Type 1 Diabetes in Children: Bryson's Story

Type 1 Diabetes in Children: Bryson's Story (00:03:21)
Video Transcript

[Host] When you learned that your  child has type 1 diabetes, you were probably given a lot of information—from  medicines to how and when to eat. It's a lot.

But watching this video as a family  may help. This is Bryson's story.

[Bryson] "Hi! I'm Bryson.

Not long ago, I wasn't feeling great. I  found out that I have type 1 diabetes.

It was tough at first, but now things are better.

Type 1 diabetes means my  body doesn't make insulin.

Insulin is a thing that helps turn the  sugar from food into energy I can use.

Without insulin, my body can't use the sugar  from food. And that can make me feel sick.

Like a lot of kids with type 1  diabetes, I have a pump and a CGM.

My doctor calls it a continuous glucose monitor.

Because of the pump and CGM, I don't have to do  finger-stick tests or give myself insulin shots.

But a few of my friends with diabetes  test their blood and use insulin pens.

It didn't take long for me to learn how  to keep my body feeling good and healthy.

I pay attention to the foods I eat.

My CGM checks my blood sugar, and my  pump gives my body the insulin it needs.

And just in case my pump or the CGM breaks, my parents and I know how to do the  finger-stick test and give insulin shots.

Here's how I would test my blood if I needed to.

First I poke my finger with  this thing called a lancet.

Then I put a drop of blood in a little machine  that checks how much sugar is in my blood.

After I test my blood, a grown-up helps me  figure out how much insulin my body needs.

Insulin gets into my body through a shot.

The shot has a really small needle.

And now that I'm used to the shots,  I don't even feel them much anymore.

At school, I go to the nurse's office a few  times a day to make sure I'm doing okay.

When I started going to the nurse's  office so much, some kids wondered why.

They were worried about me, because  they thought I might be sick.

So I told them about diabetes. And I told them  that you can't catch it from somebody else.

Having diabetes means I am more careful about the food I eat.

But it doesn't mean I can't have treats.

I just have to make healthy  choices most of the time.

And I have to remember that if I eat some  types of food, I might need more insulin.

My family helps me by eating healthy too.

We try to make dinner together,  and we all help with the cooking.

I can keep doing all the activities I like to do.

Like playing football! Because  exercise helps me stay healthy too.

Oh! And I learned I'm not the only kid on my  team who brings medicine to play football!

Arthur brings an asthma inhaler,  and Kate brings a bee sting kit.

We help each other remember to bring the things  we need when we have practice and games."

[Host] Thank you to Bryson and his  family for sharing their story.

It may not always be easy, but just like Bryson's  family—with information and a little time— you and your child can manage type 1  diabetes and live healthy, happy lives.

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