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~ Diabetes, Cancer Fighter, Father of Twins, Kayak Fishing, Woodcrafter, Lover of Life

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Tag Archives: Life

The Phone Call That Changed Everything

17 Saturday Jan 2026

Posted by Tim Hughes Living with CML in Cancer, Depression, Diabetic, Disability, Leukemia, Life, Weather

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Anniversery, Cancer, Celebrate, Chemotherapy, CML, Depression, Doctor, health, Lab Work, Laughter, Leukemia, Life, Medicine, Oncologist, Weather

It’s hard to believe, but I’m coming up on my 12th anniversary of being diagnosed with CML (Chronic Myeloid Leukemia). My most recent lab work showed my cancer as undetected—which is always good news… with an asterisk. In my case, “undetected” can be a little sneaky. It can be undetected on one visit and pop back out of range on the next. I wish I could tell you why there’s such a swing, but I don’t do anything differently from month to month. Same diet. Same routine. Same bad jokes. The only thing that really changes is what the numbers decide to do.

I will never forget the day I found out. Or the days leading up to it.

I had gone in for a routine six-month checkup when my GP called and asked me to come back in for more lab work because something looked “off.” Then on February 14, 2014—Valentine’s Day—my wife and I were getting ready to meet one of my daughter’s newest boyfriends. He was coming to pick her up for a high school date, and I was in the important stage of fatherhood known as trying to find the right words to mildly terrify a teenage boy.

That’s when my phone rang.

Keep in mind, this was late on a Friday afternoon, when most doctors’ offices are already mentally in their cars. The nurse told me my white blood cell count was extremely high and that they wanted me to see an oncologist.

At that moment, I had never heard the word “oncologist.” I didn’t know what kind of doctor that was.

During the phone call, my wife quietly looked it up and said, “Tim… that’s a cancer doctor.”

Needless to say, my carefully rehearsed intimidation speech for my daughter’s boyfriend completely left the building.

My appointment was scheduled for the following Tuesday at 10 a.m., which made that weekend the longest weekend of my life. A thousand scenarios ran through my head. I didn’t sleep much. I just wanted Tuesday to get there so I could talk to someone who actually knew what was going on.

Tuesday morning arrived with snow and ice. I kept calling the office. No answer. The hospital sat on top of a steep hill, and the road was iced over. No one was going up it, including me.

Later that day, the temperatures rose, someone finally answered, and my appointment was moved to 2 p.m.

I’ll never forget meeting my oncologist. He made a lasting impression. My wife decided that day she didn’t like him from the start.

I had a thousand questions loaded and ready. I opened my mouth to ask the first one. He held up a finger and said, “I’m talking. When I’m done, I’ll answer your questions.”

And just like that, I realized I was not in charge anymore.

He’s an older doctor, and sometimes I worry that one day I’ll walk in and find out he’s retiring. I’ve been with him nearly the whole time—nearly because there was one stretch when he tried to pawn me off on another doctor at another hospital because my numbers wouldn’t behave. But that’s a story for another time.

The time after my diagnosis was one of the darkest periods of my life. I slipped into a depression I had never known before. I truly thought CML was a death sentence. I was afraid to buy anything because I figured it would just have to be sold or given away. There were days I stayed home—not because I was sick, but because I didn’t want anyone to see me fall apart.

And honestly… at that time, I didn’t care.

Through some very serious conversations with my wife, my parents, and my oncologist, I slowly crawled my way out of that hole. It didn’t happen quickly. It didn’t happen neatly. But it happened.

They say laughter is the best medicine, and while my insurance company may disagree, I’ve found it to be pretty true. If you go back and read some of my early posts, you’ll notice they don’t carry the same humor as the ones I write now. There’s a reason for that.

I still have days when the weight hits harder than others. I still have moments of fear, frustration, and fatigue. But I’ve learned that sometimes it’s better to laugh at life’s situations than to let them crush you. Humor didn’t remove cancer from my life—but it did give me a way to live with it.

