I am a wreck. I feel like my world just came crashing down. I got a call this morning that the results came back high risk. I am 40 my u/s looked good 1.6 - 1.8 neck measurement saw the nasal bone and s/he was moving everywhere. Blood work came back Pap A: .4 HCG: 4.2 which brought my risk of having ds greater than 1/10.
Going for a CVS in two days. sick to my stomach. Any one have a risk for downs worse than 1/10 and have a normal healty baby?
what else can cause a low PapA and high HCG?
I need positive support right now... I am a mess.
Re: NT results
Me:40 AMA, DH:36 0% morph, TTC#1;
BFP#1 4/2011, MMC 6/2011 11wks Trisomy 13;
BFP#2 11/2011, CP
FSH: 17.9, AMH: 2.2
IVF#1 w/ICSI: ER 4/3: 5R,4M,4F
ET 4/6 All 4 (1-8A+, 2-8A-, 1-3A) BFP#3
Two weeks of beta hell = Blighted Ovum
IVF#2 Aug/Sept: ER 8/27: 4R,3M,3F
ET 8/30 (1-8A+, 1-6A+)
Beta#1 9/10: 350; Beta#2 9/12: 796; Beta#3 9/20: 9155
Expecting Boy/Girl Twins! My babies were born 4/23/13 at 36w1d!
BFP #1 - missed m/c 4.18.11 found @8w3d, d&c @13w
BFP #2 blighted ovum found 8.2011 @8w, misoprostol
BFP#3 - missed m/c 6.11.12 @ 9w3d, d&c revealed extra chromosome 15
BFP#4 8.10.12, DD born 4/26/13
Over-40 parents...what we lack in vigor, we make up for with cunning.
Make a pregnancy ticker
I had awful results at first too....I am 39 and my blood work numbers apparently made the risk even worse. But. my sonos were always perfect. My DH and I made a decision early on that what will be will be. We didn't want CVS or amnio. We had each NT scan, then the genetic sono at 18 weeks and our 20 week anatomy scan. Each one was perfect. Not a single soft marker for a child with Downs or any other issues. Doctor told me he would rather have me have lousy blood numbers and perfect sonos than other way around. I am now 35 weeks and doctors tell me this is a very healthy baby based on sonos and weekly monitoring,
Hang in there. The wait between my first NT results and 20 week anatomy scan was brutal, but the blood results often give many false positives, especially in the over 35 group.
Me 41 DH 46 Not actively ttc, surprise BFP on 1/6/11! 4/1/11 m/c our sunshine at 16wks after complications from CVS test. TTC #2 **5th cycle 12/6/11 BFP! Missed m/c at 9 weeks 1/21/12, trisomy 14. Two Chemical PG 3/12&7/12
** BFP 8/16/12 beta #1 148! beta#2 407 beta #3 4000 u/s 9.10 1 lovely hb 126, Baby Boy is due 04/28/13!!
I am 37 with my first. Last week my NT scan was measured at 3.9 mm. My blood work brought my odds to 1:4. We had a CVS, results came back Friday and we are having a healthy baby girl.
These are fairly new tests, some "bugs" still need to be worked out. IMO the invasive tests give more concrete results.
I am sending you good thoughts. I know what you are going through.
I have no experience but I wanted to wish you the best of luck. I agree with PP sometimes age, right off the bat, skews the odds against you. GL and I hope it's just a false alarm.
JM
That is not true. Our son, who had Down Syndrome, had a nasal bone. That said, if NT is normal AND a nasal bone is present, it significantly reduces the instance of chromosomal abnormality. I think it goes down to 4% if I remember what my MFM quoted.
My results with my son were 1:10. We did the amnio (were 17w when we got results). Amnio came back totally normal and he certainly doesn't have Downs Syndrome.
What tanked me was my PappA as well. I can't recall if mine was high or low though. What I've learned since then though is that abnormal PappA (again, I can't recall if it is high or low PappA) can be an indicator of a risk for Pre-Eclampsia. I developed Pre-E in my 37th week. Talk to your doctor about this so they are aware to keep on the look out if it applies to you.
I hope your CVS went well and that you've already gotten results back that you are in the 90% like I was that have a perfectly normal baby.
BFP#2 2.5.11 (EDD 10.15.11) DS born 9.28.11
BFP#4 8.27.13 (EDD 5.6.14) DD born 4.23.14
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