Every child is different, but this timeline provides a general overview of what you can expect during your child's first year in the Texas Children's Celiac Disease Program.
Program Coordinator Outreach
Introduce your care team
Provide educational resources and school support forms (e.g., 504 Plan)
Schedule your gluten-free nutrition education visit
Answer questions and discuss your family's needs
Nutrition Education
Meet with a specialized pediatric dietitian to learn the fundamentals of a healthy gluten-free lifestyle, identify hidden sources of gluten, and develop a nutrition plan tailored to your child.
Coordinator Check-In
We'll check in to see how your child is adjusting, answer questions, and connect your family with additional resources if needed.
GI Follow-Up Visit
Your child's gastroenterologist will monitor growth, symptoms, healing, and nutritional status, repeat any necessary laboratory tests, and review the ongoing treatment plan.
Coordinator Follow-Up
We'll help ensure your child's annual follow-up is scheduled and address any new questions or concerns.
Once your child's symptoms have improved and celiac disease is well controlled, follow-up visits typically transition to an annual schedule. In selected cases, your physician may recommend a repeat endoscopy to confirm intestinal healing.
