I have been on this board on and off for a few years as
you can see from my history as I have had four losses. I hope it's
alright that I post here asking for some advice. I hope to get back to this board some day as PGALer.
We have been going to an RE since our second loss. Then, we
lost our daughter in September to a Trisomy during the second trimester
and recently had another early loss. We have no living children. I had a D & C for my second loss at about 10 weeks or so and the chromosomes were normal. The first and most recent losses were too early to get testing done on.
We just had karotyping done on both me and my husband and everything came back normal which is hopeful. It is also important to note that even though our daughter had a trisomy it was said that it was a fluke. I have had everything else tested from blood clotting to autoimmune to thyroid etc.I have also had an HSG, and SHG and everything was normal there too. The only thing that came up is that I have MTHFR (compound het for the A and C genes). I am on extra folic acid, B-complex and baby aspirin for that along with my prenatal.
Is there anything else that I am missing here? It has to be something other than bad luck at this point. It is just such a mystery and we are starting to feel so hopeless. We are meeting with our new RE in July so hopefully she will be helpful but if there is anything else that your doctors have done for you, please let me know. We haven't had my husband's sperm tested. We don't have an issue getting pregnant but unfortunately I just can't seem to keep the pregnancies.
I know that you aren't doctors but perhaps you have had some testing done that provided some answers for you that you feel comfortable sharing.
Anyway, sorry for venting here. I really appreciate any advice that you have to offer. Congrats to you all. I hope to be back here soon.