Columns

“Thanks for putting into words my experience with Parkinson’s. I’m going to share your column with my doctor.” Readers of my “Possibilities with Parkinson’s” column have often made such comments. It’s a sincere compliment, and I’m very grateful that my words resonate with others. However, I can’t help but wonder…

Spring is finally here, and when I think spring, I think baseball. Just like in baseball, where each team has a roster of players, Parkinson’s patients have their own teams of professionals in their lineup. Let me tell you about my team and its batting order. For my team, the…

In a four-part audio series for Newman Catholic Campus Ministry called “Nothing to Fear,” the Rev. Mike Schmitz delves into several elements of fear: vulnerability, rejection, inadequacy, and the future. The series led me to ask, “How do we view fear?” I believe many people see fear as something…

Every year in April, Parkinson’s Awareness Month comes and goes, and I find myself wondering if anything has changed. Did the temporary boost of attention spark change in the medical community? Did fundraising efforts make a difference in our pursuit to end this disease? How might we maintain our…

My sister, Bev, 84, was diagnosed with Parkinson’s disease (PD) in 2017 after having undiagnosed symptoms for about eight years. She told me that while working as a nurse and then as an echocardiography technician, she experienced the shaking of her head and left hand. Bev also had some…

Notable events, like my granddaughter’s school play, often are not scheduled to accommodate my Parkinson’s disease (PD). Usually, early evening events seem to occur exactly as I reach the peak of my worst “off” period. But will I miss these types of activities? No! I need to be out…

Keeping adequate reserve in our personal reservoir of energy helps us to be available for the lucid times. We need to minimize fatigue and add richness to life despite living with a chronic illness like Parkinson’s disease (PD). Managing the well of resources involves not only filling up the well…

For many of us with Parkinson’s disease, traveling can trigger anxiety, but a successful trip is still possible. While extra planning, extra time, and good shoes are a great place to start, sometimes they are not enough. The method of travel that suits our needs may require asking for help, or as we…

My experience with Parkinson’s disease was limited until my dad was diagnosed with it in 2013. A man in our church had it, and I used to notice his unsteady hand. Eventually, he stopped going to church. I remember feeling incredibly sad about how a disease could make people retreat…

Parkinson’s disease (PD) is a tough life and not to be taken lightly. With all the serious aspects of PD that manifest in our lives and the effort needed to manage them, it’s hard to find time to be light and playful. With tongue in cheek, following…