Cody has cancer and also has had a hard tough taking his medication. He has to swallow many large pills for his medication. While this has been difficult, Cody has learned some tips and ways to help get him used to swallowing medicine. Watch as Cody walks through a few different techniques.
You can also learn more about medicine and what it does for you in our health library!
Diabetes is a disease that affects how the body uses glucose (pronounced: gloo-kose), a sugar that is the body’s main source of fuel. Like a CD player need batteries, your body needs glucose to keep running. Here’s how it should work.
You eat. Glucose from the food enters your bloodstream. Your pancreas makes a hormone called insulin (pronounced: in-suh-lin). Insulin helps the glucose get into the body’s cells. Your body gets the energy it needs.
The pancreas is a long, flat gland in your belly that helps your body digest food. It also makes insulin. Insulin is kind of like a key that opens the doors to the cells of the body. It lets the glucose in. Then the glucose can move out of the blood and into the cells.
But if someone has diabetes, the body either can’t make insulin or the insulin doesn’t work in the body like it should. The glucose can’t get into the cells normally, so the blood sugar level gets too high. Lots of sugar in the blood makes people sick if they don’t get treatment.
There’s a lot of diabetes information out there — unfortunately, not all of it is based on facts. Although you can find a lot of good information about diabetes on the Internet, you can also find bad information. Following bad advice could actually harm a person with diabetes. Sometimes you don’t even need to log onto a website to get incorrect info — family members or friends can give out information that’s incorrect, inaccurate, or misleading without even knowing it!
It’s a good idea to talk to your diabetes health care team if you ever come across information that doesn’t seem quite right or sounds too good to be true. And be cautious if someone tells you to do the opposite of what your diabetes health care team has told you — always check with your doctors first to get the scoop on what’s helpful and what’s harmful. Learn more
Does your child have type 1 or type 2 diabetes? Learn how to manage the disease and keep your child healthy. Check out these helpful tools.
The Pediatric Endocrinology service at Kosair Children’s Hospital provides diagnostic and therapeutic services for children with disorders and diseases including:
We provide diagnostic endocrine tests for patients in the areas of endocrinology and carbohydrate, amino acid, and mineral and lipid metabolism. We can also address growth abnormalities and the range of conditions that can cause them.
Georgia is 14 years old and is living with Crohn’s disease. In this video Georgia answers the questions of ‘how does Crohn’s affect what you eat?’, ‘what about stress?’, ‘how do you handle the pain?’, ‘what are the side affects of steroids?’, and ‘how do you just live life?’. Listen and watch as Georgia explains her situation and provides encouragement to others that are dealing with Crohn’s.
View Part 1 of Georgia’s story
The two most common types of IBD are called Crohn’s disease and ulcerative colitis (say: ul-sur-uh-tiv keh-lye-tis).
Crohn’s disease most often develops where the small and large intestines meet and usually causes all layers of the intestinal wall to become sore, inflamed, and swollen. Crohn’s disease can affect any part of the digestive tract, including the mouth, esophagus, stomach, small intestines, large intestines, and anus.
Unlike Crohn’s disease, ulcerative colitis inflames only the inner lining of all or part of the colon and rectum. Sometimes, only the rectum is affected. In both Crohn’s disease and ulcerative colitis, inflammation may stick around for many years, flaring up over and over again.
Georgia is 14 years old and has Crohn’s disease. In this video, which is part 1 of 2, Georgia answers the question’s of ‘what is Crohn’s disease?’, ‘how did you learn that you had Crohn’s disease?’, ‘what was it like being in the hospital for so long?’, ‘what helped you cope?’, ‘how do you manage day-to-day?’, and ‘how did kids at school react?’. Watch as Georgia carefully explains how she has overcome great difficulty to live happier and healthier while managing her disease.
View Part 2 of Georgia’s story
The two most common types of IBD are called Crohn’s disease and ulcerative colitis (say: ul-sur-uh-tiv keh-lye-tis).
Crohn’s disease most often develops where the small and large intestines meet and usually causes all layers of the intestinal wall to become sore, inflamed, and swollen. Crohn’s disease can affect any part of the digestive tract, including the mouth, esophagus, stomach, small intestines, large intestines, and anus.
Sometimes all you need to relax and calm down is to focus on taking deep breathes. Watch as Amber shows us some techniques for deep belly breathing.
What’s something that you do all day, every day, no matter where you are or who you’re with?
(a) think about what’s for lunch tomorrow
(b) put your finger in your nose
(c) hum your favorite song
(d) breathe
It’s possible that some kids could say (a) or (c) or that others might even say — yikes! — (b). But every single person in the world has to say (d). Breathing air is necessary for keeping humans (and many animals) alive. And the two parts that are large and in charge when it comes to breathing? If you guessed your lungs, you’re right!
Your lungs make up one of the largest organs in your body, and they work with your respiratory system to allow you to take in fresh air, get rid of stale air, and even talk. Let’s take a tour of the lungs!
