Bitty Buddha 101: What to Do When You Meet Someone with a Bad Name

"Dickbutkus" by photo by Alan Light. Licensed under CC BY 2.0 via Commons -

“Dickbutkus” by photo by Alan Light. Licensed under CC BY 2.0 via Commons –

I think being part of the human tribe is hard, but for my seven-year-old Buddha, it seems kind of cake-walky. It’s not that nothing bad ever happens to him. I mean, a few weeks ago he breathlessly announced that he was pretty sure he’d met a bully at school. Yet his thrilled expression matched that of someone who’d spotted a Yeti. Some boy had cornered him at the water fountain and said, “ME NO LIKE YOUR NAME!'” (Maybe it was a Yeti.) My son happily added, “I just ignored him.” He saw the whole situation as an opportunity to exercise his willpower and kindness.

If my genetic matter had any bearing on the situation at all, there would have been some spitting of warm mouth-water into certain people’s too-close-together eyeballs. But that, of course, is half the reason I’m so fascinated by his insights into a life well-lived. He really addresses some of the most basic and troubling challenges of living among others. Case in point: what he shared with me during the three-minute car ride from school today…


Mom, they moved me to a new bus this week.


Yeah, but I feel really bad for her, because she has a really bad name. It’s MISS DIRTY. That’s a REALLY bad name to have. Well, actually, I guess it’s not so bad. It’s kind of pretty if you just say it—misterdee! But then if you think about what it means? Well, it’s a pretty bad name, so I feel really bad for her.

No, because that would hurt their feelings. Just pretend you didn’t notice.

Sure. You could do that. It would probably make them feel good.

Sometimes there’s such a thing as a good lie.

Pretty much. Yup.

Like, maybe if someone’s really naughty, you tell them, “Hey, there! You do a really good job following the rules!”


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Bitty Buddha 101: How (and Why) to Make a Mean Person Your Friend

I can’t count how many times someone’s called my first-grader a little Buddha. He’s an insightful little fart, often boiling down life’s tough stuff into the simplest terms from the backseat of my Hyundai. And he’s always unusually happy, even when his nose is bleeding like a scene from the Colosseum. One could argue that all first-graders have a happy nature, but that’s simply not true. I know, because my sixth-grader came out of the womb with her cup already half empty. (Boy, did THAT hurt. Rimshot!)

As a result of the constant flow of weird and wonderful things that come out of my son’s mouth, something awful happened: I became One of Those Annoying Moms Who Quotes Verbatim Conversations with Her Child on Facebook, like this one:

“Mom, I love you more than you love me.”
“Impossible. I love you times infinity.”
“Well, I love you times googol.”
Then, after much back and forth about I LOVE YOU googolplex, googolplex plus one, infinity plus infinity, he says, “Just kidding. I actually only love you about 10 percent.”

And this one:

“Mom, I think sometimes it’s better to be a kid than a grownup, because if you’re a kid and you punch someone, you just get in trouble. If you’re a grownup…JAIL.” 

And this picture:

Dodge Ram

With this caption:

“I think that guy really wants you to honk at him. It says, ‘Big Horn’ right there on the back, Mom.”

Look, I’m not saying he’s a total wizard, but he’s kind of growing on you, right?And sometimes he does make some amazing observations, about which I post things like this:

Playing a silly game of “what’s your favorite…” at bedtime, I asked my son, “What’s your favorite booger?” He said, “The not-bloody ones.” And when I laughed, he said, very seriously, “I’m not kidding. They’re gross. The blood tastes so bad on the booger!”


I could go on, but I won’t, because starting today, I’m just going to put the virtual microphone right under his chain. Today, Bitty Buddha wisdom, as dispensed to me from the back of my Hyundai and repeated to me for transcription when we got home–because he thought “we should probably put that on Google, to help people.”

