Is there such a thing as too much Levodopa? In this honest, experience-driven episode, Bryce dives into the reality nobody talks about: knowing when your medication is helping—and when it’s starting to hurt. From the early days of chasing “control” with more pills to the wake-up call of dizziness, exhaustion, and dyskinesia, Bryce shares real stories and practical signs that it’s time to rethink your dose.

Whether you’re newly diagnosed, deep into your Parkinson’s journey, or a caregiver wondering what “too much” looks like, this episode unpacks:

• Why there’s no universal max dose for Levodopa (and what really matters)
• The hidden signs you might be overmedicated—like hallucinations, sleepiness, and impulse control issues
• What it feels like to “hit your peak dose” (and why tracking your symptoms is everything)
• How your medication needs will change as Parkinson’s progresses
• Why being your own advocate—tracking, journaling, and speaking up—makes all the difference

Bottom line: The goal isn’t just to survive, it’s to function and live. Sometimes, that means having tough conversations, adjusting your dose, and remembering: more isn’t always better, but less isn’t noble if you’re struggling.

Bryce-ism of the Episode:
"More medication isn’t always more freedom. Sometimes, it’s just more noise your body has to shout over. Tune in, track it, and find your real balance."

👇 What’s been your Levodopa journey? Drop your experiences in the comments—I read and reply to every single one!

Inner Circle 

💬 Want a safe, private space to connect with me and others on this journey? Join my Inner Circle for live monthly calls, support, and 24/7 community:
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💬 I read and reply to every comment
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⚠️ Important Note
 This is my personal Parkinson’s medication journey—what works for me may not work for everyone. Parkinson’s is different for each person, and medication plans should always be tailored to individual needs. Before making any changes to your medication or treatment, consult with your doctor o

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