MENUMENU
  • contact@thefpiesfoundation.org
  • Sign up for updates!
The FPIES Foundation
MENUMENU
  • Home
  • About FPIES
    • What is FPIES?
      • About the Diagnosis
      • Adult FPIES
      • Symptom Checker
      • Glossary of Terms
    • FPIES Q&A
      • What is FPIES?
      • Common Symptoms
      • Common Triggers
      • Diagnosis and Testing
      • Management Strategies
    • Online Learning
      • FPIES Medical Literature
      • FPIES Learning Library
    • Life with FPIES
      • Advocacy
      • Doctor Visits
      • Provider Directory
  • Resources
    • For Families
      • FPIES Toolbox
      • Emergency Care
      • Cooking and Nutrition
    • For Practitioners
      • Health Professionals Home
      • Nutrition Professionals
      • Join the Database
    • For Kids
      • Kids' Corner
      • Ways to Cope
      • Meet the Treatment Team
      • School Support for Kids
    • Resources
      • Web Resources
      • Awareness Posters
      • Global FPIES Patient Registry
  • Get Involved
    • Share Your Story
      • Inspiring Family Stories
      • Research and You!
      • Starting the Conversation
      • Support Groups
    • Outreach
      • Raise Awareness
      • Be a Volunteer
      • Volunteer application
      • Be a Partner
      • Medical Nutrition Equity Act
    • Events
      • Food Allergy Awareness Week
      • Global FPIES Day
      • Rare Disease Day
      • Fundraisers
    • Social Media
      • Support and Awareness
      • Facebook
      • Twitter
      • Instagram
      • Linked In
      • YouTube
  • About Us
    • Leadership
      • Meet our Team
      • Meet Our Founders
      • Connect with Us
    • Programs
      • Accomplishments and Goals
      • Global FPIES Day
      • Research
    • Site Content
      • Authorship and Review
      • Terms of Use
      • Copyright
      • Site Map
    • Policies
      • Medical Disclaimer
      • Privacy Policy
      • Link Policy
  • Blog

Empower

Helping families

Talking About FPIES- Part Three: Explaining FPIES to Your Child

Talking about FPIES is a 3-part blog series by Angelika Sharma, FPIES Foundation volunteer. Explaining FPIES to your child You may not have conversations with your baby or small child yet, but you are already communicating with them about their FPIES every day. In part three of our Three-Blog-Post Series Read more…

By thefpiesfoundation, 3 yearsSeptember 24, 2022 ago
Helping families

Talking about FPIES- Part Two: Effectively Sharing Your Needs with FPIES.

Talking about FPIES is a 3-part blog series by Angelika Sharma, FPIES Foundation volunteer. Effectively sharing about your FPIES needs In the early days after an FPIES diagnosis, parents learn so much: from information about the diagnosis to navigating their new everyday life. As their days are re-shaped and the Read more…

By thefpiesfoundation, 3 yearsSeptember 17, 2022 ago
Helping families

Talking About FPIES- Part One: How to Explain FPIES to Others

Talking about FPIES is a 3-part blog series by Angelika Sharma, FPIES Foundation volunteer. How to Explain FPIES to Others As the parent or caregiver to a child with FPIES, you regularly find yourself having to explain the needs of your child: first with family and friends, then in places Read more…

By thefpiesfoundation, 3 yearsSeptember 9, 2022 ago
Living with FPIES

“A Mothers Guide to FPIES”: Interview with the Author

Recently, we learned of a parenting book for parents of children diagnosed with FPIES. We had an opportunity for an interview with author, Angelika Sharma, and here is what she shares about her book, “A Mother’s Guide to FPIES”. Tell us a little about your book and your aim in Read more…

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

Planning Your Summer Adventures: When FPIES is Your Uninvited Travel Companion

Planning Your Summer Adventures, When FPIES is Your Uninvited Travel Companion Backpacks are starting to gather dust, you’ve inflated the kiddie pool . . . . summer must be here! At our house, we are always thrilled for the arrival of summer. It allows us to take a breath, stock Read more…

By thefpiesfoundation, 3 yearsJuly 19, 2022 ago
Living with FPIES

All About Cross Contact

A FARE Collaborator blog Most of us don’t think twice about going on vacation or attending neighborhood barbecues, but for people managing food allergies, having others provide meals requires extra vigilance and planning. Those not living with food allergies are typically unaware of how easily and quickly an otherwise safe Read more…

By thefpiesfoundation, 3 yearsJuly 7, 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
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

5 Unexpected Ways to Help School Children Living With FPIES

Planning meals for children can be challenging. You have to come up with a dish that is not only appealing to them but is also packed with nutritious ingredients that sometimes your child probably doesn’t like, and these difficulties grow tenfold when it comes to prepping meals for children with Read more…

By thefpiesfoundation, 6 yearsFebruary 2, 2020 ago
Helping families

A Peek Into ‘FPIES – The Mystery that Made My Brother Sick’, a Children’s Book

We are so excited to share with you that a children’s book about life with FPIES was recently published! The book, “FPIES  – The Mystery that Made My Brother Sick“, was written by a fellow parent of a child living with FPIES and is a real-life story about her son.  Read more…

By thefpiesfoundation, 6 yearsJanuary 19, 2020 ago

Posts navigation

Previous 1 2 3 … 9 Next
  • Facebook
  • Twitter
  • Instagram
  • LinkedIn
  • Pinterest
https://youtu.be/JitPvOMjHlY
https://youtu.be/DDNVNbjLNhY

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.


MENUMENU
  • Home
  • What is FPIES?
  • FPIES Patient Registry
  • Our Blog
  • Terms of Use
  • Privacy Policy
  • Authorship and Review
  • Site Map
Hestia | Developed by ThemeIsle