Type 1 diabetes in children

Type 1 diabetes in children is a condition in which your child's body no longer produces an important hormone (insulin). Your child needs insulin to survive, so the missing insulin needs to be replaced with injections or with an insulin pump. Type 1 diabetes in children used to be known as juvenile diabetes or insulin-dependent diabetes.

The diagnosis of type 1 diabetes in children can be overwhelming, especially in the beginning. Suddenly you and your child — depending on your child's age — must learn how to give injections, count carbohydrates and monitor blood sugar.

There's no cure for type 1 diabetes in children, but it can be managed. Advances in blood sugar monitoring and insulin delivery have improved blood sugar management and quality of life for children with type 1 diabetes.

The signs and symptoms of type 1 diabetes in children usually develop quickly, and may include:

• Increased thirst
• Frequent urination, possibly bed-wetting in a toilet-trained child
• Extreme hunger
• Unintentional weight loss
• Fatigue
• Irritability or behavior changes
• Fruity-smelling breath

When to see a doctor

See your child's health care provider if you notice any of the signs or symptoms of type 1 diabetes.

The exact cause of type 1 diabetes is unknown. But in most people with type 1 diabetes, the body's immune system — which normally fights harmful bacteria and viruses — mistakenly destroys insulin-producing (islet) cells in the pancreas. Genetics and environmental factors appear to play a role in this process.

Once the islet cells of the pancreas are destroyed, your child produces little or no insulin. Insulin performs the critical job of moving sugar (glucose) from the bloodstream to the body's cells for energy.

Sugar enters the bloodstream when food is digested. Without enough insulin, sugar builds up in your child's bloodstream. This can cause life-threatening complications if left untreated.

Type 1 diabetes most often occurs in children but can occur at any age. Risk factors for type 1 diabetes in children include:

• Family history. Anyone with a parent or siblings with type 1 diabetes has a slightly increased risk of developing the condition.
• Genetics. Certain genes indicate an increased risk of type 1 diabetes.
• Race. In the United States, type 1 diabetes is more common among white children of non-Hispanic descent than among children of other races.
• Certain viruses. Exposure to various viruses may trigger the autoimmune destruction of the islet cells.

Type 1 diabetes can affect the major organs in your body. Keeping your blood sugar level close to normal most of the time can dramatically reduce the risk of many complications.

Complications can include:

• Heart and blood vessel disease. Diabetes increases your child's risk of developing conditions such as narrowed blood vessels, high blood pressure, heart disease and stroke later in life.
• Nerve damage. Excess sugar can injure the walls of the tiny blood vessels that nourish your child's nerves. This can cause tingling, numbness, burning or pain. Nerve damage usually happens gradually over a long period of time.
• Kidney damage. Diabetes can damage the numerous tiny blood vessel clusters in the kidneys that filter waste from your child's blood.
• Eye damage. Diabetes can damage the blood vessels of the eye's retina, which may lead to vision problems.
• Osteoporosis. Diabetes may decrease bone mineral density, increasing your child's risk of osteoporosis as an adult.

You can help your child prevent diabetes complications by:

• Working with your child to maintain good blood sugar control as much as possible
• Teaching your child the importance of eating a healthy diet and participating in regular physical activity
• Scheduling regular visits with your child's diabetes health care professional

Children with type 1 diabetes are at risk of other autoimmune disorders, such as thyroid disease and celiac disease. Your child's health care provider may recommend tests for these conditions.

There's currently no sure way to prevent type 1 diabetes, but this is a very active area of research.

The antibodies associated with type 1 diabetes in children who have a high risk of the disorder can be detected months or even years before the first symptoms of type 1 diabetes appear. Researchers are working on:

• Preventing or delaying the start of type 1 diabetes in people who have a high risk of the disease.
• Preventing further destruction of the islet cells in people who are newly diagnosed.

There are several blood tests for type 1 diabetes in children. These tests are used to diagnose diabetes and to monitor diabetes management:

• Random blood sugar test. This is the primary screening test for type 1 diabetes. A blood sample is taken at a random time. A blood sugar level of 200 milligrams per deciliter (mg/dL), or 11.1 millimoles per liter (mmol/L), or higher, along with symptoms, suggests diabetes.
• Glycated hemoglobin (A1C) test. This test indicates your child's average blood sugar level for the past 3 months. An A1C level of 6.5% or higher on two separate tests indicates diabetes.
• Fasting blood sugar test. A blood sample is taken after your child hasn't eaten (fasted) for at least 8 hours or overnight. A fasting blood sugar level of 126 mg/dL (7.0 mmol/L) or higher suggests type 1 diabetes.

Additional tests

If blood sugar testing indicates diabetes, your health care provider may recommend additional tests to distinguish between type 1 diabetes and type 2 diabetes because treatment strategies differ by type. Additional tests include blood tests to check for antibodies that are common in type 1 diabetes.

