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Grayfeathersblog

~ Diabetes, Cancer Fighter, Photographer, Exercise, Twins, Boy Scout Leader, Kayak Fishing, Lover of Life

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Tag Archives: Blogging

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.

Life is an Adventure Part 1

17 Wednesday Jul 2019

Posted by Tim Hughes Living with CML in Cancer, Leukemia

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Tags

Blogging, Cancer, CML, Hairloss, Hospital, Leukemia, Tests

Life is certainty an adventure.  One that rarely disappoints.  That is, if you life long enough to live through it.  If you’ve been following my blog for any length of time, you should know by now that I am cursed with the dreaded “C” word, Cancer.  I have what is known as CML.  Chronic Myeloid Leukemia.  I was diagnosed with CML back in February, 2014, Valentines day to be exact.  Since my diagnosis, I have been on three different types of oral medications, the preferred form of chemotherapy for this type of Leukemia.  Each one with it’s own faults.  With each medication, it would start off working but for some reason the med would stop working and I’d be left with months of trying different dosages trying to find a happy medium.  When this last drug bit the dust, my oncologist gave me the dreaded news that he would be deferring me to another oncologist, one who specializing in bone marrow transplants.  At this writing, I have an appointment this Friday with an oncologist at another hospital.  However, this doctor is not part of the transplant team.  So, I’m somewhat concerned as to why I’m seeing him.

This is the end of Part 1.  Part 2 will come after the meeting with this new oncologist.  If things go according to the way I think, I will be going through the transplant soon.  I’m not sure when but I know it will be soon.  Donors will have to be found,  tests will have to be run and so forth.  I will keep this blog going as long as I feel like blogging.  Pray for me during this time._2TH1271_tonemapped

365 Day Photo Challenge 294/365 “Day at the Gardens”

20 Tuesday Oct 2015

Posted by Tim Hughes Living with CML in Photography

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365 Day Photo Challenge, Blogging, Botanical Gardens, Flowers, Roses, Television, Weekend

https://tchphotography.smugmug.com/Botanical-Gardens/i-x8CcWK9/A

First of all as of today I’ve been “Blogging” for two years.  Never thought that would happen.  Secondly, I’ve been too negative lately in my posts and I apologise for that.  It’s for that reason I won’t be posting things about work for a while.  I will simply have to find another outlet for my frustrations.

This past weekend I had about two hours that I was able to spend with my wife.  Normally while at the house, she has her papers that she has to grade while I’m either on the computer doing emails or watching television.  Either way we’re not doing anything together.  I’ve found that we have nothing in common when it comes to watching television.  In order for us to spend any time together we’re simply going to have to get out of the house. That way it’s just her and I and we’re “forced” to spend time together.

Thanks for following me!!

21 Sunday Sep 2014

Posted by Tim Hughes Living with CML in Uncategorized

≈ 3 Comments

Tags

BCR ABL, Blogging, Blood Cancer, Cancer, CML, Leukemia, Oncologist

Went to the my oncologist last Wednesday.  He was not happy with my last results that was taken over two months ago. BCR ABl test results was .73% which I thought was pretty good until he told me it HAD to be down to zero and had to be within the first six months.  I was diagnosed in February so six months would make it in July.  I’m currently waiting for the doctor to call me to tell me what my results were last week.  If it’s not zero then I’m going to have to get on some other type of meds.

I don’t do this or any other blog for followers but just to be able to get things off my chest.  As I am honored to have each of you follow me I am somewhat surprised to see some what I would call super bloggers that are following me.  I’m really glad to have each and everyone of you on board.

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