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In Loving Memory of This Treasured
Trisomy 13 Child

< Memories Page

 Nathan David Bouligny

February 8, 2007

  San Diego, California (CA) - Full Trisomy 13
Becca Bouligny bbouligny@yahoo.com

Nathan means Gift
David means Beloved
He was our “Beloved Gift”

Why would a good God allow these type of things to happen?  
As you’ll read in John 9   The Man born Blind.  As he walked along, he saw a man who had been blind from birth.  His disciples asked him, “Rabbi, was it his sin or that of his parents that caused him to be born blind?”  “Neither,” answered Jesus:  ”It was no sin, either of this man or of his parents.  Rather, it was to let God‘s works show forth in him....”
Click here to listen to Larry's message about his son Nathan (In Audio) Also ~ The "powerpoint presentation" for the Sermon
 
 

Hello friends,
Our little Nathan David was born this morning at 3:15 a.m., weighing in at 4 lbs. 11 oz. my husband and I enjoyed him for an hour and 45 minutes and then he went home to be with our Heavenly Father.

He was sweet and wonderful and breathed all by himself. He struggled a tiny bit, and eventually just decided he would rather be with the Lord. He went very peacefully. We are so blessed to have met him and spent the time with him that God granted us.

The Lord is good and answered so many prayers through our little Nathan.

Becca
mom to angel Nathan David, 2/8/07

- - - - -
11-25-06
Thanks so much to everyone for loving and praying for us and the other prenatal families.  We certainly appreciate it and can feel the Lord moving in our lives.
 
An update on Nathan David: We went for an echocardiogram about ten days ago.  It went...as we expected.  at this point, no news is really "bad news"...it is all just plain news!  Nathan's heart has a number of issues.  they originally said HLHS, but the cardiologist said it is possible that his heart is "flopped" (yes, that is the proper medical term - haha!), and that it is the right side that is underdeveloped.  They think they saw the aorta, but could not find the pulmonary artery.  They believe that is because it isn't there, but aren't sure.  so at this point they are calling it pulmonary artesia and truncus arteriosis.  They said we could come back for another echo if we like.  not sure if we will go or not.  I tend to try to gather every ounce of information possible, whereas my husband doesn't really see the point of going back in, seeing they will do an echo when Nathan is born.
 
Right now there appears to be a small artery that is looping around and pumping to the lungs.  If we do have a live birth (hopefully!), the valve that usually closes in the first few days will pose a huge threat to his life if it actually closes (sorry, forgot the name...but you all know it!) .  however, we know that we are not dealing with "normal" anatomy...so it is possible that it won't close.  only God knows and He has finally taken me to the place where I am GLAD to not be in control! 
 
During the echo Nathan's heart rate went way down for extended periods of time (down to 60 for a number of minutes).   The doc said this could be an indication of a problem, or it could be an exaggerated slowdown that every baby has.  He was nice and vague!  We'll see.  God is SO good and we know that Nathan will be with us for the appointed amount of time that He ordained before the creation of the world.  He is gracious to give us the fulfilling peace that comes in knowing and understanding Him. 
 
We're having turkey dinner tonight...so back to work!
 
Blessings to all, i am so appreciative of the support we have here.
Becca, wife to Larry, mom to Nathan David (full T13 due 2/21/07) and furbabies Samson and Delilah

Becca Bouligny bbouligny@yahoo.com

 

 

 

 

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Text and graphics © LivingWithTrisomy13.org 2005-2007 All information found on this site was submitted to us directly by the families and used on this site with their permission.
Cover photo of Pamela Sullivan & her precious daughter Maria, copyright Pamela Sullivan 2004, used with permission.
If We Hold On Together  Song Copyright 2002 by Patricia Welch, Ltd. All rights reserved.   Used with permission.
 
*Disclaimer
All material on this site reflects our personal journey with raising a Trisomy 13 child. It is not meant to replace any medical advise of a professional familiar with your specific condition. The personal journeys of any parents on this site are only their opinions and their own journey with having a Trisomy 13 child. You should consult with your own physician or other medical professional regarding the opinions or recommendations expressed within these pages as to your own child's symptoms and medical condition.
 

Looking for ALL families who’ve had a trisomy child of any number. Whether you terminated, miscarriage, had a stillbirth, live birth - living or deceased. Including adoptive and Foster parents. Please fill out the TRIS survey  to help update the medical literature and to improve the quality and availability of medical care. Tracking Rare Incidence Syndromes (TRIS)  Click here to add your information

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