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! 
Last Post: FPIES aND IgE?
Last Post: Possible FPIES?
Last Post: formula assistance
Last Post: Aloe Vera Juice with FPIES
Last Post: New bread recipe!
Last Post: Second Child with FPIES - Help!
Last Post: SLC, Utah
Last Post: Phoenix az
Last Post: Minnesota
Last Post: Upstate NY Area
Last Post: North Carolina anyone?

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. 

Last Post: FPIES Started at 5 and getting worse

Where are you from?  Make local connections by listing your Country/State/Region here! 

Last Post: Where are you from?
Last Post: Rare Diseases Day Feb. 29, 2012
Last Post: NAET's
**The FPIES Foundation does not provide medical advise, diagnosis, or treatment. ******THIS INFORMATION HAS NOT BEEN REVIEWED BY THE FPIES FOUNDATION'S MEDICAL ADVISORY BOARD.********* Terms of Use: