Tag: Dame Anne Begg

Clause 99, Catch 22 – State sadism and silencing disabled people

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Here is the Hansard record of The Work Capability Assessments – Mandatory Reconsideration adjournment debate – it’s the 6th debate about Employment Support Allowance (ESA) tabled by Labour MP Sheila Gilmore, who has worked very hard to present her gathered and substantial evidence to an indifferent government about the terrible consequences of their sadistic sickness and disability “reforms”.

Section 102 and Schedule 11 of the Welfare Reform Act, (Clause 99) is the (State) power to require revision before appeal. People who wish to challenge a benefit decision will no longer be allowed to lodge an appeal immediately. Instead, the government introduced mandatory revision or review stage, during which a different Department of Work and Pensions (DWP) decision maker will reconsider the original decision and the evidence and, if necessary, send for more information.

We have campaigned since 2012 to raise awareness of Clause 99. During the Consultation period, I wrote a response to the government’s proposals, which many people used as a template for their own responses. I remember that Black Triangle, amongst others, ran a campaign also, and I remember that we ALL RAISED THE SAME CONCERNS.

In summary, the main concerns were that basic rate ESA was to be withdrawn during the mandatory review period, leaving sick and disabled people with no money to live on, whilst the DWP reconsidered their own “fit for work decisions” that were wrong.

I know that our Consultation responses were ignored by the government. The changes were introduced anyway, despite our grave concerns. Since October 2013 people have to apply for mandatory reconsideration separately before they can lodge an appeal. We were also very worried that no time limit was established for the DWP to undertake and complete the mandatory review. Our concerns were fully justified, as it’s emerged that people are waiting 7-10 weeks for the mandatory review decision. Meanwhile, these people cannot appeal. And have no money to live on.

An added concern is that this system as it stands demands such a lot from people who may be very vulnerable, seriously ill and/or have mental health problems. Their difficulties are exacerbated by cuts in legal aid for welfare rights advice and cuts in local authority grants. There is a significant contraction of the availability of help for those who need it the most from advice agencies.

Last year, Lord Freud suggested people awaiting their mandatory review should apply for Jobseekers Allowance (JSA) and then re-claim assessment-rate ESA if they have to appeal. However JSA claimants have to be available for and actively seeking work, and this is beyond people with disabilities or health conditions. As a result, many are ending up without any support at all from the State, having been deemed too “fit” to be eligible for ESA, but too sick or disabled to claim JSA, because these people cannot meet the high level of conditionality or remain available for work.

These people are left with NO lifeline benefits for periods as long as ten weeks. It seems Penning is oblivious to the fact that DWP “decision-makers” are demonstrating quite clearly that their initial “fit for work” responses are plainly and fundamentally wrong, it seems that Tory Ministers have engineered a situation that places some of the most vulnerable disabled people in a nightmarish situation where bureaucrats tell them they are both fit and unfit for work. Both contradictory decisions are then used to withdraw lifeline benefits. That’s not only grossly unfair, it’s terribly cruel. It also demonstrates how completely arbitrary DWP “decision-making” is, in order to justify removing people’s support.

Even when it’s the case that someone manages to make a successful claim for JSA, they are greatly at risk of being sanctioned because of the high level of conditionality, and the requirement to be available for work, in order to remain eligible for the benefit.

Furthermore, there is growing evidence that the DWP are closing existing ESA claims when a person successfully claims JSA during the mandatory review period, on the grounds that it isn’t possible to have two ongoing claims for two separate benefits open at the same time. This effectively means that people lose their right to appeal for the reinstating of their ESA, as their original ESA claim has ended.

This is how disabled people, amongst whom are some of our most vulnerable citizens, are being treated, what kind of government would allow such an utterly unacceptable degree of absolute callous indifference into what was originally designed as a system of support? A system that is now punishing people because they are sick or disabled? And what sort of government ignores the evidence of the extreme suffering and distress they are causing people?

