Join us Sunday, November 8th (1-7pm) at Padel39 East for our fifth annual Padel 4 Parkinson’s event!
It will be a memorable day featuring tournaments, games, and activities for every level, alongside food, refreshments, DJ and exclusive auction opportunities.
Together, we're helping fund life-changing programs today and the search for a cure tomorrow. 100% of net proceeds support Power for Parkinson's and Parkinson's research through the Michael J. Fox Foundation.
Tournament and ticket information coming soon. Sponsorship opportunities available! For more informations or questions, email Padel4Parksinson@gmail.com.
Our Story
Padel 4 Parkinson's was born from Austin's padel community and a deeply personal connection to Parkinson's disease. Inspired by the experience of having parents living with Parkinson's, we asked a simple question: What if every point we played could help someone else? That question became the foundation of Padel 4 Parkinson’s, an annual event dedicated to turning the love of sport into hope, awareness, and meaningful action. Every serve, volley, and smash helps support Power for Parkinson's, providing life-changing exercise and community programs, while advancing research through the Michael J. Fox Foundation.
Victoria Young
I am inspired by my Dad, who was diagnosed 13 years ago with Parkinson’s Disease. There is no known cure. Everyone’s experience is unique, and because of this my dad has tried many different medications and trials (sponsored by MJFF). It is a challenge every day , but I believe we can build a future where Parkinson's is no longer part of anyone's story, where there are no
“good days and off days”. That's why I'm committed to raising awareness, supporting those living with the disease, and helping fund the research that will one day ensure all days are good ones.
Susanna Olivarez
My mom, Rosario, was diagnosed with Parkinson’s Disease nearly 20 years ago. Parkinson’s is progressive, so wherever you are today in this journey, this could be your best day. My mother is in the advanced stages, facing challenges with speech and balance, yet she continues to inspire us with her positive outlook. Our family remains hopeful and we are grateful for organizations that fund research and provide support to families like ours.
Tony Young
I hate Parkinson’s disease! Seeing what it is like for those who live with it and the fight they put up to keep going; is reason enough for the rest of us to do what we can so the world can be free of Parkinson’s.