Parents read this blog post

If you are a parent of a child with type 1 read this blog post by another parent

This blog post taps on a lot of different issues that are so important.

When I try to pull this up, my computer locks up.  Are others having this problem?  I would really like to read this.  Gina, can you possibly copy/paste it here?

I was able to read it, but I couldn't copy all of it. Maybe Gina will have better luck. It's a great story.

I was able to get to it.  Thanks for the post, GIna.  Gives me a lot to think about. 

The thing is parents are always thinking---ALWAYS---because we love our children and want them to grow up and live full and happy story that sticks in my head was from years back--when I first married.My husband had 2 cousins with type1.........The story ended years later with these words....They were both type1--one did what he should and went off to live a full good life--the other one--well I saw where he ended--in an old folkes home in his late 30's-where he lived only a few years and died.They say all the hard drinking-smoking-late nights-not caring for his d caught up with him.I am not out to scare my daughter but she knows this story.I will tell her when I see things are off--Please just take care of this.Have the really good life like your dads cousin who tried ..

This is taken from A Shot in the Dark Blog by Sandra Miller: link to the original post

Growing Pain

Over the last four years I've received messages from readers telling me how we're doing a "beautiful job" helping Joseph manage his diabetes and that I'm an "amazing" mom.

Well at the beginning of last month, I felt about as far from amazing as any mom could get — and even now, I'm still a little shaky.

You see, Joseph was sneaking food, treats mostly — but worse, he wasn't bolusing for them.

When I first found out that he wasn't being truthful with us, it hurt.

A lot.

But the not bolusing, well that just froze me in my tracks.

For several days and nights after I realized what was going on, I couldn't think of anything but what this might do to him in the long run — not just the effects of the high blood sugars, but the habit he seemed to be falling into.

And desperately, I wondered why?

We'd always worked together on this stuff, but now...

It started with small things, a candy wrapper in his room, a number of unexpected high blood sugars... coming to a head just after Halloween — when we left a bright red plastic bag filled with nearly 4 lbs of candy sitting on our kitchen counter.

(Stupid to have left this out, I know.)

Within a few days the bag weighed considerably less.

I discovered this after yet another argument with Joseph about him having eaten a snack without bolusing — this time, a chocolate chip granola bar.

His blood sugar was 404.

I asked him why he hadn't bolused.

"I don't know," he said turning away from me.

I got upset, choking out that I didn't want him to hurt himself. That if he gets in the habit of eating without insulin, he could set himself up for other health problems — serious health problems...

And when it seemed like he was tuning me out, "... some people have lost their sight because they ignored their diabetes, because they didn't take care of themselves."

Immediately, I wanted to take it back.

"Wait, Bud- "

But he was already halfway up the stairs, heading to his room.

Shaken, I returned to the kitchen to start making dinner. To calm down. That's when I noticed that red bag on the counter next to the stove, and — looking at it closely for the first time in a few days — saw the empty wrappers sticking out of the top of it. I opened it wider, and there were piles of them.

Oh no.

"Joseph," I called up the stairs, "was that granola bar the only thing you ate?"

No answer.

"Joseph— please, come downstairs."

A moment later he walked slowly into the kitchen wearing an inscrutable expression, then his eyes traveled to the red bag on the counter.

"No, I had a mini Snickers too."

"But why, Bud? It can't feel good to be high... if you eat something, please, you have to bolus for it."

"Yeah, I know." That's all he said.

The next afternoon, when he arrived home from school, I asked Joseph to sit down with me on the couch in our lower level. To talk.

"What's really going on, Bud?"

"I don't know... it's just hard having diabetes... I mean, no one else has to think about this stuff, they just eat what they want when they want. You know what B told me on the phone last night? He has his Halloween bag under his bed, his parents have no idea it's there... "

"But Honey- "

" ... and when I see your face when I have a high blood sugar, I just feel bad."

"Bud, I- I'm sorry. I don't know what to say... If I look upset when you're high, it's not you... I'm not angry or disappointed in you, I'm just worried about the high. I'm sorry that I made you feel like that. No matter what we do, there are always gonna be highs, lows — we can't make this perfect. Nothing is perfect."

"I know, I just hate having this," he said, his voice catching — and then he looked down at his hands for a few seconds before going on, "and please Mom, please don't say I'm gonna go blind."

Looking up at me, eyes wet with tears, he suddenly looked very young.

I put my arms around him— my own tears dripping down onto his shoulder as I held him close.

"I'm sorry, Bud — that was a horrible thing to say. I was so desperate to get through to you. I don't want to scare you, I just want you to take care of yourself. Listen, we are going to figure this out, I promise."

For a moment, we just sat there and said nothing.

Finally, we both stood up. "Hey, I'm hungry," he said. Then, without missing a beat, he pulled out his meter and pricked a heavily calloused finger.

"189... I can wait until dinner."

"No, Bud - go eat something now if you're hungry, just bolus for it."

"Okay," he said, "I'll have a banana," and he ran up the stairs taking two at a time.

Later, with the rich smell of ratatouille filling the kitchen, I called upstairs to the kids, telling them dinner will be ready soon, giving them the 10-minute warning. Evan clomped heavily down the stairs, shuffled into the kitchen and grudgingly agreed to try the ratatouille, but insisted that she "hates" polenta.

Shaking my head, I handed her some utensils to put on the table.

"Bud, can you do a check?" I said to Joseph, while pulling four white plates out of the cupboard.

He's 249.

"Hey, did you bolus for that banana?"

"Yes," he said, "two units." Then he filled several glasses with lime fizzy water, placed them on the table, and headed back up to his room.

A few minutes later, while standing next to Ryan at the stove, I noticed something on the floor in a corner of the kitchen— a large, empty, silver can.

