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Grayfeathersblog

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

Grayfeathersblog

Tag Archives: Memory

Missing Clyde on His 21st Birthday

25 Sunday Jan 2026

Posted by Tim Hughes Living with CML in Family, Pets

≈ 1 Comment

Tags

Birthday, books, grief, Heart, Life, Loss, Memory, Miserable, Pets, Sadness, Sounds, Weather, writing

Today’s been a tough day.

As much as I tried to keep my mind occupied, there was no escaping the fact that today would have been Clyde’s 21st birthday. And yes — Clyde was a cat — but anyone who’s ever loved an animal knows they aren’t “just pets.” They’re routine. They’re comfort. Their presence. They’re family.

The fact that today was cold, rainy, and just flat-out miserable didn’t make it any easier. It felt like the kind of weather made for staying inside, listening to the quiet… and noticing who’s missing.

He’s been gone a little over two months now. And there are days I think things are getting a little easier. Then a memory pops into my head out of nowhere — the sound of him moving across the floor, the way he looked at me, the little habits he had — and it nearly drops me to my knees. Today was a good example of that.

Grief with a pet is strange. They’re woven into the smallest parts of your life. Feeding times. Favorite spots. Empty corners. You don’t realize how many pieces of your day belonged to them until they’re suddenly not there.

I used to think time was supposed to make this hurt less. I’m learning instead that time just teaches you how to carry it. Some days it’s light. Some days it’s heavy. And some days — like today — it feels like the full weight of 21 years.

So tonight, I’m letting myself miss him. I’m letting it be a tough day. Because Clyde wasn’t “just a cat.” He was a constant. A companion. A small life that left a huge space behind.

Happy 21st birthday, Clyde. You are still loved. And you are still missed.

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

≈ Leave a comment

Tags

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.

Filing for Disablility

23 Wednesday Jan 2019

Posted by Tim Hughes Living with CML in Disability, Photography

≈ 3 Comments

Tags

Birds, Disability, Feeder, health, Memory

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Yes, I’ve filed for disability.  Let me tell you, so far, it’s been one hell of a ride.  First of all, they tell you to go online, print out the paperwork, fill it out and send it in.  I did that, and while I was getting the information,(doctor’s notes, procedures, diagnosis’) I found out that you can also fill all the paperwork online then submit it once you have it completed.  Of course, I had most of the information filled out before I knew I could do it online.  Once I completed the paperwork online, I hit the submit button and off it went.

Several weeks go by and I get a phone call stating that they had received the paperwork and they, in turn, had sent it to the appropriate people.  I thought I had already done that.  Oh well.

Another week or so goes by and I get a letter in the mail telling me that I’ve got to go see one of their doctors.  I was expecting this.  I had to send the letter back to them stating that I was to keep the appointment.  The week before the appointment I got another reminder about the appointment.

The doctor was a psychiatrist.  I had to see him because of the memory issues I guess.  He asked a lot of questions regarding my health, my daily routine and of course, my memory.  After about thirty minutes or so he was done.  Now the waiting continues.  Oh I know this could take years before I hear anything and it will probably end up being denied.  I understand that.  Of course, I willl apeal it.

Life goes on.

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