special needs

Don’t Look at the Whole Staircase

Chris Irvine, Parent CoachLeave a comment

I like to think I have some natural gifts that lend themselves to good parenting. I believe I am empathetic, creative, logical and kind, which helps me connect to people in general and my kids in particular. That’s not to say these qualities are always activated when I’m parenting. Perhaps I’m using one or another, or perhaps they’ve all flown out the window in a moment of frustration or exhaustion.

I also happen to have two of the least fickle kids on the planet. Once they decide, They Have Decided. On whatever it is. Maddie’s way of expressing her decisiveness is the simple act of refusing to bend. She has decided not go to to Thanksgiving at Grandma’s, for example, so there is nothing you can say or do, no threat of punishment or offer of reward, that will alter her decision. The answer is no, and that’s that. We can make our whole family insane trying to change her mind, and the likely outcome involves not even a glimmer of hope. There are exceptions, of course. Like when I was trying to potty train a nearly four-year old kid who just wasn’t interested in the process, so I started challenging her to race me to the bathroom. I think it worked twice, and then that was the end of that. Still, I was thrilled with my double victory.

My son’s way is different. He can argue you into a rabid, frenzied froth of frustration. You will never win that argument. You might not lose it either, but as a parent not winning is pretty much the same as losing. I had an early indication of his logic skills when he was a five-year old preschooler. He had shut the door to his room, which was unusual, so I thought I’d better investigate. I soon discovered he was in his closet, door closed. He had to be up to something. “What do you have in there?” I queried. Out stretched a hand holding a box of goldfish crackers. “Why are you hiding those?” I asked. “If you had asked me I would have said yes.” And then something dawned on me. “What else do you have in there?” Out stretched his hand with what turned out to be decoy number two: a box of Teddy Grahams. I repeated my response. I was detecting a pattern. “What ELSE do you have in there?” And there it was, a bag of chocolate chips. And that was NOT okay with me. That evil genius had rolled out his decoys in hopes of avoiding the final discovery. “We’re screwed,” I told my husband. Some years later – maybe he was eight – he effectively asked me a series questions, knowing how I would answer, so that I would actually lead myself to his desired conclusion. I don’t remember the topic, but I do remember realizing what was happening just before he succeeded.

I am reminded of our friend’s mom who early on recognized our challenge with Maddie. “Her stubbornness will serve her well when she’s grown. The hard part is getting from here to there.” Amen, Joan, amen. Same for our son, I’m sure.

So anytime I can talk my kids into anything, I’m surprised and delighted and pretty darn proud of myself.

A couple weeks ago my niece M turned 18. Maddie and M are only nine months apart and truly the best of friends. Our families live about 45 minutes away from each other. M is incredibly busy, so the girls don’t see each other as much as they’d like. So you would think, wouldn’t you, that the upcoming party and sleepover would be unmissable.

As I try to do with Maddie, I had reminded her each day for a few days to prepare her for the event. Late morning the day of the party I sat down on Maddie’s bed and said, “We should leave around three o’clock today.”

And to my surprise she responded, “I have been trying to motivate myself all week, and I just haven’t been able to do it.”

All the months since she graduated high school, I have been avoiding, as much as possible, any situation that involved making Maddie go somewhere. After all those years of morning turmoil, I realized not only did I no longer have the energy to take on that fight, but that the fight was futile anyway. So much wasted effort, so much heart-attack inducing frustration that ultimately had no positive effect—I just couldn’t go back to that. And yet here I was.  I could feel the tightness in my chest forming almost immediately. We couldn’t let our sweet M down on her big day. And I really wanted Maddie to enjoy what I was certain would be a good night. What was I going to do?

I pulled myself together enough to say, “I think it’s been about two weeks since you went anywhere. That happens to me too, like when I’m sick for a week and I’ve been at home, it’s just easier to stay home than go anywhere. Eventually I just make myself go somewhere and then it gets easier. It happens to everyone,” I assured her.

She was still unmoved.

“OK,” I said. “Forget about going all the way up to M’s house. Let’s just think of something small to do first. Like maybe we could go to the coffee shop for lunch.” Originally I had required she take a shower, but I realized that was a serious obstacle, so I let that go.

“Is How to Train Your Dragon playing anywhere?“ she asked. A glimmer of hope!

“I’m sure it is!”

So we picked a movie time that allowed us a quick lunch out and would also get us to the party in time. I said, “Just throw your toothbrush and toothpaste in your bag in case we get up to M’s.”

Don’t look at the whole staircase. Just look at the first step.

I’m sure I’d heard that before but it wasn’t until a week or two later that a motivational speaker I was watching used that phrase. I had put it into practice without naming it, and to my amazement and delight, it worked. Just like all the times I folded Maddie’s writing assignment page in half so it didn’t look so scary. “Just do a Maddie-sized essay,” I’d say. Just one small step at a time.

We had our quick lunch (delicious and fun!), drove north to the movie (love those Dragon movies!) and it was an easy and welcome third step to drive further north to see her cousin. She was happy to be there and, as expected, she had a wonderful time.

I patted myself on the back or a job well done. But not because I won a battle. It was because I used one or two of my gifts at the right time to look at my daughter and see what she needed. Just a peek at the first step!

Nailed it.

The Brave Speak for Those Who Can’t

Chris Irvine, Parent CoachLeave a comment

A friend recently asked me for advice. She has a family member whose toddler shows signs of autism. Knowing the importance and impact of early intervention, she  wants desperately to say something to the parents and suggest their child be assessed. She also has experience as an educator and parent that helps inform her suspicions. So, let’s say she brings up this tough issue and the parents take offense.  Based on what she told me, that’s not an unlikely response.

Does she risk upsetting her relationship with the parents to advocate for the child? That’s a tough choice to make, but I think that answer is yes.

Here was my reassurance to her, which I hope she can pass on to her relative:

  1. Getting a diagnosis doesn’t make autism (or whatever it may be) any truer than it is without the diagnosis.  In that moment that word is uttered in reference to a child (or adult), the person hasn’t changed. She is exactly who she was the moment before.
  2. One gift of the diagnosis is a life-changing light suddenly shone on your child. Many of the questions you may have had are quite suddenly answered. Not all of the questions, of course, because each child (on the spectrum or not) is a unique individual. But you can begin the process of understanding your child in a new way, enabling you to parent them with newfound empathy and patience.
  3. Another gift – and I cannot stress this enough – is that services become more readily available to you. Since Maddie was not diagnosed until around age 10, she struggled through elementary school as the teachers and staff struggled to understand her. And then, magically, we had the word “Asperger’s” to throw around and suddenly Maddie was less of an enigma despite having not changed a bit. Was everything magically solved at that point? Certainly not, but instead of just being the smart, stubborn kid who refused to perform, or the weird kid who repeated the word “paperclip” over and over until she was eventually sent outside the classroom, or the kid who would hide during school hours, throwing the staff into a frenzy, she became a more sympathetic person who deserved compassion and help. It makes me so sad to think about the years she was misunderstood and therefore mistreated.

