• Home
  • About
  • Blog
  • Insights
  • FAQ
Menu

Out-Thinking Parkinson's

Progressive Symptom Reduction Strategies for Parkinson's Disease
  • Home
  • About
  • Blog
  • Insights
  • FAQ
Todd Vogt.jpg

Athletics Training and Competitive Sport with Parkinson's Disease

October 18, 2019

How I Bounced Back After Parkinson’s Diagnosis to Make US National Rowing Team

by Todd Vogt

I was diagnosed with Parkinson’s Disease approximately one year ago, at age 44. I knew something was seriously wrong with me for about six months prior, but the exact cause took a while to figure out. Looking back, I can see that I had symptoms starting about two years before my diagnosis. I remember having these unusual bouts of fatigue, where I would be wiped out for a day in an unusual way. Also, during workouts, I would get unusually fatigued. Even still, getting the diagnosis was quite a shock. I was devastated. As a competitive rower, I identify so much with my physical capabilities. I exercise everyday and eat well. Physical activity is how I stay grounded. At some level, I felt pretty invincible. I thought Parkinson’s was something that happened only to older people, not to someone younger and healthy. But then I was diagnosed with early onset Parkinson’s and just felt so lost.

For a while, I didn’t know what this new situation would mean. I would try to read online about the condition to answer some of my questions, but sometimes it was too depressing. The hardest thing to deal with was the fact that I assumed my days of being a competitive athlete were over.

It seemed a given to me, as I knew I didn’t move as well and so often I felt weak and tired. But I continued to live my life the best I could, working hard at my job as a rowing coach and exercising the best I could when I could.

Around that time, about six months after my diagnosis, I started to get curious about just how much I could still do physically. I was encouraged to continue working out by my neurologist, Ronald Pfeiffer at OHSU, and my naturopath, Lindsey Fontenot. That’s when I started trying to seriously train again. It was a big adjustment, mentally more than anything. I had to be very patient with myself and what I could do. I tried not to compare my new training to what I had been able to do before. At some point during this time, I realized I could still row and exercise quite hard, albeit at a different level. It became a sort of a game to see how fast I could row and how much I could train with my condition. I started to see it as a daily challenge.

Todd Vogt 3.jpg

There were still plenty of hard days—times when I couldn’t help but feel frustrated that I had to develop this new training outlook and times when I just missed the days of not having to think about any limitations. My left side doesn’t respond as quickly leaving me feeling uncoordinated. But then, after a bad day, the next day I’d try to get back at it and do the training I could do. I found that cross-training with a stationary bike really helped me feel better about what I could do. And I also started making an effort to work out with friends as that helped motivate me on days I might have been tempted to give up. That’s when I started reading and thinking about the National Paralympic team and the rowers they had on their team. That got me really interested.

After some internal debate, I finally reached out to—the Paralympic High Performance Director, Ellen Mizner, who is located in Boston. I introduced myself via email, told her about my condition, and asked her about how one gets designated or classified as a para-rower. Her response was warm and receptive. And with her help, within a few months, I completed the qualifications to be classified as a para-rower. I was ecstatic, but also quite nervous. Now I had the chance to compete again but I didn’t know how it would go considering my new circumstances. But the next step was attending the training camp in Boston for the Paralympic National Team, so off I went.

In Boston, I was impressed and, honestly, a little intimidated at the level of ability with the other para-rowers. The training camp lasted 12 weeks and there were several other strong male rowers vying for the same five spots. I felt pretty unsure about my chances to qualify, honestly. But then in July, my partner and I, Andy Wigren, won first place at the US National Team Trials in our event, the PR3 Men’s Pair event. This earned us the right to represent the US at the 2019 World Rowing Championships. It was amazing winning the trial. I’ve never been on a national team before and I was beyond ecstatic.

The summer had so many highlights. In Linz, Austria at the World Rowing Championships, Andy and I competed against some incredibly strong rowers but still managed to finish in 6th place in our event. And then in June, a really cool thing happened. While competing at the World Rowing Cup II in Poznan, Poland in the PR3 Mixed Four event with my teammates, we won a World Cup gold medal. I was floored. That was such an awesome day.

