Children's Hospital

The first piggy bank I remember was shaped like the old Primary Children’s Hospital in Salt Lake City. “Primary” is the Mormon program for children under age twelve. The LDS church founded Primary Children’s Hospital in 1922. 

When I was a child growing up in Vancouver, we participated in “Pennies By The Inch,” which has been described as “the nation’s oldest grassroots fundraiser.” Each year all the kids in Primary received our own cardboard hospital piggy bank. We were supposed to save enough money by our birthday to donate a penny for each inch of our height. It didn’t seem weird to send pennies a thousand miles away to another country. We knew Children’s Hospital is a special place for kids with special health challenges, wherever they are. 

I never met anyone who was treated at Primary Children’s Hospital. But it felt good to send my pennies to Salt Lake, just in case. As Marlo Thomas says about St. Jude Children’s Research Hospital, “Give thanks for the healthy kids in your life, and give to those who are not.”

As a parent, my faith in Children’s Hospital has grown even more fervent. My first paternal vigil was at Seattle Children’s Hospital in 2005. When Eleanor was a month old, her infant gastric reflux spiked. Whole bottles of formula ended up on her fathers, and she stopped being her happy self. Our pediatrician assured us this was perfectly normal reflux. But it kept getting worse. Eventually we took her to the walk-in clinic. They immediately sent us across town to the emergency room at Seattle Children’s Hospital, where Eleanor was diagnosed with pyloric stenosis.

 

The pylorus muscle connects your stomach to your intestines. Sometimes the valve gets stuck a few weeks after birth. Anything you try to put into the stomach just comes back up. In the old days, infants with pyloric stenosis soon died. Fortunately, surgeons figured out how snip the pylorus and get things flowing again.

 

It took three days before Eleanor was hydrated enough for surgery. My parents came down from Bellingham, and my sainted ex-mother-in-law Judy flew in from Nebraska. Before the surgery, the nice Korean-American surgeon explained to us what was about to happen. Then he and Eleanor disappeared behind the ominous doors, and the rest of us went around to wait on the other side.

An hour later, Eleanor and the surgeon came out through the happy doors, and she began her swift and complete recovery. We went back to another eleven months of ordinary infant reflux and pediatrician visits, never again begrudging the vomit-stained clothes.

My next trip to Seattle Children’s came six years later, and involved mysterious bacterial pneumonia. I drove to the hospital. Eleanor took a helicopter.

Eleanor, Kamryn, and my ex had taken the train home after visiting Judy in the Midwest. After Oliver and I picked them up in Seattle, Eleanor began writhing in pain in the backseat. By the time we got to the Whidbey Island ferry she was burning up. We drove straight to the hospital on the island instead of going home. The doctors pumped Eleanor full of antibiotics, then put her on a helicopter to Seattle Children’s. 

It took a few days in the hospital to bring down Eleanor’s fever. We missed seeing the Broadway tour of “Aladdin.” I gave our tickets to a friend from Seattle Men’s Chorus; he gave Eleanor an oversized Tinker Bell balloon from the hospital gift shop. 

Here’s the key passage from the story of Eleanor’s pyloric stenosis surgery:

“Eventually we took her to the walk-in clinic. They immediately sent us across town to the emergency room at Seattle Children’s Hospital.”

Our upstairs neighbor in Seattle was an ER doctor at Seattle Children’s. When I complained about Eleanor’s melodramatic helicopter ride from Whidbey Island, she said “If you showed up in my Emergency Room with chest pains or a gunshot wound, I’d sent you straight to the grown-up doctors at Harborview.” Likewise, whenever a pediatrician or parent in the Pacific Northwest faces a life-or-death situation, they want their patient at Seattle Children’s.

Last spring my son Oliver started having weird stomach problems. Every four or five weeks he would develop symptoms resembling food poisoning – 24 hours of nausea and vomiting, but without a fever. We talked with our pediatrician and stayed in monitoring mode. 

When Oliver experienced more intense symptoms in November after just a two week break, we skipped school and went to the Urgent Care clinic. The doctor ordered an X-ray and labs. She described some of the potential causes, from stress to cancer to Crohn’s disease. Instead, the nurse called that afternoon to say the X-ray images showed alarming signs of intestinal blockage. CT imaging confirmed Oliver had a bowel obstruction.

The good news is a blocked intestine can be fixed with a one-time surgery. As I learned during Eleanor’s first visit to Seattle Children’s, the bad news is your child will die without surgery. The scary news is emergency abdomen surgery has only a fifty percent survival rate.

