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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.


24 April 2015


Outcomes from the first international EA survey.

In this video, Graham Slater, EAT Chairman, presents the [...] LEARN MORE

16 February 2015


EAT Medical Advisory Board

EAT is delighted to announce that the INoEA (the [...] LEARN MORE

23 December 2014


EAT online survey: a clear picture of EA patients issues.

Dear EA patient, Do you suffer from recurring reflux [...] LEARN MORE


Storify Bridging the gap – day 2 –

[View the story “Bridging the gap – day 2 [...] LEARN MORE


Storify Bridging the gap – day 1-

[View the story “Bridging the gap – day 1- [...] 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