How Punk Music Saves Lives

I live with depression and anxiety. I do All The Things to reduce the extent to which they affect my daily life but, regardless, they are my companions. So, I know, on a personal level, what it is to look for a community where I feel accepted and understood as I am.

Cover of the book 'Scream Therapy: A Punk Journey Through Mental Health' by Jason Schreurs, featuring a microphone with a tangled cord and the book's title prominently displayed.

Jason Schreurs (class of 2022) wrote Scream Therapy: A Punk Journey Through Mental Health (Flex Your Head Press, 2023) to reach out to his community. Schreurs lives with bipolar disorder. Depression and anxiety are not fun, but the roller coaster ride of bipolar disorder? As my mother used to say, “Thank the lord for small mercies.”

Scream Therapy is what Schreurs promises to be: a message to people who, at some point in their lives stumbled into punk music, often by way of skateboarding, and found their community. Punk concerts are always screaming loud, the mosh pits are nothing I could ever trust, and sometimes the live performances are improv’d by musicians who assembled just that evening, for that evening only.

I’m the first to admit I don’t like hard core music. The heaviest metal bands I’ve ever enjoyed are the likes of Steppenwolf, Rush, and the Doors—easy listening compared with punk. But the thesis of Scream Therapy is not that everyone should like punk. The thesis is that an inordinate number of punk rockers feel strongly, as Schreurs does, that punk music saved their lives. Without the community they found in punk—a community that gave them a sense of belonging for the first time … well, ever—they would have ended their own lives. 

Consider this passage about a man named Brian, now a middle-aged husband and dad with a day job that wouldn’t suggest anything about him as a person, much less how deeply he relies on punk music and the punk community for his mental health:

For Brian, leaving his parents’ house for a more stable environment allowed him to focus on turning his pain into positivity. Brian poured all he had into screaming in bands and organizing shows. At age 16, he booked a West Coast tour for Ashes, his first serious band. At 17, he went to Europe with Battery, the straight edge hardcore band his name became synonymous with for the next eight years. Between tours, Brian moved to Boston when he was 18 and set up one of the most popular recording studios of the ‘90s and ‘00s….

But depression creeped back into his life after opening the studio. He buried his internal turmoil and poured everything into the music, surrounding himself with a support network of bands like Gainesville, Florida’s Hot Water Music—unwavering rays of positivity with members that would do anything for him. It was the most amazing time of his life, but he kept his struggles hidden, stifling his inner doubt and emotional pain. “I was one of the most sought-after record producers for bands all over the world, and I felt like a failure.” Brian digs deep for the right words to make sense of that time. “The thing about depression is it’s not fucking reasonable. It doesn’t make sense.” 

(Boy, do I understand that sentiment.)

Years later, Brian’s nervous system refused to hold back his depression any longer.… “I remember my wife saying to me, ‘You need to be doing music. You need to be writing.’ I had to force myself to think about my issues and acknowledge them and not let them grow and become corrosive.” One evening, Brian picked up a guitar in his basement. Less than 10 minutes later, he had the first song he’d written in 20 years. I picture his song as a battering ram, bashing the pain trapped inside. “I can’t express to you the weight that came off my shoulders.” Brian sighs and tells me singing and songwriting for his new melodic hardcore band Be Well is his daily therapy….

“I don’t know that I’ve ever felt such gratitude as I feel toward punk and hardcore,” he says. “It gave me a family and an avenue to find myself at multiple times in my life when I needed a community to hear me, and see me, and appreciate not only my strengths but my weaknesses.” Brian chokes up and pretends to clear his throat. I do the same. His words could be mine. 

Not every type of music, or any art form, is for everyone. (I look at Jackson Pollock’s paintings and think What?) But there is a body of research on the importance of community to mental health, some of which Schreurs cites in Scream Therapy. It doesn’t matter what bring people together around as long as the community they create provides its members with a feeling of belonging, a feeling they have people to turn to as much to celebrate their victories as to seek support and reassurance when life sucks. 

I don’t imagine I’ll ever care for punk music. But if Schreurs and his peers find in the punk community what they need to get through life, more power to them. And more power to Jason Schreurs for reaching out to whomever he can reach through his book as well as his podcast, also called Scream Therapy, and letting them know there are people out there that they, too, can turn to for support, laughter, joy, reassurance—or maybe just to have a really satisfying scream. 

