I had a futher scan with two consultants on 31/12/09 and they said that they think that the fluid in the stomach looks like it has reduce a little bit but they can still she a white area coming up on the scan when they look at the bowels. They said that this is called echogenic bowel but they still could not tell me the exact reason for this. I was told that it could be that the baby had swallowed a bit of blood when i was bleeding in the first few weeks of the 1st trimester but i doubt it is this as my 12 wk scan never showed this problem. I was also told that it could be a abnormal chromosome even though i came up as very low risk when i had my n.t scan. She said that i could have a amniocentesis but was a small risk of miscarriage, 1% which is 1 out of 100 women will lose their baby but that i should think about it first.
When i previously attended my 20 wk scan when i got the news they tested my blood for any infections such as Cytomegalovirus, Toxoplasmosis and Pavovirus. Thankfully they have come back negative but im still awaiting the result for the Pavovirus but the consultant seems to think that this will come back negative as well as im no longer anemic.
The consultants then said they will refer me to UCLH hospital down warren street for me to have a cardiac scan to check the baby's heart. After leaving the two consultants i felt a tiny bit better then i did after speaking to the other consultant when i had my 20 wk scan as they were taling to me about possibly termination and about the baby dying the womb, me still having to go into laour which really, really left me and my partner in distress
on Monday 4th I saw the specialist at UCLH hospital and had a really in dept scan. He said that in his opinion he thinks the fluid in the baby's stomach is moderate and not severe as previously stated on my 20 wk scan print out. He could also still see the white area coming up on the scan over the baby's bowels. This has not got any better or worse from the 20 wk scan. he said that he is cautiosly optimistic that the baby has a perorated bowel and not an abnormal chromosome but could not be 100% sure. He said that i could still have a amniocentesis but said that having that procedure is not on his high list of priority for me to have but for my own piece of mind that i could have the test if i wanted too. We also got tested for cystic fibrosis.
Me and my partner left the room for a bit to discuss it and agreed to have the amniocentesis as the specialist was not 100% sure what the problem was which is fair enough plus i think i could of mentally handled the rest of he pregnancy not knowing.
The consultant who carried out my amnio said my chance of miscarriage was 0.5% which is 1 in 200 due to me having the test at 21wk 5days.
Anyway i got a call today saying that the first part of the test for Down's syndrome, Patau's syndrome, and Edward's syndrome all came negative which we are over the moon about the 2nd part of the test results will be back in 2-3 wks. I was told that if the first part came back ok the second part will most likely will do as well but im not too sure how true this is. I will just wait for the result
Anyway guys i just wanna thank you for your help and support over this distressing time i had to go through. Dont know what i would do without you all xxx
I will keep you all updated