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Tag Archives: Family

Catching Up, Slowing Down, and a Growing Family

07 Monday Sep 2026

Posted by Tim Hughes Living with CML in Cancer, Family, Fishing, Kayaking, Leukemia, Life, Twins

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adventure, Alarm, Bible Study, Blogging, books, Dizziness, Family, Fatigue, Fishing, health, Heat, Holiday, In-laws, John Grisham, Kayaking, Kindle, Life, love, Reading, Weather, Weddings, writing

I’m behind on my WP blog reading. It’s been a rough couple of days with this fatigue. I’ve been doing pretty well with the dizziness, but between this extreme heat we’re having and the fatigue, life has slowed down to a crawl. I haven’t been doing much more than sleeping my life away.

Right now, I’m waiting on my phone to charge enough to last through the night so I can use it for my alarm in the morning. I’m going to try to go to bed early tonight, so once I’m done catching up, I’m calling it a night regardless of how much charge is left. 4 a.m. will come early, and I need to be up and moving so I can make it to Bible study by 6 a.m. Apparently, my body and I have different opinions about what constitutes a reasonable bedtime.

Because it’s been so hot, even in my garage, when I am awake, I’ve usually got my Kindle out, and I’m reading. I’ve started reading one of my favorite authors, John Grisham, again. I’ve read just about every book he’s written. I took inventory the other day and discovered I only have ten more books to read before I’ll be completely caught up.

He just came out with his latest book, and he already has another one scheduled to be published in 2028. Yep, I’ve already got that one on my “to read” list, too. I may be tired, but apparently I’m still organized enough to plan my reading schedule several years in advance.

My wife, my twin girls, and I also met up with my son’s future in-laws. My son wanted to use today’s holiday as an opportunity for all of us to finally meet. We had a great time getting to know them. They may be a little higher class than what we’re used to, but they are really nice people and were incredibly easy to talk to. I’m hoping we’ll have more opportunities to get together before—and even after—my son’s wedding.

Oh, by the way, my son is getting engaged next week.

They’ve already set the wedding date for sometime in March of next year. So, that makes two.

My daughter, who got engaged a few months ago, will be getting married in June, and my son will be getting married in March. That means we’ll only have one more to get married off.

At this point, I’m not sure when that will happen, but we’re not in any big hurry. I’m pretty sure my daughter isn’t either.

I do have a fishing date planned for this Wednesday. It may take me a little longer to get to my fishing hole because of this fatigue, but I’ve got it on my calendar anyway. Sometimes you just have to put something on the calendar and hope your body gets the memo.

So, I guess we’ve officially entered the “planning weddings” phase of life. Between that, Bible study, reading, fishing, trying to stay cool, and trying to convince my body that sleeping all day isn’t actually a hobby, plenty is going on around here.

I just wish I had a little more energy to actually participate in it.

Listen to What Your Body is Telling You.

30 Sunday Aug 2026

Posted by Tim Hughes Living with CML in Cancer, Kayaking, Leukemia, Life, Uncategorized

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Body, CML, Dizziness, Doctor, Family, Fatigue, Fishing, health, Kayaking, Life, Medication, Mental, mental-health, Reaction, writing

I was reminded of that today while reading a blog post I follow. Hazel reminded me that no matter what I’m doing, I need to listen to what my body is telling me. Sometimes we have a tendency to push through things, thinking we’ll be okay. Other times, our bodies have a way of making it very clear that we need to slow down.

Mine has been doing a pretty good job of getting my attention lately.

I started a new medication for my CML last Thursday. I’m taking two tablets, 40 mg each. I’m supposed to take them on an empty stomach, with no food for two hours before and at least one hour after taking them. I took them at bedtime both Thursday and Friday.

Friday night was rough.

I had a very restless night and finally decided to get out of bed around 3 a.m.—or at least I attempted to.

I sat up and immediately became dizzy. I sat there for a few minutes and waited for it to pass. When I finally stood up, the dizziness returned, and I nearly hit the floor. I grabbed the wall to keep myself upright and waited another couple of minutes before attempting to move.

Eventually, I made it to the den and collapsed into my recliner. I was exhausted. I felt like I had absolutely nothing left in the tank.

I tried going back to sleep, but I couldn’t get comfortable. I decided I would read for a while, but, of course, my glasses were in the bedroom.

