You have guest access to browse, login, or register.

WelcomeAboutShare With CareHelp
Share Your Story. Participate in online discussions about premature babies, start a blog, or just meet other NICU families. March of Dimes  
HomeCommunity CenterShare Your StoryParent to ParentGet Involved
 
SHARE HOME >  SHARE YOUR STORY >  ALL SHORT STORIES >  SHORT STORY ARCHIVES - 2006

Our TE fistula miracle

Diana G - 02:27pm Jul 3, 2009 EST

Our beautiful little boy was born this past December. The next day (after trying unsuccessfully to convince the nurses that something was wrong the entire day before), he was diagnosed with TE fistula with esaphageal atrasia. We had him transferred later that day to a better hospital with a top ped. surgeon. His surgery took place at 3 days old. He had a G tube put in and the TE fistula was repaired. The G tube was removed shortly before his discharge and he has been nursing beautifully. He left the hospital at almost 4 weeks old and is being followed by his surgeon, neonatologist, and ENT for laryngo-trachea malasia. His cry still sounds as if he's gasping but his voice and noises are greatly improving. His 3 year old sister fed him a raisin once when my back was turned and it got stuck in his esaphages but at his next feeding he threw up with lots of force and luckily the raisin came out. He has not started solid food yet and I'm a bit nervous to start but otherwise he's doing great.



  OutlineAll MessagesOlder ItemsOldest ItemsNewest ItemsNewer Items

ehbeagle - Jul 3, 2009 4:41 pm (#1 Total: 5)  

 

Welcome to Share and congrats on the birth of your son. I am glad that he is doing well. I do not have any experience with TE fistula. I will keep you all in my prayers. God bless,

Elizabeth

Angel Love - Jul 3, 2009 5:13 pm (#2 Total: 5)  

Looking forward to seeing you at Shareunion October 1-3 in Atlanta, GA!!  

Welcome to Share!

I posted on the other entry that you posted in the Parent to Parent section, but wanted you to know that we're here to listen any time you need someone to talk to. There are others here who have experience with this situation with their own children and I'm sure they'll be posting soon as well. I look forward to hearing more about your little man!

Tracy

vicki stewart - Jul 3, 2009 5:52 pm (#3 Total: 5)  

 

Hi and welcome to SHARE! My daughter was also born with a TEF and esophageal atresia. She is now 16 months old and doing great. I understand you being nervous about starting sold foods~ I was too. For us taking it slow was the best way to go. We would offer baby food, but didn't try to force it. She recently made to transition to table food about a month ago. I'm glad he is doing so well! I would love to hear more about him
Vicki

KHolley - Jul 5, 2009 6:48 pm (#4 Total: 5)  

 

Welcome to Share. I am so glad to hear that your son is doing so well after such a scary start. Thank you for sharing your story!

Katie

Grace's Mom - Jul 7, 2009 9:38 am (#5 Total: 5)  

^i^D'Lon Grace^i^ ~ Forever 3 ~ Missing you every second of every day! (I HATE PH!)  

Hello and welcome to Share. It is nice to hear that your little boy is doing so incredible after a very scary start. Thank you so much for sharing your story!

Take good care,
Yolonda



  OutlineAll MessagesOlder ItemsOldest ItemsNewest ItemsNewer Items


To post, please login or register.



 
We are pleased to provide a forum for sharing, and remind everyone that the viewpoints, opinions and actions expressed here are those of the individuals themselves, and may not reflect March of Dimes policies or positions. Information on this site does not take the place of guidance from your health care provider. Always verify information with your health care provider before taking action. Any messages or stories shared on this site may be used in other March of Dimes marketing activities.

Donate now!