Hi, welcome dazed, jelly, Erica, sorry that you find yourselves here. To those who were asking, the basic RMC tests are: Blood tests: hormones, thyroid, clotting, possibly karyotyping for you and OH. A scan for uterine abnormalities. Karyotyping of 'products of conception' wherever possible, to check for chromosomal abnormalities. For at least 50% of people, no cause is found. Many on here have got to that point then self referred as private patients to the implantation clinic in Coventry.
I have been lurking on and off recently (will have a good read through soon) due to being mega busy. Great to hear Tanny and tiny are doing so well, and there seem to be lots of other bfp's on here...hang in there everyone. just thinking of you on Thursday, and boozle your RMC sounds a little frustrating. Sorry to anyone I have left out.
Me, aged very nearly 41
DS 2011, straightforward, no problems, now 3yrs 7mnths
1)MMC June 2012 at 11 wks, died 7.5 wks, ERPC
2)TFMR Sep 2013 at 13 wks due to serious abnormalities at 12wk scan - 90% chance of death in-utero - chromosomes normal
3)Jan 2014 MMC at 10 wks, sac only at 8wk scan - Trisomy 22, natural mc
4)June 2014 MC 8wks, HB seen around 7 but behind for dates - medical mc, chromosomally normal
The 4th one really changed things. Have been to Coventry and am awaiting results. My whole mind set has changed since the last one, and I feel increasingly hopeless. It really really may never happen, and I am starting to adjust to that, and even doubt the decision to keep trying for a second child. I do know how lucky I am to have DS.
longest how are you doing?
cloud I get the struggling feeling. Hope you're ok
Sorry yet another long post from me...