Showing posts with label kids. Show all posts
Showing posts with label kids. Show all posts

Wednesday, December 29, 2010

Childhood illness

A coworker's 13-year-old child was recently diagnosed with Type 1 Diabetes. This discovery will change the child's life, as well as the family's, for the foreseeable future.

Learning about this caused me to reflect on my own experience at that age; one that I haven't shared with many people, for no other reason than its impact on my life has drastically diminished since I reached adulthood. But perhaps that in itself can be reassuring to my coworker and her kid -- that after awhile, it just becomes a part of life that you don't even think about.

I'm sure everyone remembers the annual or semi-annual elementary school health screenings. Vision, hearing, lice (ew), scoliosis. Not sure what they're screening for these days. But no doubt everyone remembers "that kid" who had to be pulled out of the classroom a day or two later by the school nurse for re-screening.

7th grade. I had pink glasses then too.
Having to get re-screened for vision wasn't a big deal. In fact, it was kinda cool to get glasses. At least, I thought so. I got lots of compliments on pink squarish plastic frames that were very stylish in fourth grade. Even my bus driver noticed.

But getting pulled out of class for re-screening of anything else was horrifying. I remember we all got kind of tense and uneasy when the school nurse popped her head in the door. "Whose name is she going to call? Please don't let it be me! Please
don't let it be me!"

"I need to see Emily Cole, please."

NOOOOOOOO!!!!!!!!! 

The stares, the whispers (mostly, I suspect, from my fellow classmates vocalizing how happy they were it wasn't them), the teacher restoring order.

That time, I had to be called back for a scoliosis re-screening. And, oh, I had it alright. Big and bad. After the visit to our family doctor, I was referred to a spinal specialist in Minneapolis. I was 10.

Being a kid and getting diagnosed with a chronic disease is awful. Granted, mine wasn't life-threatening. But it did mean some changes were coming my way. And when you're a kid, it is earth-shaking. The most resounding question in my 10-year-old head was,"WHY ME?!"

Not my x-ray, but mine is similar.

Turns out I have double-primary idiopathic scoliosis. In layman's terms: two curves in my spine, which looks like a big S. Looking at me, you probably wouldn't know anything was wrong. But upon closer inspection, you might notice that one shoulder is higher than the other, one pants leg hangs lower than the other and that I tend to stand with all my weight on one foot.

This "hidden" disease was the cause for multiple trips to Minneapolis to the spine specialist. I missed school. Was questioned by classmates. And worst of all, I was terrified that I would need to wear a brace. Think Joan Cusack in Sixteen Candles. The ultimate humiliation.

For awhile, it looked like I wasn't going to need "treatment." My spine was border-line. Each visit to the specialist necessitated x-rays, upon which Dr. Lonstein (who had a fabulous British accent) would draw, using a slide rule and protractor, to determine the severity of the curves and whether they had worsened.

A couple years passed and my spine stayed just inside the safe zone. Until I hit a growth spurt. Then the curves went crazy. "Well, I'm afraid we need to talk about treatment." I was 13. Junior High, where it's torture just trying to act normal enough to fit in and make it through unscathed.

I saw my future flash before my eyes. I was already kind of a nerd. I liked to read and play the flute and paint my nails different colors. And now I was going to have to wear an obnoxious, uncomfortable brace for 23 out of 24 hours each day until I stopped growing. Any shred of social acceptance I had earned for myself would surely be dashed the day I returned to school.

But ---- what's this? There's an alternative to a brace? A new experimental technology called Electro Spinal Orthosis, or ESO for short? And this meant no brace??? SIGN ME UP!

Like this, but on the right side only
And, seeing me on the verge of tears at the idea of wearing a brace, my parents did sign me up. An ESO was basically an electrode muscle contractor. Yes, not unlike those silly "workout your abs without doing a single sit-up" contraptions. Two electrodes were positioned on my back and would contract the muscles at intervals, essentially pushing my spine over and, in theory, preventing the curves from worsening. Since most adolescent growing happens during sleep, the thought was that the muscle contractions / spinal correction would also be most effective during sleep.

So, each night, my mom would slap the electrodes on my back, which had long wires that connected to a control box that I would then turn on and attach to the side of my bed. And my back muscles would contract all night long. Every night. For 1,095 days (give or take).

