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LeighAnnK

Avarey Grace Champagne~Mommy's Angel

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Where do I even start? This is the first time I have ever done anything like this, and trust me, I'm a rambler so this may take a while. My Avarey Grace is coming Feb 8th or 9th of 2012 and I couldn't be more excited and scared. My Fiancee, Kevin, and I first found out about Avarey's CDH on Sept 9th 2011. Let me tell you, there is nothing like seeing your first baby for the first time, then being told it's a GIRL , and then being told there may be a problem. Talk about something to bring you down. You spend the moment from the first time you find out your pregnant until the BIG ultrasound day imagining how your baby is going to look and what it is going to be, and then all of that is forgetten given a few simple words. It truly crushes your heart. Kevin and I had not heard of CDH until that faithful day and since then my whole world has been upside down. Avarey has left sided cdh and only her stomach and part of her intestines are up in her chest. Her heart is pushed all the way to the right, but it is full size, beating correctly, and pumping blood great! We have been told by doctor's that we have "the best case" for a "life threatening" birth defect. Being CDH parents we all know this still does not mean she will make it. I find that trying to explain it to people is one of the hardest parts. You never want to tell someone that you are having an unhealthy baby, and then further on trying to explain exactly what is wrong complicates things. As great as it is to hear "Oh babies make it all the time, babies that are born 3 months premature live to have perfectly healthy lives..."so on and so on. Or even worse, "Oh it's a simple surgery, babies are fighters, they always come out on top. She'll be just fine." No It's not OK, no it's not that simple. There are 1,000,000 things that could wrong, and the surgery is the least of the complications, she has to be able to breath in the first place. But people who are not CDH parents are supporters just don't get it. I know they mean well, but it's just not that easy. Or maybe this venting is just all the built up resentment.... I try to so hard to stay positive and i try so hard not to be angry, but it is nowhere near easy. Never in my life have I known what true heartache is till now. Never in my life have I ever cried to the point it hurts, and now it seems to happen day in and day out. I am finally moving forward somewhat, the mornings aren't as sad and the days don't seem as long. I know she still has a chance, but there is also that chance of what if. What if my angel doesn't make it, what if I decorate a nursery and no sweet baby girl to bring home to it, what do i do with all the cute pink baby clothes and the christening gown and her blankies? How do I ever move on? My support group from home is great, I could not ask for a better fiancee or grandparents for Avarey, but sometimes they don't can't quite get it. I'm her mommy, I'm suppose to keep her here, and what if I fail at that? Avarey's due date is fast approaching, as I much as I cannot wait to see her pretty little face and hold her tiny little fingers, I want to keep her inside as long as I can, that way I know she's safe. But until till I guess it's doctor appointments every week and a BPP test on Monday the 5th! (Prayers for that are more than welcome) And in the time being I'll enjoy every last kick,flip, and turn she makes and every last ultrasound screen I get to see her pretty face through! May God Bless each and every one of you!

Mommy Loves you Angel Avarey <3
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  1. Kara Mohmand's Avatar
    Hi, I understand how you are feeling. Although this isn't my first pregnancy I am still feeling all the things you have written. I'm due with my son Caleb on January 23 but am told I will probably be induced a week early just so everyone is prepared. This is a scary thing to be facing and the hardest part seems there are no "real" answers until the baby is here. All of the uncertainty is hard to deal with sometimes. I completely understand how you feel anout keeping your daughter safe inside for as long as possible, for me the time just seems to be passing too quickly. Just know that even though you might feel alone there are others who understand and can relate. I will keep you and Avarey in my thoughts and prayers daily.

    Kara
  2. JadeHunt's Avatar
    LeighAnn,
    Your entry brought me to tears, as I know exactly how you are feeling. I have thought those same thoughts, had those same feelings, and cried that many tears. My son, Liam passed away on June 25, 2011. He was one month old. He was born with CDH, though we had no idea he had this birth defect. For nine months, my husband and I had doctor after doctor tell us that we were having another perfectly healthy baby boy. When Liam was born, our excitment turned into complete devastation and shock.

    Liam was at Children's Hospital Boston and was doing rather well. He suddenly took an odd turn. He nurse thought he had an infection- she was right. The infection was bigger than any antibiotic and five days later, Liam was gone.

    You are right in that 1,000,000 things can go wrong- this is true for any pregnancy. I guess as parents, we assume the risk. I want you to know that you are not alone and that there are many mom's like myself who are here to offer any and all support we can. Please don't hesitate to contact me. I try to write a blog on Liam's page once per week, but I'm making it a priority to do this every day. It's becoming therapy for me, and helps me to feel closer to Liam.

    My thoughts and prayers are with you, Avarey and your entire family! God Bless and take care of yourself!

    Jade
  3. Chris and TracyMeats's Avatar
    Praying for Avarey and strength for you. Love that baby girl and cherish every day with her. Believe in the strength of your baby girl. I pray you are surrounded by much love this holiday season and feel the love from your unborn daughter. (((HUGS)))