I really, really didn’t want to get back up.

I knew what was probably going to happen.

Sure enough, when I stood up, the dizziness hit again. I nearly fell backward into the recliner. I grabbed hold of something and waited for it to subside. After a minute or so, I was able to make my way to the bedroom, retrieve my glasses and return to the den.

By the time I got back to my chair, I was wondering if I had enough energy to make the trip again if I had forgotten something.

Around 5 a.m., I finally decided I needed to find out exactly what might be going on. I made my way to the kitchen and retrieved the medication information packet that came with the prescription.

I started reading through the list of possible side effects.

Number three was dizziness and feeling faint.

Bingo.

Unfortunately, there was nothing listed specifically about fatigue. Later, I learned that fatigue is a side effect associated with many cancer medications, so apparently I managed to get a two-for-one special.

Dizziness and fatigue.

Just what I was hoping for.

I texted the guys in our Saturday morning Bible study group and told them not to expect me. I explained that I believed I was experiencing side effects from the new medication and that I simply wasn’t feeling well.

I spent most of the rest of the day in my recliner, getting up only when I absolutely had to.

I slept a little better Saturday night, but I’m still dealing with the fatigue and dizziness when I stand. Because of that, I didn’t go to church this morning either. Thankfully, I was able to watch the service on YouTube.

I had been thinking about going fishing Monday.

I’ve changed my mind.

At this point, I seriously doubt I’ll feel up to it. And honestly, I don’t think getting into a kayak while I’m dizzy is exactly what my doctor would recommend. Besides, I’m pretty sure the fish would take advantage of the situation and laugh at me.

I don’t have any appointments until Tuesday morning Bible study, and I’m really hoping I’ll be feeling better by then.

I’m also not taking any more of this medication until I speak with my oncologist on Monday. I want to talk with him about what happened and see what my options are. Maybe there is a way to adjust the dosage so that the medication can still do what it’s supposed to do without making me feel like I’m one wrong step away from becoming a human tumbleweed.

I’ve spent a lot of years dealing with CML and everything that comes with it. I know how important it is to take the medication and follow the treatment plan.

But I’m also learning that following the plan doesn’t mean ignoring what my body is telling me.

Sometimes you have to stop, pay attention and say, “Something isn’t right.”

That’s where I am right now.

So, for the moment, I’m going to listen to my body, stay in my recliner, and let my oncologist help me figure out what comes next.

Maybe the fishing rod can wait a few more days.

The fish aren’t going anywhere.

Well… at least I hope they aren’t.

I Hate Hospitals

24 Monday Aug 2026

Posted by Tim Hughes Living with CML in Family, Life

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Bloodwork, Complications, Daughter, Doctor, ER, Family, health, Hospital, Irritated, labs, Life, love, Mono, Scans, Sick, Sickness, Tests, writing

Hospitals are not my thing.

I ought to know. I’ve spent my fair share of time in them over the past several years.

For the last few years, it’s been my mom who has had to spend time in the hospital for one reason or another, and my siblings and I have spent plenty of days sitting beside her during her stays.

And honestly, it’s one of the worst things I’ve ever had to do.

Not because I don’t want to be there for my family—I absolutely do. But sitting in a hospital room all day trying to make small talk is just not my idea of a good time.

When I’m the one in the hospital, I’d much rather be left alone. Give me a book, a television, and a pillow, and I’ll be perfectly happy to entertain myself. When people come to visit me, I feel like I have to entertain them, and that’s the last thing I want to worry about when I’m sick.

Unfortunately, for the past few days, I’ve found myself spending quite a bit of time in a hospital.

This time, it wasn’t for me or even for one of my parents.

It was for one of my daughters.

She has been in the hospital because of complications from mononucleosis—Mono, for short. Her spleen is enlarged, and she developed an infection that the doctors wanted to make sure wasn’t being caused by something other than the Mono.

Exactly why it took several days to figure all of this out is still beyond me.

Her boyfriend took her to the ER Thursday afternoon around 2:00. She wasn’t seen until sometime after 6:00 and wasn’t admitted to the hospital until the following day.

Four hours just to be seen, and then another night before they decided to admit her. Maybe I’m just impatient, but that seemed a little ridiculous to me.

