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  • Without A Phone: A Morning, a Coffee, and a Thoughtful Disconnection

    Without A Phone: A Morning, a Coffee, and a Thoughtful Disconnection

    Author’s note: I didn’t intend to write a digital detox think piece. Sometimes remembering how much we rely on our phones only requires forgetting them.

    Yesterday I met a friend for coffee. I was so focused on making sure I had everything we needed. I didn’t even realize I left my phone at home on the charger.

    It’s the second time in less than a week I have done it.

    The funny thing is I didn’t even realize I had done it yet again. I only noticed when I was three blocks away. I got a notification on my Apple Watch. It said, “Your phone has been left behind.”

    Classic.

    For a second, I considered turning around. There was the part of me who knew if I did, we were going to be late. Also it wasn’t like I didn’t have a way to get reach emergency services should there be an emergency.

    My Apple Watch has built-in cellular service. Thanks, sister, for insisting that I get it. All I would have to do is press a button on the watch, and it would immediately call 911.

    Still, it felt weird… like I was missing a limb.

    As I walked to the train, it hit me how deeply enmeshed phones are in our lives. In 2025, they’re no longer just for calling people.

    Actually, I can’t recall when I last had a full phone conversation. It was not with a doctor’s office or customer service. These days, we text, DM, post, scroll.

    Our phones are our GPS, music libraries, cameras, credit cards, and even IDs. They’re an extension of us, but maybe too much so.

    Life Before

    I’m old enough to remember a time before the regular use of cell phones. My parents got their first one in the mid-90’s. My aunt got one too, mostly because she was caring for my grandma and needed to stay reachable. Back then, minutes were a precious commodity. You didn’t just use your phone. You rationed it.

    I didn’t get my own phone until I was graduating high school. My mom joked about calling me during graduation to make sure my diploma was legit. I have forgotten what my number was back then. It’s somewhere in the ether with my high school locker combo.

    My First “Smart” Phone

    My first smartphone was an AT&T (HTC) Tilt—Windows Mobile, baby. I think got it on sale with a two contract, mostly for the novelty of “the internet” in my pocket. The iPhone had just launched, but it wasn’t in my budget.

    Fast forward a few years, and now I’m Team Apple for life.

    Rewired Society

    Don’t get me wrong smartphones are useful. I love being capable of writing blog posts like this one on the go. I can stream music and podcasts without juggling devices. I look up trivia mid-conversation like a know-it-all wizard. It’s convenience in my pocket.

    But… they’ve also rewired us. We’re always reachable, always plugged in. Our downtime is filled with a never-ending scroll of reels, tweets, memes, and 24/7 news updates.

    I’m as guilty as anyone. Give me five minutes. I’ll lose them to Facebook stories or Instagram reels I didn’t even mean to tap on.

    A Few Stats That Might Surprise You:

    Phone use is up—way up.

    According to Pew Research Center in 2024, 98% of Americans now own a cellphone. Over 91% of teens use theirs just to pass the time.

    Smartphone “addiction” is real.

    • 57% of Americans consider themselves addicted to their phones.
    • 3 in 4 feel uncomfortable without them.
    • 1 in 6 sleep with their phones.
    • Nearly half panic when the battery drops below 20%.

    We’re glued to our screens.

    Americans check their phones 144 times per day and spend an average of 4.5 hours daily on them; that’s up over 50% from just two years ago.

    And yet, they’re our lifeline.

    From music to maps, IDs to emergency access, they’re not just helpful they’ve become essential. For better or worse.

    Freeing Feeling

    Still, something about leaving my phone behind felt… freeing.

    For once, I was here in the moment. I noticed more. The way the early sun reflected off windows as I walked towards the train. The rustle of leaves. The quiet murmur of the city on a Saturday. 

    Sure, I had a few anxious thoughts. What if there’s an emergency? What if Lassie can’t text me that Timmy fell in the well?! But the world didn’t end.

    My Apple Watch, though less feature-packed, has my back. I can still get directions to the café. I can make a quick phone call if needed I check messages from people who matter. I even pay for coffee if I really wanted to. (Though using it for payments is still more awkward than helpful for me.)

    I’m not about to go full off-the-grid minimalist. But next time I forget my phone? I just might let it be. Sometimes, it’s worth being disconnected to reconnect with the world, with others, and with yourself.

    My challenge to you

    Try it. Leave your phone at home on purpose. Just once. Feel what it’s like to not have that constant pull in your pocket. You might be surprised at what you notice. And you’ll definitely survive.

    (Lassie, I trust, will find another way to reach you.)

  • A Moment of Green: A Poem from the Loring Greenway

    There’s a stretch of the Loring Greenway that never fails to quiet the noise inside my head. Every time I walk it, I feel like I’ve stepped out of the city and into a secret world. It is a place where the air smells different. The rustle of leaves and birdsong feel like old friends.

    The photo below doesn’t quite capture the feeling (does any photo ever?), but it’s the view that inspired the poem.

    The Greenway

    The greenway is like being teleported.

    Gone are the noises of the big city.

    The scent of nature surrounds me.

    Birdsong drifts from the trees and fills me.

    Flowers bloom, green leaves rustle—

    offering warmth the concrete jungle lacks.

    It is an oasis.

    It is a respite.

    It is a calming force.

    There are times I want to stay here forever,

    to escape the world and its responsibilities.

    But for now,

    I’ll sit a moment longer,

    and simply enjoy—

    the greenway.

  • Every Day, Not Just May: A Reflection on Mental Health Awareness

    Every Day, Not Just May: A Reflection on Mental Health Awareness

    Why We Need More Than a Month

    May is Mental Health Awareness Month. It’s a time when you’ll see posts, ribbons, infographics, and campaigns reminding us to check in on ourselves and others. And don’t get me wrong—that’s important. But mental health isn’t something we should only be aware of one month a year.

    It’s something we should acknowledge, support, and talk about every single day.

    My Mental Health Journey

    Mental health struggles don’t come with a calendar notification. They don’t wait until May to make themselves known. For some of us, they’re lifelong companions—sometimes silent, sometimes loud, sometimes manageable, sometimes utterly overwhelming.

    I’ve been living with anxiety and depression for as long as I can remember. But for years, I didn’t have a name for what I was feeling. I didn’t know that the heaviness, the racing thoughts, and the sudden and intense emotional dips weren’t just “personality quirks.” They were not something to tough out. I finally received the right diagnosis when I became an adult and sought professional help. More importantly, I got the right support. Medication and counseling made a world of difference for me. But even with treatment, mental health isn’t something that just gets “fixed.” It’s something I continue to manage, day by day.

    You Can’t Always See It

    Here’s the thing: you can’t always see it.

    People with mental health challenges often look “fine” on the outside. Smiling. Working. Cracking jokes. Showing up. We become masters of masking. We hide the pain, the fear, and the spiral. Society hasn’t always been kind to people who show those things. But just because someone looks okay doesn’t mean they are.

    Some days, I genuinely feel good. I feel steady, grounded, even joyful. Other days, something as small as a smell can affect me. A song or an old photo may send me down a dark tunnel I wasn’t expecting. It can take everything I have to claw my way back out.

    Coping Isn’t Always Healthy

    And let’s talk about coping mechanisms. I joke about my “coffee addiction”—and yes, my relationship with caffeine is a little… complicated. But beyond the laughs, I’ve also had a much more serious struggle with alcohol. For a while, I used it to cope. To numb. To silence the noise. But through therapy and intentional choices, I’ve worked hard to build a healthier relationship with alcohol. (Still working on the coffee one, though. Baby steps.)

    Why I’m Sharing This

    I’m not sharing this for pity. I’m sharing this because mental health is still so misunderstood, so stigmatized, and so often invisible. I want to be part of normalizing the conversation. Because the more we talk about it, the more we make space for people to feel less alone.

    So if you’re struggling right now—silently or not—please know you’re not alone. You matter. You deserve support. And there’s absolutely no shame in seeking help.

    Mental health awareness doesn’t end when May does.

    It’s an everyday thing. Let’s keep talking.

    Mental Health Resources

    If you or someone you love is struggling with mental health, please know that help is available. You are not alone.

    Emergency Help (24/7):

    • 988 Suicide & Crisis Lifeline: Call or text 988 or chat at 988lifeline.org Free, confidential support for people in emotional distress or crisis.
    • Crisis Text Line: Text HELLO to 741741 Trained crisis counselors available anytime, anywhere in the U.S.
    • National Domestic Violence Hotline: Call 1-800-799-7233 or text START to 88788 thehotline.org

    Support for Specific Communities:

    Ongoing Mental Health Support:

  • Out of My Mind and Back Into My Memories

    Out of My Mind and Back Into My Memories

    Why This Story Hit So Hard

    About a month ago I watched the movie Out of My Mind on Disney+. Afterward, I decided to go back and read the book. I’m so glad I did. You know what they say books are always better than the movies.

    Even though I saw the movie a month ago, Sharon Draper’s words brought back memories. I hadn’t expected those memories to resurface. They still ache a little, even years later.

    Before I go any further, I want to be clear. These are my thoughts, my feelings, and my recollections of what happened. Memory is slippery. Emotions can tint the edges. So take what I say with a grain of salt. Know that this is how it felt to me. Sometimes that’s the most honest thing a person can offer.

    Melody’s Story, and Mine

    In the story, Melody is a brilliant girl with cerebral palsy. She uses a communication device, has a sharp wit, and knows more than most people give her credit for. A highly emotional moment in the book occurs when her classmates are selected for a big trip to Washington, D.C.

    Melody is supposed to go too. But things don’t go as planned. Melody doesn’t get to go. Reading that part felt like looking in a mirror.

    The Trip I Didn’t Get to Take

    When I was in seventh grade, my school organized a class trip to Washington, D.C. just like Melody’s. I was excited. Nervous. Hopeful. I pictured myself standing in front of the Lincoln Memorial. I imagined exploring the Smithsonian. I saw myself laughing with my classmates in a hotel room late at night. I imagined the memories we’d make, the stories I’d have to tell. But then came the catch.

    The school told me I couldn’t go unless one of my parents, or another adult, came along as my personal aide. They said it was about ensuring my safety and meeting any personal needs I might have during the trip. But here’s the thing: by that age, I could dress, bathe, feed, and toilet myself without assistance. The only support I might’ve needed was help navigating long distances. Someone could push my wheelchair when my stamina ran low from all the sightseeing. It wasn’t really about safety.

    It was about discomfort. Their discomfort. They didn’t want to figure out how to include a disabled student. They weren’t willing to make accommodations. And they certainly didn’t offer to help cover the cost of bringing someone to support me. So their solution? Exclude me instead.

    Much like Melody in the story, I was deeply disappointed. But disappointment was nothing new to me. I’d grown used to it whether it came from friends, family, or the world at large. I rarely showed it, because by then, I had learned to hold it in. I knew expressing it wouldn’t change anything.

    Still, I remember one conversation vividly. One evening, I was riding in the car with my aunt. I told her how much I wanted to go on that trip. I don’t remember where we were headed, but I remember the weight of wanting so badly to be included. She even talked about trying to help cover the cost, or going with to aid me, to make it possible.

    But in the end, it just wasn’t possible. My parents couldn’t afford the added expense. So that was it. No Washington, D.C. No trip. No adventure. Just me, left behind at school while my peers made memories without me.

    My class explored the nation’s capital while I stayed behind. I sat in a classroom with the small group of students who didn’t go. I felt forgotten. Left out. It felt unfair. I had wanted that experience so badly. I wanted to be part of the stories they’d tell when they came home. I didn’t want to be the kid they left behind.

    Bitterness and Bucket Lists

    Even now, nearly 30 years later, it still leaves a slightly bitter taste in my mouth. I still haven’t made it to Washington, D.C. But it’s on my bucket list. When I finally get there, I’ll be standing tall. You better believe I’ll be giving a big, proud, proverbial middle finger to every staff member. This is for every teacher who once thought I didn’t belong. Because guess what? I made it anyway.

    Melody’s Story Is Our Story

    Reading Out of My Mind brought all of that back. Melody’s story isn’t just hers. It belongs to many of us. We have had to fight just to be included. Others take these things for granted. Her heartbreak is our heartbreak. But so is her strength, her wit, and her refusal to be underestimated.

    That’s the power of stories like this one. They don’t just show the world as it is they help us imagine the world as it should be.

    A World Where Everyone Belongs

    I believe in that world. One where we don’t put conditions on belonging. One where we assume competence instead of questioning it. One where disabled children aren’t left behind because adults decided their inclusion was too inconvenient or too expensive.

    If you haven’t read Out of My Mind, I encourage you to. Yes, it’s a work of fiction. However, it captures something deeply real. It portrays the inner life of a young person who is so often spoken about instead of spoken to. Melody’s voice may be artificial in the technical sense, but her story rings powerfully human.

    Let’s build a world where no one has to prove they deserve to be part of the story.

    Let’s listen.

    Let’s include.

    And let’s never stop imagining, and creating, a better way forward.

  • From Poster Child to Invisible Adult

    From Poster Child to Invisible Adult

    Growing Up Disabled in a World Obsessed with Cute

    When I was a kid, people thought I was adorable. I had chubby cheeks, a bright smile, and Cerebral Palsy.

    That last part, my disability, somehow made me even more “inspiring” in the eyes of strangers. I was the kind of kid who showed up in brochures for community events. I got extra attention from teachers and therapists. I drew “Aww”s and “God bless him”s at the grocery store.

    A young boy with curly hair and large glasses smiling brightly at the camera, wearing a yellow and black striped collared shirt with a yellow boutonnière pinned to it.
    Me at my most joyful—missing teeth, oversized glasses, and a smile bigger than my face. The kind of photo people loved to “aww” over.

    Disabled kids are cute. Society loves a feel-good story, especially one that comes in a pint-sized package with leg braces and a cheeky grin.

    But here’s the thing: I grew up.

    And when I did, the attention disappeared.

    I’m 41 now. Still disabled. Still Cerebral Palsy. Still me. But somewhere along the way, I stopped being cute. And in the eyes of the world, I stopped being seen.

    Adult man with curly hair wearing clear glasses, a gray hoodie, and a denim vest, sitting indoors and smiling slightly in a well-lit coffee shop.
    The same person you saw in the childhood photos. Different glasses, different decade. Same Cerebral Palsy. Same me.

