Many losses are associated with Parkinson’s disease, some more impactful than others. So far, because of deep brain stimulation (DBS), which I had in 2021, I’ve had more gains than losses in the past couple of years. It’s changed my life for the better in so many ways,…
My husband, John, and I got our cat Rosie from the animal shelter many years ago. She was a muted calico, the smallest and prettiest of all our indoor cats. What a sweetie she was. We called her my daemon, after the animals that were a physical manifestation of a…
Note: This column describes the author’s own experiences with deep brain stimulation. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. When I was diagnosed with Parkinson’s disease in 2015, I thought deep brain stimulation (DBS) was a last…
When I was diagnosed with Parkinson’s disease in 2015, I was alone. I had an appointment with the neurologist, and I never even considered bringing somebody. My husband, John, was working as a vendor at a farmers market, so I drove straight there after the appointment. He was busy…
My husband, John, was leaning over me and saying, “What happened?” I looked up at him and said, “Why?” What I was trying to say is, “Why did you wake me up?” But I couldn’t get the words out. Then my arms, which hadn’t tremored since my deep brain…
Since my diagnosis of Parkinson’s disease in 2015, my sense of smell has been nonexistent. Overall, I have to say the loss hasn’t bothered me too much, especially when compared with other Parkinson’s symptoms, such as tremor, slowness, and stiffness. The only time it does bother me is…
When my daughters were young, I used to joke that my superpower was the ability to worry. Now that they’ve grown into capable young adults, I don’t worry quite as much. Plus, what’s left to worry about? I already have an incurable illness, as I was diagnosed with Parkinson’s…
It’s hard work being an optimist when you have a disease that is progressive, neurodegenerative, and — wait for it — incurable. So what do I do? I work hard at it! The work began in 2015, when I was diagnosed with Parkinson’s disease. There is nothing like a…
Before I knew I had Parkinson’s disease, or even what it was, my family lost their collective mind. They insisted I was whispering and they couldn’t hear what I was saying. I still remember thinking they were all crazy. Were they gaslighting me? Why would they do that? Was…
Twenty years ago, I developed frozen shoulders. Yes, plural. Over the course of a year, both of my shoulders locked up, causing me to gasp in pain when doing the simplest tasks — brushing my teeth, putting on deodorant, combing my hair. It took months of physiotherapy, and then…
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