They did scans. They drew blood. Tests were run. Promises were made—and apparently forgotten.

Once she was finally admitted, it seemed like the hospital had no idea what the ER had already done. So, they started doing tests all over again.

It was almost like she had checked into the hospital and said, “Hi, I’m here. Let’s start from the beginning.”

On Saturday afternoon, the hospitalist came in and said she wanted to keep my daughter one more night for observation. She assured us that, barring any problems, she should be able to go home the next day.

The next morning, my other daughter said she could stay a little longer so she could take her home when she was discharged.

My wife and I went to church and then went out to eat afterward. We hadn’t planned on going to the hospital that afternoon, but eventually made our way there so we could relieve my other daughter.

Several hours passed.

Still no word about my daughter going home.

Finally, I went to the nurses’ station and asked what was going on.

That’s when we found out the doctor had actually decided earlier that my daughter was NOT going home.

Wait… what?

When exactly were we going to be told this?

If I hadn’t gone to the nurses’ station and asked, there’s no telling when we would have found out.

Needless to say, I was livid.

The doctor finally made her way into the room about three hours after I had made my inquiry. After expressing my disappointment that no one had bothered to keep us informed, she explained that she was trying to consult an infectious disease doctor to make sure there wasn’t something else going on.

That’s when my wife pointed out that an infectious disease doctor was already supposed to be involved.

Apparently, the hospitalist wasn’t aware of that.

The ER doctor was supposed to have already ordered the consultation, but somewhere along the way, someone dropped the ball.

And unfortunately, my daughter was the one lying in that hospital bed while everyone tried to figure out whose ball it was.

This morning, the infectious disease doctor finally reviewed her bloodwork and assured my daughter that there was nothing else going on. Everything she was experiencing was related to the Mono.

Her instructions?

Go home.

Rest.

Give it a week or so.

That’s exactly what she’s doing now.

She’s home, resting, and hopefully on the road to recovery from what has been a pretty debilitating illness.

I know hospitals and healthcare workers are dealing with tremendous workloads, and I appreciate the people who take care of us when we need them.

But sometimes I really do wonder how we’ve managed to make it this far in our healthcare system.

Maybe I’m just getting old.

Or maybe I’ve spent enough time in hospitals to know that sometimes the biggest challenge isn’t figuring out what’s wrong with the patient.

It’s figuring out what everyone else is supposed to be doing.

For now, though, I’m just thankful my daughter is home.

And I think we’ll all sleep a little better knowing she’s there.

When Good Days Take Unexpected Turns

24 Friday Jul 2026

Posted by Tim Hughes Living with CML in Family, Fishing, Kayaking, Life, Nature, Twins, Uncategorized

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AC, adventure, Air Conditioning, Appointment, Costly, Daughter, Doctor, Family, Fishing, Hardware, HVAC, Kayaking, Life, love, Nose, parts, Phone, Tether, Thermostat, writing

Tuesday was spent at the doctor’s office with my dad, following up on his broken nose. After examining him, the doctor decided not to do anything since he could still breathe through it without any difficulty. Dad actually broke his nose when he was a kid, so it was already a little crooked. I guess he’s had decades to get used to a nose that doesn’t point due north.

My plans to go fishing on Wednesday changed when my son called early that morning saying his air conditioner had quit working.

I haven’t had to do much HVAC work since I retired, so it took me a little longer than usual to diagnose the problem. It didn’t help that there were actually two problems. After several hours, two trips to the hardware store, a new thermostat, and a new capacitor, his air conditioner was finally back up and running. It felt good to know I hadn’t forgotten everything I learned after 32 years in the business.

My daughter told me on Sunday that she wanted to go fishing. Since she had a hair appointment on Thursday, she decided to spend the night and get an early start the next morning.

We fished for several hours before either of us had any luck. Her luck changed first when she hooked a big fish, but it got off before she could get it to the kayak. Then my luck changed when I finally landed one. Unfortunately, my good fortune lasted about five seconds.

As I was handling the fish, my phone slipped out of my pocket and disappeared into the lake, never to be seen again.

My daughter actually climbed out of her kayak and tried feeling around with her feet to find it, but it was gone. This is the second time my phone landed in the water, and you’d think after the first time I’d have learned my lesson. I have a phone tether on order now that should arrive tomorrow.

