Here you will find other FPIES families who offer a community of support, as well as a wealth of FPIES knowledge. Each child's situation is unique, so treatment plans must be individualized. Get started by reviewing and compiling information, then plan to meet with your doctor and/or medical team. We are a group of parents, just like you, so cannot give a diagnosis, nor dispense medical advice, but hope to be a valuable resource none the less!
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Adults with FPIES symptoms and/or diagnosis can exchange information here!
Last Post: Medical Literature
A place to connect families with children beyond Infancy and Toddlers, who either are still affected by FPIES or are just beginning this journey.
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Where are you from? Make local connections by listing your Country/State/Region here!
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