease (PD) didn’t begin in a doctor’s office — it began at home, with my wife.

In December of 2022, she was the first to notice the changes: a slight tremor in my hand, stiffness in my movement and a slowing that I tried to explain away as stress or age. She told me I needed to see a doctor, and, as usual, she was right. It wasn’t until January 5, 2023, that I heard the words that would change everything: “You have Parkinson’s disease.”

In that moment, I felt both relief and fear — relief because I finally had an answer, and fear because I knew nothing would ever quite be the same. Parkinson’s isn’t a condition with a simple fix. It’s something you learn to live with, day by day, through patience, adaptation and perseverance.

Michael Sierchio headshot

My first major hurdle was finding the right neurologist. The first two didn’t feel like the right fit. I needed someone who understood not only the science of Parkinson’s, but also its impact on my daily life — someone who saw me as more than a set of symptoms. I finally found that person on my third try, at the Cleveland Clinic in Las Vegas, a Parkinson’s Foundation Center of Excellence. The Cleveland Clinic quickly became my lifeline — a place where I felt truly understood and supported.

That neurologist offered me something unexpected: the opportunity to participate in a clinical trial for a new medication called Tavapadon. Joining the trial was a turning point. It gave me purpose and a sense that I could contribute to progress — not only for myself, but for the broader Parkinson’s community.

Over time, I began to notice improvements: steadier movement, clearer focus and, most importantly, a renewed belief that science and hope can walk hand in hand. Although the trial I joined has not been FDA approved yet, the experience strengthened my faith in research and the value of participation.

But medication alone wasn’t enough. I needed connection. Through my involvement with the Parkinson’s Foundation, I became a research advocate and ambassador and later joined the Parkinson’s Foundation Southwest Chapter Board. That experience opened my eyes to the strength of this community — individuals facing the same challenges, each one finding their own way to adapt and thrive.

Advocacy became a form of therapy for me. It turned my diagnosis into action. I started speaking up, sharing my story, and helping others understand that Parkinson’s doesn’t erase who we are — it simply reshapes how we show up in the world.

My wife has been my greatest support, encouraging me to stay active and consistent. I walk about two miles every day and track my sleep with an Oura Ring to manage my energy and symptoms.

Living with Parkinson’s has taught me that hope isn’t something that just happens; it’s something we build. It’s built by showing up to appointments, by volunteering for research, by offering encouragement to someone newly diagnosed, and by choosing, every day, to keep moving forward. There are frustrating days — with symptoms, medication changes, and uncertainty — but I remind myself to keep learning, stay curious and use technology as an ally.

My wife’s intuition started this journey, but the people I’ve met along the way have given it meaning. I still have hard days — moments of frustration, fatigue, and uncertainty — but they’re balanced by purpose and perspective. Parkinson’s may be part of my story, but it isn’t the whole story. It’s a chapter I continue to write with courage, gratitude and hope.

Explore ways to get involved with the Parkinson’s Foundation today and find your local chapter.

Videos & Webinars

Los ejercicios recomendados para el Parkinson

No importa en qué punto se encuentre en su recorrido por la enfermedad de Parkinson, el movimiento habitual es una buena medicina. Los estudios demuestran que la incorporación de una rutina de ejercicio es esencial para el manejo de los síntomas de la enfermedad de Parkinson.

Back to Top