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Parkinson’s Doesn’t Just Affect Me — It Affects Us

Parkinson’s Doesn’t Just Affect Me — It Affects Us

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This episode is a love letter to the unsung heroes — the care partners, the spouses, the friends, the ones who stay.

Bryce opens up about how Parkinson’s affects everyone, not just the person diagnosed. From disappearing friendships to the invisible emotional toll on partners, this is a deeply honest conversation about what it really means to live with Parkinson’s in a relationship, in a family, in a community.

He explores guilt, grace, burnout, and how the strongest relationships learn to adapt — not by going back to what was, but by finding a new rhythm.

❤️ “You don’t have to fix everything. Your presence changes everything.”

This one’s for every caregiver who’s ever Googled symptoms late at night, for every partner who sits in the waiting room, and for every friend who keeps showing up. You matter more than you know.

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📌 Products I Personally Use & Recommend:
All products Individually Links:
☀️ Light Therapy Wake-Up Alarm Clock – https://amzn.to/41MP5zP
😍 Magnesium Spray – https://amzn.to/3XYuoyy
💊 Vitamin D3 (5,000 IU Daily) – https://amzn.to/4kCRJ2E
⚡ Vitamin B12 (1,000 mcg Methylcobalamin) – https://amzn.to/4kyJZ1z
🧠 Vitamin E (400 IU Daily) – https://amzn.to/41CEwhv
😴 Melatonin (1–3 mg for Sleep, If It Works for You) – https://amzn.to/3FNTxWl
⏰⌚ Projection Alarm Clock – https://amzn.to/3QSxBf1
🆒📔 Cooling Comforter – https://amzn.to/3QVu1Ro

💬 I read and reply to every comment
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▶️ Video Podcast Playlist: https://bit.ly/4h27D3y
🎧 Audio Podcast: https://feeds.buzzsprout.com/2466483.rss

⚠️ Important Note
This is my personal Parkinson’s medication j

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General Inquiries: office@bryceperry.org

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Disclaimer:

The information shared in this podcast is based on personal experiences and opinions. I am not a medical professional, and this content should not be considered medical advice. Always consult with your doctor or a qualified healthcare provider before making any changes to your treatment or lifestyle.


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