Thankful for Parkinson’s? Yep, and here are 5 new reasons why

Last year at this time, I posted five reasons I’m thankful I have Parkinson’s disease. Finding them required a spoonful of creativity and a bucketful of optimism.

This year, I super-challenged myself to come up with five more

A person holds a sign that says "grateful."

A tall order? Yes, but in my experience, putting gratitude front and center helps me focus on the positives, the gifts, the people, the blessings that I sometimes take for granted. That’s a good reason to continue the list.

Of course, this challenge comes after another year in which Parkinson’s rudely has made itself tougher to manage, and the symptoms have progressed in a most inconsiderate manner. (I can be grateful for Parkinson’s, but I don’t have to be polite to it.) 

Some days are good, others are “stinky dog,” to borrow a phrase from a friend. Sometimes the medications work, other times they are off.

My optimism endures regular pushback. 

Last year’s five reasons were tough enough to find, and any low-hanging fruit is gone. To double the list of reasons that I’m thankful for Parkinson’s disease required some deep thought about what’s going well – and not so well – in my life. But I have met the challenge! Read on.

As a reminder, here are the 5 from last year

Having Parkinson’s disease:

  • teaches me empathy for others who suffer
  • has led me to interesting people and a vibrant community
  • provides an opportunity to try new things
  • allows me to help others with the disease
  • helps me value my mortal existence, what I have left of it

And now, reasons 6-10

I’m thankful I have Parkinson’s disease because…

6Having PD helps me develop a stronger sense of hope.

Let’s face it. Parkinson’s is a degenerative disease. It’s a one-way street to worse. You don’t get better from it, and there’s no cure. 

 A woman goes backward off a cliff hang on to a rope.

I have a mental picture of myself rappelling off a cliff, waiting for the belayer up top to gently lower me to the ground. If the belayer represents a cure, then in this metaphor I will be suspended on the rope for a long, long time! 

It’s unlikely I’ll ever be free of Parkinson’s. But I can hope for more effective treatments. I can hope for improved diagnoses so if a grandchild sees signs of PD someday, the disease can be stopped in its tracks. Hope is a powerful companion to gratitude.

7. Having PD changed my priorities.

Shortly after my diagnosis, I noticed certain parts of my life were becoming more important, while others now carried less weight. So I reorganized some things. I dropped hours at work. I began journaling again. I paid more attention to what I ate. I studied scriptures. I reached out to extended family.  

The problem now is choosing which of these priorities to focus most on. I still have only 24 hours in a day!

8.   Having PD encourages me to educate others about the disease.

Two women talking together inside the house.

Telling someone about your Parkinson’s disease is one thing; it’s another to teach them about it. I’ve enjoyed learning all I can about PD, and then taking the role of educator when people ask me about it. It may seem like an impossible task to counter the misinformation out there, but I’m trying to do my part.

9Having PD forces me to slow down.

By nature I am a busybody. There are days I put bees and beavers to shame. From the time I was little, my mom was always telling me to slow down. 

Well, Mom, I couldn’t do it on my own, so Parkinson’s is doing it for me. Bradykinesia (slowness of movement) is a major symptom, and I’m feeling it. All that busyness isn’t good for you anyway. It’s important to stop and smell the roses. Oh wait. Not easy when people with PD lose their sense of smell!

10  Having PD brings my blessings into focus. 

While Parkinson’s disease is, as Michael J. Fox says, “a disaster,” I gratefully recognize what I do have and what I can do.

I have many loving and supportive family members, including a husband already proving that he intends to be a devoted care partner for the long haul.

Beyond the richness of family relations, I have a living space that provides creature comforts, a church community, access to medical care, and loyal friends.

There’s always someone worse off than me. It’s useless to compare, but when I’m feeling like I drew the short stick in life, I know I’m in the company of many good people who don’t deserve what they got.  

And a bonus reason …

A woman holds purple flowers wearing a ski cap with trees behind her.

Exercise is a crucial therapy for people with Parkinson’s disease. As an unshakable hiker, I acknowledge that living with PD has increasingly brought me outdoors for beautiful hikes throughout the country and beyond. I’ve also tried new types of exercise, like boxing, tai chi, and yoga, and some have stuck. 

I’m grateful for the extra push to stay fit.


What’s on your mind during this season of thankfulness? Drop a thought in the comments.

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7 Comments

  1. You have reminders for everyone, Colleen: the value of time, slowing down (a little 😉 ), and beauty in the world.

    1. You’re right, Neil, it applies to almost anyone. And I probably should have heeded my own advice pre-diagnosis, too!

  2. I am grateful for your courage and tenacity. Though you may have slow days or setbacks, you grit your teeth and soldier on. That inspires me for my challenges and trials.

    1. Thank you, Bryan, you are very kind. We all have challenges, trials, and setbacks. I try to remember that each person I meet is carrying a burden I probably don’t know about.

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