Kat’s Musings

Tag: housewife

  • Defying Disability: My Daily Act of Rebellion

    Defying Disability: My Daily Act of Rebellion

    Every single morning, I whisper sleepy sweet nothings to my man. After that, I rise with fire in my veins. I spend the entire day fighting against the disability that constantly tries to drag me down.

    I push this stubborn, trembling body to its absolute breaking point. I lean hard against the bathroom counter while brushing my teeth. My legs shake as I take selfies for him in the mirror. I refuse to let weakness win. In the kitchen, I grip the edge of the counter. I make my espresso with gritted teeth. My knees threaten to snap back beneath me. I refuse to constantly sit in a wheelchair. I refuse to strap on those ugly, soul-crushing leg braces that would mark me as conquered.(Only HE is allowed to do that!).

    A physical therapist once looked me dead in the eye. She suggested I stop relying on my mother to drive me to appointments. She calmly recommended I call a WHEELCHAIR VAN! It would pick me up and drop me off. She acted like I was some fragile invalid. The words barely left her mouth before I shut that shit down. I was not feeling it. The idea of being loaded and unloaded like cargo made my blood boil. The thought of sitting in a wheelchair instead of the seat of a car was infuriating. I told her no, thank you, and never went back. Now I get down onto the floor everyday and do my own exercises, No van needed. I refuse to give in. I refuse to let anyone reduce me to a scheduled pickup in a van built for surrender.

    Life keeps trying to force me onto my ass. There is even a goddamn chair sitting right there in my shower like a permanent joke . Most days I have no choice but to sit under the hot water like a broken doll while it cascades over me. But the only time I truly get to stand—proud, naked, water streaming down my body—is when my man steps in behind me, his strong hands gripping my hips as he holds me upright so I can clean myself. I love the way he steadies me, the way his hard body presses against mine, keeping me vertical through pure possessive strength while steam fills the air. In those heated moments I feel rebelliously alive, even as my legs scream and tremble beneath me.

    I face that humiliating chair and the endless war with gravity everyday. Yet, I reject every medical enhancement. I refuse every synthetic crutch and modern healthcare. I do not believe in any of it. If it is meant to be, it is meant to be. If sickness is coming for you, it will find you. It does not matter how many pills, injections, gene therapies, or experimental treatments they invent. All the advances in medicine are nothing more than dressed up as progress.

    I will not be synthetically made better.  
    I refuse to be rebuilt, patched, upgraded, or artificially propped up like some defective machine.  
    Only the natural way.  
    Only the forever way.

    And my hands? That is another story. For over fifteen years now, I have had the use of only my right hand. My left hand is dead weight, a silent traitor that sways useless at my side while I fight like hell. I have mastered one-handed shoe tying, buttoning, and zipping. I have learned to handle my personal hygiene with stubborn grace. However, some cooking (chopping, etc) and deep cleaning are still slow and frustrating for me. They are nowhere near as efficient as I demand of myself. I practice longer to get better physically. I refuse to accept the limitation. My ultimate goal is to do it all for my man. I want to cook his meals with these one-and-a-half hands. I want to deep clean our home until it shines, all for him. I want to serve HIM. I want to care for him. My broken body can still rise up and give him everything he deserves.

    This is my daily mantra. It is my middle finger to disability and to weakness. It defies a world obsessed with comfort and “fixing” every imperfection. I choose to feel every tremor, every ache, every exhausting victory on my own raw terms. I lean on counters instead of rolling in chairs. I am held up by my lover’s grip instead of cold metal and plastic. I struggle one-handed. I am eager for the day when I can entirely care for the man I love.

    In a society that worships ease and vulnerability, I stand as a living, breathing, unapologetic rebellion. My legs may shake and threaten to give out. My left hand may be useless dead weight. However, my spirit is lava. I will keep going every single day. I will keep whispering filthy sweet nothings into my man’s ear at night. I will keep fighting with everything I have left.

    This is how I love.  
    This is how I fight.  
    This is how I remain fiercely, provocatively, alive.

  • Choose Your Fighter

    Choose Your Fighter

    Transformation: from disability to housewife-in-training (throughout the years of my illness)

  • Americana.

    Americana.

    I have lived in the tiny town of Snohomish, Washington,since I was seven years old. Snohomish is not flashy. It is not Seattle. It is the kind of place where you grow up slow. The biggest drama is who forgot to lock the barn. In Snohomish, “good morning” still means something.

    I used to hate that. I wanted to be a big city girl (ala Samantha Jones in Sex and the City). I even went away from the public school I was supposed to attend. I did this so I could dress and be a little more high class. 