Treatment for type 1 diabetes includes:

• Taking insulin
• Monitoring blood sugar
• Eating healthy foods
• Exercising regularly

You'll work closely with your child's diabetes treatment team — health care provider, certified diabetes care and education specialist, and registered dietitian. The goal of treatment is to keep your child's blood sugar within certain numbers. This target range helps to keep your child's blood sugar level as close to normal as possible.

Your child's health care provider will let you know what your child's blood sugar target range is. This range may change as your child grows and changes.

Insulin

Anyone who has type 1 diabetes needs lifelong treatment with one or more types of insulin to survive.

Many types of insulin are available, including:

• Rapid-acting insulin. This type of insulin starts working within 15 minutes. It reaches peak effect at 60 minutes and lasts about 4 hours. This type is often used 15 to 20 minutes before meals. Examples are lispro (Humalog, Admelog), aspart (NovoLog, Fiasp) and glulisine (Apidra).
• Short-acting insulin. Sometimes called regular insulin, this type starts working around 30 minutes after injection. It reaches peak effect at 90 to 120 minutes and lasts about 4 to 6 hours. Examples are human insulin (Humulin R, Novolin R).
• Intermediate-acting insulin. Also called NPH insulin, this type of insulin starts working in about 1 to 3 hours. It reaches peak effect at 6 to 8 hours and lasts 12 to 24 hours. Examples are NPH insulin (Humulin N, Novolin N).
• Long- and ultra-long-acting insulin. This type of insulin may provide coverage for as long as 14 to 40 hours. Examples are glargine (Lantus, Toujeo, other), detemir (Levemir) and degludec (Tresiba).

Insulin delivery options

Insulin delivery options include:

• Fine needle and syringe. This looks like a shot you might get in a health care provider's office, but with a smaller syringe and a much thinner, shorter needle.
• Insulin pen with fine needle. This device looks like an ink pen, except the cartridge is filled with insulin. A needle is attached for injection.

• An insulin pump. This is a small device worn on the outside of your body that you program to deliver specific amounts of insulin throughout the day and when you eat. A tube connects a reservoir of insulin to a catheter that's inserted under the skin of your abdomen.

  There's also a tubeless pump option that involves wearing a pod containing the insulin on your body combined with a tiny catheter that's inserted under your skin.

Blood sugar monitoring

You or your child will need to check and record your child's blood sugar at least four times a day. Typically, you or your child test his or her blood glucose before every meal and at bedtime and occasionally during the middle of the night. But you or your child may need to check it more often if your child doesn't have a continuous glucose monitor.

Frequent testing is the only way to make sure that your child's blood sugar level remains within the target range.

Continuous glucose monitoring (CGM)

Continuous glucose monitoring (CGM) devices measure your blood sugar every few minutes using a temporary sensor inserted under the skin. Some devices show your blood sugar reading at all times on a receiver or your smartphone or smartwatch, while others require that you check your blood sugar by running the receiver over the sensor.

Closed loop system

A closed loop system is a device implanted in the body that links a continuous glucose monitor to an insulin pump. The monitor checks blood sugar levels regularly. The device automatically delivers the right amount of insulin when the monitor shows that it's needed.

The Food and Drug Administration has approved several hybrid closed loop systems for type 1 diabetes. They are called "hybrid" because these systems require some input from the user. For example, you may have to tell the device how many carbohydrates are eaten, or confirm blood sugar levels from time to time.

A closed loop system that doesn't need any user input isn't available yet. But more of these systems currently are in clinical trials.

Healthy eating

Food is a big part of any diabetes treatment plan, but that doesn't mean your child has to follow a strict "diabetes diet." Just like the rest of the family, your child's diet should regularly include foods that are high in nutrition and low in fat and calories, such as:

• Vegetables
• Fruits
• Lean protein
• Whole grains

Your child's registered dietitian can help you create a meal plan that fits your child's food preferences and health goals, as well as help you plan for occasional treats. The dietitian will also teach you how to count carbohydrates in foods so that you can use that information when figuring out insulin doses.

Physical activity

Everyone needs regular aerobic exercise, and children who have type 1 diabetes are no exception.

But remember that physical activity can affect blood sugar. This effect on blood sugar levels can remain for hours after exercise, possibly even overnight. You or your child might need to adjust your child's meal plan or insulin doses for the increased activity.

If your child begins a new activity, check your child's blood sugar more often than usual until you and your child learn how his or her body reacts to the activity.

Make physical activity part of your child's daily routine. Encourage your child to get at least 60 minutes of physical activity daily or, better yet, exercise with your child.

