Apologies for the AW post. I wasn't sure the best place of this, as it's not really a check in, wto, or tww question....
My 2nd loss was a miscarriage at 20 weeks due to chromosomal disorder that resulted in the baby developing hydrops. From the time I found out something was wrong (12 weeks) to the loss and D&E procedure (20 weeks), I saw the Maternal Fetal Medicine specialist weekly.
After the loss, she said she was very hopeful for the next pregnancy and that it did not appear to be a reoccurring issue. However, she did recommend I meet with her for a consult before trying again. My consult meeting is this Thursday.
H and I had our DNA tested, and everything came back normal, so it wasn't likely something that is our DNA to pass along.
Anyone else been through this? Any suggestions on questions to ask the MFM before we try again?
** December BMB Siggy Challenge - Animals in Pools **
Me: 31+ H: 32
TTC Since 11/2015
#1 - MMC 6.5 weeks (2/16); #2 - MC due to cystic hygroma at 20 weeks (10/16); #3 CP (2/17); #4 - Due 12.16.17