We discovered at our 10w scan last week that I'd had a MMC - no fetal heartbeat and baby measured only 9+3 (after seeing and hearing a beautiful heartbeat at 7+1 and 8+5)
We had the ERPC done privately so we could get the tissue testing done to see if it would give us any answers (BUPA paid for the ERPC but won't pay for investigations so I'm expecting a bill for the histology and cytology testing)
The histology report said they were able to retrieve 'products of conception' for cytogenetic testing, which I think means they were able to find tissue that was definitely pregnancy related and not just maternal tissue
There was also no evidence of molar pregnancy
Has anyone had the tissue testing done? What kind of information should we be expecting it to give us?
I'm assuming that if there were chromosomal abnormalities then it will hopefully be able to identify this, and ideally which ones?
I'm told it will also tell us whether it was a baby boy or girl, although I'm not sure I'm ready to know that. Although if the mc was due to something like Turner syndrome that's obviously only carried on the XX chromosome so pretty damn self evident
We asked the Dr not to send the cytology report through in the post but to give us them in person at our follow up consultation. If the baby was chromosomally normal and it's my body that rejected it, I need to be given that information in context where we can discuss it
The histology report was pretty grim reading, as you'd expect from an autopsy of your dead baby. No nice way to dress up phrases like 'Partially necrotic decidua' and 'Multiple fragments of pale brown tissue' 
So if anyone has any experiences of having the tissue testing done post mc, I'd be very grateful for any insight you can share so we can prepare ourselves as best we can. TIA