It is hard to see, but on the left side of the "The Gad About Town" tab (at least on a Windows browser) there is a little square box that looks like a blob of brown and green. I first placed it there as an inside joke with myself, but the story is worth sharing.
It is a photo of a duck.
In 2012, I was diagnosed with a still-undetermined form of spinocerebellar ataxia. (I just noticed that the word "spinocerebellar" now freely flows from my fingers as I type it; I insist on Wikipedia'ing it to check the spelling--to preserve the illusion to myself that this is still new to me--but it is now forever in my vocabulary.) This disease, which I have written about before ("Ataxia") and will again, is progressive, degenerative, affects my sense of balance, and is robbing me of my physical control of my legs.
My symptoms first appeared in 2006, I now realize, when my walking began to slow. I was always a rapid walker, and I felt like I was moving my legs in the same way I had always moved them, but the time it took for me to complete familiar walks was getting ever longer. Even in 2005, while mowing a friend's lawn, I noticed that it took me longer than it "ought to" have. My legs were tiring easily. Finally, I started to run late for appointments (most hazardously, my job across town) and was perennially underestimating the time it would take me to walk somewhere.
All this was new. I shared what I was experiencing with no one, except to promise when my lateness was noticed that I would "do better" next time.
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A blue heron, patrolling the shore like a cop on the beat.--Photo by Mark Aldrich |
There are usually a few breeds of duck on the pond, and my friends and I became "expert" in observing the inter-species social behaviors of the different breeds. (In a word, some breeds are just bullies, even to humans who are feeding them breadcrumbs.) We developed story lines about each duck family's day.
One family of five, a mother duck and her four ducklings, became "my" family. This was because one of her offspring was lame. He or she--I decided he was a he, but I believe it is a she (those who know about such things can tell immediately when looking at the photo below)--appeared to have a broken right leg. Cute and small as they all were, the four of them fuzzy and adorable like they were posing for a children's book cover, the siblings would push him away from our breadcrumbs, but he always fought hard for his share.
Broken or born that way, he held his leg tucked alongside, which forced him to remain seated on the ground when the others were toddling towards the crumbs. Then, in a flurry of action, he would start to wobbly waddle, but he was perpetually a few steps behind. He was slow in other ways, too: by the time his siblings were free of their baby fuzz and displaying more grown-up plumage, he still had some fuzz.
I saw that, even with his right leg held in a crook, even sitting awkwardly on the ground, once he started walking, after a few unsteady strides he would catch up to his siblings. But he honked just as loudly as they did, each of them telling the others to mind their manners at the top of their voices. In the water, he appeared to swim as quickly as the others.
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In 2008, the bizarre sensation of being always on the edge of a fall became a part of my life. I could not walk across a parking lot without first looking across it to plan which cars I would use as targets for potential falls. I started walking with a cane.
Faced with the prospect of crossing an empty parking lot (I worked for an electronics retailer that frequently locates its stores in open-air plazas, so that is why I have twice mentioned parking lots), I would look for an abandoned shopping cart (there was a grocery store nearby) and use that as a walker.
As before, I shared what I was experiencing with no one, except sometimes I made jokes about walking with a cane--I named it "Michael," as in the actor--and I did not have a doctor, because I was 40 and a guy and why bother?
I did not have a doctor, because 40. I was 40 and my legs felt like they were in boots nailed to the ground. I would take a step only to find that neither leg moved.
By 2011, completely foreseeable circumstances had given me the beautiful gift of poverty and thus Medicaid. Now able to afford a few visits to a neurologist, I underwent the series of tests that led to my diagnosis.
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On our next visit, two weeks later, he was still there. Of course. He was still missing every first chance at breadcrumbs--even those tossed specifically at him--but fought his siblings to get his crumbs once he started moving. They still pushed him away from their second and third chances at crumbs on the ground, but he was louder than the others and was getting faster, even limping, but doing something like using his lame limb like a cane. He was using his lame leg.
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I use a method of walking that I devised without knowing what I was doing back at the electronics store: I push off with my right leg, like a right-handed pitcher, and swing my legs under me, using the cane to tap a rhythm. Once I get myself up to speed, I can outpace many of my friends. It is difficult for me to stop suddenly, like when I am jay-walking, so I do not do that. There are days where I do not know what my legs are going to do and we seem to educate each other.
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Two friends who walk with me step by step. |
Because I have a diagnosis, I know why I am experiencing these things, and new developments can no longer be as surprising as the discovery in 2008 that it seemed that I could no longer walk. Because I have friends in whom I confide (like you who may be reading this), any new development will not be experienced like running head-first into a wall, which is how it felt for me in 2008.
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My buddy.--Photo by Mark Aldrich |
This is the photo that accompanies this blog, next to "The Gad About Town" name. He is my duck about town.
It is now December and I hope he is still with us, but in the warm south, ornery at his siblings every staggered step of the way.
Thanks, Mark. I'll be thinking of your duck.
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