Disability Employment Gap Debate
Full Debate: Read Full DebateJo Stevens
Main Page: Jo Stevens (Labour - Cardiff East)Department Debates - View all Jo Stevens's debates with the Department for Work and Pensions
(8 years, 2 months ago)
Commons ChamberI find nothing in the hon. Gentleman’s comments that I can disagree with, but the fact is that they do not have that confidence at the moment. That is clear from the examples I am giving and from the expert third-sector organisations. They do not have the confidence because of the way they have been treated throughout their lives in having to fight for appropriate wheelchairs and go through traumatic work capability, PIP and DLA assessments, which they find demeaning. The whole process reduces their confidence not just to enter the workplace but to maintain a dignified level in society. I take his point, but there is far more for us to do.
This view is echoed in many ways by Sue Bott, deputy CEO of Disability Rights UK, who said:
“It is bad enough that the government spends so much of its time and resources on finding ways to deny”
disabled people
“benefits and support but then not to put measures in place that would increase employment opportunities really is a double whammy for disabled people. The fact is that it is only when we see a government seriously committed to equality will we get progress.”
Last Friday, I saw a constituent, a 37-year-old man with Parkinson’s disease, who had gone through a PIP assessment. The assessment report described him throughout as “it” rather than “him”. Does the hon. Gentleman agree that that is an example of exactly how the approach he advocates is not being put into practice under this scheme?
That is absolutely sickening, and it should reduce us all to shame. That goes to the heart of why we have said throughout the election campaign in Scotland that when we create our social security agency we will put dignity and respect at its heart for those very reasons. Sadly, in some cases—not all, but some—those things have been lacking.
There was another case that I wanted to highlight about the work capability assessment, but time is pressing. Suffice it to say that the failings of the assessment stage make it far more difficult for the Government to achieve their goal of supporting disabled people who, with the correct support and guidance, would be able to find employment. Jobcentres, which are there to provide such help and support, are dealing with people who are not capable of working because of their ill health and disabilities, but who have mistakenly been sent there as a result of the flawed ESA decision-making process.
Another disabled constituent of mine who is in work contacted me regarding problems with the progress of his DLA and PIP application. He informed me that he had had numerous problems with the process. Despite supplying detailed medical evidence of the effect the health problems had on his life and the type of support he requires—the evidence clearly highlighted why that support was needed—he was told that he had to attend an assessment with ATOS. My constituent requested that that be carried out at an assessment centre, but was sent a letter by ATOS telling him, in language that he found threatening, that it would need to be a home visit.
Given that my constituent is trying to maintain a full-time job, the unavailability of weekend appointments makes it very difficult for him to adhere to strict appointment times during the week. The assessor did not attend on the day that was eventually scheduled. When my constituent inquired about that, he was told that no appointment had been made for him. This led to ATOS stating that it would consider the application on the basis of the evidence that my constituent had supplied, which left him understandably confused about why that had not been done in the first place. Supporting people with disabilities who are already in work is essential to ensuring that the disability employment gap is not widened still further. The Resolution Foundation referred directly to that in its report yesterday.
In conclusion, I hope that the Secretary of State will reflect on the personal testimonies that I have presented, as others across the House no doubt will, as he progresses towards the Green Paper. SNP Members are committed to seeing disabled people supported into employment when they are able to be, but that can come about only through appropriate support, and not simply by honouring the rhetoric of getting people off benefits and into work.
If the hon. Lady will forgive me, I will not, because I understand that we are only about 20 minutes away from the closing speeches and I want to give everyone the opportunity to speak.
Secondly, the motion says that the House
“regrets that the Government has not yet published its White Paper”.
That does not even take account of the Secretary of State’s clear statement that he now intends to bring forward a Green Paper. I am surprised to hear the Labour party say that we should be doing this quicker, because its usual complaint is that we do not listen enough. Now, it appears to want us to rush out proposals without talking to the people we should be listening to. A proper consultation in which we talk to people with disabilities and the third-party, voluntary and charity sector organisations that represent them will take time. It is absolutely right for us to do that.
The motion goes on to note
“with concern that commitments made in the Autumn Statement 2015 to help more disabled people through Access to Work and expanding Fit for Work have not materialised”.
I have the autumn statement here. It is clear in its commitment that there will be
“a real terms increase in spending on Access to Work…to help a further 25,000 disabled people each year remain in work”.
It talks of
“expanding the Fit for Work service”
and of
“over £115 million of funding for the Joint Work and Health Unit”.
I say gently to the Labour party that the autumn statement is still in place. We are still in the period that it covers. I do not understand why Labour is suggesting that we are in some way reneging on it, when the period is still current.
If the hon. Lady will forgive me, I will not give way for the reasons I have given. I am sorry.
The motion
“further notes that the Government is reducing funding”.
That just does not add up. We are increasing spending on disability support. In the last Parliament, spending rose by £3 billion. We are now spending £50 billion on benefits alone to support people with disabilities and health conditions.
