Dear Monoamniotic Monochorionic Families,
We haven't been very active on this site but success stories meant so much to us while we were expecting. We'd like to update the blog with some recent stories. If you want to share your success story please email us at monoamniotictwinmoms@gmail.com and we will be happy to share it! Email your story as well as a picture (or a few pictures) if you want to share your beautiful MoMos!
Monoamniotic Twin Moms
We are a group of moms with monoamniotic monochorionic twins, also known as mo/mo, mono mono, MCMA or monoamniotic twins. We've posted some medical studies to review and you'll find our success stories, and we hope this gives you courage and something positive to think of during your journey. Success stories are posted at the top but use the menu to the right to navigate the site. If you have momo twins and want us to share your story email us at monoamniotictwinmoms@gmail.com.
Tuesday, April 4, 2017
Oh my goodness, Twins!!! (August 2015)
I was about 20 weeks pregnant when I went to my first pregnancy
appointment with my OB. Since this was
my sixth pregnancy, I felt like I knew what to expect, so didn’t feel the need
to make any appointments earlier in the pregnancy. My doctor joked with me about my being too
busy to bother with appointments, since I work full time. I complained to her about my new health
insurance, which had a high deductible, so she commented that we’ll have to
make sure this is a vaginal delivery (cheaper than a c-section), and I remember
thinking, “Of course it will be vaginal, all of my others were...” Then she started doing the ultrasound scan,
and she turned to me and said, “There’s two”, and I responded, “You’re joking,
right?”, thinking that she was teasing me.
She turned the monitor to me so I could see the two fetuses, at which
point I said “But, twins don’t run in my family”. “They’re identical; it’s not genetic, just
chance” was her reply. I was so surprised,
I think I said “But it should be genetic!”
As my doctor kept scanning, her entire demeanor changed from the light,
friendly attitude, to a very serious one.
She told me that she didn’t see a dividing membrane, but at that point,
I really had no idea what the implications of that were. She hurried me out of her room and called a
maternal fetal specialist for me, and got me an appointment the next day for
the 20 week detailed anatomy scan.
I went to the anatomy scan blissfully unaware of the high
risks of my pregnancy. After a long
appointment, during which both fetuses were scanned very carefully and were
thank God found to healthy and defect-free, the doctor came in and explained in
a very matter-of-fact manner that my twins were monochorionic monoamniotic,
which is high risk for cord entanglement that can lead to fetal death, and if
one twin dies in utero, that frequently causes brain damage to the other twin. He told me there is no treatment or “fix”, we
just monitor weekly until ~28 weeks, at which point in-patient monitoring is
recommended, and that delivery is via c-section between 32-34 weeks. I remember my head was kind of in a whirl
after the appointment. I went out to my
car, called my husband, and told him the whole thing. Then, wanting to share with someone else, but
not yet ready to freak out my mother, I called my friend, who happens to be a
nurse. We talked, and I was feeling a
little better, until I checked out a link that she had emailed to me, which
quoted a 40-50% fetal mortality rate.
That’s when I remember that it really hit me, “Oh my goodness, my babies
can really die in utero at any second!” I
spent the rest of the day, although I was at work, googling monoamniotic
twins. I also read a lot of case studies
and articles published in medical journals, since I have access to those via my
workplace.
For the next eight weeks, I went to weekly ultrasounds,
praying each time that the babies would be alive. At 28 weeks, I checked in to the hospital for
in patient fetal heart rate monitoring.
It was really weird checking in to the hospital, since I felt totally healthy,
and wasn’t in labor, so it felt wrong to be in a hospital. But I kept reminding myself that this isn’t
for me, it’s for the babies. Initially,
I was on intermittent monitoring for one hour, three times a day. Every evening I would pray that my babies
would survive through the night, and every morning, when the heart beats were
found on the monitor, I would thank God that they were alive. I also had weekly ultrasounds in the
hospital, and got steroid shots when I first arrived.
Although
it was much more comfortable to be monitored only three
times a day for one hour, I didn’t completely understand how that would
help if
the babies were in distress at some off-monitor time, and I had lengthy
discussions with my OB and the specialists about whether cord knotting
is
sudden, or are there detectable signs of fetal distress prior to
something catastrophic. The difficulty is that since monoamniotic
twins are so rare, there’s just not a lot of data. Also, my specialist
group had three doctors,
and each had a slightly different opinion, which added to my confusion.
One felt that the way the cords were tangled
in my particular case, which was a big ball, not a long twisted braid,
was
actually more favorable, and he felt one hour 3x a day was sufficient.
