From Boy Scout to Brain Games: How I Found Clarity in Pips

Constellations are a hoax.

As a Boy Scout, I joined other boys in looking up at the sky, straining to see the Big Dipper. The other kids claimed to recognize it. They were, I am sure, just sucking up to the Scoutmaster.

I, by contrast, reported that the Big Dipper did not exist. I couldn’t see it, which meant it wasn’t there. I explained that constellations are a ruse concocted by Big Astronomy, which just wants to sell us telescopes and planetarium tickets.

The Scoutmaster, clearly compromised by the Space Cartel, rejected my argument. I did not make Eagle Scout.

Maps are another mystery for me. I can handle written directions, but when someone offers to draw me a diagram, I check out.

Words I understand. Pictures? Nope. Where’s Waldo? I haven’t a clue.

It’s not a Parkinson’s thing — I was born this way.

Which Brings Me to Pips

Since my Parkinson’s diagnosis, my #1 fear has been cognitive decline. Although research on the benefits of “brain games” is inconclusive, I took up Sudoku a few months ago. Can’t hurt, might help.

Recently, the New York Times launched an online dominoes game called Pips. My wife, the talented and patient PDXKnitterati, attempted to show me how to play it.



Ms. Knitterati can interpret pictures — she’s a knitting instructor and pattern designer. She sees things I don’t see.

Our Pips lesson did not go well. The instructions made no sense to me. Even in “Easy” mode, I couldn’t figure out where to put the dominoes or why. I quickly lost interest, and after a while we gave up.

Before Parkinson’s, that would’ve been the end of it. But I spent the next morning stewing about the experience.

Would it have made a difference if the dominoes had numbers on them instead of dots? Was my problem with Pips the same one I’ve always had, or was this a sign I was slipping?

If I tried again, could I figure it out? If I figured it out, would that be a sign I was still ok?

I fired up my iPad, went through the Times game tutorial, and tried “Easy” mode again. No luck.

I went to YouTube, found a couple of “How to Play Pips” videos, and watched them both. Went back to “Easy” mode and… completed the puzzle.

Self-diagnosis: cognition intact.

Pips is now part of my daily routine, and I’ve move up to “Medium” difficulty. Perhaps someday I’ll look at a map.

The other night I went outside and looked for the Big Dipper. It wasn’t there.

Hoax.

.

Bonus for Those Who Read to the Bottom

.

“House of the Rising Sun,” but catchier than you may remember it.

.

An acoustic guitar army tackles “Walk This Way.”

.

A “progressive bluegrass” take on the Peter Gabriel classic.

.

The moon landing? Also a hoax. Here’s what really happened.

8 responses to “From Boy Scout to Brain Games: How I Found Clarity in Pips”

  1. homewizard Avatar

    I salute you for trying, and trying again. Perseverance!

    I am playing Pips as well, but I am still distressed that I do not need to match one end of a domino to another.

    Like

    1. shakinstreet.com Avatar

      I’ve never played dominoes, so I had no preconceptions about how the game was supposed to go. Still not 100% sure I like Pips, but it feels like maybe my brain is expanding.

      Like

  2. Kevin Rowan Avatar

    Fine work this week. Being more of a “word guy” I have taken up Quartiles. So far it has kept me from lapsing into dementia. You might give it a try. Via Apple News/puzzles.
    Regarding this week’s video offerings, my fav was the Aerosmith cover. “House” was good also, and “Sledgehammer” was clearly written as a bluegrass song. Trains, hammers, sure. Country stuff.
    Neil Armstrong really did go to the moon. How else did he get moon rocks?

    And you couldn’t see the Big Dipper last night because it was here in McMinnville. Come down. I’ll show you.
    Take care and happy Pip-ing.
    Kevin

    Like

    1. shakinstreet.com Avatar

      McMinnville is a long way to drive — couldn’t the Big Dipper come up to Portland for a few days?

      Like

  3. Gail Avatar
    Gail

    Now that you’ve conquered PIPS, try The Almanac. Free app on my iphone. 4 games that I can usually get done in less than 10 minutes. (Yesterday I think it was more than 20 minutes!)

    Like

    1. shakinstreet.com Avatar

      Gail, thanks for your confidence in me, but I have not exactly conquered Pips yet. I’m still working on the “Medium“ level, and it makes my brain hurt. So I’m going to put The Almanac on the “try some time in the future” list.

      Like

  4. jchrisanthony Avatar

    I worry about cognitive decline as well. I’m not much of a gamer-I get bored quickly. I’ve noticed that my memory is getting worse, but it is hard to know if it is PD or just the aging process. I’ve always joked that I suffer from CRS (can’t remember sh*t) syndrome. Since my diagnosis, I notice these changes and view them through a different lens. I read about cognitive decline and PD, but I can’t remember where.

    What were we talking about?

    It’s not funny, but I have to be able to see a little humor in it.

    Chris

    Like

    1. shakinstreet.com Avatar

      I have also never been fond of online games — but unusual times call for unusual measures. Some people whose advice I respect spoke highly of Sudoku, and my wife made a good case for Pips. Both of them force me to think, and that can’t be a bad thing.

      I have a long and well-documented history of absentmindedness. As you point out, it’s hard to pinpoint where my usual cluelessness ends and Parkinson’s decline begins.

      Like

Leave a reply to Gail Cancel reply

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