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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.


10 July 2019

Children’s book Havva, the giraffe that can’t eat leaves.

When our beautiful twins, son Mats and daughter Jinte, [...] LEARN MORE

07 August 2018

Useful TOF/OA Terms in various languages

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

06 August 2018

ERNICA has launched its website ! The European Reference Network for Rare Inherited Congenital [...] LEARN MORE

Record number of Adult TOFS attend 2018 Adult TOF Seminar

A record number of adults born with Tracheo-Oesophageal Fistula [...] LEARN MORE

Glossary on Esophageal Atresia in 9 languages

For the EA travelers, here are 70 keywords translated [...] LEARN MORE

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