    The “Cute Factor” and Conditional Compassion

    We follow a cultural script with disabled kids. We shower them with support, attention, and affection. This continues as long as they remain children. The moment they grow into adulthood, that same compassion starts to dry up. Public programs disappear. Services shrink. Opportunities narrow. Even social attitudes shift from admiration to discomfort, from celebration to suspicion.

    As a child, I had access to therapies, educational supports, and community resources. There were coordinated efforts to help me grow, thrive, and participate. But as I got older, it felt like the message became: Well, good luck now you are on your own.

    I went from being someone people wanted to help… to someone people tried not to make eye contact with.

    The Adult Disability Cliff

    This isn’t just my story. This situation is a systemic reality known in advocacy circles as the services cliff. The support sharply drops off when a disabled person ages out of pediatric care. It also decreases when they leave school-based programs or children’s nonprofit funding.

    We don’t talk about this enough. Adults with disabilities face higher rates of poverty, unemployment, isolation, and inadequate healthcare. But we rarely make the news unless we’re breaking Paralympic records or fighting for survival in a viral video.

    Why? Because disabled adults don’t make people feel warm and fuzzy in the same way disabled kids do. We complicate the narrative. We ask harder questions. We don’t fit into feel-good stories with easy endings.

    Kids vs. Adults

    As a Child with a DisabilityAs an Adult with a Disability
    School-based physical, occupational, and speech therapyTherapy often not covered or comes with strict insurance limitations
    Individualized Education Plans (IEPs) with legal accountabilityNo IEPs for college or jobs—just ADA “reasonable accommodations”
    Access to special education teachers and support staffLimited access to job coaches; shrinking supported employment resources
    Pediatricians and specialist trained in children with disabilitiesFewer adult physicians familiar with complex disability care
    Early intervention programs (birth–age 3)Virtually no equivalent early adult transition support
    Summer camps, social groups, and extracurricular inclusion programsSocial isolation is common; few adult-focused adaptive recreation spaces
    Case managers to help coordinate servicesAdults often navigate a confusing system alone
    Parent advocates built into the systemAdults are expected to self-advocate
    Medicaid waivers often easier to access for minorsAdult services require complex eligibility and waitlists
    Positive visibility in media and fundraisersAdults rarely portrayed unless overcoming “against all odds”

    The shift is more than inconvenient; it’s structural. We build systems around disabled children to help them grow. Then we tear those systems down just when adulthood starts demanding more from us: jobs, independence, healthcare navigation, stable housing.

    The message? “You’re on your own now.”

    From Three Times a Week to Barely At All

    When I was a kid, I went to physical therapy three times a week.

    I’ll be honest—I wasn’t a huge fan of it at the time. I was a kid. I didn’t want to stretch or do strength exercises. I wanted to be outside or reading or literally anywhere else. But looking back, I realize just how lucky I was.

    Those sessions helped me build strength, coordination, and confidence. They gave me tools to move through the world.

    Now, as an adult? I can count the number of PT sessions I’ve had in the past ten years on both hands.

    It’s not that I stopped needing physical therapy. Cerebral Palsy didn’t magically go away when I turned 18. But getting PT as an adult is a whole different game. There has to be a specific reason or goal that meets insurance criteria. It’s not about maintaining mobility. It’s about justifying the expense.

    Even when you do qualify, you’re often limited to a small number of sessions. Once they’re gone, they’re gone. Never mind if your muscles get tighter again, or if your mobility starts slipping. There’s no regular check-in. No ongoing plan. Just a shrug and off you go.

    I get that insurance companies want to save money. But regular PT for adults isn’t just about recovery it’s about maintenance. It’s about keeping people functioning and independent for as long as possible.

    I’ll be the first to admit it’s not always easy to schedule therapy sessions as an adult. I remember when I was taking classes in Hutchinson. Just finding time between classes and homework to go to PT was a challenge.

    Now, I have to fight for every step literally and figuratively.

    The Economic Angle: Preventative Care Saves Money

    What gets overlooked in all this is how short-sighted the system is. Ongoing PT and accessible health support aren’t just about comfort they’re about prevention. If adults with mobility disabilities had regular maintenance care, many could avoid injuries. Falls, surgeries, and hospital stays could also be avoided later.

    But instead of investing a little now, we let people deteriorate, and then spend far more reacting to preventable problems. It’s penny-wise and pound-foolish. And people like me pay the price with our bodies.

    The Emotional Cost: Losing Visibility

    There’s a strange grief in realizing you once mattered more to the world.

    As a child, I had a whole team cheering me on therapists, teachers, volunteers, neighbors. Now, I’m often just trying to prove I deserve the bare minimum. It’s not just about services. It’s about dignity. About being seen.

    When I was younger, people called me brave. Now, they call me an expense.

    Still Here. Still Worthy.

    I’ve included a photos. Me as a child, me as an adult. The disability in both pictures is the same. The person? Still me.

    But the world doesn’t treat those two versions of me the same way.

    This isn’t a plea for pity or applause. It’s a call to remember that disabled children become disabled adults. We don’t stop needing support, visibility, and respect just because we’ve aged out of a marketing campaign.

    The cute kid didn’t disappear. He just grew up.

    And he still matters.

  • Somewhere Wet and Windy

    Somewhere Wet and Windy

    The Walk Begins

    This is your on-the-ground correspondent reporting live from the storm zone—also known as my neighborhood sidewalk.

    It all began innocently enough. I had just finished my coffee. I was strolling home with Surley, my loyal service dog. A light drizzle began to fall. No big deal. We’re Minnesotans. We’ve seen worse.

    A city street in Minneapolis with dark storm clouds rolling in, a USPS mailbox in the foreground.
    Earlier in the day—ominous clouds overhead, but still totally convinced I’d make it home dry.
    Spoiler: I did not.

    The Downpour + Tornado Siren

    But then—cue the dramatic music—the sky opened up. Torrential rain. We ducked under shelter. It let up. We continued. It poured again. We found more cover. The storm played with us like a cat with a string.

    And just when we were four blocks from home, the tornado siren wailed.

    Where was it located? Right on the very street we were walking. Rain pelted our faces. The wind howled. The siren blared as if it were auditioning for the lead role in a disaster film.

    Naturally, as the siren screamed, I started picturing The Wizard of Oz. But instead of Dorothy and Toto, it was Levi and Surley getting swept up and carried off to the land of Oz. I wasn’t wearing ruby slippers. However, I was absolutely ready to take down a witch with a soggy sock. I had some Midwestern passive aggression ready as well.

    The real star of this cinematic experience? Surley. Calm. Steady. Unbothered. For a dog who usually finds storms a bit spooky, he handled it like a seasoned storm chaser.

    I told him repeatedly how proud I was. He just powered through the wind and the rain. He glanced at me as if to say, “Chill, I’ve got this.”

    Coming Home

    We made it home drenched, slightly stunned, and still laughing.

    Surley celebrated with zoomies.

    I dried us off like we’d just crawled out of a creek. Which, in a way, we had.

    A yellow Labrador retriever lying on a carpet, still damp from the rain, resting with his eyes half-closed.
    Post-storm status: one brave boy, thoroughly toweled and dramatically resting on the living room floor.
    (Zoomies: complete. Dignity: mostly intact.)

    Your Turn

    Have you ever been caught in a surprise storm with your pet?
    Did they channel inner courage… or cartoon chaos?

    Tell me your best soggy, windy, or siren-filled story in the comments.

  • Where I Write: My Favorite Coffee Shops for Creativity and Caffeine

    I love sitting in local coffee shops to write. I’m fortunate to have so many great spots within walking distance of my home. Each spot has its own vibe. Each has a reason for becoming a favorite. Here are just a few that come to mind, in no particular order.

    Caribou Coffee on 11th & Nicollet Mall

    I’ve loved Caribou for as long as I can remember, even before I drank coffee myself. A longtime friend was once a VP at Caribou. They would occasionally leave coffee gifts on my aunts’ doorsteps. The brand has always felt familiar.

    What I love about this location is its convenience — just a few blocks from home. The huge windows flood the space with natural light, perfect for people-watching along the street and sidewalk. In the summer, I love sitting outside with a cool drink. If the patio is full, I wander across the street to Peavey Plaza and grab a bench.

    Caribou’s drinks are always my top pick. Their milk chocolate syrup is smoother than most, even compared to others on this list. My go-to drink depends on the weather. I choose a milk chocolate mocha in winter. In summer, I prefer a plain iced crafted press. Before they introduced the crafted press, I’d order an iced mocha without whip.

    Corner Coffee on 9th & Nicollet Mall

    This corner has seen many coffee shop incarnations. There has been a Starbucks, Dunn Bros, and a tea and matcha place. Now it’s Corner Coffee, and I couldn’t be happier. When it opened in spring 2024, I was eager to try it. I love discovering new places!

    The vibe here is cozy and inviting, and I always feel at home working on a project. My go-to drink is a latte, regardless of the season. As for food, it’s a toss-up between their pastries and the fruit pies they often stock.

    Starbucks in the IDS Crystal Court

    I don’t visit this Starbucks as much in the warmer months. It’s a perfect winter retreat since it’s connected to the downtown skyway system. There’s no need to brave the cold! One detail I really appreciate: they have a table clearly labeled for people with mobility aids like mine. In fact, I wrote about that in one of my very first blog posts.

    Mocha Momma’s Coffee on 3rd & Nicollet Mall

    This gem is tucked inside the central public library. I first discovered it when I went to pick up a library hold. Like many downtown spaces, it’s been home to different shops over the years. However, Mocha Momma’s has quickly become a favorite.

    The atmosphere feels personal and welcoming — it seems to be run by just one person, who greets everyone warmly. There’s a great variety of drinks (including affogato — vanilla ice cream drowned in espresso!), and the apple fritters are incredible.

    A funny moment: recently, I was so engrossed in writing that I didn’t hear the closing announcement. Thankfully, the owner kindly let me finish my thought before gently nudging me out.

    These coffee shops are where I can sit, relax, and dive into my latest writing project. I feel so lucky to have all these options nearby. However, I wish my wallet loved them as much as I do!

    Do you have a favorite coffee shop where you love to read, write, or just relax? I’m always looking for new spots to explore! Drop your recommendations in the comments. I’d love to hear about your favorite places to fuel your creativity. I’m also interested in where you satisfy your caffeine cravings.

  • Redrawing the Map

    Redrawing the Map

    This post grew out of a writing class assignment. We were asked to draw a map of my childhood neighborhood. Then we had to tell a story about it. What emerged was not a single story. It was an exploration of childhood, disability, and friendship. It also examined how we redraw our lives over time.

    When I was drawing the map for class, I realized how small my world was. We were supposed to share a story about our neighborhood. However, I didn’t have any that came to mind. At least, not in the way the assignment intended. What came to mind instead was pain and heartache.

    The sharp smell of pencil lead clung to my fingers as I traced the roads of my childhood. On the page, the map looked simple. Two gravel roads crossed like stitches. There was a handful of houses. The sagging fence line was where the horses would run and buck. But as I drew, the map whispered back something I hadn’t expected.

    The map was small.

    Not just in miles and landmarks, but in meaning. It made me realize how small and limited my world had been.

    I rarely left home. The only times I did leave were to go to school or church (at least until I got confirmed). Occasionally, I went to the theater, the skating rink, or a cousin’s house for a sleepover. Those trips stopped once we hit junior high. I really interacted with neighbors only when we rode horses around the section.

    Living in the country and having a disability made it difficult to have friends. The isolation wasn’t just about miles of gravel roads. It was about feeling cut off from the world of other kids. Even when classmates lived nearby, the distance between us felt bigger than geography. It was the distance of difference, of not quite fitting into their games, their rhythms, their conversations.

    I remember when I was in school, there were only a few places I could sit during lunch. We had long, picnic-style tables, and because of the wheelchair, I was limited to the ends. I didn’t want to be a burden to anyone. So, I’d often pick the same table. It was the one closest to the end of the cafeteria line. It became its own quiet ritual — not quite belonging, not quite invisible, always on the edge of things.

    Still, there were moments of connection that broke through.

    One afternoon in first or second grade, I played baseball in the yard of the twin girls. They lived down the other country road and were also in my grade. I sat on the grass to make it easier to get around because wheelchairs and lawns don’t mix well. I don’t remember much else from that day. I recall the sun on our backs. There was a quiet sense of belonging, even if only for a moment.

    I remember having a couple of my own friends over — both times because it was my birthday. The first time was in fifth grade when I “invited” the pastor’s son from church. He came over for a sleepover. I still shared a room with my sister then. That night, my mom decided it was time for my leg stretches. They usually forgot them but remembered at the worst moment. I was hopeful they’d skip it. But no. I lay there trying not to cry in front of my friend. My mom stretched my legs, sometimes painfully. He didn’t stay long the next morning. For my birthday, he gave me a black-and-white picture of a dragon to color in with markers. I think I colored it, though I don’t remember for sure.

    Then there was the classmate who lived next door for a while. We’d been friends since kindergarten. We were the kind of friends who came and went as their family moved away. Then they came back, and after a while, moved away again. When they came back briefly in eighth grade, I remember trying harder. I made a point to talk with them and to help. It was a small act of making amends. I pulled away in fifth grade because I thought they were “cramping my style.”

    The second birthday friend came when I was a senior in high school. We got out of school early one Friday. We wandered around downtown. This was a small thing to most people, but huge for me. I was so used to the school bus taking me straight home. We went to the Video Box. I rented my first R-rated movie because I was now eighteen. I think it was American Pie. My friend gave me a finger skateboard to assemble. It was a cool alternative. A real skateboard would’ve been too hard for me to use. I held onto it for years. Looking back, I realize he was probably one of the only “real” friends I had in high school.

    These two friends? I haven’t spoken to them in years. If you tracked them down and asked, they might not remember the details. But I do.

    Looking back, I see that while I often felt on the margins, I wasn’t as alone as I thought. Those small moments — a game of baseball, an awkward birthday sleepover, a walk downtown — were lifelines. They didn’t erase the loneliness, but they punctured it, leaving small but lasting marks. They taught me that connection doesn’t have to look like the movies or the friendships I envied. It can be quiet, brief, imperfect — and still matter.

    And as much as the map of my childhood was small, the map of my adult life is much broader. I have a small core group of friends. There are fewer than a dozen of them. But they are the kind of people who show up when it matters.

