Just be aware that the medical staff with call you an AMA -- for advanced maternal age. You will have more tests. They will monitor you much more closely at 35+. You will undergo chromosomal testing, the full workup, and probably go over the results at an appointment with a genetics counselor who interprets the findings. You have a X% chance of this genetic condition, an X% percent chance of that condition. Just know this going in. |
I'd be a little weary of listening to an expert who uses a hard cutoff like this. |
Hi. Mom of the kid with Down syndrome here. Let's not start a debate on the ethics of having a child with Down syndrome; that's getting too far off topic. The point is that abnormalities like Down syndrome can happen to anyone at any age, but the risks increase as you get older. And despite what people on here are saying, there is nothing you can do to guarantee it won't happen to you. You can do the pre-conception genetics counseling (we did that), take the vitamins (did that, too), give up alcohol (yes), live a healthy lifestyle (yep), and do everything "right," and still end up with something wrong. Sometimes issues can be detected during pregnancy, and sometimes they can't. For anyone interested, there is a good essay on this topic called "Super Babies Don't Cry," by Heather Kirn Lanier: https://velamag.com/superbabies-dont-cry/ And to those who have said, "Just get an abortion if something goes wrong," I'll say this: It isn't an easy a decision for everyone. Most people don't find out there's a problem until the second trimester, past the point where they assume they are "safe" and have started to get attached. I was 17 weeks along when I found out. It's not an experience I would wish on anyone. Whether you are pro-choice or pro-life, a prenatal diagnosis can cause you to question all of your values. Ultimately few people regret their decision, whatever that decision may be, but it's a hell of decision to make. And you will be judged for it, no matter what you pick. I'm not trying to scare anyone. I just don't want anyone to take the risks lightly. Your chances of a problem are low, but they are not zero. That doesn't mean you shouldn't try for another kid. Just make sure you have these difficult conversations with your significant other ahead of time. Where do you stand on terminating, and under what circumstances? Do you have the resources to care of a child with special needs? Talking about these concerns won't prevent a problem nor the emotional upheaval of a diagnosis, but at least you will have a framework to go off of should the worst happen, so that you aren't making life-changing decisions in crisis mode. And if you disagree about how to handle a situation, better to know that before you conceive. Good luck to all would-be mothers out there. May you all have healthy children. |
Really? Perhaps your child is very easy going, has a very mild condition, or a combination of the two. I do not imagine most siblings of a person with a significant disability will claim that it has little/no effect on them. Sometimes the effects are actually really positive but a lot of times with really serious conditions they are not. I'm glad your family is not affected. |
Hi OP, I had my kids at 36 and 39, so I generally would say go for it! But if your husband’s anxiety about the risks is very strong—even if there’s good data that might show that the risks are much lower than he’s assuming—that might be an indication to stop at two kids. I don’t know your husband of course, but I wondered if in expressing his anxiety he is trying to communicate that he would rather stick with two kids. |
Is it much more tiring to be pregnant at 39 than 36? Did you notice/feel a difference? |
I had my first at 37 and am pregnant with my second now at 40. PP sounds like it’s a hassle but it’s anything but. I got a blood NIPT test at 12 weeks and they left a voicemail and sent an email with results. I also found out the gender then. Because I was AMA my insurance fully covered it automatically. My doctor has never said anything negative about my age. Only a matter of fact comment like “because of your age insurance will cover XYZ”. At 40 they said they “won’t let me go past my due date” at my first visit at 6 weeks but haven’t mentioned it again and I’m now 25 weeks. We had the option (like every pregnant person) to do genetic testing but opted to skip it. |
I was 37 and the fetus tested positive for Down syndrome, the genetic disorder caused when abnormal cell division results in extra genetic material from chromosome 21. Although chances are very low, I was one of those due to advanced maternal age. It happens. |
Hard to say—I was definitely more tired the second time but I had a toddler so that was a huge factor! |
I’m sorry about your situation. This is the risk with every pregnancy. |
There's nothing magic about turning 35.
I'd go ahead and do all genetic testing/NIPT and make sure your anatomy scan is scheduled as early as possible. |
Learning Disabilities are much more common among children born to mothers over 35. In most cases these are mild and wouldn’t be obvious to anyone who wasn’t intimately familiar with the child’s academic performance. |
Not everyone is this cavalier about ending the life of their fully formed fetus. |
I’m the PP who was pregnant at 37 and again now at 40. So far this pregnancy has been easier except that I sustained an injury unrelated to pregnancy so I’m already waddling like I’m 42 weeks along. 😂 |
OP it’s important to remember that nothing is ever guaranteed with kids. A friend had her first at 25, totally normal pregnancy, nothing to be concerned about. Went to hospital for labor and had a bad delivery and child ended up disabled with cerebral palsy. It has a hard few years for them parenting. There are thousands of things that can go wrong with a kid and very few of them are related to maternal age. It’s just a gamble. |