Last Friday, I attended a meeting of the North Devon and Torridge disability access forum. It was an extraordinarily positive meeting. Yes, it has concerns about the people it represents, but it wants to have a positive way of working with me and, through me, with the Government. That is typical of the positive attitude in North Devon. In Ilfracombe just two months ago, I organised a Disability Confident event, which the Under-Secretary of State for Disabled People attended. It was an extraordinarily positive event that showed what can be done when people get together and work for the good of the majority of people. That is what we should be do doing.
I am pleased to be able to speak briefly in the debate and to follow the hon. Member for Plymouth, Sutton and Devonport (Oliver Colvile). I want to use the opportunity to describe the experience of one of my constituents, who came to see me because of her concern and frustration about the Fit for Work scheme that is mentioned in the motion.
My constituent is a highly trained occupational therapist with decades of experience. She was employed by Fit for Work, the company under the umbrella of Health Management Ltd which is part of Maximus, the company to which the Government have awarded a lucrative contract to work with people with disabilities to get them back into work.
When the Secretary of State for Work and Pensions was the Secretary of State for Wales, he announced that the Fit for Work service was to be provided in Wales. The service was to provide support and advice to employed people if they had been or were likely to be off work for four weeks or more. According to Government statistics, about 48,000 Welsh workers a year are off sick for that length of time. Fit for Work was to be gradually rolled out across Wales and England. It was seen as a particularly important scheme in Wales, where a higher than average proportion of the workforce is employed in smaller companies, which do not have occupational health services to support absent staff.
The then Welsh Secretary said:
“The Fit for Work initiative will give tens of thousands of people across Wales the support they need to return to their jobs more quickly. This is clearly good for the Welsh economy.”
GPs in Wales were to offer patients a referral to the service, which included an in-depth assessment, followed by a personal return to work plan and managed support to get back to their jobs. That was in June 2015.
My constituent came to see me because, as she put it, both as an employee of Fit for Work and as a taxpayer she was concerned about how that contract was being delivered. She started working for Fit for Work in November 2015, a few months after the Secretary of State’s announcement, at the centre in Nantgarw in the constituency of the shadow Secretary of State, my hon. Friend the Member for Pontypridd (Owen Smith). However, by April 2016 Fit for Work was making staff redundant because of insufficient referrals of clients, and the centre was closed.
My constituent asked me why the Government were not supporting a service that they had instigated. Twelve months after the start of the scheme the public, GPs and employers did not appear to know about it on any kind of meaningful scale. It was inadequately advertised, so it is little wonder that the number of referrals was too low. She told me that Fit for Work did only a few employer engagement activities. The implementation was poorly managed and badly promoted. Matters even got to the stage where highly qualified medical assessors—case managers like my constituent—were taken off assessments with clients and told to ring round employers to tout the service.
Fit for Work had been predicated on 13,500 referrals a month, but the service was getting only about 450 referrals. Not only had it been badly advertised and implemented, but the process that case managers implemented was not effective in helping people achieve the aims of the scheme. My constituent described it to me as very standardised and commoditised. Speed and light touch were its hallmark.
The assessments were expected to be carried out very strictly, which had the effect of diluting the wealth of professional experience that my constituent could bring to her role. Assessors were expected to complete six assessments a day. She told me that she struggled to even do two or three properly because of the time it took. Everything is done over the telephone. Calls are meant to take 45 minutes and the referrals were supposed to be for people who had, for example, back pain, depression or anxiety and had been off work for four weeks. However, some of the people being referred had been off work for two years and their problems were much more complex.
I was just thinking about how one would try to gain, in 45 minutes, not only the trust of the person but sufficient information to understand properly their condition and the context they were living in. To do the assessment properly, my constituent felt it required preparation, including: reading all the information from the employer and the GP; making the telephone call; gathering the information from the client; considering all that evidence; considering what a return-to-work plan might look like; transcribing that information; and giving recommendations and an opinion within the production of that return-to-work plan. She told me that to do that properly would take three hours.
The targets set for the Fit for Work programme had the effect of removing much of her clinical judgment from the process. Fit for Work auditors would listen in on the calls with clients and tell the case manager whether the call they had made had passed or failed the requirements of the process—not whether it would deliver a proper return-to-work plan. It was very difficult to pass the test. She described the scheme and its implementation as being entirely data-driven, rather than people-driven. On his appointment, the Secretary of State said, laudably, that he wanted to ensure his Department realised there was a human being behind every DWP number. This direct account from someone who was employed to deliver his Department’s scheme flies in the face of that.
My constituent left me with a message for the Secretary of State. She says she is convinced of the need for this service. It could help a lot of people to get the right help and get back into work sooner after illness or injury. Her team was a fantastic group of highly skilled, empathetic and knowledgeable health professionals. They had very many valuable strengths and experiences to make people’s health and wellbeing better, allowing them to return to work at a time that was right for them. They were not utilised. They lost their jobs, the centre was closed and that support did not materialise.