Disabled people are able to work in many ways, that's true niceguy. I have disabled friends, and actually worked in employment supporting people with long term health conditions and disablities into work. I still support people with mental health difficulties, though not directly with employment issues. I have worked in this field for 6 years now.
But, how many employers do you think want to employ disabled people?
I can tell you: very few. And look at the current economic climate, which has lead to many workplaces becoming cut throat and pared back. These are not good environments for encouraging employers to take on people where they may need to make adaptations, or allow flexibility in working.
What's more, many disabled people, once out of work, tend to remain out of work for longer, and this negatively affects their CV and job prospects. 11% of visually impaired people are in paid employment. Not because they are incapable of work. But because they are incapable of getting an employer to take them on.
You may also be confusing DLA with other benefits. DLA is (was) payable to all persons with a disability, it has nothing to do with employment. In fact, the figures put out by the present government around the 'cost' of disability benefits are highly misleading: less than 2% of DLA claimants have been found to be fraudulent, it is a very hard benefit to obtain. And being made harder.
Affordability may - may - come into it, yes the figures look high (when we talk about millions) but you need to look at it in context. Can we as a society afford to pay DLA to enable people with disabilities to engage meaningfully in life i the way people without disabilities take for granted? I would hope we could.
Atos, let's face it, get incentive payments for every person they deem as 'fit for work'. Their procedures are highly suspect. Take, for example, my patient, Mr X. Mr X was deaf in one ear. On top of this he suffered from depression. And arthritis. He had lost his job a year before I met him. He qualified for IB and DLA. As he moved to ESA he had an assessment. The 'doctor' spent the whole assessment shouting at him. He did his best to lipread. The form she completed deeming him 'fit for work' declared he had no hearing problems at all. He lost his benefit and had to submit an appeal or claim JSA (which takes 3 months to be processed). Mr X never said he was not 'fit for work'. He was actively looking for work. He wanted ESA because it provided him with extra support to help him find work because he had a registered disability (hearing impairment) which affected the type of jobs and employers he could approach. The distress it caused, and the affect on his depression, set him back and he relapsed. He won his appeal, because his wife was at the assessment and witnessed all the shouting going on.
The structure is not fit for purpose. It was set up to prevent people who were entitled to a benefit getting it. This is true of the many mllions of pounds of unclaimed benefits remaining in the treasury every year.
Believe me, once you scratch the surface of this debacle you quickly realise the nonsense spouted by the tabloids has very few grains of truth in it.