Living in Lessons

Tree of the Knowledge of Good

I don’t tend to be a mourner. I shed a few tears, maybe a sob here and there, and then the person I love lives on in my memories and, if I’m lucky, in the lessons I’ve absorbed from them.

I’m blessed to have been born with a small army of Great Aunts. I don’t mean that  they were a generation removed from mine. I mean that they were and truly are great – awesome. They adventure. They dive into learning. They are helpers and nurturers. They have always been what I want to be when I (eventually) grow up. Kind. Brave. Extraordinary.

One of my League of Extraordinary Women passed away on Sunday night. She was a prominent fixture in our lives when Thing1 was born, helping us navigate the German healthcare system (where he was born). A counselor and mother, she helped me learn to trust myself and my love of Thing1 when I was getting my parenting sea legs.

I am thinking of her even more intensely this evening as I take a break from writing IEPs to absorb Thing1’s news from his latest visit to Dartmouth Hitchcock where he spent a good part of his senior year and what should have been his freshman year of college. We are learning, yet again, that having a chronic illness means that he has, what his doctor once warned was, a permanent diagnosis, inspite of having had a colectomy.  Now, instead of thinking about summer jobs, he is faced with another, riskier surgery or the very real possibility of cancer by the time he’s in his thirties.

He always seems to take the news in stride, but I know he’s frustrated and a little frightened. Hidden in my office where he can’t see me, I give into a few sobs before acting on the lessons my very awesome aunt taught me everyday.

I know if she were here, she would offer a hug and tell me to trust my love for Thing1 as we help him over this next hurdle. She would remind us that we have the strength to get through this together and that it’s okay to cry. And, as she showed us everyday of her life, even when her own child faced a debilitating illness, she would remind us to care for others around us. She would show us how not let fear steal the happiness we do have with each other.

I will sob for a few more minutes before I get back to writing IEPs, and then I’m going to remember her by living her lessons.

 

What Next?

This time last year, I was holding Thing1’s hand as he recovered from major surgery and navigating an unwanted gap year. I was still working at home, and Thing2 was still getting his feet wet in middle school. They were the center of my world and the center of my life, and I thought I knew who I was – a mom, writer and artist. The last twelve months, however, have changed all of that.

When I first started this blog seven years ago, I was a work-at-home-mom. The boys were 12 and 6 and, in addition to being the center of my world, were the centers of my days. At the time, the messes and chaotic rituals that go with raising creative kids in the country were endless sources of entertaining and, sometimes, heartbreaking, inspiration for post after post. Trying to preserve the moments, I got back to drawing/illustrating and then found my way to painting.

While Thing1 and Thing2 starred in many posts, I resisted making this a “mommy blog“ for reasons I couldn’t explain then but, after this year of change, I am starting to understand now.

I changed work venues and careers at the beginning of summer. Then Thing1 left for college after a summer of work. Thing2, a case study in extroversion, waded enthusiastically into the middle of middle school, and, while they are still the centers of my life and my heart, they are not always at the center of my day. Thing1 is carving out his own life. Thing2 is working his heart out to be better than his brother at everything. I’m getting to know them both as young adults, and it is an exhilarating experience. It’s also a confusing one.

The kids seem to be forging their identities almost effortlessly. I’ll always be a mom, but with each snip of the apron strings, my ‘mommy’ days seem to be slipping away. I’m still new enough at teaching to think of it as something I do and not yet as something I am, and that distinction has, over the last few months, repeatedly prompted a question about the other important part of my life of “What do I create?” Am I a writer who paints or an artist who writes?

With our family stories evolving away from the kitchen table near the wood stove, for the first time in seven years, I don’t know what to write. I don’t know what to paint. I even started taking internet personality tests (always a reliable source of wisdom), hoping the results would spur an obvious answer and direction.

Then a friend reminded me that an artist is an artist, regardless of the medium. That meant the answer was simply in getting back to creating again. The task, now, is to start with writing something – anything – every day.

I know he’s right.

I know that the act of creating will be the discovery of the next stage of life. So bear with me as I get my new bearings. All topics are on the table, and the journey has just begun.

Pie in the Sky

I went out for a treasure hunt after work, sure the entire blueberry crop would have been poached by Japanese beetles. Fortunately, the heat that every Vermonter has sworn they won’t complain about and the humidity we will gripe about seems to have produced a harvest big enough for us and the bugs. I should be happy with enough for a few desserts, but, this year, I want more.

