A Chance to Reinvent Ourselves

Life is about not knowing, having to change, taking the moment and making the best of it without knowing what’s going to happen next.

Gilda Radnor

One thing that I have noticed in the Parkinson’s Community is that so many of us have used our diagnosis as a means to reinvent ourselves. No matter what your stage of life, change is possible. I have seen many with young onset change the course of their careers due to PD, often doing something related to Parkinson’s. Some have become Rock Steady Boxing coaches and personal trainers. There are others who have taken their professional skills and adapted them to be able to help others with PD. And there are some who have become world class athletes. We have all heard about people with PD who could not draw a straight line before and now have become accomplished artists. There is no stopping a Parkie when he/she decides to try something new.

Photo by Andreas – on Pexels.com

From a previous post “Is there anything good about Parkinson’s“, I wrote:

“I think that having Parkinson’s allows us to see the world differently.  It also gives us the chance to reinvent ourselves, over and over again, as the disease progresses.  Many of us are doing things now that we never would have imagined doing. Why not try that boxing class and see what the buzz is all about?  You have a sudden urge to play an instrument?  Go ahead and do it.  It is good for your brain.  Same for learning a new language.  Learning new skills can help reconnect some of the neural pathways in your brain that have been damaged by PD.  The most interesting thing to me is that so many of us have found new interests, often showing creativity in the arts where there was none before.  Is it the added dopamine that we are taking? Or the lack of dopamine?”

I have seen this phenomenon happen to people with Young Onset PD as well as those of us who are older, like myself. We are not content to sit around and do nothing. So we find something new to set our sights on. For me, at some point after my diagnosis, I realized that I could write about having Parkinson’s Disease to educate others about the disease. Imagine my surprise to find out that people actually read it and seemed to enjoy it. I had never considered myself a writer before, but now, apparently, I was.

In my previous incarnations, I had been an audiologist, mom, calligrapher, volunteer, museum docent and now a writer. When the pandemic hit 3 1/2 years ago, I once again reinvented myself, this time as the host of a bi-weekly webinar for women – which in turn led to greater advocacy on behalf of the Parkinson’s Community at large. So do we, like cats, have 9 lives? More? Maybe the possibilities are endless. I wonder what is next for me.

Have you had the opportunity to reinvent yourself since your diagnosis? Have you changed the focus of your career? Done something completely different? I would love to hear from you about this.


Some exciting news

Join me for this terrific program on October 29, 2023 at 1:00 PM ET

In 2010 British comedy writer Mayhew-Archer was told
he had PD and decided to find it funny.  
If you’re worried or in need of a laugh, join us.  
THIS PROGRAM IS OPEN TO EVERYONE
Please note that there will be no recording allowed.  
You must be present on Zoom that day for the performance
REGISTER HERE for this free event

2 responses to “A Chance to Reinvent Ourselves”

  1. Elisa Peterson Avatar
    Elisa Peterson

    I have been a visual artist my entire life. I smiled at your remark about not being able to draw a straight line; I have fought the urge to draw straight lines in order to make what my artist mother called “the living line”, which is a wiggly interesting line.
    I am two years into my PD diagnosis, and I think that I was showing symptoms about four years ago when I began finding it harder to venture out on long walks. I was about 76 years old and suddenly I began writing short essay memoirs.
    I was possessed by a creative urge to write down the defining transformative moments of my life, as honestly as I could. I was acutely aware of time passing and wanted to leave behind a record: evidence that I had struggled, been injured and triumphed. I wanted to leave a chronicle for my granddaughters.
    Some of my writings have been published. I have been invited to perform by reading some of them. Some are poems. Some are small illustrated humorous zines. People have laughed at them and people have cried when I performed them aloud.
    I call these collections ” Unreported Damages and Retroactive Repairs”. They are the true stories of the buried pain and the moments of revelation that created my character, also the hurters and the helpers.
    I encourage people to write little pieces about the moments in life that stand out vividly for them; the first kiss (mine was terrible), the teacher that inspired you (mine was mean, but she called me an artist and I believed her) secret shaming events, abuse (if you can bear it).
    We all have stories to tell. Since I began writing I have become interested in all the hidden stories that walk by me daily. I use my camera to photograph interesting people and then I paint them in my studio. I keep my ears open for interesting remarks and then go to the studio and draw or paint them as cartoon characters. My sidekick is a precocious 8-year-old granddaughter who prods me to take my meds, keep moving and creating.

    1. Sharon Krischer Avatar

      Elisa,
      thank you for sharing your story. If you have not already found it, check out The Quiver, which is an online magazine for people with PD to contribute artwork, poems, stories, etc.
      Sharon

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I’m Sharon

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