Second Battle, Same Me

Tag: cancer again

  • Today I Choose Joy

    This morning I sat in the almost-dark and watched the sky split itself open. Every day really is a blank canvas, but let’s be honest—most of the strokes are thrown on by things I’ll never control. Life doesn’t exactly wait for my approval before it slaps paint around.

    So I start where I can: ordering the little pieces that actually belong to me. Call it self-care, call it survival, call it refusing to let the day turn beige.

    As the sky softened into light, I decided—resolved, even—that I’d throw some light of my own around today. Maybe for myself, maybe for anyone who crosses my path. The geese flew overhead in their messy V, reminding me that forward is the only direction that counts. And the blue heron strutted across the water like it owned the place, reminding me to stay exactly where I am, no apologies.

    So here’s the palette I’m grabbing: joy.

    • Joy in the fact that I woke up vertical.
    • Joy in feeling well enough to move, not just moan.
    • Joy in time with my granddaughter—even at 25, when she’s not giggling but building her own damn life and still making me proud.
    • Joy in collapsing for a nap without guilt.
    • Joy in dancing if the music insists, even if it looks like a medical emergency.

    That’s today’s order. Joy, bold strokes, no beige allowed. Maybe you should order some too.

  • Self Care This Morning

    Photo by Photo By: Kaboompics.com on Pexels.com

    There is no blog post today because, at this very minute, I’m enjoying the most relaxing massage — a gift from a very dear friend.

    After listening to my heart, I realized I need more of this: more quiet moments, more relaxing adventures, and more time with dear friends who remind me to pause. 💚

  • Hearing Your Heart

    Today, a friend I haven’t seen in a long while reached out. She didn’t know my cancer was back. She didn’t know I was in treatment again. She just said, “I would love to hear your heart.”

    That line stopped me cold.
    Not “let’s catch up.” Not “tell me what’s been going on.”
    She wanted to hear my heart.

    And that got me thinking: what kind of peace, what kind of love does a person carry when they care less about your circumstances and more about your heart?

    Do I even listen to mine?
    Sure, when it comes to the big-ticket items—marriage, kids, family, love. Those are the moments when you’re “supposed” to listen to your heart.

    But do I listen to it daily?
    When I wake up bone-tired.
    When the chemo wall hits and knocks me flat.
    When Sassy drags me down the driveway like a reluctant sled dog.
    Do I stop and check in?

    Truth: most days, my head is way louder than my heart. My head is bossy. It says:

    • Take the meds.
    • Keep walking.
    • Don’t puke in public.
    • Try to be funny about this so people aren’t uncomfortable.

    Meanwhile, my heart whispers. And I ignore it. Because sometimes, my heart says stuff I don’t want to hear—like “rest” when I’d rather power through, or “cry” when I’d rather throw up a sarcastic one-liner. Or, “it’s ok to be mad about this” when I don’t want to think about that.

    But my friend’s words have been simmering all day.
    Maybe what she really offered me was permission.
    Permission to pause. Permission to tune in. Permission to let my heart speak, even if it doesn’t have the right words, even if it stutters.

    So I asked myself: what does my heart say right now?

    And here’s the messy, beautiful, unfinished truth:

    • I’m still here, even if this is not what I planned to do this year.
    • I’m still fighting, and will not stop.
    • I still love, and need to show myself a little more of that.
    • I still have stories to tell.

    That’s my heart.
    Maybe small. Maybe quiet. Maybe shaky.
    But it’s still beating. And today, someone wanted to hear it.

  • And just like that –

    The Wall Meets Udenyca

    Within 24 hours of slamming face-first into The Wall, it retreated.
    I give full credit to the tiny (yet monstrous) contraption known as the Udenyca On-Body Injector—a device slapped onto my arm right after chemo. Supposedly, it waits 18 hours before releasing its magical (and slightly terrifying) payload of medicine. If you’d like the medical mumbo-jumbo, you can check the official site here: udenyca.com.

    But if you’d rather hear it the way it really went down, buckle up.

    How It Works (According to Me)

    On Friday, they stuck this little white box on the fatty part of my arm (nurse’s words, not mine). Imagine half a computer mouse, only bulkier, and now imagine me banging it into every wall, chair, or doorframe in my house. Chemo makes me clumsy; add a plastic box to my arm and I become a human demolition derby.

    The device waits. Then, exactly 18 hours later—2 p.m. on Saturday in my case—it explodes into action. Note the description explodes please!

    The Moment of Truth

    I was napping, minding my own business, when suddenly:

    • A jet engine fired up inside my arm.
    • A samurai sword stabbed me in the exact same spot.
    • And then, as if I’d just licked a battery, I could taste the medicine.