As the saying goes, a day late and a dollar short.

Needless to say, we called it a day and headed home.

After unloading the truck, I spent the next several hours at the phone store getting everything transferred to a new phone. It wasn’t exactly how I had planned to spend my afternoon, but at least I got to spend the morning on the water with my daughter.

I’d gladly trade a phone for memories like that… although I’d really prefer not to make it a habit.

Benadryl, Broken Noses, and a Busy Day

20 Monday Jul 2026

Posted by Tim Hughes Living with CML in Boy Scouts, Family, Leukemia, Life, Uncategorized

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adventure, Appointment, Benadryl, Calendar, Cancer, CML, Doctor, Drugs, Family, health, infusion, Kindle, Life, Nose, Reading, Therapist, writing

Today started out busy, and judging by my calendar, it’s only the beginning.

I had two doctor appointments today—one at 10:00 a.m. and another at 3:00 p.m.

My first stop was my oncologist’s office for an iron infusion. They usually take about two hours, so I figured I’d have plenty of time to get home, eat lunch, and make it to my physical therapy appointment.

Well… that was the plan.

The infusion ended up lasting nearly three hours, which turned my carefully planned schedule into a race against the clock.

Before the infusion, they always draw blood to check my iron levels and determine if—and when—I’ll need another treatment. Then comes the fun part. They hook me up to a small IV bag of Benadryl.

They use Benadryl to offset any reaction I may have to the infusion.

I don’t know about everyone else, but Benadryl absolutely knocks me out. I’m talking “you could redecorate the room around me, and I’d never know it” kind of asleep.

I had brought my Kindle to pass the time, but after the Benadryl started flowing, I don’t remember making it past the second page.

A lady sitting next to me was receiving three bags of chemotherapy. I knew I’d been asleep for quite a while when I woke up, and she was already on her third bag.

When I finally came to, my iron infusion was almost finished. I did my best to stay awake long enough for the nurse to remove the IV. Truthfully, I could have happily curled up in that recliner and taken another nap, but I had places to be.

Downstairs, I stopped to pay for parking. An elderly lady ahead of me was having trouble with the payment machine. Her card wouldn’t work, and she didn’t have another card or any cash. I asked her to cancel the transaction, scan her ticket again, and I paid for her parking.

Four dollars wasn’t going to make me go broke.

My good deed for today.

She thanked me several times before heading on her way, and then I paid for my own parking.

My physical therapy appointment went well, although concentrating wasn’t exactly easy with all that Benadryl still floating through my system. I think my therapist took one look at me, decided I wasn’t going to set any personal records that afternoon, and let me go home about ten minutes early.

Tomorrow will be another busy day. I’ll have to miss my Tuesday morning Bible study because I’m taking my dad to the doctor to have his broken nose checked after his fall.

He’s already informed me that he has no intention of letting them reset it.

According to him, he broke it as a kid, it’s been crooked ever since, and he doesn’t see much point in making it straight now.

At 87 years old, I guess he’s decided that a crooked nose has become part of his identity. Who am I to argue with that?

When Plans Change in an Instant

17 Friday Jul 2026

Posted by Tim Hughes Living with CML in Family, Kayaking, Life, Uncategorized

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adventure, blood, Broken Bones, Dad, Doctor, Fall, Family, Fishing, Hospital, kayak, Life, love, Nose, Parents, Preparation, writing

It doesn’t matter how carefully you make your plans—one phone call from one of your parents can change everything in the blink of an eye.

I had planned on going fishing today. It had already been a challenge just getting ready. I had a meeting Thursday night, so I wasn’t able to load my kayak until I got home late. I loaded everything else beforehand, leaving only the kayak for when I returned.

We’re also down to one vehicle right now, so after my physical therapy session, I needed to take my wife grocery shopping. Then I had to drive across town to exchange my shoes before I could even think about heading to the water.

Then the phone rang.

It was my mom.

She told me my dad had fallen outside. According to her, there was blood everywhere. She had already called 911, and the paramedics were on their way to take him to the emergency room.

I left the house immediately. I got to the ER so quickly that I actually arrived before the ambulance did.

A short time later, my mom and my nephew arrived, and Dad came in around the same time. He had a pretty nasty gash on his forehead that had cut open a blood vessel. He also broke his nose and badly bruised his right arm.

