It's no secret on here that I am suspicious of most doctors.
Went to the MFM for the first time yesterday. The doctor told me that he was mildly concerned about baby A being significantly smaller (visually not just by measurement) than baby B. I am 19wks1day. Baby B measures @ 19wks3days. Baby A measures @ 18weeks0days
He feels better because:
1) "A" has been smaller since day 1 and nothing has changed about how she measures in comparison to baby B. In other words they grow at the same rate.
2) The fluids around them are totally fine. Also blood flow through their chords are normal.
3) A is not too small she's just smaller than her sister. And her first anatomy scan came back completely healthy. They see no problems.
His concern also includes the fact that A's chord connects to the left side of the placenta and this could cause TTTS.
He explained that TTTS is a four stage condition and he wouldn't even put us at Stage one at this point.
Oh also I have placenta previa, which a technician at my regular OB told me I didn't have so MFM dr said he'll look again next week before diagnosing me with that definitely. Now I'm scheduled for monitoring almost every week.
Does anyone have experience with this? I don't know what to think or do.
Re: One modi twin is smaller than the other.
what are you wondering about? are you not happy with the plan? I know its scary when there are unknows with our babies, but in my experience the very best thing is a doctor who is honest about these unknowns and does their best to look at all the evidence to decide on a treatment/monitoring plan which it sounds like your dr is doing
Peanut Butter and Jelly!
<a href="http://s568.photobucket.com/albums/ss122/AliceNP/?action=view
He wouldn't answer me because we had already been there for 3 hours. And I think he didn't want to freak me out in an uncessesary way. I told him I wouldn't and I just want to know.
It sounds like your doctor is proactive and aware of the risks of TTTS. Not every doctor is, so that's a plus for you. I believe the occurrence of TTTS is 10-15% in mo/di multiples (not exactly sure on that statistic). There is no way to prevent it, but you can educate yourself on the warning signs. Frequent monitoring is very important. This is a good website to check out:
https://www.tttsfoundation.org/
I don't think there's any reason to freak out yet. Try your best to trust the experts but also ask questions until you understand. I've done lots of my own research about mo/di and ttts pregnancies after I went through it. While it was happening I was too afraid to look much up and I felt very alone. My MFM said he sees about 1 or 2 cases like mine per year. Discordant growth between mo/di twins doesn't always lead to ttts, sometimes one twin ends up with a larger placental share. However both can occur simultaneously so they should monitor as such. If you have ttts they will likely send you to a specialist to evaluate you for surgery to ablate the abnormal vessels between the twins. I didn't do surgery because the fluid levels improved with bed rest. I did have to be admitted to the hospital at 24 weeks for monitoring because they were very worried about the smaller twin and his blood flow.
Peanut Butter and Jelly!
<a href="http://s568.photobucket.com/albums/ss122/AliceNP/?action=view
It sounds like you are in good hands w/ your MFM. The most important thing at this point is that you are monitored frequently. It can be nerve-wracking, but it's also nice to know exactly what's going on with your babies. T&P that everything continues to be fine and that the worst part is just the annoyance of all the doctor visits!
Mono/Di Twins - Due March 3, 2014 (Realist EDD - Feb 5, 2014)
Mommy to Jericho - 2 Years Old.
As far as the actual appts are concerned, the every other week ones didn't take a toll. It was nice for my sanity. The fluid and bladder checks were a quick and I was on to work with a stop for breakfast
Mono/Di Twins - Due March 3, 2014 (Realist EDD - Feb 5, 2014)
Mommy to Jericho - 2 Years Old.
@Jenyoung5 I am 22w with mo/di twins with a 25% discordance in growth as well.
Welcome!
Mono/Di Twins - Due March 3, 2014 (Realist EDD - Feb 5, 2014)
Mommy to Jericho - 2 Years Old.
Peanut Butter and Jelly!
<a href="http://s568.photobucket.com/albums/ss122/AliceNP/?action=view
Also the Bolthouse protein drinks are great.
If the fluids are good, don't worry about TTTS.
That is Stage 1 - when the donor's fluid (most vertical pocket measurement) is less than 2, and the recipient's is greater than 8. My twins had TTTS. It only happens in 10% of identicals. So not very often. We ended up having surgery to correct, which was successful. Not sure about cord placement being an indicator, that's the first I heard of it. TTTS has to do with shared blood flow within the placenta. ID's share blood vessels. Most of the time (90%), they figure out the balance. 10% of the time, they don't, and one tends to give it all up (donor), and the other takes it (recipient). It's good for neither. At any rate, TTTS would see grow discordance along with the issues in fluid, lack of a visible bladder (Stage 2), and cord flow issues (Stage 3). And let's just not discuss Stage 4. My girls didn't really show any growth discordance before surgery. The donor just started to slip behind the recipient when we had surgery, and she was only 3 oz less than her sister at birth (5.1 and 4.14).
BTW, my surgeon said that all the protein drinks in the world wouldn't correct a chronic TTTS like I had. Protein is definitely important, but don't kill yourself over it. I tried upping my protein too, and it didn't make one iota of difference.
TTC since May 2006. After 3 failed Clomid cycles, 2 failed Injectibles/IUIs, 2 failed IVFs and 1 failed FET, we moved on to adoption!
Last ditch FET resulted in BFP, and identical twin girls!