INTRODUCING! Parent-Led Virtual Support Group for Families Affected by FPIES We’re considering starting a parent-led support group (virtual) designed to offer compassionate, peer-to-peer support for parents and families of children with FPIES. This group would Read more…
"I Have FPIES" is a rhyming story from diagnosis to learning to live with this rare food allergy condition. It is filled with universal experiences that children and families navigating FPIES will understand and relate to. It provides a sense of community for children who may feel different than their friends and family and a sense that they are not alone with their feelings!
Navigating your child’s Food Protein-Induced Enterocolitis Syndrome (FPIES) can be tricky, but know that many parents face this challenge, so you're not alone. A 2021 review shows that FPIES may not be as rare as it once was. This diagnosis may feel limiting for parents who want their children to explore new foods. However, proper research will help you make informed decisions, so your child still enjoys a tasty and balanced diet.