I don't typically post here (I'm usually on the Nov 12 FB group) but thought you ladies would probably have more experience than anyone. I have the heterozygous MTHFR mutation was am 35w5d. Just had my weekly ob appt., and they are having me go for weekly BPP. Dr. didn't really give a good reason for doing this (don't get me wrong, I will cherish any moment to take a peek at LO) other than he wanted to make sure everything was okay with the baby. Since there is little research in general about MTHFR, he basically wants to cover his butt. Anyone else have to do this? Just curious...
BFP#1 1/27/09 :: Natural m/c 2/6/09 @ 6w
BFP#2 5/11/09 :: Natural m/c 5/27/09 @ 5w5d
BFP#3 7/24/09 :: Missed m/c, baby stopped growing at 6w4d :: natural m/c 8/28/09 @ 8w6d
BFP #4 11/27/09 :: DD born 7/27/10
BFP #5 2/29/12 :: DD born 11/6/12


Re: MTHFR moms & 3rd tri
BFP #2 10/29/08 ...stillborn via c/s @41w 7/20/09
missing my baby everyday
BFP #3 1/20/10 My angel's little sister Grace Madison was born September 8th 2010 @37w. We're so blessed! Thank you angel for getting her here safely.
BFP #4 12/30/11. Jackson Christopher 8/22/2012 via repeat c/s @ 37w 3d
I am 30 weeks and hetero MTHFR, I just had a regularly scheduled appointment with my MW yesterday and she didn't mention anything about this. BUT I did have to be cleared by my MFM to go to this birthing center and he took me off lovenox at the same time (13 weeks), so maybe since he cleared me I don't have to do the BPP, which I was under the assumption was reserved for high-risk pregnancies, which I am not since I was removed from the lovenox. My RE and MW don't consider MTHFR alone to be high-risk.
Are you on enoxaparin/lovenox?
So, I am really not any help - sorry!
#1 BFP 1/10/11; missed m/c discovered 7w5d
IF Dx: Endo, hetero MTHFR mutation, poor morphology
#1 IUI: 1/18/12 = BFN
#1 IVF/ICSI 4/2/12 = 2 x 7-cell and 1 x 5-cell transferred (3dt) = BFP!!
H was born at 41w2d on 12/29/12 - be still my heart!
#2 IVF/ICSI 1/19/14 = 2 x 8 cells transferred (3dt) = BFP!! EDD 10/09/14
M&W born at 37 weeks on 9/18/14 - I am the momma of 3 boys!!!
My doctor didn't call it that but based on the other ladies responses I guess I am. I know starting at 30 weeks I'll be doing twice weekly NSTs and I will have an u/s every other week. He never said anything specific about the ultrasounds that I'd be getting but he did send me for a "growth scan" on Monday where the tech checked the baby, placenta, fluid and my cervix. I believe this is what my other scans will be like as well.
I am homozygous for MTFHR (I can't remember which one right now I think the A one?) and I had pre-eclampsia and a stillbirth with my last pregnancy so I'm not sure if it is just because of the MTFHR. I also take daily low dose asprin and have been since I was TTC. My doctor talked about lovenex but decided the asprin was enough.
No problem! Thanks for the response! I'm only taking baby aspirin (which I will be stopping this week) since I do not have any other symptoms/diagnosis. I was not high risk for my daughter or this pregnancy, so I'm not quite sure why he's being so cautious at this point. Similar to you, just having the MTHFR did not make me high risk.
BFP#2 5/11/09 :: Natural m/c 5/27/09 @ 5w5d
BFP#3 7/24/09 :: Missed m/c, baby stopped growing at 6w4d :: natural m/c 8/28/09 @ 8w6d
BFP #4 11/27/09 :: DD born 7/27/10
BFP #5 2/29/12 :: DD born 11/6/12