Saturday, August 20, 2011

One month old.


She is over 8 pounds now and is even starting to get a few little baby fat rolls on her legs. She had her real first smile; she looked right into my eyes and smiled. I don't like it when people see a little baby smile and say, "Oh, she must have gas." Why does it have to be gas, can't she just be smiling?

School has started and we are settling into a schedule again. It was nice to have the girls stay at grandma and gramdpa's for over 2 weeks; the house was so clean. We really did miss them and are glad they are back. Even with a messy house and all their drama.

I love to hold Ginny on my shoulder after she nurses and rock her. What is it about holding a little baby against you? Her feather-soft hair, her warm skin and her little sigh. It seems that everything else just melts away and you are so close to heaven. I still look into her eyes and see the signs of Downs. But my 5 year old says, " I love Ginny's eyes, they are so cute." She doesn't see Downs, she just sees her baby sister. There are time that I can see her as just Ginny, sometimes I even forget for a while about Down syndrome. I can see that I need to be more like my 5 year old, like a little child. It is a slow process but it is happening, slowly. I feel like this is my opportunity, my blessing, to re-learn why we are here on earth.

I have always know the "Sunday School" answer to this question but now I am learning it on another level. We are here to gain a physical body. It doesn't have to be a perfect body and He never said it would be a body without ailments or imperfections. We suffer pain that we might be more able to show compassion and empathy for others. We are also here, without a memory of our pre-earth life, to be tested and learn to serve God, serve those around us and to follow the path He set for us. He did not send us here to get the newest and coolest stuff, to look good is society's eyes and find success in the world's eyes. It is how we are seen through His eyes that really matters. We should be humble so we can accept that He knows more than we know. We should acknowledge His hand is all things and we will know we are not alone. We should know that He loves us enough to allow us to feel pain so that will ulimatly be for our good. He also send His Son into the world knowing that He would suffer and that He would be ridiculed unjustly. I am sorry if this is turning into a Sunday School lesson but these are things that I feel deeply and it is part of my journey that I am taking with Ginny. I think sharing my feelings also helps me really believe them.

Friday, August 12, 2011

Ginny's Birth Story

Everything seemed to stop. Even with all the nurses running in and out of the room and all the commotion; I just started to fade away. I could hear people talking. “She has a chin like mine.” I heard my husband, Tim, say. But I didn’t see anything, except for her eyes. They had placed her on my stomach and we looked into each other’s eyes. Her eyes were wide open and she wasn’t crying. She was just looking at me with her beautiful but ever so slightly upward slanted eyes. Then there was nothing. In my heart I knew. I think I had known for a long time now. Why else would I have kept myself from ever letting my heart fully embrace the anticipation of a new baby? Why else was I so guarded about even telling people I was pregnant? Because I knew, I knew she might have Downs. And there she was, looking at me. Her eyes were the eyes of a baby with Down syndrome.

It was a high risk pregnancy based on my age and I also suffered from gestational diabetes again. I had an ultrasound in Denver. They told us the baby was a girl, girl number 5. “We only do girls,” we joked. We already he a name picked out, Ginny. My Aunt Ginny, whom I had dearly loved, died several years ago and I wanted to name her after my aunt. After another month or so I had one more ultrasound and that is when it started. The doctor that read the ultrasound called me later that day and left a message asking me to call her back and page her at the hospital. I felt the urgency in her voice and my heart skipped a beat. When I spoke to her later she said that there found 2 markers for Down syndrome and that I needed to make a decision. A decision? About whether or not to continue the pregnancy she explained. I was shocked, of course I did. Besides they were only risk factors not a diagnosis. I was strongly encouraged to have an amniocentesis but ultimately decided not to have the procedure. The test could result in a false positive and there was a risk of harming the baby. But I could feel the possibility of Down syndrome nagging in my heart for the rest of the pregnancy. I cried about the possibility for a few days but then pushed it to the back of my mind and would not let it occupy my thoughts. I had too many other things to worry about right now. Tim had been suffering from chronic severe back pain even after back surgery and had lost his job the previous month.

