Good morning, ladies! For anyone who is deemed high-risk or is receiving additional monitoring.
How far along are you?
Why are you considered high-risk / getting increased monitoring?
What type of additional testing, monitoring will you be getting?
Any questions / rants / raves?
Re: High Risk Check-in 6/6
5 weeks
Why are you considered high-risk / getting increased monitoring?
Spondylilothesis and Hypertension
What type of additional testing, monitoring will you be getting?
I will have biophyiscal profiles in 3rd tri multiple times for the hypertension. As for the spondy, this is my first pregnancy post fusion so we will see....
Any questions / rants / raves?
Not yet.
I'm eager to get my medical team assembled, and feel like I'm in limbo, but I just had an ultrasound last Thursday, so I don't feel anxious about being between doctors. Yet.
Also, I'm 40, Rh neg, with a donor egg from my Rh pos wife, and I carry the MTHFR gene, compound heterozygous, with normal homocysteine levels. And I'm overweight. Those are all factors that bump me towards high risk, but it's the mo/di twins that put me solidly in that category. So far, my RE put me on baby aspirin and prescription prenatals (with the good folate) for MTHFR.
7 IUIs, 7 BFNs.
2 IVF attempts, both cancelled and converted to IUI, both BFNs.
Decided that my tired old ovaries are ready to retire.
Next step- reciprocal IVF, using my wife's eggs, my uterus!
fresh 5 day transfer (2 embryos) 4/17/17- BFP!
Identical twins "due" 1/2/17 (but anticipated arrival sometime December)
Why are you considered high-risk / getting increased monitoring? I'm AMA, there are congenital heart defects on my mom's side of the family, history of LEEP(x3) for cervical dysplasia, and I had preterm labor with DD.
What type of additional testing, monitoring will you be getting? I'll be followed by MFM, with extra ultrasounds to check for heart functioning and also cervical length.
Any questions / rants / raves? Not yet! My 1st appointment with MFM is June 26th.
I use Hypnobabies! http://www.hypnobabies-store.com/link.cgi?affiliateID=472
J18 December Siggy Challenge: Christmas Movies!
EDD: 1/6/2018
Eva Jane: 7/23/2014
How far along are you? 10 weeks, 1 day
Why are you considered high-risk / getting increased monitoring? Previous Pre-E requiring hospitalization and induction. Also Class D drug taken during 1st trimester
What type of additional testing, monitoring will you be getting? All the genetic testing plus 4 additional US before the 20 week AS. Looking for any Neural Tube Defects from the medication. Later on extra BP monitoring
Any questions / rants / raves? Just praying for a healthy baby with no problems
How far along are you?
7w6d
Why are you considered high-risk / getting increased monitoring?
5 previous 1st tri losses, AMA, elevated CRP (inflammation issues), and an as yet undefined immune issue - the CRP issues commonly contribute to pre-e, low birth weight, pre-term labor and other fun stuff. Like @smorzandoj, I will be required to have multiple 3rd tri biophyiscal profiles to keep an eye on the babe.
What type of additional testing, monitoring will you be getting?
Feel like a pin cushion! Lots of blood draws, monitoring of CRP level, white cell and complete blood counts, among other profiles. ETA: also getting weekly ultrasounds right now, for which I am sooo grateful.
Any questions / rants / raves?
Sad to be talking about graduating from my RE (because he is amazing), but trying to keep perspective that it is an incredible thing to be making progress! Trying to keep looking forward - will be meeting my MFM and getting back to my regular OB in a couple of weeks.
Me: 40, DH: 35 / Married: 2009; TTC #1: 2013
2013 - 2015: 5 pregnancies —> 5 miscarriages
TTCAL with RE (RPL specialist): February 2016
2016: 3 medicated TI cycles —> 3 medicated IUI cycles: All BFN
Donor Egg IVF Transfer: May 1, 2017
May 11, 2017: BFP!! Beta #1: 449.1, Beta #2: 844, Beta #3: 1714
EDD: 1/17/18, it's a GIRL!
E. L. A. born 12/7/2017
10+2
Why are you considered high-risk / getting increased monitoring?