I was recently talking with a friend in her 40s who has chosen not to have children. If she ever changed her mind, she said, she would want to go right into the teenage years, skipping right past all the noise and messiness that comes with babies and young children. We agreed adopting an older child is fraught with uncertainty, but then I pointed out that even when you have a baby, it’s still a roll of the dice. Your child might become an Oscar-winning actress, or a homeless addict, or a high school valedictorian who goes on to solve world poverty or goes to jail for insider training. Or she might have autism. Or some combination of those things.

Certainly the dreams of an expectant couple do not include addiction or a prison sentence. Or autism (to be clear, I’m not equating autism to either of those things). And yet a diagnosis of autism is an increasingly likely outcome of an assessment. Awareness and the ability to diagnose autism have improved dramatically over the last decade or two, but depending upon the trajectory of a child’s development, and depending upon their gender (boys are more likely than girls to get an early diagnosis), a chid may still go for years without getting a diagnosis and therefore the appropriate help. I know because that’s what happened to us. So many years of pain and frustration and confusion could have been avoided. There are so many things I would have approached differently if only I had better understood the daughter I so desperately wanted to know.

For my entire life deep in my soul I have believed in speaking up for those who cannot speak for themselves. If anybody qualifies for that, it’s a young child with autism. It might take some real courage to speak the words, “Have you thought about having Reilly assessed?” Or “I’ve heard of some services that might benefit Sophia.” But remember, you might be the only person to utter the magic words that eventually open the door to early intervention, a deeper understanding of that child, and continued services throughout that child’s educational experience and beyond.

If you know a family who needs help navigating this special realm of parenting, or who hasn’t dared consider autism or a learning difference a possibility, look into yourself and see if you can find the courage to speak up as an advocate for that child. A gentle observation or suggestion, or a connection to a free assessment, could change the lives of the whole family forever.

Be brave. Speak up with love and compassion. And know in your heart you’re doing the right thing.

And even if you can’t, I still love you.

The Experiment Continues

Chris Irvine, Parent CoachLeave a comment

In August 2015 I had what turned out to be a knee-slapper of an idea: The school year that was about to begin would somehow be The Big Experiment. Maddie was about to to start public high school as a sophomore after three years at a private special education school, and after a year of battling with her over attendance on a daily basis, and years of thinking and thinking and wondering and planning and getting disappointed and crushed and then reviving myself for the next round, we had decided This Was It: It was either This (the public high school)—or boarding school. The idea behind boarding school was since the kids sleep and wake up AT school, they can’t not GO to school. They’re already there! And that’s what I so desperately wanted for my bright, talented, interesting, lovable kid: to GO to school.  Well, and to not have to freak out every single morning over her refusal. I had felt the years of my life slipping away from me as the stress built up in my body and mind. It really was taking a toll, so something had to be done.

Nearly three years—and another new school—later, I realize how naive and narrow-minded my thinking was. The idea that somehow it would all sort itself out in that defined period of time is absurd to me now. What was I thinking? I don’t know exactly, but let me tell you, it got a whole lot worse before it got better.

I’m not sure how many times my therapist had to tell me that just because going to school was what I would have wanted, just because I thought the social part was important, or just because I really thought going to a dance was an important part of the high school experience, those things would necessarily have any meaning for Maddie. It wasn’t until Maddie basically quit going to school in October of her junior year (2016), and I fully gave in to the concept of her not going to school, that I also fully comprehended not only how differently we are made but also how perfectly fine those differences are.

We worked with the school to complete her junior year’s coursework basically in a home-schooling capacity.  But at the end of the year we had to make a decision. The public school is not in the business of home-schooling, we were told. The teachers and administration had been so accommodating! They had bent over backwards to make things work for us, but they could not continue merely sending home work for Maddie to complete without having her attend at least part of the time. They had revised schedules, reduced schedules, minimized the amount of time she would need to be there, but ultimately it just wasn’t happening, so we absolutely had to take another route.

If you are the parent of a child with special needs, you can imagine my mental state at this point. Every new attempt to make things work is fraught with anxiety because you know it may or may not work and then you’ll have to go through the process all over again. You’ll have to rethink and rework and research and try, yet again, to make the best choice for your child, knowing full well this may be just another attempt in a long line of failed attempts to get it right.

With the help of two consultants, we landed on public online high school for senior year. Online because Maddie could literally do school in bed. Public for several reasons: she would have an IEP and they would have to make accommodations; it follows the state curriculum so she would have a diploma from an accredited school in case she wants to go to college at some point; and it’s free. We still pay a lot of money to the educational consultant who works with Maddie twice a week and manages her workload, so free is a welcome bonus.

And guess what? It’s working! There have been ups and downs, particularly for me. Last summer during a meeting with our consultants, one of them mentioned she thought my motivation was to manage all of Maddie’s schooling for this year. “Um, nooooo!” I clarified. “If I had my choice, I would have literally nothing to do with it.” And I meant that. I’ve had it “up to here” with the stress of it all and would gladly have gone on my merry way and let those two ladies work it all out with Maddie and I could just make her food, badger her into taking showers, and then have fun with her. That sounded perfect! “You all just work this out, and call me when she graduates!”

As it turns out, I have participated quite a bit, but our educational therapist is the Overseer of Things, and for that I am grateful. The stress of the school battle was quite literally killing me and I needed to hand over part of the responsibility to somebody else at least for awhile.

I’ll write more about the experience of online school later, but for now I’ll just say this: What I thought was going to be an experiment with an end date and some sort of answer was indeed an experiment, but one without an end. This whole parenting thing is an experiment. I’m still working on it. We are still working on it. There is a lot of talk about what’s next (that’s another blog entry), and I don’t know what that is yet, but it will be something and then something after that and then something after that. And we will forge on, trying to have fun along the way and not losing sight of the end goal: a content, fulfilled, secure human being. In that part of the experiment, I’m pretty confident we’re succeeding.

And Maddie will graduate on June 14th – her 18th birthday.

P.S. Special shout-out to those who encouraged me to start blogging again. Thank you!

The Art of Acceptance

Chris Irvine, Parent CoachLeave a comment

One of the many concepts I have struggled with and contemplated over the years of parenting my autistic child has been the difference between giving up and acceptance. I have come to the conclusion that it’s simply a matter of mindset because the outcome of giving up and acceptance is the same: you recognize there is a reality you probably can’t change, so you put your energies elsewhere.