My sister arrived shortly afterward, and then came the waiting. Anyone who has spent time in an emergency room knows that waiting is just part of the process.

After about two hours, I knew Dad was stable and being well cared for. Since there wasn’t much more I could do, I left to attend my meeting.

A couple of hours later, after the meeting ended, I called to check on everyone. Thankfully, they were already back home.

I called Dad again this morning, and I’m happy to report that he had a good night. He’ll see a doctor on Tuesday to have his broken nose evaluated. I offered to take him, but my nephew may be able to do it. We’ll know for sure in the next couple of days.

Days like yesterday are a reminder of how quickly life can change. One minute you’re thinking about fishing, and the next you’re sitting in an emergency room with your family.

I’m just thankful the outcome wasn’t worse. At 87 years old, a fall can be life-changing. God was watching over Dad, and for that, I’m incredibly grateful.

A Calendar Full of Red

15 Wednesday Jul 2026

Posted by Tim Hughes Living with CML in Diabetic, Disability, Family, Fishing, Kayaking, Life, Pets, Retirement, Uncategorized

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Appointment, Bible Study, Calendar, Car, Cat, Doctor, Family, Fishing, Life, Meeting, Shoe, Shoe Store, Therapist, Travel, writing

My cat Sophia must have decided I needed the extra rest because she let me sleep until 6:30 this morning—an hour later than my usual wake-up call. I don’t know what got into her, but I’m not about to question a miracle.

My wife had a physical therapy appointment today, so I didn’t get much accomplished before it was time to chauffeur her to the appointment at 11:00. While she was with her therapist, I stayed in the truck. I used the time to go over my upcoming Bible study lesson. It was a productive way to pass the time.

I had planned to take my new shoes back to the store because the longer I wear them, the more my right foot hurts. I was hoping I could simply exchange them for a 7E width, but after doing some research online, I discovered that width isn’t available in the current style. Since my wife also had another appointment later in the day, I couldn’t make it to the shoe store. That means I’ll have to make a special trip tomorrow and hope I can find a pair that actually fits.

I have physical therapy in the morning, and afterward I’ll head across town to the shoe store. Once that’s done, I’ll come back home, pick up my wife, and take her grocery shopping.

After we get back, I’ll start loading what I can for Friday’s fishing trip. Unfortunately, I have a late meeting across town, so I won’t be able to load my kayak or fishing rods until I get home around 11:00 that night. Thankfully, it only takes a few minutes to load everything, so I should still be able to get to bed early enough for my 4:00 a.m. alarm.

I looked over my calendar for the next month, and it’s covered in red. I mark all of my appointments—and all of my wife’s appointments—in red so they stand out. Right now, there’s something scheduled at least three days every week, and several days have two appointments. Retirement sure wasn’t supposed to involve this many waiting rooms.

I’ll be glad when my wife gets her car back. Sharing one vehicle has made scheduling everything a lot more complicated. I know it’s only temporary and it couldn’t really be helped, but it has definitely added a layer of inconvenience to our daily routine. Hopefully, things will get back to normal soon.

One Day at a Time with Mom and Dad

11 Saturday Jul 2026

Posted by Tim Hughes Living with CML in Family, Life, Uncategorized

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Ageing, Arthritis, Dad, elder, Family, gardening, Grass, health, Lawn Mower, Life, Mom, Nature, Pain, Parents, Scoliosis, writing, Yard, Yard Work

Yesterday I got off to a later start than I had planned. I rolled up to my parents’ house a few minutes before 9:00 a.m. My goal had been to get there by 8:00, but I just couldn’t get moving. By the time I had eaten breakfast and made my second round of coffee, I was already running behind.

When I arrived, I didn’t see my parents’ car. Sometimes they park inside the garage, but most of the time it’s sitting just outside.

I unloaded the lawnmower, which takes a few minutes since it’s on a trailer. Once it was off, I moved it onto the driveway to make a few adjustments to the mower deck and ensure it was level.

Normally, by this point, Dad is already outside with me because his driveway alarm lets him know whenever someone pulls up. Since I hadn’t seen either of them, I figured one of them must have had a doctor’s appointment and had forgotten to tell me.

