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This is an archive of the LivingWithTrisomy13.org site (2005-2010) for current information please see:
http://www.livingwithtri13.org

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please email Vanessa@livingwithtri13.org

In Loving Memory of This Treasured
Trisomy 13 Child

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JayLynn Burbidge

Click here to send an update or photos

August 25, 2009
lived 2 hours

  Tooele, Utah (UT) - Full Trisomy 13
7 lbs and 8 ounces at 20.5 inches
 
 



9-2-09

I just wanted to give you a final update on JayLynn. Our sweet angel JayLynn Mia was born August 25th at 11:52 am at the University of Utah hospital. She surprised us all by weighing 7 lbs and 8 ounces at 20.5 inches long. She arrived in her daddy's arms warm and full of life. Cooing and breathing was the sweetest sound in the whole operating room. We then welcomed her into our family only a few short minutes later.

Everyone was overjoyed to see her and hear her. JayLynn received her blessing and continued to surprise us all. She fought so hard to do all the things we had hope she would. She enjoyed getting her first bath with daddy and grandpa Rick, cooing and being ticklish the entire time.

We were all surrounded by so much love even the photographer felt it. JayLynn finally went back to her heavenly father two amazing hours after being born and filling our hearts with so much joy and love. We didn't think it would be more than seconds and we were blessed with hours.

It was her big amazing heart that finally said it had enough. She passed in my husband and I's loving arms so peacefully. We were very grateful for the time we had and enjoyed kissing, loving and holding JayLynn.

Monday was JayLynn's funeral, I don't think there could have been any other mother so happy with the way things went. Lots of family and friends came to show their support and love for JayLynn. And she looked so peaceful that I will always remember the look on her beautiful face. Both of JayLynn's big sisters got to say goodbye and they told us all how much they loved her. JayLynn has forever touched our family.

She is an angel and she is looking over us telling us that she is at peace. My husband and I are so grateful for this website and all the support we have received though it. We know that our love was never about how many chromosomes we have but about the way life works and how much JayLynn changed our lives.

Thank you all and God Bless. We know we will see JayLynn one day and she will be just as perfect as she was the first time we saw our angel. xoxo The Burbidges

   

Update 8-17-09

Dr. Byrun decided that since I delivered my other two pregnancies at 38 weeks that we are going to take JayLynn at 36 weeks. So the 25th of this month we are going to be having our bundle of joy come into our lives and stay for how ever long she is willing to be her with us.

The excitement and nerves are kinda overwhelming. I'm excited to meet her and see this little person who has put so much faith into me and my husband. I'm very nervous that I won't be able to say goodbye and I know that when the time comes I won't want to.

JayLynn has been a blessing to us and she has forever changed our lives. We had some pictures done and I am enclosing a few. With only a week left we are taking our time enjoying what time we have as a family.

My brother recently had a baby and I thought I would have a very hard time seeing him but it turns out that I'm overjoyed that he is healthy and beautiful. It helps me to deal with JayLynn and her passing to know that she will be watching over us, knowing we will think of her everyday with love and joy. I'm very grateful for the experience to have someone so special come into our lives and the fact that I've meet some of the most supportive people.

Thank you very much all of you for everything the prayers, the gifts, and the joy of knowing I helped someone as you have all helped my family.

Pictures: Blonde is BriLeigh Brunette is Trinity my husband Cortney and myself Jessica


 

 

Update 7/28/09

I just wanted to give you an update once again. JayLynn has Holoprosencephaly and full trisomy 13. Her facial features haven't developed as much as we had hope. I'm struggling with the gestational diabetes once again. My blood sugars are really high so we might have to try insulin which is one more thing to add to that long list of stress lol.

We are enjoying the rest of the short time we have with her which will be about a month. Dr.Buyrn wants to take JayLynn at 37 weeks so that i won't put so much stress on her little body. We are doing this by c-section.

We have been told we will have a short amount of time with our beautiful gift so it seems like I'm not ready for this month to fly by. We have been meeting with the Angel Watch ladies and they have been a great support for both me and my husband.

We did our maternity pictures with Now I Lay Me Down To Sleep which was a wonderful experience once I get them I will email then so you can post a new picture. I want to thank everyone who has been an ear, a shoulder to cry on or someone who has just touched our hearts with this experience. Thank you all our best the Burbidges

Jessica
Boo_Baby05@hotmail.com

Update 6-24-09

I just wanted to update you on our progress!! We found out she has full Trisomy 13 and she also has a disorder I forget the name but it means the fronter part of her brain (in Latin) and before the doctors said JayLynn (that is what we are naming her) was almost a month behind well we had another ultrasound and she is only a week behind so she has caught up!!! We still have hope and we are sticking with our goals, we found a new doctor her name is Dr. Buryn, an amazing lady!!

Our main goal is to get her home so she can be with everyone who loves her. and the doctors have been very understanding and are going to try to help us reach this goal. We are still preparing for the worst but hoping for the best. we are doing fund raiser because the funeral is expensive but I feel her moving everyday and I'm so grateful for the wonderful people this has brought into our lives!

I know JayLynn is going to be a fighter I can feel it and I know our family is going to fight for our newest blessing!

I just wanted to thank everyone who has come into our lives and helped us through this it means a lot and we are all very grateful!! thank you for your time hope everything is well xoxo

Jessica
Boo_Baby05@hotmail.com

5-17-09

Hello my name is Jessica Burbidge. My due date is September 14th 2009 but the doctor say I’m measuring small and moved me back about three weeks. My husband and I just found out at our 20 week ultrasound that our daughter has Trisomy 13. We don’t know any more that it’s the 13. We go to the doctor tomorrow to find out all the information, our options, and try to figure out where to go from here.

At first we were heart broken and didn’t know what to do the doctor strongly suggested that we abort the baby but I felt in my heart that it was not an option. We have two other children both girls BriLeigh is 3 and Trinity is 2 they are very excited to be big sisters.

Our entire family supports us and wants all the information they can get their hands on as well as ourselves. We don’t feel it is our choice to give up on our little girl before she has a real chance to show us how strong she is. And we feel that in every way she is a blessing and can’t wait to have her in our lives.

We live in Tooele, Utah and our e-mail address is Boo_Baby05@hotmail.com or cortneyburbidge@yahoo.com Jessica

 

Submitted 5-17-09

 

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All text and graphics © LivingWithTrisomy13.org 2005-2010 - all rights reserved
Use prohibited without permission
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 (Patau Syndrome) - 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.
 
 

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