How can this government show no remorse whatsoever, or decent and normal concern in the face of so many accounts of such human suffering and desperation – and heartbreaking comments such as “one constituent sold off his few remaining possessions to survive.” 

Many are relying on already stretched food banks, whilst others are taking out high interest loans. This situation is being exacerbated by growing delays. As we’ve pointed out, the law needs to change so claimants can be paid ESA at the assessment rate during the reconsideration process. This shouldn’t actually cost any money, as it is paid at the same rate as JSA – that benefit officials suggest claimants should receive anyway. I know that Sheila Gilmore is pushing to see basic rate ESA reinstated. She is also demanding that a statutory time limit is set on how long reconsideration decisions take. But Penning remains adamant that this isn’t going to happen.

Sheila notes that this issue was raised with Ministers when the legislation was going through the House and in subsequent sittings of the Work and Pensions Committee, for example. In April 2012, the Administrative Justice and Tribunals Council warned that the absence of a time limit could have the effect of “delaying indefinitely the exercise of the right of appeal to an independent tribunal”.  

Many of the key issues with the mandatory review can be seen summarised herehere and here. Sheila Gilmore and Anne Begg have covered these extensively during the ongoing Work and Pensions Committee ESA inquiry, as well as during the course of the many separate tabled debates.

Penning, I’m sorry to say, remained indifferent when he was confronted with evidence of the unforgivable suffering, the links to suicide, the links with high risk of homelessness, hunger, anxiety and stress, and the exacerbation of illness and mental health conditions in vulnerable people – this government’s policies are creating these extreme hardships. Bearing in mind this is meant to be our government’s support for very vulnerable sick and disabled people, his position is indefensible. So are his objections to answering these questions before. He said: “Actually, this is a bit like groundhog day. According to my file, this is the hon. Lady’s fifth debate on the subject. She said that it was the sixth; perhaps we missed one….

I am slightly concerned, because I said many of the things that I am about to say to her Committee only a few days ago. I hope that its members will pay attention to what I say, because during the speech of the hon. Member for Edinburgh East I feared that the report might have already been written.” 

Perhaps if he told the truth, listened and did his job properly, there would be no need for us to raise the same concerns again and again.

I doubt I could be an MP, I probably lack the necessary constraint, I’m afraid the sneer in his words, given the gravity of the situation for so many sick and disabled people, would have possibly elicited an out of character, but unstoppable, spontaneous punch in his spiteful, indifferent face, such is my anger. And really it’s impossible to see the welfare “reforms” as anything other than callous, spiteful and scripted sadism and indifference to people’s pain and desperation. I’ve always loathed bullies.

Sheila Gilmore said she had been told by Mark Hoban previously – last September – that claimants could request “flexible conditionality”, to avoid the difficulties imposed by JSA conditionality criteria. However, DWP’s Director acknowledged in April – some seven months later – that “not all advisors had been aware of this”. As Sheila Gilmore responded: “It is hard to have confidence in the Department, given that previous assurances were clearly unfounded.

Penning said: “As a Minister in the DWP, I am absolutely determined that we will ensure that taxpayers’ money is spent wisely; that it goes to the people who need it; that we put in place training for the right people…”

He seems to have overlooked the fact that most people claiming ESA have worked, paid income tax, and are still contributing proportionally more tax than those on the highest incomes pay, via VAT, Council Tax, the Bedroom Tax and an array of other stealth charges

And very clearly, the “people who need it” are NOT getting the support they need.

As Sheila Gilmore points out: “There is also an administration cost involved in a claimant receiving the assessment rate of ESA, ceasing to receive it, claiming JSA and then potentially claiming the assessment rate of ESA again. These are significant costs when multiplied by the number of people involved. In addition, if everybody claimed JSA successfully, they would receive benefit at exactly the same rate as they would have been getting on ESA, so if there are any savings to be anticipated, is it because ministers thought that people would, in fact, struggle to claim JSA during the reconsideration process, given that administration costs are likely to outweigh anything else? ”

“I am sure that cannot be the case.” she added.