I agree. Without further adieu…


Hello, everybody. This is how you make a mean person into your friend. The reason you want to make them into your friend is because it’s hard to make friends with people who are mean. It’s really hard, because you think they’re so mean. That’s what most people think, so then the mean person doesn’t get friends, and they become sad. Try to make friends with them, so you don’t get hurt. But be careful, so you don’t get hit. These are the instructions:

First, you need to make friends with them.

Then, you need to help them become good, because friends normally obey each other and like to have fun, so he might obey you and be nice and be a good person.

Also, this is all how it started. Because I had a bloody nose at school, because another boy slapped me in the nose on accident. We were playing cops and robbers. He gets in a LOT of mischief almost every day. After the nosebleed, since I didn’t want to lose him as a friend—because it’s hard to make friends with people that are naughty—I had to make him better. I plan to stay friends with him so I can try to do that.

Put that in your pipe and smoke it.

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You’re Doing It All Wrong: Parenting in the Information Age

The choice is obvious.

The choice is obvious.

To circumcise or not, to vaccinate or not, to breastfeed or not, to co-sleep or not: Parenting young kids has become a series of capital-W watershed choices that are presented as ways to make or break your child—physically, emotionally, developmentally. The stakes are always portrayed as the highest of high, with nearly every single debated issue (and there are LOTS of them) leading to this one conclusion: “If you do [or don’t do] X, your child will suffer grave consequences or even death.” But, hey, no pressure, right?

Since there are always horrifically true cautionary tales on both sides of every single one of these debates, both sides have plenty of ammunition to scare the bejesus out of parents. From deciding whether to let baby sleep on his back or tummy, to deciding whether to let older children walk to the park alone, mom and dad repeatedly get the message that life itself hinges on their decisions. It’s exhausting, and brand-new parents definitely bear the brunt of it. So, to me, it feels cruel to wag an angry finger at those parents who, for example, didn’t vaccinate their kids at the height of McCarthy-ism (Jenny, that is, not Joseph). We’re all just trying to figure out what information to trust, and make sure our kids don’t get toasted.

Parenthood is a series of forks in the road, and I suspect the signage we face at these forks has become much messier and more involved than it was for generations past. It’s damn scary to keep trying to play by ever-changing road rules, as information keeps getting repackaged, reversed, or revised. It’s also scary to realize that even if we play by the numbers—or, on the opposite end, just sit at the fork and hope the winds will decide the proper tine to blow us down—there is the potential that we’re going to harm our children. Damned if you do. Damned if you don’t. Your actions can lead to horrible consequences. Your inaction can lead to horrible consequences.

The Disney measles drama is what’s on my mind as I write this blog. To me, it’s just one more reminder that, in the Information Age, a Critical Thinking class should be required coursework for parents. Heck, why not for everyone? As a society steeped in information and with crisis after crisis being presented to us in a steady flow, we need now more than ever to be better equipped to separate data from opinion, judge for ourselves what deserves our attention, recognize a spin when we see it, and draw logic-driven rather than mob-driven or fear-driven conclusions. That’s not an easy task if you aren’t taught the skills to accomplish it. I for damn sure could use a refresher course,  much more than I needed one of those cute little hospital classes on taking care of a newborn, as it turns out.

I write these words after reading this angry dad’s article. I’m not cheerleading everything he wrote (as there are many parts where I find the data points interesting but don’t draw the same conclusions as he does). I certainly haven’t walked a mile in his shoes, but I can see he’s wearing his thinking cap and trying to encourage critical thought. That deserves some praise. As he put it in his intro: “I hope when you’re done reading that you say to yourself, ‘he gave me a ton to think about.’”

Mission accomplished.

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All Better

My son wept today. Even though he’s six, such displays are rare with him. The tears were over a Lego creation he worked on for maybe an hour, tops, something he very generously called a Transformer. To me, it looked like it could be a Lego anything: a building, a sandwich, a tribute to Tetris.

“This right here? It’s a shooter. It grows at night, when the bad guys are out, like this—vvvvssshhoowwww, bachonk, bachonk—with wings that can’t be broken. AND it defends against rockets. Pah-kew! Pah-kew!”

