Parkinson’s Sweating? Here’s What’s Really Happening

One minute you're sweating. The next minute you're freezing. And everyone around you seems perfectly comfortable.

Meanwhile, Carmen is asking me to pick a temperature.

Believe me, I'd love to. But apparently Parkinson’s has taken control of my body's thermostat!

In this episode of Living with Parkinson’s: The Good, the Bad, and the Reality, we're talking about something many people don't realize Parkinson’s can affect: your body's ability to regulate temperature.

We explore seven surprising things:

• Excessive sweating: Why you might suddenly start sweating even when the room isn't hot.

• Uneven sweating: How some parts of your body may sweat too much while others sweat too little.

• Heat intolerance: Why warm weather can leave you exhausted, dizzy, or feeling completely drained.

• Feeling unusually cold: Why your hands, feet, or entire body may feel freezing when everyone else is comfortable.

• Medication-related sweating: How sweating can sometimes be connected to OFF periods or dyskinesia.

• Night sweats: Why you might wake up soaked even when your bedroom isn't particularly warm.

• When temperature problems become serious: Why severe overheating, dehydration, confusion, or sudden major changes require medical attention.

And here's something that surprised me:

Sometimes excessive sweating in one part of your body may happen because other areas aren't sweating properly!

I also share a simple way to recognize patterns by tracking three things: time, medication cycle, and environment.

You'll also hear Carmen’s Care Partner Corner, where Carmen explains why temperature problems can be frustrating for both people.

Because apparently my internal thermostat is broken, and Carmen has become the customer service department. 😂

The biggest takeaway?

You don't have to silently put up with temperature problems just because you have Parkinson’s.

Recognizing patterns, making practical adjustments, and talking with your healthcare team can help you manage them.

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“With Parkinson’s, medication is like coffee. It’s not about how strong it is. It’s about when you take it.”

⚠️ Important Note

This is my personal Parkinson’s journey. What works for me may not work for everyone. Parkinson’s is different for each person, and medication plans should always be discussed with your doctor or healthcare provider.

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