Hi all
Have been silently reading posts for sometime now.
Apologies for the long post in advance..
My story in short. Diagnosed with endometriosis and went through laproscopy in 2021. AMH significantly reduced. Was advised not to go for ivf with own eggs due to low AMH plus needed PGTA for a cardiac mutation I carry.
March 22, went for DE PGTA tested euploid embryo (Only 1 normal out of 5). Positive test but ended in blighted ovum as it did not progress.
Changed clinics, new donor, FET Jan 23.
Everything was fine until 12weeks and we were over the moon to hit the milestone, and that everything was planned for next few weeks in terms of scans and tests.
At a 16weeks scan couple of weeks back there was a bombshell dropped on us that the baby had an abnormal heart and it will need one or more surgeries and lifelong monitoring.
We are completely devastated as we choose the DE route to avoid any heart or other health issues I have and yet we are facing this. We are at a complete loss of ideas as to where to start next.
This is most likely heading towards a TFMR.
My question to you all is:
I'm increasingly feeling that there is something wrong in me that fetuses are not able to develop properly. Are there any tests any one can suggest I could look into?
We would be giving one last try with the frozen embryo and hence wanted to do everything I can.
It cannot be an inherited genetic issue as husband and donor are normal karyotype and no genetic mutations from whole exome tests. It could be a random genetic issue which I cannot believe.
Any pointers much appreciated.
Love and baby dust to all.