This seemed like the day to begin this - my daughter's funeral.
I never would've thought that at 26 I would have been planning a funeral and much less a funeral for my baby. But that's where I've found myself this week.
My now husband and I got engaged in September 2012 after over a year of living in our new home. We began planning a very small, intimate wedding but could not decide on a wedding date. I bought a wedding dress in October. We finally decided on a spring wedding.
Thanksgiving was the first day I thought something was...off. There began my weeks of "morning" sickness that I chalked up as the flu. I missed a few days of work here and there, but never thought anything of it at first. Finally in December, my fiancé suggested we pick up a pregnancy test.
The next morning, December 11, 2012, I took a test before work. Positive. I stared at the pregnancy test in complete shock - I had no idea what to do. The pregnancy was completely unplanned (I was on birth control!) but we were no less overjoyed. We got married a month later on January 12, 2013 and I was 12 weeks and 1 day.
Though I had terrible morning sickness that lasted well into my second trimester and heartburn that consumed me if I even thought about spicy or acidic food, I had a fairly normal pregnancy. Nothing seemed unusual until 19 weeks when we went to our ultrasound to find out if we were having a baby boy or girl. It was then we were told we were having a girl! - and that her limbs were measuring a bit behind. I originally thought nothing of it as I myself am barely pushing 5 feet.
We were sent to a perinatal office where we were told our baby girl may have a type of skeletal dysplasia known as achondroplasia (dwarfism) or she could just be short like her mama. It wasn't until 29 weeks and 6 days - after we had named her Kennedy, finished her nursery, sent out invitations for our baby shower, bought a new family-friendly SUV - that we were told by another doctor at our perinatal office that her skeletal dysplasia appeared to be lethal - her lungs would not support her and she would be stillborn or pass shortly after birth. I broke down and sobbed - I felt as if the wind had been knocked out of me. That was the first time I had ever seen my husband cry.
I was out on bed rest due to emotional distress by my OBGYN. We met with a neonatologist at our delivery hospital to discuss our birth plans and were told he believed our little Kennedy had thanatophoric dysplasia. We began planning for the worst, but other than immediate family and a few close friends, kept it to ourselves. There were so many days we didn't leave the house.
At exactly 33 weeks, I had been feeling very uncomfortable and decided to go to the hospital just in case. To my surprise, my water had broken and I was in labor. I had an emergency c-section that night (my doctors believed a c-section was the best chance we had at meeting our daughter alive).
My husband paced the hallway. I was so overwhelmed with fear. Kennedy was born crying - a sound I never thought I would hear! I cried tears of joy. The joy grew stronger as we were told she needed little help and would be going to the NICU. She shocked every doctor and nurse there.
After 3 days in the hospital, we were transferred to our local children's hospital NICU for further research on her skeletal dysplasia. We spent the rest of Kennedy's short little life there. On her 35th day of life, they confirmed that she did have thanatophoric dysplasia. We were lucky for every day we had with her.
The next few days were the beginning of the end of our time together. On her 38th day of life, Kennedy passed in her sleep. She had been sleeping most of the day, but she opened her eyes, looked right into my eyes, and smiled one last time. I held her tightly in my arms as she passed.
We had her visitation last night and her funeral this morning. I still can't believe she's gone. I am trying to find