He had just finished describing this terrifying beauty to me, in great and passionate detail, when he went running off, tripped, and sent the whole thing flying. When it landed on the ceramic tile in our kitchen, his creation shattered back into all its original pieces. There were maybe a hundred, all told. We had to get out the dustpan and everything.

The weeping that ensued wasn’t a goldfish-died kind of weeping, and he didn’t seem particularly interested in having an audience. It was more like a crop-is-ruined-better-get-a-second-job sort of stoic sadness you might see from a farmer at the end of a particularly bad summer. Yeah, things got kind of real for him for a few minutes there.

Instead of running to comfort him, I watched from the next room. I know he’s only six, but I wanted to see what he’d do with the ordeal. Because, you know, life is like that. Shit randomly breaks and goes wrong, and you can’t always repair it. Whether it’s shattered glass, a dropped egg, or something intangible, like a friendship, some breaks won’t mend. That’s a hard and important lesson to learn. This was a decidedly privileged and painless way to start teaching it. I’d be a fool to pass that up.

When I was in the fifth grade, I won a raffle for a beautiful porcelain figurine. Among the entire school population, there were only two winners—two such figurines—and to be one of those winners felt like winning a Pulitzer. I’m sure I didn’t think of it in those terms at the time, maybe more like meeting Olivia Newton-John or waking up with boobs. About five minutes after I retrieved the doll from the school office—she had this flowing blue gown, long black hair, and sultry eyes with eyeshadow—some kid on a BMX bike came tearing through the breezeway where I was standing, crashed into me, and sent her flying. She completely shattered, save for her sad head.

“Can we glue it?” I sobbed to my mom. She had witnessed the whole scene unfolding as she walked from her car to pick me up. “We can, right!?”

No way in hell could my mom put eight million shards of porcelain back together to look like Catherine Zeta-Jones in a ball gown. That doll couldn’t be glued. She couldn’t be replaced. It was time to let disappointments just be disappointing. My mom knew (or just learned) what I’m continuously learning: Parents can fix only so much, and that’s actually a good thing. Because real life has curves and ditches that cannot be avoided. You gotta practice for them when you can.

I could see that today was that kind of training day for my son. When he was ready, I took him up in my arms and hugged and kissed him and told him how much it sucks when something you work so hard on gets ruined. But I didn’t make it “all better” for him. I didn’t even try. That’s his job, and he figured out how to do it all by himself.

Transformer II: The Second Coming

Transformer II: The Second Coming


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Real Life

Three years ago today, on my mom’s birthday, I received a call that punched me in the gut during a business lunch: It was my dad, letting me know that a possible donor heart had been found for him.

In the business of heart transplantation, the person in need of the heart lives in a kind of limbo as a name on a registry of potential recipients. My dad was fairly high on the registry because of the severity of his condition, but many months had passed since he was placed there. And until that phone call, every time his name showed up on my caller ID, my stomach would do a flip.

My lunch partner, a client, had the uncomfortable job of watching me cry into my sushi after I hung up. As I apologized for my blubbering, I remember him saying, “It’s okay. This is real life!” He was exuberant, and I knew what he meant: It’s so easy to forget that life isn’t a collection of errands and pastimes and lunch dates and things that merely add up to a day and another day and another one after that.

En route to the hospital, I picked up my kids from school. They were giddy as just-fed hamsters, not being old enough to fully grasp the complexity of what was happening. I’d say the glee was slightly more than they show at the county fair when I let them eat cotton candy, and slightly less than they show on Christmas morning. Gently I explained that our excitement came at a very high cost: Their grandpa was about to gain a heart because someone had died, and the surgery he was about to have was incredibly serious. It was important to me that they regard the gift much differently than ones left under Christmas trees. This was no Lego set or American Girl doll. This was real life.