So here I am, almost twelve years in. Still showing up. Still rolling the dice on lab work. Still grateful for “undetected,” even when it comes with an asterisk. Still learning. Still stumbling. Still here. And still trying to laugh whenever possible… because some days, laughter is the only thing in the room that reminds you you’re still alive.

If you’re reading this and you’re walking through cancer, or any other terminal or life-altering diagnosis, let me tell you something I had to learn the hard way: don’t give up. Don’t give up on tomorrow. Don’t give up on joy. Don’t give up on the people who love you. And don’t give up on yourself.

There will be dark days. There will be scary appointments. There will be lab results that knock the wind out of you. But there will also be days you never thought you’d see. Conversations you didn’t think you’d have. Laughs, you didn’t think you were capable of anymore. Life doesn’t end when a diagnosis begins. It just changes.

Hold on. Ask questions. Lean on the people God has put in your life. Celebrate the good days. Endure the hard ones. And if all you can do on some days is get out of bed and breathe, then that is more than enough for that day.

Almost twelve years ago, I thought my story was coming to an end.

It turns out that it was just the beginning of a very different chapter.

And as long as there’s breath in your lungs, there is still a reason to keep turning the pages.

Please Hold…My Brain is Loading

11 Sunday Jan 2026

Posted by Tim Hughes Living with CML in bariatric-surgery, Cancer, Family, Leukemia, Weight Loss

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B12, blog, Brain Fog, Buffering, Chemotherapy, CML, Concentrating, Diary, Drugs, Forgetfulness, gastric bypass, health, Leukemia, Life, Medications, Memory, Memory Loss, Mental, mental-health, Sleep, Sticky Notes, Venting, writing

When I started this blog some years ago, it was mainly meant to be a diary of sorts — a place to vent and to voice my opinions. Gaining an audience was never part of the plan. This was more “Dear Diary” than “Dear Internet.” It wasn’t until I was diagnosed with CML that I decided to use this platform to write about my experiences with cancer and maybe, just maybe, help some other poor soul going through the same thing.

As with most things in life, plans change. Sometimes gently. Sometimes with a two-by-four.

Not only was I dealing with CML, but I also decided to write about my experiences with gastric bypass surgery. When I was doing my research, I noticed there really wasn’t much content out there. And what I did find often ended shortly after surgery, for whatever reason — almost like everyone vanished once the anesthesia wore off and nobody ever came back to update the internet.

There’s something else that’s been going on for quite some time, and I’ve finally decided to put it down on paper. I’ve been experiencing brain fog for several years, and over time, it has gotten worse. “Brain fog” is a term used to describe symptoms such as difficulty concentrating, memory problems, mental cloudiness, confusion, and trouble finding words — essentially, feeling like your brain is running Windows 95 in a world that expects fiber internet.

I notice it most when I’m trying to carry on a conversation and, right in the middle of it, my mind just… leaves. Names vanish. Phone numbers disappear. Sometimes I forget what I was saying while I’m still saying it. Short-term or long-term, it doesn’t matter. It’s there… then it’s not, kind of like my car keys.

What makes this so difficult isn’t just the symptoms themselves, but how they sneak into everyday life. I’ll walk into a room and forget why I’m there. I’ll open my phone to look something up and immediately forget what I was looking for. I’ll stand in the kitchen staring into the fridge like it’s going to explain my life choices to me.

Conversations that should be easy sometimes turn into mental obstacle courses as I search for words I’ve used my entire life. It affects my confidence more than I care to admit. When you can’t trust your own memory, you start second-guessing yourself. You hesitate before speaking. You rely more on notes, reminders, and the people around you. I’m grateful for their patience, but it’s a strange feeling when your own brain doesn’t always show up prepared.

