I will be 32 at time of delivery, no history of losses but had to do IvF due to male factor. Which I think should warrant pregnancy/fetus genetic testing, but apparently I'm the only one.
Other than the regular NT-finger stick and second trimester quad, I don't get the option of insurance paying for genetic testing for chromosome abnormalities (and the selfish bonus of sex identification).
Anyone else in this boat? Anyone considering paying cash oop to get a genetic work up?
I want to be as prepared and informed as medical technology allows.
Re: Age 32, no high risk, don't get genetic testing covered? Anyone else in the same boat?
if your NT results show high odds for one of the chromosomal abnormalities, at that point they'll offer you additional testing to verify, and it'll be covered.
I think what is being covered is standard of care and it's pretty good.
I was pregnant with my first at 32, and was happy with the NT Scan as my pre natal testing.
Plus major physical, medical problems of every organ system .
Just stinky to be in that grey area of 32 with Ivf, progesterone supplement til 7 weeks, seems like it warrants done testing. I'll chill. Just jealous of those 35 year olds....
I had a dating U/S at 8w and won't have another U/S until 20w. We will do the quad screen at 16w, but until then nothing.
I'm high risk because I have severe HG (been admitted several times for fluids and vomiting control). I'm on a continuous Zofran pump now which has kept me out of the hospital. But while HG makes me high risk, it doesn't have any effects on the babies genetics, so they don't offer extra testing (the real worry with HG is maternal health, and low birth weight of baby, which is monitored at the anatomy scan and later).
It's hard waiting, but I count myself lucky. To only "need" an U/S at 8w and not again until 20w is a good thing. I had quick U/S at 10.5w, but that was in the ER and only because they couldn't find the HB on Doppler (I was there for HG complications). Baby was fine tho.
TL:DR.... It's a good thing to not need the extra screening, but yes, waiting, worrying, and thinking what if is brutal. I try not to think about it. Our quad screen is in Jan at 16w and I'll make my self neurotic if I obsess over it. I totally understand how you feel :-/
My OB told me that IF the blood test came back and didnt look so good the additional tests she would send us to get WOULD be covered because it would make me be considered a "High Risk" Might be someone to look into.
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I've heard that as well. But I'm definitely not going to sit around hoping that the NT scan uncovers issues that would make the full genetic screen covered. I'd prefer to have my NT scan look super low risk. :-)
Counsyl informed preggo test is 1000$.
Everyone else is about the same, try said on websites that if Insurance states they will cover, if they back out, the most you will be stuck with is $250.
I even looked up all recruiting clinical trials to see if any cell free DNA trials were occurring within a 2/3 hour drive of me.
Guess I'll just have to rely on praying and healthy diet with plenty of organic vegetables and exercise...
Meh. Thanks for the cool stories ladies. Except you, miss 29 year old with testing covered. I'm envious.
Go eat some yummy romaine for dinner ladies, I'll catch you all later.