For me, switching to CREXONT has made a significant difference.

Before CREXONT, my OFF periods could last around an hour and a half. I would lose energy, my voice would get softer, finding words became harder, my walking slowed down, and falls became a real problem.

Since starting CREXONT, my OFF time has dropped dramatically—sometimes to around 15 minutes—and I’m getting close to four hours of ON time between doses.

It has also allowed me to reduce or discontinue other Parkinson’s medications that were contributing to problems like low blood pressure, night sweats, dyskinesia and night terrors.

This video is simply my personal experience. Parkinson’s affects everyone differently, and medication decisions should always be made with your neurologist or movement-disorder specialist.

But when something makes this much of a difference in my life, I believe it’s worth talking about.

We are Unshaken—sharing the real side of living with Parkinson’s, supporting caregivers and families, and reminding each other that a diagnosis does not get the final word.

Subscribe and follow along as we continue building the Unshaken Parkinson’s community.

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After years of unexplained pain, countless doctor visits, and more questions than answers, I finally heard the words: "You have Parkinson's."

This is the true story of my diagnosis, the hope I found in finally having an answer, and why that journey inspired the creation of the Unshaken Parkinson's Foundation—a place where no one has to face Parkinson's alone.

If this conversation resonates with you and you'd like to help us build a place where no one faces Parkinson's alone, we'd love to connect with you.