Tabitha is 15 years old and has both cystic fibrosis and diabetes. Despite her illness Tabitha is extremely positive and some great words of encouragement for others that are going through a tough time or dealing with illness. Watch more videos from Tabitha!
Kids who have CF have to take care of themselves, but thanks to a better understanding of what causes CF and improved treatment, they can go to school and do regular stuff, just like other kids. Meanwhile, researchers are working on even better treatments and hoping that one day there will be a cure. Learn more
Tabitha is 15 and has cystic fibrosis. In this segment Tabitha shows us how she puts together her acapella treatment at home. Watch more videos from Tabitha!
Approximately 30,000 people in the United States have been diagnosed with CF, which affects both males and females. It’s not contagious, so you can’t catch CF from another person.
Cystic fibrosis is an inherited disease caused by mutations (changes) in a gene on chromosome 7, one of the 23 pairs of chromosomes that children inherit from their parents. Cystic fibrosis occurs because of mutations in the gene that makes a protein called CFTR (cystic fibrosis transmembrane regulator). A person with CF produces abnormal CFTR protein — or no CFTR protein at all, which causes the body to make thick, sticky mucus instead of the thin, watery kind. Read more
Juliana is a brain tumor survivor. She talks about the complications through the years and how she has used art and family to help her through tough times.
A tumor is any mass caused by abnormal or uncontrolled growth of cells. Tumors in the brain are categorized according to several factors, including where they’re located, the type of cells involved, and how quickly they’re growing. Learn more
Watch as Tabitha shows us how she does her vest treatments at home for cystic fibrosis. See more videos from Tabitha.
What is Cystic Fibrosis
Cystic fibrosis (CF) is an inherited disease that causes the body to produce mucus that’s extremely thick and sticky. The mucus in people with CF is thicker than normal because CF affects cells in the epithelium (pronounced: eh-puh-thee-lee-um), the layer of cells that lines the passages in the body’s organs. In a person who does not have CF, the epithelial cells produce a thin, watery mucus that acts like a lubricant and helps protect the body’s tissues. In a person with CF, however, the thicker mucus doesn’t move as easily. This thick, sticky mucus clogs passages in many of the body’s organs and infection sets in.
If you use the computer to play and talk with friends, you also have an online identity. That means you have an identity that’s related to how you look, what you do, and what you say when you’re using the computer. If you play on Club Penguin and put seven disco balls in your igloo, that says something.
Sites like Club Penguin and Webkinz let you create an avatar — a character that represents you. It’s fun to dress up that character and maybe give it a sense of style you’d never try at school. Would you like a rainbow mohawk hairstyle? It’s yours at the click of a mouse.
Avatar games, instant messaging, and chat rooms also let you choose your own screen name. If you want to be known as King_of_Ketchup, that’s your new name. Maybe your little sister will want to be the Mayor_of_Mustard.
So if you start calling yourself the King of Ketchup, does that mean you really like ketchup? Should you tell your new online friends how much you love ketchup and all the foods you like to top with ketchup? That’s up to you, but it brings up a good point: How much should you share about your real self online? Read more
Tabitha is 15 years old and has diabetes and cystic fibrosis. In this segment she discusses how she stays motivated to do her treatments and how she manages her illnesses. She has great tips for those that are struggling to comply with medications and treatment.
When people are first diagnosed with diabetes, they might be nervous about getting shots or medical tests and scared about how diabetes will affect their future health. Learn more
Dominique helps us understand the fears of cancer and explains ways in which he deals with fear.
Fear is one of the most basic human emotions. It is programmed into the nervous system and works like an instinct. From the time we’re infants, we are equipped with the survival instincts necessary to respond with fear when we sense danger or feel unsafe.
Fear helps protect us. It makes us alert to danger and prepares us to deal with it. Feeling afraid is very natural — and helpful — in some situations. Fear can be like a warning, a signal that cautions us to be careful. Learn more
Dominique was diagnosed with Hodgkin lymphoma cancer. In this segment he talks about ways that he is able to cope with the disease and encourages others to look on a brighter side.
Lymphomas that involve a particular type of cell, called a Reed-Sternberg cell, are classified under the heading Hodgkin’s disease. There are several different subtypes of Hodgkin’s disease, based on how the cancerous tissue looks under a microscope. Learn more about Hodgkin lymphoma.
Decades of pediatric expertise, comprehensive treatment and support services make Kosair Children’s Hospital an excellent choice for the treatment of all forms of childhood and adolescent cancers. For more information on our Cancer Care services, call (502) 629-KIDS.
Dominique discusses how he was diagnosed with cancer and what he first treatments were like. Make sure you check out all of Dominique’s videos on CopingClub.com to hear his full story!
Hodgkin’s disease is a type of cancer called a lymphoma, which is a cancer of the lymphatic system. (The disease is sometimes also referred to as Hodgkin’s lymphoma.)
