Showing posts with label FPIES Now I Know. Show all posts
Showing posts with label FPIES Now I Know. Show all posts

Friday, January 31, 2014

Join Together for Better Care: Rare Diseases Day 2014

World Rare Diseases Day February 28, 2014

Rare Disease Day 2014 focuses on care and encourages everyone in the rare disease community to
Join Together for Better Care.

We are not alone. Here at The FPIES Foundation that is something we feel every parent and caretaker should realize. Not only are there other families dealing with the same challenges FPIES poses, but if you add in other families also dealing with a rare disease the numbers are staggering.
Rare Diseases Day 2014 is fast approaching and this year we encourage the FPIES community to join your voices with these other families. Our diseases are different, but many of our struggles are the same and together our voices are strong and clear.
Rare Diseases Day was created and is coordinated internationally by EURORDIS. It was started by patient organizations and continues to be patient led. It is a great way to let decision-makers know about the challenges and impact facing a family dealing with a rare disease like FPIES.
Did you know there are 6000 different rare diseases affecting over 60 million people across Europe and North America alone??? EURORDIS tells us, "Most of these diseases are genetic, serious, chronic and debilitating. Each disease is different, but they affect people in similar ways. Experience shows that bringing together scattered knowledge and resources for people living with rare diseases is the most efficient and effective way to mobilize the care patients and families need and deserve."

How Can You Get Involved?


  • Wear that you Care:
“The Global Genes Project is one of the leading rare and genetic disease patient advocacy organizations in the world. The non-profit organization is led by Team R.A.R.E. and promotes the needs of the rare and genetic disease community under a unifying symbol of hope – the Blue Denim Genes Ribbon™. Get your Care about Rare ribbon here.  



  • Join Hands: Raise and Join hands to show your solidarity with rare disease patients around the world! Upload your photo directly to RareDiseases Day, share it with us on FB, or send to us for FPIES Community display submission to HandprintsAcross America, as part of Rare Diseases Day USA. 
  • Show support in Social Media:

ü  Join us on Facebook and ‘like” Rare Diseases Day and Global Genes Project
ü   Retweet and share rare disease news from Rare Diseases Day and Global Genes on Twitter, use hashtags #raredisease,  #Careaboutrare and #WRDD2014 
ü  Check in on YouTube: Watch the videos, comment and link to the many videos and upload your video to the Rare Disease Day channel. 

  • Tell your story:
    • FPIES Foundation Inspiring Family Stories page - Sharing both our trials and successes gives a voice to all those struggling with this invisible diagnosis, and is a valuable tool for other families as well.  This is a unique opportunity for families to learn from one another and continue to grow together as a supportive community.  Write to us at contact@thefpiesfoundation.org for more information on joining the Inspiring Families!
    • With Rare Diseases Day directly – upload your photos, video or submit story here
    • In a “Patient Letter to Representative” - fill out the form and fellow rare disease advocates from Global Genes Project will hand deliver your personal story with your “legislative ask” to your members of Congress. 
  • Involve your local Media – write and share your story and what Rare Diseases Day means to you. The media is the best way of reaching the general public and serves to shape the opinions that will convince policy makers.

For more ways to get involved:



Global Genes


This post was written by the Executive Board of The FPIES Foundation 



Tuesday, November 19, 2013

FPIES Awareness cards!

With the help of this caring community of families living with Food Protein Induced Enterocolitis Syndrome, we have developed a set of new awareness cards for families living with FPIES, inspired by families.


The business card-sized awareness cards are great for providing simple explanations of FPIES for friends, family, babysitters and so forth. Keep them in your wallet, car, or taped to the fridge to promote awareness and understanding where needed!




This postcard-size FPIES awareness card is great for keeping in the diaper bag or a purse. It not only provides information in plain language about FPIES and how to identify a reaction, but also gives tips on ways others can help to keep children affected by FPIES safe. This is great to share at playgroups, with family or with caregivers!


Along with these newly developed cards, we continue to have the FPIES Awareness rack card, a great at-a-glance explanation about FPIES.   These and more printer-friendly awareness materials are available for downloading and printing (or save the photo and share it in your social media- Facebook, Twitter, Pinterest and more!) from our Raise Awareness page of the website.

