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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

14 August 2017

Useful TOF/OA Terms in various languages

Terminology Glossary English Turkish Terminology Glossary English Spanish Terminology [...] LEARN MORE

20 July 2017

AFAO Family Weekend, every year, on the last week-end of June…

Meet and exchange with others, hear personal accounts, attend [...] LEARN MORE

10 July 2017

Professor Cattan talk about Tissue Engineering

25 April 2017

Celebration of the CRACMO Birthday, Lille, France.

The National Reference Centre of Congenital conditions and Malformation [...] LEARN MORE

22 April 2017

Storify on ERNICA kick-off meeting

[View the story “ERNICA: Kick-off meeting in Rotterdam” on [...] LEARN MORE

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

The 5th International Conference on Esophageal Atresia will be held in Rome, Italy, 2019