only just picked up on this thread and haven't read all posts sorry. my nephew (now aged 2) was born with hare lip and cleft palate. it hadnt been picked up on any scans and was a complete shock to my brother and SIL. they found it very hard at first but have had nothing but wonderful support from the NHS and CLAPA throughout. Harry has now had two major ops now (first to create his top lip as there really wasnt anything there at first, and the second to join his palate as the cleft went all the wat front to back).
He is doing so well now and, unless someone told you, there is no visible signs left. His ops were done in Manchester on a specialist unit and the staff were / are fantastic. At the moment the only slight concern is he still is being quite slow at developing his speech - but the HV's say there is nothing to worry about. we know he will have to have more ops well into his teens (until his growth settles) but so far fingers crossed he is being an absolute star.
I can only agree that this story is worrying and upsetting and sit here thinking of my nephew feeling glad he is in the world.