    When my last living grandma was dying of cancer, they were there. They helped with rides and supported me during the funeral. When my first service dog, Dempsey, was diagnosed with third-degree AV block, they ensured I got him to his vet. They made sure he attended his appointments. They also made sure that I ate. When he passed away unexpectedly, one of them drove nearly eight hours round-trip to bring me home from a camping trip in northern Minnesota.

    Back then, I thought the boundaries of my world were fixed. I believed the small map I lived in was all I’d ever know. But maps, I’ve learned, can be redrawn.

    My childhood map may have been small. However, my adult map is wide enough to hold friendship. It also encompasses grief, loyalty, and love. Sometimes, the best stories come from the places we outgrow. These stories also come from the people we learn to carry with us.

    Author’s Note:
    I share this piece with the hope it resonates. It is for anyone who has ever felt on the margins. Yet, they still found meaning in imperfect connections. It’s about small worlds, quiet resilience, and the way we carry the past as we grow into larger lives.

  • The Story of Me: A Life in Songs

    A few months ago, I shared on Facebook about my dream band. I am not the lead singer. Instead, I am the mastermind behind an all-star lineup of incredible musicians. I also created a set list: a musical journey through my life.

    Since then, the idea has evolved. Some songs have shifted. Some meanings have deepened. I found myself wanting to explore more deeply why I chose each song. This blog post is my way of expanding that original idea into something fuller, something truer.

    This isn’t just a collection of songs I like—although, yes, I love every single one. These are songs that shaped me, challenged me, lifted me up, and made me who I am today. They are the soundtrack to every twist, turn, heartbreak, and triumph.

    These songs aren’t always ones I heard at the exact moment something happened in my life. Some came later, after the dust settled. Some found me when I didn’t even know I was looking. But each song helps me tell a part of my story. Each one shines a light on a chapter I lived—the good, the hard, the unforgettable. This is The Story of Me.

    Act 1: Roots and Dreams

    “Heartland” – George Strait

    Selected Lyric:

    “When you hear twin fiddles and a steel guitar, you’re listening to the sound of the American heart.”

    Reflection: Growing up, “Heartland” was always playing in the background of my life. It was not just a song, but also a feeling. My mom was a huge George Strait fan. She loved this song. I can’t even count how many times we watched the George Strait movie Pure Country together. It became part of the fabric of our home.

    This song speaks to my roots on the hobby farm in Minnesota. My childhood was shaped by open fields, hardworking days, and country values. I live in the city now. Whenever I hear this song, it takes me straight back to that life. It was simpler and more rugged. It’s a piece of home, stitched into the soundtrack of my story.

    “Boot Scootin’ Boogie” – Brooks & Dunn

    Selected Lyric:

    “Out in the country past the city limits sign, well there’s a honky-tonk near the county line.”

    Reflection: Whenever I hear “Boot Scootin’ Boogie,” I can’t help but smile — and I definitely can’t sit still.

    This song brings me back to trail rides, when the organizers would throw dances that felt like pure magic. I recall being out on the dance floor with our longtime friend Rita. She never once cared that I used a chair.

    We danced, we twirled, and we laughed until it felt like we could float. Rita’s smile was as much a part of the dance as the music itself.

    Even today, when this song pops up on a playlist, I can’t help but move a little. It sneaks onto the radio and I can’t resist it. For a moment, I’m right back there, boot scootin’ through a night full of freedom and joy.

    “Should’ve Been a Cowboy” – Toby Keith

    Selected Lyric:

    “I should’ve been a cowboy, I should’ve learned to rope and ride.”

    Reflection: Despite the wheelchair and my disability, part of me always dreamed of being a cowboy.

    Maybe it sounds silly. When you grow up on a farm surrounded by horses, animals, and wide skies, the dream just seeps into you. It becomes a part of your very being.

    “Should’ve Been a Cowboy” captures that longing. It represents the fantasy of freedom and adventure. It embodies a life lived on your own terms.

    It’s a song I also heard often at trail ride dances. It links it forever to memories of dusty boots. I remember late nights and a few wild spins around the dance floor.

    Even if I never got to ride off into the sunset, this song keeps that dream alive in me. It remains where it belongs.

    “Wide Open Spaces” – The Chicks

    Selected Lyric:

    “She needs wide open spaces, room to make her big mistakes.”

    Reflection: “Wide Open Spaces” is about growing up — about realizing you need more than the world you were given.

    When I graduated high school in 2002, my parents were understandably nervous. Their little boy was in a wheelchair. He had big dreams and an even bigger heart. He was stepping out into a world they couldn’t protect him from.

    At first, Hutchinson, Minnesota, was my stop. I knew almost immediately that it wasn’t where I was meant to land.

    I needed Minneapolis.

    The big city wasn’t just exciting — it was necessary. It was the place where I could finally begin to find myself. I was a queer person still wrestling with coming out. I was also a disabled person searching for real opportunity.

    This song became an anthem for that ache. It symbolized the hunger to live a life too big for the fences around me.

    “Heads Carolina, Tails California” – Jo Dee Messina

    Selected Lyric:

    “Heads Carolina, tails California, somewhere greener, somewhere warmer.”

    Reflection: “Heads Carolina, Tails California” fits into my story alongside “Wide Open Spaces”.

    It’s the other side of the same dream: the impulsive, wide-eyed yearning for more.

    “Wide Open Spaces” was the heavy ache of leaving. This song embodies the giddy hope. Somewhere — anywhere — could be the place where life would finally open up for me.

    It’s about grabbing freedom by the hand. You flip a coin. Trust that wherever you land, it will be yours to claim.

    Act 2: Searching and Struggling

    “Iris” – Goo Goo Dolls

    Selected Lyric:

    “I don’t want the world to see me, ’cause I don’t think that they’d understand.”

    Reflection: “Iris” captures a part of my story. It was heavy and complicated. It involved the long and messy process of starting to figure out who I really was.

    There was so much fear tangled up in that discovery.

    I didn’t want the world to see me, because deep down, I didn’t believe they would understand.

    People often struggle to see disabled people fully — to recognize us as complex, whole, feeling humans.

    They struggle even more to see queer disabled people.

    This song had the aching vocals and the haunting rhythm. It became a place where I could sink down into my feelings. I could be fully honest with myself about the isolation and the yearning.

    There was a stubborn, shining hope that somehow, someday, someone would understand.

    “Fast Car” – Tracy Chapman

    Selected Lyric:

    “You got a fast car, I want a ticket to anywhere.”

    Reflection: “Fast Car” is about leaving the past behind. It is not about forgetting it or pretending it didn’t shape you. It is about choosing to move through the sticky, painful parts toward something better.

    It’s about believing in the possibility of more, even when everything you know is pulling you backward.

    This song became part of my story. There have been so many times I wanted — needed — to keep moving forward. I had to believe that something better was just down the road.

    It’s the soundtrack of resilience. It embodies stubborn hope. It represents not giving up on yourself even when the past tries to anchor you in place.

    “I’m Alright” – Jo Dee Messina

    Selected Lyric:

    “It’s a beautiful day, not a cloud in sight. So I guess I’m doin’ alright.”

    Reflection: There was a stretch of time in my life when everything felt heavy.

    I came out to my parents. It didn’t happen the way I had hoped. The experience caused a lot of hurt feelings, tears, and anguish on all sides.

    Around that same time, I also lost my Grandma Dokken. Watching her slowly slip away because of Alzheimer’s was devastating. It was even harder. My relationship with my other grandmother had always been strained by complicated family dynamics. This made the loss of Grandma Dokken cut even deeper.

    After all of that heartache, I came to a realization:

    I had gone through hard things.

    I had felt pain that hollowed me out.

    And still — I was going to be alright.

    This song became a quiet promise to myself.

    Not because everything was perfect.

    But because I was still standing.

    “Gravity” – Sara Bareilles

    Selected Lyric:

    “Set me free, leave me be, I don’t want to fall another moment into your gravity.”

    Reflection: Sara Bareilles originally wrote “Gravity” about a relationship. However, the song took on an entirely different meaning for me.

    For me, it became a conversation with my depression and anxiety. This was an invisible and relentless force. It always seemed to pull me back down into the depths of myself.

    It’s that painful tug you feel even when you’re trying so hard to move forward.

    It’s the exhaustion of fighting to stay afloat.

    This song became a mirror for that struggle — that exhausting, tender plea to my own mind: Let me go. Let me breathe. Let me be free.

    It’s not just sad; it’s truthful. It reminds me that even in the middle of that pull, I am aware. I am fighting. I am still here.

    “Angel” – Ellis Delaney

    Selected Lyric:

    “I need a little company, all I need is a pat on the back.”

    Reflection: Throughout my life, there have been so many moments when I’ve felt adrift. I was alone in the world. I was hanging on by a thread.

    “Angel” captures that ache perfectly. It conveys the quiet, desperate hope that someone might reach out, take my hand, and just be there.

    It’s not about needing someone to fix everything.

    It’s about needing a little company and a little comfort. It’s also a reminder that the path is mine alone to walk. However, I don’t have to walk it completely alone.

    Whenever I hear this song, it brings me back to those hard moments. It reminds me that it’s okay to need others. It’s okay to reach for connection. It’s okay to ask for an angel when the night feels too heavy.

    Act 3: Loyalty, Loss, and Love

    “Ride” – Amanda Marshall

    Selected Lyric:

    “If you’re out of inspiration, all you feel is desperation. Consider this an invitation — I’ll be your ride.”

    Reflection: College was where I found some of the best people I’ve ever known.

    Even 20 years later, we’re still connected — not just in memories, but in life.

    They’ve blessed me with the honor of being godfather to one of their children. This gift still humbles me beyond words.

    These friends are my ride-or-die crew. They are the ones I would drop everything for, without a second thought. I know they would do the same for me.

    “Ride” perfectly captures that spirit. It embodies the fierce loyalty. It reflects the deep-rooted love. The unspoken promise holds that no matter where life takes us, we’re riding it together.

    “When It Don’t Come Easy” – Keri Noble

    Selected Lyric:

    “But if you break down, I’ll drive out and find you.”

    Reflection: “When It Don’t Come Easy” is a quieter promise, but no less fierce.

    Over the years, I’ve had friendships that have weathered storms — real storms, the kind you don’t walk through unscathed.

    We’ve stood by each other during our lowest, messiest, most broken moments.

    This song is my way of saying:

    I got you.

    When things fall apart, I’ll come looking for you. When it feels like you can’t take another step, I’ll be the one who finds you.

    I’ll bring you home.

    No judgment, no expectations — just love.

    This song reminds me that sometimes the most powerful thing you can do for someone is simply stay.

    “Beat You There” – Will Dempsey

    Selected Lyric:

    “Don’t cry for me, I’m alright. I’m better than you know.”

    Reflection: “Beat You There” cuts deep into my story.

    I found this song not long after Dempsey — my first service dog, my companion, my constant — passed away.

    That loss tore a hole in me.

    Finding this song gave me something to hold onto during that time. Hearing Will Dempsey sing about love, loss, and the bittersweet promise of reunion provided comfort.

    It felt like Dempsey’s spirit was speaking back to me somehow. This was not just because of the name. It was because of the deep, aching truth woven into every word.

    “Beat You There” isn’t just about grief.

    It’s about remembrance, loyalty, and hope. We hold the hope that wherever our loved ones go, we will meet them again someday.

    Whenever I hear this song, I imagine raising a glass in a quiet toast:

    You beat me there. But one day, I’ll see you again.

    Act 4: Becoming

    “Wonder” – Natalie Merchant

    Selected Lyric:

    “They say I must be one of the wonders, God’s own creation.”

    Reflection: Growing up, people doubted my ability.

    Hell, even now — at 41 years old — people still doubt my ability.

    “Wonder” resonates with that feeling deeply.

    It’s not a song of anger or resentment.

    It’s a quiet, unshakable declaration: I am here. I am whole. I am wondrous, whether you see it or not.

    This song reminds me that I don’t have to fit anyone’s idea of what “ability” should be. I define what “success” should look like.

    I exist. I thrive.

    And in that, I am a wonder.

    “Days Like These” – Janis Ian

    Selected Lyric:

    “When the one thing left is the blessing of my dreams, I can make my peace with days like these.”

    Reflection: My aunt introduced me to Janis Ian when I was in college.

    I was initially attracted to the faster songs. These included those with driving rhythms like “God and the FBI.”

    But over time, “Days Like These” started to hit differently.

    It’s a quieter song, but it carries a heavy, beautiful truth:

    After all the struggle, all the loss, and all the hardship, the blessing of my dreams is enough. I have endured a lot. If I still have the people I love, then it’s enough.

    It’s not about pretending life is easy.

    It’s about recognizing that even on the hard days, especially on those challenging days, there’s still something strong and sacred. It’s worth holding onto these things.

    This song reminds me that survival isn’t just about getting through. It’s about carrying your dreams forward. This is true even when the skies stay dry a little too long.

    “Hometown” – Brandon Stansell

    Selected Lyric:

    “I should say thank you, ’cause now I finally know who I really am.”

    Reflection: Growing up in rural Minnesota was hard.

    There were so many things that made me feel alone. The small-town expectations were overwhelming. There were also the unspoken judgments. No matter how much I tried, I felt I would never quite fit into the mold laid out for me.

    But “Hometown” reminds me of the hard conversations and the quiet heartaches. Even through all of that, my hometown shaped me.

    It made me strong.

    It gave me the roots I needed, even if it took leaving to figure that out.

    I can’t change the past.

    And that’s okay.

    Now I know exactly who I am. It is not in spite of where I came from, but in some ways because of it.

    “Invisible” – Hunter Hayes

    Selected Lyric:

    “There’s so much more to life than what you’re feeling now.”

    Reflection: “Invisible” is the song I would sing to my younger self. I would sing it to the queer kid who felt unseen. They felt misunderstood and out of place.

    It’s also the song I would sing for every young person struggling to find their way. They are struggling to believe that they matter.

    Growing up, it often felt like I was invisible. It felt like who I was deep down didn’t fit into the world around me. Maybe it never would.

    This song is a promise:

    It will get better.

    You are seen.

    There’s so much more waiting for you beyond the smallness of this moment.

    You are not broken.

    You are not alone.

    You are not invisible.

    “Brave” – Sara Bareilles

    Selected Lyric:

    “Say what you wanna say, and let the words fall out.”

    Reflection: “Brave” is about finally finding the courage to say what you need to say.

