I'm more of a lurker than a poster but this subject is one I feel very strongly about.
Let me say, first of all, that I do have an agenda and its not hidden. Way back in the dim and distant days of the 70s as a new mother of just 20 I had the terrifying experience of trying to get help for my newborn's projectile vomiting only to have the professionals to whom I turned fail to believe me and suggest I was imagining the problem due to my "obvious" PND. After six nightmare weeks and numerous visits to the GP, talks with the HV and a near nervous breakdown he threw up all over the GP and was diagnosed with pyloric stenosis, a well known condition which the HV should have recognised from my description. He was operated on the following day. I was told by the surgeon that if diagnosis had been made a few days later he would have been at risk of dying during the operation as he was undernourished and very dehydrated. If DS had been born thirty years later I have no doubt I would have been diagnosed with MSbP as the symptoms somehow never showed themselves when the HV was present. I would have found myself involved with social services before you could say "Roy Meadow" and God knows what would have happened from then on.
I do not say this to attack HVs, GPs, or social workers for that matter. I tell this story to illustrate that institutions can, and do, make mistakes and parents should never abdicate their responsibility for their child's welfare to a professional as professionals, too, are only human.
The other point I wish to make leads on from this and it is that it is our duty as citizens to keep questioning our institutions. It is only by doing this that errors can be uncovered and injustices remedied.
So carry on asking questions, Elizabeth. Your are obviously passionate about this issue and to me that's a good thing.
MM