How much testing did you do after your first (& hopefully only) loss? I am torn whether to do more testing. I already had a bunch of bloodwork done & was diagnosed with a heterozygous Factor II mutation, but when I went to an IF doctor yesterday he told me that is not what caused the m/c since it was in the 1st tri & it usually causes 2nd tri losses (more great news!)
I am just wondering how many people were recommended/chose to do a lot of testing. Thanks!
Re: How much testing after first loss?
My doctor said my insurance wouldn't cover any testing since it was my first m/c, so we opted not to test. Kinda sucks, just wondering, though.
I'm really sorry for your loss.
This.
My insurance won't cover testing until 3 losses. I hope I don't get to that point.
BFP #2 4/13/10. Bridget born 12/28/10
BFP #3 Finn born 8/11/15
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Same for me as well.
AlpacaBunny - Don't worry, the picture does not bother me...your kids are beautiful! Congratulations on your success!
I have not gotten the pathology results for the baby yet which seems strange since my d&c over 3 months ago (sept 11th) I plan on calling the office tomorrow again to see if they came in & just have not called me yet. I believe I probably had the same blood profile done along with a few auto-immune disorder tests. They want to test me for a few more auto-immune disorders (ANA, thyroid antibodies, & celiac disease) as well as some hormonal things (FSH, estradoil, prolactin, TSH & mercury levels) They also want to do a chromosomal check (karyotype) on my husband & I.
The names of the tests came from the IF doctor. I am not sure what all of them are.
My loss was in my 2nd trimester so maybe things are a little different for us but we're able to get a full battery of testing. Right now we're waiting for the autopsy results, which they said can take up to 3 months to come back. The extent of testing is going to depend on what the autopsy results are.