|Baby's 1st picture|
They also gave us all the information for all the testing you can have done. She mentioned the First Trimester Screening. I had not had this done w/ my other two, but thought what the heck...I'll get to see the baby again on an ultrasound. So we scheduled that for May 2nd.
I never thought I'd get a call from Maternal Fetal Medicine, that my baby had a 3% chance of having Down Syndrome. Just that phone call had me hysterical. I called Tim bawling. After I talked to him and my sister and my bff Sara, they all assured me that these test are often wrong, there's not a likely chance that "I was the 1". I mean after all I knew in my heart my baby was fine, right? Well we met w/ the genetic counselor, who pretty much just went over the results of the First Trimester Screening, told me we had a 3% chance of having a baby w/ Down Syndrome and what our options were. We could have the CVS test (Chorionic Villus Sampling) done which would need done right away, we could wait until I was 16 weeks along and have the amnio, or do nothing and just wait and see. Well I needed to know right away. I was 13 weeks 4 days and had to have the CVS before I was 14 weeks. So they got me in later that day to have this procedure done, where they put a needle through my stomach and take a sample of the placenta.
|Picture they took before the procedure started|
Now I had to wait a week to 2 weeks for the results... but again I "knew" everything was fine! I kept calling (because they said I could, lol) and they didn't have the results yet...But on May 24th, I got the call... the call you never expect to get. The genetic counselor said, "Lindsay, it's not the news you were expecting, your baby has Down Syndrome", I was in shock. All I said was "ok". And then I asked what the sex of the baby was and she said "it's a girl", I said "of course". I lost it. I think I cried uncontrollably for most of that day. My sister and Sara came over and we talked about it, made me feel a little better, but it all didn't seem real. The counselor wanted us to come in and discuss the results, so Tim and I went in later that afternoon. They first told us that this was not our fault, there was nothing we did to make this happen, or nothing we could have done to prevent this. Of course we were give all the statistics and what our options were w/ my pregnancy. I was still in a fog. We had so much to think about. Would we keep the baby, what does this mean for our family, what financial hardships will this bring on, what about our other 2 "healthy" children, and a lot of other things. We decided to wait to make "that" decision about our baby girl until later. I couldn't with all the life in me terminate a pregnancy. Emotions were everywhere. I'm not a big "GOD" person, but I kept asking him for direction. To tell me what I was supposed to do with this information. Did I know about this now so I could terminate or prepare. I wanted a sign! But I knew the answer was in my heart the whole time. We didn't plan for this pregnancy, it was given to us for a reason. I was chosen to bring this special girl into this world.
The next step was the "big" ultrasound, where they could see if she had any other "markers" for down syndrome. But in the mean time I started reading. Mostly blogs and message boards, because these are real people that are living w/ children w/ down syndrome. I needed to know what my state offered for help. I found most of the information I needed and I've really accepted that we are having a very special little girl. She will be a baby, a toddler, an adolescent, a teen, an adult. She will do most of what my other children have done, just might take her a little longer to get there... and I'm a pretty determined person, so I will help her get there! She will still look like us, act like us and be as much a part of our family as Andrew and Jake are. She will go to preschool, elementary school, middle school, high school, and if she wants college... There are so many opportunities out there for her it's amazing. Maybe more than for Andrew and Jake. I've really started to get excited to meet our little girl. I'm still scared of the unknown, but I don't know what is in the future for any of us, so I can't let that keep me from living my life.
We had our "Big" ultrasound on June 17th. We were nervous of what they were going to tell us. Some things they were looking for are heart defects. Children w/ down syndrome have a 40-60% chance of having one. They would look for blockages in the bowel, kidney problems, shortened bones, cyst on the brain and several other things. So what did they find... well she does have a hole in her heart, a VSD (ventricular septal defect ), and some fluid on her left kidney. The doctor didn't seem overly concerned w/ these findings and said we'll watch them. But he kept saying "this baby looks good". She had no other "markers".
We will go back on July 25th to have an Echo cardiogram of her heart and will be able to better see the hole and how big it is. For now I am happy. I don't want people to be sad for us. I'm past the sad part of this diagnosis. I want to move on to the fun part of being pregnant. I'm feeling her kick, we're picking baby names, and I've started a collection of pink things. I want people to educate themselves on what down syndrome is and I hope they will and will want to be a part of my daughters life and love her for who she is, not judge her for having that extra chromosome and looking a little different.
Here are a couple things I've read along the way that have kept me encouraged:
This is called Welcome to Holland, love the perspective it gave me. And the way I've figured it, I've been to Italy twice, so why not check out what Hollands like :)
downsyndromepregnancy.org has been a great resource too.
There are more that I will update with later. I need to find them again, lol...
Stay tuned for updates :)