Multiples

What is TTTS?

I know I'll kick myself once someone tells me but, I can't figure it out.  While I'm at it, I'll ask what is it?  TIA.
Warning No formatter is installed for the format bbhtml

Re: What is TTTS?

  • Twin-to-twin transfusion syndrome... when twins who share a placenta have unequal nourishment.

    Here's the TTTS Foundation's website if you'd like to know more:

    https://www.tttsfoundation.org/

  • imagejacobandcrystal:

    Twin-to-twin transfusion syndrome... when twins who share a placenta have unequal nourishment.

    Here's the TTTS Foundation's website if you'd like to know more:

    https://www.tttsfoundation.org/

    This.  I am getting monitored for it every 2 weeks.  My Dr. says there is a 15% chance of us getting it (with our twin type).  One of my twins has cord insertion at the edge of the placenta, which worries me too.

    Love: 8/2000 | Marriage: 7/2005 | Baby makes three: 3/28/2007 | And one more makes...SIX?
    image
    Steal my kids picture or pretend they are yours, I will find where you live and ship all of their dirty diapers to your doorstep. Promise. image
    image
  • Loading the player...
  • imageMrsAmyB:
    imagejacobandcrystal:

    Twin-to-twin transfusion syndrome... when twins who share a placenta have unequal nourishment.

    Here's the TTTS Foundation's website if you'd like to know more:

    https://www.tttsfoundation.org/

    This.  I am getting monitored for it every 2 weeks.  My Dr. says there is a 15% chance of us getting it (with our twin type).  One of my twins has cord insertion at the edge of the placenta, which worries me too.

    Same here.  My Baby B has a marginal cor insertion, but she is actually the bigger twin now.  :)


    After 2 rounds of IVF & 2 rounds of FET, we were blessed with identical twin girls!
    image

    Lilypie Third Birthday tickers
  • Our friends are going through it right now. It can only happen with identicals who are sharing the placenta - one baby basically receives too much of everything while the other is basically not receiving any nutrients etc....

    She & her baby girls had to go through "in utero" surgery at 22weeks to separate their blood vessels - baby A has an enlarged heart from excess blood and B was so tiny with a large head from lack of blood, nourishment etc... it is so heartbreaking.  Now her water broke at 25weeks so it is a waiting game to see if the babies can make it to at least 28weeks. 

     

    I hope no one on this board has to go through TTTS

    Lilypie Second Birthday tickers
  • There's a few of us on here who have TTTS survivors.  We were diagnosed with it at 24 weeks, and I was put on complete bedrest.  I delivered at 34w, and my girls were 2lb 13oz and 4 lbs 9 oz.

    littlewonders also has TTTS survivors, and they flew to Texas to have the laser surgery.

    Warning No formatter is installed for the format bbhtml
  • We are TTTS survivors also! Well I haven't delivered yet but I'm almost 32 weeks and the boys look fantastic- as if they'd never had it. We also flew to Texas for the surgery. Its scary but there are treatment options out there if caught early.
  • My boys are survivors as well. They didn't have TTTS until 27 weeks. So we were to far along for the surgery or to even fly anywhere for it. So they did an amniotic reduction and watched me very close. We made it to 33 weeks. The boys were 4lbs 6oz and 2lbs 14oz. However looking at them today you wouldn't even know that they dealt with this. They are now 20lbs and 17lbs. 
This discussion has been closed.
Choose Another Board
Search Boards
"
"