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Over time, I have learned that the non-motor symptoms of Parkinson’s disease especially those caused by a malfunction in the autonomic nervous system can be more challenging to live with than the traditional motor symptoms associated with PD. These symptoms include everything from drooling to increased urgency and frequency of urination, to too much or too little sweating. My faulty thermostat has me living in what feels like a constant state of heat exhaustion, and I’ve yet to even experience the joy of menopause. Hot flashes that come and go would be a welcome relief from feeling “hot, hot, hot” 24/7. I am certain that one day the sun and moon will align in such a way that these conditions will collide head on, giving rise to an internal inferno that will melt down what Parkinson’s has left of my brain. Even on Chicago’s coldest days, when the winds howl and the temperature feel like double digits below zero, I am comfortable in my warm-up suit. For months, my winter coat sits like a prop in the back seat of my car in case of emergency like should I hit one of Chicago’s bottomless potholes and find myself with a flat tire. Strangers stop me on the street to ask, “Aren’t you cold? Where’s your jacket?” Do they think I don’t know when I’m cold, or are they worried that I can’t afford a winter coat? I tell them my mother lives in Florida and offer them her phone number so they can rat me out. They shake their heads in disgust and walk away.
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