October 10 is World Mental Health Day. Here are some other books by MFA grads relating to mental health and the role of community in maintaining it: 

About mental health and its impact on one family:

Run, Hide, Repeat: A Memoir of a Fugitive Childhood, by Pauline Dakin.

About the importance of building community around almost anything:

The Fruitful City: The Enduring Power of the Urban Food Forest, by Helena Moncrieff.

Just Jen: Thriving Through Multiple Sclerosis, by Jen Powell.

The Heart of Homestay: Creating Meaningful Connections When Hosting International Students, by Jennifer Robin Wilson.

About the power of community, as well as the challenges it can present:

The Minister’s Wife: A Memoir of Faith, Doubt, Friendship, Loneliness, Forgiveness, and More, by Karen Stiller.

Must-Read Books from Recent Canadian Graduates: Part 2 of The List So Far

So many new authors on this list! (For comparison, see the first list here.) Congratulations to all the newly published authors (at least since the first list), to all the authors who were published long before I reviewed your books, I’m reading as fast as I can, and to all the authors who’ve been published that I still haven’t got to … I’m reading as fast as I can! And to anyone reading this, if I’ve missed anything, gotten any details wrong, or in some cases don’t know the year you graduated, please let me know. And the winners are:

(Edited to add: Apparently I missed quite a few books that should go on this list. I’ve added them at the top of the list so you won’t miss them. There have been several more deals but the books aren’t out yet and I’m unable to find complete information about them.)

Barone, Rina (class of 20??) Art Always Wins: The Chaotic World of Avant-garde Pioneer Al Hansen, (press and year?)

Jaffer, Taslim (class of 2022) with Omar Mouallem, Back Where I Came From: On Culture, Identity, and Home. Book*hug Press, 2024.

Kierans, Kim (class of 2025), Journalism for the Public Good: The Michener Awards at Fifty. Bighorn Books, 2024.

Kuzmyk, Emma (class of 2025) with Addy Strickland, This Wasn’t On the Syllabus: Stories from the Front Lines. Simon & Schuster, 2024.

McKay, Lori (class of 2020) Searching for Mayflowers: The True Story of Canada’s First QuintupletsNimbus Publishing, 2024.

Moore, Chris (2024) The Power of Guilt: Why We Feel It and Its Surprising Ability to Heal. HarperCollins (Canada), BenBella (US), August Books (UK), 2025.

Moscovitch, Philip (2019) Adventures in Bubbles and Brine: What I Learned from Nova Scotia’s Masters of Fermented Foods—Craft Beer, Cider, Cheese, Sauerkraut and More. Formac Publishing, 2019.

Simpson, Sharon J. (class of 2021) The Kelowna Story: An Okanagan History, 2nd Edition. Harbour Publishing, 2025.

John Larsen’s (Class of 2023 I think) book is not out yet–due in 2026 I think. 

Book cover of 'Black Cake, Turtle Soup, and Other Dilemmas' by Gloria Blizzard, featuring a colorful abstract background with wavy lines.
Book cover for 'Press Enter to Continue: Scribes from Babylon to Silicon' by Joan Francuz, featuring an image of ancient scribes on a laptop screen.
Book cover for 'The View from Coffin Ridge: A Childhood Exhumed' by Gwen Lamont featuring a black and white photograph of a corridor with scattered leaves.

Book cover design for 'The Fruitful City' by Helena Moncrieff, featuring colorful illustrations of leaves and flowers, with the subtitle 'The Enduring Power of the Urban Food Forest'.
Book cover for 'Overrun: Dispatches from the Asian Carp Crisis' by Andrew Reeves, featuring various species of fish against a light blue background.
Book cover of 'Peace by Chocolate' by Jon Tattrie, depicting the Hadhad family by the sea, highlighting their journey from Syria to Canada.

Understanding Disability: A Journey Through Parenthood (and other essays)

The closest I can come to understanding what it’s like to have a child with a disability is that all three of my kids, when they were very young, were in and out of hospital with asthma, and felt like they stuck out at school because they were the only ones with food allergies, some of them life-threatening. 