I was allowed to skip a night here and there, for the occasional sleepover. But otherwise, the electrodes accompanied me on family vacations, to long weekends at relatives', everywhere.

I experienced several fitful and sleepless nights at first. And I think I can speak for my mom when I say it took her awhile to get the hang of positioning and attaching the electrodes every night. But eventually, I got used to it and what started out as an ordeal became a 5 minute addition to my sleeping and waking routines.

Physical effects of scoliosis
For me, the treatment was successful. I think the curves maybe worsened a degree or two during that time, but it was considered acceptable. However, ESO was discontinued as a treatment option shortly after I stopped using it. The research had determined that users experienced mixed results and it was not a reliable method of treatment. I'm just glad it worked for me.

As an adult, I suffer from periodic neck, lower back and hip issues, for which I see a chiropractor. I do a lot of back stretches, which have become second nature. I still have a hard time wearing certain styles of dresses, and my pants will never be even at the cuff, which is frustrating. But, all in all, I consider myself pretty healthy.

My "illness" didn't scar me for life. But I do think it gave me a perspective that I wouldn't have had otherwise. And while each person's situation is different and each experience is unique, it is my hope that the similarities can be reassuring in the end. All we can do is experience it, learn from it, live our lives and in the process, try to help others do the same.

Thursday, July 1, 2010

That'll learn me

It seems I have received my comeuppance. See, in my last blog post, I commented on how Robb & I would have to get our fill of nature during our weekend at Philpott Lake because we'd be spending the following weekend at Shenandoah National Park with three little kids who were sure to scare away any and all signs of wildlife with their rowdiness.

HA!

Reality couldn't have been any more blatantly ironic. After winding through random rural roads, over the river and through the woods, Robb & I finally arrived at the Salthouse Branch campground at Philpott Lake (near Fairy Stone State Park). It was indeed beautiful; the campsites were arranged on terraced loops overlooking the lake and the woods were thick and green.

And then, there were the rebel flags. And rebel yells.

Ah yes, it seems that Philpott Lake is a haven for redneck weekenders. (And I'm only using this term because the people there proudly proclaimed themselves as such.) Noisy trucks, mullets, grubby chubby children, confederate flags, cigarettes, beer bottles, hootin' & hollerin' filled our weekend. The only thing missing were gunshots.

Robb and I were lulled to sleep our first night by the sound of our neighbors --
a father and son spending some quality time together for Father's Day weekend. This invovled drinking, cussing, guffawing, and then wretching until 2 a.m. What better way to say, "I love you," then to holler "DRINK! DRINK! DRINK!" at your dear ol' dad as he is bent over puking his guts out.

I won't elaborate on the rest of our weekend there, but suffice it to say everything was beautiful, except the people. We saw no deer, no birds, no wild animals at all, except for squirrels chasing each other through the treetops and vultures circling overhead. Appropriate.

Our next weekend at Loft Mountain, however, couldn't have been more pleasant. The boys were eager to help and learn and the baby was a happy camper (sorry, couldn't resist). Deer, rabbits, birds and butterflies were plentiful, as were the black raspberries. The weather was warm but comfortable and our mostly-secluded campsites backed up to the woods.

We went on a nature discovery hike with Ranger Georgette (with whom Caleb, the future biologist, instantly bonded) and Nathan was busy helping build campfires and naming boulders (here he is at right, standing on "Kid Mountain"). Eleanor toddled and giggled and picked raspberries. At the risk of speaking for Bill and Jennifer, I think they had a pretty good time themselves. Robbie & I definitely did.

All this to say, touché! Lesson learned! 

The Pattersons at Loft Mountain

Friday, February 12, 2010

Kid art

I love kid art, especially when given to me. Any of these could be framed, hung in a gallery, and sold for a million dollars. However, I'm perfectly content letting these masterpieces adorn my home.

 
fish ink print from neighbor Dameon (age 10), on the refrigerator


abstract painting by niece Gabbi (age 3), on the back of my front door 
[I think it looks like a mushroom on a blue & red background]


  
marker drawings by Katherine (age 3), in the living room
[the left one is my name, and the right one is a picture of her family's house in Idaho,
because I've never been there and she wanted me to see what it looks like.]

What I love about them: no inhibition, no fretting over composition, technique, medium, or whether or not it's any good. Pure and selfless creative expression in the moment, intended as a gift for someone else. 

We adults could take a lesson.