June 2015 Moms

First trimester screening

Have we discussed this? Sorry if we have. Is anyone doing this? My doc asked me about yesterday at my appt. I didn't do it with my son but considering it this time. My insurance covers it also, which is nice. What are everyone's thoughts?
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Re: First trimester screening

  • We did it with DS bc DH is adopted. He knows his birth mother, but nothing about his birth father. We did genetic counseling too. We will do it again with this baby.
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  • I will do it. I want as much info as I possibly can have. If something were wrong I wouldn't want to find out in the delivery room.
  • We did it for peace of mind with DS, so we'll probably do it again with this one.

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  • We just did ours on Thursday.
  • We haven't done it with any of the others and won't this time. Partially because insurance doesn't cover much of it, partially because we have almost zero risk factors for most things, and partially because it would cause more stress. I know me, and I'd be anxious about the results and I'd be more stressed out if it came back with any elevated risks. It's strange I know, but I would do better finding out later on if something was wrong than if I discovered it early.
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  • We are doing the cell free dna test at 10wks this time. We didn't last time but I feel like now that we already have one, we need to be more prepared. It's a fairly new test and has a 99% detection rate and a 0-0.07% false positive, which makes me feel better. And it's just a maternal blood test. The things they do now are crazy.... It also tells the sex. Not sure if we'll find that out so soon though....
  • We may do the harmony blood test, it gives definitive results. Our ins won't cover it, so it will depend on how much it is.
  • SoCalGal915SoCalGal915 member
    edited October 2014
    We are doing the testing. I don't know if my insurance covers it. My appt is set for 10w6d. @willowprincess‌ Unless cost is a huge impediment, I see no reason not to do this testing. Some genetic diseases are totally random. Wouldn't you like to know ahead of time if your baby has Downs Syndrome so you can plan or take appropriate action? I think it's foolish NOT to test.
  • My dr does the panorama which is just like the materni21. I have experienced a genetic defect in a prior pregnancy so I need the peace if mind. A lot of genetic diseases will cause late term miscarriage, stillbirth, or cause the baby not to live long once born. Others, like Down syndrome are manageable. I think every child has the right to the best possible care and sometimes that means a lot if research and preparation ahead of time. Ignorance is not bliss when it comes to things like this.

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  • Does anyone know what the cost difference is between the different tests? I'm considering doing one of the fetal DNA tests but am thinking none of them will probably be covered by insurance. Maybe I'll just do the first trimester screening depending on the cost difference.
  • My first appointment isn't until 11/11 but I plan to ask about this then. I definitely want to do it for peace of mind/to be prepared. Also I like that many of them can tell you the sex early. Normally, insurance only covers this for high risk or advanced maternal age moms. A friend of mine gad her first at 35 and it was covered for her. I'll gladly pay the few hundred bucks for it out of pocket if I need to.
  • We did this with our DD because they thought, from our 9 week sonogram, that she had Gastroschisis, so they suggested further testing, she was totally healthy. We haven't discussed doing it this pregnancy or not.
  • We might if it's offered. H has CF and I'm not a carrier, but we might be able to get it covered by insurance because of his genetic disorder.




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  • @SoCalGal915 no I don't necessarily want to know way ahead of time. I likely would discover it at the anatomy scan and that's early enough for me. That still leaves time to prepare before birth. I'm not saying people shouldn't get the tests. If you do, then please do. But we choose not to. Nothing wrong with that.

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  • We'll get the blood test done around 11weeks to find out the blood type (I'm RH-) but I don't know about the other tests. My OB said I wasn't high risk with my son so I didn't do anything but verify I am not a CF carrier. This time I'll be 3.5 years older, but still not 35 until April so I don't know if she'll reccomend it or not.
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  • I'm 36, so yes please I will take advantage of the advanced maternal age stamp that goes on my chart! Take that insurance!

    We'll opt for whatever version of the Materniti21 test that my OB uses. My first appt isnt until 11/13 at 8weeks though, so I have to wait to find out what it will be.
    DS1 born 3.15.2011
    DS1 edd 6.21.2015
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  • Planning to do MaterniT21 at exactly 10 weeks.  We did it the last time and had results in about a week and a half.  I felt much better knowing that baby was genetically normal and that the potential for a healthy pregnancy was very high.  
    TTC #1 12/2009
    BFP #1 1/2010, M/C 6 weeks
    BFP #2 6/2010, DD lost to
    congenital heart diseasewe are heartbroken.