Lymphoma is a disease in which cancer cells form in a person’s lymphatic system and start to grow uncontrollably. There are several different types of lymphomas, and they are divided into two broad categories: Hodgkin’s disease and non-Hodgkin’s lymphoma.
Decades of pediatric expertise, comprehensive treatment and support services make Kosair Children’s Hospital an excellent choice for the treatment of all forms of childhood and adolescent cancers.
Watch as Deontay talks about having Hodgkin lymphoma.
Hodgkin disease, or Hodgkin lymphoma, is a type of cancer that affects the lymphatic system. This highly sophisticated filtering system helps the body’s immune system remove bacteria, viruses, and other unwanted substances.
The lymphatic system includes the lymph nodes (glands), thymus, spleen, tonsils, adenoids, and bone marrow, as well as the channels (called lymphatics or lymph vessels) that connect them. When lymphoma occurs, cancer cells develop in a person’s lymphatic system and start to grow uncontrollably. Learn More
Hayley was in an accident that caused severe burns. Here she talks about how she deals with dressing changes and also teaches us how to relax.
From kids washing up under a too-hot faucet to an accidental tipping of a coffee cup, burns are a potential hazard in every home. In fact, burns, especially scalds from hot water and liquids, are some of the most common childhood accidents. Babies and young children are especially susceptible — they’re curious, small, and have sensitive skin that needs extra protection. Learn more about the causes of burns and how to treat them.
Tabitha has cystic fibrosis and has quite a few different medications that she has to take throughout the week. Watch as she offers tips on ways to remain diligent and organized throughout the treatment process. Watch more videos from Tabitha!
Medicines are chemicals or compounds used to cure, halt, or prevent disease; ease symptoms; or help in the diagnosis of certain illnesses. Advances in medications have enabled doctors to cure many diseases and save lives. Learn more about medicine.
When was the last time you had a stomachache? It’s normal for all kids to get bellyaches once in a while. But some kids get bad stomach pain all the time. They are tired and even feel like they might throw up. Some of these kids may have what’s called inflammatory bowel disease (or IBD).
About 1 million Americans have IBD, and 30,000 new cases are diagnosed each year. IBD, which can be diagnosed at any age, most often affects people between 15 and 35 years old but has even been found in babies as young as 18 months old! In the United States, it’s thought that as many as 100,000 kids younger than 18 years old have IBD.
So, just what is IBD? How do you know if you have it? And what help is available if you do? Learn more
Watch as Hayley talks about dealing with cystic fibrosis and goes through her treatments.
Doctors and people with CF can do several things to slow the progression of the disease and fight its complications. To loosen mucus, people with CF exercise regularly and may use inhalers (like kids with asthma use) or nebulizers that help deliver medication to the lungs.
Coughing helps people with CF clear the mucus from their lungs. They may also take antibiotics to prevent or fight lung infections. Chest physical therapy may also be an important part of a person’s CF treatment routine. After lying down in a position that helps drain mucus from the lungs, the person has a helper, such as a parent, gently bang on his or her chest or back to loosen the mucus. And a newer device called a therapy vest that shakes the chest allows teens to be more independent by doing their therapy on their own.
Seth Jacobs has cystic fibrosis and has created this video to explain how he deals with CF.
Right now, there is no cure for CF. Even if symptoms are mild at first, they get steadily worse over time.
But there is hope. Fifteen years ago, most children with CF would die before reaching their teens. Now, with new treatments available, more than half live into their thirties, and new research is leading to the possibility of a cure. Statistics now show that nearly 40% of the people living with CF in the United States are 18 years or older.
Learn more about living with CF.
Lanie is 12 years old and has cystic fibrosis. Cystic fibrosis (CF) is an inherited disease that causes the body to produce mucus that’s extremely thick and sticky. The mucus in people with CF is thicker than normal because CF affects cells in the epithelium (pronounced: eh-puh-thee-lee-um), the layer of cells that lines the passages in the body’s organs. In a person who does not have CF, the epithelial cells produce a thin, watery mucus that acts like a lubricant and helps protect the body’s tissues. In a person with CF, however, the thicker mucus doesn’t move as easily. This thick, sticky mucus clogs passages in many of the body’s organs and infection sets in.
Learn more about living with cystic fibrosis.
Nashawnte is a 9 year old diagnosed with pancreatitis. When her pancreatitis flairs up she has a lot of pain and has to go to the hospital. Sometimes she has to have an NJ tube inserted which requires sedation. She’s SCARED of sedation but has been working very hard to overcome her fears! Learn more [...]
Cody has cancer and also has had a hard tough taking his medication. He has to swallow many large pills for his medication. While this has been difficult, Cody has learned some tips and ways to help get him used to swallowing medicine. Watch as Cody walks through a few different techniques. You can also [...]
Tyler’s gives tips and advice to kids and parents who are going through divorce. Divorce is stressful for parents and kids alike. Although reactions will depend on a child’s age, temperament, and the circumstances surrounding the split, many kids feel sad, frustrated, angry, and anxious — and it’s not uncommon for them to act out because [...]
