Sarah, Our Shooting Star |
With the help on my husband, my doctor, amazing nurses, and a kind friend, I labored to bring Sarah into the world. We were only 22 weeks and 3 days along and did not expect her to survive for even a few minutes, as some babies do at that gestation.
It's amazing how quickly things can change. A week and a half before had been Valentine's Day. We celebrated love, we celebrated our daughter Bridget's first birthday, and we celebrated having our ultrasound which told us we were expecting another daughter. The ultrasound is how we ultimately learned the worst. Somewhere early in pregnancy, Sarah had stopped developing properly. Her brain had not fully divided. It's a disease called HPE or holoprosencephaly. She also had hydrocephaly, an encephalocele, and problems with her heart and placenta. The placenta kept pulling away from the uterine wall, causing bleeding during my pregnancy. The wide range of problems led them to believe Sarah likely had a chromosomal issue of some kind. We never were able to find out for sure, due to a lab error.
Holding Sarah for the time I could |
At first that was all that mattered. Our daughter's health. Then I found out that carrying her to term would be risky for me. There were a number of possible issues that might arise. The one that scared me the most was the idea that as the placenta grew, and continued to pull away from the uterine wall, I could hemorrhage. We believed that Sarah's life was a gift, even if she would never live outside of me. But my life was a gift, too. And we felt strongly that I couldn't risk it. Not to prolong her death. Not when it meant that my daughter might suffer. This was a very personal decision, and I don't believe that there is a right or wrong answer. You have to do what is best for you and your baby.
Sarah's Marker |
Sarah was warm and beautiful with her button nose, long perfect fingers, and great big feet. It was so wonderful to have her in my arms. I touched her face, played with her ears, marveled over her little mouth, and kissed her tiny sweet face. The hard part came when I handed her back to the nurse to take away. She told me I could have her back if I hadn't had enough time. But there can never be enough time with your baby. Nothing short of taking them home to love forever is good enough.
The angel who watches over the children's cemetery. |
We buried her in the Garden of Little Angels in the nearby cemetery. Through all of this I have learned that neither Sarah, nor Dominic and I are alone. Sarah is in the company of so many other precious children whose mothers miss them, and I have joined a sisterhood of mothers of loss. I would give anything to take away their grief, but I am thankful for their support and the support of so many people who offered me encouragement and kindness when the world seemed to have turned upside down. I still miss her everyday.
Thank you for sharing her with us. Having other people know her story, keeps her alive for us.
For anyone who wants to read our whole journey with losing Sarah, please see "Losing Sarah" in the labels section of my sidebar.
For anyone facing this kind of decision, or a difficult pregnancy, please feel free to contact me, via the tab in the sidebar. I received some unkindness as we went through this, but I received much more support. After losing Sarah, and then having Liam, I feel very strongly that it's my duty to pay that support forward to other moms and families.
I really appreciate your words. We recently lost our angel due to an encephalocele and there are not many people to talk to or supprt groups to turn to. Thank you for telling your stories.
ReplyDeleteI really appreciate your words. We recently lost our angel due to an encephalocele and there are not many people to talk to or supprt groups to turn to. Thank you for telling your stories.
ReplyDeleteAmanda, if you look on my encephalocele page, I provide a link to our support group for parents. We have parents who have also experinced loss due to encephalocele and would love to support you.
ReplyDelete