If Oliver needed surgery, we wanted it to happen at Seattle Children’s. Our pediatrician and I spent the next few weeks folding bureaucratic red tape into holiday bows. Oliver’s insurance approved a referral to the Seattle Children’s Gastrointestinal Clinic – but the first available appointment was in April. Meanwhile, we watched for a return of Oliver’s symptoms. My friend Dr. Ken did his pediatric residency at Seattle Children’s. When I described the test results, Dr. Ken echoed our local healthcare providers:  “it’s probably not an emergency emergency right now, but if symptoms return or pain he should go to the ER right away!” Not just any Emergency Room – everyone told us we should go directly to the ER at Seattle Children’s if Oliver’s fever spiked. 

Eventually someone looked at Oliver’s X-rays. On Friday, December 6, as I was heading up to Canada for Vancouver Men’s Chorus’s (and Taylor Swift’s) last three concerts, I got a call from Seattle Children’s. The told me Oliver could skip the Gastro Clinic. Instead they scheduled us for a surgery consultation in Seattle on Monday. 

Oliver and I met with Dr. Steven Lee, the Korean-American Chief of Seattle Children’s Surgery Division. Dr. Lee told us Oliver needed surgery as soon as possible. A week later, Seattle Children’s called to tell me Dr. Lee would be performing Oliver’s surgery on December 30. 

After thirty years in gay choirs, a handful of songs inevitably reduce me to tears whenever I try to sing them, such as the coming out anthem “Michael’s Letter to Mama”; the AIDS-era funeral staple “I Shall Miss Loving Him”; and the homesick ballad “Un Canadien Errant.”

This year Vancouver Men’s Chorus closed the first act of our holiday show with a Cher song: “DJ play a Christmas song, I wanna be dancing all night long.” The chorus repeats the words “that’s the only thing I want this year” as if in a trance. When we began rehearsals in September, Cher felt like a total bubble gum number, just like our Dolly Parton encore “Baby I’m Burnin.’” Then I saw Oliver’s x-ray report, and realized my son needed abdominal surgery to save his life. 

Since November, I’ve been unable to sing or hear “DJ Play a Christmas Song” without weeping. I don’t know what Cher is wishing for on the dance floor. But all I wanted for Christmas last year was a surgery appointment at Seattle Children’s. 

Oliver and Papa’s story continues in “Abdomen Whisperer”

Heaven Together

We chose my daughter Eleanor’s name even before I watched her birth nineteen years ago.

 

Three and a half years later, I got a call from the State social workers asking if we would take a girl from the foster system who was sixteen days older than Eleanor. We weren’t fond of her birth name, which had already been used by another family member as a boy’s name. Instead we chose “Rosalind,” which I thought was another strong woman’s name.

 

My son was a year old when he arrived from the foster system. We’d already used our top two boy names (“Graeme” and “Henry”) on failed adoption attempts. This time around “Oliver” was everyone’s second choice. My first pick was “Cameron”; my ex favored “Emerson.” So we put all three names into a hat and let Eleanor draw.

Rosalind came out as queer in middle school. A couple of years ago they identified as nonbinary, so we learned to change pronouns. They said “Rosalind” felt wrong and too girly, but they hadn’t chosen a new name yet. Instead they finished high school with the nickname “Lynn.”

 

Earlier this year, Lynn came into my room and asked “Papa, how do you feel about the name ‘Emerson’?” (Apparently Lynn didn’t remember Eleanor picking “Oliver” out of the Sorting Hat.)

 

I smothered a laugh. I told Lynn my ex was fond of “Emerson” because he liked Thoreau, Emerson, and the American transcendentalists. But I’m more of an English-y English Major. Plus I find Emerson too patriarchal. 

 

Lynn thought for a moment. “How about ‘Cameron’?”

 

This time I laughed out loud.

I’ve been waiting my whole life for a child named Kamryn. (That’s how they spell their name.)

 

I was ten or eleven years old when I saw my first musical. It was a touring show at Vancouver’s Queen Elizabeth Theatre called Saturday’s Warrior. After the Broadway successes of Godspell and Jesus Christ Superstar, a group of musicians from Brigham Young University attempted to translate Mormon culture into musical theater. Saturday’s Warrior is about a family resisting worldly temptation and trying to get back to heaven together.

