Hi all,
I had genetic testing done following my recent MMC of twins. The result stated female genetically normal pregnancy tissue was found. As I understand it this is kind of inconclusive because:
A) The tissue tested could have been mine; and
B) There were two embryos and only one result.
Does anyone have experience of such results and how to interpret them? The letter I got just said the tissue tested was genetically normal and to get a referral to a Gyne Consultant from my doctor as I’ve had 2 MMCs (one pre my son and this recent one post). I had just chalked it up to chromosomes given my age.
That said, I took Clexane, asprin and prednisone for the first 12 weeks with my son (precautionary) and with the latest pregnancy was just advised to take Clexane and asprin as all the research on prednisone points to assistance with implantation (which had already happened). Now I wonder if I’d been taking it whether the outcome would have been different.
Anyway, I’m getting a copy of the actual result and will speak to my IVF consultant about it.
However, can someone let me know what tests are worth doing following repeated miscarriage? I’ve had my thyroid levels checked recently and take loads of vitamin D. It would be helpful to be informed, as it might be worth getting checked out before we do any more FETs.
Thanks in advance!