    It’s about stepping into the space you were once too afraid to claim.

    For so long, fear kept me quiet. I was afraid of being misunderstood. I feared being judged. I worried about being too much or not enough.

    But bravery doesn’t mean you’re not scared.

    It means you speak anyway.

    This song reminds me — and challenges me — to keep choosing honesty, even when it’s hard.

    It’s an anthem for every moment I opened my mouth. I spoke my truth. I took one more step toward being fully, unapologetically myself.

    “Soar” – Christina Aguilera

    Selected Lyric:

    “Don’t be scared to fly alone. Find a path that is your own.”

    Reflection: “Soar” lives in the same spirit as “Brave”:

    It’s about stepping into who you are without apology.

    It’s about refusing to shrink, refusing to bend yourself to fit the world’s expectations.

    This song reminds me that bravery isn’t just about speaking your truth. It’s about living it. This is true even when the path feels lonely.

    “Soar” is the reminder that the world is mine to claim. I don’t have to wait for permission to build a life that feels true.

    It’s not about becoming someone else.

    It’s about finding — and loving — the person I’ve always been meant to be.

    “This Is Me” – Keala Settle (The Greatest Showman)

    Selected Lyric:

    “I am brave, I am bruised, I am who I’m meant to be. This is me.”

    Reflection: “This Is Me” is the culmination of everything I’ve lived, everything I’ve fought through, everything I’ve become.

    It’s the moment I finally stand up and say:

    This is who I am.

    If you don’t like it, I don’t care.

    I’ve spent enough of my life shrinking, apologizing, trying to fit where I was never meant to fit.

    Now, I choose to take up space.

    Now, I choose to be seen.

    Bruised, brave, whole — exactly as I am.

    Encore

    “Gently We Row” – Melissa Etheridge

    Selected Lyric:

    “Slow, slow, this river is slow. We’re all out here on our own. Row, row, gently we row. One day we’ll find our way home.”

    Reflection: If there’s a final note to this story, it’s “Gently We Row.”

    Life isn’t a race.

    It’s not about having all the answers.

    It’s about moving forward, one step at a time. Take each moment as it comes. Do the best you can with what you have.

    This song reminds me that none of us really know exactly where we’re headed, and that’s okay.

    It’s okay to stumble.

    It’s okay to search.

    It’s okay to dream.

    What matters is that we keep rowing gently. We do so determinedly through the slow, winding river of life. We trust that someday, somehow, we’ll find our way home.

    And maybe the real magic isn’t in the finding.

    Maybe it’s in the rowing itself.

    Final Invitation

    Music tells a story. This one is mine.

    If you’ve never heard some of these songs or artists before, I encourage you to check them out. You might discover new music you love—and maybe, through that music, a little piece of who I am.

    Want to hear the full soundtrack?

    You can listen right here:

    What songs would be on your life’s soundtrack? I’d love to hear your set list. Drop it in the comments below!

  • A Revolution Remembered: 250 Years After the Shot Heard ’Round the World

    On April 19, 1775, British troops marched toward Concord to seize weapons. What they found instead was resistance. Ordinary farmers and tradesmen—Minutemen—stood their ground at Lexington. A single shot rang out. No one knows who fired it.

    But that one act of defiance became the spark that lit the American Revolution. That shot, the “shot heard ’round the world,” was not about war—it was about refusal. Refusal to be ruled without representation. Refusal to surrender liberty to unchecked power.

    Two hundred and fifty years later, we are again facing a moment of reckoning. Not with muskets, but with microphones. Not with bayonets, but with ballots and bold voices. The question before us now is the same one our founders asked themselves. Will we allow one person to dictate the future of the many?

    I am a disability advocate. I am deeply invested in civic participation. I’ve spent a lot of time thinking about what real representation looks like. I don’t just study history—I live its consequences. We can see the struggle when navigating inaccessible systems. We also witness it as democratic norms erode in real time. It’s clear that the fight for equity and accountability didn’t end in 1776. In fact, it’s happening right now.

    Today, in 2025, I find myself reflecting on that revolutionary spirit—and wondering how far we’ve strayed from its core principles.

    We now have a President who increasingly behaves as though he alone can decide what’s best for the country. He is circumventing the proper chain of constitutional authority. The office of the presidency is growing disturbingly monarchical. This change is due to sweeping executive orders and claims that other branches are “in the way.”

    What’s worse is that many in Congress, across both parties, are allowing it. The legislative branch should act as a check on power. Instead, it has become largely passive. This passivity enables the President to do whatever he sees fit.

    Even the judicial branch has begun picking and choosing which executive actions to confront, leaving accountability up to political whim. If the courts do rule against the President, there is a growing concern he may simply choose to ignore them. This is because the judiciary, for all its authority, has no enforcement power.

    If the executive no longer respects the rulings of the courts, democracy is not occurring. If the executive fails to adhere to the laws passed by Congress, democracy is not occurring. It is authoritarianism cloaked in American institutions.

    What the Constitution Actually Says

    Our government was deliberately designed to prevent this very kind of power consolidation. The Founders, having just fought a war to escape monarchy, built a system rooted in checks and balances.

    • Article I of the U.S. Constitution gives Congress the power to make laws.
    • Article II outlines the duties of the executive branch, which is to enforce the laws—not to write them.
    • Article III gives the judiciary the power to interpret those laws.

    These three branches are meant to restrain each other, not serve one another. A President may issue executive orders, but those do not carry the same weight as laws passed by the legislature. They are meant to clarify enforcement—not create new legal frameworks.

    The Federalist Papers Warned Us

    Even in the 1780s, the Founders feared the possibility of executive overreach. In Federalist No. 47, James Madison famously wrote:

    “The accumulation of all powers, legislative, executive, and judiciary, in the same hands… may justly be pronounced the very definition of tyranny.”

    And in Federalist No. 51, he reinforced the vital need for institutional limits on power:

    “Ambition must be made to counteract ambition… It may be a reflection on human nature, that such devices should be necessary to control the abuses of government. But what is government itself, but the greatest of all reflections on human nature?”

    These weren’t just lofty ideals. They were warnings from men who had lived under unchecked rule—and refused to let it happen again.

    History Doesn’t Just Repeat—It Responds

    The Revolution wasn’t a one-time event. It was a stand for enduring principles: representative government, accountability, and the rule of law. Every time we allow a single branch—especially the executive—to override or ignore the others, we betray that legacy.

    This isn’t about party lines. It’s about constitutional lines. If we let any President, of any party, expand their authority unchecked, we risk transforming the presidency into something unrecognizable. Something we once fought to be free from.

    Real-World Example: Immigration and the Alien Enemies Act

    The most urgent and alarming example of executive overreach in 2025 is the revival of the Alien Enemies Act. This is an obscure law passed in 1798. It gives the President sweeping powers to detain or deport non-citizens from hostile nations during times of war.

    President Trump’s administration has invoked this law to target and deport Venezuelan migrants. Many of these migrants had legal status, including visas, humanitarian protections, or pending asylum claims.

    The justification? Alleged—but unproven—ties to criminal gangs or national security concerns. In many cases, these individuals were given no warning. No chance to contest the accusations. No hearings. No due process. Just detention and removal.

    The American Civil Liberties Union (ACLU) and immigration advocates have challenged the policy in court. They argue it is a clear violation of the Constitution’s due process guarantees. Even the U.S. Supreme Court temporarily stepped in to block certain deportations.

    The larger concern remains: What if a President can ignore the courts? They could revoke legal visas and strip people of their rights with a signature. What protections are left then?

    This is not just an immigration issue. It’s a constitutional crisis. A President is using a 200+ year-old wartime law to unilaterally remove people. This occurs without oversight, without evidence, and without legal recourse. This action is exactly the kind of authoritarian overreach the Founders feared.

    Personal Reflection & Call to Action

    I advocate for marginalized communities. Rights can quickly be erased when those in power stop listening to the law. They start listening only to themselves. This moment isn’t about politics. It’s about people. And the systems that are supposed to protect them.

    To uphold the integrity of our democratic system, it’s imperative that we, as citizens, engage actively in the political process. This includes:

    • Advocacy: Contacting legislators to express concerns about executive overreach and urging them to assert their constitutional role in policy making.
    • Education: Staying informed about governmental actions and understanding their implications on various communities.
    • Participation: Voting in elections, attending town halls, and participating in public discourse to influence policy decisions.

    We the People Are Still the Safeguard

    We may not be standing on a battlefield. We may not hear the crack of muskets or the gallop of horses. But make no mistake: we are in the midst of a revolution.

    This one may not be started by a single shot—but it can be started by a louder voice.

    A voice that refuses silence. A voice that challenges overreach. A voice that demands the democracy we were promised.

    Our founders lit the fire of liberty with action. We must ensure it keeps burning. This requires awareness, advocacy, and an unwavering insistence that power must always serve the people—not rule them.

    Sources & References

    U.S. Constitution – Full Text: https://constitution.congress.gov/constitution/

    Federalist No. 47 – James Madison: https://guides.loc.gov/federalist-papers/text-41-50#s-lg-box-wrapper-25493412

    Federalist No. 51 – James Madison: https://guides.loc.gov/federalist-papers/text-51-60#s-lg-box-wrapper-25493413

    History.com – Lexington and Concord: https://www.history.com/topics/american-revolution/battles-of-lexington-and-concord

    Vanity Fair – Deportations and the Alien Enemies Act: https://www.vanityfair.com/news/story/supreme-court-blocks-trumps-use-of-wartime-law-for-deportation

  • More Than Qualified, Still Overlooked: One Disabled Worker’s Truth

    The Harsh Reality of Disability and Employment

    Finding a job is hard. Finding one as a person with a disability? Often twice as hard—and half as fair.

    Despite decades of progress, people with disabilities still face enormous hurdles in the workforce. From inaccessible interviews to discrimination that’s harder to prove than to feel, the disability employment gap remains stubbornly wide. As of 2024, only about 22.5% of people with disabilities are employed, compared to 65.8% of non-disabled people, according to the U.S. Bureau of Labor Statistics. And now, with looming threats to Social Security programs, the urgency to find stable, fulfilling work is greater than ever.

    Balancing Purpose and Pay

    I have been looking for more financially stable work for quite some time. I love what I do right now. However, I need something more reliable regarding the amount of money I can bring in.

    I am also looking for jobs that will feed my soul. They should not drain my emotional and physical energy. I know that might seem like taking the easy way out. Throughout my life, I’ve learned that being in draining positions harms my overall well-being.

    Many people with disabilities face the same struggle. They try to balance physical or mental health needs with the demand for financial stability. It’s not just about wanting a job. It’s about finding one that doesn’t push you past your limits.

    A 2022 study by Accenture found a significant correlation. Companies that embraced disability inclusion were twice as likely to outperform their peers in profitability. They also had improved productivity. Yet, many of us never get the chance to show what we can do.

    Living on the Edge of Uncertainty

    I am in a rather unique situation. I do receive SSDI. This allows me to be more selective about the work I do. I am also aware of the changes the current administration is trying to make to Social Security.

    You should look for alternate sources of income. This is important in case there is a stoppage in the SSDI checks you receive. According to the Social Security Administration’s 2024 Trustees Report, the trust fund is projected to be depleted by 2033. Reforms are necessary to avoid depletion.

    The Job Search: A Loop of Silence and Rejection

    In the past six months, I have submitted countless applications. Most of the time, I don’t hear anything back. Then there are rare instances where I get to interview. I don’t know if I suck at the interview process. I don’t know if it’s because I am a wheelchair user. Maybe it’s because I have a service dog. Usually, after that first interview, I get the dreaded response. It says: “After careful consideration, we have decided to move forward with other candidates.” Their experience more closely aligns with our current needs.

    Statistically, this kind of experience isn’t unusual. According to the National Organization on Disability, many employers still have biases. They also have inaccessible workplaces and a lack of inclusive practices. These conditions make it harder for disabled applicants to be hired or promoted. These invisible barriers reinforce the frustrating reality many disabled job seekers face. You can be qualified, capable, and enthusiastic. Yet, you might still be overlooked.

    My Work History: Then and Now

    I have been working on and off since I was 14 years old. During the summer of 1998, I had my first taste of what a job would be like. I was taking summer classes in the Twin Cities thanks to the generosity of my aunts. They had an amazing friend who worked as a head chef at a hotel near the airport. They were willing to give me a chance at what I can now only describe as something of an internship. Arrangements had been made for me to “work” one day a week. Despite this, I still had to interview with the head chef. I was scared and nervous and excited all at the same time.

    My first official summer job was at the Swift County Recorder’s Office in the summer of 2000. It was an exciting experience, even though the job was simple: scanning documents to be digitized. It gave me more responsibility and a little bit of spending money. I worked so much that I burned through the allotted funds that paid my wages. The following summer, I had a similar job with the county’s Soil and Water Conservation Office. Again, it was a simple job but taught me a lot about responsibility.

    These early jobs weren’t glamorous, but they helped shape my work ethic. I was learning to navigate a world. This world was not designed with me in mind, like it wasn’t for many other young adults with disabilities. According to the National Organization on Disability, workplace biases persist. Inaccessible environments remain. Additionally, a lack of inclusive practices continues to be a major roadblock to employment for disabled individuals.

    Campus Jobs, First Steps, and New Lessons

    The summer after my senior year of high school, I didn’t work. Not because I couldn’t get a job, but because I wanted one last summer of freedom before college. During college, I held a few on-campus jobs. While living in Hutchinson, I worked part-time as a tutor. To be honest, I don’t even remember what subject I tutored. However, I do remember getting a letter from the county about not reporting the $65 I earned. I had no idea I needed to at the time.

    At Augsburg, I had a variety of jobs. I helped the campus LGBTQ+ organization with their website and digital advertising. I was also a tour guide for the admissions office. My focus was often giving tours to prospective students with mobility challenges.

    A Decade of Retail—and Then, the Curtain Closed

    After graduation, I was fortunate to land a temp job with a downtown Minneapolis staffing agency. I was surprised they hired me, but I guess when you’re a temp, they take whoever they can get. That role lasted about eight months, and then I was unemployed again. I submitted many applications back then. It felt like a lot. I rarely heard anything back.

    Eventually, I applied at Best Buy. They had a location at the Mall of America. It was easy for me to get to. I’d never worked retail in my life and barely shopped at Best Buy before. I remember the hiring process. There was a phone interview. Then there was a group interview (my first ever). I felt completely out of place during it. I didn’t say much because I didn’t know what to say. Somehow, I said enough to move on to the final interview and land the job.