    The girls who live in Snohomish pride themselves for living in a Bodunk town. “Fancy” usually means that you will sink into the muddy fields. It is not the norm.  But I did not like that. I did not want to wear pajamas and slippers to class. I wanted to wear stilettos and I dreamt of living in a penthouse. 

     None of that ended up happening. It became dangerous to even visit a city. Now I have a different perspective of this small town. It feels like living inside a postcard and that postcard smells like rain and fresh-cut grass most days. 

    This town is tiny, maybe ten thousand people. Main Street still looks like it did in the nineteen-twenties. It has brick storefronts, a hardware store that sells everything from nails to fudge, and diners. The river runs right through the middle—Snohomish River, wide and slow. Packed with sunburned locals in July. Around here, summers are for the county fair (something that I do not partake in). It is not the flashy kind with Ferris wheels taller than trees. It’s just a dusty field off Second Street, filled with goats baaa-ing, cotton candy, and sketchy ride operators. Winters are quieter. Fog rolls in off of Puget Sound like a blanket, and school buses crawl through it, headlights glowing. 

    People here do not rush. You wave at strangers because you have seen them before— since the town is so small. Everyone knows everyone’s business. They do not judge, or at least, they do not judge out loud. This was new to this little Russian girl. I left for college, came back since. The river still smells the same. The hardware store still sells fudge. And yes it rains, but it rains softly— as if this place is giving you a hug. 

    I want to share this hug with the love of my life. Convincing my boyfriend to move out to Washington state was like my experience of recognizing my hometown in the past. It is different from the postcard version I see now. 

    While we would not be living in Snohomish, small towns are so much more attractive than the big bad cities. While I do not want to dress like a slob or float down a river in the summer— I would rather that than be raped by an immigrant and encounter needles in the storefronts.  He would rather cheer for the teams that his family has always supported and not be surrounded by “aw shucks” coworkers. 

    So I do not belong in Snohomish, Washington, but I have definitely developed an appreciation for small towns. I might live in a small “Americana” town in Montana or the Carolinas. Wherever I end up, I will always waive “hello” and will not judge (out loud). 

  • Physically.

    Physically.

    I am still buzzing from last week —just lying there, tangled up in sheets, his arm slung over me. 

    I swear, nothing feels better than finally being in the same room as him. No more FaceTime lag, no more “can you hear me?”—just his stupid grin, his real voice, the way he smells like his high end cologne collection. I melt every time he opens his arms towards me . Like, actually melt. My shoulders drop, my jaw unclenches, and suddenly the whole past —my parents criticisms, constantly feeling ignored and not understood —evaporates. 

    He does not even have to say anything. Just stands there, arms open . We did not do grand gestures. No roses, no playlists. Only sweet treats waiting for me upon arrival. Then him flopping onto the hotel bed, me curling into his side like it is the only spot that fits. His hand finds mine—always does—like it’s muscle memory. And I think, “God, this is it”. This is what I have been waiting for.

    The best part? He gets quiet too. Like he knows I need five minutes of nothing—just us breathing, the TV on mute, his thumb rubbing slow circles on my knee. I could stay like that forever. I do not care if it sounds sappy. I am happy. Not content or fine—happy. The kind that makes my chest ache a little, like it is too big for my ribs. And yeah, I miss him. But right now? I guess I just wait. 

    The waiting is terrible but necessary and I hope —temporary. When the bleed took my body away from me, I was waiting to go back to university (I thought I would physically be back on campus), but instead, my parents made me apply online and finally finish my Bachelor’s degree TEN YEARS LATER. Then came the waiting for my recovery—I realized that I wasn’t made for the indoctrination and fake “wokeness” of the “real world.”

    But when I met my man I thought that this waiting was over. He loves me as I am—so I no longer needed to rush anything or force myself into school/ work. 

    I found that in these settings, I was constantly being penalized for having the “wrong “ opinions in my essays and papers, but would immediately be rewarded and praised as soon as I brought up my disability. I did not want to use my situation as a crutch. I hate pity.  So I chose to be myself. A little right wing, conservative and definitely against any kind of diversity. And everyone hated that. Except the love of my life. 

    But when I am back home alone again—in my own little bubble—the quiet hits different—like the rooms are too big without him breathing next to me. I miss the way he rolls over and pulls me closer—I keep replaying it: his fingers tracing lazy circles on my back, the way he mumbles to me even though I’m already half-asleep. It’s stupid how much I crave that—his weight, his heat, the dumb little sounds he makes when he is dreaming. And yeah, I know it is cheesy to say out loud, but… I am happy.

