I doubt any DLA claiment would mind being checked if they had any confidence in the system Jade.
The worry is that decisions are not made by medical staff. It seems entirely hit and miss and you really can never tell what they are going to do next.
I know of children who receive the higher rate of care for fairly mild disabilities whilst others cannot get DLA at all. Even those with severe and complex needs.
You can fill in the form, send it off, get turned down, appeal and be awarded DLA. Infact a huge amount of claims are awarded on appeal. How can that be? Either the intial decision making is wrong or the appeal decision is wrong.
I know people with the same conditons, affected in the same way - one will be awarded DLA, one will not.
I failed an ATOS test because I turned up for it. I couldnt be suffering from what I said I suffered from because I turned up for the test!. I turned up for it because they told me I had to and if I didnt I would lose the benefit I was on.
A bit like the drown the witch test. If you float you are a witch and will be killed, if you drown you are innocent but are dead anyway.
People are scared because DLA always has been hard to get and hard to keep. If its been such a lottery up till now what the hell is going to happen next?
Those making decisions appear to know so little about the lives they are tampering with. They wanted to stop mobility allowance to anyone living in residential care. That would mean that they couldnt choose when they wanted to go out. Their carers could not have them home for weekends, their lives would be entirely dictated by the availability of minibuses and staff ratios.
I have no confidence at all that the right thing will be done by people with disabilities.