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
Resources and support for providers caring for patients affected by FPIES
Join the Global FPIES Patient Insights Network, adding your voice to FPIES research
Tools to navigate school for kids, parents, and the teachers who support them
Kid-specific FPIES resources for affected kids, as well as their siblings and friends
Support and connect with other families affected by FPIES in a private forum
Expand your knowledge of FPIES with FREE online and printable resources
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.
The Medical Nutrition Equity Act (S-1194, HB-2587) is a piece of legislation currently being championed by medical professionals and patient advocacy groups that aims to improve coverage of medical nutrition (such as elemental formula) for individuals affected by a variety of conditions, including FPIES. Learn how you can get involved TODAY!
Do you ever wish you had more opportunities for raising awareness about FPIES? Are you ever unsure of where to get started with raising awareness? The last day of February each year is “Rare Diseases Read more…
Happy 2021 to all! Now a full month into our New Year, we want to invite our community to join us in resolutions to spread FPIES education and awareness throughout 2021! With the state of Read more…
With a vision to learn more about the microbiome and its potential impact on individuals affected by FPIES, we invite you back to our Global FPIES Patient Insights Network (www.fpiesregistry.com), through our partnership with Invitae, Read more…
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