And immediately I knew. Because Ryan's mom had called me earlier that day to ask if she should bring more cookies when she comes down in a couple of weeks. I'd checked that can and told her "yes" — because there was one cookie left.

I walked upstairs, knocked on Joseph's bedroom door and just asked him.

"Yeah, I had one," he said without looking up.

"When you had the banana?"


"And you didn't bolus for it."

"No, I didn't," he said quietly.

"But, why?" I asked, desperate for an answer.

"Because I knew you wouldn't want me to have one. That you'd rather I made a healthy choice."

"Bud, even if you didn't have diabetes, I'd encourage you to eat healthy — that's what Mom's do — it's the not bolusing that really scares me."

Then I turned around, and walked back down the stairs, a massive lump sticking at the back of my throat.

I don't understand — he can have treats . . . when we have dessert, he has dessert; when he wants to go get ice cream with his friends, I let him...

His last A1c was 8.7

It's been creeping up again, thanks to many unexplained highs— highs I thought were due to the hormones of a growing teen (and maybe that's at least partly true), but now I don't know.

Joseph and I have always been able to talk about things, about almost anything, really. But lately, we've been arguing a ton.

I don't know what to do.


I wrote much of this post about three weeks ago — since then, I've done a good deal of crying and a lot of thinking. I've also gone online and — among other things — read this thread on I discovered that what we've been going through is fairly common.

Just knowing we weren't alone gave me strength — and made me believe that we could get through this.

It took a lot more talking — and far more listening — before it finally hit me:

Joseph's sneaking food and not bolusing for it may have had less to do with deprivation than it did with him needing more independence.

(Yes, I realize to some this may sound counterintuitive, but hear me out.)

I honestly believe that by making choices he knew I wouldn't like, by not bolusing, he was struggling with us — with me — to "take the wheel." To show us that if we continue to drive this thing and not trust him to do it, we are going to crash.

He's going to crash.

(Does this make any sense?)

Joseph knows more about nutrition than most people and eats healthy food at home; he knows how to count carbs and how to bolus for food better than we do.

He has a good foundation.

Now, while we've let him eat like a kid and, more recently, like a teenager, he's always asked or sent a text to one of us when he's going to eat a snack, with carbs and a bolus calculation — and for a long while now, 99.9% of the time we text or say "go for it."

And I think it's that routine that needed to change.


Two weeks ago, I went up to his room, sat down next to him on the edge of his bed and took a deep breath.

"Bud, how would you feel about eating snacks and not calling or texting me about them? About coming home from school and getting something out of the pantry without checking with me or Dad first?

Still checking your blood sugar and bolusing, but not checking with us?"

His face lights up.


"Yes, really. Bud, I've been stupid. I should have done this a long time ago. You know, when I was your age I used to eat these things called "Hot Fries"... Andy Capp's Hot Fries. Never asked my mom, I just walked down to Prevites Market, bought a bag and ate them. And I loved Nestle Crunch bars, too. Now don't get me wrong," I add quickly, "I didn't sit down and eat masses of them, but I ate treats when I was a teenager. And I didn't ask for anyone's permission to do it... I want you to be able to do that too."

I'm about to say more, but I can't — because Joseph has me in a bear hug.

"Mom, I love you," he says, holding me tight, "and I'm sorry about not bolusing. I'm really, really sorry."

Then he pulls away from me, suddenly looking much older.

"I can do this, Mom."

And for the first time in weeks, I feel like I've done the right thing.

Gina - thanks for posting as I was having trouble with the original site crashing too.

It is a great blog - so much to think about and learn from, even as a parent to a 4 yr old - they are always growing up and becoming more capable each day. Sometimes I think we miss the things they have grown into being able to do, because we get focused on the things they haven't; the things that we want them to do on their own (like chores without a million reminders). It usually happens to me that all of a sudden my kids have mastered some new skill without me noticing and I need to praise and be proud of them for that and be willing to keep helping them with the skills I 'think' they should have by now. And a lot of times, getting them to do the things I want just means giving them more freedom to do it their way - and sure enough in a few days or weeks, they end up doing it the way I want too.

Thanks for reminding me that we're not the only ones in this situation, and for giving me ideas for the future. My daughter started sneaking juices and hiding the empty boxes behind her rocking chair when she was 4.. and I couldn't figure out why she was so high in the night.  And then when I found them, she blamed them on her daddy drinking them all.. lol  Anyway, we got through it and we explained that if she's hungry she needs to tell us, not just take something in a sneaky way and not get insulin. We had a similar situation where she was at her grandparents sneaking candy off the table (supposedly running in to use the bathroom) while we were all outside.. so none the wiser until sky high readings and trying to figure out why..  She's a smart girl too, and I think you hit the nail on the head, it's hard for them to have diabetes  (she tells me all the time - it's not fair) and they need some freedom to prove they can do it.  My daughter is older now, and tomorrow is the first time she'll get to sleep (possibly) at her grandparents house.. which is a super big deal for her.  Her older cousins are going to be there, and although she's trained on her pump, meter, & cgm, everyone else is trained too because I need to know she's in good hands regardless of how much I trust her to care for herself.  One never knows when she isn't going to be able to care for herself - due to a crashing low, or whatever may be the case.  It's harder on me leaving her there for a few hours (and possibly the night) - but the freedom she gains from being a "normal" kid for once, is priceless.  I can't imagine not being able to spend the night at my grandparents as a child; she needs to have those same experiences too.  It's moving into the trust phase though... Do you trust them as much as you trust yourself to care for this precious child of yours? And in truth, if I didn't she wouldn't be going. And what a big step for all of us that is.  Like the big step you're making with your son, to give him the opportunity to prove that he is capable of managing his diabetes (to some extent) because in reality, that's what he is going to have to do when he grows up and what better time to do it.