The Pancreatic Disorders Program at Children's Wisconsin is unique for its deep experience treating acute and chronic cases. Our team gives you and your family the best and safest care possible.
In addition to world-class care, we have many resources for kids and families. We provide a comfortable and welcoming place for every step of your journey. We’re here for you, from finding out what’s wrong to long-term care.
Before Your First Visit
For your first visit to the Pancreatic Disorders Program, make sure to bring:
- Your child’s medical history
- Past test results
- List of medicines
- Reports from previous procedures
Our team offers many services to diagnose and treat health issues of the pancreas and gallbladder.
We work with Children’s Wisconsin experts in:
- Diagnostic and interventional imaging
- Advanced endoscopy
- Nutrition
- Genetic testing and counseling
- Chronic pain care
- Surgery
We look at every part of your child’s health to find answers and provide the best care possible. This helps us find the cause, even with hard-to-diagnose cases.
If you have any questions before your first visit, please contact our team.
After Care
Whenever possible, we treat the root cause of pancreatic insufficiency. This way, your child can recover and go on to a normal life. If the cause is genetic, we work with your family to manage it and make your child comfortable so they can grow.
Patients who are missing enzymes because of genetic issues will need to stay on PERT for life. Make sure your child takes their pills. It’s the best way to manage their symptoms and help them grow.