This is our second missed m/c. With this pregnancy we saw the h/b twice. Last time we saw it about a week ago. Yesterday there was none.
I mentioned to my doctor the idea of testing the remains to see what happened. Did the baby have a genetic problem? He seemed to think that because I have had one sucessful PG in between my m/c's it wasn't something necessary. However, he later said that since we saw the h/b several times and the baby measured a bit small he thinks that perhaps there was an issue.
I wanted to address it with their office when they call today for my D&C time. I was just curious who has done this and what were your findings? A friend of mine who is an OB suggested that DH and I also get testing. Anyone done that?