Once at the hospital, I realized the kids would need some diversions. There would be hours of waiting for screening results. The surgery itself could take well over a dozen hours. So, I left to buy some coloring books at a drug store up the road. On my way back in, waiting by a set of interior elevators that would take me up to my dad’s room, I overheard a somewhat hysterical conversation taking place between two women. They were huddled together on a bench, shoulder to shoulder, heads bowed. One was telling the other what a beautiful thing she’d done, what an amazing choice she’d made. She said to take comfort in it, because it meant someone else out there would get a chance to live. The sobbing was unbearable. My chest dropped into my ankles. Was this the donor’s loved one?

Because his donor’s survivors opted not to respond to the letter my dad was allowed to write several months after surgery, we still don’t know who my dad’s donor was. We might not ever know. But I have my suspicions.

The day my dad had his transplant, there was an accidental death here in town, a young woman hit by a car. I read about it in the news the next day, noting how close the time of death was to the time my dad got his call. Was it her? My dad’s donor was classified as “high risk,” which can mean any number of things, one of the typical ones being a history of IV drug use. The obituary of the woman whose death was reported in the news included a request that donations be made to a foundation for diabetes research. Surely she’d been a diabetic. Did she receive insulin by IV?

I don’t actually know if this woman was my dad’s donor, but I feel sure that those women in the hospital atrium were her loved ones. So, I feel sure she was somebody’s donor. That’s why I keep a photo of her on my desktop. For the past three years, her face has greeted mine at some point nearly every day, every time I fire up the machine where I write these words. Every time I look at her face, cupped in her own hands with a playful light in her eyes, I say a little prayer for her and the people she left behind. I wonder if she did what she wanted to do before she died. I feel grateful. And sometimes I linger a little longer on the picture, remembering that this is real life. We each get just one to call our own. Mine is nobody else’s, and I get to choose what becomes of it, at least until I die and leave a little piece of it to someone else.


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My Cantankerous Little McCain

If you came here looking for a political spar, sorry. Being a new mom during major elections sucks: I mean, I know what sounds like bullshit, but I’m in no position to debate the finer points and could only rely on invective to back myself up. In other words, I’m like most voters I know (except that I tend to keep my political opinions to myself when they’re just that: opinions). This is particularly crappy, because I’m all for allowing only demonstrably informed individuals a vote. If it weren’t for party platforms staying basically the same, I’d have to sit this election out.

Anyway, I noticed a few weeks ago that my baby boy looks like John McCain — not in the face but in the arms. All newborns do. Those stiff little curled things, held a few inches from the body: Aren’t they cute? Even on McCain.

Do you think it would be inappropriate for me to dress my baby up as John McCain for Halloween? I could give him a little white comb-over, and the slightest hint of melanoma. To wit, when I wear my glasses and pull my hair up, I bear a fair resemblance to Sarah Palin. I’m totally going to do this thing.

Don’t think I won’t. Our firstborn bore a great resemblance to Der Fuhrer when she was a baby. You bet your buns we scribbled a dark moustache on her little upper lip that Halloween. Because that’s politically correct, right?

Posted in babies, general mockery, politics, speed-posts | 3 Comments

Unbreakable Girls: Lessons in Extraordinary Resilience

Kendall Smedley was just twelve years old when a latent snarl of malformed vessels in her brain—there since birth—ruptured and left her lifeless in the ER at a children’s hospital in Madison, Wisconsin. That night, whether by chance or providence, a respected neurosurgeon fresh out of a late-night surgery got the midnight page. At Kendall’s bedside, he swiftly made the call: Emergency surgery would be necessary to relieve brain pressure. Nurses ushered Kendall’s parents from the room just before she coded.

Kendall after brain surgery

Kendall after emergency brain surgery

Kendall’s mom, Susan, didn’t know her firstborn had crossed over that night. Neither did her father or her stepfather. They were too preoccupied with the post-surgery prognosis: There was a mere 20 percent chance Kendall would survive the 24 hours ahead. She came out alive, but Kendall can’t remember any of it, not even the hours before she’d lost consciousness, not even calling home from the slumber party where she’d been trying to fight off a headache.

