Hello,
I had blood work done at 14 weeks and they told me that I have an increased risk for my baby girl to be born with Turners Syndrome. I really wanted to do the Amniocentesis to find out if she had it but my husband did not want me to have it done due to the risk of miscarriage. So I chose not to. Now here I am....waiting.... driving myself nuts not knowing. I am only 24 weeks and I am so scared she is going to have it. Does anyone have a daughter with Turners syndrome or do you know someone with it? If so how are they doing?
This is my second pregnancy and I feel slightly disconnected, with this particular chromosome abnormality only 1-2% of babies make it full term...Majority pass before hand. I catch myself wondering when the last time she moved was. it's mentally exhausting preparing for a stillbirth when there could be absolutely nothing wrong. I kind of wish i did the amnio instead of listening to my husband.
Thanks for listening.
I had blood work done at 14 weeks and they told me that I have an increased risk for my baby girl to be born with Turners Syndrome. I really wanted to do the Amniocentesis to find out if she had it but my husband did not want me to have it done due to the risk of miscarriage. So I chose not to. Now here I am....waiting.... driving myself nuts not knowing. I am only 24 weeks and I am so scared she is going to have it. Does anyone have a daughter with Turners syndrome or do you know someone with it? If so how are they doing?
This is my second pregnancy and I feel slightly disconnected, with this particular chromosome abnormality only 1-2% of babies make it full term...Majority pass before hand. I catch myself wondering when the last time she moved was. it's mentally exhausting preparing for a stillbirth when there could be absolutely nothing wrong. I kind of wish i did the amnio instead of listening to my husband.
Thanks for listening.