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LivingWithTrisomy13.org

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In Loving Memory of This Treasured
Trisomy 13 Child

< Memories Page
 

 Amaya Faith Lynch

August 12 2006 - August 20, 2006
With us for:  7 days 19 hours and 44 minutes  

  Sheridan, Oregon (OR)
 

 

 
 

"She was our true joy.  We will always be thankful for the time God allowed us with her and will continue to seek His will.  

God's plans are always perfect and we know that Amaya's life will be used in a glorious way.  We have already seen her make such an impact on so many people and will be looking forward to the continuation of God's plan as He reveals it to us."

Aaron & Gina Lynch (available for immediate support)
503 843 0987
aaron.gina@gmail.com
If anyone wants to talk feel free to call.   


Amaya Faith came into this world on August 12th 2006.  She was barely breathing, not crying and not responding to stimulation from the  doctors.  My husband and I cried and prayed and waited, and than there was a faint cry. What a wonderful sound, one that brought even more tears to our eyes. After two failed intubations Amaya began to breathe on her own and I was able to hold her for just a brief moment before they rushed her and my husband off to the NICU.  As lonely as that feeling was I insisted that my husband stay with her, thank God for friends.  I was so thankful to hold her before they took her way, but how empty a feeling it is to be pregnant, give birth, and than sit in a hospital bed with nobody but a good friend.  You are suppose to be cradling your newborn close on your chest as your husband looks loving down at both of you.  I was determined to get to the NICU asap and was out of bed within a half an hour.  

After my one hour check I was ok'd to make the wheel chair ride over to see my precious baby and husband.  She weighed 4lbs 5oz and was 17 1/2 inches long.  She had had a difficult hour and they had to try to intubate again, but once again the attempt failed and she started to breathe on her own again.  We were able to spend a glorious week with our baby girl, holding her, loving her and treasuring every moment God allowed us to have with her.  Through the week we encountered lots of trying times, there were two nights when Amaya had to be  resuscitated 3 times.  The 2nd night on the 3rd time it took chest compressions to get her to come back.  The next night we had to make the hardest decision of our lives, we decided that if she had another episode that we were going to just hold her and love her.  

We knew that she couldn't be intubated and having watched them do chest compressions and knowing how hard they were on her little body, we couldn't put her through any more pain.  We also knew that she was God's child, given to us to care for until He chose to bring her back to him.  We had two and a half more wonderful days with her after that and were blessed by every minute with her.  On Sunday morning at 6:30am her oxygen alarm started beeping and within minutes her heart rate was dropping, my heart raced as I held the oxygen right up to her mouth and rubbed her back as vigorously as I could, we tried repositioning, 100% oxygen, and lots of stimulation.  

My husband and I cried and prayed and tried, but knew God was saying it was time.  We got her out of bed and I held her as Aaron stroked her cheeks, with the sun shining in our window we rocked our baby girl in her last half hour with us.  We cried and prayed as we treasured and thought of each moment we had been blessed with. She left our arms and went to be with Jesus at 7:07am on August 20th 2006.  She was our true joy.  We will always be thankful for the time God allowed us with her and will continue to seek His will.  

God's plans are always perfect and we know that Amaya's life will be used in a glorious way.  We have already seen her make such an impact on so many people and will be looking forward to the continuation of God's plan as He reveals it to us.  The pain of losing a child, a baby, is indescribable.  The hurt is so deep and the pain so overwhelming that it takes a constant reminder to trust God and His sovereignty.  God does not make mistakes, He creates all life and knows each one of us inside and out.  We are honored that He chose us to be Amaya's parent's, even if the time seemed to short, it was a wonderful week.  God's strength and comfort will sustain us in this time, as well as the faithful friends and family He has placed in our lives.  I know that every day will bring new reminders and new tears, but we will forever be thankful for the life of our little Amaya Faith.  Aaron and Gina Lynch

 

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August 26, 2006

Amaya Faith lived 7 wonderful days and now rests in her heavenly home with Jesus.  More on her 7 days of life http://amayafaith.com/

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Update: August 5, 2006
Thursday we had an ultrasound and growth check, our little girl surprised us with a 12oz. weight gain (which for her is good) in only 2 weeks.  She is measuring at 3lbs 14oz., but still about 5 weeks behind in growth.  She was as stubborn as usual and wouldn't show us her face, but were able to see her cleft lip a little bit.  

After our ultrasound we had an exam and found out that I was almost 4cm!!!!  The doctor went ahead and scheduled our induction for the 18th, but told us not to be surprised if she arrives earlier.  We are awaiting her arrival eagerly and can't wait to meet her.

Thank you all for your prayers and support.  We continue to pray for Amaya's healing and trust God completely with her life.  We love her so much and are planning to bring us home a new addition in the next couple of weeks.

- - - - - - - - - -
" We are so blessed by her already and God has given Amaya to us for a reason."
~ Gina Lynch

Hi ThereseAnn,  this is Gina Lynch.  I spoke to you back in April about our little girl Amaya Faith.  I just saw that this has been added to the website so I wanted to pass on our information.  We do not have an official diagnosis, choosing not to do the amnio, but the doctors feel certain that she has trisomy 13.  We are due on August 30th but planning to deliver on the 18th of August.  

Amaya is doing well, each kick and squirm is a delight.  She is so strong and kicks me harder than any of my other 3 girls, it is hard to imagine that anything could be wrong.  We are so blessed by her already and God has given her to us for a reason.  

God remains faithful to give us strength, comfort, scriptures and songs to remind us He is in control.  We are believing that God can do a miracle, He is the creator, the comforter and perfector of all things.  

Proverbs 3:5 says

"Trust in the Lord with all your heart and lean not on your own understanding.  Seek his will in all you do, and he will direct your paths." (NLT)

We live in Sioux Falls, SD our email is aaron.gina@gmail.com
Amaya's website is http://amayafaith.com
Our number is 503 843 0987,  if anyone wants to talk feel free to call.   

 

 

 submitted: 6-10-06

 

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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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