 

This time most summers we’re planning a trip out to Lake Michigan for an almost annual, unofficial family reunion near South Haven, Michigan. We’re not this year.

 

I’ve been going to that spot in Michigan since I was a fetus. My grandparents are buried there. We’ve solved the world’s problems sitting around the table on the porch there, watching the sun set over the lake, noting how much the wind in the trees sounds like wave lapping the shore. We’ve forgotten the answers before bed and celebrated the fact of family there for almost every summer of our existences.

 

But It holds another meaning for me.

 

Eighteen years ago, the Big Guy and I missed Michigan for the first time. In April, my job had moved us to Germany while I was six months pregnant, and Thing1 was due at the end of July. There would have been no travel that summer.

 

Thing1 refused to vacate my womb until the last possible minute. The extended family had convened along the lake. Early in the morning the first week in August, the Big Guy phoned th gang in Michigan. They huddled around their speaker phone, as the Big Guy, Thing1 and I took turns talking, crying and babbling about the newest member of the family.

 

The next year we were all together along the lake.

 

We celebrated Thing1’s first birthday there.

 

We celebrated his second birthday there and, because his birthday falls smack dab in the middle of blueberry season, we celebrated with blueberries and cake.

 

Thing1 has celebrated almost every birthday there with his parents and grandparents and cousins, always with blueberries, and for the last four or five years, blueberry pie.

This summer when Thing1 turns eighteen, we won’t be in Michigan because the Big Guy is getting ready to get a new knee. It’s a good reason to stay home.

 

As I write this, however, we’re getting ready to take Thing1 back to the hospital for the second time this week to address his anemia, to talk about a new medication and possibly stronger measures to get his auto-immune disease under control.

 

He is barely eating. He is getting winded after short walks. He is not looking like his normal almost eighteen-year-old self, and we need for him to get at least a little of his own back before he flies our coop.

 

Last summer, just before we left for Michigan, Thing1 marked his birthday with a hike up the back of Equinox Mountain. He texting us updates of storms and bears on the path until his cell phone died and shortly before he home announcing that he felt truly alive.

 

We don’t know what the next few weeks or even months hold, but, barring a miracle in the next few weeks, there will be no 10 mile hike. There will be no blueberry festival or typical 18th birthday bash.

 

There will be a celebration, however. Even if it’s just our family of four cuddled on the couch, we will make sure he knows that, no matter what the circumstances, his being part of our clan for the last eighteen years, his having made us a clan, is something worth celebrating. And, if I have any say in the matter, it will be with blueberries.

The Living is Living

Thing 1

Thing1 Keeping his Eyes on the Future

Summer camp hasn’t started yet, so the boys are enjoying the fully unscheduled portion of summer. They go to bed, mostly, when they want. They get up when they’re done sleeping, lately, only time to binge watch Avengers movies together until friends call or dinner time.

This morning Thing2 was finishing up the umpteenth viewing of Spiderman – Yet Another Spider-Man Origins Movie and getting ready to move onto The Unknown Hero – A Filler Episode About A Guy we just made up but that You Need Your Parents to Buy If You Want to Understand All The Sequels when I realized I hadn’t heard the gentle sounds of found two boys not arguing all morning. I checked the clock and realize it was lunchtime.

Thing1 is normally very good about getting himself out of bed early enough in the morning to make sure he gets enough food to get his medication. At ten I had texted him it was time to get up. I saw the text was delivered, but by noon, it still hadn’t been read, and I knew today he needed a push.

I called up the stairs to his bedroom but got no answer and climbed up as quietly as possible. When I got to the top, he was curled up on his side, and, knowing he usually favors sleeping on his back, I got nervous. I called him again and still got no answer. Resisting the urge to channel my inner all Shirley MacLaine in Terms of Endearment, slapping my kid awake to be sure he hadn’t croaked in the 4 hours since I’d first called to him, I went over and gave him a gentle nudge on the shoulder. He didn’t answer, and I called again.

I knew he wasn’t dead. Very few people die from his disease. I did know his medications have been as reliable as my first Pinto, and if his flare up was turning into a scorcher, we might need to take a drive down to the ER to treat the acute symptoms until the pharmaceuticals and cannabis oil could regroup in his intestines.

