If you have a child, (or loved one, friend, etc.) born with Tracheoesophageal Fistula and/or Esophageal atresia, I would love to be of help to you. My son 3, was born with both of these birth defects, and I would love to answer any questions that you may have regarding the surgical procedures, what the future holds, etc. Feel free to ask anything, or share your own experiences...it's very therapeutic! 
[This message was edited by JorJor on 02-25-01 at 09:16 PM.]
[This message was edited by JorJor on 02-25-01 at 09:16 PM.]