I’m not bound by Parliamentary codes of conduct, as Sheila is. So I can say freely and categorically that it IS the case, and we anticipated this at the Consultation stage. Furthermore, the government know that WE know this, but they remain unremorseful, refusing to re-introduce assessment rate ESA, and to place a time limit on the reconsideration process.

Clause 99 has been introduced to make appealing wrong decisions that we are fit for work almost impossible. Sick and disabled people are effectively being silenced by this Government, and the evidence of a brutal, de-humanising, undignified and grossly unfair system of “assessment” is being hidden. More than 10,600 people have died  between 2010 – 2011, this a significant increase in mortality because of the current system, (the government have refused to release the data regarding ESA-related deaths since 2011 despite numerous Freedom Of Information (FOI) requests) and it is absolutely terrifying that our Government have failed to address this.

Instead, they have made the system even more brutal, de-humanising and unfair. What kind of Government leaves sick and disabled people without the means to feed themselves and keep warm? Clause 99 is simply an introduction of obstructive and Kafkaesque bureaucracy to obscure the evidence of an extremely unfair and brutal system. By creating another layer of brutality, the Government is coercing people into silence.

Successful appeals were evidence of an unjust system, and now, having made the process of appeal almost impossible, we have ministers trying to claim that suddenly the system is fine.

It’s FAR from fine.

430847_149933881824335_1645102229_n (1)Thanks to Robert Livingstone for his brilliant artwork.

I would also like to say a BIG thank you to Sheila Gilmore, Dame Anne Begg, Debbie Abrahams and all other MPs who work tirelessly in challenging and opposing the avalanche of social injustices and authoritarian policies this government have inflicted on those least able to fight back themselves.

PIP and the Tory monologue

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Here is a very important leaked correspondence between Dame Anne Begg and Esther McVey regarding PIP. (Personal Independence Payment, which is to replace Disability Living Allowance.) The correspondence flags up some serious concerns regarding a lack of transparency and accountability, responsiveness and a basic lack of following established democratic norms and protocol on the part of  the current Government. Mounting successful challenges to reform requires having detailed information regarding that reform. Here is clear evidence that the Conservatives are intentionally stifling democratic dialogue.

There are some serious issues raised in Esther McVey’s response that signal some very worrying changes to advisory groups and their role in how they influence policies. Esther McVey is indicating that the Secretary of State has already moved away from dialogue with, and paying heed to independent groups, as well as secretly deciding that any input and advice at all does not need to be published and open to public scrutiny. It signals that the Government will no longer be obliged to do anything more than pay lip service to consulting independent groups. Of course such consultations are crucial mechanisms of democratic process, scrutiny, the safeguarding of human rights, as well as Government transparency and accountability. Here we see evidence that these mechanisms are being very quietly dismantled. This clearly signals an authoritarian turn on the part of the government.

McVey has managed to avoid going before the Work and Pensions Select Committee, and she is telling the Committee that she intends to publish the Government’s response the SAME DAY as the secondary regulations are presented to Parliament. This gives us no time whatsoever for scrutiny, analysis, preparation or effective challenge.

Letter from Anne Begg to Esther McVey:

Dear Minister

Disability Living Allowance and Personal Independence Payment (PIP)

You will be aware from the debate in Westminster Hall on 25 October that the Committee has a number of outstanding concerns about the eligibility criteria and plans for implementation for PIP. As you know, we had hoped to explore these issues in an evidence session with you in November. Committee staff had been in the process of trying to identify a suitable date through your officials.

We first invited you to appear during the week of 5 November but you did not have a diary slot available that week. You then offered 9.00 am on 12 or 13 November, but neither of these was possible for Committee members (particularly as one was a Monday morning when we are travelling from our constituencies). Our next suggestion was 21 November.

