Food Allergy News and Research

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...

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Kids With Food Allergies
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