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So as I mentioned in a previous post, I was not at all happy with my OB for my first appointment on 1/6 and decided to switch when I was told that would be my one and only ultrasound. My appointment with the new OB is on February 1st. However, the appointment is with the OB nurse, not the OB at all.
I'm concerned because for my first appt on 1/6, not a single thing was mentioned about genetic testing. No background history about my family was taken. I talked to my SIL and she mentioned that she had an NT done at 12 weeks to test for Down's, Trisomy 18, and the like. She mentioned that Tay-Sachs is more prominent in our French-Canadian heritage. I had never even heard of this test, or any other genetic testing. I'll be 11 weeks at my next appointment with the OB nurse, so I won't even have the chance to get anything done then because I won't be seeing an actual OB.
Is it common to just not inform moms-to-be about genetic testing? I'm 30, have two cousins with Downs, and apparently have a heritage that has a higher propensity for a genetic disease. As I sit here thinking about this, I'm getting angrier and angrier that nothing was ever mentioned to me so far about testing of any kind, with either OB. I know the chances are slim that there will be a problem, but if I hadn't done some research I wouldn't even know about my increased likelihood or the options that are available.
With DD they never offered 1st trimester screening with me. The first appointment was with a nurse as well. She asked all of my history. It was after I did the quad screen that levels were high and they recommended a genetic counselor. After that appointment we had the choice to pursue testing. Since I was transferred to high risk the first time I just decided to start there this time. They offered testing right away (which can be done either in the 1st or 2nd trimester, your choice) because of my history.
I hope you get answers soon. I'm sure if you express concern they will go along with your wishes. ((HUGS))
My OB talks about genetic testing at the 8 week appointment for everyone.
But, they've started a new maternal blood test now, my office is moving away from the nuchal translucency scans because the blood test is more accurate--the NT scan has a high incidence of false positives that lead to amnios that carry a risk of miscarriage. The maternal blood test finds the baby's DNA in your blood and tests it for common genetic disorders. I was offered screening via maternal blood for trisomy 13, 18 and 21 as well as CF. I don't know if they have a TS screening but I imagine they do, if you are concerned about it. The test can also tell you the baby's gender.
My ob said the test can be done any time after 7 weeks but it's better to wait until after 10 to get a better sample. I have not decided whether or not I'm getting the test done, but if you have missed your window for the NT scan to look for trisomy 21 (11-13 weeks) you could request the blood test which will be more accurate and look for more disorders anyway.
But yeah, I do think the office should have had someone call you to discuss genetic screening. Perhaps they just aren't organized enough to have it figured out yet about where you are in the pregnancy and that you're a new patient. But, at 11 weeks for your first visit you should still have time to do the NT scan if you want it.
Also, I had heard that T-S is more common in certain Jewish populations--I didn't know it was a prominent feature in the French Canadian community, too; that's interesting!
Sapphire you are very close to me! About a 2 hour drive
When I made my appt the scheduling nurse just basically told me any questions I had would be addressed at my appt. I know that When I am talking to the nurse if there is any questions they refer them to the doctor and that the doc is the one who writes the referall to the specilist for any reason. maybe at your appt your nurse does the same? maybe shes just there to do routine stuff and if something arises the doc just steps in.
Korbyn 28 week miracle 5/17/13
I heard they arent accurate at all and usually just lead to more worry. The first doc I saw pretty much told me he didnt recommend it and mumbled on and didnt say much about it. When I switched to the team of midwives, they offered it in an unbiased way and I preferred that. I still declined genetic testing as it often has way too many false positives. I would rather not worry about my baby in there and keep it close as possible to a natural birth experience with the exception that I cannot wait to know the gender.. I personally wouldn't worry about the extra testing unless you are really worried.. but it could just lead to more worry.
I asked about the CVS at my last appointment and was told that Dr. didn't recommend it, even though I am 36. I will be having bloodwork at 11 weeks and then the NT scan at 12 weeks. If there are indications that we have a high risk for genetic defects, I will go ahead with the amnio or CVS at that point.
Mama to many:
Twin DDs: 14 yo
Step DD: 15yo
Step DD: 11yo
Rayna-August 18, 2013!
With my pregnancy with chase, I was never offered one.
With this pregnancy, the Ob did talk about it and give me information and booklets on each of the available tests. She told me it was optional, and no pressure to get it done. She also mentioned that if I got it done at her office, my insurance most likely won't cover it. She said if I did it at the high risk doctor, my insurance WOULD cover it (how weird).
Then the high risk Ob scheduled it without even talking to me about it! lol (I'm okay with that, I wanted it anyway)
Sooo... I think it's just a matter of your Ob's views. Funny thing is I have the same Ob from Chase's pregnancy to this one and once they offered and once they didn't.
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personally, I never opt to have genetic/amnio testing done. When I found out the risks of harming my baby were higher than the risk of something being wrong with my baby (due to my age) I said no. I've also heard of so many false positives. There is really nothing that can be done except abort your baby and that is NOT an option for us, so we always opt out.
I have always been offered it and have always done the first trimester bloodwork and NT scan. If something were to be wrong, I like to have all the information possible so that measures could be taken to prepare for whatever challenges baby may have at birth. I do not think I would do an amnio, if it got to that point because I would be too scared and not want to risk it, especially since we would have the baby no matter what. But yes, I have always done the bloodwork/NT scan
I was offered the NT scan and bloodwork with this pregnancy and my last. I enjoy the extra peek and honestly, though it would not change my mind, I want to be prepared for the increased possibility that there may be something "wrong" (I dont like that word because it sounds so neg.) so we can be ready for that as a family. I have a family history of certain chromosone problems and spinal issues, so maybe that has some holding on why it was offered to me both times. But I enjoy it, and I have never personally known someone who had a false positive with the NT scan but it does happen. I just prefer it to more invasive testing (CVS and amnio). I asked for the materni21 but was told I was not "at risk" enough for it.
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