Some days are better than others. There are moments when everything feels clear and normal, and I start to think maybe I’ve turned a corner. Then there are days when my thoughts feel like they’re moving through mud, and even simple tasks take extra effort. Those are the days that wear on you — not with fireworks, but with a steady drip of “Seriously? Again?”

If you Google the term “brain fog,” you’ll find a long list of possible causes: lack of sleep, medications, chemotherapy, B12 deficiency, and even anemia. I’ve spoken to my doctor about it, and while some over-the-counter options might help, with my anemia and the chemotherapy drugs I’m on, they may not make much difference. In other words, this may just be part of my user agreement for now.

I don’t share any of this for sympathy. I share it because this blog has always been about honesty — the good, the bad, and the occasionally forget-why-I-walked-in-here. Brain fog may be part of my story right now, but it’s not the whole story. I still laugh, I still enjoy life, and I still manage to function… even if I need a few more sticky notes than the average person.

I’ve learned to adapt. I write more things down. I set reminders. I give myself a little more grace than I used to. And when I lose my train of thought mid-sentence, I’ve decided it’s perfectly acceptable to blame the fog, shrug, and move on. If nothing else, it gives the people around me a chuckle — and honestly, some days I’m laughing right along with them.

And if you ever see me standing in a room staring off into space like I’m waiting on divine revelation, don’t worry. I’m probably just buffering.

Unwelcomed Alarm

10 Saturday Jan 2026

Posted by Tim Hughes Living with CML in Weather

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Alarm, Challenges, Coffee, health, Life, mental-health, National Weather Service, Production, Rain, Sleep, Storms, Thunder, Weather, writing

I wrote in my last post about how crazy our weather has been. Apparently, the weather department took that as a challenge.

Last night, it decided to toss in another curveball — a cold front pushing through, dragging thunderstorms along with it. We spent most of the day and evening under a tornado watch. By bedtime, we had already picked up nearly three inches of rain, and the storms were still rolling in. The thunder wasn’t rumbling anymore; it was auditioning for a demolition crew.

Before going to sleep, I set my phone alarm for 5:30 a.m. so I could get up and get ready for men’s Bible study at 8. Responsible. Mature. Clearly overconfident.

Sometime later, I heard an alarm and woke up. I didn’t question it. I just accepted my fate. I took a long, hot shower, shaved, got dressed, and headed to the kitchen. I started the coffee and even remember thinking, “Tracy should be getting up soon. It’s got to be around six.”

The first pod finished, and I glanced at the stove clock.

4:10 a.m.

I stared at it, waiting for it to blink and say “Just kidding.”

It didn’t.

I checked my watch. Same time. That’s when it hit me — I hadn’t been woken up by my phone alarm. I’d been summoned by the weather radio.

I sat down in my recliner with my coffee and pulled up the radar. Sure enough, the National Weather Service had issued a flash flood warning at 3:45 a.m. That alert was the “alarm” that launched me into full morning-person cosplay.

So there I was — clean, dressed, caffeinated, and absolutely betrayed — living in a time slot meant only for bakers, farmers, and people who lost a bet.

There was no going back to bed. And even if I tried, I’d probably sleep right through the real 5:30 alarm just to complete the joke.

Moral of the story: I don’t need an alarm clock. I need a personal meteorologist who knows when to mind his business.

No Joy for Christmas

28 Sunday Dec 2025

Posted by Tim Hughes Living with CML in Family

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Christmas, emotion, Family, Hardships, Holiday, Joy, Kids, Life, Remembering, Resentment, Tears, Tension

I want to start by apologizing for this rant. My poor wife has listened to me wrestle with this for the past week, and I still don’t feel settled. I’m honestly at the point where I’m ready to say I’m done celebrating Christmas—and maybe even Thanksgiving—with my parents and siblings altogether.

At the center of it all are my parents, my mom and dad. They’re both in their eighties now and won’t be with us forever. That fact matters, and it weighs on me more than I probably let on. Then there’s my wife and I, and our three kids—all grown, all adults, all working and living their own lives. That still feels strange to say sometimes.

