EAT
@eatfederation
EAT is a federation of member support groups each associated with the rare congenital condition of Esophageal Atresia (EA).
ID: 1394699012
http://www.we-are-eat.org 01-05-2013 13:48:45
368 Tweet
319 Followers
209 Following
Forging new connections: Only 0.5 % of babies are born with a congenital disease, but 40 % of babies with #esophagealatresia are premature. Yesterday we were meeting up with Silke Mader, founder of EFCNI network, at #ESPHGAN to raise awareness for our cause.
We are very proud to announce that Graham Slater, former chair of EAT, was elected a member of the board of EURORDIS-Rare Diseases Europe, the alliance of over 1,000 rare disease patients organisations in Europe! Congratulations, Graham! #ESPHGAN23 #esophagealatresia #raredisease
Surgical Treatment of Esophageal Anastomotic Stricture after Repair of... sciencedirect.com/science/articl… BCH Department of Surgery #SoMe4PedSurg StayCurrentMD EAT jpedsurg
EAT at the #ERSCongress: We are proud to speak about the topic of #esophagealatresia as a lung disease on #PatOrgDay2023. European Lung Foundation
The joint meeting of the International Network of Esophageal Atresia (INoEA), the Pediatric, Adolescent and Adult Foregut Interdisciplinary Society (PAAFIS), and Aerodigestive Society will be held in Istanbul, Türkiye between April 30 and May 3, 2025. More: we-are-eat.org/news/inoea-paa…
Bronchiectasis Patient Conference 2024: Saturday 23 March 2024 from 10:00 to 16.00 CET. European Lung Foundation and @EMBARCnetworkonline present the annual bronchiectasis patient conference. Register here: europeanlung.org/en/get-involve…