The issue now seems to have moved on from being simply a diary problem. Your officials have indicated that you would prefer not to give evidence before the PIP Regulations are published because you feel you would be unable to answer the Committee’s questions. I would like to make clear that our intention was that our evidence session should inform the drafting of the Regulations, and the eligibility criteria, before they are finalised and laid before Parliament. The change in your position suggests to us that final decisions have already been made.

We would be grateful for your response to the following questions to help clarify the situation:

1. When do you plan to respond to the consultations on the draft assessment criteria and thresholds and on finalising the detailed rules for PIP?

2. Will the relevant Regulations, including the draft assessment criteria, be published in draft and subject to some form of further consultation, before they are laid before Parliament? If so, what is the timescale for this and what scope will there be to amend them further?

3. When do you expect the final Regulations to be laid (officials have been able to tell us only that they will be laid “before the end of the year”). If it is your position that it is already too late for the Committee to influence the finalising of the relevant Regulations, I would ask you to give a commitment to appear before us as soon as possible after they are laid, to explain the rationale for the final decisions you have made.

Draft Public Bodies (Abolition of the Disability Living Allowance Advisory Board) Order 2013

Departmental select committees (DSCs) have a formal role in scrutinising draft Orders laid under the Public Bodies Act. Departments are required to bring these draft Orders to the attention of the relevant DSC. The Committee has the power, as set out in Cabinet Office guidance, to recommend an extension of the laying period to 60 days if it decides this is necessary to ensure proper scrutiny.

DWP staff failed to bring the Draft Order on the DLA Advisory Board, which was laid on 15 October, to the Committee’s attention. The Committee staff only became aware of it because the House of Lords Secondary Legislation Scrutiny Committee contacted them to discuss the respective action each committee planned to take.

We are concerned about this lack of recognition by the Department of my Committee’s formal scrutiny role in relation to draft Orders under the Public Bodies Act. Officials have tried to allay the Committee’s concerns about the draft Order by saying that it does not do anything significant. I would make two points about this. Firstly, it is for the Committee to decide whether any matter within its remit is significant or not, including draft Orders. Secondly, the agreed formal procedures should be adhered to whether or not officials regard an issue as significant.

I would be grateful for your assurance that the Department will adhere to the agreed procedure on future occasions.

We understand that the Lords Scrutiny Committee has expressed concerns about the Department’s failure to carry out any consultation on the proposed abolition and has recommended an extension of the scrutiny period to 60 days [12th Report, HL 55, 1 November 2012]. We agree with this recommendation.

Turning to the substantive issues raised by the draft Order, the Committee staff made clear to your officials that we were willing to deal with these as part of the broader oral evidence session with you on PIP—if you had been able to attend a meeting before the 40-day laying period expires on 28 November.

As you no longer intend to appear before us in November, we would be grateful for your response to the following questions on the implications of the abolition of the DLA Advisory Board:

1. What measures will be put in place to protect the interests of non working-age claimants who will continue to claim DLA?

2. What measures will be put in place to protect the interests of working-age DLA claimants prior to their migration to PIP?

3. What will be the composition of the PIP advisory group referred to in paragraph 7.5 (b) of the PBO explanatory memorandum?

4. Will the advice of the PIP advisory group be published?
I would be grateful for your response by Friday 9 November.

Yours sincerely
Dame Anne Begg MP

Chair
Dame Anne Begg.

I suppose the terms of authoritarianism extend to have an impact on opposition parties and affect their capacity to gather information and organise actions much the same as they do campaigners and the general population. Again, without being provided with information and crucial detail, it becomes very difficult to mount a successful challenge against controversial legislation. This is a Government that does exactly what it chooses, and barely bothers justifying itself. Consider, for example, that no impact assessment was carried out regarding the welfare reforms. Or that the risk register concerning the Health and Social Care Bill has yet to be published and made accessible to the public.

