Hi ladies! Has anyone else had identical twins that had separate amniotic sacs but shared one placenta? We found this out yesterday, and even though I think this situation accounts for about 60% of identical twins, it has me a bit worried. They mentioned that they need to monitor me closely throughout the pregnancy to scan for the possibity of "twin to twin transfusion syndrome" (TTTS), which has scared the living daylights out of this usually chill mom-to-be.
Re: Identical twins sharing one placenta
Yup, this is how my twins are.
I am being monitored closely than I see on these other moms monitored on the boards by my MFM. They only start to worry when the discordance between the twins is between 20-25%. My twins are at 15% right now.
I started weekly cervical checks at 16 weeks and will last until I am 26 weeks. They not only look at my cervix, but also the babies size and amniotic fluid sacs. I have growth ultrasounds every 3 weeks to monitor this as well.
I know there are a few ladies on this board that actually have had the TTTS syndrome as a diagnosis. We have been lucky to avoid it thus far.
Congrats on your pregnancy and try not to worry.
Katie: 1/16/08 2lbs. 15oz.
Abby & Emily: 12/31/10 6lbs. 2oz. & 5lbs. 7oz.
Mine were not in separate sacks but they did share a placenta. My dr was also concerned with TTTS so I had a million and a half u/s to measure them. Luckily they were within a few oz of each other the entire pg and weighed the exact same at birth.
Try not to stress a lot about it. I know its hard but worrying doesnt do anything but stress you out which is not good.
Hello There,
Yes, it is scary to hear about all of the possible complications that can arise with mono-di twins (that is one placenta and two amniotic sacs). We are now 30 weeks and everything has gone well so far. My OB referred me to a Perinatologist as soon as she realized we had two LOs in there. Since that point we have had regular ultrasounds every 3 weeks to monitor for any signs of TTTS as well as regular appointments with my OB. The up side to this is that you will get very good at identifying what is what on ultrasounds and lots of opportunities to have family come and share the experience with you. My advice to you is make sure you have doctors you trust and do your homework online to make sure you understand what they are talking about. It is scary but remember what a blessing this is and keep your eye on the goal. GL
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I may never have met you, but I LOVE YOU ALL!!! Thanks so much for all of your input - I think I just needed to hear it from others who have been there.
I really am not a worrier, but this has me a bit thrown. I keep trying to remember that we keep beating all the odds (spontaneous pregnancy at 41, twins, then indentical twins...), so there is more than enough reason to believe that everything will be 100%.
Welcome to the worrying or motherhood, I suppose.
It's very common.
My girls are mono/di and I carried them to 36 weeks 3 days, when I had my scheduled c-section. You'll be monitored for TTTS, but it's no big deal. My MFM and OB were also not comfortable with me delivering vaginally b/c there was one placenta, so I had to have a c-section. You may have Drs that feel similarly. I also had my c-section early b/c they were sharing a placenta. I could have gone past the day my section was scheduled.
My girls arrived happy and healthy!
My 7 week-olds were mono-di identical girls. We were monitored closely for TTTS and had a scare around 26 weeks with discordant fluid levels which were found to be improved the next week. Never developed TTTS.
We had u/s monthly throughout the pregnancy with the MFM specialist office. One of the specialists in the group came in and reviewed the actual ultrasound before we were allowed to leave each time. Gave us a lot of reassurance that things were being followed. Make sure you are seen by a MFM/perinatologist.
My girls were born early due to pre-eclampsia. No complications developed related to placenta sharing. Worrying won't help anything, but being informed and being followed by a specialist will be the most beneficial for your babies. Good luck with your pregnancy!
The good news is that your doctor seems very proactive. That's awesome!! There are many ignorant doctors out there who ignore the risk-mine was one one them.
I was diagnosed with TTTS at 18 weeks. We had a big scare there for a while, but the treatments we got have helped and I'm now 30 weeks and the baby girls are growing well and look good.
There are ways to treat it if you do happen to get diagnosed. PP is right though it's about a 10% chance.
Good luck to you!!!
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