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Thursday, March 24, 2011

Seriously.........you need to pick a position and stay there!

First of all let’s start at last Friday night…..no sooner I posted the last post about the baby being transverse, I started feeling him shift around.  Soon the shifting turned PAINFUL and I came to the conclusion he was flipping.  For about 2 hours I was seriously uncomfortable as he maneuvered his way into whatever position he was going for.  Luckily I had read online that if a baby is transverse at the point in pregnancy, like my baby was, it could feel like you were going into labor if they move into a completely different position.  So I didn’t completely freak out when I was in a good amount of pain and my stomach looked like something from the Alien movie.  It took the baby a good 2 hours to ‘move’ positions.  My stomach, which has stretch marks just from him flipping positions, was sore the rest of the weekend.  So it was hard for me to tell what kind of position he had flipped into.  Of course I was hoping for head down!
            Fast forward to my most recent round of appointments at the Fetal Care Institute this week.  We started with another Fetal Echo.  I convinced them to use the ultrasound machine to tell me if he was head down because I couldn’t stand the suspense…………..and HE WAS!  YIPEE!  So we now run the chance of having a normal deliver (hopefully) and he better NOT be thinking of getting out of that position.  I can’t take another 2 hour round of flipping.  OUCH!
            So back to the Fetal Echo – the actual function of the heart still looks very normal.  Good good good.  The negative – it appears the left side of the baby’s heart is somewhat small.  The doctor feels that it is small due to the position it is in and room it has to grow.  She didn’t feel, at this point, it was affecting the functionality of the heart.  Since the heart is growing in a different place, it may just have to grow a little differently.  But from the testing done, even though it is slightly misshapen, it seems to be working normally at this point.
            Following the Echo we had another upper level ultrasound.  This is where things get interesting.  The bigger the baby gets, the more difficult it is to get a clear image of his organs.  I had trouble spotting things that I have become accustom to seeing on a regular basis!  And some of the organs I was hoping to see, like the left lung, we could not see at all.  The docs told me it is not necessarily because it is not there; it is because it becomes increasingly more difficult to see from this point on.  So it is somewhat of a guessing game.  The baby is weighing in at a whopping 5lbs. 4oz.
            Both Dr. Yang and Dr. Vlastos still give us a positive vibe about the outlook of our baby.  He has come a LONG way over the past 8 months.  I am just now entering the 9th month of pregnancy.  Ye Haw to that.  This has been the easy part I guess.  The hard part begins once he is born. It appears that all CDH babies go on what is best described as a roller-coaster after birth.  They have a honeymoon period after birth where they are lookin good.  Then things will go way up and way down.  You just have to hope that your baby pulls through and back into the unloading zone of the roller-coaster.  I guess where you would “get off the ride” equals getting to take your baby home.  Which is ultimately what EVERY CDH PARENT HOPES FOR, as only 50% get to do it. 
            I have been following several other blogs of CDH parents who are due close to me.   Several of them have had their babies.  Some of the babies are still in the NICU fighting the CDH battle, while others joined the other CDH cherubs in heaven over the past several weeks.  My thoughts and prayers go out to each of those families – both those who are sitting day after day with their babies in the NICU hoping for a miracle and those who are grieving the loss of their miracle.  I feel every baby is a miracle, no matter how long they are with us.  I know soon I will be in their shoes.  I have tried to prepare myself the best I can for it.  But you can only do so much when you are on my end.  The rest depends on the miracle coming into this world on or around April 26th.

8 comments:

  1. Glad the serious talk helped. Obviously, he is going to be a great listener! You all four are in my prayers...love and miss you guys.

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  2. I just found your blog through Pearson's blog and wanted to let you know that I will be praying and following your baby's journey. I am the mom to a right-sided CDH survivor who was also more than 7 weeks premature. She is now a healthy 2 year old and I feel blessed every day!
    Hugs,
    Jennifer
    Mom to Dakota 12-25-2008
    jennifertrafton@hotmail.com

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  3. That was such a touching post, especially the end. I pray the baby has your strength to get through this. And that he stays head down!!

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  4. Janna, I came across your blog a few weeks ago and I have thought of you and your family every day since. I just had a 9 pound baby boy who laid transverse through the end of his pregnancy and it is HORRIBLE. I'll keep praying for you both. Miracles happen every day. Stephanie (Moore) Fox

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  5. Hi. I just came across your blog whilst looking up info on cdh. I live in Scotland a million miles from u but gave birth to a beautiful baby boy named max with left sided cdh 6 weeks early. He is now 17 months old and although tube fed i couldn't wish for a more content laid back happier little boy. I know u already know this but these babies are tough and when they fight they go for it! We have had the roller coaster of a lifetime but with strength, patience and the love of your family u can get through about anything. I will be thinking of u all and checking your blog regularly. U should look up avas blog whose mum terri is an absolute inspiration - she answered so many of my questions and still does. My blog is wwwmiraclemax.blogspot.com I hope he gives u inspiration too. Katie x x

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  6. Praying for you as you get closer to the fight to survive this birth defect called cdh. Know you are not alone. Thanks for the support on Ava's blog. It means a lot. Prayers and thoughts headed your way.

    ~Terri and Ava Helmick
    http://avaslifewithcdh.blogspot.com

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  7. Janna...your blog is one of the great things about the Internet. Having the opportunity to share your thoughts with other cdh moms, and they with you, is a g-dsend! Although we talk daily, I learn so much by reading your blog.

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  8. I just found your blog too and wanted to drop a note to say that I'm praying for you. Dr. Yang is amazing, you are in great hands. Everyone at CHERUBS is praying and we're here for you!

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