It’s also noteworthy that Cameron is currently proposing that consultations, equality impact assessments, audits, judiciary review are all simply “inconveniences” that are (and I quote) “… not how you get things done…” 

Ask yourself what kind of things Cameron “wants to get done” bearing in mind that every single policy that this Government has designed and implemented has been about taking money away from the poorest people, and reducing the lives and experiences of the most vulnerable citizens, rather than enhancing those lives in any way.

Consider that these legislative mechanisms are important to democratic process, accountability, procedure and law, as well as being basic human rights safeguards. This is a Government that clearly is not about reflecting and meeting the needs of the public.

The Government have been made aware that sick and disabled people are dying after Atos have assessed them as fit for work. Ask yourself what kind of Government flatly and loudly denies that this is the case, without investigating the truth of the many serious concerns raised, and looking at the many cases that have been presented to them during debates in Parliament. What kind of Government tells lies about marginalised social groups, and propagates hateful stereotypes of marginalised citizens in the media to justify removing their welfare – calculated to cover basic living costs. Welfare provision is paid for via taxes, which many sick and disabled people have also paid. Our welfare support is NOT a “handout”: it is our money, our national insurance, paid by us for when we have a need of support. Social security.

Below are a couple of key paragraphs from McVey’s response to Dame Begg. These reflect the quiet dismantling of the Disability Living Advisory Committee, and the fact there is no advisory report or a formal advisory group regarding the development of PIP. Note again that the Government is not big on following procedure, or being transparent, accountable and consultative.

E. McVey: “Public Bodies (Abolition of the Disability Living Advisory Board) Order 2013

Please accept my apologies that the draft Order was not formally brought to the attention of the Committee as it should have been done. I understand that Cabinet Office made the Secretariat of the Committee aware that a draft Order was in the offing earlier in the year but unfortunately procedures were not followed through on a formal basis as they should have been. I will ensure that the Department will adhere to the agreed procedure on future occasions.

I hope my answers to your questions explain why we have taken the view that this Body which has not been asked to give any advice since 2008 had an extremely limited remit and why officials thought it proportionate to deal with the questions you raise on a correspondence basis. We certainly had no intention of disparaging the important role the Committee undertakes. I have set out my replies to your questions below.”….

“There will not be a PIP Advisory Group in the way that the Disability Living Allowance advisory group operates. In the Explanatory Document to the Public Body Order we explain that we have decided to use time-limited advisory groups and that the people asked to help us develop the assessment criteria for Personal Independence Payment (the Assessment Development Group) encompassed a wide range of expertise across health, social care and disability, including from occupational therapy, psychiatry, physiotherapy, social work, general practice, as well as representatives from Equality 2025 and Disability Rights UK. We included the Assessment Development Group in the Explanatory Memorandum as an example of how the Secretary of State is using a time-limited advisory group in policy development.”….

[Note the fact that the time limited invisible Advisory group approach doesn’t apply to just the PIP legislative development, it is to apply to ALL policy development. Also note she later goes on to say that “There was no FORMAL Advisory group, there is therefore no formal report from the Group, nor is there a requirement to publish their advice.”]

Section 89 of the Welfare Reform Act 2012 requires the Secretary of State to lay before Parliament an independent report on the operation of assessment within two years of regulations under section 80 coming into force and a second report within four years of that date.

Will the advice of the advisory Group be published?

As mentioned above there is no formal Advisory Group. The assessment criteria for Personal Independence Payment were developed in close collaboration with the Assessment Development Group. Although members sometimes submitted written comments on proposals, advice was generally given verbally and captured in meeting minutes.

There is therefore no formal report from the Group, nor is there a requirement to publish their advice, although we have published details of the development process in the explanatory notes which have accompanied the first and second drafts of the assessment criteria. The explanatory notes can be found at http://www.dwp.gov.uk/policy/disability/personal-independence-payment/the-assessment-criteria/

I hope this reply is helpful to the Committee.

