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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

27 August 2015

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EAT Medical Advisory Committee

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

26 August 2015

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AFAO families day 2015

Here is a storify summary  of the annual families [...] LEARN MORE

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Report on gastro-esophageal reflux from Shelley

Dear fellow-sufferers of esophageal atresia, I am 18 years [...] LEARN MORE

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TOF/OA Leaflets now available in Arabic!

A  TOFS member Mayyada Wazaify  translated some of the [...] LEARN MORE

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Getting ready for an EA European Reference Networks?

Yann Le Cam, Eurordis Chief Executive Officer and Matt [...] LEARN MORE

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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