A loud crack. I turned and yelled at my grandson, “Keep the billiard balls on the table!” The noise was so loud that I was sure the ball had smashed into the Sheetrock wall. I’ve been known to bounce a ball off the table practicing a special billiard shot. But,…
Sometimes you’re living life to the fullest and forgetting Parkinson’s while doing something you never expected. Recently, for me, it was fishing — something outside my comfort zone. Fishing — really? My first adventure was last summer with friends who wanted to share their love of fishing. It was a…
It was one of those “perfect storm” weeks, when everything came together in a cumulative effect to make life miserable. Too much stress on my system makes it exceedingly difficult to use the conductor due to malfunctions. This only happens to me a few times a year, but it is…
I heard something recently that was new to me — that we are living in “sandwich times.” In other words, this is the “sandwich generation.” It’s a time in history when many are simultaneously caring for both a child at home and a parent. Caring for a so-called normal…
Finding the right doctor who meets your needs as a person with Parkinson’s disease can be daunting. I have consulted with 11 neurologists, seven of whom were movement disorder specialists (MDS), in the five years since my initial diagnosis in 2015. Following are my top criteria in choosing what I…
Conductor brain training has made living with Parkinson’s disease easier for me. The most amazing thing I discovered while using what I call “the conductor” is that signals coming into my brain are sometimes distorted. This distortion can take place in the form of signal amplification or suppression. If…
It’s finally time to open the front windows. A slight breeze has arrived to cast the hot air far (I hope) into the east. With the opening of the windows comes the pulling back of the curtains, which means … LIGHT! I love the daylight pouring in through the…
“Parkinson’s will not define me.” That was my mantra when I received my diagnosis five years ago. Today, I write about Parkinson’s, participate in Parkinson’s research studies, and teach classes to help others fight Parkinson’s. So, maybe it does define me. I…
‘What is something your friends and family can do to show you how much they care?’ A while back, someone asked people with Parkinson’s disease this question on a public Facebook forum. One of the first replies was bittersweet. Bitter because of the loss that was undoubtedly experienced, and sweet…
Imagine that it is a bad day, and you are also in a Parkinson’s disease “off-period.” Normally, it would be time to rest, right? But what if family arrives for dinner? It was the only time they could manage in their busy lives, and I really wanted to see them.
Get regular updates to your inbox.
