7 Subtle Changes That May Signal Your Parkinson’s Has Progressed

Comments · 170

• DO

  @doinglifetoday · 2 months ago · pinned

  ❤ Thanks so much for watching.<br><br>Which of these 7 subtle shifts hit closest to home for you?<br><br>Just comment the number (1-7) or tell us what you&apos;ve been noticing lately.<br><br>Remember, Parkinson&apos;s progression doesn&apos;t always happen with big dramatic changes. Sometimes it&apos;s the little things that quietly creep in over time.<br><br>Your comment might be exactly what someone else needs to read today to realize they&apos;re not alone.<br><br>And if you&apos;re new here, welcome. We&apos;re a community of people with Parkinson&apos;s, care partners, and friends who believe no one should have to figure this out alone. ❤

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• JA

  @jaysjams1517 · 1 month ago

  My tip for care partners - my wife attends my neurology appointments because she can provide info on her observations to the Dr that I am sometimes unaware of.

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• VI

  @VivHolmes · 2 months ago

  I find myself nodding in agreement with everything Bryce talks about, so much that I&apos;m starting to look like one of those bobblehead toys. Thanks Bryce, for capturing all that Parkinson&apos;s is, so very well.

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• KM

  @kmcd2501 · 1 month ago

  Keep showing up; keep being real. You have Parkinson&apos;s, but don&apos;t let Parkinson&apos;s have you.<br>Make the best of a bad situation.

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• LA

  @lavontolbert3864 · 2 months ago

  This is one of your best! Will ask my husband to listen. I still can walk with my coffee cup - but I don’t drink from it until I can sit down.

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• KR

  @kristinbluhm777 · 2 months ago

  I sometimes feel like I am living my life from medication dose to medication dose. &nbsp;I have medication stashed everywhere and even though I also have diabetes, Parkinson’s requires more management than the diabetes. &nbsp;I’m one of those people who doesn’t like to be told to do something and my first instinct when my body says it’s time for medication is to say no and throw a tantrum. &nbsp;Even after two years having to take stops to take medication really kind of annoys me.

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• PA

  @padmavelaga4788 · 1 month ago

  My brother is going through this, he himself is a doctor so it is very hard on him. Wish he listens to you. He is not alone on his journey! Love your show. Camron is a rock. You are lucky. God bless you both! 🥰

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• 50

  @509susieq · 2 months ago

  Bryce, I can’t thank you enough for your encouragement through these videos! You articulate so well many of the things that I deal with. I am passing this video along to my family, both near and far. Thank you for taking the time and energy to continue your work. It is making a difference for me, and countless others I’m sure. I especially resonated with counting the cost. Having Parkinson’s doesn’t mean I can’t do things I still love, I just have to be realistic about the cost physically, mentally and emotionally. My story is similar to yours in that I first experienced symptoms when I was 45, and was officially diagnosed three years later. That was 20 years ago. I still travel quite a lot, just not as much as I used to. In my earlier days, I would fly to the other side of the world and hit the ground running. Now I don’t go as far or as often, and insist on having at least one whole day to recover from the travel and jet lag. Thank you for giving Voice to many of the things I face every day. You (and Carmen) blessing!

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• JO

  @Joe_Park1956 · 2 months ago

  Need 50% (at least I feel it) longer for most things I got to do. Especially for doing things in the household, or walking outside.

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• SA

  @sandracline1935 · 2 months ago

  This podcast is telling me not to be so hard on myself especially when I am unable to do many of the tasks I used to do or have the energy to a accomplish.

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• MS

  @MsCarilyn · 1 month ago

  I noticed my husband leaning forward and shuffling for over a year. Memory also started fading prior to the shuffling.

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• ED

  @eduardogong · 3 days ago

  Bryce, your videos are amazing and truly motivational! Thank you