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Type 3: Raising children with Diabetes

by IBD Medical on May 01, 2024

Raising children with diabetes

This Mother's Day, we’d like to send a shoutout to D-moms, or ‘type 3’ parents.

These are parents raising children who have been diagnosed with diabetes. It can be hard to find information as a mom of a child with diabetes, so we've put together a few ideas to help with the stresses of looking after a child with diabetes. From carrying juice boxes everywhere you go, to counting carbs and always being on call, being a D-mom is hard.

It can feel isolating, as a parent who doesn't have diabetes yourself, to find others going through the same things. Check out our Support Port group on Facebook to find others in a similar situation. It's also a place to share your experiences and advice to help others.

A few easy tips for first-time D-moms:

  1. Find snacks with clear nutrition labels and carb counts. It's good to mix up the snacks you give your child and keep their lunch box interesting.
  2. Many restaurant chains publish nutrition information online. Look it up ahead of time to help with carb counting and choosing options.
  3. When cooking at home, use recipes that include nutrition information to help with carb counting. Some recipes include carb counts, helpful tips and ingredient swaps. Check out the recipes on our blog, or sign up to our mailing list for new recipes!

We hope these tips help make raising a child with diabetes feel a little less challenging. Your child's diabetes care team can point you to local organizations and support networks, and talking to other parents going through the same thing can really help.

Comment below if you have any helpful tips or experiences to share — we’d love to hear from you!

Glucology
The content of this Website or Blog is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this Website or Blog.
If you think you may have a medical emergency, call 911 immediately, call your doctor, or go to the emergency room/urgent care.

General information, not medical advice. Always talk to your diabetes care team about your care.

1 comment
by Neal Van Berg on May 22, 2024

My son became a type 1, 6 days after his second birthday, at that time I had been a type 1 for 26 years. 34 years ago there was only finger sticks for blood sugar and syringes and vials of insulin, no external pumps or continuous glucose monitors.

When he wanted something sweet between meals we told him, let’s test your blood sugar and see how much insulin you’ll need. He never objected to this and we never talked about cheating on his diet.
We never forced him to give himself injections or finger sticks, plus I made it my goal to give him his injections as quickly as possible to minimize any discomfort.

I think he was in the first grade when he told me he wanted to test his own blood sugar and the second grade or third grade when he wanted to learn to give himself shots.

He transitioned nicely and has always been a model type 1, regarding: eating testing his blood and giving himself shots. He has never been in a coma or needed hospitalization due to his diabetes other than the initial visit when he was 2 years old.

I am very proud of him, even though everyone with type 1 has daily challenges as parents regardless of how you feel, you must make every effort to make your child’s diabetes maintenance be a normal matter of fact experience, so your child isn’t traumatized by their new life.

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