Home SEARCH What is Trisomy 13? About This Site Donate
Contact Us

  Embracing Life - One Moment at a TimeTM

LivingWithTrisomy13.org

Ironman for Kids - The Living with Trisomy 13 Community thanks Michael Hennessey for helping to raise awareness for Trisomy 13 and other related disorders. See Video & Details>

In Loving Memory of This Treasured
Trisomy 13 Child

< Memories Page

Lincoln Tanner Roberts
June 19, 2006 - July 7, 2006

 


 

Phoenix, Arizona (AZ) - Full Trisomy 13

Jill Roberts (Arizona) is available for immediate support
623-521-0212  jill@oneplacechurch.com


Our story began on June 19, 2006 with the birth of our precious baby boy Lincoln Tanner Roberts. I gave natural birth at 10:26 in the morning at 38 weeks; he weighed 6 lbs 5 oz and was 18 inches long.  The nurse handed me our baby and after finding out that we had a boy, noticed that he had an extra digit on each hand. We were assured this was common and that it could easily be taken care of. We had a few hours with Lincoln before the nurse change and the taking of Lincoln to the nursery. We had no idea that anything was wrong until the Neonatologist came in to speak to us and let us know that they had to put in an IV in and give him oxygen. She explained to us that she believed that Lincoln had Trisomy 13 but couldnıt give us a definite positive answer until the blood work came back. She told us that the condition is fatal and that we would probably have a few days with him.

We at once went to the NICU to spend time with him as we did not know how long we would have. It seems a blur looking back on that time. A rush of pure joy of just having a child and a rush of devastation of finding out that your child is going to pass away.
 

We spent a full week at Phoenix Baptist Hospital. The nurses and doctors were so amazing; they taught us how to care for Lincoln as he was on oxygen and a feeding tube. He was able to suck but just not enough for a full feeding. We decided to bring Lincoln home on Monday morning June 26th; it was one of the scariest days of my life. We had a rush of emotions of not feeling prepared to care for our sick baby and not knowing how long he would be with us. We did have the wonderful support of Hospice of the Valley. Having Lincoln at home was so great, he transitioned well and it was so great to be together as a family with our 1 1Z2 year old son.
 
Lincoln continued to do well, eating more and needing less oxygen. He wasnıt as sensitive to light and noise and could even tolerate his brother messing with him a little. We had so much hope that he would be with us for a long time. On Wednesday July 5th he had his first apnea episode, he couldnıt get settled down and was held his breath while he was crying and passed out from lack of oxygen. We were so shaken. The following day he continued to have
more episodes and we knew that he wasnıt doing well. We had a family friend come over to take pictures on Thursday afternoon and about one hour after she left Lincoln really started to go downhill. He stopped breathing for almost 4 minutes and we thought he had passed and then all of a sudden he took a huge gasp of air and regained breathing. It felt as though our heart was being ripped out every time this happened. This continued through the night many times over, he just kept holding on. We said goodbyes so many times, it was torture. I couldnıt let go of him, I wanted every second I could holding my incredible son. He took his last actual breath in the arms of his daddy and passed away in his mommyıs arms. I held him for a long time, rocking him and weeping. Lincoln went to be with Jesus on July 7th at 1:40 in the afternoon. We were able to have 18 days together.
 
During our journey with Lincoln there is a scripture that fully explains our feelings in all that we went through in this struggle. It is Lamentations 3:1-32, it speaks of desperation and feeling of abandonment and in the middle it starts to speak of hope and Godıs mercies and that we wonıt be consumed. This scripture was a huge encouragement to know that Godıs mercies donıt fail. I still donıt understand why this happened, Iım sure I never will. But I do know that God is gracious and He is still faithful.
 
If there is anyone that reads this and is in the Phoenix area and wants to talk to someone who has gone through the experience of having a Trisomy 13 baby I would love to talk, listen and cry with you.
 
Mark & Jill Roberts
623-521-0212
Phoenix, Arizona


 
 

 

 

 

 

 

 

 

 submitted: 9-20-06

 

Click here to download printable LivingWithTrisomy13.org "awareness cards."

Living with Trisomy 13
Focused on prayerful support and gifts of love to those touched by a Trisomy 13 child.
Inspired By An Angel
Attn: LivingWithTrisomy13
15802 Springdale St.. #68
Huntington Beach, CA  92649

info@LivingWithTrisomy13.org

 

 

Text and graphics İ 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

Translation
Search Specific Languages or Countries

 

Design & Hosting lovingly provided by::
Apke Web Services