    For one delirious second, I thought I’d dreamed it all. But the little green light that had been flashing turned solid—meaning the beast had done its job. No dream. 100% real. WTF.

    The Aftermath

    Once the pain subsided and the device wheezed its last mechanical breath, I lay there still trying to understand what happened

    Of course, being the overachiever I am, I immediately read the list of possible side effects. Big mistake. (Pro tip: if you don’t want to imagine yourself sprouting hobbit-feet hair or growing elf-ears, don’t read the fine print. These are not actual side-effects, but they are more desirable than the actual possible effects. Just saying.)

    Today

    This morning, I realized something shocking: I actually felt better. The nausea and exhaustion that had pinned me to the floor the day before started lifting.

    So here I am—up, moving, and cautiously optimistic. The Wall may have knocked me flat, but with a little help from science, samurai swords, and jet engines, I got back up.

    This cancer fight is brutal, unpredictable, and weirdly comical at times. Yesterday was down. Today is up. Tomorrow? I’ll keep fighting.

    👉 Every day is a battle. Some days I hit the Wall. Some days I walk away from it. But I’m still here—and that’s what matters.

  • The Wall

    Every cancer patient who’s ever taken chemo knows about the Wall.


    It’s out there—lurking around the corner—just waiting to remind you that chemo doesn’t f***ing play. It can show up once, twice, or stick around to let you know things are about to get real for a long-ass time.

    Yesterday, I slammed right into it.

    Clue #1: Standing up, minding my own business, feeling like my body was about to collapse straight to the floor.

    Clue #2: My personal favorite—great waves of liquid exiting my body from all possible orifices, burning like I was sliding down a razor blade the whole way.

    When that was over, I slept five more hours like a baby. (There’s always a blessing somewhere, right?)

    The rest of the day was almost normal. I ate. I kept it down. I slept well last night—though don’t get the idea that sleep was some natural miracle. It came courtesy of prescribed medication. I took the pills. I slept. I was happy with that.

    This morning, I’m trying to figure out if I’m still clinging to the Wall. Dizzy when I stood up—clue? Spilled a glass of water and felt exhausted cleaning it up—another clue?

    And then I thought of the hundreds of thousands of people who were taken on death marches by their enemies—tired, confused, sick, exhausted—yet still driven forward by the will to live.

    I have that will to live too.

    If I keep meeting the Wall day after day, I’m not going to give up. But I know I’m going to need your encouragement along the way.

    And if someone could whip up some real mashed potatoes like Grandma used to make—and a bowl of real brown gravy—and drop them off, I’m sure it would help me fight the Wall. (Or maybe it would just fly right through me. Either way, it would taste like heaven going down and that would be good enough for today.)

    If you like my blog, please share it with your friends and encourage them to subscribe. I feel bad just blurting this word vomit out on the same few people. Spread the misery, like and share! ❤️❤️❤️

  • What do I really really want

    I just want it to be over — magically over. Not some haunted, never-leaving-for-good over, but over like I don’t have to do this anymore. Plain and simple. No more appointments, no more counting pills like prayer beads, no more scheduling my life around naps and pukes. Is that too fucking much to ask?

    I know the truth: you have to go through the damn thing to get past it. You can’t short-circuit the mess. You have to slog. So here I am — slogging. Hazy brain days that feel like I’m moving through molasses. Brainless moments where I stand in front of the fridge like it’s a conspiracy. Rest when my bones beg for it; heal when my body remembers how; poison because science says so; repeat because the calendar is a cruel comedian.

    Between the bleak and the boring, what I really want is the tiny, ridiculous stuff: to write in peace and light without the guilt that I should be “doing something productive” while I wait for the next appointment. To sit at the kitchen table with my laptop and not have the cloud of “what if” hovering over every line. To drink coffee that’s still hot. To walk outside and not count steps like they’re a report card. To have a normal week that does not begin and end with an IV drip and a list of side effects.

    Also? I want to shoot a fire arrow into this cancer and blow it the fuck up. There. I said it. There’s the part of me that wants to be dramatic and violent and victorious all at once. I want a literal and metaphorical kaboom — lights, confetti, the whole over-the-top ending to this chapter. Tell me that’s unreasonable and I’ll roll my eyes and bring the fireworks anyway.

    And listen: I’m conflicted. I can want peace and quiet and also want to scream and torch the thing that put me here. I can be grateful for the hands that hold me and furious at the time it steals. I can laugh at myself for crying over a lost sock and then sob over the way the chemo makes my bones feel like someone took a jackhammer to them. Cancer doesn’t come with an instruction manual that says “how to be graceful.” It comes with a lot of improvisation, a poor soundtrack, and the occasional emergency snack saved by a patient husband I nicknamed my own Luke Skywalker.