Cover of the book 'I Don’t Do Disability And Other Lies I’ve Told Myself' by Adelle Purdham featuring a blue background with artistic illustrations of leaves, a bird, and a horse.

It doesn’t begin to compare to learning the child you’re carrying has Down Syndrome, or to waiting many extra months for your child to figure out a pincer grip. Where it does compare is the understanding that your child is your child and they are absolutely perfect the way they are (even though it doesn’t always feel like it when they’re in the middle of a raging tantrum).

In the series of essays that comprise I Don’t Do Disability and Other Lies I’ve Told Myself (Dundurn Press, 2024), author Adelle Purdham (class of 2022) walks us through the emotional wreckage of finding out that your unborn child has a disability, the prejudices we are likely to uncover within ourselves when that happens, and the fierce protective instincts that then compel that parent to become a disability activist, advocate, ally. 

But that’s not all she walks us through because these essays also cover the terrain of love and marriage, of being a mother/writer who feels guilty when she’s mothering about not writing and when she’s writing instead of mothering (boy, do I know that one well), and who tries in every moment of her life—okay, as many moments as possible—to be a good person. In a deeply touching and achingly honest essay called “A Thin Line,” she writes about an encounter with a homeless woman. 

I see her as I drive past, stumbling down the street, decrepit. Please, I think, I don’t want us to run into her. She is a mess. I’m Ronald from The Paper Bag Princess …

We are on our way to the cottage. The SUV is packed full. The girls have their cupholders folded down in anticipation the bottles of iced tea I will be buying them to go with their dinner. …

I park the car and notice the Freshii on the corner. “What about Freshii? You girls can get bowls.’

While these girls have not yet been exposed to the ways of the world, the underworld, they are well versed in the vernacular of a privileged life. They speak the dialect of healthy takeout well. As do I. … the girls and I can afford to cruise around until we find an open takeout place that suits our tastes. This idea of accessibility to food as an immense privilege will sit with me and my uneaten burrito, afterward, when I find I no longer have an appetite.

As we cross Hunter Street, directly in front of us is the woman, doubled over …

“Please, can you help me?”

She asks for money, and I immediately reach for my wallet and pull out a loonie, the only coin I have. Why have I not pulled out a bill? Is it because I believe she will use it on drugs or alcohol instead of food? Yes….

“I need help,” she repeats. “I’m scared.”

With the enunciation of her fear, that is it. The thin sheath between us slips away and the world stops for her and me. Our lines cross, her path and mine, like asteroids colliding, and intergalactic even. I feel the presence of the girls over my left shoulder, standing stone still, watching. If I turn my back on this woman and hurry the girls away, it will be like turning a shoulder on myself, on my daughter, on my daughter’s friend, on the very stardust I am made of.

“Do you need to go to a shelter?” I ask her. Clearly, I think she needs to go to a shelter. She can’t stay here … 

On my iPhone, I quickly google the number for the shelter. …

“It’s so good to see kids,” she says, squeezing her eyes shut, then opening them. “It’s been so long since I’ve seen any kids.” …

Springing into action is what privileged women like me know how to do. We ascertain the problem and create a plan. My plan is to call the shelter. Make sure this woman is safe. Show my kids that I care, that we should all care, that a person in need is a person in need. That we don’t turn our backs on a person in need, no matter how destitute, forgotten, and discarded they seem. Especially when that is the case. Why is that the case? And why do I need to remind myself of this?

I won’t spoil the outcome for you. I will just say that this is some of the best literary writing I’ve read in a while—clear, compelling, compassionate. Purdham’s voice pulls me in; I could be standing next to her, watching the scene in each essay unfold, whether it’s at the lake listening to the loons, in a rocking chair nursing an infant, or on a street trying to help an unhoused woman through a state of extreme distress.

July is Disability Pride Month. Add to your pride in knowing a bit more about disability tomorrow than you did yesterday by reading this book.

Here are some other books about disability:

Just Jen: Thriving Through Multiple Sclerosis, by Jen Powley.

One Strong Girl: Surviving the Unimaginable—A Mother’s Memoir, by S. Lesley Buxton.

Scream Therapy: A Punk Journey through Mental Health, by Jason Schreurs.