Six months into his flare up, and Thing1 has learned that he’ll never not notice it. What’s changed over the last six months,though, is how quickly we let it derail a day or a life. Without being sanguine about the need to address and treat symptoms and stay in touch with doctors, we’ve also learned when to race to the ER and when it’s okay to wait for a call from the doctor. We’ve learned to distinguish the signs of a little more inflammation merely exhausting him into extra naps for the days and when the disease is firebombing his insides until he’s on the road to anemia again.

Most mornings, my main concern is that he gets good about getting himself out of bed before he moves out in the fall. We’re still making plans for fall, not always sure if we’re being determined or a little foolhardy. The reality, however, is that anything could happen between now and September, even things that have nothing to do with a chronic illness. Those things could help him on his way or completely derail him, but until those possibilities become realities, we keep plotting the points on his journey through the summer and into his future.

Fathers and Sons

The Big Guy and Thing1 have been working to replace the radiator in Thing1’s Volvo wagon, a car that’s seen more winters than he has, gifted to him by my parents when they bought a new one two years ago.

The Big Guy went to a car show with a friend earlier in the day.  Interested more in exotic cars, our boys Stayed home while I worked. I’m working Sunday, Fathers Day, so the holiday atmosphere is a bit muted.

We’re closing out the afternoon as the Big Guy and Thing1 closed out the repair job. Thing one was so engrossed in the project he forgot to try to dodge the camera.

It’s a quiet, gorgeous afternoon, but it’s not the shared love of cars and fixing things that makes the afternoon glow. It’s watching them bond and the Big Guy’s pride as he remembers he had a big hand in raising the capable, affable mechanic next to him.

I can’t help feel like that’s the most best way to honor a relationship between father and son.

What Kind of Mother

It’s two day before Thing1’s graduation. I’m on hold with the pharmacy for the third time this week trying to find out what’s happened with the most expensive of his five prescriptions. The insurance company won’t approve an increased dosage.

I’m scrolling through Facebook while I wait, stopping to like a friend’s post about a daughter’s scholarships or add a frowny-face to a post about a shelter dog on ‘death row’. I’m thinking about Plan B and C, including a three hour drive to Montreal to buy the temperature-controlled drug there. 

The hold music is still playing as I pause at a picture of a crying toddler. I click on it and open the article.

The boy in the article has been recently separated from his immigrant mother. The article doesn’t mention if they entered the US illegally or were seeking asylum, only that he is traumatized and that his mother is now incarcerated several states away. I break a strict self-imposed rule and scroll to the comments below the article. There is outrage at the child’s situation. There is also indifference and even smug vitriol cast at the mother and, by extension at the child on whom our government is visiting this psychological trauma, for his mother’s ‘sin’, a misdemeanor at worst, of crossing the border.

The pharmacy customer service rep returns and pulls me back to my current battle, which suddenly seems almost insignificant. I harden my heart and head and click the back button, for now forgetting the child and the hundreds like him.

“I’m sorry, Ma’am,” she says, her voice almost robotic. “The insurance company has denied the claim again.”

“Well can you at least send out the original prescription?” I ask. “He’s getting way behind now.”

“I’m sorry, Ma’am,” she says again. “The old one was canceled with the new one. We’ve sent it back to the hospital to reauthorize.” 

I want to ask her if she worries about job security if medical marijuana – a derivative of which we are on now wholly dependent to stop my firstborn’s internal bleeding – ever gains real traction. Instead I thank her for nothing, knowing I’m being rude for no good reason and with no expectation of an improved result. I call the hospital as soon as I hang up. 

The nurses – there’s a special place in heaven for them – are already faxing and calling and liasoning between the doctors and the ‘experts’ at the insurance company (there’s a special place for them too). The nurses inform me that the insurance company’s chief pharmacist denied the new dose again, and they are appealing the denial a second time.

By Friday afternoon, company is due to arrive for Thing1’s graduation. I finish most of the cleaning and sit down to call the hospital before the weekend starts. I sit on hold, thumbing through the Facebook feed on my phone again, smiling in spite of my frustration. Images of kids smiling at parties and beaming parents flood my feed. I know they have their worries too, but, for a moment, I feel like I’m looking through a window at another world.

