Hello - me and my husband have been undergoing fertility treatments for almost a year now (since a lap that discovered i had severe endometriosis and removal of one ovary). They have since discovered my husband has poor morphology (2% kruger) and i have mild pcos.. We have gotten pregnant twice via IUI and follistim, however miscarried both times. The first time no bleeding at all and diagnosed with a blighted ovum, finally began to bleed at 10 weeks. The second one i started spotting and bleeding at 5 weeks, however my beta doubled every 26-30 hours regardless of the bleeding (even though i was on supplemental progesterone it dropped from the 40's at 4weeks preg, to 10 when the bleeding was occuring, but began to rise as we increased my dose but miscarried anyways)
My question is How likely is it that a clotting disorder or genetic factor caused both of these since they were both so different from each other? If it was from one problem/factor, wouldn't the miscarriages be more similiar in occurance? We are awaiting genetic testing, but my RE wants us to wait a full two months from the time my beta went to 0 so it won't interfere with the clotting tests, however its been 1.5 months and are debating continuing with the follistim in one week regardless of the testing. Thanks so very much for your time and help!