Steering Downhill: You Have More Control Than You Think

I once slid down Mount Hood on my butt.

Perhaps I should explain.

Several decades ago, I signed up for a college mountaineering class and climbed Mount Hood. On the way down, our instructor taught us to glissade.

Glissading, says Wikipedia, is

…a climbing technique mostly used in mountaineering and alpine climbing where a climber starts a controlled slide down a snow and/or ice slope to speed up their descent…

Most glissading is done in a seated position…with the legs bent to absorb shocks and bumps, and an ice axe held diagonally across the body to be in a position to perform a self-arrest if the glissade starts to get out of control.

When I first sat down in the snow and pushed, I didn’t move. Then I was flying—too fast. I jammed the axe into the slope, bounced over some rocks, and finally stopped, shaking and exhilarated.

Full disclosure: I did not slide ALL THE WAY down Mount Hood — it was maybe a hundred feet. But this is my blog, and I will exaggerate whenever I damn well feel like it.

I’ll also admit to a moment of panic… a short section where it felt like I was about to become mountain pizza.

What brought me back under control? The ice axe, and a mountaineering instructor who’d taught me to steer.

I thought about that ride as a read this passage in Lewis Richmond’s Aging As a Spiritual Practice:

Once, one of my workshop attendees raised his hand and half jokingly said, “I’m fifty-eight and I know where I’m headed – downhill. It’s all downhill from here.”

I thought for a moment and replied, “well, I’m not sure I agree, but even if you’re right, the real question is: are you going to just slide, or are you going to steer?”

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We’re all heading downhill. As we get older, the parts wear out — and not all of them can be replaced. Add a Parkinson’s diagnosis to the mix, and it’s tempting to lie down on the couch and cry.

Which I’ve done, on occasion. I’m not a pretty crier.

But as 2026 gets underway, there are many opportunities for us to influence the journey.

  • Medications and surgery to control the symptoms.
  • Exercise programs to slow the progression — sometimes for many years.
  • Support groups to put us in a room with others who understand what we’re dealing with.
  • Clinical trials testing a wide variety of therapies and potential cures.

In the r/Parkinsons subgroup on Reddit, a poster called OldRounder recently discussed his decision to take up basketball after a several-decades break. He’d been a good player into his 40’s. Now he was near 60, with Parkinson’s.

His first few times on the court didn’t go well, but he stuck with it:

 It was shocking how much my skills had degraded. My right hand was weak and uncoordinated. I could barely hit two out of 10 free throws and shot mostly air balls. Dribbling was a joke. That was in February of this year. I’ve been doing basketball workouts 3 + times a week since then.

Gradually, in fits and starts, my skills started improving. Before, shooting a basketball was something that just came second nature to me. Pure muscle memory. Never thought about it. Now I had to train my entire brain and body to move and shoot again. There were times when I would hit two or three shots in a row and then two or three air balls because I didn’t have control with my body anymore. It was like there was a blockage between my brain and my body.

Today was the first time I hit ten free throws in a row. I had to concentrate on every aspect of the shooting motion, but I was able to do it. It doesn’t sound like much of an achievement, but it literally took hundreds of hours to get here. More importantly, it took belief in myself that I could improve and do it.

A Parkinson’s diagnosis tries to convince us the downhill journey will be bumpy and painful, with an ugly crash at the bottom.

Maybe. But it doesn’t have to be passive. We have the opportunity to live well on the way down.

Every day there are tens of thousands of people like OldRounder at boxing gyms, ping pong tables and pickleball courts, dance classes, and support groups who have decided to exercise agency over the disease.

We can lie back and slide to the bottom. Or we can grab an ice axe and steer.

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Bonus for Those Who Read to the Bottom

The “Munsters” theme as a surf instrumental.

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There aren’t a lot of Toto covers played on vegetables. Or fruit. Or squash, which I have learned is sometimes classified as a fruit and at other times as a vegetable.

Anyway, enjoy “Africa,” which begins at 1:40.