Stories of children being separated from parents also appear. I don’t click on the articles; I’ve just heard their stories on the radio. A father, separated from his young son, has killed himself. Mothers in detention are being told they may never see their children again. Today, knowing I can do nothing, I choose to be blind.

The nurse picks up and tells me the insurance company is still stalling. My son is now over a week behind on the main medication he needs to know will work before he makes too many plans for fall. 

Saturday I tune out, focusing only on our small family celebration. At noon, our firstborn, my baby crosses the great divide from high school to a world that expects something of him. It is a huge step, and I constantly think how fortunate we are to have been able to travel toward and cross over that divide with him. Now, increasingly, he will travel independently. 

Once, I thought this part of the journey would be like ripping a band-aid off of an unshaved leg. 

Before Thing1 was born, I did not want kids. I was a wretched sinner. I had fornicated. I had lied — to people I hated, people I loved, to myself constantly. I had been guilty of almost every deadly sin. I was selfish. I was the worst candidate for a potential parent.

Somehow the miracle of my son happened. It would trite to say that he saved me, and he didn’t. He instead brought out a best part of me that I didn’t know existed so that I could be there to save him if the need ever arose.  

When he was first born, in my dreams, the need always arose. Shortly before I went back to work my dreams became colorful scenarios of someone pointing to my past sins. A judgmental family member or actual judge would tear him from my unfit arms, a rhythmic, colicky cry providing the nightmare’s soundtrack.

Initially, I thought these dreams were more selfishness — the fear of losing the one good thing I had ever been a part of making. Eventually, I began to see my anxieties about losing my child were really about the fear that my earlier sins, in the form of karma, delayed ‘justice’, or just incompetent mothering might threaten his foundation, that the sins of his mother would be visited on him.

Tuesday is Thing2’s last day of school. Our older son’s case is still under appeal. The three of us decide to go to lunch rather than wait by the phone. It’s a perfect Vermont summer day until we get back to the mailbox where we discover the first denial letters, signed by the insurance company’s chief pharmacy officer. 

I call the hospital for a status report. As I wait on hold, I google the pharmacy officer, a woman I discover. Knowing it’s psychotic, I get on Facebook, stalking the woman who’s denied my child’s prescription. I find her profile easily, discovering a professional portrait and a few snapshots of her with a little girl, maybe her daughter. 

I want to message her, to ask her what kind of mother can look at my seventeen-year-old’s charts and deny his chance at health. How can she be so blind to his condition?

The nurse returns and informs me that the doctors have conferred with the insurer for yet another review. We’ll know more Wednesday morning. 

Wednesday after lunch I start my daily calls. Our son is anxious to go back to work. Three weeks without his medication, however, are causing a backslide, despite the cannabis oil on which we’ve pinned too much hope.  

But I still have hope. I have a Plan B and C through Z if needed, and Thing1 knows it. That knowledge is letting both of us see his future through an optimistic lens. 

I keep Facebook open for a few more minutes after I hang up the phone. Graduation photos still appear in the feed. So do more articles about children being torn from their families in the name of national security. 

I click on a few, avoiding the comments, focusing on the families, on the children. I mull over a new Plan A, then Plan B to help safeguard those futures. They are not my children anymore than my son is the pharmacy officer’s child, but they are someone’s children. I still don’t know exactly how to help, anymore than I know if we’ll win our second appeal, but today, as I wait, I refuse to be blind.

Widgets and Wonders

The senior class graduates Saturday. The fifth grade, the elementary school’s senior class, celebrated their ‘moving up’ to middle school a few days earlier. Thing2’s graduation to the next step of his education was a huge milestone for us. It’s the first time in twelve years that we won’t have a child in elementary school. But it’s not only our perspective that made the afternoon unique.

The Big Guy and I each went to schools with thousands of kids. Graduation at mine lasted almost two hours because we had to wait for hundreds of kids to accept their diplomas. I knew the principal’s name, but I doubt he knew mine before he read it on the slip attached to my diploma. We were widgets, school was a factory.

At Thing2’s ceremony, there were songs. The music teacher handed out awards to the kids who had done chorus and band. The teachers from each 13-kid section handed out academic awards, and then, at the fifteen-minute mark, it was time to hand out the ‘diplomas’.