I started the mower and began cutting the grass. About thirty minutes later, I spotted Dad. Evidently, he had been outside the whole time working somewhere in the backyard. He was soaked with sweat. He had been picking up limbs to clear the way so I could mow the yard.

I immediately stopped the mower and told him he had done enough. I made him go inside where it was cool. I stood there and watched until I saw him walk across the deck and into the house. It was simply too hot for him to be outside doing that kind of work.

I mowed for a little over an hour before taking a break. When I went inside, Dad was sitting on the couch. He had changed shirts, but I could still tell he was overheated from being outside. I fussed at him a little for staying out there long enough to get that hot.

My poor mother was sitting on the other side of the room, bent over from the arthritis pain in her neck. She’s been dealing with that pain for several years now, and it just keeps getting worse. Unfortunately, there’s really nothing that can be done. She’s been rubbing Hemp cream on her neck, and it seems to help for a couple of hours, but the pain always returns.

Seeing my elderly parents in this condition always weighs heavily on my heart because I know the day will eventually come when they won’t be with us anymore.

Mom has been living with one kind of pain or another ever since they were involved in that terrible head-on collision back in 2014. She used to stand nearly six feet tall. Today, she’s barely five feet because of scoliosis and arthritis. She’s so hunched over and in so much pain. She refuses to just sit still. She wants to tend to her flowers and keep the house clean, but she’s reached the point where she simply can’t do those things anymore. Most days she ends up sitting in her recliner in the den, wishing she could still do what she once did.

Dad keeps talking about buying a new lawnmower. The truth is, he doesn’t need another mower because he doesn’t need to be cutting the grass anymore. But he refuses to slow down. He’s always got to be working on something. No one can convince him otherwise.

He’s a smart man. There’s a lifetime of knowledge locked away in that brain of his, and every now and then I still have to make a phone call and dig some of that knowledge out. I’ll definitely miss that someday.

After I finished cutting the grass, we were sitting on the back deck when I told him he didn’t need to worry about buying another mower. I told him I’d be more than happy to come up every couple of weeks and cut the grass for him. He seemed to appreciate that… right up until he asked if he could sit on my mower and drive it around to compare it to his old one. Before long, we were right back to talking about buying a new mower.

After everything was finished, Dad and I sat on the back deck talking for several hours before Mom joined us. A cool breeze had started blowing, making it comfortable enough to just sit and enjoy each other’s company.

We talked about life and the choices we’ve made over the years. We talked about my kids and the possibility of grandchildren someday since two of my three children are talking about getting married.

Mom quietly said she hopes she’ll still be around when my children become parents, but she isn’t sure that will happen.

To be honest, I have my doubts too.

But I’m still praying we’re both wrong.

Rolling With the Punches

09 Thursday Jul 2026

Posted by Tim Hughes Living with CML in Life, Uncategorized

≈ 1 Comment

Tags

adventure, appointments, Cutting Grass, Dead battery, Doctor Appointment, Family, gardening, Lawnmower, Life, Logestics, Nature, Parents, Troubleshooting, Wreck, writing, Yard Work

It’s been a few days since my last post, and it’s been a busy few days.

You never realize how much you depend on something until you suddenly don’t have it. Since my wife’s car is still with my daughter, we’re down to just one vehicle. That means choices have to be made, schedules have to be adjusted, and everything takes a little more planning. My daughter is still looking for another car, but she’s waiting on the insurance check before she can buy one.

On top of that, life doesn’t slow down. I’m going to physical therapy for my back twice a week, and my wife has therapy once a week. This coming week I also have two doctor’s appointments, and my wife has an appointment on the very same day. I think we’ve worked out the logistics, but if one appointment runs long, it could throw our whole schedule into chaos.

Today was my second physical therapy appointment. Unfortunately, I had already spent part of yesterday doing yard work, so I was pretty sore before I even walked through the door. After an hour of stretching and exercises, I’m even more sore now. The therapist warned me that I’d probably feel it for a couple of days because we stretched muscles that haven’t been worked like that in a while. My next appointment is Monday morning.

Tomorrow I’ll be heading back to my parents’ house to cut their grass again. I’ve already loaded my mower and weed trimmer onto the trailer. Last week I didn’t have time to do any trimming, so it’s really needed now. The biggest question is how my back is going to handle sitting on the mower for four hours. It may take me longer than usual because I’ll be stopping often to stretch and give my back a break. I’d rather take my time than pay for it later.

