• Team-based care: Specialists meet with you and your child together, in one room, at the same time.
• Family-centered approach: You are the most important part of your child’s care team.
• Expert staff: Our team includes physicians, nurse clinicians, dietitians, speech and language pathologists, psychologists, medical assistants and more.
• Consistency of care: We work closely with your child’s primary doctor and therapists.

Treatment plans will depend on your child’s specific diagnosis. Learn about what to expect at your first appointment here.

Before Treatment: Your First Visit

Your child’s care begins with a full evaluation. At the first visit, you’ll meet with a doctor, nurse and dietitian. We’ll review your child’s medical history, feeding habits and growth. We may recommend tests like blood work or imaging.

At your second visit, your full care team may also include a psychologist and speech therapist. We’ll watch your child eat, talk about your goals and answer questions. Then we’ll create a plan together.

This may include feeding therapy, changes in diet or other medical support. Before you leave, you’ll get a written summary of the plan and clear next steps.

During Treatment: Putting the Plan into Action

Once we create a plan, we’ll help you put it into action. Most families start with outpatient visits. Some kids need more support and may benefit from a short stay for more focused care.

Types of treatment include:

• Outpatient therapy: Your child comes to regular visits while working on feeding goals at home.
• Intensive outpatient therapy: Your child attends several full or half-day sessions, where they typically have 3 meals per day over five days. This is helpful if your child needs extra support or if you're coming from out of town.
• Inpatient therapy: Your child stays in the hospital for about two weeks for 24-hour care, daily therapy and family training. Patients receive 3 meals a day working with our team over the course of their inpatient stay. This is only needed if other treatments haven’t worked.

We track your child’s progress and adjust the plan as needed. You’ll get regular updates and support from the team.

After Treatment: Long-Term Follow-Up

After your child finishes treatment, we’ll keep checking in. Some kids reach a point where they no longer need therapy or tube feeding. Others need more time to grow their skills or manage health conditions.

We’ll help you know what to expect, including:

• Follow-up visits or phone check-ins
• Changes to your child’s feeding plan over time
• Support as your child transitions back to your regular care team

We’ll also give you tools to help your child stay on track at home. Our goal is to help your child eat well, grow strong and feel confident — both now and in the future.