Tag Archives: lows

Still wondering.

So… I’m somewhere around three weeks until the next appointment with my endocrinologist.

My last several A1cs have been excellent for someone living with Type 1 Diabetes.

But how have I gotten there? I wonder.

Did I get there with perfect blood sugar numbers all the time?

Did I get there with lots of lows?

If I had a lot of lows, did I do more damage to my overall health than that A1c number is worth? For the record, my basal insulin delivered versus my bolus insulin delivered always turns out to be pretty much what they are supposed to be, I’m told.

But still… What if I’m using too much insulin to knock down potential highs, leaving me with extra insulin that’s just going to get stored around my midsection? Honestly, I’m really worried about that.

What if those lows are killing off brain cells, causing other issues that I haven’t imagined up until now?

What if my A1c looks good, but my highs and lows go up and down through the day like an EKG, instead of like a normal person’s pancreas works?

I mean, look… On paper, I’ve been the model student for some time.

I’m still wondering if the truth is something different altogether.
 
 
 

Wordless Wednesday: Kryptonite.

I like to change things up once in a while. I love my Glucolifts to help get me up from low blood sugar. But every now and then I like to get something else to put in my pocket, and it provides a nice change of pace so I don’t get burned out on the Wildberry, which is my absolute favorite.

This week, I decided to get these little buggers, and I put a few in my pocket for… well, you know. I even needed a couple on my way home from work yesterday, and I couldn’t understand why they didn’t seem to bring me up at all. I also experienced some serious gastrointestinal discomfort through the night.

This morning, after closer inspection, I found out the reason why:

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After this experience, I’ll be happy to run back to my Glucolifts.

And God help me when I get older and have trouble reading my prescription bottles. I’m only half kidding about that.
 
 
 

Throw me a frickin’ bone here…

I was a victim of one of those stupid unexplained, recurring lows the other day.

Near the end of my workday, I had to excuse myself from a meeting and reschedule because I couldn’t focus. I knew something was wrong. A quick glucose check revealed a 47 mg/dL reading.

So immediately, I shut off my pump. I did not have any insulin on board at that time. I ate a fruit cup that was hiding in my desk drawer for just such an occasion, and just for good measure I ate a couple of pieces of candy too. Okay, three pieces.

I performed another check half an hour later (it’s supposed to be 15 minutes, I know, sue me), and I was at 170 mg/dL. This was at the end of my day, and figuring I was at a safe number, I turned my pump back on. I should also note that to err on the safe side, my basal setting between 4:00 p.m. and 6:00 p.m. is significantly below what my basal rate is at any other time of day, because that’s usually when I’m finishing up my day and traveling home.

I made it home, let the dog out, looked at the mail, and then did another BG check. Can you believe it?

52 mg/dL

I made my kicked-up ramen noodle recipe for dinner
, and due to the day’s previous events, I definitely under-bolused. Or so I thought. 2½ hours later? I was at 62 mg/dL.

Sometimes diabetes throws us a curve ball, and we need to try and deal with it the best we can.

It would be nice, however, if diabetes would throw me a frickin’ bone now and then.


 
 
 

Altered diabetes states.

This is one of those #makessenseifyouhavediabetes stories, and it’s also a partial chronicle (not chronic) of a dream from over the weekend.

Somewhere in the night, I started dreaming that The Great Spousal Unit and I were in a department store, shopping for shoes. These were to be new shoes for me, and I’m pretty finicky about the shoes I buy. So I was taking too long, trying on shoes, putting them back, etc., and suddenly Maureen “remembered” something she needed to look for in another department. At this point, this is not too different from the norm.

But then, for some reason, I needed to find her again, so without putting my shoes back on, I started wandering through the store looking for my wife. And, like usual, I covered every department in the store, multiple floors, asking multiple people if they had seen her. They all said no, they hadn’t seen her.

But as I was walking away from one person I had asked, I heard her mention to someone that there was a customer walking through the store without shoes on. I was violating the “no shirt, no shoes, no service” rule. Now my paranoia was kicking in, and I was simultaneously looking for my wife and trying to dodge store security, who obviously wanted to cart me off to “mall prison”.

This continued on for some time, until I made it back into the shoe department, looking for the pair of shoes I walked in with. As dreams go, this was typical: I’m frantically searching for my shoes where I had left them, and I could see store security coming right after me.

Just before they closed in on me, I woke up suddenly. Being it was a weird dream, I took a moment to do a BG check: 52 mg/dL.

Must have been all that running around the store.
 
 
 

Let’s talk.

