For those who carry a heavy load

Several weeks ago, during one of my daily sessions of mindless scrolling, I saw a job posting for a Copywriter position at a big company. It was full-time and paid well, so I applied. The weird thing is, I’m not looking for a job. I don’t even have time to have a job.

I routinely do this thing when my life starts to feel overwhelming: I start thinking that the answer to all of my troubles is to get a full-time job, because then I’d have a legit excuse to be somewhere at a specific time and the additional income would easily cover the cost of hired help to shuttle my children to and fro. It would also pay for all the Botox I need after spending two years worrying.

Also in this imaginary scene where I have a job, I could do what Robbie does every morning and just yell “Bye!” as I back out of the driveway, waving out the open window with one dry-cleaned, tailored arm.

Of course, you and I both know that adding anything extra to my plate right now would be a fatal mistake and that’s probably why I got a rejection letter yesterday from that company, despite the fact that my cover letter was fucking amazing.

“This is a form of escapism, isn’t it?” I asked my therapist during one of our sessions, which was a silly thing to ask her because I already knew the answer.

Sometimes parenting these three astonishingly bright, neuro diverse children feels like too high a calling.

No. That’s a lie.

It’s more like it feels like too damn much. I don’t think it’s just me — I know a lot of other mothers who also feel like I do, like we’re drowning in a sea of face masks and parent/teacher conferences and antibacterial wipes — but I can also say, as the parent of children who are amazing but also not exactly normal, that most of the time I am just too exhausted to talk about it.

The reason why the parents of unusual children feel lonely is because they’re too tired from parenting to discuss it or anything else with any other human being. I make myself talk about it because my therapist hounds me every two weeks at my appointment.

“Are you writing?”

She already knows the answer, but she asks it anyway, just like I did with the job application question.

“NO, I’M NOT. Because where do I even begin?”

***

Maverick is now is 13 years old, an age I’m surprised to find that I thoroughly enjoy. For so long, I dreaded parenting a teenager, but now I know my fear was based in the simple fact that I’d never done it before. He’s a joy to spend time with, when he isn’t skulking around moodily, but really, who DOESN’T skulk around moodily from time to time?

His suicide attempt in 2020 marked the beginning of a time that I haven’t fully emerged from or processed completely. It feels like the whole family was on a relatively normal plane ride and then we hit turbulence so violent I still find myself dry heaving into that little blue barf bag tucked into the seat pocket with the boring airline magazines.

The airplane straightened out a bit for awhile. We moved into a new house in a wonderful neighborhood only minutes from the school. We have a big yard and a covered porch and a big grill next to an outdoor TV. There is a community pool. Our quality of life is so much better; I am certainly happier and less frazzled now than I was when I spent 2 hours a day in the car. We love it here.

All of us, that is, except for Asher.

By the time dusk settled on Asher’s 10th birthday, the bottoms of his feet were turning black and blue from stomping barefoot as hard as he could on the slate tile in our kitchen. He was crying because it hurt, but he was unable to stop. We all stood by helplessly, unsure of what to do. I’d never seen anyone, let alone a child, in the middle of a severe obsessive-compulsive episode. Every time he “messed up” (what does that even mean? We may never know), he’d have to start over at the beginning — stomping and counting, stomping and counting. If anyone touched him, he screamed, and it would start all over again.

I have to do this! he yelled, and we believed him. It was obvious that whatever was going on was beyond his control.

Later, as we tried to sing happy birthday, he sobbed because he couldn’t stop washing his hands. He scrubbed for so long that we finally lit his candles, hoping that would help him stop, but he didn’t. He couldn’t.

The candles burned all the way down until there was nothing but a sheet of hardened wax on the top layer of his cake. By the time we finally got him to stop washing and drying his hands, they were raw and bleeding. I sliced the top layer of his birthday cake off and threw it into the garbage.

“PUT IT BACK!” he screamed. “PUT IT BACK!”

I stared into the garbage can and whispered I can’t. And we all cried, except for Robbie.

Just writing about these moments makes me feel exhausted. My arms feel like they’re full of lead. How the hell did we get here and when was the first sign that Asher was struggling? Honestly, who knows. He’s always counted, always collected, always enjoyed rituals. Where is the line between quirky and needing hospitalization?