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Fifteen years ago, some guy posted a strange-but-compelling ukulele cover of “Like a Rolling Stone.” In 2026 I found it.

6 responses to “Steering Downhill: You Have More Control Than You Think”

  1. jchrisanthony Avatar

    Great post. Note to self: procure an ice axe. 🙂

    Unfortunately, we don’t all have the resources available in our areas. I will begin Rock Steady Boxing in two weeks, as I will complete my cardio regimen next week. Unfortunately, the closest location is about an hour away. Regular exercise is key, as you well know. I find that skipping for even just a few days sets me back, which is good reason to not skip.

    I notice that you travel a bit. How do you keep up with your regimen when you are globe-trotting? We are scheduled to go to Europe for a couple of weeks in July. Hoping I can find a way to stay active.

    Like

    1. shakinstreet.com Avatar

      I am always nervous about skipping a day — I’m convinced Parkinson’s (“Phil” to you, “Ohtani” to me) is waiting for me to slack off so it can take a bite.

      Traveling is one of those “do the best you can” situations. I’m partial to the road-warrior hotel chains — a Hampton Inn or Holiday Inn Express will usually have some sort of gym. Even the bad gyms generally have a treadmill, and some of them are pretty well-equipped.

      In Kona last month I found a gym with Rock Steady Boxing classes twice a week. I bought a one-week pass, went to RSB twice, and used the treadmill three other days.

      For what it’s worth, Rock Steady Boxing claims to have programs in several European countries, although you may encounter a language barrier. Worth investigating, anyway.

      https://members.rocksteadyboxing.org/internationaldirectory

      Like

  2. Adventure Friendship Avatar

    Wonderful post—informative, exciting, and enjoyable to read.

    Like

  3. Sharon Bergman Avatar
    Sharon Bergman

    I enjoyed reading your inspiring and encouraging post. OldRounder’s experience getting back into basketball makes me want to take line dancing lessons again. I stopped because it wasn’t as fun anymore due to losing some coordination. I’d like to try it again and see if I can build some new neural pathways. There’s also contra dancing which got too fast for me and I miss it so much. I’d like to see if the organizers for the dance I used to attend would include an occasional slower paced dance for ones like me.

    To make up for losses I have added in some new hobbies such as ping pong and wall climbing both of which give me a lot of joy and also improve my symptoms. Overall, I’m doing my best to steer and I try to put fun in every day.

    And I always enjoy your videos. My favorite this time is the Munster theme song. Love it. I grew up watching The Munsters at dinner time. : )

    Like

    1. shakinstreet.com Avatar

      Thanks for the insightful comment Sharon.

      We all have to negotiate with our expectations and our bodies. Adjusting our expectations is a challenging exercise, but a necessary one. OldRounder built some new neural pathways and managed significant improvement — but he recognizes he’ll never be the basketball player he once was. 10 free throws in a row is a huge achievement for him, and he seems reconciled to the possibility that he may be approaching his post-diagnosis upper limit.

      The Parkinson’s challenge is to negotiate a way to enjoy line dancing or contra dancing even if you never regain 100% of your old skill. The opportunity is there.

      Like

  4. […] reading my post about Redditor OldRounder’s return to the basketball court, Shakin’ Street subscriber Sharon Bergman writes that she’s thinking about taking up […]

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I’m Phil Bernstein

I was diagnosed with Parkinson’s Disease on May 25, 2023. At the time, I was only vaguely aware of Parkinson’s — primarily from articles in People about Michael J. Fox. And I didn’t know anyone with the disease.

Now, I know a lot more about the illness, and I’ve joined the Parkinson’s community in my hometown of Portland, Oregon.

I’ve found that writing helps me think through challenges, and this illness definitely qualifies as a challenge. I’ve started Shakin’ Street to help me think through the various obstacles, tools, and resources that a newly-diagnosed Parkinson’s patient encounters along the way.

I hope some of these posts help you address and tackle your own challenges.

Let’s connect