 

The curtain opens on what Mormons call the “Pre-existence,” the period in our souls’ eternal progression before God created the physical universe. After kicking Lucifer and all the fun angels out of Heaven, our spirits wait around to see who will end up with the hot bodies when we arrive on Earth. Or as the Wikipedia plot summary for Saturday’s Warrior begins: 

 

While waiting in the pre-mortal Life to be born, a family of eight children promise each other that they will always be there for each other (“Pullin' Together”). The youngest, Emily, is afraid that when her turn to be born comes around, their parents will be tired of having kids, and she won't be born into their family. The oldest, Jimmy, promises Emily he will personally see to it she will be born into their family. Julie—the second-oldest daughter—and Tod—another spirit in the pre-mortal life—promise each other that, while on earth, they will somehow find each other and get married (“Circle of Our Love”).

 

Saturday’s Warrior is Mormon folk art, loosely based in church doctrine but deeply intertwined with Mormon culture. And an intense spiritual experience. Ever since I saw my first musical, I’ve always had the same vision of the family I was supposed to build when I came to Earth:  I’m going to have twins. I’m going to have one of each. The other person has a blur for a face. Vancouver is home.

 

Five decades later, I sing in Vancouver Men’s Chorus. Bear and I can see Canada on our walks. My parents live across town. I’m a disabled gay single father. And I have the best daughter, son, and child in the world.

After people find out I grew up Mormon, they often ask if I know David Archuleta, the earnest and talented American Idol alumnus and BetterHelp spokesperson. This March, David shared a personal video after releasing his newest single (and showing up online in numerous shirtless photos):

 

“When I came out I also left my church, and when that was made public I didn’t hear from my mom for a few days,” Archuleta says to his friends in a car in the video he shared. “I thought, oh no, she's probably so upset with me but then she sent me a message saying that she also was stepping away from the church.”

 

“She’s like, ‘I don't wanna be somewhere where you don't feel welcome and if you'’re going to hell, then we’re going to hell together,’” he continued. “So the song is based off of that and it’s called ‘Hell Together.’”

 

Although I don’t know David Archuleta, I’ve known a lot of gay Mormon Baby Boomers, and fellow gay Mormon Generation Xers, and gay Mormon Millennials like David. Many endured similar experiences, and some didn’t survive. Change will come eventually. Maybe Gen Z is different. But I don’t need the church to change anything, because our Mormon family has always found a way to support each other. 

My brother Doug died last year from spine cancer. In my eulogy at the Mormon church in Bellingham, “Fathers and Brothers,” I summarized our heritage:

 

When my sister-in-law posted the announcement on Facebook letting folks know Doug had died, I was moved by the outpouring of comments. Three or four repeated words stood out:  “Nerd.” “Smart.” And “funny.” I realized that’s what the comments would say for all four Leishman brothers.

 

The other words Doug’s friends repeatedly used to describe him on Facebook were “family” and “father.” Fatherhood is at the center of all my brother’s lives. That is the great gift our parents gave to each of their sons, and now to each of their grandchildren and great-grandchildren.

 

Church policies and meeting schedules come and go, but the fundamentals are eternal, like the familiar Mormon slogan “Families are forever.” I recognize “forever” is way too long for some families. But not for us.

Hopefully

Last year my one of my children told me they identified as nonbinary. I’m that kind of a father.

 

They also said “Rosalind” felt like “too girly” a name. So at school this year they went by the nickname “Lynn.” In the meantime, because they still haven’t picked a new permanent name, I have a free pass using “Rosalind” at home. (They said old people can only handle so much change.)

When I was looking at baby names long ago, “Rosalind” seemed like a name that said “strong woman” – with shout outs to Shakespeare and Auntie Mame. But I remember how uncomfortable my child felt sitting in the audience at As You Like It five years ago when everyone kept referring to the main character with their name. Of course, Rosalind cross dresses for most of the play....

I have seen anti-trans headlines many times before. 

 

As Co-Chair of the Federation of statewide LGBT advocacy organizations during the 1990s, I was among the voices loudly insisting on full inclusion for trans voices and trans issues in our advocacy. There will aways be whispered (and often shouted) temptations to leave some folks behind. Instead, I’m proud to have been part of welcoming communities and organizations for the last thirty years. 