Esther McVey MP
Parliamentary Under Secretary of State and Minister for Disabled People

Anne Begg : “Disability groups have not been consulted about the framing of the PIP assessment contracts or the guidance to assessors, so, although there has been limited consultation, the wider implications of how the measure will work in practice have not been subject to any kind of co-production. In one meeting, the Disability Benefits Consortium told us that the documents had been counted in and counted up, and that it had been given 15 minutes to look at them. That, again, is hardly co-production.

On the PIP assessment, the Government have said that there will be a requirement for face-to-face assessments for most claimants. That also raises a number of questions. On what basis did the Government come to that conclusion? Will the Government not be able to take account of existing evidence in most cases? That leads me to a question on a slightly different point: will there be any transfer of information already held by the Department for Work and Pensions, so that people do not have continually to remind it of such things as, “This is a glass eye, and of course I am not going to see out of it.” That is not as daft as it sounds. Sometimes, when people have gone for a WCA they have been asked what vision they have in their left eye when they have not had a left eye for decades.” – Dame Anne Begg, Daily Hansard – Westminster Hall 25 Oct 2012 : Column 319WH Westminster Hall.

Here is the full response from Esther McVey :

Dame Anne Begg MP
Chair
Work and Pensions Select Committee
7 Millbank
LONDON
SW1A 0AA
8 November 2012

Dear Anne

Thank you for your letter of 1 November. I am sorry we have been unable to identify an opportunity in November for me to appear before the Select Committee to discuss the PIP assessment criteria and regulations.

The Department has taken considerable time to develop the assessment criteria, throughout which we have sought to be transparent and to engage with and seek the views of disabled people, their organisations and parliamentarians. Our initial proposals for Disability Living Allowance reform, including the high-level principles of the assessment, were published in December 2010.

We published a first draft of the detailed proposals for the assessment criteria and regulations in May 2011, a second draft in November 2011 and ran significant consultations on both. The consultation on the second draft ran from January to the end of April this year, during which we received around 1,100 written responses and met with around 60 disability organisations.

Since the consultation closed on April 30 the Department has been carefully considering the responses received to identify any areas that we need to change to ensure that the assessment is both fair and operates effectively. As part of this we have also considered the comments made in the Select Committee’s report of 19 February and during the evidence session attended by my predecessor in December 2011.

We have also been working to test proposals for change, so we can understand the likely impact of the revised assessment. This work has now concluded and we have reached conclusions on the content of the finalised assessment criteria and regulations. We are now in the process of finalising the drafting of the government response and regulations and discussing the detail with colleagues across government.

We intend to publish a joint response to the consultations on the assessment criteria and benefit rules as soon as it is ready. While we do not yet have a firm date for publication, I am confident that it will be before the December recess. I do appreciate that many people would have liked an earlier response but it has been essential to take our time on this important issue and make sure we get the decisions right.

We have also not yet reached any final decisions on the publication of the PIP regulations but I think it likely that the key regulations will be published and laid on the same day as the government response.

Given the significant engagement that has already been undertaken, we are not intending to carry out any further consultation on draft regulations. However, we agreed during the passage of the Welfare Reform Act that the key regulations on PIP relating to benefit entitlement would be affirmative, which will allow Parliament further opportunity to scrutinise them.

I realise that this response is likely to be disappointing. However, I do consider that the development of our proposals for PIP has been carried out in a transparent and consultative fashion and that there has been full opportunity for the Committee to comment and offer suggestions for changes over the two year development process. We will be offering briefing sessions to MPs and Peers to explain the government response and regulations before the regulations are debated and I would be very happy to appear before the Select Committee to do the same to explain the rationale, as you suggest.