    So I keep going. I show up for the naps and the meds and the ridiculous moments because there’s still light to find. There are small mercies — a friend who drops off a pie, a dog that insists on dragging me outside, a good TV show that distracts for forty blessed minutes. There are stories I didn’t think I could finish that surprise me by being halfway decent. There are mornings when my head clears and I can see color again, and those mornings are holy.

    Mostly I keep going because I refuse to let this story end with me never coming back over it. I want the ending where I walk out the other side — bruised, scarred, wiser, still snarking — not looping back into the same damn place. That’s the stubborn part of me speaking: I want life after this. I want the pages after the battle. I want to play, to laugh, to be boring and ordinary and loud and alive.

    So yeah — I’ll keep slogging. Hazy brain, brainless days, rest and heal, poison and repeat. I will draw in the light where I can. I will fire the arrow in my imagination and shout when I need to. And I will keep looking for the little lights that make the whole thing bearable until one day—God willing—the arrow does its job and this is over for real.

  • Drops of Fears

    Photo by Ali Hassan on Pexels.com

    Tears falling—
    Drops in the vein.
    Never staying, never staining,
    Never easing the pain.

    Drops sliding
    Through the vein:
    Maybe a cure,
    Maybe more pain.

    Tears, fears, flips—
    Drops, stops. Cancer quits.

  • Dry Mouth, Dark Humor, Still Alive

    The day after: the poison comes back to visit like an unwanted in-law.
    It wades where it pleases — stabs, jabs, puddles of outrage in my bones.
    The shoulder cedes first, a tiny drill bit burrowing in until it’s bored its way to the middle of my back.
    My head’s a foggy TV zone and all I want is a long nap, but then the hips join the pity party.

    Is there a silver lining? Sure — it’s passing through. Slowly. Like a moving train that refuses to be quiet.
    Nausea tags along like a bad joke. Dry mouth, too. The more I drink, the more my stomach stages a protest.
    I don’t want to sleep away the days I still own. I don’t want chemo to be the weather report for my life.

    No Tylenol, no Motrin, no miracle dime-store fix. The pain pools and pounds and nobody gets to leave early.
    But here’s the part I keep repeating until I believe it: I am stronger than the fear in my head.
    I can fight harder than my doubts allow. I am more than a count on a lab sheet.
    More than nausea. More than a chair in an infusion room.

    I want to live — not someday, not after the list of “ifs” — today.
    I will live. And if the poison thinks it can make me quiet about that, it can try.

  • The Power of Female Friendships

    Every now and then, my friends and I manage to pull off a miracle—we get together. Not the everyday friends you bump into at the grocery store. Nope. These are the women I see maybe three times a year, if the planets align and nobody’s kids, grandkids, or husbands derail the schedule. We missed some friends this time, but we will catch up next time.

    But here’s the thing: they are my friends. The kind that, when you finally sit down together, it feels like no time has passed at all. This time, we even had a new lady join us—and boom, instant friend. That’s how women work. We don’t need a blood oath or a secret handshake. Just pass the coffee, and welcome to the circle.

    We started with breakfast, and when the sun hit us full in the face, we moved tables. When the sun found us again (because apparently it was stalking us), we moved again. And we just kept talking—about life, kids, grandkids, husbands, hopes, frustrations, the whole messy, beautiful pile. I never really thought much about cancer at all that day.

    There’s something magical about these kinds of conversations. They flow so naturally with women who care, who understand, who aren’t afraid to be real. You don’t need warm-up questions or polite small talk—you just jump right in. And somehow, even though we don’t see each other all the time, there’s always too much to say and never enough time.

    Because here’s the truth: women need other women.
    And I need these women.

    So thank you, my friends, for the laughter, the honesty, the tears, the shifting tables, and the reminder that I’m not doing this life , or in this battle, alone.

    I love you all. (You too Dougie.)


  • Live Life or Stay

    Photo by Jenny Uhling on Pexels.com

    Today is the day.
    What will the numbers say?
    Do I pack my bag for a trip,
    Or do I, once again, stay?

    Plans were made—
    Before he arrived.
    Plans for living life,
    Not just fighting for it.

    If the numbers are good,
    I’m going.
    Because life is too short.

    If the numbers are bad,
    I’m staying put,
    Gearing up,
    And fighting for life.

    So y’all—say a prayer,
    Send a wish to the universe.
    This girl needs to get out and live.
    Because life is too short.