We have an appointment scheduled with our RE next week and we were told that we'd receive the results of the genetic testing at that appointment but my RE nurse just called me with the results. She said the RE will go over everything with us in detail next week but she didn't want to keep us waiting.
The baby had Trisomy 16. And it was a boy.
I really know nothing about this (since in 5 years I've never gotten this far) and I know the RE will fill us and I'm certain I'll do my fair share of research between now and then, but any info you ladies can share would be appreciated. Like, is this something that is generally just bad luck? Or is it a genetic condition that he or I have that causes (and will continue to cause) our babies to have this? Those are the types of questions I have for her, but a week is a long time to wait, as you all know.
Re: D&C genetic testing results in
My little girl had trisomy 12. The doctor said it is something that will not happen again, it is rare. I know it's not the same diagnosis as your little boy. They ran karyotyping on DH and I about a month ago and we will get our results at the end of the month.
I hope your RE can give you some answers.
BFP #1 9/6/2009 EDD 5/29/10. Missy Moo born 5/12/10 after 3 months of bedrest due to PTL, IC and a bicornuate ute causing IUGR
BFP # 2 1/28/12 EDD 10/6/12 No heartbeat seen @ 10 weeks, Autumn
BFP #3 8/18/12 EDD 5/2/13 No heartbeat seen at 7w3d, Mae
BFP #4 01/31/2013 EDD 10/15/2013 No HB seen in our little girl at 10w2d due to trisomy 12, Abigail
BFP #5 6/27/2013 EDD 3/10/2014 diagnosed with protein S deficiency heparin twice a day. Luke's HB stopped at 8wks
BFP#6 12/22/2013 EDD 9/4/2014 No HB seen at 7w2d, Leia
BFP #7- 5/12/14 EDD 01/2015, ruptured ectopic 5/31/14
Me: 38, DH: 40 | Married April 2012 | TTC since October 2012
DX: Hypothyroid, DOR, Right Tube Blocked, Uterine Fibroid (awaiting hysteroscopy) | DH: Beta Thal Minor, ED (Cialis)
OCT - DEC 2012 | TI | BFN
JAN 2013 | BFP ~ EDD 9/23/13
MAR 2013 | MMC due to Trisomy 10 ~ D&E MAR. 8
APR - JUN 2013 | TTA
JUL - NOV 2013 | TI | BFN
NOV 2013 | HSG & SHG ~ Right Tube Blocked & "Thickening" of Uterus
DEC 2013 - JAN 2014 | NTNP | BFN ~ Switched to new practice
JAN - FEB 2014 | 3-D u/s & SHG ~ Uterine Fibroid ~ Awaiting Hysteroscopy
***All Are Welcome!***

Our doctor is happy that our baby came back with a chromosomal issue over a genetic one because I also test positive heterozygous MTHFR and they were worried that may be the issue. It means that our chances of conceiving a healthy baby are better and there's absolutely nothing we did wrong or could have done differently. I know how much it stinks to lose any child, but I have hope that our results mean we still have a chance, even after 2 losses. I hope your RE can answer all of your questions and concerns for you and give you hope and closure. Don't be afraid to ask about anything on your mind when you go and know we're here for you.
BFP #1 11/19/12 EDD: 7/25/13 Natural MC on 12/31/12 at 10w4d
BFP#2 3/1/13 EDD: 11/5/13 Missed MC 4/9/13 at 10w D&C 4/11/13
Baby #2 diagnosed with Trisomy 16. Diagnosed Hetero MTHFR.
BFP#3 8/5/13 EDD: 4/13/14 Team Green Turned Team Blue! Our rainbow baby, Griffin R arrived via c-section (breech since 20w) on 4/11/14.
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~~Everyone Always Welcome~~
My Ovulation Chart
BFP #1 3.16.12. mmc 5.7.12 at 11 weeks ~Avery Cameron~
BFP #2 12.12.12. mmc 1.22.13 at 10 weeks ~Theodore Michael~
D&C #2 Chromosome analysis results: Translocation Trisomy 14
My RPL Testing: Homozygous MTHFR, normal karyotype
DH's karyotype results: Robertsonian Translocation 13:14
BFP #3 9.10.13 mc at 4 weeks~Our little May Flower~
BFP #4 10.13.13- Our Rainbow Baby, a little girl, arrived June 25, 2014!