“I’m not going to stay,” she’d told her mom as the rest of the girls played in the background. “This is a really bad one.”

Headaches had long been typical for Kendall but were usually nothing Ibuprofen or chiropractic adjustments couldn’t shake. During the week before the party, they were happening daily. She’d even gone to the chiropractor the afternoon of the brain bleed. After the adjustment, she’d felt well enough to jump on her trampoline before heading to her friend’s home. Kendall’s last memory of the night was of ordering pizza with her friends. She doesn’t remember the string of calls she made to her mom, the last one in hysterics as Susan steered down Highway 12/18 toward the Madison suburb of Oregon.

“Hurry, Mom!!!” Kendall had screamed. “I feel like my head’s exploding!!!”

Then, she just went quiet.

“She’d been having headaches off and on for years,” recalls Kendall’s mom, a vibrant lung-cancer survivor who now works as manager of national events for the National Lung Cancer Partnership. “They weren’t debilitating to the point that she’d just lay there, but they were consistent. I’d taken her to her pediatrician, and at the time we were looking at hormones, because she was at that age. How many pre-teen girls have headaches, you know?”

The culprit behind Kendall’s headaches was actually an AVM, or arteriovenous malformation. This rare congenital defect can go undetected for years or even a lifetime. And it can present as a single tangle or many clusters in the brain’s circulatory web. Some are expansive, others small. Though AVM ruptures are generally less deadly than other types of strokes, Kendall’s was the exception.

Two Years Later

On a sunny winter day in Madison almost two years after her surgery, Kendall is visiting her neurosurgeon, Dr. David Niemann, in his University of Wisconsin Hospital office. Looking at her, nobody would guess she’d been to the brink here just two years earlier, head shaved and stitched on one side, saddled with speech loss, memory loss, and a dismal prognosis. Though Dr. Niemann continues to monitor what remains of Kendall’s AVM, today’s business isn’t medical. She’s interviewing him for a school report about someone who inspires her.

“Patients like you, who just were so sick,” he says, “to be able to really make an impact and see someone get back to normal when they were really not normal or almost dying—it’s a really great thing. Just treating patients and seeing them get better is one of the most motivating things for me.”

Dr. Niemann says AVM ruptures are uncommon and have just a 10 percent mortality rate. Only part of Kendall’s AVM ruptured, which is not unusual, and only part of what remained could be embolized. Shaped like a jellyfish, it presented as a central snarl with a long tangle of vessels meandering along one side of Kendall’s head. The snarl is what ruptured.

“Your story is a little more unusual,” Dr. Niemann tells Kendall. “If you didn’t get treatment right away, you wouldn’t have made it. Yours was more unusual in the severity and then also in your recovery. You’ve really had a remarkable recovery…and your story isn’t over yet.”

Kendall’s only lingering symptom is short-term memory loss. Emotionally, she’s rebounded with superhuman calm, even though medically she’s not out of the woods. Early on, once she regained verbal expression, she says she’d ask the same question seven or eight times in just a few minutes. But working with a memory specialist, she’s made leaps in improvement and honed extraordinary coping skills. Her lifeline is a notebook for jotting important information: homework, test dates, plans. She recently made High Honor Roll at her middle school.

“There was not a single I can’t go back to school or I don’t want to do this,” says her stepfather, Trent Gerber. “No, it was when can I go back to school? That isn’t any different than she was before, except she works harder now because she wants to maintain the same high level.”

On a cold January day as I visit their suburban home, Kendall stands with her arms wrapped around Trent in the front doorway. She’s all sandy hair and freckles, melting into him as she readies to be interviewed. Unlike Kendall’s mom, who’s more a kindred spirit to Kendall, Trent seems somewhat stupefied by Kendall’s sweetheart-warrior nature: timid but strong, threatened but unafraid, so utterly un-childish. She’s a force, a child who leaves adults in wonder.

