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Tag Archives: labs

I Hate Hospitals

24 Monday Aug 2026

Posted by Tim Hughes Living with CML in Family, Life

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Tags

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.

Under the Microscope… Again (Apparently I’m Now 5.9% Banana)

06 Friday Feb 2026

Posted by Tim Hughes Living with CML in bariatric-surgery, Diabetic, diet, Life, Uncategorized, Weight Loss

≈ 4 Comments

Tags

addiction, Appointment, Bloodwork, Change, Coffee, craving, Doctor, Food, health, labs, labwork, Life, lifestyle, pottassium, relationships, Surgery, writing

Lab results are in, and just like that… I’m under scrutiny again.

When I got the email with the results, the first thing that jumped out at me was my potassium. High. Again.

This isn’t new. It was high before, then magically went back to normal on the retest. Go figure. But here we are again. My doctor called yesterday and told me my potassium was elevated to an “extremely high” level. Naturally, I went digging through my past labs, and I noticed a pattern — since my weight-loss surgery last April, my potassium has been slowly climbing.

And I have absolutely no explanation why.

For those who don’t live their lives waiting on lab portals to refresh, high potassium — or hyperkalemia — means there’s too much potassium in your blood. Normal is between 3.5 and 5.0 mEq/L. Mine? 5.9 mEq/L.
Apparently, that extra .9 is where doctors start using their serious voice.

Now here’s where it gets interesting.

The only real lifestyle change I’ve made since surgery is that I’ve apparently developed a full-blown relationship with coffee. Before surgery, I had never enjoyed a single cup in my life. Not one drop. Loved the smell. Hated the taste. But after surgery? My body apparently said, “You know what we need? Coffee. All of it.”

Those pre-surgery classes warned me this might happen. Foods you hate, you’ll crave. Foods you love, you might hate. They never warned me I’d wake up one day emotionally attached to a coffee mug.

I’ve asked other doctors if coffee could be the culprit. Most said, “Probably not,” though they also gently hinted that maybe I shouldn’t be drinking coffee like it’s my full-time job. This latest doctor, however, seems less convinced.

The nurse asked how much coffee I drink in a day.

I was honest.

  • 22 oz before breakfast
  • 22 oz with breakfast
  • 22 oz sometime after supper

Apparently, this is not the answer they were hoping for.

And it doesn’t stop there.

If I go somewhere, I have a freshly made 22 oz riding with me in the truck. I also have what can only be described as a coffee emergency kit — a toolbox with all the fixings — just in case I get stranded somewhere that doesn’t have a coffee shop with my brand of coffee.

Yes. I know. It’s really sick.

Some people say caffeine keeps them awake. Not me. I can drink coffee at 9 PM and be asleep by 11 like a toddler after a long day at daycare. I’m not wired all day. I’m not bouncing off walls. I’m just… caffeinated and functional.

Her suggestion?
Limit myself to one cup per day.

Not one 22 oz cup.
One. Cup.

Friends… that is simply not going to happen.

Today I tried. I drank only one 22-oz cup. And I spent the rest of the day thinking about coffee like it was an ex who still had my hoodie.

I go back to the doctor next Tuesday for more labs. Hopefully, I can make it until then. And maybe — just maybe — they’ll tell me it’s not the coffee doing this.

So now I wait. More labs. More monitoring. More trying to figure out what exactly my body is doing and why it suddenly decided potassium is its favorite hobby.

In the meantime, if you see me walking around slightly jittery but emotionally stable, just know I’m doing my best… and possibly negotiating with myself about a second cup.

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