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What to Expect at your Cystic Fibrosis Appointment

Diagnosing cystic fibrosis in your child - what to expect

Diagnosing cystic fibrosis is a multi-step process. It usually starts with a newborn screening test performed by the state. If the screen is abnormal, infants and children are then referred to a Cystic Fibrosis Foundation-accredited care center like Children’s Mercy for further testing.

Your first appointment

When you come for your first appointment, the CF specialist will do a comprehensive examination of your child. We will do a sweat test and genetic testing along with your child’s clinical evaluation.

Although most people are diagnosed with CF by the age of 2, some are diagnosed as older children or as adults. A CF specialist can order a sweat test and recommend additional testing to confirm a CF diagnosis at any age.

Our team approach to ongoing care at Children’s Mercy

If your child is diagnosed with CF, you will have regular appointments with a team of specialists who will get to know your family and work closely to coordinate care for your child’s specific needs.

At the Children’s Mercy Cystic Fibrosis Care Center, we take pride in our diverse group of dedicated CF experts and the outstanding care we provide for children with CF. Our care team includes providers, nurses, respiratory therapists, social workers, dietitians and pharmacists.

We have four pediatric pulmonologists and one pediatric nurse practitioner who provide care in CF clinic. Several team members travel to our outreach clinic in Joplin, MO once a month for families who live closer to that location.

Once you have established care in our CF clinic, we encourage you to pick a primary CF provider. That provider partners with a nurse, social worker, and dietitian so a core team of people provide expert care for your child. This approach allows for our team members to develop close, long-term relationships with you and your family.

Health education at each visit

Your family will come to Children’s Mercy for a comprehensive CF clinic visit approximately every three months. We work hard to streamline your time in the CF clinic while making it a worthwhile and valuable experience.

Our CF Care Center uses a Quarterly Visit Curriculum. This means that during each clinic visit, we choose to focus on a different aspect of CF care:

  • Respiratory Care
  • Nutrition Care
  • Psychosocial Care (mental and emotional health)
  • Annual Review (focusing on medications and overall health)

During these visits, one team member will spend extra time with your family to focus on education in their area of expertise and planning for your child’s upcoming growth and development milestones.

Our goal is to teach your family everything you need to know about CF and how to best manage it. Even if your visit focus is on a different aspect of care, you can always see other team members, such as the dietitian, pharmacist, or social worker, if you need to.

Coordinated care for all your child’s needs

The Children’s Mercy Cystic Fibrosis Care Center has strong collaborations with other specialists that may be important for your child’s care. We have Children’s Mercy specialists who are familiar with CF care in the following areas:

Hepatology (Liver Care)
Otolaryngology (Ear, Nose, and Throat)
Gastroenterology (GI)
Psychology and Psychiatry
Infectious Disease

Education day

We also offer an annual education day for family members and caregivers of children with CF. This event provides the opportunity to hear from both local and national experts in CF care. It also allows for networking with others in the CF community.

Family members and caregivers of children with CF are encouraged to attend. Adolescents and young adults with CF are encouraged to participate remotely using our telecommunication platforms.