So many times I have felt like I was giving up. Or perhaps just giving up too soon. I was hard on myself, too. Remember my failure to chart? I felt so guilty when every single professional we worked with, including psychologists, psychiatrists, and occupational therapists, insisted that making reward charts was the answer. THE answer. It never was the answer for us, and I knew it. But I would often try for a week, and then just bail out. Was I giving up? I didn’t know. I just knew it wasn’t working. It seemed futile. Maybe I wasn’t trying hard enough. Maybe I wasn’t organized enough or disciplined enough. Maybe it felt too difficult for me (it is true it’s not in my nature).

I realized at some point, however, that it wasn’t my failure. Charts were meaningless to Maddie. So I could release myself from guilt because really what I was doing was recognizing what was true (acceptance!) and acting accordingly. Maddie didn’t give a shit about a reward chart and she never would, so why keep trying? I could release myself. And guess what? That is not the same as giving up!

I also remember deciding there would be no more fights about homework. And in our house, that meant no homework at all. It wasn’t going to happen without a lot of pushing on my part, and often my energy was wasted. I really should have made that decision when Maddie was in first grade, when homework first came into our lives. What should have taken ten minutes (an appropriate length of time for a six-year-old, if they absolutely must have homework at all) took a full hour because of the Asperger’s (and with it, ADHD) I didn’t know she had. I don’t know why I didn’t just tell the teacher, “Look, this is killing us.” I now realize years later that she would have most likely said “No problem.” But I was fighting it, swimming upstream in a deluge, losing my mind over something that was at the time both impossible and unnecessary. If only I’d had the wisdom of acceptance back then. Or the next year, or the next year, or the year after that. And on and on.

Finally, after more than eleven years of this struggle, two weeks ago we began the new phase of Maddie’s education. She hasn’t set foot on a campus for months, and in fact she took a couple months off to do whatever the heck she wanted. Which, by the way, was awesome for me, too. I realize parenting involves occasional conflicts with your kids. You will inevitably be at odds at least once in awhile. But the daily grind of morning-long battles, fraught with anxiety on both our parts, was just too much. For both of us. I got to say at least a temporary goodbye to migraines. And, it turns out, Maddie was able to to go off the Prozac she’s been taking since she was nine.

I noticed a few days ago that her prescription bottle was still in the Ziploc bag she had taken to camp last month. She had been a bit less reliable with her nightly medication since she quit school. I was no longer managing my teenager’s bedtime, which involved watching the clock, telling her five times to brush her teeth, cleaning off her bed, filling her water bottle, reminding her to take her medication, and hanging out for a bit (I do miss our nighttime conversations) before turning off her light and saying good night. So I wasn’t aware she had simply stopped. Fortunately, unlike many similar medications, you can apparently just stop cold turkey without withdrawal symptoms.

After I spotted the neglected bottle, I casually asked Maddie if she had been taking her medication. “No,” she said, matter-of-factly.

“I thought so. Are you feeling okay?” I asked.

“Yup!” Clearly she was feeling better than OK.

“If you start feeling any anxiety or if you feel a little depressed, you need to tell me, okay?”

“Yup!” And I know she will. I’m so grateful for that.

And so here we are. Her decision to quit school relieved me of that two-month migraine and apparently freed Maddie from the anxiety, in particular, that had been plaguing her since the fourth grade. Seven years later (SEVEN YEARS!), we figured out together that “giving up” on school was really just accepting that it wasn’t working, and then making the choice to do something else, and rather magically, we are both okay. After all these years of struggle, all these years of meetings and IEPs, and then no IEPs, and then IEPs again, after traumatizing experiments with ADHD meds, after all those fights and struggles and tears and digging in on her part and frustration and yelling on my part, and frustration and even the occasional physical outburst on her part, and my trying and trying and feeling like a failure, and wondering what I should do, and then trying something and finding that doesn’t work, and trying something else and then something else, and feeling defeated and exhausted and afraid and discouraged, Maddie and I found acceptance.

And so, for now, we are free!

The difference between giving up and acceptance, it turns out, is in your feeling of power. When you give up, you are admitting defeat. The thing, whatever it is, has won. And so you shrug and say, well forget it. With acceptance, you are making a choice. You are not a victim. You are in charge. YOU say, I have decided this thing, whatever it is, is happening, and you find a way to embrace it, and hopefully, to make the best of it and find a new path to peace.

Finding My Voice

Chris Irvine, Parent CoachLeave a comment

Recently I wrote about what’s been keeping me from writing. A few personal distractions have factored in to be sure.

Now I have realized there has been another big distraction from my Asperger’s parenting blog. And that is the current election.

I won’t go into my opinions here. Suffice it to say they are strong. They are burning. They are becoming increasingly consuming of my mental energy. I have always had opinions about these things. I have some very firm beliefs, which have developed over the years as I have grown and matured and become more open-minded and more worldly. I would say they are mostly fully formed.

But like many of us, I have refrained from engaging in discourse about those taboo subjects: religion and politics. I think money is one too. I still don’t really want to discuss religion. That’s personal. Another person’s religious beliefs are their own. I respect them and value our differences. I am certainly curious to learn about various religions, but I don’t feel the need to convince anybody one way or the other or to be converted, either. And money is just not that interesting to discuss.

But politics has become something else for me all of a sudden. I am so fired up I feel like I might explode. And guess what? Sometime over the last year, I have found my voice. Partly it’s probably due to my age. I turned 49 last month. I still feel 25. I’m still goofy and silly and jokey and dancey and sing-y and face-makey and all that good stuff. One of my purposes in life is to have fun with my people. I want us all to enjoy ourselves. I put a lot of myself into that mission on a daily basis, particularly with my family. We dance with the dogs, and say “That’s what she said” as often as possible. I crack myself up, to be honest. Seriously, I am HI.LAR.I.OUS.

But this 49 thing has given me something very powerful. Maybe it’s courage. Maybe it’s kind of the old-lady-who-doesn’t-care-what-anybody-thinks attitude, even though I don’t exactly feel old. Maybe those are one in the same.

Or maybe writing 100 blog posts about my life, letting down my guard to expose my fears and failures and weaknesses and hopes, has given me the courage to speak my mind about other things.

Or maybe it’s because things are falling into place with my kids, which have been the consuming force in my life.  I’m learning to accept the challenges of my 16-year-old daughter, and my nearly 14-year-old son is becoming more independent. So I have this freed up energy, energy that is searching for a purpose. And I’m finding that purpose.

Whatever precipitated this development, here it is. I have found my voice. And I really do mean found. I have had this voice my whole life, but I’ve kept it quiet. I’ve been polite and diplomatic and quiet. I have sat around a table full of people who shared a singular viewpoint while I most vehemently but also silently disagreed. I didn’t want to stir up trouble. Oh, the fire burned in me, but my desire to be polite and maybe, I hate to admit, to be liked, has suppressed my voice.

