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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 www.we-are-eat.org 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.

News

16 February 2015

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EAT Medical Advisory Board

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

23 December 2014

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

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

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Storify Bridging the gap – day 2 -

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

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Storify Bridging the gap – day 1-

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

24 October 2014

SONY DSC

Posters exhibition – 3rd international conference on esophageal atresia- Rotterdam

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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