Gosh I'm pleased to have missed this.
snickersack - vitamin A is a good treatment for measles - you don't need too much, but when your baby has measles some doses of cod liver oil will help (if you can get it into him).
Glad some people have recommended Halvorsen's book (have barely skimmed thread, but saw his name mentioned).
I'd also recommend reading the CryShame hearing diaries. CryShame does have an agenda, so certainly can't be claimed to be neutral but the hearing diaries are currently the only way to find out what is going on at the GMC trial day by day. When the trial started I thought Wakefield, Murch and Walker-Smith were stuffed, I was sure they would be picked up on something with such a long list of charges (and having spent the last 2 weeks trying to get the answer to a very simple ethics problem and failing miserably I was pretty sure they'd be able to pick up on something technical if they needed to). Now I'm not so sure. I can't imagine that they'll be allowed to be let off because politically that would be disastrous but the reports from the hearing make it difficult to see exactly what the defendants are going to be picked up on. From Richard Horton (editor of the Lancet, no friend of Wakefield's) saying the Lancet paper was excellent science and still stands, to the unravelling of the financial issues (money was not paid to Wakefield personally as has been claimed) to what seems to be a lot of evidence that the doctors acted entirely reasonably throughout.
You need a spare day, but if you really want to find out the story behind the headlines (well some of it, the families involved - i.e. the supposed 'victims' were not allowed to give evidence, although some GP's did) it's worth a read.
If anyone ever tells you it's an easy and black and white decision to make they're lying. The more you know the harder it gets. Following the US payment for MMR damage to a girl diagnosed with a mitochondrial disorder (and originally autism) lots has been written about the incidence of mitochondrial disorders in autism- the truth is no-one knows. They can be hard to diagnose, especially in the UK where it often takes years to get through all the genetic tests -if you ever get offered them.
Yes the risk overall is very small, but some children are at a much higher risk. It's identifying them that's important. I knew when ds2 and ds3 were born that they were at a far higher risk of autism (think its something like 1 in 20 - think about the panic attack that that sort of result would induce in someone having a nuchal fold screen- then remember that ds1 is affected far more profoundly by his autism than any of the people I've so far met with Down's Syndrome are affected by their condition). We took a decision when ds2 and ds3 were born to be very careful with things that could affect their immune system and their gut. Vaccinations were included in that list (and remain so). We never say an outright no to anything, but we don't have the luxury of assuming that everything will be fine. Either way. Disease versus vaccination. A true rock and hard place for us. We lost the certainty of an independent future for our children when ds1 regressed and lost his speech.
I don't expect anyone else to necessarily make our decisions (not sure what ours is long term anyway), but likewise I don't really expect to be criticised when most people have no idea of the realities of profound autism. Or of the fear that a sibling might regress.