The principal started with a gentle reminder of the rehearsal instructions the kids had received earlier, producing a chorus of giggles from the risers behind her. She started to read out a name and the first boy climbed down to accept his certificate, but then she stopped.

“Wait a minute Mr. Smith,” she said, holding up her hand and seeming to wipe a speck of dust from her eye. The grinning boy froze, watching her as she stopped to tell the parents a story about his first day at preschool. It took less than thirty seconds, and the entire diploma handoff took less than thirty minutes for all thirty kids, even though, for most of them, the principal paused to recount a special moment or running joke.

Even for a small state like Vermont, we know our school system is on the very small side. It’s small enough that, despite ranking second in the state, there’s been a push from above for improved efficiency and lower costs by consolidating with other districts. Our district has strenuously resisted that push, and much of the resistance has focused on the school’s academic achievements. The district has also conducted more than one study to justify its existence financially.

It was Thing2’s commencement that reminded me that, in education, value can’t be determined solely by efficiency, or even scores.

The principal and teacher to student ratio won’t be any different on Saturday when Thing1 is climbing the risers. The high school principal has taught each of the kids, has coached many of them in little league, has been a presence in most of their lives for the last thirteen years. The teachers have been coaches, are parents of their classmates.

The whole ceremony, if history is any judge, will take 30-45 minutes. In those 45 minutes, however, will be packed thirteen years of phone calls and parent-teacher conferences, of field-trips and spur-of-the-moment meetings to talk over a parent’s concern, of newsletters and community service days, of nurses calling to make sure everything’s still alright, of teachers saying ‘he can do better’ because they absolutely believe that their students can. Those 45 minutes will be the result of thirteen years of creating young adults invested in a community that they know has invested in them. They will be the results of a community saw something more important than widgets.

It saw the future.

Summer Breaks


It’s the week before graduation. Thing1 and the Big Guy are working together to disassemble a third-hand swing set that has become too tired and worn to allow even the cats to play on. The swing set arrived at the house when we did, when Thing1 was in first grade and Thing2 was on the way. This weekend, both boys are too big to use it, and watching the Big Guy and Thing1 work together as equals to take it apart and clean up the rest of the yard for next weekend is making my eyes sweaty.

Thing1’s on weekly Humira now. The levels still aren’t high enough to make a difference, and he’s using cannabis oil to handle the inflammation. I get to make the odd joke about being mom of the year for getting my kid to use pot (it’s not, it’s hemp), but it is working to a degree. He’s weaning off of Prednisone which isn’t working, still taking Lialda, which isn’t working and waiting for the next blood test to see if we’ll stick with Humira or move on to the next trial-and-error.

And he’s waiting for his life to begin.

Except a funny thing has happened in the last few weeks. In between the phone calls and the daily inquiries into his bowel movements, he’s managed to get to alumni dinners for this year’s grads. He’s helped plan and pull off a senior prank centered around screwing up a parking lot for a day. He’s scheduled a new student orientation day for college.

We don’t know if he’ll be going to college in the fall. We don’t know what his future holds. The reality is, however, even if he weren’t sick, we wouldn’t know that.

Next week his grandparents and aunt will come to see him graduate. We’ll have a small party at home with a burger bar, music and a slide show of the most embarrassing moments of his first 1.78 decades.

It’s been hot the last few days. We all laugh as we realize the snow tires just came off a week or two ago. It’s springing into summer, and, just as quickly, Thing1 will be into his ‘real’ life. He’ll take his Ulcerative Colitis with him. We’ll help him fight for as much as we can for as long as we can, but, in the long run, the bulk of the battle will be his.

Hopefully he’s heading into a long summer, but the nature of his disease is that he will see winter again. Some winters are easy. Others throw a Nor-easter at you every week until you think you’ll throw in the shovel and let the winter bury you. This winter, he learned how to dig.

Because he also learned that, for the people who can and will dig, the winter does end. It always ends.

How to Raise a Parent


Thing2 is sitting across the couch from me right now tapping on an old laptop my parents bequeathed him when they upgraded theirs. He’s working on a project, talking through the lines as he taps and proving I know nothing about parenting.

I’ve worked in some sort of IT for the better part of the last 25 years. I’m the last person to tell a kid they shouldn’t play on a computer, but Thing1 got sucked into Minecraft in middle school, torpedoing his grades for over a year. It’s safe to say, the Big Guy and I are wary of Thing2 acquiring a tech addition.