Speaking of my mower…

It’s about four years old. After I finished mowing my own yard yesterday, I drove it over to my outdoor hydrant to wash off all the grass clippings. I do that every single time I use it. I think it looks better when it’s clean, and maybe—just maybe—it’ll help it last a little longer.

When I finished spraying it off, I climbed back on, turned the key…and absolutely nothing happened.

For the next hour, I started troubleshooting everything I could think of. Eventually, I convinced myself the starter had gone bad. I began pricing replacement starters and quickly discovered they aren’t cheap. I finally found an aftermarket one that appeared to fit my mower, but something kept nagging at me.

“What if it’s not the starter?”

I’ve been down that road before—buying parts I didn’t actually need. I’d hate to spend the money, wait for the part to arrive, install it, and discover the mower still wouldn’t start.

So I called my dad.

He suggested I try one more thing before ordering a starter. I’m glad I listened.

Earlier in my troubleshooting, I had tried jump-starting the mower with my jump box, thinking the battery might be weak. It still wouldn’t even try to turn over. I checked the battery with my meter, and it showed what appeared to be enough voltage, so I ruled it out. Just to be safe, I put it on the charger while I went inside for lunch.

After lunch, I spent a few hours doing other things around the yard before checking it again.

Surprisingly, the battery voltage had actually dropped even lower than it was before I put it on the charger.

Well, there was my answer.

The starter was fine after all—it was the battery.

That meant another trip to the auto parts store for a new battery. While I’m certainly glad it wasn’t the starter, I still wasn’t thrilled about spending money on a battery that I hadn’t planned on buying.

Sometimes life has a funny way of piling things on all at once. Between juggling one vehicle, therapy appointments, doctor’s visits, back pain, cutting my parents’ grass, and now replacing a mower battery, it has definitely been one of those weeks.

Hopefully next week will be just a little less eventful…but somehow I doubt it.

A Morning on the Water and an Evening Under the Fireworks

05 Sunday Jul 2026

Posted by Tim Hughes Living with CML in Boy Scouts, Family, Fishing, Kayaking, Life, Photography, Retirement

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250 Years, adventure, America, Boy Scouts, Family, Fireworks, Fishing, Independence Day, Kayaking, Life, river, River Life, Summer Camp, Travel, writing, Youtube

I hope everyone had a wonderful weekend!

I took advantage of the few hours I had available to go fishing Saturday morning. I didn’t invite my friend Rick on this trip because I wasn’t sure how long my back would hold up. Since the ablation, I haven’t been able to sit in my kayak for very long before the pain starts bothering me.

I launched on the river around 5:30 a.m., and by 10:30 I was ready to head back to the launch. I knew that if Rick had gone with me, he would have wanted to stay out all day, and I knew that just wasn’t going to be possible for me.

The other reason I went alone was that I didn’t want to have to track him down when I was ready to leave. Last week, I told him I planned to head home at 2:00 p.m. By 2:30, he still hadn’t made it back to the launch. I finally left without knowing where he was, and that made me feel pretty uncomfortable.

At least until my back gets better, I think my fishing trips will end around 11:30 each morning. That’s quite a change considering we normally stay on the water until around 4:00 p.m.

Saturday evening, we went to my in-laws’ house on the river. They invited us, along with eight couples from their Bible study group, over for a barbecue and the annual fireworks show put on by their next-door neighbor.

I was genuinely surprised by the quality of the fireworks. It looked like something you’d expect to see at a professional display. I started recording about ten minutes after the show began, and it continued for another ten minutes or so after I stopped. My arm finally gave out from holding my phone up for so long, so I had to call it quits.

https://youtu.be/hIVYBx3J-Q8

As you’ll see in the video, we were very close to where the fireworks were being launched. In fact, I think we may have been a little too close at times!

This was also the first time in about ten years that I was able to spend the Fourth of July at home. In years past, I was always away at Boy Scout summer camp. That meant leaving my wife at home with our two cats, who were terrified by the thunderous fireworks our neighbors set off every year.

It felt good to spend Independence Day with family, enjoy some great barbecue, watch an incredible fireworks display, and still squeeze in a few hours of fishing that morning. Even though my back limited my time on the water, it was still a day well spent.

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