We welcome requests or materials via e-mail or postal mail.  Simply contact us at: contact@thefpiesfoundation.org and we will be happy to send you an awareness packet! 

This post was written by the Executive Board of The FPIES Foundation 

Sunday, August 25, 2013

The FPIES Foundation Celebrates Anniversary

The FPIES Foundation Celebrates Anniversary with Huge Social Media Awareness Day
Allows families to Text-A-Wish to support Foundation’s Efforts

August 25, 2013 The FPIES Foundation is excited to celebrate its second anniversary of empowering, educating and helping families navigate Food Protein Induced Enterocolitis Syndrome, or FPIES. 

The Foundation is planning a week-long celebration leading up to August 31, 2013 honoring the medical professionals, volunteers, and most importantly, the families who help raise awareness.  These amazing, strong families live with this rare allergy every day and are the reason the FPIES Foundation exists.

The week launches Sunday, August 25th, 2013 with an exciting social media campaign filled with inspiring stories and the latest FPIES information and awareness opportunities.

The week caps off with the most aggressive FPIES Foundation fundraiser to date.  On Friday, August 30th we team up with the Wish Upon a Hero Foundation for a special social media awareness day.  FPIES Awareness will race across Facebook, Twitter and personal cell phones as people participate in our Text-to-Donate day.  Just text WISH on August 30th to 80077 to donate $5 to the FPIES Foundation and its efforts to help families.




FPIES is a rare and often difficult diagnosis.  It is a delayed food allergy affecting the gastrointestinal tract, typically diagnosed in infants and young children.  Classic symptoms of FPIES include profound vomiting, diarrhea, and dehydration. These symptoms can cause severe lethargy, change in body temperature and blood pressure, and often lead to hospitalization. Unlike typical food allergies, symptoms may not be immediate and do not show up on standard allergy tests.

The FPIES Foundation’s roots lie with families, started by moms who saw a vital need for information and resources.

Foundation Chair Joy Meyer says, “As we go into our 3rd year I am even more inspired to be a member of this community.  Families and medical providers come together every day to help children living with FPIES thrive.  We have this great community to thank for these growing resources, building awareness and support.”

Highlights this year include:

  • 501c3 Non-profit designation
  • A newly expanded website with an extensive FPIES “toolbox” to help families check symptoms, journal foods, and prepare for doctor visits
  • A provider directory filled with FPIES knowledgeable doctors and specialists
  • Launching “FPIES, Now I Know” an awareness video inspired by real FPIES families
  • Awarenessis Action” campaign with brand-new resources families can print out to help educate medical professionals and raise awareness in their communities
  • An expanding Medical Advisory Board dedicated to a multidisciplinary approach to FPIES
  • The formation of a Volunteer Advisory Board made up of active members of the FPIES community
  • Social media outreach through Facebook/Twitter/Pinterest and the FPIES Foundation blog
  • Awarded certification from HON (Health on the Net) Code, “the commitment to reliable health and medical information on the internet.”
  • FPIESFoundation supported regional monthly gatherings, and tools to help families start their own FPIES Foundation meet-ups
  • Participation in Feeding Tube Awareness Day, Rare Disease Day and Food Allergy Awareness Week
The work doesn’t stop here.  The FPIES Foundation is excited for the year ahead with plans to launch a first of its kind ‘For Kids’ page, including a Child Ambassador program where the focus is entirely on the child, and not only on the child’s FPIES.
We will continue partnering with organizations to increase awareness and education while lobbying to create standardized practices for FPIES diagnosis and treatment.


The FPIES Foundation is an Incorporated 501(c)(3)Non-Profit Foundation. It is a collaborative effort of several families affected by FPIES whose relentless journey has sparked the desire to help other families find their way. FPIES is often under recognized and poorly understood. The organization's founders identified a dire need for tangible support resources for both the affected families and the medical community. The FPIES Foundation is committed to providing a credible and interactive support resource for this rare, oftentimes isolating diagnosis. It strives to make the everyday lives of FPIES children and their families easier.

This post was written by the Executive Board of The FPIES Foundation