Trans journalist Evan Urquhart recently published a chilling essay in Slate under the headline “Many Queers Can’t Bring Themselves to Face the Emotion They’re Really Feeling Right Now. We Must.” According to Urquhart, “the word for what we’re feeling right now is ‘despair’: 

 

I first had the idea to write a piece about despair more than a year ago. Let me leave you with the knowledge that none of this was unexpected. For many in the queer community, we’ve moved well past the point of fearing something might happen, and on to figuring out how we’re going live through this. Our despair is grounded in grim acceptance and practicality. We are learning that life goes on after you accept the fact that no help is coming, and you’ve been left alone to defy or defend or escape, or just bear witness.

 

It is 2023, and I weep to see children used as punching bags by evil politicians and the Republican Party. But I refuse to despair.

Fathers and Brothers

My brother Doug Leishman died on April 25, 2023 after enduring spine cancer for the last six years. Doug asked that each of his brothers speak at his memorial. This is what I shared at the Mormon church in Bellingham on May 16, 2023.

I’m grateful for this opportunity to meet together as Doug’s family and friends. Gatherings of our extended family always have one very obvious impact on me and many other Leishmans, including Doug. After listening to everyone’s stories, I forget how to pronounce my own last name. It will take several days to switch back from Lishman to Leashman.

 

Leishman is an ancient Scottish surname. It’s been pronounced the same way for hundreds of years, since before Shakespeare and the King James Bible. But our branch of the family met the Mormon missionaries in Scotland during the 1850s. They sailed across the ocean and walked across the prairie. When they reached Utah, Brigham Young sent them north to settle Wellsville, in Cache Valley. They became a peculiar people, and developed a peculiar dialect. “Roof” became “ruff.” “Creek” became “crick.” And “Leishman” became “Lishman.” That’s how my brothers and I grew up pronouncing our last name.

 

When I began my professional career, I made a conscious choice to introduce myself as “Roger Leishman.” Just like I don’t say “crick.” But we don’t make a big deal about pronunciation, and respond politely to anyone regardless of how they say our name. Except for “Leischman,” of course.

 

Like Doug, on days like today we are all “Lishmans.”

When Kyla posted the announcement on Facebook letting folks know Doug had died, I was moved by the outpouring of comments. Three or four repeated words stood out:  “Nerd.” “Smart.” And “funny.” I realized that’s what the comments would say for all four Leishman brothers.

 

Folks often remark on how much we resemble each other and both our parents, but they struggle to put their finger on the specific similarity. Folks would say we are even more similar in our personalities. Especially my sisters-in-law, and our children.

There are differences. Yes, we’re all nerds, but Doug is the Dungeons & Dragons nerd. We’re all funny – but Doug is the master of sarcasm.

On the wall at my parent’s house there is a framed series of pictures of the four Leishman Brothers. The same series of photos hangs on the wall in my living room. They were taken a few years ago near Lake Whatcom. It was the only time when the brothers, parents, and grandchildren were all in the same place at the same time. So we hired a photographer. 

 

There are four pictures in this series. In the first picture Roger, Doug, Brian, and Warren are all smiling appropriately for the camera.

 

In the second picture, Doug has a quiet grin. He is sticking his finger into Warren’s ear.

In the third picture, Warren has his finger in my ear, and everyone is grinning.

 

In the fourth picture, the brothers have all burst into laughter. 

 

If you look close, you can see differences between the Leishman Brothers. Warren went bald early. I’ll always be the oldest, and the gay one. And as Brian is quick to point out, he is the tallest brother.

 

A couple of months ago, I had the opportunity to drive to Kamloops with my parents. Doug looked about the same as the last time I’d visited:  lying in a hospital bed on his stomach in the corner of the living room, surrounded by his children and grandchildren. Before we drove back to Bellingham, I reached in for a goodbye hug. I was struck by how thick and curly Doug’s hair had gotten. And still so dark. 

 

Technically, I am now the least bald Leishman brother, and Warren is the least grey. But I think we should retire the hair titles with Doug as champion.

Gatherings like this are important because we can help each other remember the real Doug.

I often find it a challenge to recall stories from the past without a picture or something to remind me. Faces are especially hard. Last month when my parents called to let me know Doug had died, I lay in bed weeping because I couldn’t remember what Doug looked like before cancer.

 

Doug spent the last few years of his life being seen from a strange angle. Spine cancer prevented him from walking or lying on his back, so we only saw him lying on his stomach. That’s how I noticed his dark curly hair.

