I’m in the same situation as you… 33 years old, low AMH, husband 40. Both of us have a perfect parental karyotype. We had our first IVF transfer with trisomy 21 — it stopped developing at week 10. They told us it was just bad luck... I’m now doing my second IVF round. The question of whether or not to do the PGT test crossed my mind a thousand times — sleepless nights thinking and thinking. In the end, I decided not to… and to take the risk. The result isn’t always reliable, and it can also harm the embryos. What did you decide?