I hope I'm doing this right. I saw this as a post topic idea and browsed a few other month groups to see how they did this. I figured since AMA Mom's tend to have to go through some extra testing and things it might be nice to talk about them especially for those of us like me who are first time AMA Mom's but not necessarily first time mom's too.
Anyways I'm Jasmine and clearly since I started this thread I'm advanced maternally as they call it. I'm 38 and this is my surprise 4th. My youngest is 4 and will be almost 5 by the time this one arrives so it's been a while for me and now add on all the AMA stuff and I'm overwhelmed slightly. I just had my first sonogram and everything looks on track they said. My next appointment is the 23rd and I'll be 10 weeks 2 days by then but I'm going to try to go in the week before just to get a blood draw for the Panorama testing in hopes that maybe it will be ready at my next appointment the week after. I'm very anxious to know the sex this time which is weird to me as I was team green for my last and first baby but since we need to do a bedroom shuffle eventually with this one I feel I need to know sooner than later to mentally prepare. The doctors sent my info over to the high risk doctor they said as well so I'm going to have to see them for the first time soon and I'm totally not sure what to expect. Any idea from anyone else who has done this before maybe?
I'm not sure what else to write so I'll stop here but looking forward to talking about all those extra appointments we all have to look forward to.
Re: AMA Mom's Check In
First BFP on 1/4/22. Due date 9/13/22.
First BFP on 1/4/22. Due date 9/13/22.
First BFP on 1/4/22. Due date 9/13/22.
I'm glad I waited until I was good and ready. When I was in my 20s I was more concerned with getting my party on! Now I'm much more settled.
And excited to have you all to navigate through it!
**BFP#1 9/5/12 EDD 5/15/13 changed to 5/25/13 after u/s, missed mc 10/19/12. D and C 10/22/12**
BFP 4 10/28/19 EDD 7/6/20
I'm sure I win most AMA award at 44 yo and I'll be 45 when baby comes in July. Both this baby and my 15-month-old were conceived via donor egg IVF. My first pregnancy was pretty normal but I did have the MaterniT21 test for genetic testing and I had extra ultrasounds toward the end. I did have an amnio at 19 weeks but that was not due to my age - they found an abnormality at the anatomy scan and wanted to make sure it wasn't something more serious.
I'm a really young 44 year old and the egg used to conceive this baby is from someone in their 20's so hopefully this will be a delightfully boring pregnancy.
2017 - egg retrieval #1 - 3 eggs, 0 embryos appropriate for transfer; ER #2 2 eggs, 0 embryos on day 3; ER #3 1 egg 0 embryos
moved to donor egg in summer 2017; 35 eggs retrieved; 19 fertilized; 9 total embryos
Fresh transfer Dec 2017= BFP! baby boy born 8/22/18
May 2019 - surprise natural pregnancy ended in MC
Nov 2019 FET; MC at 9 weeks
May 2020 FET; BFN
July 2020 FET; CP treated with methotrexate
Oct 2020 BFP!
Take a look at my blog
Natural MC 10/01/14
I'm curious to know, for those of you who are/ have done genetic testing what led you to that decision? If you don't mind me asking of course. Was it purely age related or were there other factors that influenced your decision?
I totally get why many women skip the test. It’s such an individual decision and really depends on what kind of info you’d find helpful vs anxiety-producing.
(TW)My fist was a 32 week preemie so I'm unfortunately familiar with getting scary news around delivery. I went into labor at 31w5d. The neonatologist talked to us about possible complications and it was the scariest conversation I've ever had.
I think that since I already have anxiety regarding having and sustaining a healthy pregnancy (I had a mc between my sons) I'd rather wait to hear bad news. I definitely see the merit in being prepared and did consider testing this time around because of AMA.
I'll cross my fingers and pray for those boring and scare-free pregnancies for us all as well!
Also, I have 4 recent friend examples of (3 who didnt test). The first three had no genetic testing ever or with prior pregnancies.
- friend found out her son at 2 weeks-1 month old had cystric fibrosis. This was kid #2 and she had no clue she and her husband were carriers
- friend found out kid #3 at 2.5 yrs old is hemophiliac (no clue she and husband were carriers and other kids are fine)
- friend found out at birth baby had down syndrome. She wished she knew bc she said it stole her joy of having new baby. If she'd known shed known to mentally prepare herself (and sometimes there are medical things too)
- another friends son was born with a host of genetic problems. They knew of just the hydrocephalus seen on ultrasound.
My first child was at 38 and this hopefully 2nd (and last) one will be at 40. Bc we struggled with infertility for years and bc we are also data people like @rachelredhead, we first had genetic testing done to understand what we might be carriers of, then also had genetic testing on our embryos pre-IVF. All that said, I’m still nervous about this pregnancy for some reason...and will be doing NIPT at my 12 wk appt as a first screen (and strongly hoping not to need more invasive testing from there... but if it’s inconclusive I NEED answers).
Now that we have a healthy & happy child, I feel like we would want to even more carefully consider if we would bring a severely disabled child into the mix or not...
I think for that reason I’ve been pretty emotionally disconnected and plan to remain so for several more weeks.
Natural MC 10/01/14