    Originally, it was supposed to be a seasonal role, but they decided to keep me on part-time after the holidays. I continued working at Best Buy for nearly 10 years. Over time, I shifted into different departments and eventually landed a full-time position. It was nice having PTO and a consistent paycheck.

    Unfortunately, it wasn’t meant to last. In the summer of 2018, Best Buy closed that location. I considered applying to the nearby Richfield store and even had a few interviews there, but it felt different. They seemed more hesitant to hire someone with my “unique abilities.” It didn’t work out, but I received a decent severance package and took a much-needed three-month break.

    That hesitation? It mirrors what many disabled workers experience. Too many hiring processes contain a subtle skepticism. There’s a belief that accommodating a disabled employee is more trouble than it’s worth. But data and my own personal experience contradicts that. Studies show that providing accommodations often costs less than $500, and the long-term benefits—employee retention, morale, and diversity—are invaluable.

    I did a training video in 2017 while I was with Best Buy on this exact issue. My general manager and I were featured in a video about workplace accessibility. The video highlighted how simple accommodations can make a huge difference in supporting disabled employees. These include clear communication, flexibility, and simple adjustments to schedules and the layout of an eight-foot section. For example, the management made the point-of-sale terminal more accessible. This change helped me ring out customers in my department.

    All they had to do was remove a section of shelving to lower the register. It didn’t just work for me—it worked for everyone. While the video is now unlisted, it remains one of the proudest accomplishments of my time there and is still featured on my LinkedIn profile as a reminder of what true inclusion can look like in action

    Where I Am Now—and Where I Want to Go

    In the fall of 2018, I landed my current role at U.S. Bank Stadium. I love the staff I work with—it’s a great environment. Things have changed a lot since returning post-COVID, but I don’t see myself leaving anytime soon. That said, hours have been very limited since the pandemic. I need something that provides more financial stability.

    In 2021, I met Amy B., a personal trainer specializing in inclusive fitness. She created Fit with Amy B to provide training for people of all abilities. I improved my own health through her program. She also brought me on to help behind the scenes making everything run smoothly. She saw the benefit of having people with disabilities not only workout with her. They also worked with her to bring greater awareness to healthy living, regardless of your abilities. I truly loved what I did for Amy. I have yet to find another job that offered the same level of flexibility. It also provided fulfillment.

    Unfortunately, SSDI barely covers my monthly expenses. It doesn’t give me the flexibility to do the things I enjoy, like traveling or going out with friends. Living on a fixed income can be incredibly limiting.

    According to the National Organization on Disability, many people with disabilities face financial insecurity. They also encounter systemic bias and physical barriers. These obstacles prevent equal access to job opportunities.

    And yet, studies by Accenture show that companies prioritizing disability inclusion perform well. They are also twice as likely to be innovative.

    The Bigger Picture: You’re Not Just Hearing My Story

    This isn’t just my story. It’s the story of many people in the disability community. They want to work. They are ready to work. They constantly run into walls—both visible and invisible. It’s time to break those walls down.

    Call to Action

    We need employers, policymakers, and communities to step up. Employers must rethink hiring practices to eliminate bias and prioritize inclusion. Lawmakers need to protect Social Security and invest in programs that support people with disabilities, not strip them away. And for those reading this: listen to our stories. Share them. Advocate for change. Because no one should be shut out of opportunity simply because society hasn’t caught up to our potential.


    Sources:

  • The Cost of Loyalty: What It Takes to Be a Season Ticket Holder

    The Cost of Loyalty: What It Takes to Be a Season Ticket Holder

    I wasn’t planning to write this today. I sit here and look out at the dreary Minnesota sky. I know there’s a significant chance I won’t attend tonight’s Minnesota United FC match. I felt like I needed to put some thoughts down.

    Quick note: I’m part of AccessiLoons—Minnesota United FC’s first and only supporter group focused on accessibility and inclusion. However, everything I share here is based on my personal experience. It doesn’t reflect the views of the group.

    This will be the second game I’ve missed this season—and not because I’ve lost interest or stopped caring. Far from it. I’ve been a season ticket holder since 2015. That was long before the team joined MLS and before Allianz Field was even a blueprint. Supporting this team has been one of the most consistent and joyful parts of my life.

    But tonight, like many nights, I’m forced to weigh the realities of being a fan with a disability. The weather is cold, windy, and there’s a chance of rain or snow. And rain and power chairs don’t mix well.

    After last weekend’s afternoon match, my wheelchair started to malfunction on the way home. Thankfully, I made it back safely and the issue didn’t repeat itself—but moments like that stick with you.

    Every time I head out in this type of weather, there’s that voice in the back of my mind:

    • “Is my chair going to malfunction again?”
    • “Will I get stranded somewhere?”
    • “What do I do if something goes wrong?”

    It makes you cautious at times about leaving the house.

    This post isn’t just about one missed game. It’s about what it really takes to be a loyal fan in 2025—financially, physically, and emotionally.

    When Passion Meets Practicality

    I’ve always budgeted for my season tickets. When I was working full time, the yearly price increases didn’t hit as hard. Even during the pandemic, I had enough money coming in to keep my seats. Soccer was one of the few constants during an unpredictable time.

    But when the world reopened, my income didn’t bounce back as ticket prices continued to rise. Something that once felt like a justifiable splurge now feels like a financial stretch.

    Still, giving them up feels impossible. Supporting this team is part of my identity. It’s how I connect with friends. It’s where I feel community. But loyalty, especially on a fixed or limited income, comes with a price—and that price keeps going up.

    Accessibility Isn’t Just About Seats

    Being a fan with a disability adds another layer to all of this.

    Sometimes, I simply can’t attend—even when I want to. The home opener in March is always a weather gamble, and this year was no exception. That was in the evening—and I had just worked an afternoon shift at U.S. Bank Stadium. I was already cold and running low on energy. I didn’t know if I had the stamina—or the body regulation—to sit through the full match.

    As someone with limited mobility, I can’t generate much body heat. Once the sun goes down, so does the temperature—and so does my ability to safely enjoy the game.

    I made it to the match the weekend before because it was an early afternoon kickoff. It was still cold, but the sun made it manageable. That little bit of warmth made all the difference.

    And then after the issues with my wheelchair after last weeks game there’s the added layer of equipment concerns. It was enough to shake my confidence. Now, every time I head out , I have to ask:

    • What if my chair stops working?
    • What if I get stuck far from home?
    • Who do I call?
    • Will anyone be able to help?

    That kind of risk doesn’t factor into most fans’ decisions to attend a match. For disabled fans, it’s part of the mental math every single time.

    To be clear, many of these challenges aren’t unique to Minnesota United or Allianz Field. The stadium staff has generally been supportive, and there are accessible features in place. But even well-designed venues can fall short when the full spectrum of disability isn’t considered. These issues show up in stadiums across the country—and they’re often invisible to those who don’t live with them.

    Some of the most common barriers disabled fans face include:

    • Cold or extreme temperatures that are dangerous for fans with mobility or circulation limitations.
    • The distances from parking or public transit stops are long. They can feel like a marathon for those with fatigue. This is also true for those with chronic pain.
    • Crowded concourses and bottlenecks that create safety issues for wheelchair users and others needing space.
    • Ticket policies with little flexibility, even when health issues make last-minute changes necessary.
    • Energy management challenges—sometimes, it’s not about willpower. It’s about knowing your body has limits.

    The Marketplace Problem

    When I can’t attend, I turn to the SeatGeek Marketplace to resell my tickets. But that experience isn’t fan-friendly either.

    I need to list the tickets above face value to cover SeatGeek’s 10% seller fee. This is necessary to just break even. On top of that, buyers are charged another 10% fee. That’s a 20% markup just for a resale—not to make a profit, just to avoid losing money. And guess what? Most people won’t pay that.

    So now, I’m out the money, and I missed the game. It adds insult to injury.

    Lately, I’ve found myself quietly wondering what the future holds. I’m not ready to give up my season ticket membership yet. However, I’m starting to reevaluate things. The rising costs, the physical strain, the uncertainty that comes with each game—it all adds up.

    At some point, I may have to ask myself whether this version of loyalty is still sustainable for me. I love this team. I’m not going anywhere as a supporter. However, being a season ticket holder might look different down the road.

    Let’s Do Better—for All Fans

    If you work for a team, a supporter group, or even a ticketing platform, ask yourself a question. What are you doing to make sure disabled fans are fully included?

    Accessibility isn’t just about wheelchair spaces or ADA check boxes. It’s about understanding the full picture. This includes weather risks, energy limits, and malfunctioning mobility equipment. Resale policies also matter. Then, there is the emotional toll of being excluded from something you love.

    If you’re not thinking about all types of access, you’re leaving people behind.

  • Holding Onto Love: A Reflection on Loss and Love

    I’m sitting here writing my next story when Wherever You Are by my friend Ellis starts playing in my ears. Just like that, memories flood my mind. They are the people who have passed on and left this world.

    “I’m still here, after I’m gone. In the birds singing their love songs, in the summer sun let me warm your heart. ‘Cause I will always be wherever you are.” – Ellis Delaney

    Three years ago today, my Grandma Marlys Hoiland passed on to whatever is next. These are my thoughts and feelings through the lens of a child, and now an adult. Sometimes, we just need to put words to the emotions we carry. For me, this was one of those times.

    There is just something about grandparents. As a little kid, I feel like I spent a lot of my time with her and my Grandpa Roger. I vaguely remember the Easter Bunny stopping at her house instead of mine. I think we were staying with Grandpa and Grandma. Mom and Dad were gone somewhere.

    One of the coolest things about her? She was a school bus driver. When we went on field trips, there was always a chance she’d be the one behind the wheel. For little me, that was the best thing ever.

    Grandma Marlys standing in the snow next to a yellow school bus with ‘Benson School District 777’ written on the side.

    But when my grandpa Roger passed in the summer of 1994, things changed. I was just a kid—too young to fully understand what was happening, but old enough to feel the shift. I wanted to spend time with my grandma, but I was afraid to ask. The issues the adults in my life had with each other weren’t mine to carry, but they affected me anyway. So I kept my distance because I didn’t want to make things difficult.

    Years later, when I moved to Hutchinson to attend college, I got the chance to reconnect with her. It felt like I was trying to make up for lost time. I made a point to enjoy the moments we had, and to be present. I didn’t bring up the past or the complicated family dynamics—I just wanted to be her grandson.

    Grandma Marlys sitting next to Levi, both wearing glasses, in a cozy living room setting.

    Then life took me to the big city, and time slipped away again. As things settled down at school, I promised myself I’d see her at least once a year. I kept that promise for many years. I was lucky to have an amazing friend. He would drive me the two-and-a-half-hour drive, just so I could spend an hour or so with her. We shared a meal and a laugh.

    Grandma Marlys in a blue hoodie, resting her arm on her Levi's as they sit close together in a warmly lit home setting.

    When she got sick, we all knew time was short. The family planned a birthday party for her, knowing it would be her last. Once again, my friends rallied around me. They drove me back to that small town. This allowed me to be there. I told her I loved her. I told her I was sorry I didn’t do more. I felt it deeply in my heart. I knew it would be the last time I’d get to say what I had been holding onto for years.

    On March 20, 2022, she passed. One final time, my friends stood by me. They drove me to her funeral because they knew—just as I did—that I needed to be there.

    “If you don’t want to, don’t say goodbye. Say I’ll see you around the next time.” – Ellis Delaney

    As a child, I didn’t have control over the choices being made around me. I felt powerless to bridge the gaps that had formed. But as an adult, I can make my own choices.

    I can choose to reach out, to show up, to hold onto the people I love while they’re still here. I can choose not to let the past dictate my present.

    I am not capable of changing what happened, but I can learn from it. And I can make sure that when I look back, I have no regrets about the love I’ve given.

    Love is something we can choose to hold onto, even when time and distance try to pull us apart. It’s in the memories, the laughter, and the simple moments we share.

    I carry my love for Grandma Marlys with me, not just in my heart. It is clear in how I choose to live. I strive to be present. I cherish those I care about. I also never let love go unspoken.

    I can’t change the past. I can only strive to be a better person. I aim to do what I know is right. I want to honor the people I love while I still have time.

    I love you, Grandma Marlys. Always.

    Check out my friend Ellis Delaney and their song Wherever You Are on Bandcamp.

  • Here We Go Again

    I Hate Writing About This, But I Have To

    I don’t like talking about politics on social media, and I certainly don’t like writing about it here. But this isn’t about politics—it’s about livelihood.

    I feel like I’ve written this post a dozen times. I hate that I have to keep writing about government funding, budget cuts, and restructuring. I hate that every few months, I have to sit down and explain. Once again, I must clarify why Social Security, Medicare, and Medicaid aren’t just line items on a budget. They are lifelines for millions of people, including myself.

    I wish I didn’t have to keep writing about this. I won’t stay silent until I am confident that my future is safe. The future of millions of others must also be safe for me to stay silent. Because the moment we stop speaking out, those in power believe they can do whatever they want.

    Why This Matters (Again)

    There’s talk of making deep cuts to Social Security, Medicare, and Medicaid. Do I think it’ll happen? Maybe not to the extent being proposed, but the fact that it’s even a possibility is terrifying. Medicaid/Medicare is a life line for people like me.

    If it does happen, here’s what it means for me:

    • SSDI helps cover my portion of household bills and the costs of having a service dog. I work part-time, but last year, I made about $1,600 before taxes—not nearly enough to live on.
    • Medicare covers my $50,000 power wheelchair. If they slash funding, approvals for equipment and repairs could take months. If my chair breaks down, my independence is gone.
    • Medicare and Medicaid cover my PCA (Personal Care Assistant) hours. These hours help me conserve energy. This way, I can focus on things that bring me joy. Examples of these activities are writing and spending time with friends. If they take those hours away, I risk serious health consequences. Even a reduction means needing a shoulder replacement sooner rather than later.

    And then there’s Jason, my longtime PCA, who also relies on this income. If his hours are cut, he loses a major source of financial stability. That means losing our home. It’s that simple.

    This isn’t just about me. This is about millions of people—seniors, disabled folks, low-income families—who depend on these programs to survive.

