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Good afternoon everyone! My wife and I have recently been thrust (totally against our wills) into the world of Type 1 management. It has been a major lifestyle change. We were preparing for my new job/relocation and were about 2 weeks from the big day when we took her to the doctor. Here's a bit of the story.

We have a 20 month old daughter. In April, she caught a cold. Then she didn't get better. She had the wettest diapers we had ever seen. Some nights, we would change her 3 or 4 times. We thought we had bought some very poorly made diapers and vowed never to buy that brand again.

One day, she was having a good day, so we changed her diaper and took her to the zoo. When we got back to the car she had soaked through her diaper, her clothes, and the stroller in less than 4 hours.

She was fiercely thirsty. She would suck down an 8 ounce sippy cup full of milk/juice and barely even breathe. Then she would throw up. Then she would scream for more. We started limiting her to two ounces an hour.

As the days passed, she became more inconsolable. She wanted to be held all the time, yet would be fidgety, irritable and uncooperative.

She lost 3 or 4 pounds, which was a big deal because she only weighed something like 24 pounds to start with.

Finally, my wife said it was time to go to the doctor, this just wasn't right. The doctor did a simple fingerstick blood test with the same kind of monitor a diabetic would use at home. I said "Whatever." I was in full-on denial at that point that diabetes could possibly be the problem. I was a bit incredulous that the doctor would even suggest it. The result was 334. I said "Well, that's not right." The nurse got a different brand monitor and did it again, 324. Uh... Alrighty then... She was in moderate ketoacidosis.

We spent 3 days in the hospital where she got insulin and fluids, and we got to learn a lot, really fast. We cried, we hugged her, and we loved her. We're still learning.

She has turned back into her normal, bubbly, adorable self. It's a lot of work, but we do what we have to do.

Since our move, we have found a pediatrician that's comfortable taking care of diabetic kids for the normal kid stuff, and we have a pediatric endocrinologist who can speak in plain-people language. Our diabetic educator is the absolute best.

Because I have a clinical pharmacy background with a solid understanding of basic nutrition, the dieticians weren't so helpful. I was hoping they would be able to tell me how to look at a plate of food and correctly estimate the carb count. Silly me. They wanted to explain the difference between carb, protein, and fat. And stop there. The diabetic exchange lists based on 15g carb counts weren't so helpful, either, because her sliding scale is based on 35g carbs, and she never eats that much, anyway.

She's still in her honeymoon phase, and producing just enough of her own insulin to really mess with us. As a toddler, I'm sure that's all part of her master plan to take over the world.

Her current regimen goes something like this:
1 unit of Lantus in the morning.
1/2 unit of Novolog for every 100mg/dl over 200. We change this to every 150mg/dl over 200 at dinner/bedtime.
1 unit of Novolog for every 35 grams of carb she eats. Of course, there is just no way she'll eat that much unless it's straight candy. Hooray for 1/2 unit syringe markings!
We test her at mealtimes and snacktimes. If bedtime is significantly later than dinner (more than 2 hours) we'll test then. And we wake her up at 1am to test her and give her a protein snack. So around 6-8 times daily. Our primary management problem is preventing lows.
Our goal is an A1C that's 7-8 and BG 100-200. We aren't shooting for tighter control than that because of the danger of hypoglycemic consequences to her developing nervous system.

Sometimes people ask us if it's hard to poke her fingers for the blood tests or if it's hard to give her injections. Yes, it's hard. She doesn't like it. She doesn't fight us, though. And it's a lot harder to watch our child deteriorate into a life-threatening case of ketoacidosis or worse.

Research I'm truly hoping for: a self-running glucometer (perhaps the glucowatch) that speaks with an intelligent insulin pump making essentially an external pancreas. I think we'll see this happen before we see a cure.

Anyway - I just thought I'd share our experience. I realize that type 1 and type 2 don't have a lot of crossover concepts, but our goals are the same - to live happy, healthy, productive lives.

And oh yeah - the Pink Panther book rocks!
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good luck buddy, sound like you're on track. my thoughts are with.
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What a challenge!

I have a cousin, now nearly 50, who was diagnosed as a toddler.
That was before nearly as much was known as now.
While I wouldn't wish this on ANYONE, I'm so glad that more can be done now.
I also hope "they" are able to move right along on the no-stick testing and no-injection insulin. Sounds like you would appreciate that as much as your poor daughter

{{{Randy & family}}}
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Thanks for posting. It seems like you and your wife are keeping level-headed about this whole thing, which is great.

I'm a Type I (have been since age 9), and must reconfirm that your approach is absolutely correct. When they're so small, they can't tell you that they feel funny -- so preventing major lows is key. Soon -- though it may seem like ages away -- she'll be able to tell you how she's feeling and monitor herself more, not that it'll make it at all easier on you.

Please let me know if you have any questions about Type I. Age 9 seems so very long ago, but I remember handling my diabetes as a child and perhaps have some good tips. Perhaps. :)


Editor (Stock Advisor and Rule Your Retirement)
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Our primary management problem is preventing lows.

Your primary goal is normal sugars and the only way known today is Dr. Bernstein's methods.

He's has some patients that are as young as your daughter. If you do this right, it's as easy as tying a shoe.

In addition, there is some research for newly diagnosed diabetics that certain autoimmune drugs can reverse the error.
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So is Dr. Bernstein a friend or a family member? All I ever see you do is shill for his book.
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So is Dr. Bernstein a friend or a family member? All I ever see you do is shill for his book.

You can look it up yourself and decide for yourself.
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Welcome to the board. The good news is you found out early and she will grow up not knowing any other way of life than managing her diabetes. I have often heard that it is easier growing up with a challenge or disability than having to learn to deal with one after having previously lived a "normal" life. Having lived a normal life for over 30 years, I am not sure what it would have been like to have had diabetes since I was an infant instead of being diagnosed after having established my adult life.

This board is for Fools with diabetes and those Fools living with family or friends diagnosed with diabetes. You will find a lot of opinions as to how diabetes is to be treated. I think the most important thing is that you are happy with the medical support you have found in your new community and that your daughter has quickly responded and adapted to the changes to her life. Just make sure you and DW are taken care of too. As you note, it was a major shock for you as parents. Don't just shove your needs to the side by focusing on your daughter. Make sure you are dealing with her disease in a healthy manner as well.

Who hopes you will find support in sharing the highs and lows of your experience...
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