Thank you for the questions. On your final point, there's a recognition that we seek to achieve a cultural change. This isn't simply about families with people with autism, but actually about the support they receive in the workplace and the attitudes of different employers. Within the report published today, you see direct examples of people who have been helped by the service to remain in employment if they are in employment, or to seek employment as well. The challenge is how we don't set up a service to fail, but how this is part of wanting to change our national conversation and trying to change the amount of practical support that is available to businesses and to their employees. But I recognise that there is a significant road to travel here, just as there are in a number of other areas, but that is part of the commitment that was set out in the integrated service.

I'll deal with your point about waiting times now. The 26-week target: there will be more information available internally, within the Government, this autumn as we look again at the roll-out of the waiting time standards. We need to be certain, before we roll out the target and we start publishing information, that it is robust and reliable. All of us have had experience in the past of trying to roll out waiting time standards with them not been available, and then—where they've not been ready in the robust way that they should be, rather—that then causes a lack of confidence in what the figures are. I'm not trying to hide the figures; I’m not trying to make sure that they only come out when they look good for me. I'm really interested in making sure that they're actually genuinely reliable, because I expect there will be a variation in learning between different parts of Wales. But I want to make sure that they are robust, that they can be relied upon, and that they help to drive some improvement in measures that actually matter and have real impact on families.

On your point about the cost to legislation, there is always a cost to legislation, not just a cost to this place in the mechanics of running, but there's a challenge here in terms of the cost and in terms of the time and resource that is available to practitioners, to the policy team here centrally, and what that then means in terms of diverting that attention to go into a legislative process as opposed to being focused on improvement. Legislation won't produce more money. We will still have the sum of money that we have available to the Government, and we'll still have to make choices about that, together with our partners in other services. I'm most interested in understanding for the people delivering the service and taking part in it the difference it's made, and what our real prospects are for delivering the sort of improvement that, as I say, each of us in this room would want to see.

Your point about statutory services—we already have statutory requirements for ourselves, the health service, local government and partners to achieve and to deliver on. We need to make sure those are made real, and that's part of the reason why I'm moving forward with the code of practice, because I do recognise that there will be people who will understand and who will tell their own story about what has happened, and about where their needs have not been met in the way in which we envisaged the legislation would do. I think we have to get that legislation right and make those rights real, and that would, could and should make a real difference to those families as well.