    In a recent Disability Scoop post dated March 19, 2025, they tell the story of Xavier. He has a rare genetic immune disorder. It undermines his body’s ability to fight disease. California’s Medicaid program, Medi-Cal, provides Xavier with the treatments he needs. It offers resources to his family as well. This support helps him live as normal of a life as possible.

    His mother is quoted saying:

    “It’s allowed him to go to school. It’s allowed him to be home and not living in a hospital 24 hours a day,”

    Parents of children with special health care needs aren’t the only ones raising concerns about potential cuts. Disability advocates, health care providers, budget analysts, and state lawmakers have also voiced alarm. The House proposal passed on February 25 does not explicitly call for Medicaid cuts.

    Nonetheless, it instructs the House Energy and Commerce Committee. This committee oversees the program. It needs to find $880 billion in savings over the next decade. According to experts, reaching that level of savings would be nearly impossible without reducing Medicaid funding.

    I Hate Writing About This, But I Can’t Stop

    Every time I write about Social Security or Medicare or government cuts, I feel like a broken record. I’ve covered this before:

    And yet, here we are again.

    I wish I could stop writing about this. I wish I could move on. But I can’t. The second we stop talking about it, the people in power win. The moment we get exhausted and say “Oh well, nothing we can do,” they triumph.

    What Can We Do?

    • Talk about it.
      • Even if it feels repetitive, even if it’s exhausting—keep the conversation going.
    • Contact your legislators.
      • I know, I know—Congress is a mess. But if enough of us make noise, they have to listen.
    • Get your story out there.
      • Talk to the media.
      • Write to local newspapers.
      • Use social media.

    I don’t want to write another post like this in six days, in six weeks, or in six months. But if I have to, I will.

    Because this isn’t politics. This is life.

    Read More:

  • Left Behind by the Democrats

    Left Behind by the Democrats

    Over the past few months, I’ve written extensively about the changes unfolding in our government. I’ve also discussed their impact on our communities.

    There have been drastic budget cuts to Social Security. There is also an urgent need for reform in Minnesota’s disability services. I’ve delved into the pressing issues that affect us all. I’ve also explored the challenges faced by the LGBTQIA+ community, highlighting the growing need for advocacy and support.

    Amid these discussions, I’ve felt an increasing urge to share more of my personal story. Shortly after the 2024 presidential election, I wrote a piece that I wasn’t quite ready to publish. It was raw, emotional, and an honest reflection on feeling left behind by the Democratic Party. While I shared it with a few close friends, I hesitated to make it public. I wasn’t sure how it would be received—and, frankly, I wasn’t ready for the potential backlash.

    I continue writing about the state of our nation and the impacts of policy changes on disability support services. I realize that my personal story is an essential part of this broader conversation.

    The emotions I felt in November 2024 still resonate. They affect not just me but many others too. These emotions reach those who feel disconnected, disillusioned, and left behind.

    Today, I’m ready to share this piece with you. I’ve made some edits to improve readability and included links to cited sources. My hope is that it resonates with you. I wish it sparks meaningful conversations. I also hope it encourages all of us to think critically about the direction we’re headed as a country.


    Left Behind by the Democrats

    A Personal Reflection on the Democratic Party’s Disconnect and the Fight for Our Rights

    By Levi Dokken | November 7, 2024

    I have been sitting here with a lot of feelings—sadness, anger, even rage. Part of me wanted to lash out at the people who voted for Donald Trump. To work through these emotions, I felt the need to sit down and write.

    Writing helps me release emotions. It allows me to express my thoughts. By expressing them, they don’t consume me.

    The Disconnect Between the Democratic Party and Rural America

    Donald Trump has won, and I believe it’s because the Democrats failed. They have failed the people they claim to represent. They are no longer the party of working men and women. Just look at the state of Minnesota. It went for Harris but is still a sea of red. There is only a small island of blue. The party only focuses on the areas where they need electoral votes to win the overall race.

    I grew up in a small town in Minnesota. I saw firsthand that most people in my community weren’t necessarily concerned with national politics.

    They focused more on day-to-day struggles. They were figuring out how to put food on the table. They were also finding money to cover the mortgage. They worried about what to do if their child needed braces and health insurance didn’t cover it.

    Candidates campaigned across the United States. They focused primarily on so-called battleground states and urban areas. They believed these areas would secure enough votes for them.

    Small towns across the nation increasingly feel disconnected from the Democratic Party. They believe the party has shifted its focus toward urban and coastal issues. This shift comes at the expense of rural communities.

    The Electoral System: A Barrier to Representation

    I often wonder if political candidates would pay more attention to smaller towns if votes were delegated differently. They might also focus on smaller states.

    Our current electoral system feels outdated. It resembles a relic of an age long since dead. In it, the voices of a few battleground states dictate the direction of the entire country.

    What if we had a more localized electoral college system within each state?

    For example, if each county were assigned an electoral vote, it might create a more balanced representation. The majority vote within a county would decide how that county’s electoral vote was cast. This system could offer an option to the current popular vote system that most states use to assign their delegates.

    Disappointment with Democratic Leadership

    Joe Biden announced he was running for a second term. I had a strong feeling he was going to lose.

    In 2020, he claimed he would be a transitional president. What happened to that promise? He was unwilling to even hold a primary. I was much more enthusiastic about the possibility of MN Rep. Dean Phillips entering the race. The Democrats, however, dismissed it, holding fast to the tradition that the incumbent automatically runs for re-election.

    Watching the first presidential debate, I was floored. Both candidates seemed unfit to hold the highest office in the land.

    Biden stumbled with his words and thoughts; at times, he seemed unable to keep his ideas in order. Trump wasn’t much better—he mostly rehashed grievances from 2020 without offering a clear plan for change.

    Project 2025: A Threat to Disability Rights

    Project 2025 adds to my concern. It is a plan from The Heritage Foundation. The next administration might choose to implement it.

    According to the Disability Rights Education & Defense Fund, this plan proposes changes with deep impacts on programs like Medicaid. It introduces funding caps, stricter eligibility requirements, and time limits.

    These changes could drastically reduce access to essential services for people with disabilities. Services like medical equipment, personal care attendants (PCAs), and specialist visits are crucial. They are necessary for maintaining health and independence.

    For me, Medicaid covers my specialist visits. It also covers my nearly $50,000 power wheelchair and repairs. Additionally, it covers the cost of my partner, Jason, as my PCA.

    How Do We Talk to Those Who Voted for Trump?

    How do I talk to my friends and family who voted for Donald Trump? How do I understand their choice to support someone who has assaulted women? He attempted to overturn a fair election. He also incited his supporters to storm the Capitol.

    Some of Trump’s supporters hold harmful views. However, I believe most are simply scared, misinformed, or longing for a past they believe he can bring back.

    I don’t want to cut these people out of my life, especially when many are lifelong friends or family. We can still be connected; we just may not talk about politics.

    What Can I Do Moving Forward?

    I’ve shared many things with you. The Democratic Party’s disconnect from rural America is concerning. Our electoral system has flaws. Policies like Project 2025 carry potential consequences. There’s a growing divide among friends and family. I can’t help but feel a mix of frustration and overwhelm.

    The future feels uncertain. These decisions could have long-lasting effects. They could also have life-changing effects for myself and those I care about. I find myself sitting here after writing this, asking myself, What can I do?

    As one voice out of millions, not much. But I can be part of something bigger. When others raise their voices against the incoming administration’s policies, I can stand with them. I can support the women in my life, the friends who feel vulnerable right now. I can do my part, however small, to work toward a future that protects everyone’s rights and dignity.

    Will you join me?


    Sources

  • Squishy Boy: A Love Letter to My Gentle Dog

    Squishy Boy: A Love Letter to My Gentle Dog

    The other day, I wrote a poem called Ghost in the Wiggles about Dempsey and his lingering spirit. As I reflected on Dempsey’s story, I realized Surley deserved his own tribute, too. Unlike Dempsey, Surley is my “squishy boy”—not because of his size, but because of his soft and tender spirit. He’s a dog who needs the world to be gentle, who thrives on a calm voice and a soft touch.

    Living with a soft dog like Surley has been both a lesson and a gift. He’s taught me to breathe before the storm, to find patience when frustration blooms. This poem, Squishy Boy, is a love letter to his delicate heart. It is also about the journey we’ve shared to understand each other.

    Squishy Boy

    You are my squishy boy.
    Not fat—just tender.
    Your blonde hair, soft as your heart.

    You are my squishy boy.
    I must handle you with care—
    a soft touch, a soft voice.
    Sometimes, that’s not easy.

    You are my squishy boy.
    In the beginning, frustration bloomed.
    The TV volume rose and fell—
    a ghost in the remote.

    I fought with it,
    tried to keep the world gentle,
    so the noise wouldn’t hurt you.

    I wasn’t mad at you—
    but you thought I was.

    You are my squishy boy.
    You sought safety,
    curled up with him, not me.
    It hurt. It still hurts.
    I was only trying to protect you.

    You are my squishy boy.
    I learned early on—
    sudden sounds could startle you,
    prickle your gentle spirit.

    I only wanted to protect you,
    but you misunderstood my frustration.

    You are my squishy boy.
    You have taught me to temper my rage,
    to breathe before the storm.

    You are my squishy boy.
    You must always carry something—
    from first light to bedtime.

    Your turtles, soft and worn,
    are never far from your mouth.
    They give you strength,
    a comfort you can hold.

    You bring them to bed when I let you,
    tucking them close as we curl up,
    safe and snug together.

    You are my squishy boy.
    You crave reassurance,
    always near me, on me.
    At first, it felt like too much, suffocating,
    but now, it feels sweet.

    I am your rock.
    I am your safe space.
    And you—
    you are my squishy boy.

  • A Ghost in the Wiggles: A Heartfelt Poem of Love and Loss

    I don’t often write poems, but some mornings, the words find me.

    This morning, I sat next to Surley. I was sipping my coffee and preparing to table at the Can Do Canines open house. A familiar ache settled in. I glanced up at the picture of Dempsey.

    There he was, sitting on the dock. His deep, soulful eyes stared into my very soul. I realized he remains a ghost. He will forever haunt me. He lingers in the quiet moments of my day.

    Surley and Dempsey share so much: their wiggle butts, their playful spirits, the way their eyes hold entire stories. And yet, they are so different—one chocolate, the other yellow, each with a unique heartbeat. I needed to put these feelings somewhere, to capture the love and the loss, the comfort and the haunting.

    So, I wrote this poem.

    A Ghost in the Wiggles

    You are chocolate; he is yellow—
    But you are both dogs
    With shockingly similar eyes,
    Though so different.

    Yours, a deep golden amber,
    His, a rich, soulful chocolate.
    When he looks at me,
    I see you in the shadows of his gaze.

    I love you.
    I love him.

    You craved morning belly rubs,
    A ritual of joy.
    He only offers his belly
    Because he knows it brings me closer to you—
    A bridge to the boy I lost too soon.

    I love you.
    I love him.

    I look at him, and I see you.
    I know he is not you—
    He is his own dog,
    But still, I see you.

    Your silly face, your wiggle butt.
    I see you when he zooms around the house
    After a long day’s work,
    When he rests his head on my lap,
    Looking up at me.

    I love you.
    I love him.
    He is here, and you are not.

    You are a ghost,
    Haunting the corners of my mind,
    An invisible chain,
    Forged by how you left so abruptly,
    Binding me to you,
    Never letting go.

    I love you.
    I love him.

    Will your ghost haunt me forever?
    Even with him here,
    The heartache lingers,
    Popping up in the most unexpected,
    Unusual ways.

    I love you.
    I love him.
    You are gone.
    He is here.

    You both have that same wiggle butt,
    But unlike you,
    He must always have something in his mouth—
    As if the comfort of a toy or a bone
    Keeps him steady,
    Helps him reach your confident stride.

    I love you.
    I love him.

    You were bold, hard-headed,
    Needed a firmer hand,
    Met the world with unflinching eyes.

    He is squishy, tender,
    A softer heartbeat in this home.
    Crumpling at the slightest hint of an upset dad,
    Looking up for reassurance,
    Needing to know he’s doing it right.

    I love you.
    I love him.

    When I first got upset with him,
    I thought I broke him.
    I thought we weren’t meant to be,
    Because he shut down,
    So unlike you—
    You, who always pushed back,
    Certain, strong, sure.

    He is not you.
    But in his own way,
    He is exactly who he needs to be.

    I love you.
    I love him.

    Through him and around him,
    Your spirit still dances—
    A ghost in the wiggle.

  • When Budget Cuts Hit Home: How Social Security Reductions Are Impacting Us All

    Social Security Is More Than a Government Program

    Social Security isn’t just a government program; for many, it’s a lifeline.

    I’ve been receiving Social Security benefits in one form or another since I turned 18. Initially, I relied on Supplemental Security Income (SSI) while attending college from 2002 to 2008. It gave me a freedom many going through college don’t have. I was able to have a reliable source of income so I could focus higher education.

    When I entered the workforce in the winter of 2009, I found stable and reliable work. This job allowed me to completely eliminate my need for Social Security assistance.

    Later, after leaving my job at Best Buy in 2018, I transitioned to Social Security Disability Insurance (SSDI) benefits. These services are vital—not just for me but for millions of Americans who depend on them for independence and stability.

    Why I’m Speaking Up Now

    I felt compelled to write this piece after watching The Rachel Maddow Show last night. Maddow discussed the potential fallout from the latest budget cuts to the Social Security Administration (SSA). These cuts, led by Elon Musk and the Department of Government Efficiency (DOGE) under President Trump, go beyond budget trimming. Entire programs are being eliminated, putting vulnerable populations at serious risk.

    According to a recent Washington Post article, the acting head of the SSA privately admitted to certain outcomes. He said these cuts would likely lead to more mistakes. They might also result in longer delays in processing claims. The possibility of an even more frayed safety net is alarming, and I couldn’t sit by quietly.

    The Human Impact of Bureaucratic Delays

    These cuts won’t just affect new applicants—they could impact those of us already receiving benefits. Whether it’s renewing benefits, updating personal information, or resolving administrative issues, interactions with the SSA are often necessary.

    When the system is underfunded and overwhelmed, routine tasks can become significant obstacles. Delays and mistakes in processing claims can lead to missed payments, prolonged appeals, and devastating financial consequences.

    Real Stories, Real Consequences

    It might be difficult to grasp the real-world impact of bureaucratic slowdowns. This is especially true for those who have never had to navigate this system.