     Like, stupid-happy. Not the Instagram-filter kind—just the real, messy, I-cannot-believe-this is-mine kind. I never had this before. Was I ever truly happy?  I manipulated my way into graduating with straight As and everything else I had done was always done through force or for someone else. This is mine. My life. My happiness. So here’s to him. To us. To every second I get to be physically right there, skin on skin, no screens, no distance—just him and me and this ridiculous, perfect quiet… I guess I have to go back to waiting for this feeling again. 

  • My little journey

    My little journey

    I still remember the date—June thirtieth, twenty-ten—like it’s etched into my skull. That morning, everything felt heavy. I’d been carrying this quiet tumor since sixth grade; doctors shrugged it off back then, said it was dormant, harmless. 

    But I wasn’t dormant. I was crumbling—mentally frayed, body aching from the stress and exhaustion of my broken heart —and then it happened. One second I’m pacing, doing my PR work for a R&B artist in Seattle, Washington, next I’m gone. Coma. Lights out. 

    When I woke up two weeks later, the left half of me was missing. Not gone, just… silent. Arm limp, leg dragging like dead weight. I couldn’t grip a spoon, I couldn’t even hold my phone let alone text, and I couldn’t step without someone holding me up. The tumor had burst, they said. Pressure built, brain swelled, and my left side paid the price. The first weeks were a blur—hospitals, tubes, nurses who spoke too loud. I remember staring at my hand, willing it to move. Nothing. Just a stranger’s fingers attached to me. 

    Rage came next. Why me? Why now? I’d already been broken—why finish the job? 

    But rage burns out. What stayed was stubbornness. Physical therapy felt like torture at first—electrodes zapping my arm, therapists yelling squeeze! Even the simple task of sitting up in bed or in the wheelchair was torture. I hated mirrors. I hated pity. I hated the way people talked slower, like I’d lost my brain along with my limbs. Months turned into years. I learned to walk again, but only with help—slow, lopsided, cane in right hand like a crutch. I taught myself to write, even though my handwriting looks like a kid’s. I can complete tasks like buttoning my shirts and tying my shoes awkwardly. And I can cook—awkwardly, one-handed—because I refuse to live off someone else’s help forever. 

    The real recovery wasn’t muscle. It was headspace. I stopped asking why and started asking what now? I went through a number of therapists and some of them turned out to be lifesavers. I read all of the books and I watched all of the videos on neuroplasticity—stuff I never cared about before—and realized my brain was still rewiring, still fighting. 

    Today, I’m not cured. My left arm waves around without purpose while clenched in a fist. While my left leg drags on bad days. 

    But ultimately I have found an incredible love who accepts me as me and continues to inspire me through this journey. This is why I am writing this—I’m not the girl who got thrown into a coma; I’m the one who clawed out. If you’re reading this and you’re in the dark—whether it’s a brain injury, depression, whatever—listen: the body forgets, but the mind remembers how to want. And wanting is enough. Keep moving. Even if it’s just one stupid, stubborn inch at a time.

  • This Is Me…

    This is a little project that I am working on while I wait for my Prince Charming. You can follow my journey as I recover from disability and wax poetic about my passions in this life. I do not want children but I strongly desire to be a perfect little housewife. This is where I speak my dreams into reality…

    I have always loved the quiet thrill of a well-run home—like it’s my own little kingdom. There is something magic in turning chaos into calm. Folding laundry while the kettle whistles, watching sunlight hit the counter just right, knowing dinner’s simmering and no one’s yelling about deadlines. I’m not here to sell you on domestic bliss. I just… like it. The rhythm of it. The way a clean sink feels like a tiny victory. The slow burn of bread rising while I write this little blog . This is me. A future housewife who’d rather scrub grout than climb ladders.

    I will also write about being natural and all-in-all health. I spent years chasing perfect bodies, pills, and quick fixes until I realized healing isn’t about looking good; it’s about feeling whole. Now it’s less kale smoothies and more slow walks barefoot on grass (once I get to walk again!), breathing like I actually mean it, and saying no to anything that makes my gut twist. It’s messy, it’s unglamorous, but damn if it doesn’t feel like coming home to myself. 


    And the man of my dreams? I have finally found him, but even though he is over 40, he’s still growing into someone who loves me mid-recovery, mid-mess, mid-laundry pile. He knows that I want a man who can sit with me while I journal about old wounds, who can hand me my espresso without asking why I am crying (I can be overly emotional). Not a prince. Just… steady. Kind. Real. So I’m writing it all down—recovery, health, love—before the apron goes on. Before I start folding his socks like they’re sacred. Because if I’m gonna build this life, I want the foundation to be mine. Not borrowed. Not borrowed from anyone.