I have two brothers and a sister. One brother is married with kids, two of whom are now adults with their own jobs. Watching the next generation step into adulthood really drives home how quickly time passes. My youngest brother is also married, but his family is in a completely different season—three young kids, full of noise, energy, and chaos. I recognize that life because I’ve lived it.

Then there’s my baby sister. She’s married and has a son in his twenties who is autistic. While his age says “adult,” his needs and world often look more like those of a teenager. He’s special—everyone knows it, including him—and I think he’s figured out just how wrapped around his finger the family really is.

The real issue, though, isn’t any one person. It’s the expectation that everyone must be present at every family function. My mom believes that if something is planned, everyone has to be there—no exceptions. For years, Christmas has been pure hell because of this mindset.

If someone couldn’t make it, she would get upset and cry. As the oldest, I’ve tried to talk to her calmly, suggesting she pick a date and let people work around it. But there are two things she refuses to accept. First, our family has grown, and people now have other obligations—spouses, in-laws, jobs, kids, and schedules that don’t revolve around one household. Second, if Christmas falls on a weekend, many people still have to return to work on Monday. She cannot understand why they can’t “just ask off.”

Here’s the part that still stings the most. I’ve been married since 1991, and from day one, my wife and I always gone to my parents’ house for Christmas lunch. Always. My wife’s parents also had lunch every year, but we never went there first. We would eat at my parents’ house, open gifts, then rush out and head to either her parents’ house or her brother’s—arriving late every single time. They would be waiting on us.

Year after year, this happened. And not once did my wife complain, because she understood exactly how my mom would react if she didn’t get her way.

Now things have changed. My wife’s parents have both passed away, and her family now gathers at her sister’s house. That house is in the opposite direction from where my family meets. Trying to fit both sides of the family into one day is no longer just stressful—it’s impractical. What used to be exhausting is now simply unreasonable.

About five years ago, something finally changed for the better. My mom told me she and my sister had talked and decided that the Saturday after Christmas would be our official family Christmas. It felt like a miracle. Everyone could make it. No tears. No drama. No guilt. It worked.

Until yesterday.

My youngest brother’s wife, who works as a prenatal nurse, had to work late. My mom went hysterical. Suddenly, Saturday “won’t work anymore.” According to her, the solution is that we’ll all meet the day after Christmas because she’s convinced a future executive order will make it a federal holiday.

I tried explaining—calmly—that even if something like that ever happened, it wouldn’t affect healthcare workers, and many employers wouldn’t observe it anyway. Changes like that take years, if they happen at all. None of that mattered.

And just like that, we’re back to square one.

What makes this so hard is knowing that my parents are aging. Time is limited. I don’t want resentment to be what I remember. I don’t want the holidays to feel like obligations instead of moments. Honoring our parents shouldn’t require everyone else to bend themselves into knots, sacrificing peace and fairness to avoid tears.

Wanting boundaries doesn’t mean I love them any less. It means I’m trying to protect my wife, my kids, and myself from decades of emotional strain that always seems to fall on the same shoulders.

I don’t have all the answers yet. I just know I’m exhausted. And for the first time, I’m seriously questioning whether continuing these holiday traditions—exactly as they’ve always been—is worth the emotional cost.

With time being what it is, I want whatever holidays we have left to be filled with meaning, not tension. Maybe stepping back isn’t giving up at all. Maybe it’s the only way to find peace while there’s still time to appreciate one another.

Holiday Doldrums

17 Wednesday Dec 2025

Posted by Tim Hughes Living with CML in Depression, Family, Pets

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books, Cats, Christmas, Doctor, emotion, Family, Gifts, Home made, Kids, Life, Ornaments, Pets, writing

Christmas is a little over a week away and as usual I’m struggling to get everything bought. This year I’ve decided to make several of my gives to my friends and family. I may end up being that person that no one wants a gift from next year but it is what it is. I made my wife and kids Christmas ornaments honoring my cat that just recently passed. I’m really hoping that everyone likes them.