 

I knew if I got out of bed and walk into the living room, the pictures on the wall would help me remember laughing together with Doug. But I wanted to conjure the memories on my own. Eventually I was blessed to remember two images of the real Doug.

The first memory was from the spine floor at Vancouver General Hospital. A year and a half ago, Doug was paralyzed by a new tumor in his neck. He was airlifted from Kamloops to Vancouver, where two separate teams of surgeons worked from both front and back, removing the cancer and reconstructing his vertebrae. Doug spent the next hundred days at VGH.

 

I sing in Vancouver Men’s Chorus, which rehearses on Wednesday evenings. Each week I would drive up early and spend time in Doug’s room. He was propped up on his back in a hospital bed. It’s the only time in the last few years when I got to look Doug in the face. It also gave me the opportunity to sit down and spend hours talking with my brother, sometimes with other family and sometimes just the two of us.

 

We discussed our challenges living with cancer and with PTSD. But mostly I remember sitting together face to face with Doug, and talking about what it means to be a father.

Spine cancer targets the parts of the body that signal pain. In addition to dealing with Doug’s underlying symptoms, his healthcare team always focused on making him comfortable. Greedy pharmaceutical companies and irresponsible doctors have created the terrible opioid epidemic that is ravaging our communities. But modern opioids are also miracle drugs that make it possible to endure to the end.

 

While Doug was at Vancouver General, three separate teams were responsible for the opioids in his IV drip, his pillbox, and the little pump installed in his chest. I happened to be visiting the hospital when the pain management teams realized not only were they not communicating clearly with each other, but they were using three incompatible measurements to track dosages. One team would give Doug enough medicine for him to sit up all the way for a meal. After a few minutes they would have to crank the bed back down for him to rest, which would react with the medicine from the other teams. Sometimes Doug would overdose. And then they would start over.

 

While visiting the hospital, I also observed the laborious process of putting Doug in a wheelchair. I listened to presentations about grueling rehabilitation programs at inconveniently located facilities. 

 

After more than three months at VGH, Doug was finally stable enough to leave the spine floor and return home. When I visited Kamloops with my parents a few months later, there was no sign of the elaborate rehabilitation programs we’d heard about at the hospital. Instead, Doug used every ounce of his energy to spend as much time as possible with his family. His world was tiny:  a bed in a corner of a living room. But Doug’s world was as large as eternity because he was at the center of his family.

As I lay in bed last month grieving, I remembered a second image of Doug, from a couple of summers ago. It was the height of the pandemic. Nothing was harder for our family than the Canadian border being closed for the first time since the War of 1812. Doug was stuck in a bed in Kamloops, and my parents and I were stuck in the States. 

 

Like everything else, the Mormon temples closed. But by a miraculous convergence of circumstances, Katie and Christian were able to get married in my parents’ backyard in the strangest Mormon wedding ever. I will always remember the last time I ever saw Doug walking:  he staggered down the aisle, holding on to his daughter, the happiest man and the proudest father in the world.

 

Besides “nerd,” “smart,” and “funny,” the other words Doug’s friends repeatedly used to describe him on Facebook were “family” and “father.” Fatherhood is at the center of all my brother’s lives. That is the great gift our parents and now Doug and Kyla have given to each of the “Lishmans.” 

Church policies and meeting schedules come and go, but the fundamentals are eternal, like the familiar slogan “Families are forever.” I recognize “forever” is way too long for some families. But not for us. 

 

When I was young, the president of the church was David O. McKay. He delivered a similar message, but with more words in it:  “No other success can compensate for failure in the home.” (It was the Mad Man era – our ad slogans were longer than my kids’ generation, just like our attention spans.)

 

My brother Doug lived a successful life when it comes to what really matters. I hope we can all remember and be inspired by Doug’s example.

Douglas Todd Leishman

1967-2023

 

Let the World be Kind

The annual Sehome High School yearbook displays free “advertisements” where parents salute their graduating seniors with embarrassing baby pictures and a short message. My daughter Eleanor is on the yearbook staff. She chose our photos, nagged me about submitting my advertisements before the deadline, and lent me a couple of old yearbooks to see examples of previous contributions from parents.

 

“We are so proud of you” and “We love you” were the most common messages. Quotations came from Maya Angelou, Shel Silverstein, Led Zeppelin, John Quincy Adams, and the Old Testament. Several parents loved their children to the moon and back, while others chose to signal their affection with a dense forest of exclamation marks.

