Hi ladies -
Anyone here do PGS?
I just did our last FET yesterday - 2 6-plus day blasts that were deemed "normal" via PGS
I know it still may not work (and that's ok) but it occurred to me that I don't even really know what "normal" means .... Does it mean I don't have to do MaterniTI or CVS or worry about the NT screening?
I know I'm getting ahead of myself but I'm just curious. Essentially I barely got a look at the results - we didn't want to know genders and so all of the sudden when we realized it was there and we didn't want to know it all went really fast...
Anyway.. Just curious if anyone had anyone had gone through this?
Re: PGS PGD Question
Maternit21 only screens for 3 trisomies - 13, 18, and 21. PGS is not 100 percent guaranteed, but I would probably be confident enough to skip maternit21 and the like. The NT scan is primarily used to detect the most common chromosomal abnormalities, but can also be used to detect non-chromosomal deformities (these would also likely be apparent at your anatomy scan, but sometimes people want to know as early as possible for planning or termination purposes). Sometimes people just like the extra ultrasound to see the baby, too.
Cvs and amnio aren't routinely done unless you have other tests or ultrasounds showing abnormalities, and these can also be used to diagnose a whole host of other, non-chromosomal genetic diseases.
3/22 ER: 25R, 20M, 15F. 9 genetically normal, and 3 survived to Day 5
3/27 ET: transferred 1 embryo, beta 9dp5dt=163, 12dp5dt=639
4/25 1st ultrasound at 7 weeks = identical twins with heartbeats?!!!
3/22 ER: 25R, 20M, 15F. 9 genetically normal, and 3 survived to Day 5
3/27 ET: transferred 1 embryo, beta 9dp5dt=163, 12dp5dt=639
4/25 1st ultrasound at 7 weeks = identical twins with heartbeats?!!!