Paying people to assess disability on a bonus scale is madness.
Therese Coffey was on Peston last week, and she said that the rate of UC is so low that people can't live on it, so they try to get PIP, and instead of using it to help with their disability they buy bread and milk with it.
If that is the case, the obvious answer is to increase UC, but that brings us back to the unfairness of someone on benefits getting more than their neighbour who gets up early to work a hard shift on minimum wage. It's obvious to me why people resent that. I think the rise in the MW is a step in the right direction, but it probably needs to be higher - it's either that or keep claimants in poverty - and I think the top up benefits were a very bad idea. I fully understand that people need them, but that's because employers are allowed to get away with paying too little, and landlords charging exploitative rents. Maybe the housebuilding will help with that, but not if the houses being built are all detached 4 beds instead of affordable ones.
I don't know whether people get PIP too easily. I know a couple of people who get it and really do need it for mobility aids and so on. They both had to jump through hoops to get it and stressed every time the renewal interview was looming, but I also know that a relative of my daughter's ex claimed to have agoraphobia but regularly turned up at their house asking for a lift home after she'd spent the day at the shops and been out for lunch. I also know someone who did an MA whilst claiming enhanced benefits as he'd left work because of stress. I couldn't help thinking that if he could travel in for lectures, do all the required work and cope with the stress of assignments and exams he could have held down a job of some sort.
Both of those people got various grants and discounts as a result of their benefits, which meant that they'd have to earn a reasonable wage to maintain their lifestyle. I think that sort of thing should stop. I'm not sure how it could be done though, as nobody wants to see people with incapacity forced to work and getting worse.
I wonder whether a more 'kind' approach to MH has made people see themselves as disabled when they wouldn't have in the past, and they genuinely believe that they are unable to work? I do know that as soon as anyone says something along those lines, however, they are accused of being intolerant and discriminatory.