Shaking Things Up - a Column by Mary Beth Skylis

Many Parkinson’s caregivers report seeing changes to their loved ones as the disease progresses. Some people experience more irritability. Others might see apathy. Maybe it’s just that there’s been a subtle adaptation to how they experience the world. Since my dad’s diagnosis in 2013, I’ve definitely seen changes in…

When I was a kid, my dad was always in motion. If he wasn’t hard at work in the office, he was mowing our 10-acre lawn or cleaning the chicken coop. It was only in the evening that I’d finally see him at rest when he’d pop in a video…

Hi, everyone! If we don’t know each other already, I’m Mary Beth. I’ve been working as a columnist and a forums moderator for Parkinson’s News Today for a fair amount of time now. But I’m still learning. I set out here to explore my dad’s journey with Parkinson’s…

When I stumble through the door on my recent visit home, I’m not entirely prepared for the sight that greets me. My dad looks like he’s walking through molasses, and my mom is hobbling around on a bad hip. I’d seen them both just a few months earlier. Mom’s…

It is a Thursday evening when my sister asks me to come up with fake illnesses to give my dad. He has just received his first dose of the COVID-19 mRNA vaccine, and my sister, ever the practical jokester, wants to tease him.

Last weekend, I was exploring a South Carolinian swamp when my phone buzzed. It was my dad. “Call me after 2,” the text glowed on my phone. “OK,” I responded. After I’d wiped the swamp juice from my shoes and peeled back my muddy socks, I dialed my dad. Usually…

While I was home last Christmas, I had an argument with a loved one that caused tensions in the household to rise. The disagreement wasn’t with my dad, who has Parkinson’s disease. But I realized later, after speaking to him, that the situation had negatively affected him, too. In fact,…

I don’t have Parkinson’s disease, but my dad does. And sometimes I wonder how lonely it can be. Even when we as loved ones try to understand the disease, experiencing the symptoms seems really isolating. No, I don’t know what it’s like to struggle with tremors, dyskinesia, or freezing. Random…

When we’re born into this world, it takes us about seven months to sit up for the first time. It takes about a year to learn how to walk. The learning process is long and difficult, and riddled with unsuccessful attempts and blunders along the way. The act of walking…

The morning is crisp and the ground is frozen by the brutal Michigan winter temperatures. I pile my belongings into the back of my Subaru as I prepare to say my goodbyes, again. In 2020, I spent nearly three months here, the most time I had been at…