There is nothing to love about falls in Parkinson’s disease
“Parkinson’s is like falling in love — without the love.” I saw this quote on social media a few months ago, and it made me chuckle. I thought it would be good to…
Living My Best Life — Christine Scheer
Christine Scheer was diagnosed in 2015, at the age of 54, with Parkinson’s disease. She is a retired chef who lives on a farm with her husband, John, in London, Ontario, Canada. She firmly believes in the power of exercise to slow down the progression of Parkinson’s. Her hope for her column, “Living My Best Life,” is that she can get conversations started and raise awareness by engaging those in the PD community and beyond.
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The things we don’t like talking about, part 2
Last in a series. Read part one. Recently, I had terrible abdominal pain in the middle of the night. It was so bad that I was doubled over and couldn’t sleep. I thought…
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Newly diagnosed with Parkinson’s disease? You’re not alone.
Do you remember those early days when you were newly diagnosed with Parkinson’s disease? Can you think of anything someone could’ve said to make you feel better? What do you wish they would’ve…
With Parkinson’s, Botox isn’t a walk in the park, but it helps me walk
Note: This column describes the author’s own experiences with Botox. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. The best way I can describe…
I’ve vowed to not let Parkinson’s prevent me from enjoying life
Is there something you’ve always wanted to do but never got around to doing it? For me, that thing was pottery. I believed it was something I could master, and that it’d fill a…
Navigating the effects of Parkinson’s disease on speech, part 3
Last in a series. Read parts one and two. Before I was diagnosed with Parkinson’s disease in 2015, I used to love getting in front of people to talk to them,…
Navigating the effects of Parkinson’s disease on speech, part 2
Second in a series. Read part one. Every Tuesday I go on a walk with my Parkinson’s buddies. I started this “walk ‘n’ talk” group after my deep brain stimulation (DBS)…
Navigating the effects of Parkinson’s disease on speech, part 1
First in a series. I recently heard a rumor that I wasn’t doing very well. An old friend dropped by and spoke to my husband, John. The friend said he’d heard from someone else…
How I’m changing my mindset to realize my full potential
In the fall of 1986, I worked as a chef at the Black Swan Café in London, Ontario, Canada. The café was on Richmond Street, one of the city’s busier streets for restaurants and…
Advocating for yourself as a patient can be hard, but it’s crucial
In 2015, during the early days of my Parkinson’s diagnosis, everything was a blur and I didn’t know where to turn. I had just started seeing a new physiotherapist whom I immediately…
Fitness, friendships, and fun: The benefits of boxing with Parkinson’s
When I was diagnosed with Parkinson’s in 2015, I didn’t know anyone else with the disease. Then I joined Rock Steady Boxing, a program designed specifically for those of us with…
Parkinson’s disease fundraisers can actually be fun, I’ve found
It’s that time of year again: time for our annual Walk for Parkinson’s. I hate asking people for money, even for such a worthwhile cause as our local Parkinson’s Society here in…
How I’m doing 3 years after deep brain stimulation for Parkinson’s
Note: This column describes the author’s own experiences with deep brain stimulation for Parkinson’s disease. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a…