Since returning home from my travels, I’ve continued to connect with more athletes in the Parkinson’s community. I’m still coaching as well which I love. It brings me so much joy to share my passion for the sport with others. Some days are harder than others, but it really helps to have these goals to look forward to. Right now I’m training hard to hopefully earn a spot on the US Paralympic Team that will compete in Tokyo next summer. Ultimately, I’m excited for what’s ahead. And, looking back at all the ups and downs of this last year, I’m really proud of all that I’ve accomplished.

This last year has taught me a lot. I know I have a much better appreciation for each day of my life now, and, specifically, time spent with my loved ones. I don’t take for granted the moments I get to enjoy with my spouse and my dog. They’re so precious to me and now I can’t help but stay aware of how much I value those times. I’m grateful for that awareness.

Getting diagnosed with Parkinson’s will never be easy. My heart goes out to anyone who has to go through that. But I hope my story can maybe make someone feel less alone and inspire them to seek out a community and stay curious about what they still can do. Over this last year, I’ve had the opportunity to meet so many awesome people and athletes, people who have become a part of my family. Everything considered, I’d say things are looking up and I think they can for you too.

Todd Vogt 2.jpg

Follow Todd on Instagram where he blogs about his rowing training and living with Parkinson’s Disease



In Biography, Exercise, Mental Health, People, Re-thinking Movement, Therapies Tags Rowing, Sport Therapy, Mindset, Motivation
← Brain Healing and Parkinson's DiseaseFascia (Connective Tissue) and Parkinson's Disease →

ABOUT

Out-Thinking Parkinson's
Out-Thinking Parkinson's Research

 Join my Facebook Group

Follow me on substack:

BLOG

  • Re-thinking Movement
  • Digest
  • People
  • Mental Health
  • Diet & Supplements
  • Therapies
  • Toys
  • Exercise
  • Video
  • Assistive Technology
  • Music
  • Biography
  • Brain Science
  • Books
Parkinson's Disease Carousel: Original Articles and Ideas
Jun 6, 2025
Waking Up the Senses and Parkinson's Disease
Jun 6, 2025
Jun 6, 2025
Feb 19, 2025
The Nervous System and Parkinson's Disease
Feb 19, 2025
Feb 19, 2025
Sep 19, 2024
Hope and Parkinson's Disease
Sep 19, 2024
Sep 19, 2024
Aug 3, 2024
DAT Scans and Parkinson's Disease
Aug 3, 2024
Aug 3, 2024
Jun 23, 2024
Dopamine Breakdown and Parkinson's Disease: Part 2
Jun 23, 2024
Jun 23, 2024
May 3, 2024
Stuck on Pause with Parkinson's Disease
May 3, 2024
May 3, 2024
Apr 10, 2024
Dopamine Breakdown and Parkinson's Disease: Part 1
Apr 10, 2024
Apr 10, 2024
Jan 2, 2024
Fright and Parkinson's Disease
Jan 2, 2024
Jan 2, 2024
Sep 16, 2023
Acetylcholine, Dopamine and Parkinson's Disease
Sep 16, 2023
Sep 16, 2023
Jul 24, 2023
Sleep and Parkinson's Disease, Part 2
Jul 24, 2023
Jul 24, 2023
Jun 4, 2023
Emotional Armouring and Parkinson's Disease
Jun 4, 2023
Jun 4, 2023
Apr 2, 2023
Histamine, Allergies and Parkinson's Disease
Apr 2, 2023
Apr 2, 2023
Feb 8, 2023
Fascia Decompression and Parkinson's Disease
Feb 8, 2023
Feb 8, 2023
Dec 30, 2022
Lack of Oxygen to the Brain in Parkinson's Disease
Dec 30, 2022
Dec 30, 2022
Dec 13, 2022
Constipation and Parkinson's Disease
Dec 13, 2022
Dec 13, 2022
Oct 19, 2022
The Endocannabinoid System and Parkinson's Disease
Oct 19, 2022
Oct 19, 2022
Aug 21, 2022
Tremors and Parkinson's Disease
Aug 21, 2022
Aug 21, 2022
Jun 29, 2022
The Neck and Parkinson's Disease, Part 2
Jun 29, 2022
Jun 29, 2022
May 17, 2022
Reducing Stress and Parkinson's Disease
May 17, 2022
May 17, 2022
Apr 7, 2022
Thiamine and Parkinson's Disease
Apr 7, 2022
Apr 7, 2022
Mar 6, 2022
Stress, Situations, Symptoms and Parkinson's Disease
Mar 6, 2022
Mar 6, 2022
Feb 18, 2022
Early Retirement and Parkinson's Disease
Feb 18, 2022
Feb 18, 2022
Feb 3, 2022
Survival Instincts and Parkinson's Disease
Feb 3, 2022
Feb 3, 2022
Dec 13, 2021
Feeling Trapped and Parkinson's Disease
Dec 13, 2021
Dec 13, 2021
Nov 4, 2021
Motivation, Pleasure, Pain and Parkinson's Disease
Nov 4, 2021
Nov 4, 2021
Oct 2, 2021
Dopamine Cell Receptors and Parkinson's Disease
Oct 2, 2021
Oct 2, 2021
Aug 15, 2021
Dopamine and Parkinson's Disease
Aug 15, 2021
Aug 15, 2021
Jul 26, 2021
Visual Cues and Parkinson's Disease
Jul 26, 2021
Jul 26, 2021
Jul 10, 2021
The Eyes and Parkinson's Disease
Jul 10, 2021
Jul 10, 2021
Jun 25, 2021
Eye Exercises and Parkinson's Disease
Jun 25, 2021
Jun 25, 2021

