Hi ladies, I'm back from my gyne....
Nothing much can be done now. I would need to do an amniocentesis test to see if bb has chromosome defect before we can decide what to do next.
The hole in the heart is a small problem. It can be treated once she is out.
The problem now is the cleft on the brain. This clefting would affect bb's mobile co-ordination [eg: movement or muscles control] which could in return affect her speech, maybe her swallowing and IQ as well. So to do the amniocentesis is to determine if she has chromosomal disorders. If she has chromosomal disorders then we would not want to do any surgery on her to repair the faults cos she would just pass on maybe in a few days or in a years' time.
If she does not has any chromosomal disorders then when she is born, she would need to have a tube inserted to her brains to drain out the excess fluid to her tummy to discharge out and it would be that way for life and maybe other surgery to correct her other faults.....
And she also has single artery umbilical cord, which is usually a sign of chromosomal disorders. As for her being undersize, that can be solved after she is born.
As for my excess of amnio fluid, maybe during my amniocentesis test, if the doc can draw out more fluid, he would do so for me.
And my amniocentesis test is on next Wed at NUH [not again!!!!]. I hope I do not have to wait for an hr before it is my turn. Yesterday, I waited for about 1hr 15mins and had my tummy exposed and scanned for another hour. And the scan was so damn painful lor! They press that "thgy" so hard onto my tummy, even hb asked if I'm in pain. Even hb knows that they pressed that "thgy" so hard. Hai...... Now I worry about the pain for the amniocentesis test.