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Our Blog -A Network of Caring

Living with FPIES

Living with FPIES: Halloween Ideas!

Halloween is one of my favorite days of the year. I love holidays in general, and even though Christmas will always have a special place in my heart, there are some pretty big expectations wrapped up (pun intended) around December Read more…

By thefpiesfoundation, 8 yearsOctober 25, 2017 ago
Helping families

Embracing the Gadgets

Before I had my two children, I was never much of a kitchen gadgets or appliances person. Most of what I needed to do in the kitchen, I could do by hand, and I didn’t want to pay for them, Read more…

By thefpiesfoundation, 8 yearsOctober 1, 2017 ago
Living with FPIES

Someone’s In the Kitchen with FPIES: Animal Cookies/Crackers

One of the things that I find I struggle with as an FPIES mom is making food fun for my kids. My youngest can eat very few packaged foods, and so anything fun he gets has to come from me. Read more…

By thefpiesfoundation, 8 yearsSeptember 16, 2017 ago
In The News

Raising FPIES awareness on The Mighty!

A diagnosis of FPIES can be life-altering.  So, when The Mighty asked our community for some of the things parents of children living with FPIES are doing, because of the diagnosis, that other people may not realize, the response was Read more…

By thefpiesfoundation, 8 yearsAugust 30, 2017 ago
FPIES Registry

Power of the PIN!

In 2013 we, at The FPIES Foundation, presented the first-of-its-kind FPIES Global Patient Registry through the Patient Crossroads CONNECT program a patient registry platform company.  Last year, Patient Crossroads underwent a rebranding to become AltaVoice.  Through Altavoice we were introduced to the Power of the Patients Read more…

By thefpiesfoundation, 8 yearsAugust 16, 2017 ago
Helping families

A Mom-Inspired Food Allergy Journal

Here, at The FPIES Foundation, we love food journals!  You can find a page in the FPIES toolbox dedicated just to food journals and we are inspired everyday by the food journals you have created and have shared with us.  We have Read more…

By thefpiesfoundation, 8 yearsMay 4, 2017 ago
Helping families

5 Ways to Thank a Doctor!

March 30th was National Doctors’ Day. Doctors across our country were recognized for the dedicated and tireless work they do each day. Everyday, we acknowledge and appreciate the contributions of the many great practitioners that support our children and families affected Read more…

By thefpiesfoundation, 8 yearsApril 23, 2017 ago
In The News

Jeanelle Boyer, PhD and an FPIES Research Update

Have you ever looked back upon your life and been in awe as to how everything seems to have worked out for some higher purpose? I am still amazed at how many of my life choices were, unknowingly, preparing me Read more…

By thefpiesfoundation, 8 yearsApril 10, 2017 ago
Helping families

10 Winter Crafts for Hospital Stays

Hospital stays can happen all too often for many families living with FPIES and we know it can be difficult to keep your little one occupied. FPIES parent Zack Skrip gave us some really great ideas back in June on Things Read more…

By thefpiesfoundation, 9 yearsMarch 5, 2017 ago
Support our Cause

10 Things You Can Do to Spark the Conversation About Rare Diseases

The FPIES Foundation has joined forces with 30 million Americans and health care advocates around the world for Rare Disease Day® on February 28.  Rare Disease Day is an annual awareness day dedicated to elevating public understanding of rare diseases and calling attention Read more…

By thefpiesfoundation, 9 yearsFebruary 2, 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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