My wife and I are still dealing with the loss. We’ve also noticed that our other cat, Sophie, has started acting differently. I think it’s her way of dealing with his absence and the solitude she experiences when we’re not here. We’ve talked and I’d like to go ahead and get another little kitten but we’re not sure how Sophie will respond. She “tolerated” Clyde and was not really the best of friends but they got along for the most part. I think my wife will eventually agree but it will take some time for her to come around.

This will be Clyde’s marker for his resting place. I’ve been real busy and haven’t took the time time to get the marker done. If the truth is known, every time I sat down to work on it I got upset and couldn’t bare to think about it. There is currently a little wooden cross that my wife placed there until I could get this made. Once I have the marker in place I think this will be the closure that I will need. I will place the marker tomorrow after I get home from my oncologist appointment tomorrow afternoon. Maybe the rains will have moved out by then.

I’m sure I’ll post again but in case I don’t, I hope everyone has a happy holiday and a Merry Christmas.

A Little Health Update (Spoiler: I’m Still Kicking)

11 Thursday Dec 2025

Posted by Tim Hughes Living with CML in Leukemia, Cancer

≈ 2 Comments

Tags

Life, health, Pain, update, Iron, mental-health, Potassium, Oncology, Kidney, Melanoma

I haven’t posted about my health in a while, so here’s your semi-regular episode of “What’s My Body Doing Now?”

First up, the oncology report: still no detectable blast cells for about eight months. 🎉 I’m not throwing a party just yet, because last time I got excited, my labs basically said, “Surprise!” and did their own thing. But for now, we’ll call it a win.

Iron levels? Yeah… those are still on strike. I’ve officially been diagnosed with chronic anemia, which explains why I’m always freezing and walking around the house like it’s January in Alaska. I’ve had so many iron infusions I’m pretty sure I’m 3% metal at this point. Waiting on Marvel to call.

And then there’s the potassium situation. Apparently my potassium levels have been creeping up. My oncologist thinks it’s tied to the kidney failure. Meanwhile, I barely eat any high-potassium foods, so my best guess is that my body is just freelancing at this point.

Skin cancer update: I had a melanoma spot and another bonus cancer removed from my left arm a little over a month ago. They left some lovely scars, which I now refer to as battle wounds because that sounds way cooler than “my dermatologist wanted a closer look.”

Now they’ve moved on to my back. I had a spot removed Tuesday that they think might also be melanoma. We’ll know more when the biopsy comes back, but let me tell you… back pain is a whole different universe. I slept approximately 12 minutes that night because I couldn’t get comfortable. Tylenol and I are in a committed relationship now.

Anyway, that’s the latest episode. Thanks for tuning in. Same time next month for whatever plot twist my body decides to add next. 😅

Family, Chaos, and Gratitude: Reflections After Thanksgiving

28 Friday Nov 2025

Posted by Tim Hughes Living with CML in Photography

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Birthday, Blogging, Christmas, Family, Gatherings, gratitude, Holiday, Life, Thanksgiving, Traditions

Opening Thoughts

Thanksgiving has a way of making you pause and take stock of what really matters. For my family, it’s more than just turkey and pumpkin pie—it’s about showing up, keeping traditions alive, and sometimes surviving the chaos that comes with it. Yesterday was no exception. Between navigating crowded tables, debates over who’s bringing what, and the inevitable “pass the mashed potatoes” shuffle, I found myself thinking about why we bother with all of it. And the answer, as always, came back to one simple thing: family.


Why I Write

It’s been a while since I’ve written this much on the blog. Lately, sitting down and putting my thoughts and feelings into words has been surprisingly therapeutic. I’ve always said that this space isn’t really for anyone else—it’s my diary, my outlet. If I gain followers, that’s great. If I lose them, that’s fine too. This is for me, and that’s enough.


