The main goal of type 1 diabetes treatment is to control high blood sugar levels with insulin therapy. People with type 1 diabetes don’t make enough insulin on their own. As a result, their cells can’t use sugar for fuel, and blood sugar levels rise. Several types of insulin and insulin delivery systems can help treat type 1 diabetes.
In addition, lifestyle changes and appropriate diabetes education can boost the overall management of type 1 diabetes. If you or your child is diagnosed with type 1 diabetes, you’ll work with your doctor or your child’s pediatrician to find the best treatment plan.
This article will discuss the eight things you need to know about type 1 diabetes treatments.
When you or your child first receives a type 1 diabetes diagnosis, it’s important to learn as much as you can about insulin. This hormone is normally made by the pancreas and helps the body’s cells use sugar for energy. People with type 1 diabetes can’t make insulin, so they need to give it to themselves as treatment.
The Centers for Disease Control and Prevention (CDC) provides information on the different types of insulin. Each type is classified by how fast it begins working and how long its effects last. Doctors choose a certain type of insulin based on many factors, including a person’s:
They’ll also consider how long it takes the body to absorb insulin and how long its effects last.
The seven types of insulin are classified by how fast they begin working and how long their effects last.
In addition, it’s important to familiarize yourself with some terms that describe how insulin works:
Your child’s doctor will explain each kind of insulin and its use. This table provides an overview of the types of insulin your child may be prescribed:
People with type 1 diabetes need to keep a close eye on their blood sugar levels. Levels that are either too high (known as hyperglycemia) or too low (hypoglycemia) can become dangerous. Your child can use their blood sugar level to determine how much insulin they need to take. They should also know that if their levels are too low, they need to eat to bring their sugar back up.
Your child’s pediatrician will likely recommend checking blood sugar at least four times a day. The American Diabetes Association (ADA) recommends testing before eating, exercising, and sleeping. If your child uses an insulin pump or takes insulin injections at least three times a day, they may need to check more often.
Blood sugar levels can be checked in two ways. Your child will likely start out using a blood glucose meter. They’ll prick their finger and put a few drops of blood on a test strip attached to the glucose meter, which gives results in a few seconds.
A continuous glucose monitor (CGM) checks blood sugar levels every five to 15 around the clock. The device has a sensor that sits underneath the skin and measures blood sugar. A fingerstick check will still be needed from time to time, but a CGM can help if your child has hypoglycemic episodes or their blood sugar levels fluctuate quite a bit.
A continuous glucose monitor checks blood sugar levels every
five to 15 minutes around the clock.
Insulin can be taken in one of four ways — using a syringe, a pen, a pump, or an inhaler. The treatment method depends on the type of insulin your child uses and their comfort level. Their pediatrician will discuss which options may work best, and your child’s needs and treatments may change over time.
Insulin injections use either a syringe or pen to deliver insulin. To use a syringe, you’ll accurately measure the amount of insulin needed from a small vial. It’s best to inject insulin into the belly and rotate the injection site with each shot. This prevents small, hard lumps from forming under the skin that are difficult to inject into. Your child may need more than one shot to meet their target blood sugar level.
Insulin pens come prefilled with insulin or with prefilled cartridges to deliver the correct dose. Pens are typically easier to use than injections and are more convenient to carry around, but they can cost more than syringes. Some children may prefer using an insulin pen because it looks less intimidating than a syringe.
Insulin pumps are small devices that provide a steady dose of insulin all day long. Your child can adjust the dosing according to their blood glucose levels. They can also give themselves extra insulin before mealtimes.
Some pumps use a very small plastic tube that runs insulin from the device underneath the skin. The dose is adjusted using a programmable machine attached to a belt or placed in a pouch or pocket.
Another type of insulin pump attaches directly to the skin with adhesive, usually on the upper arm or belly. A very small tube sits underneath the skin, and a wireless handheld device controls insulin dosing.
The U.S. Food and Drug Administration (FDA) recently approved a new technology known as an artificial pancreas. This system uses three devices — a CGM, an insulin pump, and a specialized program on a smartphone or the pump.
The CGM monitors blood sugar levels and sends information to the smartphone or insulin pump. If glucose levels are too high, the pump calculates how much insulin is needed and delivers it.
An artificial pancreas can help people better manage their type 1 diabetes and improve their overall quality of life. It also helps prevent hypoglycemia and hyperglycemia because it constantly monitors blood glucose levels.
Some adults might opt to use an inhaler to deliver ultra-rapid-acting insulin right before eating. Insulin inhalers are typically used with injectable forms of long-acting insulin to control blood sugar levels. However, this method is less commonly used than injection.
In late 2022, the FDA also approved teplizumab-mzwv (Tzield) to slow progression from stage 2 type 1 diabetes to stage 3. Adults and children ages 8 and older can receive teplizumab-mzwv.
Type 1 diabetes has three stages. The second stage occurs when immune system proteins called autoantibodies attack the pancreas. The pancreas then makes less insulin, and blood sugar levels start to rise. At stage 2, symptoms haven’t yet developed.
People with stage 3 type 1 diabetes can no longer make enough insulin on their own, and they begin experiencing symptoms. Doctors and researchers have found that teplizumab-mzwv blocks the immune system from attacking the insulin-producing cells in the pancreas (beta cells). This delays progression to stage 3 type 1 diabetes.
Along with insulin treatments, some lifestyle changes can help you or your child live a healthier life with type 1 diabetes. It’s important to work closely with your diabetes care team or your child’s team. A diabetes educator can demonstrate how and when to test blood sugar and how to administer insulin.
A dietitian can also teach you or your child how to count carbohydrates to calculate how much insulin is needed. By learning how to properly treat and manage type 1 diabetes, you or your child can continue living a healthy life.
On myT1Dteam, the social network for people living with type 1 diabetes and their loved ones, members come together to ask questions, give advice, and share their stories with those who understand life with type 1 diabetes.
Are you or your child living with type 1 diabetes? What treatments have best helped manage the condition? Share your experience in a comment below, or start a conversation on your Activities page.
Get updates directly to your inbox.
What To Do When Your Sugar Is 600+
Can A Type 1 Diabetic Benefit From Eating Fat Bombs As A Snack?
How Is Answering Our Questions?
Become a member to get even more:
A myT1Dteam Member
Just the observations of 54 T1D years and lots of experience and research.
The goal of T1D management using insulin is not to control, but to manage BG to keep it in a healthy or even normal range… read more
We'd love to hear from you! Please share your name and email to post and read comments.
You'll also get the latest articles directly to your inbox.