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Living with FPIES

Allergen Cross Contact: A 6th Science Fair Project

Recently, we learned about an award winning Science Fair project that raised awareness to food allergies. It was done by a 6th grade student and today we’d like to share a little about that project with you! Tell us a little about yourself. I am Ameya Balaji, studying in 6th grade, and Read more…

By thefpiesfoundation, 3 yearsJune 8, 2022 ago
Living with FPIES

Navigating FPIES in the Classroom– Preparing for a new school year!

I sat nervously at the conference table, introducing myself to a room of new faces, new faces that I sincerely hoped would help to make accommodations for my daughter when she entered kindergarten in the next year. I had reason to be nervous—we had never found a preschool willing to Read more…

By thefpiesfoundation, 3 yearsApril 1, 2022 ago
Living with FPIES

Rare Disease Day 2021

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 Day;” this awareness day sponsored by NORD (the National Organization for Rare Disorders) is a Read more…

By thefpiesfoundation, 5 yearsFebruary 16, 2021 ago
Helping families

Happy 2021 to All!

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 the pandemic and many of us being homebound, outreach may be a bit of a Read more…

By thefpiesfoundation, 5 yearsFebruary 2, 2021 ago
Helping families

COVID Conversations– Through an FPIES Lens: Food Labels.

From every corner of our world, COVID-19 has impacted us all in one way or another. As I sit here in my living room, in a state particularly hard hit, the evidence of this impact is all too clear. The stress, the risk of catching this illness, the changes in Read more…

By thefpiesfoundation, 5 yearsMay 28, 2020 ago
Helping families

FPIES Workbook for Parents and Caregivers: An Interview

This spiral-bound Workbook was created specifically for families managing FPIES, to help parents and caregivers stay organized and keep track of everything in one place!

By thefpiesfoundation, 6 yearsSeptember 12, 2019 ago
Helping families

Make Like A Zebra and #ShowYourStripes

Make Like A Zebra and #ShowYourStripes Every year, my daughters and I look forward to Rare Diseases Day. It is such a great opportunity to raise awareness, but I feel like it also is a wonderful reminder to them that they are not alone– there are kids all over the Read more…

By thefpiesfoundation, 7 yearsFebruary 26, 2019 ago
Helping families

FPIES: This is How We Do It

As we celebrate our seventh anniversary at The FPIES Foundation, I have been looking back over the years since our beginnings and since the start of my own family’s FPIES journey. I smile as I remember families that have come and gone from our community. Even though they may have Read more…

By thefpiesfoundation, 7 yearsSeptember 3, 2018 ago
Helping families

Paying Medical Bills as Simply as Possible

Paying Medical Bills as Simply as Possible By Margaret Hancock For those navigating FPIES – or any rare disease – hospital, specialist, nutritional, and additional medical bills can be quite confusing and time-consuming. I am grateful for a brief stint that I had with an insurance firm as I learned through Read more…

By thefpiesfoundation, 8 yearsMarch 23, 2018 ago
Helping families

Preparing for a Food Challenge

When navigating through the FPIES reality, one of the more regular activities is a food challenge. When we began introducing foods to our son, several challenges resulted in days worth of medical attention. Now, each and every food introduction we do (whether the food is a typical FPIES trigger or Read more…

By thefpiesfoundation, 8 yearsDecember 3, 2017 ago

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The FPIES Foundation is an Incorporated 501(c)(3) Non-Profit organization. The FPIES Foundation does not provide medical advice, diagnosis or treatment. Information provided is intended for supportive, awareness and educational purposes and not as medical advice.


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