I wish I had found it sooner. It seems like I wasted so much time being afraid to speak up. I was a painfully shy child, fearful of adults in general, even the lady at the Taco Bell window waiting to take my order. Or my neighbor’s grandma, who insisted she pull that sort-of loose tooth out of my five-year-old mouth. I was too timid and shy to stop her. Or my teachers, who just might call on me to speak. Even though I knew the answer or had something important or meaningful or even brilliant to say, the fear of having to open my mouth and expose myself was overwhelming. So first, I had to overcome my shyness, and that has been a lifelong journey.

But there is a lot of room between not being shy and being bold. I think I just figured that out.

So now, finally, as 50 looms, I have decided it’s time to be bold and use my voice for good. Do I still want people to like me? Well, sure, I suppose everybody does. But I want to be liked for what’s truly inside, and that’s coming out, people! It’s coming out! 

I want my kids to see me this way. I want them to see a fearless woman who speaks her mind, who stands by what she believes in. A person with a passion and a voice and the courage of her convictions. A person whose words can make a difference. Because words are my medium.

This particular blog will continue to focus mostly on parenting. No politics here, unless they involve autism or special needs or kids. I have decided, after 100 entries, that this blog is really about my journey as a mother more than Maddie’s journey as a teen, and this newfound courage is part of that journey. It’s my coming out, as they say. My declaration of strength and power and intention. My declaration of purpose. And it feels good.

 

 

 

 

 

 

 

 

Back on the Horse

Chris Irvine, Parent CoachLeave a comment

It’s been several months since I’ve written. I’m not completely certain why I’ve had such a dry spell. Certainly life has continued to provide challenges, failures, successes, more questions–with or without answers–and even some adventure.

I have my suspicions, though.

This blog has been primarily about raising Maddie. And in the last several months, although she has provided many an interesting moment, there have been some other serious issues on my mind, and I didn’t want to necessarily write about them.

One is my health. I’m one of those people who always has an issue. Or two. Or three. It’s my back. And migraines. And terrible allergies. And unexplained and ongoing gut issues. And my ankles are messed up. And I have an allergy-related sleep apnea that makes me so tired all the time. I might sleep for ten hours and still feel exhausted all day. It sucks. I’m slowly trying to address all of those things, but I’ve found it hard to say, stick to a Pilates schedule when my stomach hurts so bad all the time. I’m finally figuring that one out, so maybe it’s time for those Pilates classes again. And yes, I have to do something like Pilates where I’m less likely to aggravate my ankle or back or hip or whatever. I have one of those bodies.

Second is my marriage. It’s a struggle sometimes. Statistics show a greater risk of divorce among couples with special needs children. Boy, ain’t that the truth. As if being parents isn’t hard enough, you throw in some extra challenges that nobody’s really equipped to deal with, and you’re rolling the dice.

Third is the other kid. Our son. He’s almost 14. He’s such a cool human being. I’ve been challenged with two completely opposite children, so parenting each one is an adventure, to put it nicely. H is intelligent, thoughtful, philosophical, and deep. Sounds awesome, right? Well, those qualities are admirable and desirable and all that good stuff, but parenting a kid like that is hard. He can argue you into a corner, for one thing. And he never ever gives up. While I admire his persistence, sometimes it’s just exhausting. More on him later, though.

Also my parents. I love my mom and dad. They live about 45 minutes from us. I wish they were closer. So I could help them. On the other hand, they’re not super great at accepting help (like mother, like daughter, I’m afraid). My dad has suffered from debilitating depression and anxiety for many years. My therapist thinks he’s agoraphobic, among other things. The word “bipolar” has reared its ugly head of late. I suspect he has some PTSD from a few episodes from his younger life. Whatever the diagnosis, and whatever the cause, he is severely disabled. He rarely leaves the house. It’s too stressful. Just riding in the car is often more than he can bear. He hasn’t driven for years even though he is only just turning 70. So I worry about my dad. But even more so, I worry for my mom. She is a doer. A worker. A creator. She likes to make things, so for several years she has been sewing items to sell at a local consignment store. Or two. Or three. She also refinishes furniture and makes things like framed chalkboards for kids’ rooms. She cooks up a storm, too. She recently completely re-landscaped their front yard so it’s more drought-friendly. She likes to be industrious. She has also spent her life without a lot of extra money, so when something needs doing, she does it, for the most part, rather than paying somebody else to do it. Every once in awhile, there is something beyond her scope (particularly since becoming permanently partially disabled some years ago because of chronic wrist pain in both arms) and she’ll have to hire somebody. But her go-to is “just do it.” How do a person who can’t do anything and a person who only wants to do things live together? Guess what? The doer, my mom, adjusts her life to suit the other. There is a lot of going nowhere. Particularly because Mom worries about what might happen when she’s gone. Dad’s just not reliably level-headed anymore. I want to help them so desperately, but it seems to be out of my hands. I want my dad to be well and, even if he can’t be well, I want my mom to have a life.

So I’ve been distracted, I guess. And I haven’t felt compelled, or maybe just comfortable, putting all this in writing. I don’t want to “expose” anyone. I also don’t want to make this blog a tribute to all my problems, and most of all I think some of this stuff is kind of private. At least the other parties involved might think so.

And then there’s Maddie. She’s still exactly Maddie. She’s at camp right now, the camp she absolutely lives for the rest of the year. When we were anticipating a New York-London trip we took last month, I asked her if she was excited. “Meh,” she said. “CAMP!” That pretty much sums up her experience of our trip (another blog or two will cover that). She just wanted to get it over with and go to camp. So right now I can rest easy knowing she’s in her happy place. She’s probably filthy and she probably has terrible B.O., but it’s out of my hands, and isn’t that a beautiful thing!

And before that, of course, the infamous school year (the actual “Year of Living Hopefully”) came to a close. More on that in another entry, too.

So today I’m back. I remember now that I can write and I like to write and I have something to say. A lot of somethings to say.

The story continues.

Swimming Upstream

Chris Irvine, Parent Coach1 Comment

I don’t know if I’ve mentioned this before, but I love to shop. I know it’s stereotypical and not necessarily admirable, but it’s the truth. I love clothes, I love shoes, I love jewelry, I love purses. I also love to decorate my house. I love to buy gifts. If you mention you’re looking for a particular dress, I will take it upon myself to search to the end of Google to find it.

It’s satisfying. It’s a way that I express myself. And even if I’m not buying, it gives me pleasure to look at and feel pretty things. I can visit the Prada department at Neiman Marcus (just because my friend works in the department next door), and enjoy the beautiful fabrics and stunning details and superb craftsmanship without feeling sad for one second that Prada clothes are out of reach. That’s OK! It’s like art to me. Do I got to a museum and lament the lack of a Monet or Rodin in my house? Of course not!

