Where did you see a child dying of measles? Was this abroad soozywoozy?
We avoid antibiotics as well. Obviously if they are absolutely necessary they will be given, but ds2 has had one round, ds3 none (he's now 7). This is no longer out of kilter with medical opinion. When ds1 was little he had about 8 sets of antibiotics by the time he was 2 - mainly for repeated ear infections. Ds3 had repeated ear infections & burst ear drums, we decided not to treat with antib's. When he was hospitalised following a seizure from the ear infection I was given a long lecture in hospital about how they would not prescribe antibiotics and there was no need to give them for ear infections. (They didn't seem to notice I was agreeing with them, and saying we didn't want them anyway).
I do know a few people who's children ended up in ITU after the MMR and are now autistic (three people I think). In two cases they were told the trip to ITU was definitely not associated with the MMR. Not sure how they could be so confident without investigation, but still. In one case the paediatrician did say a few later he felt the MMR had probably led to the ITU trip and resulting autism, but it wasn't possible to say for sure.
I do know that the population of ds1's SLD school has changed over the last thirty years, and during the last 15 years there has been a big increase in the numbers of children with severe autism. There used to be about 1 or 2 in the school, now there are two classes (plus a few others in mixed classes). These are children who are non-verbal, in many cases still in nappies as teenagers and who have no dysmorphic features and nothing indicative of a syndrome, nor were they damaged at birth. Everyone I have spoken to who has been involved with the school over that long period of time has commented. Locally social care provision is changing as well to recognise the increased numbers of individuals with severe autism coming through the system (and to try and make it slightly cheaper for the council - there are now too many kids to keep sending them out of area for social care). Now the numbers coming through still aren't huge. But the lifetime cost of caring for a non-verbal individual with severe autism is huge, so I'm vaguely surprised that no-one is tracking these children/young adults or investigating where they're coming from really. Especially as social care and education funders talk about the increase as it if exists.
Please not I am not talking about Aspergers or even HFA in the above. Only the most severely affected group.