Living Well with Parkinsons Disease

Dancing in the Rain: Lessons Learned on my Personal Journey with PD (more at www.PDPlan4Life.com) Copyright 2013-20 Sheryl Jedlinski

Give thanks to “the village people”

Helping people with Parkinson’s disease live well longer takes a village working tirelessly towards a single goal. This Thanksgiving, on behalf of the millions whose lives have been touched by … Continue reading

November 25, 2014 · 4 Comments

Celebrating life’s milestones with a cause

I met my friend Claudia when she was passionately encouraging others to take part in Parkinson’s research and clinical trials. “When they see a middle-aged woman, mother and wife participating … Continue reading

November 18, 2014 · 3 Comments

Courage and team work help us conquer our fears

Courage took center stage at Chicago’s inaugural Partners in Parkinson’s (PiP) event, sponsored by the Michael J. Fox Foundation and Abbvie. Not the kind of courage that roars, but the … Continue reading

November 5, 2014 · 2 Comments

Chance encounters offer opportunity to help

Helping other people with Parkinson’s make a positive difference in their lives often requires nothing more than being in the right place at the right time, and saying the right … Continue reading

October 17, 2014 · 2 Comments

Who says physical therapy can’t be fun?

My physical therapist suggested we have a “play date” at my house so she could evaluate how well I was mastering my virtual reality-based sports games and home exercises. As … Continue reading

September 25, 2014 · 6 Comments

Walking to the beat

As much as I resisted using a walking aid, it was love at first try for my aluminum walking sticks, which are the perfect complement to my bionic knees. I … Continue reading

September 1, 2014 · 3 Comments

“Your Stamina Sucks”

“Sheryl’s stamina sucks.” These were the exact words my physical therapist wrote on my reevaluation form. She drew a grumpy face for added emphasis. “I hope that’s a new medical … Continue reading

August 23, 2014 · 5 Comments

Talk of using walker abruptly ends PD honeymoon

My 15-year honeymoon with Parkinson’s disease ended unexpectedly when my new physical therapist, Mia, completed a three-hour evaluation and recommended I start using a walker. Her words hit me like … Continue reading

July 24, 2014 · 12 Comments

My computer mouse is out to get me

Lately, it seems my computer mouse is out to get me, much like the blood thirsty plant, Audrey II, in the classic story, Little Shop of Horrors. My mouse prefers … Continue reading

February 25, 2014 · 1 Comment

Friends smooth our journey with Parkinson’s

If there is a bright side to living with Parkinson’s, it is the friends we make on our journey, who help us live each day to its fullest – laughing … Continue reading

January 13, 2014 · 3 Comments

This seat is taken!

How many of us, exhausted from running errands, have opted to wait in the car while our spouse handles the last few stops on their own? I do this often, … Continue reading

December 28, 2013 · 2 Comments

Keep fighting the good fight

Early in my journey with Parkinson’s, I drafted a list of potential motor and non-motor symptoms that I feared most. I designated the top three – dementia, hallucinations, and dyskinesia … Continue reading

December 9, 2013 · 3 Comments

Parkinson’s means always having to say, “I’m sorry”

Parkinson’s disease means always having to say, “I’m sorry.” I’m sorry I spilled my drink. I’m sorry I dropped my napkin. I’m sorry I don’t remember, I fell, I had … Continue reading

November 5, 2013 · 6 Comments

Living with Parkinson’s disease colors our world

Things happen that color the way we see the world from that day forward. Learning we have a progressive, incurable disease is one of these things. Although we have good … Continue reading

August 11, 2013 · 8 Comments

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Read more of Sheryl’s humorous stories and helpful tips at PDPlan4Life.com