Myself and DH have been trying to conceive for over 4 years now (I'm 34) and went down the IVF route last year following my endometriosis diagnosis (kissing ovaries, endometrioma etc.).
We've had a BFN, missed miscarriage (anembryonic) and a few weeks ago another BFN. After chatting to our consultant in the week she said everything was textbook (blastocysts have all been of good quality, lining good etc.) but obviously that they just weren't going to term. She seemed reluctant but said we could go for further tests if we wanted to but that she didn't see a need to do so at this stage and basically to try another round (1 embryo transferred each time, last 2 rounds have been natural FET).
So my question is, at what stage did you look into further testing and would you consider testing the remaining frosties? Obviously I'm mildly paranoid there's a genetic / chromosomal issue going on.
Thanks xx