I feel like this must be Hypoglycemia Week or something. I’ve already read two excellent posts on the subject this week, which I’ll link to during my post today. First, let me share a few photos with you:

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I received these scrapes and bruises (plus a couple of bruises on my head) thanks to a Sunday night low that happened around midnight. I was alone in the house, and I fell down once getting to the kitchen, and once in the kitchen. I never lost consciousness, and everything turned out okay in the end. But I had a serious fog that lasted for a while. I also spent some time after cleaning up spilled juice and a broken candy dish, so I wound up getting about 4 ½ hours sleep before heading to work on Monday.

I should mention that I believe this low was a mistake on my part, borne out of frustration for a remarkably stubborn high the previous Sunday. I didn’t want to face that again, so I over bloused. When Allison Nimlos wrote of her Sunday low, she did a great job of describing, clinically, what I think happened to me on Sunday night too.

For me, writing about this now is more of a thought process, stream of consciousness thing rather than a “Look at my bumps and bruises, feel sorry for me” thing. Scraped knees, bruised elbows, and a bruised head just serve as outward reminders of what happened. But how do I talk about it?

When I put on a pair of shorts and go outside, what do I say to my neighbors when they ask what happened to my knees? Do I come right out and say what happened? If I do, I don’t want to invoke pity. I don’t handle pity well. I don’t want to draw attention to myself that way. But I also don’t want to admit to a mistake in front of someone who doesn’t know me well and doesn’t live with diabetes day after day. Because the truth is, I can have 364 great days of diabetes management in a row, and one bad night can happen anyway. Every day is different. I don’t want someone thinking that the bad night is the norm, or something they have to worry about.

It’s weird because I want to look like I’m handling my diabetes well, but I need to be realistic and recognize that I’m not perfect. I think this is the kind of thing that people mention when they talk about wanting to be “normal”. We just want to live our lives, and not do or show anything that makes us stand out. We just want to be seen as “normal”, when really, our life is already normal. For someone living with diabetes.

So we keep it all inside, which leads to frustration and feeds the feeling of guilt over what happened. And the feeling of being alone, because we’re keeping it all to ourselves. Let’s face it: I made a mistake. I can’t make that mistake again! If I do, I’m less than perfect! No one will appreciate me or love me if I’m not perfect! If anyone knows about it, they’ll know I’m not perfect!

Then we complicate things by thinking: What does it hurt if no one really knows? If I don’t talk about it, no one will know that even though I’m doing better than ever in my constant battle with this condition, I still screw up one percent of the time (or maybe two percent). Or maybe I do everything right and my endocrine system doesn’t cooperate anyway. But as long as I don’t say anything about it, they’ll think I’m sitting at 100 mg/dL all the time. Problem solved, right?

The hard reality is that if I’m going to own my diabetes, I need to own 100 percent of it. One hundred percent of the time. That’s really difficult to admit, and even more difficult to put into action.

But if I don’t, I’m being less than honest with myself. It’s hard to keep that up for very long without imploding. And if I’m less than honest, less than forthright with my story, I miss the opportunity to share how incredibly dangerous living with diabetes every day can be. I miss the opportunity to explain why new technology, new drugs, and new therapies are crucial to saving lives, and in our country, saving money.

Understand me: It is really difficult for me to share a story like Sunday night’s outside of a forum like this one. But… It is very, very important for me to do so. People need to know how serious diabetes is on an everyday basis, and the damage that it does. I think many don’t know, or they forget. Not everyone is going to give us a pass for one slip-up. But if we’re honest with ourselves and others around us, the truth is that some people will. I also know this: Every generation that doesn’t bring their diabetes out in the open means another generation goes by thinking everything is just fine with us. And not understanding when it isn’t.

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I’m doing the best I can. But every day is different with diabetes, and so every day the potential exists for me to kill myself with too much or too little insulin. Sometimes that happens because we can’t get the supplies we need to test our blood sugar as often as needed. Sometimes that happens because people are over 65 and Medicare won’t approve a CGM. Sometimes that happens because my body used insulin a lot better today than it did yesterday, and different from the way it will use it tomorrow.

And sometimes, it’s because I made a once in a year (or five years, or ten years) mistake.

I’m not perfect. Diabetes is unpredictable.

Smarter, more accurate technology will help minimize those errors and keep me out of the emergency room. Better coverage for CGMs will help seniors live longer, more meaningful lives. Better drugs and delivery systems will help me live a more normal life. More diabetes research will help today’s children achieve more than anyone can imagine. And why not? Why shouldn’t they?

I know… life is tough, and we all have our problems. Why shouldn’t we all have the same opportunities? My pancreas has failed. I am not a failure.