    TTC #2 4/2011, diagnosed MTHFR, FVL
    Four natural cycles BFN; Clomid IUI BFN; Follistim IUI BFN;
    1/2012 IVF #1 BFN
    4/2012 FET BFP #3
    5/2012 7w1d u/s: anembryonic demise; M/C @ 8w.
    6/2012 found Stage II/III endo on laparoscopy, removed w/ laser.
    8/2012 IVF #2 epic fail: no viable embryos.

    Vacation, break, second opinions, on to new RE.
    1/2013 Surprise chemical pregnancy BFP #4 (break cycle), IVF #3 postponed.
    2/2013 TI w/ hormonal support, prednisone, aspirin, Lovenox, acupuncture gave us a miracle BFP #5!
    Heartbeat on U/S at 6w1d!
    Baby,please stay!!
    Our miracle baby boy arrived 10/2013!  We are so in love!!

    10/2014 Surprise BFP #6
    Our second daughter arrived in May 2015!  We are so grateful!  

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  • Does anyone know what the cost difference is between the different tests? I'm considering doing one of the fetal DNA tests but am thinking none of them will probably be covered by insurance. Maybe I'll just do the first trimester screening depending on the cost difference.
    I believe that several of the tests offer a pretty reasonable cash price, like $200 or so.  However if you have any risk factors or are over 35, your insurance very well may cover it.  
    TTC #1 12/2009
    BFP #1 1/2010, M/C 6 weeks
    BFP #2 6/2010, DD lost to
    congenital heart diseasewe are heartbroken.

    TTC #2 4/2011, diagnosed MTHFR, FVL
    Four natural cycles BFN; Clomid IUI BFN; Follistim IUI BFN;
    1/2012 IVF #1 BFN
    4/2012 FET BFP #3
    5/2012 7w1d u/s: anembryonic demise; M/C @ 8w.
    6/2012 found Stage II/III endo on laparoscopy, removed w/ laser.
    8/2012 IVF #2 epic fail: no viable embryos.

    Vacation, break, second opinions, on to new RE.
    1/2013 Surprise chemical pregnancy BFP #4 (break cycle), IVF #3 postponed.
    2/2013 TI w/ hormonal support, prednisone, aspirin, Lovenox, acupuncture gave us a miracle BFP #5!
    Heartbeat on U/S at 6w1d!
    Baby,please stay!!
    Our miracle baby boy arrived 10/2013!  We are so in love!!

    10/2014 Surprise BFP #6
    Our second daughter arrived in May 2015!  We are so grateful!  

    Lilypie Angel and Memorial tickers


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  • I do not think we will be getting the testing done. I'm in the whole "It would cause me stress/anxiety and that would be worse for the baby overall" camp.
    I have one friend that always has gotten it and one that says she did it and regretted it because it stressed her out so much.


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    BFP on Sept 29, 2014: our 2 year anniversary


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  • @willowprincess‌ If something is wrong with the baby, we will terminate the pregnancy. I don't think it's fair or right to knowingly bring a mentally challenged child into this world. If I waited until the anatomy scan and god forbid, found out something detrimental, it would be too late to terminate the pregnancy. (I understand and respect if you don't believe in this. We can agree to disagree.)
  • @SoCalGal915 I can understand why you would get testing in that instance, but you are right in that we disagree there. We would not terminate no matter what. So that definitely factors in our decision. It is definitely a personal decision for everyone.
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  • We decline all optional tests each time. I have know way too many people whose results were high risk when nothing was wrong, and for some this impacted the rest of their pregnancy - worry, stress, high risk, extra testing, and even early induction (leading to a Caesarian). And I know of 2 times where the results were low risk but the babies actually were born with ds. So either way I wodnt believe the results. And finally the diagnostic tests (amnio and cvs) carry a small but real risk of miscarriage. My mother had a stillbirth immediately following an amnio, as did my aunt. Years ago, but still not something I could ever consent to given that (to verify results).

    Im not high risk so the new blood tests aren't covered, and Im not concerned enough to pay an addl hundreds of $ oop.




    11/18/16 missed m/c 9w1
    05/2017 cp
    08/03/17 no hb 8w

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