I’ve learned that it’s impossible to know until you get there.

Both of my sons see a psychiatrist. Asher attends Occupational Therapy twice a week and he started talk therapy today. His new counselor’s views line up with my own in that she feels it’s vital that a child understand how his or her brain works so they can learn how best to manage their own symptoms and triggers. He emerged from her office with a pocket full of random items that he picked up in there — a popsicle stick, a paintbrush, some random colored beads.

“I need my paintbrush back,” she said, extending her hand. He wordlessly handed it back to her, and I detected the slightest hint of a dimpled smile underneath his face mask.

I hope this means they will get along.

***

There is more. Pepper can’t hold scissors correctly or tie her shoes and no one knows why. She struggles with executive functioning and we suspect something might crop up in the future, but in the meantime she’s starting Occupational Therapy and continuing with talk therapy and somehow, between all of the damn appointments, I worry that I’m not doing enough or enough of the right things.

Sometimes I miss drinking. Sometimes I have crazy ideas like I SHOULD GET A FULL TIME JOB and I run with that until I come to my senses. I cry in the bathtub. I talk to people. I sit in the sun.

I take my meds.

I see my therapist.

When I was growing up, people didn’t know as much about mental health, and we certainly didn’t talk about it. Things are different now, and I’m grateful. We are very big on mental health in this house — and the fact that my kids have differently wired brains is something we’re proud of. There’s no shame here.

What do I have, though, is a monstrous, invisible backpack that feels like it’s filled with rocks and I wear it all the time. I’m writing this for the other people out there who have a heavy load, too.

I see you.

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Life As A Sober Mother

My writing is so sporadic now that I’m sober. I used to have a routine: get the kids off to school, gulp a few cups of coffee, take an amphetamine, and write. I was fast, certainly. I continued to meet deadlines under some really bizarre circumstances, which is part of why I was able to keep my addictions a secret for such a long time.

In sobriety, my urges to write are calmer and my thoughts have more clarity. I like to think that when I make it to the other side of this phase of being newly sober, I’ll actually be better at my job, but time will tell. In the meantime, I have to tell you about a man named John.

John is quirky and old and speaks metaphorically. I noticed his unusual behavior right away and identified him as an autistic even before he mentioned it. His mannerisms and verbiage gave it away – I know what to look for. John is a retired university professor. He wears suspenders and large spectacles and calls himself a feminist. Sometimes he wears ironic t-shirts and carries a briefcase. He stoops over a little.

I like John.

Part of the dilemma I face as a sober mother is the fact that I have a child who was recently diagnosed with Autism Spectrum Disorder, and even though we already know that parenthood doesn’t come with a handbook, if it did, parenting a child on the spectrum would mean that I would have to throw that hypothetical handbook into the garbage can and set fire to it.

And also? I have no idea how to be a parent sober. I also don’t know how to be a sober wife, a friend, or a human being, because I have spent the past 15 years (with a few brief breaks known as pregnancy) numbing my feelings with alcohol. Some days, I just hug my kids a lot and feed them Pop-Tarts and call it good. A sober mother isn’t perfect, but she is present.

Maverick’s psychologist told me when he first presented us with the diagnosis that we needed to toss out everything we thought we knew about parenting. We are truly starting over from scratch, and I have a lot of wrongs that I need to make right. It’s kind of nice to just sit next to my 8-year-old and admit out loud that life is really hard but it’s also beautiful, and it’s going to be okay because we are finally on the right track. I think both of us are relieved, each in our own way, to finally have a label to attach to ourselves. There is freedom in having a concrete reason why I feel like I don’t belong anywhere, even though that reason is that I’m an alcoholic.

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I know I need to clear away the old ideas I had about what should be expected from my child (and from me), but I still feel like I’m rooted down in fear. Letting go of my old ideas means that I have to figure out what to do instead.

WHERE IS MY AUTISM PARENTING HANDBOOK?

Oh, that’s right. There isn’t one.

Today, I told John about Maverick. His eyes misted over and he leaned down intently, looked me directly in the face, and said the following words:

“You need to nurture him.

