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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

19 January 2021

EAT has a brand new YouTube channel !

To share its videos with its members, the EAT [...] LEARN MORE

30 December 2020

The TOF Book

Most people have never heard of oesophageal atresia (OA) [...] LEARN MORE

29 December 2020

2 books for EA children : I am a TOF kid / Abigail’s Smile : A story about a child with EA

I am a TOF kid This book has been [...] LEARN MORE

20 December 2020

An ERNICA animation for parents and families

CAN EAT – Care and Nutrition in Esophageal Atresia [...] LEARN MORE

25 November 2020

Little Info cards make life easier for German patients with esophageal atresia

A lot of patients with esophageal atresia have a [...] LEARN MORE

23 November 2020

Rare Disease Week 2021 : save the date !

EURORDIS (a non-governmental patient-driven alliance of patient organisations) organise [...] LEARN MORE

06 November 2020

09/11 Kids art auction for OATSA – South Africa

On the 9th of November, OATSA organize a kids [...] LEARN MORE

26 October 2020

Care recommendations for the respiratory complications of esophageal atresia-tracheoesophageal fistula

The International Network of Esophageal Atresia, Respiratory Complications Working [...] LEARN MORE

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