Family Gatherings: Love and Logistics

For my family, Thanksgiving is one of those holidays where we make an effort to come together around the table. Mostly, we do it for my mom. Honestly, if she weren’t around, I doubt very seriously that these gatherings would still happen. It’s funny how one person can be the glue that keeps everyone connected, isn’t it?

We also try to celebrate birthdays together. Usually, a date during the month is picked for a small get-together. But, for some reason, we never seem to meet in August for my birthday. I’ve never quite figured out why, but I’ve stopped letting it bother me.

I don’t mind the big holiday gatherings like Thanksgiving or Christmas, but birthday get-togethers can start to feel like a logistical challenge—expensive, time-consuming, and sometimes exhausting. Sometimes it feels like we’re traveling every few weeks, and, of course, the house we end up meeting at is always the farthest from mine. I swear, it’s like my GPS secretly enjoys making me drive in circles.


The Chaos Is Worth It

Despite the chaos—the crowded tables, the debates over who’s bringing what dish, and the inevitable “pass the mashed potatoes” race—there’s something special about these gatherings. Being around family, even if just for a few hours, reminds me of what really matters.

The laughter, the shared memories, the small moments of connection—they’re worth every mile traveled and every effort spent. Even when someone accidentally drops the cranberry sauce on the floor, or Uncle Joe tells the same story for the hundredth time, it all adds to the experience.


Reflections on Gratitude

The best part is that no matter how hectic it gets, or how many extra servings of pie I have to endure, we’re all still together. These little imperfect traditions are what anchor us. They remind us that family isn’t about perfection—it’s about showing up, supporting each other, and sometimes laughing at ourselves along the way.

So, as I sit here reflecting after Thanksgiving, I feel grateful. Grateful for my family, for my mom, for the chance to keep these little rituals alive, and for this blog that allows me to put my thoughts into words. Sometimes, writing is the best way to understand what really matters—and right now, family, chaos and all, is at the top of that list.

A Week Without Clyde

26 Wednesday Nov 2025

Posted by Tim Hughes Living with CML in Photography

≈ 2 Comments

Tags

Cat, Clyde, Death, Depression, emotion, Goodbye, grief, Heart, Life, Loss, Mourning, pet, Pets, writing

Clyde January 25th, 2015 - November 15th, 2025

It’s been a little over a week since my wife and I said goodbye to our little buddy Clyde — and even now, it still doesn’t feel real. The house is quieter. Our routines feel incomplete. And the space he once filled in our daily lives has become an unmistakable emptiness we carry with us everywhere we go.

Losing a pet isn’t just losing an animal. It’s losing a tiny familiar heartbeat that anchored your mornings, evenings, and even the simplest moments in between. Clyde didn’t just live with us — he lived in us. And that is why the silence left behind is so loud.


The Questions That Follow Loss

Grief invites doubt to the table whether you want it or not. In the days since losing Clyde, I’ve replayed memories and asked myself the kind of questions only guilt-ridden love can produce.

Did I fail him by not rushing him to the vet that morning when I knew he felt off? Could a vet have even helped him, or was his final moment simply his time, no matter where we stood when it came?

And then, unfairly, I asked myself even bigger questions.

Did we deprive him by loving him indoors his entire life? Should we have forced adventure on a cat who once sprinted away from his own reflection? Did we rob him of butterfly chases and bird pursuits, even though the world outside the glass clearly felt too vast for his brave-but-tiny soul?

The hardest twist of all is this:

Now that he’s gone, Clyde rests outside in the very outdoors he avoided his whole life. His body lies in the earth, a couple of feet underground, beneath open sky he never trusted long enough to explore. And somehow, that irony stung deeper than the loss itself.

