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
Create a Page for My BusinessReport Page
 
KellyandAndy Rackley

KellyandAndy Rackley Hello...My name is Kelly and my husband is Andy...My son Peyton was born July 2007 with tef/ea...He is still on stage 3 baby foods and can eat crackers or vanilla wafers smashed up..he does love juices from peas or spag sauce...He only says a few words and is not potty training yet...He is supposed to be starting half ...day at day care on Monday(if they will take him not potty trained). Im excited and nervous all at the same time...Are most kids with this slower to develop then others....we have NEVER had anyone to talk to who is going thru the same thing so it is GREAT to find this on facebook.

See More
November 5, 2009 at 1:15pm · Report
Lori
Lori
Hi Kelly my son Brandon was born on 4/9/07 with TEF/EA and severe tracheomalcia, my son did not start walking until he was 18 mos and talking until he was almost 2. We had ALOT of help from early intervention and he caught up very quickly! Our son is in daycare and from all his hospitalization I feel it is TRULY the best thing for him to be around other children since all he's had his hospitals and docs most of his life!
November 8, 2009 at 2:15am