Carnitine deficient (an enzyme essential to the metabolic process...the absence of which can lead to heart issues, among other things) and ulcerative colitis.
What type of additional testing, monitoring will you be getting?
CONSTANT blood draws to check carnitine levels. Lots of extra pills too. I'll be meeting with a perinatal doctor for regular ultrasounds and genetic counseling. I also will be having my heart checked/monitored to make sure I have no effects from my carnitine deficiency. My ulcerative colitis will just be monitored to make sure I have no flares. Right now, things are pretty well controlled in that arena (thank goodness)!
Any questions / rants / raves?
I'm already sick of all of these extra appointments. They are really hard to juggle with a toddler!
@missblaze What congenital heart defects run on your mom's side of the family? I can sympathize. That's something we have far too much experience with now, unfortunately.
@burnsmommy27 How are you going to do your genetic testing--CVS or amino? I don't know anyone else doing CVS. It's lonely here in genetic mutation land!
How far along are you? 8 weeks today!
Why are you considered high-risk / getting increased monitoring?
It's all in my signature, but…
*TW* our first child had HLHS (two heart chambers instead of four heart chambers) and a randomly occurring genetic mutation called CHARGE syndrome. He died when he was three weeks old. Also, I developed postpartum preeclampsia a week after he was born, and I went into full-blown congestive heart failure. It was like a damn episode of Lifetime television. So much drama.
What type of additional testing, monitoring will you be getting?
We're doing chorionic villus sampling at 12 weeks to test for CHARGE syndrome. Our geneticist says there is a 1-3% chance of recurrence. We will also do a full genetic microarray and test for trisomies 13,18, and 21. As well as a variety of X chromosome linked genetic disorders. Because we're going to have the genetic material, so why not do all the testing?
We're also going to do early fetal echocardiograms, between 16 and 18 weeks, to make sure this little one has a healthy heart.
Any questions / rants / raves?
Please don't think I'm evil, but we love this little one so much that if he or she has CHARGE, we won't let him or her suffer the way our first child did. He experienced far too much medical trauma in his short life. I'm terrified we won't get to bring this baby home. I'm afraid to get too excited about this pregnancy until I know everything is ok.
I'm also super pissed that my home state just passed a law strictly banning abortion at 20 weeks, with NO EXCEPTIONS for severe fetal anomalies. It's that last part that infuriates me. It puts families like us in a really tough bind, racing against time to get the information we need. Because some genetic tests take a LONG time. For example, the CHARGE test takes 4-6 weeks. Yesterday I met with our geneticist, and she told me many of her clients like us are freaking out and begging to get the 20 week scan at 16 weeks or 18 weeks instead. This new law makes a sad, tough situation even harder and scarier.
8w5d
Why are you considered high-risk / getting increased monitoring?
AMA, history of LEEP, and pre-term labor with DS (born at 35w)
What type of additional testing, monitoring will you be getting?
Counsyl testing, extra ultrasounds and referred to high-risk OB
Any questions / rants / raves?
We told our family last weekend (after 8 week confirmation/ultrasound/heartbeat) and now the next few weeks will be kinda tough- waiting to get to 12 weeks and waiting to results of the extra testing!
Girl I don't judge you at all, we are in the same boat. If there is anacephaly the baby won't make it anyways. If there is Spina Bifida I would like to know the severity before making a decision. But praying for a healthy little one.
I'm glad I'm not the only one in this situation. I will pray for your little one to have a perfect heart.
I use Hypnobabies! http://www.hypnobabies-store.com/link.cgi?affiliateID=472
J18 December Siggy Challenge: Christmas Movies!
EDD: 1/6/2018
Eva Jane: 7/23/2014
@burnsmommy27 Maybe it was the MSAFP test? I believe your doctor does a blood draw from your arm to test for that one. That test looks for a certain protein in your blood; it isn't a genetic test that looks at the baby's DNA. But if the protein level is too high or low, it may indicate a neural tube defect or a DNA problem. (Can you tell I geek out hard over all the science? Haha!)