Another doctor felt, the more monitoring the
better. I actually found out that my
friend’s cousin had monoamniotic twins a few years ago, and I spoke to
her to
hear her experience. She was in a top
hospital in NY, with a top doctor, and she was monitored basically 24/7,
with only
5 minute breaks here and there for bathroom, etc. Hearing that actually
made me more nervous,
since it seemed like my monitoring protocol was too lax relative to
that! In the end, my OB and I settled on as much
monitoring as I could tolerate, with freedom to unplug whenever I
wanted, for
however long, and no monitoring at night.
I kept myself busy with lots of reading, talking on the phone, surfing
the web, and praying.
It was really hard being in the hospital away from my
husband and kids, and I missed them terribly, especially at nights. They came twice a week to visit, but when
they left, it exacerbated the loneliness.
They would call me every evening, and I would read them a bedtime story
that I found online. That was my virtual
parenting, and I even told the nurses that I coined a new term “teleparenting”.
After I passed the 29, then 30 week mark uneventfully, thank
God, I started pressuring my OB about a decision as to whether to deliver at 32
or 34 weeks. She wanted a wait and see
approach, but I’m very goal oriented, and needed a date to look forward to. My OB pretty much left it up to me, so I
asked for a consult with the neonatologist to hear about the difference, both
short and long term, between a “32 weeker” and a “34 weeker”. In the middle of the consult, when I was 31
weeks, Baby B began to have decelerations.
There’s nothing as nerve wracking
as hearing from the monitor the sound of your baby’s heart rate drop. The nurse rushed in, put me on oxygen, rolled
me on my side, and was grabbing for the phone to call the attendant OB. I remember thinking “Oh my, it’s too early, I’m
not ready!” and praying to God that my babies stay in a little longer. After a tense minute or so, Baby B’s hear
rate picked back up. I was put on IV to
increase fluid intake, and remained on the monitor the rest of the day. Thank God, both babies heart rates looked
fine for the rest of the entire day, so the decision was made not to
deliver. Based in the discussion with
the neonatologist, and after reading whatever relevant journal articles I could
find, my OB and I kind of settled on delivery at 33 weeks.
At 32 weeks, I got another round of steroid shots. The next day I had an ultrasound, and though
the heart rates and blood flow looked OK, both babies appeared to be sleeping, as
there was no movement, and no visible chest rise indicating breathing. We waited about 40 minutes, which is the
typical in utero “nap time”, and we prodded and vibrated, but got only minimal
movements. The specialist concluded that
since the main risk in my case was cord entanglement, and blood flow and heart
rate look good, we don’t need to be concerned.
He mentioned something about steroid shots potentially making the fetuses
sleepy, so he dismissed me back to my room.
The heart rate tracings for the rest of the day were in the right range,
but had much less variability (rises and falls) than before, which isn’t a good
sign. I went to sleep praying that my
babies will be OK.
The next morning, at 32 weeks and 4 days, the specialist
turned up in my room with the portable ultrasound machine. I remember thinking, “Wait, you said
yesterday that you weren’t concerned, so why are you here now?”. He scanned me, and it was much the same as
the day before - good heart rates and blood flow, but minor movement and no
breathing. Again, he reached the same
conclusion as before, and left. About an
hour later, Baby B had a decel, and I was rolled on my side and put on
oxygen. At this point, my OB was getting
worried about the whole situation, and decided that was it, I was being
delivered. I remember thinking “wait, we
wanted to get to 33 weeks, it’s still early!”, but I trusted her call.
I called my husband and informed him that they wanted to
deliver me now. He didn’t realize that
now meant “now”, and by the time he dropped off the kids at various locations,
he arrived after the delivery. Meanwhile,
I was prepped for a c-section, given some terrible tasting antacid to drink,
since I had eaten lunch (a no-no for anesthesia, but we hadn’t planned on
delivering today!), then rushed into the OR for delivery. Everything was super quick, and within the
same minute, doctors delivered two 3 lb. baby girls. I didn’t hear the babies cry, and wasn’t
given the babies to see or hold, so I was a little concerned. At that point, my husband showed up, and told
me that the neonatologists said the babies seemed “stunned” and not very
responsive. Both babies had very low initial
APGAR scores (I think 1 and 2), and were put on CPAP right away. Later, I was wheeled in to the NICU to see
them in their isolettes- it was so hard not being able to hold them after the
whole stressful pregnancy!
The next morning, I got the report from the neonatologist,
and thank God, both girls had perked up after their first few hours of life,
and become more responsive. At one point
during the night, they thought they might have to intubate Baby A, but then she
started breathing OK again with the CPAP.
After about 2 days on CPAP, they were switched to room air. After a head ultrasound at two days of age, I
was finally able to “kangaroo” them, though only one at a time. They stayed in the NICU for only two and a
half weeks to learn how to feed and gain weight. They went home on the same day, weighing
approximately 4 lbs. And they’ve been
doing amazing ever since! Every day,
when I look at them, I thank god for my miracle girls!
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