(12 years ago)
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My hon. Friend is quite right. Even if the Government learn lessons from the pilot, will they be ready to go back to the drawing board to look at the role of assessors? Somehow, I doubt that they will be.
We need excellent assessors, who can see the nuances of difference between disabilities and are fully trained to identify and advise those they assess. That is the first issue that I hope will be addressed by April 2013. The guidance provided to assessors is another source of concern for disabled people and charities. I am interested to know whether the Government have changed their mind on whether they will consult on the guidance once it has been drawn up. Assessors would be helped greatly if they had clear and effective guidance in front of them.
An aspect of the issue that is close to my heart, as hon. Members may be aware, concerns the identification of mobility issues for blind and partially sighted people. I campaigned for an automatic entitlement to the higher rate of mobility allowance for cane and dog users. That is being lost in the PIPs system, along with many other automatic entitlements. Many people are concerned that that will create an unnecessary burden for disabled people, whether or not they eventually receive the higher rate. Will the Minister restate her reasons for creating that additional burden?
There is also concern that, under the new guidance for PIPs, guide dogs will be seen as the only evidence of mobility issues for blind and partially sighted people. I have heard rumours that the final guidance will include canes as well as guide dogs, but I would like reassurance from the Minister that that will be the case. We cannot go backwards when dealing with such people.
The guidance must be all-encompassing and provide for all types of disability. It must also recognise that being disabled can be a lifelong condition and a lifelong drain on income. The Department for Work and Pensions has published various case studies that show how PIPs would work. For example, referring again to blind and partially sighted people, one of the studies shows someone who has been living with sight loss for some time receiving a lower award than someone with the same impairment but recently diagnosed. Costs do not diminish over time, and as people learn to live more independently, they might need more help and money to deal with what they can then do. The Government want to put those people back rather than help them to go forward. People should not be penalised for having learnt to live with their condition, and the Government must consider that.
Regarding the guidance that assessors receive, I have raised a number of points that concern many of my constituents. Again, I would be interested to hear some assurances from the Minister that the guidance will be designed to reflect the multitude of disabilities. I have spoken about how we can ensure that the 1,260 people in my constituency who will lose out on PIPs, along with the hundreds of others who will not qualify for higher rates, do not lost out because of untrained assessors or inadequate guidance. We must now address what happens to the people who do not qualify for PIPs.
The hon. Gentleman makes some important points, and I look forward to the Minister’s replies. Does the hon. Gentleman accept that it is unacceptable that 48% of disabled people should not have employment, along with the well-being and stronger financial position that comes from that, and that PIPs, with the regular reviews, are a step in the right direction for many disabled people who want to work and are able to do so?
I totally agree with the hon. Gentleman, but we see Remploy factories being closed down and other areas where there is no work for disabled people, yet we try to tell them they have to find employment. If there was employment, believe me, most people who are disabled would want to take it up, and right away. Unfortunately, the realism of the work market at the moment is that there are not the jobs for every person who would like one, never mind every person who is disabled.
I asked a question about the notice given to someone who is not eligible for PIPs and was told:
“Where entitlement to personal independence payment has not been established the DLA will stop shortly after the decision notice has been sent.”—[Official Report, 23 October 2012; Vol. 551, c. 837W.]
The vague “shortly” shows an absolute lack of evaluation of what it will mean in practice. I have subsequently received another letter in which the same word is used as a time frame. That is not good enough. Far more thought and consideration needs to be put into what that will mean for people who lose their benefit. How long will they have to find another source of income? Will there be enough time for them to find other sources of benefit from the Government?
In oral evidence to the Work and Pensions Committee, Professor Roy Sainsbury said that based on the 1990s take-up rates of between 50% and 70%—we can probably assume that the rate has increased a little—perhaps as many as 25% of disabled people still do not claim DLA. We can therefore only assume that the people currently claiming DLA are those who need it most, and we can therefore also assume that they will be the people most affected by its loss. Some of the most vulnerable people in our society will now have the complicated responsibility of navigating the PIPs system, and those who have already been identified as vulnerable should be given specific attention during the handover. We need clearer answers on how long DLA claimants will have before the benefit is stopped and on what kind of help they will receive to get them over the initial period.
We can also assume that a number of appeals regarding PIPs are likely. In most places, the assessments are to be administered by Atos—a company that is notoriously bad at making accurate assessments. We already know that it got one in five ESA assessments wrong between October 2008 and November 2011, so I am certain that many people who are not eligible for PIPs will want to appeal the decision. In Scotland, the system will now be run by Salus, but I am sure that many people there will still look to appeal. We must ensure that the lessons learnt from the ESA and work capability assessments are not lost. I would like to ask that the process for people who are appealing their decision is properly conducted. Will their DLA be cut, and will they be expected to find another source of income?
I would also like to ask about how the loss of DLA and the higher or enhanced rate of mobility for PIPs will impact upon carers. I have more than my fair share of carers in my constituency, and if money is lost to them what do they do about caring, and how will carers be looked after? I am sure that they will continue to care, but they will struggle to pay their bills at the same time. We must give carers the respect that they deserve. They save this country billions of pounds every year. I am interested to hear how the Minister will deal with that.
My final point is on passported benefits—a key concern for my constituents that alerted me to the practical problems with PIPs. The Motability scheme, for example, is paid for through the higher rate of benefits. As I explained earlier, 280,000 people will lose their entitlement to higher or enhanced rate mobility, and a large proportion of them are likely to have their Motability vehicle seized. They will be unable to make the payments for the vehicle, and if they have already been relying on it—I am certain that some people will still need such a vehicle despite not being eligible for the higher rate—what will they do to get around? Will they be left in a state of isolation? At what point will their vehicle be seized? Will they be given time to get another mode of transport?
I hope that the impact of losing the higher rate of mobility has been carefully considered, because it will make a massive difference to the lives of hundreds of thousands of people. There will also be an impact on blue badge holders and concessionary travel benefits, and holding separate assessments for passported benefits will not only cause stress for people who have lost their DLA, but incur extra costs for the taxpayer. As I have said before, the aim of the policy is to save money, so this all seems pointless and unnecessary.