But grief has a way of writing stories backward. We judge ourselves not on what a life asked for, but on what it might have wanted if it had been someone else’s.


The Challenge We Loved Through

The older Clyde got, the more life asked of him — and of us.

He developed heart problems and thyroid issues that, if left untreated, triggered seizures. He depended on daily medication. Three pills a day, one so bitter it had to be hidden in a capsule like contraband medicine you smuggle past a taste border.

My wife, endlessly patient and unshakably devoted, became his pharmacist, caretaker, and protector. She never missed a dose. Not once.

As arthritis stole his ability to handle stairs, we improvised with litter boxes everywhere upstairs… which Clyde promptly judged as unacceptable. His counter-proposal? Our bed. Repeatedly. His negotiations included tarp treaties, blanket peace accords, and enough towels to open a small linen kiosk.

Deep sleep brought bladder leaks. Mobility struggles required strategic towel placement. Planning ahead became second nature. Laundry day became every day. And love translated into accommodation after accommodation.

Yes, Clyde was a challenge. But challenges don’t leave holes this big — connection without conditions does.

We didn’t put up with him. We adapted for him. Because loving him was never the question. Protecting his comfort was the answer.


The One Time He Went “Outside”

One memory has surfaced more than any other this week.

Years ago, my wife and I sat on the front porch enjoying the evening when I noticed Clyde inside, parked at the glass door like a museum curator observing a world exhibit titled “Nope.”

I opened the door, fully expecting him to reconsider.

He stepped onto the porch as if crossing an international border without a passport. Cautious. Curious. Politely concerned. He sniffed around like an overworked detective suspecting a plot but gradually accepting the peace of the moment.

And then — overwhelmed by the sheer intensity of everything existing simultaneously — he retreated indoors at high speed.

Because that was Clyde.

Brave in pixels. Overstimulated in 3D.

He didn’t want the outdoors. He wanted the safety of observation. The comfort of closeness. The reassurance of familiar floors, predictable humans, and climate-controlled affection.

And we gave him exactly that.


The Truth Beneath the Guilt

Here is what I finally realized once the guilt’s microphone ran out of batteries:

Clyde wasn’t an adventure cat. He was a heart cat. A soulmate with paws. A small emotional support mammal who didn’t read self-help books, but did master deep listening through silence and presence.

We didn’t confine him. We protected his peace.

And maybe the real guilt isn’t about the outdoors he missed.

Maybe it’s about the world not getting more time with the little cat who quietly made ours better.


We miss you, buddy.
More than you ever would have understood.
And exactly as much as you deserved.

Until we meet again. 🌈🕊️🐾

Clyde
January 25th,  2015 - November 15th, 2025

A final goodbye to my buddy Clyde

16 Sunday Nov 2025

Posted by Tim Hughes Living with CML in Family, Pets

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Tags

Cats, Death, Family, Life, Loved, Old Age, Pets

This has got to be one of the hardest posts I’ve ever had to write. Around 3:30 p.m. today, my buddy Clyde crossed the rainbow bridge.

The day began with the first sign that something wasn’t right. Every morning for as long as I can remember, Clyde would wait for me to get out of the shower. That was his way of letting me know he wanted to be picked up and placed on the bathroom sink so he could drink from the faucet—his little daily ritual. But this morning, he didn’t come.

Instead, I found him lying on the kitchen floor next to the air vent, his head down. When I reached down to rub his head, he didn’t give his usual loud purr. That told me more than anything that he just wasn’t feeling good. My wife mentioned that he’d eaten a little, but nowhere near his usual amount.

I had a craft fair to prepare for and some coasters I needed to get printed. Between the power going out mid-print and the rush to get everything finished, I didn’t get the chance to check on Clyde again before leaving. But once I arrived at the fair, I called home. My wife told me he had eaten a bit more and was lying at the end of our bed, where he always slept. Still, something in the back of my mind whispered that we might be nearing the end. I told my wife she should let our daughters know so they could come spend some time with him.

