Hi All, so just wanted to give you all an update now that we have a better idea of what's going DD2. Got the full amniocentesis report back earlier today after the most agonising 11day wait and there are no underlying chromosomal problems. Utterly relived doesn't even come close to describing it because it means that what we are dealing with is purely structural and there are well established treatment pathways with good long term outcomes.
So what we know at this point - after meeting with the Fetal Cardiology Team at Evelina's and some detailed scans we have an official diagnosis of Tetralogy of Fallot - however its very much on the mild end of the spectrum or "Fallot Lite" as coined by one of the consultants - as only 2 of the 3 characteristics of the condition actually present in any meaningful way (i won't go into the technical stuff unless anyone is particularly interested!)
So what's next? We are very likely to be looking at planned csection so there is a booked bed in NICU for her to be monitored for a little while but they anticipate that she wont actually be unwell or at immediate risk as such when she is born (a lot of time this condition isn't even discovered until after birth) so hopefully she will be able to come home relatively quickly and then will be regularly monitored and need to come back for open heart surgery at around 6mnths old to repair things.
Still a long journey to travel ahead of us but today's news means that the road is far easier to face.