I read somewhere that we spend our lives before we become parents running away from trouble, and our entire lives after becoming parents running towards that same trouble. For example, when I heard a scream back in the day I would move away from it, with the thought that whoever’s causing the screams might decide I’m a better source of torture. If there’s a messy situation with a spider crawling on the bathroom wall, well, that’s what parents are for. “Mooooom!” I’d say, and it would be taken care of while I was cowering in my bedroom.
Now I’m the one taking care of the problems, and I’ve learned to run to the source of those screams instead of away from it. It’s funny, but when I first became a father, my first inclination just switched. Like flipping a wall switch, actually. And all the parents I knew told me “several things will happen the moment you become a parent.” Here’s a comprehensive list:
“You will learn to awaken at odd hours and sleep when you can. And be able to operate off of whatever sleep you (don’t) get.
“You will suddenly become a safer driver.”
“Your current fears will become secondary to your kids’ fears.”
I have to admit that my nearly 8-year old (her birthday is Friday) never ceases to amaze me with what she thinks about. Once, about a month ago, I brought up the idea of making difficult hypothetical choices, such as, “What would you rather be, stranded on a desert island or stuck in a building … Continue reading Chatting With Lexi: On Spending Time
My wife heard back from the doctor a week after the testing was done to see whether or not Alexa had Cystic Fibrosis, and the word back was that the test was inconclusive. They would have to do genetic testing to see whether or not she tested positive, and in the meantime we would have to keep waiting. Over a month later and we were still in that holding pattern, completing the treatments twice a day, and dealing with the weight of knowing we were one step closer to our child possibly having CF, something we were supposed to be “simply ruling out” with the initial test.
And during that time period we worried. What you need to know about my wife is that in our relationship she’s the worrier on the outside, and me, I’m the worrier on the inside. I might look like I’m doing just fine, but underneath the facade I’m freaking out. In fact, sometimes I just sit still and shake because I’m so worried. It happened when I was so worried that Madeline might have DS, but then when she tested positive for it it was okay. I was able to deal with it, and I figured that would be the same way with Alexa and the possibility of CF. The possibility worried me a lot more than the actual diagnosis, because if the diagnosis came back that she had it then I could make a plan, then I could deal with it.
But Heidi, she worries from the start, and it shows on her face and in her demeanor. Reading about all the issues that children with CF have, she had driven herself into the cycle of “what if.” And don’t get me wrong. I’m not saying her way of dealing with it is wrong. It’s just different how we approach things, but we eventually get to the same place. If that place is acceptance, then we work on it, and if it’s a sigh of relief then we sigh at the same time. We were both preparing ourselves for the possibilities during that month, just in our different ways. Continue reading “Disturbance at the Heron House: Volume 3”
I am constantly astounded by the resiliency of children, the way they can adjust to just about anything, no matter how odd it is or how much it differs from their previous pattern, even my children. Now, if you know my children at all you’ll realize that they are pretty rigid in the things they do and like. For example, my 5-year old, Madeline, likes to play CandyLand, followed by Chutes & Ladders, and it has to be in that order. She also likes to try and cheat at both, but we’re working on keeping her honest. My 7-year old, Alexa, refuses to eat homemade macaroni & cheese (unless bribed with the promise of some sort of desert at the end of the mac and cheese rainbow), but she absolutely adores boxed mac & cheese with the fake orange “cheese.”
They are both also relatively stubborn when it comes to activities to do. Alexa likes to be in charge, but Madeline is not your classic follower. If there’s something she doesn’t want to do, she just won’t do it, even if they’re in the middle of it already. So, when Alexa came home from the hospital after her bronchoscopy in November, it was interesting to note how quickly both of them adjusted to the new way of life around here. I’ll explain…
Alexa had to have two “vest” administrations per day, one in the morning and one at night. The “vest” is an actual vest that inflates using two tubes attached to a powerful little machine that pushes air into the vest. It operates on escalating levels of what equates to vigorous shaking of her body in order to break up whatever mucous remained in her left lung.
Alexa also needed to have various inhalants as treatments, all of which were designed to open up her airways so that when the mucous was broken up by the vigorous shaking it would come out of the lung altogether and she would aspirate it. These treatments were also twice a day, and generally took place at the same time as the vest treatments.
During all of these treatments Alexa was far and away our focal point, which was a massive change from how things had been to that point. Because Madeline has Down syndrome it had become routine to focus on her health more so than the health of Alexa, and the issues that sent Alexa to the emergency room and then to surgery woke us up to that.
While Alexa was in the hospital, my wife Heidi stayed with her for the entire five tumultuous days, and I was back and forth from the hospital, to home, to work, and back to the hospital. It was ironically reminiscent of when Alexa was born. We weren’t sure of the time of her operation, or even what we were really dealing with for a while, and during the whole back and forth Madeline was with me, and then with her grandmother, and then back with me. Continue reading “Disturbance at the Heron House: Volume 1”
I am partial to spanking. Please don’t hit me for saying that, but it’s true. I mean, you know as well as I do that most people are forgetful, especially when it comes to things they don’t want to remember, especially kids. So, why not use the method most likely to get them to remember: the physical reminder? I learned from an early age to equate getting hit with having done something bad.
My childhood was memorable for many reasons, not the least of which were the spankings I received quickly and often. Both of my parents grew up in the school of “spare the rod and spoil the child.” In fact, I heard that exact phrase more times than I would care to admit. Of course, even when they weren’t beating me and I was well-behaved (admittedly not that often), I don’t think anyone would have classified my existence as spoiled. So, to me that didn’t fly, but it didn’t stop them from spanking me when I was bad.
I dreaded those four words. Separately they weren’t so bad. I could adjust to them if they were attached to other words, but when they were put together, back to back, they inspired a sense of helplessness, of uncertainty, and mostly of frustration. And, ironically, I heard them more often than not the older I got, whenever I asked my mother a question. Because I said so.
You’ve heard it before. You’ve probably even used it before. Believe me, I have. But have you ever really stopped and wondered why parents tend to rely on this classic gem when answering their children’s fervent questions?