I remember when I got pregnant that I wished so much for a girl. Having grown up with two sisters and no brothers, girls were what I knew and understood. And then at that 20-week sonogram, my wish came true. There was a little tiny girl growing inside me. Boy, we were going to have a good time, mother and daughter, doing all that fun girly stuff together.

And then I had Maddie. Sure she’s a girl, but she’s not especially girly. Which is perfectly fine. I absolutely love her the way she is and wouldn’t dream of changing her, but there has been a little bit of mourning over the loss of some dreams. She’s a lot of fun, but we don’t share many interests. She loves to craft. To me crafting is like getting whacked in the head with a hammer: I’m just glad when it’s over. She loves comic books. I actually do like superhero movies, but that’s about the extent of it. She doesn’t care about her hair or her clothes or her shoes or getting her nails done. At least she likes to color her hair. That’s kind of fun.

The real problem with her disdain for shopping, though, really comes into play when she actually needs something. Like bras. Or shoes. Or swimsuits. Or a graduation dress. I do all the legwork, trying to find something that will fit her rather short but curvy body and meet all her sensory requirements as well. It’s not easy. But I do it. I scour online shops and Target and Old Navy and whatever else I can think of for jeggings with a short rise, swimsuits that cover her up in all the right places, shoes that fit her terrible feet, and most challenging of all, bras that meet her many particular needs. It’s a chore. It could be fun, actually. And today it kind of was.

Saturday we leave for our spring break trip, this year to Mexico. Our week will be spent swimming and reading and playing games together. It’s a week of relaxation and quality family time (I hope). And suddenly, a couple days ago, it occurred to me that the kids have probably grown since last year and might not be properly outfitted for a tropical vacation. So yesterday I somehow got Maddie to try on the few things we could find that would be suitable for warm weather. And I was glad I did. We found two swimsuits that were way too small and a few dresses, only two of which fit. And one pair of shorts.

So here I was, six days before we leave, with a bit of a problem. A hard-to-fit teenager who refuses to shop in need of, all things, a swimsuit. Or two. Or three. Plus some clothes. So my wonderful niece, Rachel, who’s living with us right now, helped me pick out eleven swimsuits on Amazon for Maddie to try on when they arrive in the next couple of days. I have no idea what size she is, so it’s a bit of a gamble. But with a girl who won’t shop and few places nearby that offer full-coverage suits, Amazon was the answer for sure. That’s what I did last year.

And then we spent some time in Target looking for sundresses. I found some great stuff, including a Batman night shirt and a tee shirt with a Dia de los Muertos-style Darth Vader and the words “Yo soy tu padre” on it. Genius. Perfect. Also some comfortable tee-shirt dresses. I was so happy. I felt like we nailed it. I even declared our outing a success on our way home.

And then I presented the dresses and shorts to Maddie. She was not impressed. She was not interested. In fact, she was pretty rude about it.

“I don’t need any dresses,” she said flatly, not looking up from her computer screen.

“Well, you do need a couple things for Mexico,” I said. “Plus I got you a couple other things I think you’ll really enjoy.” I showed her the Batman and Star Wars items. Those got quiet approval. But she refused to even acknowledge the other stuff. Or the effort I had put into it. No gratitude, no sensitivity to my feelings, no real acknowledgement that I had done anything for her.

“I’m not trying anything on,” she announced.

I grabbed her stuff. “Well, then I’ll take it all back,” I said.

“No!” she spat, and grabbed the whole pile of clothes.

“Well, you don’t have to try everything on, but anything you are interested in keeping you have to try on. That’s just the way it is.”

No response. So I left. I don’t know why this particular exchange affected me so much, but in that moment I felt the wind just leave my body. I went from feeling so pleased to feeling utterly deflated in the matter of moments.

I also don’t know why I expected that to go any other way. She doesn’t care about clothes, unless it’s a really cool tee shirt. So not only does she not get particularly excited when I buy clothes or shoes for her, she sometimes actually gets angry. Yes, angry. As if I have wasted whatever time and money on picking out that rather than something she’d really enjoy. Okay, I get that. But this time she actually needed some clothes. (Fingers crossed at least one of those swimsuits works out!) And I took it upon myself to get her what she needs and she couldn’t have cared less.

I realize that’s probably not unusual for a teenager, the lack of gratitude and grace. But perhaps it’s the relentless feeling of swimming upstream that I experience on a daily basis that has left me feeling so deflated after this particular exchange. Deflated. Demoralized. Depressed.

The truth is, she may never develop the gratitude and grace I wished for in that moment. That would require a level of perspective taking that is not necessarily natural for people with autism. She will probably never think to herself, “Gee, Mom is so nice to me I ought to reciprocate, and go to school/try on clothes/clean my room.”

Why do I try so hard? I wonder sometimes. It’s the same old battle inside me: how do I both accept my child and refuse to give up? If you wanted to learn how to ride a bike, but knew the chances were slim that you would ever succeed, how long would you keep trying? Eventually, I suspect, a person would accept their fate and give up. And, frankly, that would be the logical thing to do. How much effort do you put into something that’s unlikely ever to come to fruition? There has to be a limit, right?

But when it’s your kid, there is no limit. How can there be? You just keep going, even if you are swimming upstream. You have to come up for air once in awhile, but you dive back in and swim harder. You accept that it’s going to be a struggle, you accept that you may never ever reach your destination, but you have to believe, at least some of the time, that the swim is worth it.

But sometimes you just get tired. Today is one of those days. My fins need a rest. I need to breathe freely. And I’ll be back in the stream tomorrow. After all, we will have swimsuits to try on.

Another Spectrum

Chris Irvine, Parent CoachLeave a comment

Spectrum:

1. A band of colors, as seen in a rainbow, produced by separation of the components of light by their different degrees of refraction according to wavelength.

2. Used to classify something, or suggest that it can be classified, in terms of its position on a scale between two extreme or opposite points.

How I felt the true meaning of that word this last week!

One moment I was holding Maddie’s hand while she struggled to tolerate the miserable sensation of “buzzing” in her face, begging me to somehow help her. In another moment I engaged in conversation with Maddie and her cousin about how one of them wished she knew herself better and the other had learned in the last couple of years how to feel more comfortable presenting her true self. From helpless young child to self-aware, philosophical teenager all in the matter of a weekend. A spectrum, indeed!

Yesterday I drove about an hour to have Easter with my parents. Maddie had spent the night with my sister who lives near my parents, so we all met for a casual afternoon celebration including lunch and multiple eggs hunts. And, as is always the case when my niece is involved, board games. We struggled through a few rounds of Apples to Apples (if you don’t have it, get it!) because we just couldn’t stay on topic for some reason. Suddenly, Maddie announced, holding her belly, “Ugh. My stomach hurts.”