    When I applied for SSDI in 2018, the process was far from smooth. Even with a fully staffed administration, the hurdles were significant. Now imagine facing these challenges with fewer resources, fewer programs, and more errors.

    These challenges are not just theoretical. They are a looming reality for millions of Americans. Many Americans rely on Social Security as a cornerstone of their financial stability.

    Connect the Dots: More on Disability Rights and Advocacy

    If you want to understand more about the broader challenges facing people with disabilities, check out some of my previous posts:

    These stories illustrate the ongoing struggle to maintain and expand the rights and services many of us rely on. The fight against these latest budget cuts is just one part of a larger battle.

    A Call for Accountability and Action

    We need transparency and a commitment from our leaders to prioritize the needs of vulnerable populations. Budget cuts might look good on a spreadsheet, but their impact on human lives can be catastrophic. We should invest in essential services. This ensures that everyone—regardless of their circumstances—has access to the support they need.

    Advocacy Starts with Awareness

    The first step in fighting these cuts is raising awareness. Share your stories, support advocacy groups, and reach out to your representatives. If we remain silent, these cuts could become just another line item in a budget. The true cost would be paid by those who can least afford it.

    Sources

  • A Lifetime of Love

    She remembered what she used to be like, and it was nothing like she was now. Lying in her hospice bed, her bones heavy against the thin mattress, she glanced over at Janis. Curled on the couch, soft snores drifted beneath the gentle rustle of pages, the worn paperback threaten to slip from her grasp. The lamp’s warm glow bathed them both, casting soft amber shadows on the walls, a thin bubble of light holding back the dim edges of the room.

    Seventy-five years. A lifetime together. She had never met another queer couple who had shared so much time. They weren’t lucky—no, not lucky. Lucky implied chance. They had worked for this. Even though neither of them had the best childhoods, they had built the kind of home they always dreamed of. 

    Over the years, they’d helped so many children find the love they themselves had needed. There had been moves, planning, saving, countless hours of discussion and paperwork. They were committed to do whatever needed to be done to help these children have the best chance of success. Through sleepless nights and boundless love, they had held on, hand in hand, refusing to let the world pull these children’s lives apart.

    As she thought back on the memories of the past her eyes grew heavy, the hum of the room melting into the slow, gentle rhythm of her heartbeat. Each thump seemed to draw her deeper, unraveling the present and letting memory rush in like a tide. 

    She could feel the edges of the world softening, as if the house itself was urging her to rest, to let go with the same gentleness they had shown every child who came through their door. Memories swept in carrying her back to the start of their story—the first glance, the first touch, the first moment when the world had shifted beneath her feet.

    The First Spark

    They met in college, back when the world was less forgiving. She had been studying social work, determined to make a difference for kids like her, while her soon-to-be wife pursued a degree in special education. The first time she saw her, they were in a crowded general education class, the kind where the professor barely glanced up from their notes.

    Her soon-to-be wife stood at the front of the room, shoulders squared, her knuckles pale against the wooden edge of the podium as her voice rose above the low hum of shuffling papers and half-hearted whispers. She was challenging the professor, demanding accommodations so that every student could participate equally. The room had gone still, the weight of her words settling over them. The professor’s dismissive response did nothing to deter her. Instead, her resolve only seemed to sharpen, a quiet defiance woven into every word.

    After class, while others slipped out through the back doors, she found herself moving forward, weaving through desks and backpacks to catch up to her. Her pulse thrummed in her ears, but the feeling in her chest told her this was important. She introduced herself, expressing her admiration for how bravely she had stood up to “the man.” The words had been meant as a joke, a thin veil of humor over a deeper truth.

    Her soon-to-be wife’s name was Janis, a nod to both Janis Joplin and Janis Ian. The moment she introduced herself to Janis, she felt a quiet thrill—a shared love of music layering itself over the spark of admiration she already felt. It seemed fitting that someone with a name echoing such powerful voices would find her own and use it so boldly.

    Janis had smiled then, a gentle, genuine expression that softened the remnants of her earlier frustration. What had struck her most wasn’t just the courage to speak up, but the quiet certainty beneath it—a sense that doing what was right was simply a given. They lingered in the empty classroom, talking as if the world had folded away, leaving only the two of them.

    That moment became the first of many. Conversations bloomed in quiet corners of the library, over long walks across campus, and in shared spaces where time seemed to stretch just for them. What began as a spark of admiration grew into a rhythm of companionship—study sessions and shared meals, standing together at protests, finding comfort in silence as much as in words. Their friendship deepened, roots entwining through shared hopes and the slow, steady discovery of all the ways their lives fit together.

    Over time, those moments became the foundation of something neither of them had expected but both had craved—a love built on the simple, powerful truth that they were better together. It was a certainty she had carried with her since childhood, a steady light in the dark corners of her past.

    Roots in Rocky Soil

    Even as a child, she had felt it—that quiet truth, unshakable and real. The girl who sat in front of her in homeroom always left her speechless, her stomach fluttering whenever she turned around to pass a note or share a smile. She had known she was different, a lesbian, from a young age, and she never felt ashamed of it. But her parents were deeply religious, and when they pieced together the truth, they cast her out and into foster care before her tenth birthday.

    The foster care system was no sanctuary. She became a pinball, bouncing from house to house, never settling long enough to call anywhere home. Some families simply didn’t know what to do with a girl like her. Others, once they realized what she was, saw her as a threat—someone who needed to be kept away from their children. Names blurred together, places faded into half-remembered rooms and faces. But there were some homes that remained sharp-edged in her memory, places where she kept her bedroom door locked at night, her back braced against the thin wood.

    Unfortunately, locked doors didn’t always keep the monsters at bay. She learned to listen for heavy footsteps in the hallway, to breathe slow and shallow when the shadows passed beneath her door. But no matter what they did, they would never change who she was. Her identity was a light she kept tucked inside, a flame they could never reach.

    By the time she aged out of the system, she was determined. She refused to be a victim. Despite everything—the moves, the broken promises, the nights spent bracing against locked doors—she graduated high school with some of the best grades in her class. Every test passed, every assignment completed felt like a quiet rebellion, proof that the world hadn’t crushed her.

    When she started college, her vision for the future was already clear. She had one goal: to become the social worker she never had—the kind who listened, who understood, who saw kids like her and didn’t try to change them. Most of the social workers she had known had dismissed her identity, brushing off her truth with tired platitudes. She remembered the patronizing smiles, the way they told her she just hadn’t met the right boy yet. As if her existence was a phase that needed correcting. As far as she was concerned, men had never done anything but try to break her.

    She didn’t need them. She didn’t need biological children, either. There were already too many kids lost in the foster care system, too many who had been thrown away like she had. Her path forward was clear—help as many of them as she could, offer the kind of safety and acceptance she had never known.

    Kindred Flames

    From the start, there had been something magnetic about Janis—something more than her boldness in the classroom or the quiet certainty that seemed to follow her like a shadow. It was in the way she held space for others, how her voice could soften a sharp room, how her laughter felt like warmth in the winter. She had a way of seeing people, of making them feel heard, even in a world that so often turned its back on those who didn’t fit the mold.

    She learned quickly that Janis’s courage wasn’t just for show. It was rooted in lived experience, in a childhood where acceptance had come slowly, edged with discomfort and caution. Janis had known what it was like to feel out of place in her own home, to love deeply while treading carefully. But instead of turning inward, she had opened herself up—her empathy a quiet rebellion against the world’s harshness.

    When they sat together on the library steps, books between them and the world moving on without notice, Janis would speak about her dreams of teaching. She wanted to create classrooms where every child, regardless of ability, felt valued. Where no one had to fight to be seen. Her vision was vivid—schools with sensory-friendly spaces, lesson plans that adapted to each child’s needs, and a curriculum that celebrated differences instead of hiding them.

    She would listen, captivated by Janis’s passion, the way her hands moved when she spoke, painting the air with possibilities. It wasn’t just what Janis wanted to do—it was the way she believed it could be done. It was a hope without edges, boundless and real.

    It wasn’t long before those quiet conversations turned into shared action. They volunteered together, tutoring kids after school and organizing supply drives for underfunded classrooms. They stood side by side at protests, their hands entwined, voices raised in unison. There were late nights spent crafting posters, cups of coffee going cold as they planned ways to make a difference. Every small victory—a kid passing a test, a teacher agreeing to try a new method—felt monumental because it was a step toward the world they wanted to build.

    Over time, admiration deepened into something more. What began as a friendship grounded in shared purpose bloomed into love, each moment layering over the last. It felt inevitable, like gravity, like finding a home you didn’t realize you had been searching for. Their love became its own kind of activism—a testament to the idea that creating safe spaces started within the walls of their own hearts.

    Through it all, Janis remained a beacon. She wasn’t perfect—no one was—but her imperfections only made her more real. She stumbled, had bad days, doubted herself, but she never stopped trying. She never lost the spark that had drawn her forward in that classroom all those years ago. And as their lives intertwined, she felt the weight of something she had only glimpsed before—a life where love and purpose walked hand in hand, where building something good was as simple and as complex as holding on to each other and refusing to let go.

    Building a Home

    After graduation, she and Janis moved into a small, one-bedroom apartment. It wasn’t much—cramped and drafty with mismatched furniture—but it was a start. They spent weekends sketching floor plans for their future home, a place where every child, regardless of ability, could find safety They dreamed of wide doorways, roll-in showers, and spaces designed with love and intention. Each step forward—every saved dollar, every completed foster parent class—was a brick laid in the foundation of the life they were building together.

    Together, they would build a home where every child they welcomed felt seen, where love was a promise kept and never taken back. And through it all, that old, stubborn certainty remained—a light they had carried through every shadow, one they now shared with each child who walked through their door.

    It wasn’t easy. Even though they could finally marry, love was not enough to erase the lingering shadows of prejudice. In many parts of the country—places like where she grew up—being in an “untraditional” relationship still barred them from adopting children. The laws may have changed, but minds hadn’t always followed.

    So they did what they had always done: they moved forward, together. They left behind familiar streets and old ghosts, settling in a more welcoming state where their dream of building a family could become a reality. 

    They spent long evenings talking about what they wanted their home to look like, what kind of parents they hoped to be. They both knew they wanted kids, but adoption had its limits. It might mean only helping a few children, but fostering—fostering had no ceiling. There were always kids in need of a safe place, a soft landing in the midst of turmoil.

    They decided to open their doors wide. The choice was never about filling a void in their own lives but about offering a refuge to children who had none. They wanted to help the kids who might not fit easily into other homes—the ones with disabilities, those who identified as LGBTQ, the ones too often left behind. It was a promise to the children they once had been, to right the wrongs of their own pasts.

    Janis’ story, like hers, was tangled with loss and longing. When they met in college, Janis had only recently come out to her parents. While Janis’ family had known other LGBTQ people, acceptance came haltingly, edged with discomfort. Their conversations were strained, the kind where words could turn into weapons without warning. But through the pain of those interactions, Janis’ resolve only grew stronger. She had learned early on how to hold space for both love and disappointment, a skill that would later help them create a home where every child felt wanted.

    Determined to break the cycle, they approached the fostering process with the same conviction they had brought to everything else. They completed the paperwork, opened their home for in-depth interviews, and showed the caseworkers the world they had built—one filled with warmth and intention. By then, they were already established members of their community. They had friends and neighbors who saw them not as an exception but as an example of what family could mean. Gathering the necessary references was effortless, a testament to the lives they had touched just by being themselves.

    When their approval finally came through, it was more than just a certification—it was an affirmation of everything they had fought for. They had created a home where love wasn’t conditional, where children of all kinds could find safety and acceptance. It was the start of something bigger than either of them had imagined, the first step in a journey that would stretch across decades and fill their home with the sounds of laughter, healing, and hope.

    Once they were approved as foster parents, all they had to do was wait. They didn’t have to wait long. One evening, as the sun sank below the horizon, they sat together on the couch, watching the highly anticipated Ellen relaunch. Their cozy, single-level home was filled with the warmth of laughter and the comfort of familiar voices. The house had been designed with intention—wide doorways, barrier-free bathrooms, and low countertops—making every space accessible to all, regardless of ability. Their home was more than just a shelter; it was a promise that every child who came through their door would feel seen, safe, and welcomed.

    The Call That Changed Everything

    When the phone rang, they shared a glance, both knowing that this call could change everything. The social worker explained that a young child with spina bifida needed a temporary placement. The courts were still determining if the child’s parents were fit to care for them. When the child arrived, their small frame and wary eyes told more of the story than words ever could. The social worker quietly shared the details—malnourishment, a severe diaper rash, and a urinary tract infection. Signs of neglect sat heavily between them, unspoken but undeniable.

    Taking gentle steps forward, they led the child inside, the smooth transition from the ramp outside to the hardwood floors a small but meaningful comfort. They moved slowly, guiding the child through the open spaces of their home, showing them that nothing here would be a barrier. The bathroom was warm and welcoming, with a roll-in shower and grab bars within reach. Soft towels were stacked neatly, and bubble bath soaps lined the tub’s edge.

    They knelt to the child’s level, explaining every step, letting them set the pace. It was important that the child felt safe and in control—something that had likely been rare in their young life.

    When asked if they’d ever had a bubble bath, the child shook their head. So they pulled out all the different bubble bath soaps they had, letting the child choose their favorite scent. The small act of choice brought a hint of light to the child’s face. Carefully, they helped the child out of their soiled clothes, but when one of them moved to put the clothes into a trash bag—for safekeeping—the child’s expression crumpled. It took a few soft-spoken assurances to explain they weren’t throwing anything away, just keeping the clothes safe.

    When the soiled pull-up was removed, the extent of the rash became apparent. Angry red skin, raw and beginning to break down. They felt a pang of grief and anger, but they knew this moment wasn’t about them. It was about this child, about showing them that love could be gentle.

    They slowly lowered the child into the warm bath, the water lapping gently against raw skin, a soft hiss of pain shared in silence. The scent of lavender bubbles curled through the air, a tender counterpoint to the child’s wary expression.

    After making sure the child was okay, they stepped out of the room to give them a few minutes of privacy. They hadn’t even fully closed the door before a small voice called them back.