Just Jen: Lessons in Resilience and Inclusion

Today, December 3, 2024, is International Day of Persons with Disabilities. This year’s theme is “Amplifying the leadership of persons with disabilities for an inclusive and sustainable future.” If anyone embodied the leadership traits required to ensure inclusivity of people with disabilities, it was certainly Jen Powley.

Jen was another author in my class (2015) for the master’s program in creative nonfiction writing. I remember arriving a day late for second-year summer residency. My daughter had gotten married on the first day of the residency, so I hadn’t left Vancouver until after the reception and had only arrived in Halifax in the wee hours of the morning. 

The next day, we had our mentor groups in the morning. Exhausted by my very late arrival, I took a nap on the lunch break and overslept. So I arrived late to the afternoon large group session and proceeded to go around on the break to say hello to people I hadn’t seen since the previous year. 

When I got to Jen, she didn’t recognize me. This wasn’t a surprise. She hadn’t been in my mentor group the previous year; her quadriplegia (caused by MS) prevented her from socializing much; and my social inhibition never helps with anything. So, I don’t know if I’d ever introduced myself to her.

Approaching her to say hello, I explained that I’d missed the welcome reception the previous day as I’d been at my daughter’s wedding. Without missing a beat or cracking a smile, she said, through her assistant, “And do you think that’s a good reason?” 

Jen was famous for her dry wit. Introducing her at a conference I later attended where she sat on a panel talking about disabilities, her first-year mentor, Lorri Nielsen Glenn, talked about her remarkable ability to, among other things, say a lot with very few words. I suspect Jen had an ability to zero in on the absurd long before she developed MS, but having difficulty finding the breath to speak honed her ability to “level a room,” as Glenn put it, in just a few syllables. 

Powley’s memoir, Just Jen: Thriving Through Multiple Sclerosis (Fernwood Publishing, 2017) takes us from her diagnosis at age 15 through her adult life, boyfriends, difficulties finding work, activism in the disability community, quadriplegia, and finding the love of her life, not to mention earning several academic degrees in her spare time. (The first time I met her, she dryly described her decision to embark on yet another degree as “much to my parents’ chagrin.”)

In a chapter called Engineering Families, Jen wrote: 

“Having hired twenty-seven assistants over eight years, I was accustomed to saying goodbye. Many of my assistants were students who didn’t stay for more than the years they were in school. Others simply moved on. Working one-on-one with my assistants, I came to know them well, but they usually only knew each other through the emails they typed for me. Some of my assistants met at shift change, but if one worked on Fridays and another worked Sundays, it was doubtful their paths would cross. Occasionally, I hosted barbecues for everyone who worked for me. Introducing themselves, they would say ‘Oh, you’re blah-blah at gmail.com. I’ve read your emails.’ The barbecues were meetings of the Jen community. I would say ‘knees’—to signal that I needed to be repositioned—and four people would get up to adjust me. 

“I engineer families out of strangers, and in the time my assistants spend as part of my family, I hope they see how strong someone who appears so fragile can be. I want them to go into the world as doctors, marine biologists, academics, librarians, and artists who know that differently-abled does not mean dumb or ill-tempered. I want them to raise their children with compassion, and if their mother or brother ever needs assistance, I want them to know they’re strong enough to step up and give it.” 

This book should be required reading for high school graduation because it helps readers learn some fundamental life skills: courage, humility, generousity, humour, compassion. At the least, I hope it’s used in some certificate, diploma, and degree programs for people who wish to work with those living with physical challenges. As Glenn wrote of her former student, “Trust this writer; she’s the real thing.” 

Published in 2017, two years after our graduation from the MFA program, Just Jen went on to become a finalist in the Atlantic Book Awards. Jen Powley died on September 17, 2023, leaving an incredible legacy of warmth, wit, and wisdom. I didn’t know her well, but I know she’s missed. 

Other books on disability:

One Strong Girl: Surviving the Unimaginable—A Mother’s Memoir, by S. Leslie Buxton.

I Don’t Do Disability: And Other Lies I’ve Told Myself, by Adelle Purdham.

Scream Therapy: A Punk Journey through Mental Health, by Jason Schreurs.