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Family's Every Meal Must Cater to Rare Disorder (Eosinophilic Esophagitis)

[Our apologies!  If you are visiting this link looking for the article on FPIES, please visit this blog post: http://community.kidswithfooda...rome-baffles-doctors]

 

Thank you to the Aurit family for sharing their perspective on living with eosinophilic esophagitis and for working on passing a law that would require insurers to cover medically-necessary amino acid formula for families in Nebraska.

 

The Aurit children and their mother, Sarah, all live with eosinophilic esophagitis (EoE), which severely restricts their diets and affects their quality of life.

 

Read the full article from Omaha.com  to find out what "Taco Night" is like at the Aurit household: http://www.omaha.com/apps/pbcs...G%2F703249930%2F1707

 

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Kids With Food Allergies
A Division of the Asthma and Allergy Foundation of America
1235 South Clark Street Suite 305, Arlington, VA 22202
Phone: 1-800-7-ASTHMA (1.800.727.8462)
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