“Do you need to lie down?” I asked.

Much to my surprise, she nodded quietly and started heading toward the nearest bedroom.

“Do you need anything?” I called.

She nodded. And pointed. At me. Of course. Just like last week, when she wasn’t feeling well, she just wanted her mom.

Hey, I get it. I’m 48 years old and it wasn’t so long ago that I felt like the one person who could take care of me was my own mom.

When Maddie was born my mom came to live with us for the first week. When I was eight months pregnant with my son, and Maddie had just turned two, I had complications that made it very difficult for me to get around, so Mom stayed with us for the entire last month of my pregnancy. She did everything. She cooked and cleaned and dug up stumps in our backyard and cleaned the tops of our kitchen cabinets. She did laundry and took care of Maddie. I was so grateful to have her there.

And then, after both visits, she unceremoniously began to pack up to go home. She had certainly done so much more than I ever could have imagined. But I wasn’t quite ready to be without her, even though I was 33 and 35, and so I cried. The first time, when suddenly there I was with a newborn baby and a lot of raging hormones, I was scared. How would Jake and I manage this new life? The second time, when my son was born, I was certainly more ready, but after a number of complications (including a systemic rash and a rib cracked during my c-section) I was still pretty miserable. Maybe I was scared. Now I had TWO babies. If I thought one was challenging, how on earth would I manage two? And post-c-section with my still-cracked rib and a rash that was getting worse before it got better.

And so I cried. With Maddie I cried for two days. With my son, it was brief, but I still cried. I still wanted my mom.

And here was Maddie feeling sick to her stomach, wanting her mom. But now she wanted me for something I really couldn’t help. I finally talked her into going into the bathroom, where I thought her problems might eventually be solved. She sat there, suffering with cramping intestines, reaching out for my hand. Again. “Help me,” she begged.

“Well, I can’t really help you with this.” She’s nearly 16. I really can’t help her in the bathroom. Nor do I necessarily want to.

“Uh, I’ll sit out here and you can leave the door open,” I offered. We were in my parents’ room, so I could just close the bedroom door and we could have privacy. I sat on the couch, looking at the spines of my mom’s books for something to read. I didn’t have my reading glasses nor was there anything I was particularly interested in. (I eventually picked up a book and handed it to Maddie. Painted Crafts. The operative word: crafts. Maddie loves them. I’m allergic to them.) So I just sat and sat and waited. And tried not to listen or breathe through my nose.

“OOOOOH, help me, Mom!” she cried again. She must have had food poisoning. She was in pain and sweating and uncertain of how long this feeling was going to last.

I sighed, “Maddie!” I’m sure I was exasperated by this point. “There’s really nothing I can do for you.” Deep breaths. Of course my heart went out to my suffering child, but I was also feeling exhausted from the demands upon me over the last several days.

Eventually she was alright and we were able to make the hour drive home.

But I couldn’t help but notice how sometimes Maddie is very fifteen, and sometimes she’s very four. Teenager-y and toddler-y. And there is not a lot of in between.

And this morning there was a lot of teenager-iness.

Mondays are always hard for Maddie. Mondays are hard for most people, I suspect, and I tell her that all the time. Everybody is tired! Even your teachers! But they get up anyway!

Despite her promise that a sleepover on Saturday wouldn’t negatively impact her school week, she was unmoved this morning. I tried all the usual tricks, and eventually I managed to get her up. I wasn’t sure how I did that although some threats were involved, as was a little bit of yelling and even some counting (toddler-iness!). I had taken her electronics out of her room and promised to return them once she got up. I even let her wear the shirt and pants she slept in (just add some deodorant, please), so all she had to do was put on her socks and sneakers, grab and hat and glove, throw her backpack over her shoulder and head up the stairs.

I took the dogs and her French toast wrapped in a napkin and headed to the door. Maddie asked, “Where’s my phone?”

“In my purse. You can have it in the car.”

Shortly after getting the dogs into the backseat and settling in myself, Maddie appeared with her backpack. I looked at the clock. 7:35. We might be on time today! I thought cheerfully. It was a stressful morning but not only we were on our way to school, for once she might not be late.

Maddie opened the door, threw her backpack in, sat down, and reached for my purse. I buckled my seatbelt. And then…

She grabbed her phone and got back out of the car.

Are. You. Kidding. Me.

She did all of that in order to get her phone without having any intention of going to school. It was all a big ruse. Or at least it became a ruse. I suspect the more insistent I had gotten about school, and the fact that I had removed her phone, had somehow inspired her to dig in her heels. She was going to win this. 

I hopped out of the car but there was clearly no way for me to win this, if winning meant getting her phone back. Even if I had tried, I’m not strong enough (or willful enough) to physically extract the phone from that grip of hers. I could stand in front of her all day, keeping her in the driveway, I guess, but that’s just ridiculous.

“If you don’t get back in the car or give me your phone,” I said sternly, “when I do get my hands on that phone, you’re losing it for a month.”

“You don’t mean that,” she challenged.

“Oh I certainly do.”

Unfortunately that month includes a trip to Mexico. Oh crap. What have I done?

Seriously. What. Have. I. Done.

I fell into the trap again. She was so determined to keep her phone that even if I had promised to destroy it during the night, she wouldn’t have done anything differently. I could take away her allowance for a year. I could even take away sleepovers for a year, and she absolutely lives for sleepovers with her cousin. I could have done any and all of those things and she would have stuck to her guns because in a moment like that, her “guns” are the only things that matter.

Actually, now that I think about it, this morning’s behavior seem both toddler-y and teenager-y. Rebellious like a teenager. Unable to anticipate the future like a toddler. Stubborn like Maddie.

I guess ultimately that’s who I’m dealing with. Not an age or a phase, but just a Maddie. She’s complicated and confusing and maddening and surprising. She is a whole spectrum unto herself! And it’s very challenging.

Some people might be grateful for the challenge. Or at least they might think they would be. I’m not grateful–at least not today. It’s damn hard. Today I feel like I’m losing my mind.

But I do accept it. That’s a gift, I suppose, of having a special needs child. You learn a whole lot of acceptance. You learn to see a person for her whole self, and you love and accept all those parts. You embrace every color of the rainbow and learn to see all the colors in between.

And somehow you just keep going. You get up every day hoping for a pretty indigo or gold but knowing today might be kind of a muddy brown or a swamp green. And today the spectrum wasn’t pretty. But maybe tomorrow will be that soothing, beautiful blue or something even better.

Finding Peace in Acceptance

Chris Irvine, Parent CoachLeave a comment

Dear readers, you may have noticed I haven’t blogged in a few weeks. I have had occasional dry spells when I’ve started a bunch of posts but couldn’t seem to develop them properly. Or maybe I’ve been busy. Or tired. Or maybe I just couldn’t write one more “I couldn’t get Maddie to school” story. How boring it would be if my blog were a daily account of Maddie’s attendance, which is predictably unpredictable if that makes any sense.