Thing2 missed a fair amount of school this winter due to severe pain from inflamed lymph nodes. The pain intensified with each bout of flu or strep he contracted in the petrie dish of elementary school, and we were worried he would fall behind.

Most sick days he rested on the couch with an iPad or Harry Potter book while I worked on support tickets. I’d check during the day to make sure his latest YouTube obsession was PG-11, but for most of the day I let him take responsibility for his own amusement. They weren’t my finest parenting hours.

Thing1 got into video games about the same time, solely on the strength of his test scores, that he also got into a middle school accelerated program. He’d coasted through elementary school math, aptitude compensating for apathy. Except for mathy-science stuff, he needed serious prodding to stay on track.

When he started the more challenging program, I asked the program head how I could help him stay more organized. Her answer surprised me.

“I don’t want you to help him. He’ll learn to rise to expectations.”

So we took the hands-off approach. Bad report cards led to loss of privileges, but when he failed, he failed. When he did well, the success was his. That experience guided him like a river winnows out earth and rock to find the best route. It’s helped him learn to stand on his own two feet and, even if he stumbles, to keep trying.

I know telling the world that I let my kid spend two months playing on the iPad is inviting slings and arrows from parenting experts. Left to his own devices, however, Thing2 scurries from couch to boy-cave, moving laundry hampers and draping sheets over his top bunk to create a movie set between naps. The iPad was soon burgeoning with special effects app and ‘screen tests’. By the time he got back to school full time, he had written a script for a Star Wars fan video, complete with a mental cast list consisting of his classmates.

It’s almost Thing2’s turn to apply to that program, and, watching him create and rise to his own expectations, I’m pretty sure we’ll use the same approach. We’ll call it good parenting even though he’ll be doing most of the heavy lifting.

Cold Turkey with a side of Fries

Tomorrow is Another Diet

Most of my diets start out with the best intentions. The night before the diet, I intend to eat the best foods — and by best foods, I mean best tasting, not necessarily best for you — as I think about the foods that will or won’t be on the menu next to the chart of exercises I swear I’ll start on the same day. They usually end about 12 hours later, right about the time I congratulate myself for not hitting the snooze button at 5AM.

Day one of my breakup with solid food was only slightly different. It was Memorial Day. The Big Guy was working, but I wasn’t. I stayed up till three in the morning the night before finishing a novel and managed to sleep in until 8AM when Thing2 — fully apprised of Mommy’s diet plan for the day — came in to see if, like many holiday mornings — I would be exposing them to a balanced American diner breakfast starring sugar, fat, and more sugar. And salt.

“Is this a test?” I asked as I sat up.

Thing2 looked confused for a second and then grinned. “Oh yeah. It’s a test.” Then he disappeared, skipping down the hall to see if he could rope Thing1 into helping me get this diet nonsense out of the way bright and early. He reappeared its the unsurprising news that Thing1, whose autoimmune disorder has redefined dietary discipline over the last year, was uninterested in indulging. He thought I should stick with my plan, Thing2 reported.

“Yeah,” we both said at once.

I ended up getting Thing2 a new box of cereal and mixing my first shake for breakfast. A second shake at noon before Thing1 and I headed to the Kmart closing sale and I was feeling more than a little cocky.

The day was still young.

Shopping trips are usually like a pillow smothering my discipline. Whether I’m manic or depressed, shopping is the rush. Food is the opiate. Even scoring a purely functional $3 swimsuit for Thing1, whetted the appetite for the nearby drive-thru.

But, determined not to disappoint Thing1 who is a model of nutritional maturity, I drove past it.

We got home and promptly retreated to the sectional to enjoy the rest of the day off.

Then I saw a notification on Facebook about a petition that needed signing before Tuesday. I knew grabbing the keys, heading out for a drive to blow off steam that hadn’t had a chance to build up on a day off, would break the straw that broke my diet wagon’s wheels.

I grabbed them anyway.

I was driving to sign the petition. Really. And then I passed by the petitioner’s house. And fifteen minutes later the car pulling into a fast-food parking lot.

I knew I was disappointing Thing1 and Thing2. I knew the Big Guy would forgive. I knew I was disappointing myself and starting the best intentions all over again, the best being there would be a clean slate in the morning.

