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The Federation of Esophageal Atresia and Tracheo-Esophageal Fistula

EAT is a federation of member support groups each associated with the rare congenital condition of Esophageal Atresia (EA). Each of the member organisations of EAT operates on a charitable basis in its own country.
The main goals of are to help EA patients and health professionals share their knowledge and experience, promote awareness of the condition across the world and support worldwide research and collation of information concerning the treatment and care of people born with esophageal atresia.


26 December 2016


First 23 European Reference Networks for Rare Diseases

Great news that ERNICA, the proposed European Reference Network [...] LEARN MORE

09 July 2016


Tracheoesophageal Fistula Repair

This 3D medical animation shows a tracheoesophageal fistula in [...] LEARN MORE


EAT to be represented on the Advisory Board of ERNICA

EAT is pleased to report that ERNICA (European Reference [...] LEARN MORE


A message from the EAT board

A quick glance at the headlines and you might [...] LEARN MORE

01 June 2016


Breaking news: OA 2016 Call for abstracts extended!

Call for Abstracts deadline extended The deadline for the [...] LEARN MORE

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We are grateful to Covidien for their financial support to create the EAT website :

The 4th International Conference on Esophageal Atresia will be held in Sydney, Australia, 2016