The X Factor

It’s certainly fair to wonder if Kendall has some sort of X Factor that most people aren’t born with. You can’t call it pluck. It’s something more primordial and esoteric, a resilience like grass. After winters and fires, it’s always grass that rebounds first and without ostentation. Kendall is a force like grass. Her mom says she was just born that way.

Scientists have long questioned what makes a person resilient, and mainstream studies disagree with Susan. They report resilience is not an inborn trait, that it’s primarily gained through positive outside influences: mentors, parents, friends, and experiences crafted to impart a sense that all of life is navigable. But one has only to revisit a yearbook to find resilient, even inspiring adults that have emerged from anything-but-inspiring circumstances with scant positive influences. Clearly there are exceptions. Kendall’s story is a mixed bag, leaving one wondering: Is her resilience a product of nature, nurture, or both?

Meet Mama Tiger

Susan Smedley-Gerber is a veritable mascot for bounce-back. In her early 30s, she was diagnosed with lung cancer and had most of one lung removed. Kendall wasn’t even a year old yet and had to be abruptly weaned. The cancer was found early because Susan wouldn’t lay off the doctors; they’d not been particularly concerned about the copious blood she began coughing up one weekend. Susan pressed and pressed and pressed them. (Think well-dressed wolverine with the self-composure of Emily Post.) Her persistence was life-saving: Lung cancer has a very high mortality rate, so early detection is critical.

“Immediately after they said cancer, I went into medical shock,” Susan says. She was in a daze for half the day–long for her but arguably not much time at all for most people coping with such a scary diagnosis. “I responded much differently than I did with Kendall’s ordeal. I was just in a totally different place. With my cancer, it was mostly about leaving Kendall that I was so distraught. Being completely [mentally] unavailable for a 12-hour period like that? That’s very atypical for me.”

Just 12 hours to regroup was all it took. Imagine that. Susan would show equally remarkable resilience during a dreadful string of unrelated tempests to follow the cancer. Within a few years of her cancer recovery, she made a painful discovery about her marriage. (She sees no need to broadcast details.) By then, she had a young son, whose ADHD and violent rages required professional intervention. Susan tried for more than a year to salvage her marriage but ultimately knew it was a cancer, too. The divorce terms required her to share placement of the kids, with a man she no longer trusted. Then Susan’s mother suddenly fell ill and died.

If you’re picturing a woman broken by a deluge of heartaches, don’t. Susan bounced back with her spirit not only intact but deeply strengthened after each blow—even, eventually, after Kendall’s brain hemorrhage.

Imagine the night of that hemorrhage. When the neurosurgeon was called in for emergency surgery, Susan felt like a dark thundercloud was condensing onto the head of a pin. Releases were hurriedly signed, machines and trays wheeled about in a flurry, and according to Susan, the staff dropped all eye contact with the family. There wasn’t time enough even to move to an actual operating room. In the midst of that firestorm picture this: The mother calmly leaning over her twelve-year-old daughter, warming the freckled cheeks not with tears but whispers of encouragement:

“I know you’re probably scared,” Susan said. “I know you can hear me. The doctor is going to make you feel better. We have to leave the room now, but we’ll be back as soon as we can. They know what they’re doing. And if you have to cross over, Gram will be there. She’ll keep you safe…but you have to come back.’”

The Science behind Resiliency

Just what makes a person capable of standing up so tall in the storm? Despite mainstream science’s tack that it’s about positive childhood influences, behind-the-curtain science tells a different story.

Michael Brandt, a psychologist at the Tomah Veteran’s Assistance Hospital in Wisconsin, says mainstream science often dishonestly shies away from crediting genetics even when credit is due. He takes issue with that. Brandt has long been engrossed in resilience research and is the Wisconsin National Guard’s go-to guy for training on the subject. His opinion: Save for slight points that can be gained by regularly getting outside one’s comfort zone, resiliency is pretty much a steady-state affair, and certain people—like Susan and Kendall—are just more predisposed to it.