I checked into the hospital a little before 6pm on July 18th, 2011. I was given the ever so fashionable gown to change into and the nurse started an IV. The doctor came in and gave me a dose of Cytotec to help my ripen my cervix and induce labor. Then before he left he said, “I’ll see you tomorrow morning.” Things were moving along fine, I even watched some TV for a while. Around 11:00pm the contractions got stronger. I had to breathe through them as I clung to the side of the bed. The nurse came to see if I needed another dose of Cytotec. She was shocked to see that I was 90% effaced, dilated to a 7 and had a bulging bag. Within just a few minutes the contractions got much more intense and I wanted an epidural. They called for the doctor and the anesthesiologist and the nurses came in to start prepping the room for delivery. Then the contractions were so strong I could not control my breathing anymore and I started screaming with every contraction. My water broke and pain ripped through my body. The anesthesiologist came in but I was crowning and it was too late for an epidural. I realized I was going to have this baby without any pain medication and panic set it. The pain was like nothing I have ever felt before and I completely lost control. Screaming, writhing, begging and calling out to God for help. At 11:36pm the doctor walked in and as he sat down he said; “You need to push.” and with one big push Ginny literally shot out onto the bed. It wasn’t over; I still had to deliver the placenta and be sewn back together since I had a significant tear during the delivery. It was a horrific experience. I felt as if someone else had taken possession of my body. The pain lingered and I could not stop shaking. The nurse finally gave me some pain medication in my IV but all I could think was, “too little too late, lady.”

“Here she is, the incredible one,” the nurse said as I was wheeled down the hall to my new room. I didn’t feel incredible. I felt like my insides had been ripped out all I could do about it was to scream at the top of my lungs. I was embarrassed at how I had totally lost control. But it was over now and I couldn’t change the past. They settled me into the bed and took Ginny to perform the normal newborn procedures; at least that is what I tried to tell myself. Alone in the room I asked Tim if Ginny looked like she had Downs. He said she looked perfect, but I was scared. Later, they brought Ginny into the room and I held her close. Finally a Neonatal nurse came in and wanted to “talk” to us. She asked if I knew why she was there. “She has downs,” I said. It was almost a relief to say it. She went on to describe why they thought Ginny had Down syndrome. Skin folds in the corner of her eyes, crease in hands, larger space between big toes, etc. I faded away again. I don’t remember her leaving the room. My body rocked with sobs as I just let my emotions boil over; Tim tried to comfort me but I wouldn’t be comforted. I was afraid. Afraid of the unknown; afraid of what kind of life Ginny would have. I loved her, like I had loved all of our newborn children, but all my dreams for her seemed to come crashing down.

The nurses said they were having a hard time keeping her temperature up and bundled her in heated blankets. She was sleepy but able to nurse right from the beginning. They took her to the nursery and didn't bring her back for several hours said she had a high hematocrit. She spend about 6 hours under the bilirubin lights to help with jaundice. I walked down to the nursery and held her as I nursed her. She was hooked up to wires and the monitors would sound when her oxygen got too low. I had seen the twins under the lights and hooked up to multiple wires so it was a familiar feeling. I couldn't help but wish that they were wrong, maybe she didn't have Down syndrome. She had an open PDA in her heart but there really didn't seem to be any obvious differences between her and my other newborn children. We found out later that the PDA had closed on it's own and the cardiologist said that her heart looks great.

I was able to take her home with me the day I checked out of the hospital. The blood tests did confirm her diagnosis and I mourned again the child I had thought would come to our family. I had dreams and hopes and ultimately a plan for each of my daughters. But that is what they were, MY dreams and MY hopes. The plan for her life will be my Heavenly Father's plan and she will have her own dreams and hopes. She has alrady taught me to look at what this life is really about and that I needed to change some things about myself. I hope I can become what I should be as her mother.