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What Parkinson’s Has Taken… and What It Has Given

by Frank Antonicelli | July 28, 2026

About Frank Antonicelli

Frank Antonicelli is from Mechanicsburg, Pennsylvania, and was diagnosed with Parkinson's disease in 2007 at the age of 43. His experiences living with Parkinson's inspired him to create the Embracing Parkinson's project, where he shares practical insights and encouragement for others facing the disease. Following deep brain stimulation (DBS) surgery in 2020, Frank rediscovered his creative side by revisiting poems he had written over the previous 30 years and transforming them into songs for his music project, Animal Speak. Through his advocacy and music, Frank hopes to encourage others to focus on what they can still do rather than what Parkinson's has taken away. His personal motto, "Patiently Persistent," reflects the mindset that continues to guide him each day.

I was 43 years old when I was diagnosed with young-onset Parkinson’s disease in 2007.

Like everyone living with Parkinson’s, I’ve lost things along the way. I’ve lost the ease of simple movements I once took for granted. I’ve watched symptoms slowly change the way I work, exercise, and go about everyday life. There have been difficult times when Parkinson’s seemed to take more than I thought I had left to give.

Over time, though, I realized Parkinson’s wasn’t just taking. It was giving me things I never expected.

It gave me a greater appreciation for the ordinary moments I used to overlook. It taught me not to take a good day for granted. It introduced me to friendships I never would have made otherwise and connected me with a community that truly understands what it’s like to live with this disease.

It also helped me rediscover a part of myself I’d set aside for years. I’ve always loved writing, and after my Parkinson’s diagnosis, I found my way back to it in a new way through songwriting. Creating again reminded me that Parkinson’s hadn’t taken away my ability to learn, grow, or express myself.

If I could erase Parkinson’s from my life and the world, I certainly would. But since I can’t, I’ve chosen to focus on what I still can do instead of what I’ve lost. That simple shift has made a big difference in how I live each day.

When I was first diagnosed, I felt like there were a lot of questions nobody could answer and not many people I could reach out to. Resources for young-onset Parkinson’s seemed very limited at the time.

More than anything, I wish I’d had the chance to learn from people who had already been living with it. That’s one of the main reasons I started sharing my own experiences. If something I’ve learned helps someone who’s newly diagnosed, then it’s 100% worth it. These days, I’m proud to see how much the Parkinson’s community has grown and how willing people are to support one another.

Parkinson’s has taken a lot from me. But it has also given me perspective, purpose, meaningful friendships, and a deeper appreciation for the life I still have.

That’s why I keep moving forward, one day at a time, patiently persistent.

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