zoefromsussex
Mother
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- Mar 29, 2010
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Well three months after delivering our son George as a result of a tfmr at 18 weeks, the postmortem report is FINALLY ready! We have an appointment with the consultant obstetrician on thurs afternoon and I'm a bundle of nerves. On the one hand, I really want to know the exact cause of his anomalies but on the other hand I'm scared in case it turns out to be a genetic condition which could occur again or (even worse) in case it was somehow my fault.
I'd love to hear from anyone who's been through the same thing or knows someone who has.
The facts we know are that George's chin/jaw hadn't formed, his joints appeared to be 'set' and there were problems with the amniotic fluid partly because he was unable to swallow. The geneticist we saw suspected Sicklers Syndrome but nobody could say for sure.
I'd love to hear from anyone who's been through the same thing or knows someone who has.
The facts we know are that George's chin/jaw hadn't formed, his joints appeared to be 'set' and there were problems with the amniotic fluid partly because he was unable to swallow. The geneticist we saw suspected Sicklers Syndrome but nobody could say for sure.