And still I ordered and indulged.

As I drove home, I debated if I should write about it. Should I tell the truth like a recalcitrant child when I got home? On one hand, why not? It wasn’t as if this was the first time I washed out of a diet. It probably won’t be the last.

Usually, however, this stage of the diet happens in secret. I say nothing and then next day I’m off it. No one says anything or even looks at me disapprovingly. But I know Thing1 worries his mom won’t be around for his college graduation. He worries I won’t be able to hike with him on his eighteenth birthday. I know I have some early signs of pre-diabetes, and the only ‘cure’ is control.

So I decided to be honest. On my blog and when I got home.

“I had fast food,” I said as soon as I got in the door.

“That’s okay,” said the Big Guy.

“I’ll start again,” I said as Thing1 said, “You can just start again. It’s a day off.”

Tonight I’m going through the intentions. I’m back on the wagon before I go to bed, and, with any luck, I’ll stay on tomorrow.

It won’t be the first battle that wasn’t won with a single skirmish.

Strange Territory

The other Friday night, Thing2 had a school dance.  Thing1 went over to SuperGal’s house for a quiet pre-prom night hang out.  The Big Guy went to play music with his traditional music band at the Wayside Country Store. For a few minutes, work was finished, school was out and I was somehow alone.

Then at 6, Thing1 texted he was starting home early, so he and I went to a new food truck discovery in Cambridge, NY. We got back just before the Big Guy finished up his gig. Thing1 went to bed early as he has been these days with his hair-trigger colon still sapping his endurance.  The Big Guy and I suddenly had the giant sectional all to ourselves. I had to keep reminding myself that Thing2 was going a sleep over after the dance since, even with the TV turned up to 50, the silence blared, heralding a new era.

When I started this blog about 6 years ago, Thing1 was just starting to pull at the fraying edges of my apron strings.  This year, despite the needs created by an acute episode of his illness, he’s been shredding the one on his side. What I hadn’t expected — but should have — was that Thing2 would start chewing at his share of the strings at the same time.

I’m wearing my UMass Mom t-shirt as I write this. It’s my new apron. There are no strings on it. Like that apron, it’ll get a few tears on it over the next few years, and, hopefully it will have a companion when Thing2 flies the asylum in a few years.

The geography of our new lifestyle is similar to when we were double-income-no-kids (DINKS) even if the absence of money reminds us that no matter where our kids are, there it is. Still, penniless or not, it feels like we’re entering new territory.

Curating Memory

Between skipping dinners at fancy restaurants and driving themselves rather than the limos featured in every movie about proms in ‘middle class’ America, Thing1’s and SuperGal/SeriousGirlfriend’s prom expenses hover far below the $1000+ average we hear about on the news.

Even the least expensive tux rental, however is a budget buster for us. Last year Thing 1 was tall and broad enough that we altered his dad’s tux down to fit him. This year he’s 60 pounds lighter but still has his prom and hers to go to.

I finally break down and buy him a suit that can go to prom and beyond, but it isn’t just about the money.

The two of them haven’t seen each other much this winter. She was under the weather in April. He’s been trying to have a complete week of school since two days after Christmas. The last week or two, we’ve juggled his medications a few more times. Tonight he has enough energy to drive the two of them in our 20-year-old Volvo wagon.

Her mom and I are feeling unusually normal. We snap as many pictures as we can fit in our phone and camera. The kids smile at us and each other the entire time, exchanging tolerant glances as their moms and dads laugh and cry and wonder aloud where the time went.

SuperGal playfully pretend-jabs Thing1 in the chest when he makes a joke intended to provoke the females.

“Careful,” he laughs. “That’s near my bleeding intestine.”

My antennae go up.

“I thought we were done with this,” I want to say.

He was done with this morning. Now, apparently, it’s back.

I don’t go to bed early on any prom night. Until the key turns in the door, I’ll be mentally replaying every news story of every kid that’s been in a prom-related car accident (even though I’ve been comparatively calm when he drives to work at night through most of the Nor-Easters we had this winter).

This prom night when he walks in the door, I’ll ask him if they had fun. Who did they see? Was the music good? Did you have snacks?

The question that has to come, that has become part of our new normal, will have to wait until morning. Whatever the answer will be, it will not become part of his memory of this night.