The FPIES Foundation is excited to
celebrate its third anniversary of empowering, educating and helping families around the world to navigate life with Food Protein-Induced Enterocolitis Syndrome (FPIES).
This past year was packed with numerous
accomplishments, big and small. The FPIES Foundation achieved its goal of
launching a first-of-its-kind FPIES Global Patient Registry. The registry is a
ground-breaking opportunity to directly bring families affected by FPIES
together with doctors and researchers interested in learning more about this
rare allergy.
We are also excited to announce that
The FPIES Foundation has established October 14th as Global FPIES Day. Global
FPIES Day honors families by giving the opportunity to bring specific awareness
to what FPIES is to the general public.
“There are days to recognize other food
allergies and rare diseases, but FPIES is unique and the children are
extraordinary. They deserve this day just for them,” says Joy Meyer, Executive
Director of the FPIES Foundation. Meyer says, “October 14th was chosen
specifically because the first research paper to mention the features of FPIES
was published in October.”
In addition to establishing
the FPIES Global Patient
Registry and Global FPIES Day, achievements by
the Foundation that were accomplished this year include:
- Releasing a Free Educational Webinar, “Advocating for your child in the Healthcare System” made possible through our partnership with ThriveRx. Find the recording to this webinar along with documentation resources and educational tools for becoming an advocate on the Advocacy page of the website.
- Launching ‘The Kids Spot’. This section created just for kids, older FPIES children and their siblings can find support in a fun, interactive way that shows them they are not alone. Here they can find support for school, hospital stays, and social situations. Also, be sure to check out the Brag Board and Kids in Action pages!
- Engaging the community in “FPIES Be the Voice,” “FPIES Share how you Care,” and “Love your FPIES Selfie” social media campaigns. Hundreds of families helped us raise awareness in conjunction with Rare Diseases Day and Food Allergy Awareness Week
- Designing new FPIES Awareness Flyers and Cards
- Participating in the Free Allergy Day at Boston’s Franklin Park Zoo and the Food Allergy Support Group of MN Food Allergy Resource Fair
- Partnering with Sarah's FPIES Clubhouse, a great place for kids to share fun stories and activities!
- Supporting teams raising awareness in the Food Allergy community by participating in various FARE walks nationwide.
- Appearing in the Advocacy Month Feature in Complex Child E-Magazine, "FPIES: The Formation of a Foundation."
- Engaging in Social media outreach through Facebook/Twitter/Pinterest and the FPIES Foundation blog
- Expanding our online Provider Database to increase the number of FPIES informed providers committed to helping children living with FPIES.
- Achieving the Top-rated Non-Profit award from Great NonProfits, a distinction given to less than 10 percent of eligible non-profits.
- Appearing in “Big Y’s Dietitian’s Corner” and “Today’s Dietitian” articles, prominently featuring FPIES and The FPIES Foundation
- Participating in Feeding Tube Awareness Day, Rare Diseases Day and Food Allergy Awareness Week
The work does not stop
here. The FPIES Foundation is excited for the year ahead and plans additional
announcements in the coming weeks about our latest efforts in raising FPIES
Awareness.
This post was written by the Executive Board of The FPIES Foundation
