As many of you may know my youngest was diagnosed with FPIES (Food Protein Induced Entercolitis Syndrome) as an infant. FPIES forever changed our lives. The outside world suddenly became a terrifying place to bring my infant son because all it would took was a single crumb to turn our day into a medical nightmare. The FPIES foundation was not only an amazing resource but also a ray of light in the darkness of this disease. They became our only support and guided us to where we are today. I am forever grateful for them, their support and their resources.
Recently, the FPIES foundation reached out to me and asked if I was interested in writing a blog article for them about traveling with FPIES. Not only was I honored to have the opportunity to give back to them for all they have done for us but they also asked me to write a Disney article! (One of my favorite subjects!) Please join me in spreading FPIES awareness. I hope you enjoy my article Traveling to Walt Disney World with FPIES