Hi everyone.
Yesterday we found out that my baby girl, who we lost at 16 weeks, had trisomy 21 (Downs). I'm not sure what to do with the news. We don't know yet if it was because I passed on a translocation - I had my blood drawn after we got the results so we can find out. Of course I'm very nervous that this will be the case, but also very hopeful that this will turn out to have been a random mutation and I am "normal." If that happens, then our next pregnancy will have a low risk of 1% of this happening again. If I do have the translocation, I guess I have a 10-15% chance that this will happen again and might need to consider PGD and IVF.
Does anyone have any experience with a MC from trisomy 21, or any information on the odds of it being random vs. a translocation? I've been reading a lot about it online but with all the medical jargon, sometimes it's hard to distinguish the facts.
Thank you.
Re: UPDATE: Got a partial answer after 2nd tri missed MC?
*************Siggy Warning. Loss mentioned.************
Me: 36, DH:37
Married 4/2010, TTC since 7/2011
Dx: Officially Unexplained (I have Polycystic Ovaries diagnosed via ultrasound, but few classic PCOS symptoms, he has mild MF issues. So... not issue free, but nothing so severe as to explain IF)
I also deal with post-surgical Hypothyroidism following Thyroid Cancer in 2009, but under control with Levothyroxine
4 months Clomid (thinned lining) and 10 months Letrozole (every indication that I responded perfectly)
6 failed IUIs in 2013, 3 with trigger
IVF #1 in March 2014
ER 3/21/14, 31R/21F, 12 frosties!
ET 3/26/14, 1 perfect blast transferred: BFN
FET#1 5/28/14, 2 "beautiful" early blasts transferred. BFP!!
Beta #1 (6/11/14) 798; Beta #2 (6/18/14) 7,966.
1st u/s (6/25/14) showed 2 sacs, 1 empty & 1 with a beautiful little bean doing what it needs to do!
EDD 2/14/15, missed miscarriage, DX: Trisomy 21. D&C 8/1/14
FET#2 Transferred 3 embies, 2 looking pretty good, one not so much. BFN.
IVF#2 January 2015, tentative ER 1/23