Pearls for Parkinson's with Dacy Reimer
Weekly Tips for Daily Living with Parkinson’s
We are excited to share a new series called Pearls for Parkinson’s: Tips for Daily Living with Parkinson’s. This is the latest addition to our educational resources, which also includes our monthly podcast entitled: EmPower Talks: Insights from the Experts.
In these new episodes, Dacy Reimer, APNP, Wisconsin Parkinson Association's President & CEO and WPA podcast host shares tips and “pearls” of wisdom for making daily living with your Parkinson’s journey just a little easier. The episodes will be short format, usually five minutes or less.
These easy-to-listen-to “pearls” air every Monday. Grab a cup of coffee or your favorite morning beverage and listen in for positive insights and helpful ideas. It’s a great way to start your week!
Pearls for Parkinson's with Dacy Reimer
Bladder Issues: Is it PD?
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Pearls for Parkinson's: Tips for Daily Living with PD.
To watch this episode on YouTube: https://youtu.be/skiqm7W8QPU
Not every bladder symptom is Parkinson’s.
And sometimes, that assumption can cause us to miss something important.
In this episode of Pearls for Parkinson’s, we talk about:
- When bladder changes are expected in Parkinson’s
- When something might be different
- And why it’s important to take a closer look
Listen in to better understand what your body may be telling you - and when it’s time to speak up.
Has this episode helped to shed light on what you're experiencing? We love hearing from you!
To support more programs like this: https://wiparkinson.app.neoncrm.com/forms/support-pearls4pd
Wisconsin Parkinson Association
website: https://wiparkinson.org/
YouTube: https://www.youtube.com/@wiparkinson
facebook: https://www.facebook.com/wiparkinson/
instagram: https://www.instagram.com/wiparkinson/
Welcome to Pearls for Parkinson's. Here is this week's Daily Living Tip. Welcome back to Pearls for Parkinson's. This month we've been talking about bladder changes with Parkinson's. And today we're going to talk about how we know that it's due to Parkinson's or something else. And this is really important because when it comes to urinary symptoms, oftentimes going more often or urgency or even accidents, it's easy to just blame it on Parkinson's. And sometimes it is, but not always. And this matters because if we assume we might miss something that's actually very treatable. Now let's start with this. When do bladder changes typically happen with Parkinson's? For many people, these symptoms develop gradually over time. They're more often noticeable as Parkinson's progresses because of how the disease affects the automatic nervous system, the part that controls things like the bladder function. But they can also show up earlier than people expect, even if the first few years after diagnosis. So the key is Parkinson's-related bladder problems tend to be gradual, consistent, and somewhat predictable over time, which is why a sudden change is something to pay attention to. So what else is going on? Some of the most common things is a urinary tract infection or UTI. That can cause increased urgency, more frequent trips to the bathroom, burning or discomfort, and sometimes even confusion, especially in older adults. And again, UTIs usually come on quickly. So if there's a sudden shift, that's something to check out. For men, another very common cause is an enlarged prostate. This can look a lot like Parkinson's related bladder problems. It has frequent urination, feeling like you're not fully emptying, and getting up multiple times at night. And it's very common as men age. So it's important to consider and rule out. Medications are another piece. Some medications can increase urgency, and others can make it harder to empty the bladder. And even some Parkinson's medications can affect fluid balance and or timing, and they can change your urinary patterns. So here's the takeaway. Pay attention to changes. Ask yourself, is this new? Is it getting worse? Does it feel different than my usual pattern? And if the answer is yes, then it's worth a conversation. Because the goal isn't to just manage symptoms, it's to make sure that we're treating the right cause. You don't have to guess your way through this. If something changes, speak up. Bring it to your neurologist or your healthcare provider. Because the more we understand what's behind the symptom, the better we can treat it. And if you've ever had a symptom turn out to be something different than you expected, share it. Your experience can help someone else ask the right question. I hope you liked this episode. If you did, hit that like button, share it with a friend or a support group, and tune in next Monday for more Pearls for Parkinson's. The Wisconsin Parkinson Association is a grassroots organization funded by people like you. To support more local programming like this, visit wiparkinson.org.
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