I'm 11 wks today and had my sequential screening. They asked me if I would like to do a test called verifi that detects higher than the normal test for down syndrome and it will detect the baby's gender. I told the Dr. Yes and we will be finding out if our baby is a boy or girl some time next week. Of course praying for a healthy baby but can't wait to know.
Re: Genetic Testing
This would be a great post for the weekly randoms thread, or your weekly ticker change group.
Son #1- 2/15/08
Son #2- 8/18/10
Baby 3 due 8/8/16
Maybe things have changed, but that was the terms. Otherwise it's out of pocket.
From my research into insurance coverage, a lot of health insurance companies cover it if the mother is 35 or over. More and more insurance companies are covering NIPT, though, since it's non-invasive, extremely accurate, and it's "cost neutral" to insurers.
You can call your insurance company and ask, but the woman I spoke to at mine had never heard of NIPT and only knew the specific laboratory names (like Harmony or Verifii) of tests that were covered (after some research). My insurance company was very nice about all my questions and did everything they could to answer them, though -- so I'd say definitely call and asking if you have questions about coverage.
I called my insurance company about it. The one my doctor recommended is called Harmony. If anything, they will go back to the doctor for justification. The doctor will have to write a brief explanation of why they recommended *this* test. And no, "The patient wanted to know what color to paint the nursery" won't fly
Usually the doctor won't recommend it unless there is some ability to justify it, for just this reason. Advanced age of either parent (in our case, my husband) a family history, etc.
My insurance confirmed they cover it, as long as it is performed at a doctors office, under a doctor's recommendation.
I admit, I am excited we're getting to peek at the sex, but mostly excited we'll be getting reassurance everything is okay. My husband has been stressing after reading a bunch of articles about how after age 36 a man is twice as likely to contribute a mutation as at age 20. I am hoping we'll be able to put his fears to rest in a few weeks.
Our little lightbulb is on the way!
12 weeks 3 days
TTC since Oct 2011
Me: 33, hypothyroidism since 14, cleared all HSG, US, Pre-pregnancy panel tests.
Hubby: 36, testicular Ca, chemo April-May 2012.
Natural cycle IUI #1 with trigger and Progesterone Suppositories (Jun 2012) Neg
Natural Cycle IUI #2 with trigger and Progesterone Suppositories (Jul 2012) NEG
Aug 2012 - break due to needing a girls' weekend in Cape Cod
Natural Cycle IUI #3 with trigger and prednisone (Sep 2012) NEGATIVE
Switched fertility clinics - forced break Oct 2012
Natural Cycle IUI #4 (Nov 2012) no trigger, no progesterone, no prednisone (Nov 2012) - Neg
1st round Clomid Cycle IUI #5 (Dec 2012) - POS
(My family history suggests that I might have a Robertsonian Translocation and I could be a carrier for Downs. So, we're keeping things private.)
I find it interesting. I've never heard of this test and will now ask my OB.
<a href="http://www.thebump.com/?utm_source=ticker&utm_medium=HTML&utm_campaign=tickers" title="Getting Pregnant"><img src="http://global.thebump.com/tickers/tt1ce3d9" alt=" BabyFetus Ticker" border="0" /></a>
I am getting the test at 12 weeks. To me and my husband it is worth it. He really wants to know the gender.
BFP #2 8/22/12 | EDD 5/5/13 | DS1 born 5/9/13
BFP #3 4/25/15 | EDD 1/7/16 | MMC 7/2/15 @ 13w1d | D&E 7/8/15
BFP #4 12/9/15 | EDD 8/22/16 | DS2 born 5/18/16 at 26w2d
Just keep swimming.
I got back my results today. Baby is very healthy and a Girl!!!! I'm so excited good luck to everyone.
BFP #2 09/03/17 | EDD 05/17/2018
I think it's a good idea to have it done early if the result will change whether or not you choose to continue with the pregnancy. Also, if the fetus has a condition that is incompatible with life outside of the womb, you're better off finding that out at 10 - 12 weeks as opposed to 16 or 20 weeks. However, if you're young and healthy with no significant family history of chromosomal abnormality, then it's probably not worth the cost.
So I called my insurance AGAIN spoke to someone different and she said the person I spoke to last time left out that its only covered if its pre-authorized, which would be the case if I was over 35 or due to medical history.
So please check with your insurance for sure if they say its covered and what authorizations if any are needed, and get a persons name (my doc said to do that lol). Otherwise the doc said the cost is very high if you aren't covered.
i had mine done yesterday, after the nuchal translucency scan. during the scan, my doctor told me he was 85% sure i'm having a girl.