Hi everyone,
We have been TTC a second baby for a little over a year now with an early MC and four CPs in that time. I’m 33, my AMH is 13.7. Me and my husband have both had hormone runs which came back fine, I’ve had a full blood run, blood clotting panel, thyroid check and pelvic ultrasound which were all ok and his semen analysis is also ok. Our first was conceived easily in 2021 and we never experienced losses until this past year.
I truly appreciate that many of you have been trying for a longer period of time and I also appreciate that IVF isn’t an easy, quick or guaranteed fix but for numerous reasons in our lives we are strongly considering the IVF route.
The thing is, every doctor we’ve spoken to and everywhere I look online there’s different advice!
We’ve had two doctors happy to go straight to IVF, one highly recommended a hysteroscopy but said it wasn’t essential. He also recommended PGT-A on the embryos but said it’s up to us.
One doctor has advised uterine microbiome testing and DNA fragmentation first.
And another has advised maybe doing a karyotype test, and possibly looking into NK cells.
All of this is private and obviously costs!
So my question is really has anyone had the suggested tests? How likely is it we might find an issue that we could resolve? Do we try a IVF round and see? I know it’s very individual of course but any help navigating this information would be appreciated.
TIA