Love and Gratitude. Irelyn’s Story.
Erin is mum to her miracle daughter Irelyn. Beautiful Irelyn was diagnosed with Hydrops just hours before her emergency delivery. Her heartwarming story is below.
When our youngest daughter was born, God intervened time and time again to make sure she would complete our little family, and encourage our family to share God’s grace.
On August 20th, 2009 at 351/2 weeks pregnant, I woke up with very mild contractions that continued to get worse throughout the morning. By 10.00am I was at the hospital in the Labor and Delivery unit thinking they would check me, say false labor, and send me home beacuse I still had 4 weeks until I was due. I am so glad God decided to lead me into the hospital that day! (Gratitude #1). They kept me there all day until 530pm when they decided I was not ready and they would discharge me. A new nurse came on shift and decided to monitor the baby a little longer. I know now this was God intervening yet again. (Gratitude #2) Thank goodness they did not send me home because it was discovered that the baby was not moving much and her heart rate was a little low. An ultrasound was ordered. (Gratitude #3). Mine and Jesse’s world changed!
The radiologist read the ultrasound and discovered a large amount of amniotic fluid, and a lot of fluid that filled Irelyn’s chest and tissues. It was explained that she had so much fluid in her chest it had displaced her left lung and heart and pushed them both over to the right side of her chest. Both lungs were also completely collapsed. Our baby was not breathing! The specialists in Missoula had no clue as to why this had happened or what could have caused it. We were given four options on how to travel the 500 miles to Seattle, but knew that we would be flown medically as soon as the discussion began. There was no way Jesse was going to be left with a lady still in labor, with a very sick baby! When we arrived in Seattle at 1.00am the doctors ordered an ultrasound hoping that the delivery could wait until the morning, when the radiologists could read the ultrasound and a team of doctors could be put together for the greatest chance of success. After seeing the ultrasound it was decided that little Irelyn would be born within half an hour. I know that God was with those doctors as they made this difficult decision. (Gratitude#4). Within that half hour a large team of specialists was formed, given the background of what they were dealing with and prepared for surgery. We will be forever grateful that all of those doctors were available and ready at 2.45am on a Friday morning!
Irelyn was born by c-section at 2.58am and immediately moved to a separate room to be put on a ventilator and have chest tubes placed to drain the fluid in her chest. We found after the delivery that had we tried to deliver Irelyn vaginally it would not have been possible because of her very short umbilical cord and incredibly swollen body. (Gratitude #5). Finally, at 24 hours old little Irelyn was given no chance of survival if she was not moved to Seattle Childrens Hospital where the ECMO machine was available. The ECMO machine is a heart -lunch machine also knows as the last step in life support. The doctors at University of Washington Medical Center knew that Irelyn’s lungs needed time to heal while the mystery of the fluid was solved.
This was most definately the hardest thing I have ever heard. It brought light to just how sick Irelyn was. At 1.00am the night after her birth the very risky job of transporting little Irelyn was underway. This was the point when I begged God to please ride along in that ambulance with our precious daughter. The preperation of moving a newborn on a ventialator and chest tubes took two hours, all for a five minute ambulance ride to another hospital. My doctor pulled some strings to get me over to the children’s hospital because he felt it was important I be there when she arrived. In case Irelyn did not make it I would be able to hold my baby and say goodbye. Thank God Irelyn is a fighter (Gratitude #6) and she flew through the transport and onto ECMO with flying colours. Irelyn was then on ECMO for 10 days in order for her lungs to heal and the fluid in her body to stop being produced due to Chylothorax (A leak in the lymphatic system).
Her time on the ECMO machine was incredibly delicate as the doctors had to make sure that her blood, that was being routed out through a vein in her neck into the machine, then back into her body, stayed at the right consistency. If it got too thick she could form clots that could travel to her lungs or brain and kill her. If her blood got too thin we could lose our precious baby to internal bleeding. Her blood levels were checked every hour and adjustments were made when necesscary. In order to be taken off the ECMO machine Irelyn had to pass a trial run of 2 hours of monitoring her lungs to make sure they could work on their own. She barely missed the first test, but the following day proved what a rockstar she is, and her little lungs were ready to breathe!
She was on a ventilator from day 1 until she was 5 weeks old. Through most of her stay in the NICU, Irelyn had 2 chest tubes, one on each side of her chest, to continually drain lymphatic fluid. Unfortunately these little tubes tend to fall out and Irelyn battled back through the loss of three different tubes. Our little miracle was also forced to fight off a terrible blood born sepsis infection with the aid of some very strong antibiotics and the grace of God.
Through all of this Irelyn continued to amaze the doctors and nurses as she charged along on her recovery much quicker than anyone expected. Irelyn checked out of the NICU after 7 weeks, and was discharged home without any medical assistance. No Oxygen, feeding tube or medications! I’ve now been giving my baby loves for a year and a half! If anyone of these things had happened different Irelyn would not be with us. God is good, and blessed us through this journey.
Irelyn today, aged 18 months.

















That is such a wonderful story! I love that it has a happy ending. We thank God for our daughter’s miraculous recovery from a hospital acquired form of staph at 6 days old. Whew! It was scary but, she fought hard and God cared for her… now she’s 8 years old! You’ve inspired me to share Abi’s story. Thank you so much.
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Tam Reply:
March 22nd, 2011 at 8:10 AM
I would LOVE to read about Abi!
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