They did. And after helping me load up my things when the fair ended around 2 p.m., they headed home but didn’t stay long.

Around 3 p.m., my wife was watching the Alabama game from our bedroom. Clyde was asleep at the foot of the bed. He woke up, stood, and looked like he wanted to go somewhere but wasn’t quite sure how. He took a couple of steps toward the edge of the bed—and then fell over.

My wife picked him up and placed him gently on the floor, but by then, he was already gone. It happened so quickly. She ran to get me, but the moment I saw him, I knew his precious spirit had already left.

We called the kids and, while they drove back, I went to the backyard to prepare his resting place. When the girls arrived, they spent nearly an hour with him—crying, talking to him, soaking up one last moment with their lifelong friend. Then we placed him in a box with his favorite towel, his favorite toy, and one of his favorite snacks (that one was my daughter’s idea).

Clyde now rests behind the shed, and we plan to place a marker after we get home from church tomorrow.

If he had made it to January, he would have been 21 years old. These last few years were challenging for him—and for us. He was on medication twice a day and had completely lost control of his bowel movements. Our bed was lined with tarps and towels so he could sleep comfortably during the day, and we had to rearrange everything at night so the wife and I could still sleep without worrying. He loved sleeping between us, so we created a little system of towels to protect him—and us—from the inevitable accidents.

It wasn’t easy. But we did it for him. He depended on us, and we loved him.

Because of his declining health, my wife and I haven’t taken a vacation in more than five years. It didn’t feel right to ask anyone else to manage his care. Boarding him was completely out of the question. With his heart condition, the stress alone would have been too much.

Now, with his passing, a huge hole has been created in our lives. The routines, the sounds, the small rituals—all suddenly gone. It’s going to take time to heal, but we’ll get there.

What I know for sure is this: Clyde was loved deeply. And he gave us more love in return than we could ever measure.

He will be greatly missed.

Hospital Visits, Craft Fairs, and Nine Hours of News

07 Friday Nov 2025

Posted by Tim Hughes Living with CML in Family

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Tags

Life, Stress, News, Family, Calendar, Hospital Stay, Siblings, writing, love, mental-health, Craft Fair

Patriotic Black Slate Coaster

If you’ve known me for more than five minutes, you know I live by my calendar. It’s not just a planner — it’s my Bible, my life map, and my emotional support spreadsheet. I color-code, I plan ahead, and if something’s not on the schedule, it’s basically not real.

So imagine my stress level when my mom landed in the hospital and my siblings decided we all need to “take turns sitting with her.”

Now, before anyone clutches their pearls — she’s fine. She’s getting great care from an entire team of professionals who actually know what they’re doing. The woman is being treated better than most people at a five-star resort.

Meanwhile, my siblings and I are out here acting like we need to take shifts in case she suddenly decides to join the Hospital Olympics. Spoiler alert: she’s not going anywhere.

The thing is, I’ve got a craft fair coming up next weekend, and that means I need to be creating — not sitting in a hospital room pretending to enjoy watching nine hours of nonstop news coverage. Nine. Hours. I don’t even like watching nine minutes of the news. I can only listen to so many “breaking” stories about things that broke three days ago before I start questioning my life choices.

But there I sit, smiling, nodding, pretending I’m not slowly dying inside while she argues with the TV. I could be home making candles, painting signs, or doing literally anything that doesn’t involve election updates.

And when I say, “Hey, my schedule’s packed,” my siblings look at me like I just said I’m skipping Christmas. Listen, I love Mom. I’ll visit. I’ll call. I’ll even bring snacks. But she’s being well cared for — by actual trained professionals — while I’m over here trying to figure out if I can make fifty more gnomes before Friday.

So no, I’m not heartless. I’m just scheduled. And if loving my mom and respecting my calendar at the same time is wrong, then I don’t want to be right.

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