Learn how to identify, manage and seek help for acute FPIES reactions
Your one-stop-shop for getting started with your family's FPIES journey
Expand your knowledge of FPIES with FREE online and printable resources
Join the Global FPIES Patient Insights Network, adding your voice to FPIES research
Resources and support for providers caring for patients affected by FPIES
Read about how others are navigating FPIES and share your story!
Kid-specific FPIES resources for affected kids, as well as their siblings and friends
Tools to navigate school for kids, parents, and the teachers who support them
Has your child experienced severe episodes of vomiting after eating infant cereal and/or first foods, or after drinking formula?
Do you question whether or not a specific food or foods may be contributing to your infant’s worsening symptoms of periodic vomiting, chronic diarrhea, reflux and/or failure to thrive?
These symptoms may indicate a need to speak with your child’s doctor about an FPIES evaluation.
August 31st marks the day The FPIES Foundation was launched. For 13 years, The FPIES Foundation has been committed to providing a credible and interactive support resource for this easily misunderstood allergic disorder to make Read more…
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.
The FPIES Foundation is proud to partner with Dayspring Pens through a donation of custom engraved pens. The team at Daysprings Pens is honored to be able to donate to an organization that works so Read more…
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