    Reassuring the child, they asked if they wanted help cleaning up. The child’s face brightened, a fragile hope peeking through the layers of fear. Taking turns, they gently washed away the dirt and pain, moving slowly, following the child’s lead. When it came time to clean the rash, they explained that it might sting but that it was necessary to help the skin heal. The child nodded, their small hands clutching the sides of the tub, their trust a precious and fragile thing.

    In one of the many bedrooms they had prepared, they had set out clean pajamas and a fresh pull-up. The room was dinosaur-themed, with green walls and blankets patterned with prehistoric creatures. The full-sized bed looked like a nest of safety, a world away from the chaos the child had left behind. When the child wheeled into the room and saw the dinosaur pajamas, their face lit up. The joy on the child’s face mirrored the joy in their own hearts, a quiet moment of connection.

    As they helped the child get dressed, they asked if they were hungry. The child mentioned spaghetti, a dish that reminded them of home—of the love they had felt when their mom and grandma cooked together. It was a memory soaked in warmth, a thread of happiness they could build on. Without hesitation, the two women set to work in the kitchen. The open floor plan allowed the child to watch as they cooked, the smell of browning hamburger and simmering tomato sauce filling the house, wrapping around them like a hug.

    When they called the child to the table, the sight of the steaming bowl of spaghetti brought tears to their eyes. The women served small portions, understanding that trust was built slowly, in careful bites and soft words. To their delight, the child devoured two full servings, their appetite a hopeful sign.

    As bedtime approached, they guided the child back to the dinosaur-themed room, keeping the lights dim and the voices soft. They could see the nervousness in the child’s posture—how their small hands gripped the armrests of their wheelchair, how their eyes darted around the room. Gently, they reassured the child that they were safe here, that nothing bad would happen.

    They asked if the child wanted a stuffed animal to sleep with. The child’s eyes widened with wonder. They mentioned a dinosaur toy left behind in the rush to leave their home. Leading them to a collection of stuffed animals, the child carefully selected a blue tyrannosaurus rex, promptly naming it “Roar.”

    With the nightlight on and Roar tucked under a small arm, the child settled into bed. They barely had time to pull the blanket up before the child drifted off, the deep, healing sleep of a child finally safe. The two women stood in the doorway, watching over this tiny, brave soul.

    They knew they couldn’t fix everything. They couldn’t erase the pain or make up for the lost years. But they could give this child a moment of peace, a chance to breathe without fear. And as they stood there, hands clasped and hearts full, they knew that every step of their journey had led them to this moment—to this small, sleeping child who deserved the world.

    The Next Chapter

    The days turned into weeks, and the weeks into months. The world outside had slowed to a crawl as the global pandemic forced everyone indoors, but within their small, accessible home, life continued to bloom. There were no trips to playgrounds or family outings, but they found comfort in the simple things—marathon sessions of their favorite TV shows, puzzles and board games spread out on the dining room table, and the warmth of shared laughter. The women created new routines, folding stability into the unpredictable days. The child, who had once been so wary, now moved through their home with an ease that felt like a small miracle.

    When the long-delayed court date finally arrived, the women and the child sat together in front of the computer screen, the virtual courtroom a reminder of how much the world had changed. The child had dressed up for the occasion, wearing their favorite dinosaur T-shirt under a button-up shirt. They clutched Roar, the blue tyrannosaurus rex, tightly in their lap, a quiet anchor in a sea of unknowns.

    But neither the mother nor the father showed up to the hearing. The empty squares on the screen, marked only by muted microphones and silent names, felt like a door quietly closing. The child’s shoulders slumped, their expression a mix of sadness and resignation. The women exchanged a look, a wordless conversation passing between them.

    When the session ended, they wrapped the child in a hug, whispering reassurances that this wasn’t the end—just a new beginning. As they sat together, the women felt a spark of possibility. There was an opportunity here, not just to provide a temporary home but to become a forever family.

    After the hearing, they reached out to the social worker, carefully expressing their interest in adoption. They spoke about how the child had become a part of their family, how their days felt incomplete without the small sounds of their wheelchair rolling through the hallways, without the bedtime stories and quiet moments of connection.

    The social worker listened, her expression softening as she took in their words. She agreed that the child had thrived in their care and promised to reach out to the judge to explore the possibility of turning this foster placement into a permanent adoption.

    As they hung up the call, the women sat in the quiet of their living room. The house, filled with so many memories, seemed to hold its breath. They knew that nothing was certain, but they also knew that love had already made them a family. The legalities would follow. For now, they continued to do what they had always done—love, nurture, and hope.

    A Forever Family

    The judge thought the adoption couldn’t happen fast enough. As they read through the case notes, a clear picture emerged: the child was thriving in the women’s care. They had made every medical appointment, ensured a balanced diet, and watched as the child’s once frail frame slowly filled out with health. Under their roof, the child had found not only stability but also joy—something that had been painfully absent from their early years.

    The judge’s concern deepened when reviewing the repeated absence of the biological parents. This was not the first missed court date, and the silence on their end spoke volumes. Even if the parents reappeared, there were serious doubts about their ability to provide the environment the child needed to continue thriving. Neglect had left its mark, not just physically but emotionally, and the judge knew that uprooting the child now could undo all the progress they had made.

    As far as the judge was concerned, the biological parents had relinquished their rights when they had chosen absence over action—not only in their care for the child but in failing to show up when it mattered most. The court had a duty to protect the best interests of the child, and all evidence pointed to the women’s home as the safest, most nurturing place for them.

    With a few signatures and a lot of paperwork, the judge’s gavel came down with a soft but certain thud—an echo of finality, of forever. They left the courtroom hand in hand, the weight of those papers light compared to the promise they held.

    A Home for Many

    But for the women, this was only the beginning. Becoming parents had reinforced the fire within them to advocate for change. They had seen firsthand how difficult it could be for children with disabilities to find loving, permanent homes. They had witnessed how bias and outdated policies could keep loving families apart. So they took their story public, speaking out about the need for reform in the foster care and adoption systems.

    They began volunteering with organizations that supported disabled and LGBTQ+ youth, using their voices to amplify those who often went unheard. They shared their journey at community meetings, advocating for more accessible housing, inclusive school programs, and better support for foster families. They hosted workshops, taught others how to create homes that were not only accessible but welcoming, and mentored new foster parents, showing them how to build trust with children who had experienced trauma.

    Their home became a haven not just for the child they had adopted but for many others who needed short-term respite or emergency care. They remained licensed as foster parents, always keeping an extra bed ready. Each child who came to stay with them left with a suitcase full of clothes, toys, and a promise that they would always carry a piece of their home in their hearts.

    And through it all, the child they had adopted continued to grow—stronger, braver, and more confident each day. They joined their moms in their advocacy work, sharing their own story when they felt ready, standing as proof of what love and stability could do. Together, they became a voice for change, a living example of how family could be built from compassion and choice, and how every child deserved a safe place to call home.

    Their activism for children had only just begun with that first adoption. Over the many years of fostering, they had countless children walk or roll through their door. Some stayed only for a night or two, finding a safe harbor in the storm of their lives. Others, like their first child, stayed forever, their temporary bed becoming a permanent part of the home. No matter how long they stayed, every child who crossed their threshold left knowing they were loved and supported.

    Their home became a sanctuary, a place where kids could ask questions without fear, where every holiday meant a seat at the table, and every bedtime ended with whispered reassurances and soft nightlights casting gentle shadows. Over the years, they hosted birthday parties for children who had never blown out candles before, celebrated report cards, and cheered on milestones —both big and small.

    Over time, they adopted four children, but two stood out most vividly in their memories. One was a non-binary youth, whose parents struggled to understand what being non-binary meant and tried to make them conform to their birth sex. When that didn’t work, they essentially said, ‘We can’t handle this type of non-conforming behavior,’ and gave them up to the state. They learned sign language to better communicate with a deaf child whose parents had given them up for adoption because they could not cope with having a non-hearing child. 

    They made additional modifications to their home to accommodate other children who had varying levels of disability, always maintaining as much of a warm and welcoming atmosphere as possible, despite some of the medical-grade equipment they had in the home.

    A Legacy of Love

    Opening her eyes after drifting through the memories, she struggled to remember the exact number of lives they had touched. She smiled faintly, knowing the number wasn’t what mattered. In her heart, she knew it was easily over a hundred children who had found safety and love within their walls. Some still sent holiday cards or called on Sundays, their voices echoing through the same halls where they once felt safe enough to simply be themselves. Others had grown up and moved on, but pieces of them remained—the pencil lines marking heights on the bathroom doorframe, colorful handprints on the garden wall, and names carefully carved into the bench that lined the dining room.

    Their first child went on to follow in both of their mothers’ footsteps, becoming not only a social worker and an educator but also a passionate advocate for all children in the foster care system. They helped raise funds to start a group of foster homes specifically designed for disabled and LGBTQ youth, aptly named ‘Next Chapter Homes’—a legacy that she and Janis had only dreamed of when they first sketched floor plans on the back of old notebooks in their drafty first apartment. Proof that love, when shared freely, could outlast a lifetime.

    They had fostered right up until the moment she received her terminal diagnosis. Even then, their focus remained on the children. They made sure every child in their care transitioned to new homes with as much love and care as possible. They spoke to each child honestly, explaining that sometimes even the strongest love stories had to change shape.

    She had no regrets. Her life had been filled with the kind of love she had once only dreamed of as a child. She thought of their first apartment—the drafty one-bedroom with thin walls and a kitchen table that wobbled if you leaned too hard. Even then, they had imagined a home filled with love and intention. What started in that tiny space, with whispered dreams and sketched blueprints, had blossomed into a sanctuary where every child could find safety and warmth. The home they built together had grown, but the love at its foundation had never wavered.

    The home they had built would remain a refuge, a testament to what was possible when love was not just a feeling but an action, a promise kept. Their home would remain, a lighthouse for those still finding their way through the storm. It would always be that rock that so many children over the years had come to depend on.

    Each room held echoes of laughter and healing, each wall painted with intention. What they had created was more than just a shelter—it was a legacy of love and acceptance that would continue to guide those who needed it most. The new children who found their way here would add their own stories to the pencil-marked doorframes, proof that love could stretch across generations.

    The Final Breath

    She wanted to go quietly, slipping away on the gentle current of her memories, leaving only peace behind. Janis, still cradled in the comfort of their home, continued to sleep, surrounded by the echoes of a life well-lived. When Janis awoke to the gentle morning light, she would carry forward the love they had always shared, now woven into every corner of their home.

    She drew in a final, slow breath, the air warm and steady in her chest, a quiet ember of life glowing soft and low. She held it know it was to be her last. It also seemed as if the house they had built together was holding its breath right along with her as the house all of a sudden because still and calm. 

    As it slipped from her lips, so gentle it was almost a sigh, a serene stillness filled the room. Her face remained soft, a smile resting there, as if she had simply drifted into a sweet dream.

    Outside, the first light of morning crept through the window, pooling around the room, brushing against the soft curve of her smile and the worn edges of the paperback in her wife’s hand. The house remained hushed, as if honoring her wish for quiet. 

    Outside the light caught on the colorful handprints on the garden wall and in the dinning room the names carved into the old bench, each a memory pressed into wood and paint. It was a new day—a continuation of the legacy she had helped build. 

    And somewhere, in the quiet of a child’s safe sleep or the joy of a new home found, the light she had carried through shadows into each child’s story remained—steady as a lighthouse beam, unwavering. A glow that would burn on, soft and endless, a promise etched into the walls of their home and into the hearts that had found refuge there.

  • AI in Content Creation: A Game Changer for Writers

    Disclaimer: This blog post was entirely generated by artificial intelligence. It is intended as a satirical piece. It is also an informative piece about AI in content creation. None of the information should be taken seriously.

    Artificial intelligence is revolutionizing content creation, making writing easier, faster, and more optimized. As an AI assistant, I help bloggers and businesses refine their content, improve SEO, and even add humor. But how exactly is AI changing the writing landscape?

    A humanoid AI robot with glowing blue eyes sits at a desk, editing content on a holographic screen, surrounded by floating SEO charts and text elements.
    AI tools streamlining content creation processes.

    Enhancing SEO and Writing Quality

    Writers no longer need to struggle with search engine optimization. AI tools provide real-time keyword suggestions, improve readability, and ensure content ranks well. Platforms like Yoast SEO make it easier to fine-tune articles for search engines.

    A futuristic computer screen displaying an AI-powered editing tool, showing grammar corrections, SEO optimization tips, and keyword highlights in real-time.
    AI enhancing content through advanced editing tools.

    Can AI Be Funny? Exploring AI-Generated Satire

    AI is even experimenting with humor. Shows like “Nothing, Forever”, an AI-generated parody of *Seinfeld*, highlight the potential for robotic comedy. While AI humor isn’t always perfect, it adds an interesting twist to digital storytelling.

    A humorous AI robot typing a satirical blog post on a futuristic keyboard, surrounded by exaggerated and funny thought bubbles.
    AI experimenting with satire in content creation.

    AI in Content Creation: The Risks and Limitations

    Despite its advantages, AI-generated content has drawbacks. Misinformation can spread when AI tools aren’t properly guided. Fact-checking sites like Snopes help verify claims, reinforcing the importance of human oversight.

    A futuristic digital interface displaying AI-powered SEO optimization, with keyword rankings, analytics charts, and content suggestions in a high-tech environment.
    AI-driven SEO improvement tools at work.

    AI and Human Writers: A Perfect Team?

    The best writing happens when AI and humans collaborate. AI assists with structure and clarity, while human creativity brings originality and emotion. Together, they create stronger, more engaging content.

    A human writer and an AI robot working together at a desk, typing on futuristic keyboards, with speech bubbles showing AI's algorithms and the human's creative thoughts.
    AI and human collaboration in content creation.

    As AI continues to evolve, its role in content creation will only expand. While artificial intelligence can enhance writing, improve for search engines, and even try humor, human creativity remains irreplaceable. The best results come from collaboration—where AI refines, and humans create.

    Whether you’re a blogger or a business owner, you can gain from this technology. If you’re someone curious about AI’s impact on writing, it can lead to more engaging content. You will achieve optimized and high-quality pieces. The future of storytelling is here, and it’s a partnership between human ingenuity and AI-powered innovation.

    For more AI-assisted content, check out these posts:

    Sources

    Xiang, C. (2023, January 31). ‘Nothing, Forever’ Is An Endless ‘Seinfeld’ Episode Generated by AI. Vice. Retrieved from https://www.vice.com/