 

As a parent and a writer, I had two favorites. The first example was exquisitely succinct:  “Well done – the whole world awaits!” 

 

The second parental advertisement sent a different message: 

 

You came into our lives, and you’ve almost been a son to us. While you may not be our number one child, you at least rate in the top three. When you return home from receiving your diploma, your stuff will be packed up for you to take away to be someone else’s problem. Please don’t try to find us. 

Love, Mom and Dad

 

Here’s what I wrote to Eleanor in the Sehome High School yearbook:

 

You are messy, passionate, determined, curious, sensitive, creative, and kind – all mixed up and baked in a beautiful pie. You’ll be gone, but you’ll always be mine.

Love Papa

 

And my message to Rosalind:

 

You are completely yourself:  brave, loyal, artistic, and kind, with a unique sense of style. Raising you has been the greatest accomplishment of my life. I will always be proud to be your father.

Love Papa

I wrote Eleanor’s yearbook message first. It’s a shout out to Waitress, her favorite musical. Before covid, I took Eleanor to a performance of Waitress at the Queen Elizabeth Theatre in Vancouver. In “She Used to Be Mine,” our inconveniently pregnant waitress lets go of the person she hoped she would become. Like many of the parental advertisements in the yearbook, the song involves a series of revealing adjectives baked together. In Waitress, the list opens with “She is messy” – which happens to fit my daughter.

 

Songwriter Sara Bareilles told the New York Times “the chasm between who we are, and who we thought we would be, is always something we’re negotiating.” New York Magazine offers its “definitive ranking” of YouTube versions of the song. (Bareilles herself only reached Number 6.) For her high school performance competitions, Eleanor chose the accompanying monologue the waitress speaks to her unborn baby. 

 

Other than my decision to describe Eleanor as “creative” and Rosalind as “artistic,” by the time I finished writing my message to Rosalind I’d forgotten which adjectives I used for Eleanor besides “messy” (which Rosalind emphatically is not). After forwarding my messages to the yearbook editors, I was struck to see the repeated adjective in both descriptions:  “kind.” 

 

When Bareilles composed “She Used to be Mine,” “kind” provided a convenient near-rhyme for “mine.” In my yearbook messages, the unconscious repetition is a reminder that my second greatest accomplishment may be raising children who aren’t lawyers.

First year law students are taught to “think like a lawyer.” Legal scholar Anne-Marie Slaughter provides an excellent summary of the concept in “On Thinking Like a Lawyer,” a short essay addressed to new law students. The phrase means, “in the first instance, thinking with care and precision.” But “thinking like a lawyer also means that you can make arguments on any side of any question”:  

 

Many of you resist that teaching, thinking that we are stripping you of your personal principles and convictions, transforming you into a hired gun. On the contrary, learning how to make arguments on different sides of a question is learning that there are arguments on both sides, and learning how to hear them. That is the core of the liberal value of tolerance, but also the precondition for order in a society that chooses to engage in conflict with words rather than guns. It is our best hope for rational deliberation, for solving problems together not based on eradicating conflict, but for channeling it productively and cooperating where possible. 

 

Professor Slaughter ends her essay with optimism about the contribution that lawyers and legal thinking can make to society: 

 

One of my colleagues at Chicago ends her first year civil procedure class by saying: “Sometimes in the first year of law school, people learn to think like lawyers, but to be a little less like people. You’ve learned the first of those things. You shouldn’t let us teach you the second.” I disagree. There is no dichotomy here. Thinking like a lawyer is thinking like a human being, a human being who is tolerant, sophisticated, pragmatic, critical, and engaged. It means combining passion and principle, reason and judgment. 

 

I absorbed a similar idealism about the legal profession when I was at Yale Law School. For me, thinking like a Lawyer or like a Writer means using words to explore and share ideas with other people, including your future self. It turns out that’s the only way I can think clearly. 

 

However, in the last few years I’ve discovered that “thinking like a lawyer” is corrosive when an attorney’s duty to vigorously advocate for the client becomes an excuse to selfishly twist the truth beyond recognition. Since my PTSD diagnosis, I’ve completed an extensive reading list in psychology and neuroscience. In the field of evolutionary biology, “thinking like a lawyer” has a much darker meaning than the ideal celebrated in Professor Slaughter’s essay. 

