I had a consultation with the specialist, and he confirmed the
TTTS diagnosis. This was not a big surprise, almost a relief after not knowing for the last few weeks. The good news is that the amniotic fluid levels are not severely imbalanced enough to warrant treatment at this time... but the bad news is that this can change within a week's time.
SOOOOO, you guessed it! I get to keep up the weekly ultrasounds. Yuck. We will be going back January 2
nd for a complete scan of both babies (weights, fluid levels and all the other goodies) and we will see how far the
TTTS is progressing at that point. I feel like a walking time bomb, since at this point the
TTTS is mild enough for both babies to survive, but just as I was drawing a breath of relief he pointed out that it can go from mild to severe in a week.
ARGH. Again, the laser surgery is only possible for another few weeks, and after that things are more dicey as far as treatment and risks for the babies.
I also need to clarify some things about the specialist. I talked to my doctor (about the things I had complained about earlier) and I found out I was not yet transferred to his practice and/or had become his patient! No wonder he never talked to me - he didn't know I existed. Poor guy, and I was so offended. My doctor simply sent me there for the ultrasounds since she wanted techs that were familiar with high-risk pregnancies. Once she clarified that, I felt much better!!! Also, he is not against the surgery, as was my initial impression, and in fact refers patients to a clinic in Ohio that performs them. Talking to him about the surgery, he seemed very well-informed about it and had indeed sent patients to get it. The only reason he only performs the
amnio reduction treatment is simply because he refers all the surgery cases to the better equipped clinic in Ohio. *Another sigh of relief.* As for not diagnosing it, my initial ultrasound reports showed such mild symptoms progressing at such a slow pace (
TTTS often develops and progresses quickly) that he did not see cause for concern. Now that the symptoms are more obvious, I am getting more detailed reports from him to my doctor and he is taking much more interest in my case... even though I am still not technically his patient. Overall, I feel much more comfortable with the situation now!!!! At least as far as trusting them with my medical information/diagnosis/treatment options.
As for the babies, I can still feel both moving around. This is a good sign!! The larger baby's heart is not quite as enlarged and does not seem to be under stress any more. Another good sign!! And the little one is still kicking and squirming (even did a somersault) which shows he has enough fluid to survive at this point.
Yay! Now just pray that they stay put in there for a few more months, and that the
TTTS stays mild enough for them both to grow strong and healthy.
Also pray for my heart condition. It is very difficult to live with and try to take care of two energetic
girlies without getting really sick. I am hoping to avoid full
bed rest as long as possible, and at this point the doctor is allowing me to do partial
bed rest. She does not want me on my feet unless necessary, and she wants my rest times to equal my activity. Again, with two little girls this is not always possible , but we are plugging along!!!
Thanks so much for all the prayers and support. I know I keep saying this, but it's true: we could not get through this trial without all the help we've been getting. I'll give you all the new info after the 2
nd, just keep in mind it takes me a while to get to a computer!!!