A sense of Humour helps me cope

My latest Parkinson’s escapade? A solo trip to town, naturally. I envisioned myself, a vision of caffeinated grace, gliding through shops, a whirlwind of retail therapy. Oh, how naive I was. Turns out, the town has opinions about my particular brand of parkinsonian swagger.

First stop, the bank. The automatic doors welcomed the person in front of me like a long-lost relative. Me? They treated me like a suspicious package. A slow, juddering shuffle later, I bounced off the cash machine and, in a move that would make a gymnast weep with envy, landed squarely in a chair by the cashier’s window. “Nailed it,” I thought, only to realize I’d just pole-vaulted over two perfectly healthy queue-standers, earning me the “you cut in line, you monster” glare.

Then, the meds decided to take a vacation. They were in my bag, of course, which was now five yards away, having staged a dramatic escape from my shoulder during my grand entrance. Meanwhile, my body had decided to audition for Cirque du Soleil, contorting itself on a bank chair clearly designed by Torquemada’s less-talented nephew. My dopamine levels plummeted faster than a politician’s approval rating, and I heard the echo of “NEXT! NEXT!” from the cashier’s desk, another five yards distant.

This cashier, clearly trained in battlefield medicine at the local GP’s office, beckoned me with the warmth of a tax audit. “I have Parkinson’s!” I bellowed, at which point the queue parted like the Red Sea, probably expecting locusts.

Finally, a manager in what I can only assume was a hazmat suit approached, cautiously retrieved my bag, and watched me down my meds like I was defusing a bomb. Then, the cherry on top: “Early closing!” I was gently ushered out the door, another day in the life of Parky Bear.
:grinning:

7 Likes

Hello Dave23. I have a neighbour with opinions about Parkinsonian swagger. I live independently doing my own cleaning, shopping, cooking etc. She thinks that “people with stuff like that” ie Parkinsons, should be put in a nursing home. I deal with it by writing very rude limericks. This gives me an important aim in life. I will have to outlive her to be able to publish.

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Morning unfortunatly we meet these so called outspoken people i meet them quite regular had the odd one quistioning my stories about Park bear but its about me as bening able to still laugh against parkinsons helps me cope Im just polite and say ita upto them if they find a problem with my stories i respect there point of view but its not mine We all deal with parkinsons diffently good luck with the limericks

In the past i’ve always poked fun at my condition & got some very strange looks but that’s me. As I am a bit older so the condition is a little worse but i’m still here to tell the tale !!

Dave23,
That was bloody brilliant. :joy:
:rofl:
I really think you should go out more and regale us with your experiences.
Laughter is a great medicine.
But seriously I totally understand the frustration and the way people behave.
We can either laugh or cry.
It is much easier to laugh.

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Hi Dave

I know where you are coming from it’s so frustrating going out by yourself. Most people don’t even give you a second look some treat you as if you are insane having a fit and should not be allowed out on your own. On the other hand sometimes see past the shaking slow speaking forgetting where you are taking about. These people probably now someone who has PD and can spot the signs. They treat you as a person and not a victim of our ailments. My close friends and family sometimes find it hard to accept I have PD and find it hard to understand why I don’t seem to be getting better?
They can’t understand why I am always try to do too much my self as I find it hard to ask.
Sorry to harp on good look Dave keep you head up high and make the smile.

Davesan

As your self I to have a wicked sense of humour