You need to let him rage and wail and say all of the things that the rest of the world will never understand. Let him feel safe with you. Be there for him. Nurture him. I can see that you’re a good mother. Forget about all the things you did wrong before today. Stop beating yourself up over the past.

Nurture your son – that’s what he needs from you.”

I’ve never talked to a man on the spectrum before about my spectrumy kid, but I am so, so glad I did. I gained so much insight from a brief conversation, and I left feeling like maybe what I’ve been doing is good enough, after all.

Nurture him. I can do that today.

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Throwing Out Everything I Thought I Knew About Being A Parent

Last week, our son was diagnosed with a form of autism. He’s 8 years old, which means that I am struggling with the knowledge that for the entirety of his short life, all I’ve done is nag and berate him for things that he truly did not know how to control.

“Parent Coaching” is a nice way of saying “You need to re-learn how to parent your unusual child.” Yesterday I attended our first coaching session alone, because Robbie was stuck at work and unable to go.

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HOLY CRAP.

I learned so much in those 45 minutes. Parenting Maverick has been a huge mystery, a constant uphill battle, and now suddenly all the information is unlocked! It’s flying at me at warp speed — all I have to do is to hang on and keep up.

I learned that when he’s beginning to get upset, we have been approaching him in a way that upsets him even more.

I learned that once the rage cycle starts, he won’t hear or be aware of anything else. That’s why sometimes he denies having said or done certain things after the fact and refuses to apologize. He honestly doesn’t know he did them. OH MY GOD, THAT IS SUCH A RELIEF. I literally thought I was raising a sociopath.

The therapist also made a huge deal over how impossibly, impossibly hard it is for any human being to handle a child on the spectrum without losing her shit. Because it’s not just difficult, and it’s not just challenging. It requires superhuman mindfulness and patience that I have not yet achieved, but hopefully, through the miracle of modern medicine and practice of breathing techniques, I will one day master it.

I learned that my expectations need to be run over, smashed into smithereens, and destroyed. I’m going to have to eradicate every idea I’ve ever had about my child and what he is capable of. I’m going to gather all of the knowledge I’ve gleaned from parenting books and articles and burn it, because none of that applies anymore. I now know that my child thinks differently and copes differently, and it is our job to be flexible.

Even though I have so much to learn, we are definitely on the right path. As the therapist talked to me, my eyes were opened to what I’ve really been dealing with all this time. We’ve already put some strategies into place, and guess what? Things in our house are already so. much. better.

I feel more hopeful than I have in a very long time, and I am grateful to be on this journey with my fascinating kid. I promise to do better now, Maverick. I promise to do better.

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Finding The Missing Piece

For almost 9 years, I’ve operated under the belief that I must be not that great at parenting, despite all my efforts. After all, I’d never changed a diaper before I had my first child, so it’s not too farfetched to assume that my struggles are due to my own ineptitude.

Despite my insecurities, part of me knew that I must be a passable mom, because when the nurse handed Maverick to me on September 3, 2008, for the first time in my life I felt a sense of purpose so distinct that it was palpable. As we stared at each other, I thought, we were chosen for each other.

As the years marched on I’ve questioned myself more and more, but that unforgettable moment of meeting my son for the first time was what I always went back to. When faced with a seemingly insurmountable situation, I remind myself that I’m meant to do this. After all, we were chosen for each other.

I was so overwhelmed with the stress of raising a child who didn’t seem ordinary (in addition to his two younger siblings), that I turned to the only thing that has ever helped me process my thoughts: writing. I wrote and I wrote, and people responded, because let’s face it — none of us know what the hell we’re doing. I needed to understand why motherhood was so hard, and why it was only becoming more difficult. I traded ideas with women from all over the world. I read all of the parenting books and applied all of the principles.

Maybe we needed more Jesus. Maybe we needed probiotics. Maybe we needed more sunshine. Maybe something was so significantly lacking that it was screwing up our family dynamic, and if I could just find that one missing piece, everything would fall into place. Maybe Robbie and I needed more date nights. Maybe we needed more money, a different house, a new school, more kids. We tried it all, and nothing worked for longer than a few days at a time.

Although Maverick does not seem overtly unusual, I knew something was off. I struggled to put my finger on what it was, and naturally everyone had an opinion. “He’s too smart,” they said. “He’s just bored.” Robbie kept telling me that Maverick probably had ADHD, just as he did as a child, and assured me that our son would be fine.