“Minimizing the genetic factor is reflective of the field in that it’s not sexy to talk about the innate qualities inherent to resiliency,” Brandt says, “in the same sense that it’s not attractive to publish studies that discuss the genetic correlates of IQ.  Researchers all know that it’s the reality, but their work has a better chance of being published if it minimizes the predisposition aspects:  Americans don’t like to acknowledge what we’ve innately inherited because it flies in the face of a self-made ruggedly independent mentality.”

Perhaps Dr. Brandt and sexy science are both right. No matter how much Susan insists Kendall was “just born that way,” one cannot overlook the powerful examples of resiliency Kendall witnessed in her mom. Susan exemplified that “self-made ruggedly independent mentality” on a daily basis. Cancer, organ loss, divorce, the fabled problem child, the loss of a parent, and the near death of her child all failed to exhaust her reserves. Instead, they somehow multiplied them.

In the moments in the ER, and in the hours and weeks following Kendall’s emergency surgery, Susan sent frequent updates to friends and family, maintaining in them the kind of composure usually reserved for world leaders in crisis situations. This was typical Susan. The feeling she conveyed wasn’t so much that Kendall was going to be okay. It was that things were going to be okay—no matter what. Nobody who knows Susan would accuse her of living in denial. She just never went to a place of fear, and neither did Kendall.

“I don’t remember ever having a thought that I wouldn’t be there the next day,” Kendall says. “I just kind of knew that I’d be okay. I knew I was going to go home and get back to my life.”

Kendall’s stepdad believes there’s a deep spiritual lesson to behold in Kendall’s recovery. “That’s something she’s taught us all lessons about—faith and strength,” he says. “It’s funny that a 14-year-old can teach a 40-year-old those types of lessons. She did it without trying, just being the person she was.”

There’s a spiritual lesson to behold in Susan, too. In light of her strong personality, it’s interesting that she chose to trust rather than panic that night in the ER when control slipped through her fingers. In doing so, she discovered that true faith makes a person fearless, and that faith is at the root of strength.

“Once I was standing in that emergency room with Kendall, there was nothing I could do,” Susan says. “Whatever was going to happen was independent of me, even though, like any mom worth her salt, I’m a ferocious mother tiger when it comes to protecting my kids.”

Obviously Susan had coped with not having control over circumstances many times in the past but never with such enormity as in that moment. The closest she’d come was with the placement of her kids. Entrusting them to a person she had no reason to trust was especially excruciating, largely because it meant a long-term lack of control. There seemed to be no working with or around it. The risks would go on and on. Uncharacteristically, she’d long been having trouble bouncing back from that one, until the AVM rupture.

“There are things that you can’t do anything about, even when you’re standing right in the room,” she says. “The experience helped me to go, ‘I couldn’t have saved her then. I didn’t save her. I didn’t have any real impact on this situation at all, except for just loving her through it. I know that if God can bring her back, all of these other issues that I feel are so ominous [referring to the split placement] are nothing. And I know now that she has her own path.”

When the headaches recently resurged—a month-long scare that turned out to be a simple vision problem—Kendall maintained her own fearless focus. Just fourteen, she proudly talks today of becoming a child-life specialist like the one who helped her and her family in the hospital. The career would give her daily opportunities to work with pediatric patients, bridging the gap between the hard corners of medicine and the soft curves of human vulnerability.

The resilience shown by Kendall and her mom raises questions of intrigue for those with less bounce-back. If we trust the word of mainstream science, we should be paying closer attention to the likes of them—not just admiring but learning. As for Kendall, whether it be by genetics, example, or the higher power she trusts, she’s in possession of all three possible wellsprings, uniquely equipped to rebound as well as pass down her gift:

“She’s never used her AVM as an excuse,” Trent tells her neurosurgeon one day. “There’s been no, ‘This is too hard now,’ never anything like that.”

“Like her mom,” her neurologist likes to say. “Just like her mom.” ᴥ

Kendall and Susan two years after Kendall's AVM rupture

Kendall and Susan two years after Kendall’s AVM rupture

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