@missblaze Oh wow, I've never heard of an atrophied or stenotic coronary artery! But that's sort of similar to one thing our son had. His aorta was under developed (aka stenotic). And the aorta connects directly to the coronary arterirs, so... Kind of similar. Does your MFM recommend a fetal echocardiogram? That will show a lot more about the heart's function then an ultrasound. And hey, on the bright side, valve replacements are starting to be done as a catheter, closed heart procedure. Even for mitral valves--that technology is brand new! So even if a heart defect is found, it can be SO much easier to fix it now than it was in the past.
9w1d
Why are you considered high-risk / getting increased monitoring?
2 previous losses, heterozygous MTHFR (C677T) and FVL.
What type of additional testing, monitoring will you be getting?
Weekly NSTs and biweekly ultrasounds in the 3rd trimester to watch for placental deterioration. I'm also on lovenox.
Any questions / rants / raves?
Lovenox sucks!
I use Hypnobabies! http://www.hypnobabies-store.com/link.cgi?affiliateID=472
J18 December Siggy Challenge: Christmas Movies!
EDD: 1/6/2018
Eva Jane: 7/23/2014
She also doesn't automatically consider me high risk because I'm 35, either.
DD2 8.22.13
MMC 1.4.17 at 16w
Expecting #3, EDD 1.29.18
Why are you considered high-risk / getting increased monitoring? History of DVT (blood clots) during and after pregnancy, FVL, May-Thurner syndrome
What type of additional testing, monitoring will you be getting? Occasional blood tests to check whether my Lovenox dose is enough
Any questions / rants / raves? I too hate Lovenox injections. My stomach looks terrible and gets these painful hard lumps under the skin - ouch.
I use Hypnobabies! http://www.hypnobabies-store.com/link.cgi?affiliateID=472
J18 December Siggy Challenge: Christmas Movies!
EDD: 1/6/2018
Eva Jane: 7/23/2014
How far along are you? 7 weeks
Why are you considered high-risk / getting increased monitoring?
T1DM (Type 1 diabetes) with decreased kidney function & FVL with a history of PEs (pulmonary embolisms - blood clots in the lung)
What type of additional testing, monitoring will you be getting?
Weekly INRs along with Cal Heparin injections 2x daily. CGM and frequent labs. Containing LCD and insulin management.
Any questions / rants / raves?
No rants but I am pretty excited. My A1C came back at a 5.2 today - which is the best I've had in my entire life!
I am MTHFR, two previous losses, and hypertension - just started after I got pregnant.
Doctor is doing increased ultrasounds through first trimester, every other week or so. We are doing screening at 11 weeks for trisomy 13, 18, and 21. I think doc will recommend more test after that. Right now he has me on progesterone 200 mg twice a day, baby aspirin, lovenox shots once a day, metanx (for MTHFR), and something for blood pressure I can't remember the name of.
I absolutely love my doctor! The first time I met with him, he basically said, "girl, we're about to change this story for you." Last week, he was so pumped about my baby's growth and heart rate, I almost started giggling.
@hesitantrenovator have you tried icing your belly before your shot? I ice mine for 10 minutes before and after my shot and only have a few very small bruises. Also, make sure you go in at an angle- that helps with the bumps.
BFP #1 Dec 2015 - CP Dec 2015
BFP #2 Jan 2016 - MC March 2016
BFP #3 May 2017 - Down Syndrome dx @ 12 wks - MC August 2016
BFP #4 November 2017
Why are you considered high-risk / getting increased monitoring?
I was diagnosed with Postpartum PreEclampsia 5 days after the birth of our DS. At 6 weeks Postpartum, I was hospitalized for severe Postpartum Thyroiditis (a near Thyroid Storm). The Endocrinologist assigned to me following the episode believes I am
an Autoimmune Thyroid patient but all labs have since been stable.
What type of additional testing, monitoring will you be getting?
All the bloodwork!
Potential 37 week induction to avoid PPPE.
No raves or rants, just wish they would find a cure or cause(s) of PE/PPPE.