“Nothing is wrong with Maverick,” he said, countless times.

Maybe something was wrong with ME. But I needed to figure it out, because we were chosen for each other.

I tried harder to create an interesting, stimulating environment at home to help satisfy his craving for information. His memory is incredible. He can recall in vivid detail the time I took him to the park when he was two years old and he had on his red t-shirt and lost his truck under the monkey bars. He quotes facts about famous scientists and the surface of Jupiter; after hearing a song only one time, he can repeat all the lyrics. He can add large numbers in his head, quickly.

I cut out red dye #40. I cut out processed foods. I limited screen time. I spanked, a lot. I tried time outs, a lot. We took away toys and privileges.

I cried. A LOT.

The older Maverick got, the harder he became to handle. His emotions were big — exuberant one minute, and terrible, raging fury the next. He was scary sometimes. Robbie works insane hours, and I was in way over my head. We now had a family of five, and while Maverick loves his siblings, he lashed out at them often. Every day was filled with drama, and I kept hitting rock bottom.

Over and over again, I found myself in terrible situations with my kid, not knowing what to do to make it better, and quickly running out of ideas. When no one has a child like yours, it’s very lonely. My friends offered support, but they had no advice.

Our pediatrician said he was perfectly normal. When speaking, Maverick makes eye contact and articulates like an adult. He understands humor — when he was 5 years old, he did a stand up comedy routine for the school Talent Show that brought the house down. Despite what the doctor and everyone else said, I knew either something was going on with my kid, or something was terribly amiss with me as a parent.

We were chosen for each other. This is what I kept telling myself.

I swallowed my pride and got professional help. By then, Maverick was 7 years old. They suggested psychological testing, but it was expensive, so we waited on that, and toughed it out through talk therapy. I hoped that they could tell me how to best parent him, because I constantly feel like our relationship is war-torn. My son thinks I do not like him. My son questions whether or not he is worthy of love.

Talk therapy, as it turns out, does not help much without a diagnosis. We said that we wanted to go ahead with testing.

“He’s a very complicated case,” said the psychologist, weeks into the testing process.

“No shit,” I replied.

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One of the best things about this kid is his zest for life.

After months of evaluation and many more issues at home, Robbie and I were called in to go over their findings. As we sat in the doctor’s office, I thought about how it took not one, but two, doctors of psychology to diagnose our son. I thought about how tired I am. I thought about how I would do whatever they said would make things better. But most of all, I thought about how we were chosen for each other.

And then he cleared his throat, and in one simple sentence, the psychologist explained why motherhood is so hard for me.

Maverick has a form of autism.

The way I felt when he told us is almost exactly how I felt when my mother told me she had been diagnosed with cancer — utter relief to finally have a reason for all the madness, followed by grief and guilt. The grief I feel over Maverick’s diagnosis is purely from all of the mistakes I’ve made over the course of his life because I truly could not understand his behavior. I misinterpreted almost everything he did and said, and that makes me profoundly sad.

Guilt and grief aside, I am incredibly proud of my kid. I’m proud of who he is and what he can and will accomplish. He has an enormous responsibility because his brain is special, and I look at this as a gift. His super brain is his gift from God, and Maverick is God’s gift to me.

We weren’t sure how or when we would tell him about what the doctors said, but it turned out that we didn’t have to. Two days after we learned of the diagnosis, I was tucking Maverick into bed when he sat up and said, “Am I autistic?”

“What makes you ask that?” I said, shocked.

“Well, I asked you that a long time ago and you said no. Do you remember?”

“I do.”

“Well, am I autistic?”

“Yes, Maverick, you are. You have a form of autism. It was hard for them to figure out, because most kids with autism aren’t as social as you are. You’re actually really lucky, because you’re good with people and you have a super brain!”

We spent the next hour lying in his bed, talking about how he’s always known he was different from the other kids, which is why he’s always gone out of his way to be kind to the weird ones. I told him that we’re going to learn about his brain, together, and that he is a very special kid.

“So special,” I said, “That it took TWO doctors to figure out what kind of brain you have.”

We were chosen for each other, and I couldn’t be more proud of us.

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