Saturday, April 11, 2009

Day 7

How do you talk about congestive heart failure in a 6 day old baby? How do you do it without chasing tears down your face, hoping to catch them before they short-circuit your keyboard?

The medical team extubated Peyton today. For 30 minutes this evening, she was breathing on her own. Then she started crashing. The extra pumping labor of her heart, as I understand, increased the pressure in the pulmonary artery (the blood vessel taking blood from the heart to the lungs to get oxygen). This increase kept her lungs wet, and she wasn't able to keep breathing on her own. It was just too much work, so they reintubated her.

Just when we had hopes for a normal day, a stable day, an uneventful day, we are told in no uncertain terms to leave the room. It was a long walk to waiting room, holding hands, choking back the tears.

The attending told us that she's going to remain intubated through the surgery. The cardiologist has ordered another echo cardiogram for the morning, and he called the cardiac surgeon, and it looks like the surgery may get pulled up to Monday. We've been told to expect to meet with the cardiologist in the morning and one of the surgeons tomorrow night.

7 comments:

  1. Karl and Rayna,
    Know that God is with you. You don't need to be strong or tough it out, just keep the line open to God. He can work miracles, just look at my nephew Rudy, rudysbeat.wordpress.com. We are praying for you. Rejoice! HE HAS RISEN!!

    Alex

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  2. Dear Karl and Rayna,
    Our thoughts, prayers and hearts are with all three of you...God is there too! We hold you in our prayers constantly. May He who is able to do all things, bring healing to precious Peyton. She is already a part of our hearts forever. May God be glorified! Love, C & B

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  3. Grandmommy and Granddaddy are shedding tears with you. And praying our guts out...for Peyton, for you (father's heart to father's heart), for Rayna (mother's heart to mother's heart), for Wayne as he works through another trauma, and for the whole rest of both families. Thanks to all who are praying with us.

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  4. Are they treating her sufficiently to keep the other organ systems functioning at an OK level?

    I'm so sorry!

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  5. Praying for your family. I heard about Peyton's heart defect from Deborah Tomei. I am a heart mom to a beautiful and happy two year old girl. She will have her seventh heart cath next month. She has had two open heart surgeries. I know how heartbreaking and confusing it can be, especially at first. Feel free to contact me at www.RamonaMae.com with any questions or just for support.

    Jane Deitrich

    P.S. What is Peyton's diagnosis?

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  6. Karl and Rayna,

    My heart dropped as I read this post. I'm so sorry you guys. We are praying for Peyton as God brings her to mind more often than I can count. We will be at the noon service tomorrow so maybe we will see you there. If not, you will be in our thoughts and prayers the entire time.

    Love,
    Jeremy and Lyndsi

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  7. Karl please keep writing...Soon the news will be good and we will praise god for the strength we have gained through these ordeals. Then we will read of hapiness and graditude. I am sure.

    Love Wayne

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