Humans are profoundly social animals. In particular, we’re deeply concerned about social status within our tribe. Evolutionary psychologist Robert Wright argues consciousness arose in human brains not to promote effective decision making but rather for “image management” – the “hoarding of credit and sharing of blame.” Like Trump University, evolution taught us “shady accounting,” resulting in “a deep sense of justice slightly slanted toward the self.” 

As Wright puts it, the “human brain is, in large part, a machine for winning arguments.” Evolution could have designed us to prioritize finding the right answer. Instead, “like a lawyer, the human brain wants victory, not truth.”

Is selfishness a bug or a feature of humanity? Is kindness?

 

Many atypical traits persist in the gene pool despite their lack of any obvious benefit to survival and reproduction, such as homosexuality, left-handedness, introversion, blue eyes, schizophrenia, and country music. In his recent book Good Reasons for Bad Feelings: Insights from the Frontier of Evolutionary Psychiatry, neuroscientist and clinician Randolph Nesse examines how evolutionary processes can explain various quirks of the human brain, including the persistence and power of altruism: 

 

For most species, close social partners other than relatives are either nonexistent or nearly interchangeable. That was probably the case for our human ancestors until some tipping point in the past hundred thousand years, when selecting especially capable, generous partners began to give advantages. The benefits of having relationships with the best possible partners shaped tendencies to generosity and loyalty.... The resulting prosocial traits are as expensive and dramatic as a peacock’s tail.

 

Common decency makes civilization possible. But no community can be healthy when it reaches the opposite tipping point, with too many individuals defaulting to lawyerly selfishness. 

David Browning, one of the second tenors in Vancouver Men’s Chorus, is a talented singer-songwriter. (In real life he’s just a doctor.) This year David set himself the personal challenge of writing a Christmas song. As any musician besides Mariah Carey will attest, composing a catchy holiday pop song presents a daunting assignment. 

 

David did an excellent job, and VMC was proud to premiere “Merry Christmas” at our recent concerts. The song’s bridge ends with the lyric “Let the anger and the tension unwind – let the world be kind.”

As Bear and I were walking through Boulevard Park last month, we met a young woman who was making a documentary for a college class. She asked if she could film me with Bear as I answered a few questions. After pointing her iPhone at us, the student asked “Are you happy?” 

 

Life has been extra frustrating lately. My family and I are beset with mounting health, personal, financial, and legal challenges. The road ahead is uncertain and confusing. Nevertheless, I am enjoying the best mental health of my life, and The Kids Are Alright. I found myself answering “yes.”

 

After I responded to a few more questions, the student filmmaker asked if I had any concluding message. I said “Be kind. And you’ll be happy.” 

Merry Christmas

Typhoid Merry

I almost got to be a super-spreader. 

 

Instead, I’m isolating in my room with Bear – the first in our family to test positive for covid despite all the social distancing, masks, vaccinations, and dodged bullets. 

I got covid without even noticing it. When Bear and I got home from our usual long walk Wednesday afternoon, I had an email from someone who attended the same festive gathering in Vancouver on Sunday. After feeling a little under weather for a couple of days, he failed a home covid test. He suggested we all check our coronavirus status. Most attendees promptly reported negative results – other than an unlucky few. 

 

I’d taken so many covid tests before. This time I squeezed four drops into the plastic well, then watched the bright red line instantly light up. 

After observing so much suffering during the pandemic, my own experience with covid has been blessedly anticlimactic. I’ve had no symptoms. The kids all stayed virus-free as we finished the last week of school. 

 

However, the December schedule is a mess. And I’m still trapped in “isolation”:  staying at home except for long walks in the woods with Bear; letting the kids feed themselves as the dishes pile up; and either wearing a mask as I try to get work done at my desk, or hiding in my bedroom while Christmas music plays on an infinite loop. 

Before the covid surprise, I was planning to drive back up to Vancouver on Wednesday night to attend a holiday sing-along event hosted by friends at a club downtown. According to the CDC chatbot’s calculations, Wednesday was my most infectious day. 

 

Ironically, I’d already decided to skip the Xmas sing-along and save myself for a New Year’s trip. Instead, I told the kids I was loopy on Theraflu. I hadn’t actually taken any. I just wanted to cover up my decision to take the day off, stay home, and do edibles while pretending to be sick. Still, I’m glad I checked my email before I changed my mind about heading to the piano bar. My boisterous caroling would have contaminated numerous unsuspecting revelers with aerosolized coronavirus.

 

Instead I’m in isolation for ten days. Blame Canada.

This is what covid looks like (Xmas 2022)