A few days ago I started thinking about my blog, and I realized what my “roadblock” has been. The reason I put quotes around “roadblock” is because that word tends to indicate something negative, something in the way of a goal. In this case, though, I think the “roadblock” has been my attitude of acceptance. I have spent so much less energy swimming upstream. I just hopped on board the raft for the ride, I guess. The ride might be tranquil and relaxing, predictably smooth. Or I might hit some Class 3 rapids, which require a bit of attention if you want to stay on the raft. Or maybe a Class 5 comes into focus, and I have to hold on for dear life despite the fear and lack of control over the outcome.

I went whitewater rafting some years ago, and, not being an especially strong swimmer, my approach was to spend the ride leaning slightly toward the middle of the raft. That way, if I lost my balance, I would (I hoped) fall into the safety of the raft, not the wildness of the river. It worked that time. Maybe that’s what I’m doing now. I didn’t fight the waters; I just tried to manage what was coming my way in the best way possible, accepting that the unknown might be around the corner.

Having a thirteen-year-old and a fifteen-year-old, I see an awful lot of orthodontic work among their peers. Braces have come and gone over the years. Many kids are on their second round. Some have even completed that.

Maddie could use braces. Her jaw is slightly off center, and although her teeth are generally straight, her canines have come in slightly above of the rest of her teeth. Braces would straighten her jaw and give her adorable face a dynamite smile. But something has been holding me back.

A couple of years ago we visited a holistic dentist for this purpose. Instead of traditional braces, the protocol involves a series of appliances that you wear on your teeth that slowly move your teeth into place. The appeal is in the outcome, which would theoretically help breathing by moving the teeth outward for a wider smile rather than inward as has been somewhat more traditional (or so I am told). I absolutely loved the idea, but I was skeptical about Maddie’s ability to manage something that was, realistically, optional. And I was right. Two years later the first appliance still sits in her nightstand, barely used. I guess I gave up. She just couldn’t manage it, and neither could I. A long and uncomfortable process that involved compliance, for an outcome Maddie didn’t even care about, was ill-advised, but I had paid the $4,000 anyway. A poor choice in every aspect.

And yet I’ve felt guilty about my failure to take care of Maddie’s smile, as if I have failed her in a measurable way. Everybody else is out there getting their perfect smiles, and every time I thought of even meeting with an orthodontist, something stopped me. After Maddie’s most recent trip to the dentist, I was determined to move ahead, but this time with braces because once they’re installed, they’re not going anywhere until the job is done. But the “call orthodontist” item on my to-do list remained untouched as the days went by. I couldn’t even make the phone call.

And then my niece Rachel, who is living with us, said something magical. She described how painful and miserable having braces was for her. I never had any orthodontics, so what did I know? I see other kids struggling on days when their braces are adjusted, but I didn’t realize how painful it could be. Nor did I realize how much tedious care was required, like frequent tooth-brushing and flossing above the braces. As I pondered the unlikelihood of braces being a successful endeavor anytime soon, Rachel said, “Maybe she’s not ready.”

YES! Maybe she isn’t ready. Maybe not now. Suddenly a weight was lifted that I hadn’t fully realized was there. She’s not ready. She’s not ready and that’s okay. She doesn’t have to be ready now. At all. Even if she’s not ever ready, so what?

And so I let it go. Perhaps in a few years we can make it happen, but the truth is it might never be worth the suffering. Maddie certainly doesn’t care if she has a perfect smile. I hope she doesn’t end up with jaw problems, but if she does, we can help her then.

Those words have sunk in and settled in my brain. Maddie isn’t ready. Maybe she’s not ready for full-time school. Maybe she’s not ready to handle homework. Maybe she’s not ready for a lot of things. And what’s wrong with that? What is the hurry, after all?

I have long realized the interesting dichotomy that resides in my daughter. She is at once 15 (“He’s hot!”) and four (“I need help shampooing!”). Right now she’s in her onesie cat pajamas, lounging in her cave-like room, playing Minecraft. I’m not sure which parts of that are four and which parts are 15, but it doesn’t matter. She’s just Maddie.

And–at least for the moment–I’m okay with that. I am trying to meet Maddie where she is. And for now it’s working. Of course it’s day eight of a nine-day vacation, during which I have required virtually nothing from Maddie, so perhaps I’m in denial. Come Monday morning, who knows how I feel?

I just take it as it comes, and there is certainly some peace in that.

The Basketball Game

Chris Irvine, Parent CoachLeave a comment

“I told Mr. L I would be at a basketball game tonight at 7.”

That was the text I received from Maddie around 10 a.m. today. I had seen emails about a basketball team for the special ed (“Bridge”) class, but Maddie hadn’t indicated she was involved so I had ignored them. I get so many emails I have to pick and choose what I read, right?

“Cool,” I replied. “Sounds fun!”

“Will you take me?”

“Of course!”

That conversation led to some of the best ten minutes of my entire life. Ten minutes because that’s how long the game was.

Maddie is not an athlete by any stretch of the imagination. Much like her mom, she has lead in her feet, and worse than that, she has bad feet. They’re flat and supernate so badly that she can’t exactly break into a full run. It’s more of a lumbering fast walk. She never really mastered catching or throwing, either. She did, however, learn to love basketball at her previous school, where she usually played during lunch with two very tall teachers and a bunch of high school boys. She’s short and slow, but she is fierce and determined. She also prides herself on being able to “take a hit,” and she most certainly did during those games, more than once resulting in a very broken pair of glasses and a pretty nice lump on her head. I wouldn’t say she enjoyed the experience, exactly, but she felt like a bad-ass for having not only survived it, but actually picking herself up and carrying on as if nothing had happened.

Most of the kids in her class aren’t athletically gifted. Lots of kids probably had motor skills delays like Maddie did, some just can’t manage the whole game concept, and many of them have probably never played basketball at all. But Maddie has quite a bit of experience, even if it was only lunchtime play.

Still, apparently she was hesitant to join until today. Somebody at the district level organized a series of basketball games between the special ed classes at the different high schools. Tonight was the first game. And it was amazing.

About twenty kids from Maddie’s school had signed up, an awfully big team for a ten minute game. The rules indicate that a non-IEP student would be on the court with four teammates to help pass and set up plays and generally keep things moving.