insights

  • Person with PD
  • Caregiver
  • Reader
  • Author
  • Therapist
Testimonials Carousel: What People Say
Mar 13, 2025
Coloring with Parkinson's
Mar 13, 2025
Mar 13, 2025
Nov 28, 2024
Very Encouraging and Refreshing
Nov 28, 2024
Nov 28, 2024
Apr 19, 2024
Stuck on Pause
Apr 19, 2024
Apr 19, 2024
Aug 12, 2023
Photobiomodulation or Red Light Therapy
Aug 12, 2023
Aug 12, 2023
Jul 7, 2022
Tremors Reduced
Jul 7, 2022
Jul 7, 2022
Mar 29, 2022
Accessible Knowledge
Mar 29, 2022
Mar 29, 2022
Oct 19, 2021
Staying Positive
Oct 19, 2021
Oct 19, 2021
Jul 28, 2021
Suggestions for Exploration
Jul 28, 2021
Jul 28, 2021
Jun 20, 2021
Educative Posts
Jun 20, 2021
Jun 20, 2021
Mar 24, 2021
Parallels with Trauma
Mar 24, 2021
Mar 24, 2021
Feb 4, 2021
Correcting Dysfunctional Sleep
Feb 4, 2021
Feb 4, 2021
Oct 27, 2020
REM Sleep Behaviour Disorder
Oct 27, 2020
Oct 27, 2020
Aug 11, 2020
Yoga Therapy
Aug 11, 2020
Aug 11, 2020
Nov 27, 2019
Strategies of Recovery
Nov 27, 2019
Nov 27, 2019
Sep 3, 2019
Applications of Polyvagal Theory
Sep 3, 2019
Sep 3, 2019
May 24, 2019
Hope and Inspiration
May 24, 2019
May 24, 2019
Feb 7, 2019
Headed in the Right Direction
Feb 7, 2019
Feb 7, 2019
Sep 10, 2018
Husband Diagnosed
Sep 10, 2018
Sep 10, 2018
Sep 10, 2018
Making Changes
Sep 10, 2018
Sep 10, 2018
Jun 21, 2018
Craniosacral Therapy
Jun 21, 2018
Jun 21, 2018
May 27, 2018
Music is Medicine
May 27, 2018
May 27, 2018
Apr 26, 2018
Social Isolation
Apr 26, 2018
Apr 26, 2018
Mar 31, 2018
From Malta
Mar 31, 2018
Mar 31, 2018
Mar 6, 2018
Impactful Discoveries
Mar 6, 2018
Mar 6, 2018
Mar 6, 2018
Co-Regulation
Mar 6, 2018
Mar 6, 2018
Feb 6, 2018
Outstanding Information
Feb 6, 2018
Feb 6, 2018
Jan 21, 2018
Slowing Down Progression
Jan 21, 2018
Jan 21, 2018
Oct 25, 2017
Exploring All the Potential Causes
Oct 25, 2017
Oct 25, 2017
Sep 10, 2017
Can-Do Attitude
Sep 10, 2017
Sep 10, 2017
Aug 28, 2017
Connecting the Dots
Aug 28, 2017
Aug 28, 2017

©2017-2024 Gary Sharpe, ©2016 Gary Sharpe and Deb Helfrich

Contact Us

Medical Disclaimer

Website Terms & Conditions