Handling challenges

Blood sugar can sometimes change unpredictably. During these challenges, more frequent blood sugar testing can help identify problems and guide treatment. Ask your child's diabetes treatment team how to handle these and other challenges:

• Picky eating. Very young children with type 1 diabetes might not finish what's on their plates, which can be a problem if they've already received insulin for that food.
• Illness. Sickness has varying effects on children's insulin needs. Hormones produced during illness raise blood sugar levels, but reduced carbohydrate intake due to poor appetite or vomiting lowers the insulin requirement. Your child's health care provider will recommend a flu shot for your child every year and may recommend the pneumonia vaccine as well as the COVID-19 vaccine if your child is age 5 or older.
• Growth spurts and puberty. Just when you've mastered your child's insulin needs, he or she sprouts up seemingly overnight, and suddenly isn't getting enough insulin. Hormones also can affect insulin requirements, particularly for teenage females as they begin to menstruate.
• Sleep. To avoid problems with low blood sugar during the night, you might need to adjust your child's insulin routine and snack times.
• Temporary changes in routine. Despite planning, days don't always stay the same. Check blood sugars often when schedules change unexpectedly. Plan ahead for holidays, special occasions and vacations.

Ongoing medical care

Your child will need regular appointments to ensure good diabetes management. This can include a review of your child's blood sugar patterns, insulin needs, eating and physical activity.

Your health care provider also checks your child's A1C levels. The American Diabetes Association generally recommends an A1C of 7% or lower for all children and teens with diabetes.

Your health care provider also will periodically check your child's:

• Blood pressure
• Growth
• Cholesterol levels
• Thyroid function
• Kidney function
• Feet
• Eyes

Signs of trouble

Despite your best efforts, sometimes problems will arise. Certain short-term complications of type 1 diabetes require immediate care or they could become very serious, including:

• Low blood sugar (hypoglycemia)
• High blood sugar (hyperglycemia)
• Diabetic ketoacidosis (DKA)

Low blood sugar (hypoglycemia)

Hypoglycemia is a blood sugar level below your child's target range. Blood sugar levels can drop for many reasons, including skipping a meal, getting more physical activity than typical or injecting too much insulin. Low blood sugar is not uncommon in people with type 1 diabetes, but if it isn't treated quickly, symptoms will get worse.

Signs and symptoms of low blood sugar include:

• Pallor
• Shakiness
• Hunger
• Sweating
• Irritability and other mood changes
• Difficulty concentrating or confusion
• Dizziness or lightheadedness
• Loss of coordination
• Slurred speech
• Loss of consciousness
• Seizures

Teach your child the symptoms of low blood sugar. When in doubt, he or she should always do a blood sugar test. If a blood glucose meter isn't readily available and your child is having symptoms of a low blood sugar, treat for low blood sugar, and then test as soon as possible.

If your child has a low blood sugar reading:

• Give a fast-acting carbohydrate. Have your child consume 15 to 20 grams of a fast-acting carbohydrate, such as fruit juice, glucose tablets, hard candy, regular (not diet) soda or another source of sugar. Foods with added fat, such as chocolate or ice cream, don't raise blood sugar as quickly because fat slows down the absorption of the sugar.
• Retest blood sugar. Retest your child's blood sugar in about 15 minutes to make sure it's back in the target range. If it's not, repeat giving a fast-acting carbohydrate and testing in 15 minutes as needed until you get a reading in your child's target range.
• Follow up with a snack or meal. Once the blood sugar is back in the target range, have your child eat a healthy snack or a meal to help prevent another low blood sugar level.

If a low blood sugar causes your child to lose consciousness, an emergency injection of a hormone that stimulates the release of sugar into the blood (glucagon) may be necessary.

High blood sugar (hyperglycemia)

Hyperglycemia is a blood sugar level above your child's target range. Blood sugar levels can rise for many reasons, including illness, eating too much, eating certain types of foods and not taking enough insulin.

Signs and symptoms of high blood sugar include:

• Frequent urination
• Increased thirst or dry mouth
• Blurred vision
• Fatigue
• Nausea

If you suspect a high blood sugar level, test your child's blood sugar. If the blood sugar is higher than the target range, follow your child's diabetes treatment plan or check with your child's health care provider. High blood sugar levels don't come down quickly, so ask how long to wait until you check the blood sugar again.

If your child has a blood sugar reading above 240 mg/dL (13.3 mmol/L), your child should use an over-the-counter ketone test kit to check for ketones.

Diabetic ketoacidosis (DKA)

A severe lack of insulin causes your child's body to break down fat for energy. This causes the body to produce a substance called ketones. Excess ketones build up in your child's blood, creating a potentially life-threatening condition known as diabetic ketoacidosis.

Signs and symptoms of DKA include:

• Thirst or very dry mouth
• Increased urination
• Dry or flushed skin
• Nausea, vomiting or abdominal pain
• A sweet, fruity smell on your child's breath
• Confusion

If you suspect DKA, check your child's urine for excess ketones. If the ketone levels are high, call your child's health care provider or seek emergency care.