Before the game started, the kids were lined up for shooting drills. Maddie was on the court talking to her teacher and then suddenly disappeared. My niece Rachel looked for her after securing a t-shirt for her (the student council brought free high school shirts for anyone who wanted one), but she had disappeared. Finally the girls found each other, and Rachel learned that Maddie had avoided the drill because she can’t shoot baskets. Moments later, there was Maddie at the front of the line anyway. She had somehow mustered the courage to face her perceived shortcomings. She stepped forward tentatively and threw the ball toward the backboard. It ricocheted right into the basket as if Maddie had done that a thousands times. Instead of jumping for joy or pumping her fist, she did a double thumb-and-forefinger point. “Yep. That just happened.” And I knew we were in for something special.

A young-looking sweet-faced boy named Nathan turned out to be a pretty good shooter. Each time he made a shot during the drill, his face lit up as the crowd cheered and he soaked up that moment with so much joy and pride. He stood there smiling, not quite knowing what to do besides enjoy his achievement.

Already I could feel the tears welling up. I came for a good time, not at all expecting the emotions that would come, too.

When Maddie’s teammate Nick dribbled down the court and made the first basket of the game, I was overwhelmed. I suddenly understood why this was happening. This was an opportunity for the kids to feel the joy of playing in front of a crowd, to be cheered when they made a basket, or just took a shot, or stole the ball. Not only that, each player was announced at the beginning of the night. Stars for an evening.

The opposing team’s “ringer” looked like a varsity player, a very tall young man with some real skills, who had to downplay his level of play and never ever take a shot. Several times he passed the ball to a very short, round girl, who ducked and flinched whenever the ball came her way. Another girl with a multi-colored braid took many shots, and missed every single one, but she just kept plugging away. I was dying for her to make a basket. She never did, but I hoped she’d felt the satisfaction of being so aggressive out there, and that she’d gained some confidence for next time. One kid one that team kept trying to steal the ball from his teammate. I guess they could use a little bit of coaching.

Primarily because of her poor shooting skills, Maddie focuses on defense. So when it was time for her to sub in, I eagerly awaited the other team’s possession of the ball so Maddie could do her thing. She was alert. She played what I would Maddie-to-Man defense, basically attempting to block any opposing team member who had the ball. I think she had the ball in her hands once, and I cheered for her to make a pass. She did, and that was the end of her ball-handling career this evening. I wondered how she would feel about her performance. She didn’t play as aggressively as I had expected. I hoped she’d feel proud of herself and want to play again, but I would have to wait until the car ride home to get her feedback.

The game was over far too soon. I guess it really only was a 10-minute game. I could have used anther 20 at least, but this was the first game for all those kids and apparently they needed to start slowly.

“I know that was only a 10-minute game,” remarked Maddie as we stood in the middle of the court, “but it was quite enough.” It turns out two or three trips up and down the court had been plenty for this evening. Clearly she needs to build some stamina. We’ll work on that.

But for tonight, it was indeed enough. Maddie’s teachers, lots of parents, the district coordinator, an assistant principal, student council representatives, varsity players and more all showed up for these kids. The gym was loud as the whole crowd cheered for both teams.

And I was elated.

For the last couple of weeks I have had trouble writing. I started and stopped several times. Parenting has mostly been a huge struggle. Maddie refused to go to school the first three days after the break ended, and then she was sick for a week, and then the struggle returned in full force. She made it to school for a half day, then most of a day, then a little more of a day, and then finally a full day.

That first successful half day only happened because I did something pretty dramatic. She had refused to go in the morning, but finally after Mr. L’s suggestion, she agreed to go to the two classes after lunch. I clinched the deal by offering to get her some fast food (a rare treat) on the way there. We had a pleasant ride. Our dogs sat in the backseat for the long round trip as well. When I parked near the office, she opened her door, and then she reconsidered.

“I can’t do it,” she said.

I went from calm and optimistic to steamed and panicked in a millisecond.

And then the shit really hit the fan. Our dog Ginger jumped out and began running around the parking lot, sniffing frantically in this new, formerly un-smelled location. My frustration doubled. Maddie rounded up Ginger and got her back into the car, and she and I resumed our conversation. Then somehow Ginger escaped again. I was simultaneously trying to manage my kid and my dog, and I thought my head would explode.

And then I realized I had an opportunity. Maddie was outside the car. So was her backpack. I coaxed Ginger into the car on the driver’s side, hopped in and shut the door. And then I hit “lock.” There I was with the dogs in the car, and Maddie was locked out. She put her hand on the window.

Boy, was she surprised. I waved at her and shook my head. “Go to class!” I yelled through the window. I wasn’t angry. I was just being loud so she could hear me.

She backed away from the car as I slowly began to pull away. I waved. She stood there.

And then I watched her in my rearview mirror. She pulled out her phone. I thought for sure she was trying to call me. But she didn’t.

I circled back through the parking lot and saw she was headed for the office, where she was to drop off a doctor’s note excusing her from the previous week. And then I went home.

I felt terrible. I had just locked my kid out of the car and driven away. Who does that? I wondered. Seriously. Who does that?

The answer, apparently, is a desperate parent who is trying to do the right thing without ever really knowing what the right thing is.

All day I felt exhausted and sad and guilty. Not for a moment did I feel especially victorious or even right about my decision.

And then Maddie got home from school. I heard the door open and close, the scramble of dogs on the wood floors and the high-pitched greetings from Maddie to Ginger and Banjo. A moment later she came to my room. I was nervous. I knew she’s be upset or mad or traumatized or questioning or something.

“How was school?” I asked.

“Good!” she answered. Not a word about the morning. Not even a “why?” I couldn’t believe it. I had felt nauseous for hours, and Maddie had turned from the car and accepted her fate. And then she had a pretty good day.

Each day has been a little more successful since then, culminating today in a on-time arrival. Mr. L assured me tonight that he doesn’t care about tardies at all. He just wants her to get there. Indeed. I don’t even really care about homework at this point. Some reasonable attempt at attendance sounds like a lofty enough goal.

Last week I was ready to give up. I began to question whether all this mental and physical effort was worth the stress if it wasn’t even helping. Why kill myself trying to get Maddie to school every day? My mornings feel almost heart-attack inducing. I’m on blood pressure medication for a reason, I guess.

After the game tonight, my niece Rachel and Maddie and I stopped for ice cream. It seemed like a good night for a special treat. “How do you feel about your performance?” I asked over ice cream.

“Good!”

“It seemed like you weren’t being as aggressive as you usually are,” I observed. I wanted to encourage her to really go for it.

“Well, I looked at the other players and thought I should go easy on them. I didn’t want to block them too hard.”

“Yeah, that’s probably the way to go,” I agreed. God, I love that kid.

At home tonight, Maddie donned a brand new costume that had arrived in the mail, to surprise her dad. She stood there holding her swords in a threatening manner, enjoying yet another special moment, and then we told him about the game.

“I feel happy,” she finally said. She loved playing basketball and was excited about her costume. It was a good day.

And there you have it. Maddie had a great day.

I had a great day, too.

And it was all because of basketball.