On Thursday 27
th December 2007, half way through our routine 12 week scan, the Doctor told us they had found a problem with our baby. That was the first time either of us had ever heard the word
exomphalos. It has been part of our daily vocabulary ever since.
The Doctor went on to explain a bit more about the condition – we won’t, the
GEEPS website does a far better job than we would (see links).The Doctor also explained that the presence of an
exomphalos is often an indicator of other chromosomal conditions. We were given a 1 in 4 chance of our baby having a serious chromosomal disorder.
At 9.30 on the Friday morning Emma had a
CVS test. Over the next couple of days, while awaiting the results, we could not be entirely sure which of the 3 possible outcomes we favoured. The choices were a baby with a serious life threatening condition; a miscarriage resulting from the
CVS or a baby with just an
exomphalos - a condition we barely understood. Though grim, at least the first two were clear cut ‘no
brainers’. The
CVS results thankfully gave us the all clear for any chromosome abnormalities.
We were then referred to Mr Matthew Coleman - Professor of Fetal Medicine at
Southamptons Princess Anne Hospital. That meeting was a real turning point and we haven’t really looked back since. We had regular scans to check that the baby was growing correctly at both Bournemouth and Southampton hospitals. Emma was advised she could have a natural birth and an induction date was booked for 7
th July 2008.