Following a diabetes treatment plan requires 24-hour care and significant lifestyle changes. Careful management of type 1 diabetes helps reduce your child's risk of serious complications.

As your child gets older:

• Encourage him or her to take an increasingly active role in diabetes management
• Stress the importance of lifelong diabetes care
• Teach your child how to test his or her blood sugar and inject insulin
• Help your child make wise food choices
• Encourage your child to remain physically active
• Foster a relationship between your child and his or her diabetes treatment team
• Make sure your child wears a medical identification tag

The habits you teach your child today will help him or her enjoy an active and healthy life with type 1 diabetes.

School and diabetes

You'll need to work with your child's day care provider or school nurse and teachers to make sure they know the signs and symptoms of high and low blood sugar levels. The school nurse might need to administer insulin or check your child's blood sugar levels.

Federal law protects children with diabetes, and schools must make reasonable accommodations to ensure that all children get a proper education.

Ask your health care provider

Contact your child's health care provider, certified diabetes care and education specialist, or registered dietitian between appointments if you have questions.

If managing your child's diabetes seems overwhelming, take it one day at a time. Some days you'll manage your child's blood sugar ideally and on other days, it may seem as if nothing works well. No one can do it perfectly. But your efforts are worthwhile. Don't forget that you're not alone and that your diabetes treatment team can help.

Your child's emotions

Diabetes can affect your child's emotions both directly and indirectly. Poorly controlled blood sugar can cause behavior changes, such as irritability.

Diabetes can also make your child feel different from other kids. Having to draw blood and give shots sets kids with diabetes apart from their peers. Getting your child together with other children who have diabetes or spending time at a diabetes camp may help your child feel less alone.

Mental health and substance abuse

People with diabetes have an increased risk of depression, anxiety and diabetes-related distress. That's why some diabetes specialists regularly include a social worker or psychologist as part of their diabetes care team.

If you notice that your child or adolescent is persistently sad or pessimistic, or experiences dramatic changes in sleeping habits, weight, friends or school performance, have your child screened for depression.

Rebellion also may be an issue, particularly for teens. A child who has been very good about sticking to his or her diabetes treatment plan may rebel in the teen years by ignoring his or her diabetes care. Additionally, experimenting with drugs, alcohol and smoking can be even more dangerous for people with diabetes.

Support groups

Talking to a counselor or therapist may help your child or you cope with the dramatic lifestyle changes that come with a diagnosis of type 1 diabetes. Your child may find encouragement and understanding in a type 1 diabetes support group for children. Support groups for parents also are available.

If you're interested, your health care provider may be able to recommend a group in your area. Websites that offer support include:

• The American Diabetes Association (ADA). The ADA also offers diabetes camp programs that provide education and support for children and teens with diabetes.
• Juvenile Diabetes Research Foundation (JDRF).

Putting information in perspective

The threat of complications from poorly managed diabetes can be frightening. If you and your child work with your child's health care provider and do your best to manage your child's diabetes, your child will likely live a long and enjoyable life.

Your child's primary care provider will probably make the initial diagnosis of type 1 diabetes. Hospitalization may be needed to stabilize your child's blood sugar levels.

Your child's long-term diabetes care will likely be handled by a pediatric endocrinologist. Your child's health care team also generally includes a certified diabetes care and education specialist, a registered dietitian, and a social worker.

Here's some information to help you get ready for your appointment.

What you can do

Before your appointment take these steps:

• Make a list of any concerns you have about your child's well-being.
• Ask a family member or friend to join you. Managing diabetes requires you to remember a lot of information. Someone who accompanies you may recall something that you missed or forgot.
• Make a list of questions to ask your health care provider. Ask your health care provider for a referral to a certified diabetes care and education specialist and a registered dietitian to provide additional education about managing diabetes.

Topics you might want to discuss with your health care team include:

• Blood sugar monitoring — frequency and timing and continuous glucose monitors
• Insulin therapy — types of insulin used, dose timing and amount
• Insulin administration — shots versus pumps and new diabetes technology
• Low blood sugar — how to recognize and treat
• High blood sugar — how to recognize and treat
• Ketones — testing and treatment
• Nutrition — types of food and their effects on blood sugar
• Carbohydrate counting
• Exercise — adjusting insulin and food intake for activity
• Dealing with special situations — such as at day care, school or summer camp; during illness; and on special occasions, such as sleepovers, holidays and vacations
• Medical management — how often to visit the health care provider and other diabetes care specialists

What to expect from your doctor

Your health care provider is likely to ask you a number of questions, such as:

• How comfortable are you with managing your child's diabetes?
• How often does your child have low blood sugar episodes?
• What's a typical day's diet like?
• How often does your child participate in physical activity?