We decided to wait a couple of years before trying to have any children. Finally we were ready and then the first positive pregnancy test! We were elated. However, a few short weeks later, I miscarried. I was devastated. After a short wait, we decided to try again. We got pregnant right away. This time, I was a little more nervous and cautious. My worst nightmares came true when after several ultrasounds, they were not able to detect a heartbeat. I miscarried again and once again my heart was broken. This time we decided to wait a little longer before trying again. Emotionally, I was a wreak and needed time to heal.
The next time we got pregnant, I hoped and prayed that this time would be different. The doctors had figured out that the cause of my miscarriages was a genetic mutation that didn't allow me to process folic acid correctly. But that could be fixed with extra vitamins and a baby aspirin daily. An early miscarriage scare left me off work so that I could be on modified rest. No strenuous activity, no standing for a long time, basically: take it easy. So I did. Things were going well. Then I got gestational diabetes and had some preterm labor. Now it was full on bedrest. However it was totally worth it when at 36 weeks and 4 days, our little Baby Z as we'd been calling the baby arrived (we didn't find out the sex of the baby and both names we had picked- Zachary and Elizabeth- both had Zs in them).
| Elizabeth Noelle, born Dec 20, 2009. 7lb 8 oz, 19 in |
| Our California Trip |
The meeting with the genetics counselor was one of the hardest things I've ever done. She was going over things that could cause short bones: chromosomal issues (like Down's syndrome, trisomy 18, etc) and skeletal dysplasias (achondroplasia, osteogenesis imperfecta, thanatophoric dysplasia, etc). She felt based on the measurements that the bones were too short for either down's syndrome or achondroplasia. That basically left the very bad or fatal diagnoses. I was sobbing and thinking "What's wrong with me? Why can't I keep my babies alive? How long will I have to hold her before she dies?" and on and on. The genetics lady said they needed more information before they could tell us more so another ultrasound and did we want to do an amnio?
Well the perinatologist did the ultrasound and the chest to abdomen ratio was not in the lethal range! Also she felt fairly sure looking at everything that our darling baby girl would have Down's Syndrome. After thinking that my baby was going to die, we were so relieved and happy. We decided to do the amnio, since it would tell us by Monday (it was a Friday) if that was indeed our diagnosis. Then we would be able to be prepared and informed. On Monday when the FISH results came back normal, I was upset. We were back to the great unknown. It could still be something very bad.
5 very long weeks later, all the tests were done. The results: achondroplasia. Trevor was relieved and happy. I was relived, happy, upset, worried, and in a little bit of shock. I guess that I has always hoped in the back of my head that everything was all right and when she was born, she would just be "normal." But after joining some online support groups, doing a lot of research, and a lot of prayer, I once again began to just be excited for the birth.
At 39 weeks they induced me (due to her large head size) by breaking my water. After less than 6 hours of natural childbirth, our Charlotte Anne arrived with a little help from a vacuum there at the end. And that is the story how we got our two little sweetie pies! Now on with life and the rest of the story!
| Charlotte Anne, March 30, 2012. 7lb 12 oz, 18 in |
| Two Sweetie Pies |
Beautiful story Allie! Your girls are gorgeous! :) Charlette's picture on FB is SERIOUSLY cute! Love those cheeks! I have three boys and my youngest was born with achondroplasia. Can't wait to see more of the blog!
ReplyDeleteAllie is there anyway that you could contact me by email I would love to talk to you about your beautiful little girl!! We have similar stories and I am currently pregnant with my first child who the doctors have diagnosed with achondroplasia. If you would email me at adirnberger@daeoc.com so I can ask for some things to expect and maybe know what I should and shouldn't register for. Thanks!
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