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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.


06 April 2020

ERNICA COVID-19 statement

Extract from  Ernica  website Posted on 02 April 2020 The [...] LEARN MORE

27 March 2020

Coronavirus / advice from TOFS website

Thanks a lot to TOFS for this article We [...] LEARN MORE

11 March 2020

Information sources related to COVID-19

We are all concerned about the fast-evolving situation surrounding [...] LEARN MORE

08 February 2020

Prix Fanny-Séléna / Fanny-Séléna Prize 2020 / Call for projects / EA research

Opening of the research projects application process DOWNLOAD THE [...] LEARN MORE

02 January 2020

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

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

The TOF book

Most parents and families have never heard of oesophageal [...] LEARN MORE

5th International Conference on Esophageal Atresia, INoEA-FATE

Thank you to Christophe Faure, MD, Division of Pediatric Gastroenterology, [...] LEARN MORE

01 January 2020

TOFS Video/easy-to-understand introduction to TEF/EA

This short animation is a comforting and easily followed [...] LEARN MORE

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The sixth international conference on EA will be held in Cincinnati, USA, in 2022.