EA/TEF Family Support Connection
The EA/TEF Family Support Connection was formed by and for families of children born with (Esophageal Atresia and Tracheoesophageal Fistula) EA/TEF and the medical professionals who treat them.
Information
Founded:
1992
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Amy

Amy Hello, I am excited that I found this facebook! My son is 11 years old, and was born with EA/TEF with severe trachia malacia. For all the new parents, grandparents, siblings, or just loved ones, please feel free to contact me, I am a research MOM, and have been down a long road! I can't wait to see everyone's story, and wish everyone a great day!

October 23, 2009 at 9:40pm · Report
Terri Housley Mullins
Terri Housley Mullins
Hi! Is your son's trachealmalacia better? Lilli really honks when she gets winded.
December 25, 2009 at 4:13pm