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The I-FPIES is governed by an Executive Board comprised of healthcare advocates and parents whose children have been diagnosed with FPIES. This committed and passionate team dedicates themselves to developing pathways to a cure for FPIES through education, advocacy, support and research.

Below are our Executive Board members and their defined roles. Any questions you have for our team may be directed to our general email at This email address is being protected from spambots. You need JavaScript enabled to view it.. We’d love to hear from you!

I-FPIES Executive Board

Fallon Schultz

Fallon Headshot

 

 

 

 

 

President and Founder

Amity Westcott-Chavez

Amity

Vice President

Amy and Jamie Barber

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Education and Awareness

Megan Parmenter

Megan Parmenter

Education and Awareness

Jennifer Lazarus

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Advocacy and Awareness

Lisa Millerick

LisaHeadshotDSC 6748

Support and Advocacy

Christine Quigley

ChristineQuigley

Support and Advocacy

Kaylee Page

kaylee-page-head-shoulders

Blogger and Editor

Evan Lazarus

Evan headshot

Web Master

Christopher Russell

ChrisRussell2

Graphic Design

Renato Ashcar

Renato

Brazilian Chair

 

Board Volunteers

Amy Gahman 

Amanda Gipson

Courtney Lopez

Tammy Nearon

 

 

International Chapters

Renato Ashcar, Brazil 

FPIES Brasil

This email address is being protected from spambots. You need JavaScript enabled to view it.

 

*I-FPIES is ever expanding and works to represent patients and families on a global level. If you are interested in chairing an international chapter, please email us at This email address is being protected from spambots. You need JavaScript enabled to view it..

 

I-FPIES wishes to pay tribute to the FPIES families who generously donated their time and talents to make this foundation possible.

Renee O'Donnell

Tricia Boskey

Lindsey Westerbeck

Lisa Woodward

Jen Buck Chapman

Jaci DeStefano

Leahan Drone

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