I'm high risk because:
-Advanced maternal age
-Hashimoto's Hypothyroidism
-obesity
-I once had an A1C reading that was SLIGHTLY high (5.8)
I'm going to be sent to the high risk clinic for all my testing. I'm a little nervous, but doing the best I can. Trying to eat really well and get plenty of exercise, and gain very little weight.
Why are you considered high-risk / getting increased monitoring? Morbid obesity and AMA
What type of additional testing, monitoring will you be getting? We will do all the genetic testing we can at 11w. Bi-weekly ultrasounds week 30-36, weekly 36+.
Any questions / rants / raves? Not yet.
I was a little irritated, however, when the receptionist started asking me if I had thought much about the Makena progesterone shot. First, I don't know much about it (was briefly mentioned by my OB at first appt), I haven't researched much because I'd like to talk to specialist first, and I don't even know that it will be an option for me yet! Anyway- not something I wish to discuss over the phone with the scheduler.
I will be placed on high risk because i had a frozen transfer ivf with icsi. Icsi transfers may have growth problems so i will have many ultrasounds and bioprofiles. Also, more than likely, i will have GD again.
I know there are increased risks of defects, which go hand in hand with identical twins. I'm trying not to worry about that. My clinic required ICSI because we had frozen donor sperm.
7 IUIs, 7 BFNs.
2 IVF attempts, both cancelled and converted to IUI, both BFNs.
Decided that my tired old ovaries are ready to retire.
Next step- reciprocal IVF, using my wife's eggs, my uterus!
fresh 5 day transfer (2 embryos) 4/17/17- BFP!
Identical twins "due" 1/2/17 (but anticipated arrival sometime December)
Why are you considered high-risk / getting increased monitoring? AMA, will be 43 at my EDD. Also, I am adopted so zero family medical history.
What type of additional testing, monitoring will you be getting? extra ultrasounds, two so far. I will also be getting genetic testing and any tests they advise.
Any questions / rants / raves? Time is too slow between appointments! I want to hear the heartbeat!
How far along are you? 10 weeks today
Why are you considered high-risk / getting increased monitoring? I'm type 1 diabetic. Even in well controlled T1Ds, we have a much higher risk of babies with congential heart defects than normal pregnancies and a much higher risk of stillbirth. I am also notorious for developing intrahepatic cholestasis, which starts around 30w, and can be fatal for baby.
What type of additional testing, monitoring will you be getting? Well, it's supposed to be an u/s by 8w, again at 10 and 12, then 16, 20, 24, 28, 32, 36, and weekly after that. Also, starting at 32w, I will have twice weekly fetal non-stress tests. Around 24w, I will have a fetal echocardiogram to check baby's heart more closely for any defects.
Any questions / rants / raves? My OB's office is not taking my concerns seriously. I just got in yesterday (at 9w6d) for my enrollment appointment. There was no u/s, nothing. They scheduled that for July 3rd. I'll be 13w2d at that point and too late for an NT u/s, which I want. I have my OB intake appointment Wednesday and let me tell you, I'm about to raise hell about it. If my concerns aren't addressed, I will be leaving the practice, which disappoints me because I had both of my kids with them.
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Currently 10 weeks 5 days
High risk due to AMA, LEEP, positive antiphospholipid antibodies (risk of clotting), sjogrens, and use of Primidone during 1st few weeks of pregnancy (risk of NT defects).
I had 2 perfectly healthy pregnancies that produced perfectly healthy kiddos (post-LEEP, btw, so not sure why that is now a concern), but the autoimmune stuff wasn't a problem until 2 years ago.
Ive already had 2 u/s and an appt with MFM. We went with the Innatal DNA this past Monday and I'll go back Wednesday (11 + 4) for NT scan, DNA results, and potential CVS. I get to stay on baby ASA for the APA disorder for now, but will be checking bloodwork to determine if I need injections. The only other thing I know will happen is a 2x week BPP starting at week 32. OB said if anything changes from appt to appt, I'll be induced.
Rants/Raves: It's a lot of time, but I'm not complaining too much because I like the constant checkups (and ultrasounds!)