When we were 12 weeks pregnant we had an ultrasound done. The doctor came in and also gave me an ultrasound which i found weird because doctors don't normally do ultrasounds. Once he was finished he said that baby showed some markers of having Down Syndrome and that i should get tested for it. We had already decided prior to this day that we did not want any testing done we would love our baby regardless. Well we were scared so we agreed to have a blood test done. I got a phone call about a week later from a nurse who worked at the hospital. She informed me that my blood test came back that my baby had a 100% chance of having Down Syndrome. I was so confused, how could just a simple blood test tell you this. The nurse had asked me four times, yes four times if i wanted to terminate my pregnancy. Of course i said no. She asked me if i wanted to get an amniocentesis done i said no but that we would need to talk about it. We opted out on having the amniocentesis done because of the miscarriage risk's. We had another ultrasound done at 20 weeks and they measured her and told us that she had an extra flap of skin on the back of the neck also that she had short humorous bones, she also had an absent nasal bone. That with these signs and the blood test that it was more likely that our baby would most likely have Down Syndrome. After hearing all of this we went home and did some research.
Myah was a NICU baby and that made it very hard for us to breast feed every day. I tried to get her to latch every day but with her low tone it was hard. Myah was not gaining as much weight as they would have liked her to so they put her on formula to get more calories in her. Myah was getting both my breastmilk and formula. I wasn't producing much in the beginning so they also had to give her formula when i had no milk to give. Myah had developed jaundice so she had to be under the light as much as possible so that limited the time i has to try and get her to latch. Myah came home after a week in the hospital and we continued to try and latch at times it was hard for both her and i, so I continued to pump and give her milk out of a bottle. I developed an over supply of milk. I was on a strict schedule of pumping every two hours during the day and every three hours at night. Myah was sleeping through the night so i had to wake her up to give her a bottles since she was stil...
Thank you for sharing your story with us.❤️❤️
ReplyDeleteThank you for reading! 😊
DeleteI love you both. Wouldn't change it for anything. Angel
ReplyDeleteWe love you too!!!
DeleteThanks for sharing. There was a brilliant documentary on BBC TV last year by actress Sally Philips called A World Without Down's Syndrome. It was incredible and well worth seeing if you haven't already. I hope it opened a lot of minds, in particular it covered the fact that termination just seems to be expected now - as you've pointed out in your blog. Am looking forward to reading more about your journey with Myah. All the best. Sally (@samesamebd on Instagram).
ReplyDeleteI will most definitely need to check it out thank you for letting me know. Ill give you a follow! Thank you for reading my blog.
DeleteGlad you said no to termination. I don't even know why they bother to ask. Will keep in reading. Thanks for sharing.
ReplyDeleteThank you for reading! Termination was not an option for us we love our baby regardless of her diagnosis shes perfect for us.
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