Draft Public Bodies (Abolition of the Disability Living Advisory Board) Order 2013

Please accept my apologies that the draft Order was not formally brought to the attention of the Committee as it should have been done. I understand that Cabinet Office made the Secretariat of the Committee aware that a draft Order was in the offing earlier in the year but unfortunately procedures were not followed through on a formal basis as they should have been. I will ensure that the Department will adhere to the agreed procedure on future occasions.

I hope my answers to your questions explain why we have taken the view that this Body which has not been asked to give any advice since 2008 had an extremely limited remit and why officials thought it proportionate to deal with the questions you raise on a correspondence basis. We certainly had no intention of disparaging the important role the Committee undertakes. I have set out my replies to your questions below.

1. What measures will be put in place to protect the interests of non working-age claimants who will continue to claim DLA?

DLAAB ‘s function is to issue the Secretary of State with independent advice. It does not exist to protect DLA claimants’ interests although of course the Board members had an interest in the integrity of the benefit system. It is not part of the decision making process for benefits and has no power to intervene in individual claims for Disability Living Allowance and Attendance Allowance. DLAAB has not provided any advice since 2008.

Work undertaken by the Board over the years concentrated mainly on medical reports on specific conditions or illnesses. This was usually because the department had detected a potential issue. For instance the department noted that DLA spending on “behavioural disorder” cases (which included ADHD cases) had increased much more rapidly than spending on other child recipients. In light of this the Board was asked to advise:

  •  whether there has been an increase in the number of children diagnosed with ADHD generally and, if so, suggest reasons for the increase; and 
  •  could the increased numbers of children in receipt of DLA be directly related to the increase in diagnosis or were there other reasons?

The Secretary of State will still commission work if he thinks this is necessary using task and finish groups as and when required and ensuring that the appropriate specialisms are covered. Even with the wide breath of professions covered by DLAAB it was still necessary on occasion to co-opt professionals with particular expertise as in the Attention Deficit Hyperactivity Disorder study where a Consultant Child and Adolescent Psychiatrist was asked to provide advice.

Claimants have always had the right to ask for a reconsideration if they are unhappy with a decision and then appeal to an independent tribunal if still dissatisfied. The Welfare Reform Act 2012 includes powers to require all claimants to seek a reconsideration before they can appeal to an independent tribunal. There is a complaints system which claimants can utilise which is advertised on the DWP website. Claimants may also apply to the Independent Case Examiner, if they consider the department has not treated them fairly or have not dealt with complaints in a satisfactory manner.

2. What measures will be put in place to protect the interests of working-age DLA claimants prior to their migration to PIP.

As explained above this was never the role of DLAAB. The same rights apply to working- age and non working-age people.

3. What will be the composition of the PIP advisory group referred to in paragraph 7.5 (b) of the PBO explanatory memorandum?

There will not be a PIP Advisory Group in the way that the Disability Living Allowance advisory group operates. In the Explanatory Document to the Public Body Order we explain that we have decided to use time-limited advisory groups and that the people asked to help us develop the assessment criteria for Personal Independence Payment (the Assessment Development Group) encompassed a wide range of expertise across health, social care and disability, including from occupational therapy, psychiatry, physiotherapy, social work, general practice, as well as representatives from Equality 2025 and Disability Rights UK. We included the Assessment Development Group in the Explanatory Memorandum as an example of how the Secretary of State is using a time-limited advisory group in policy development.

We will also continue to liaise and listen to other stakeholders of and from disability organisations including Equality 2025 which is a non-departmental public body of publicly-appointed disabled people. The group offers strategic, confidential advice to government on issues that affect disabled people. This advice can include participation in the very early stages of policy development or in-depth examination
of existing policy. The group works with ministers and senior officials across government.

Section 89 of the Welfare Reform Act 2012 requires the Secretary of State to lay before Parliament an independent report on the operation of assessment within two years of regulations under section 80 coming into force and a second report within four years of that date.

4. Will the advice of the advisory Group be published?

As mentioned above there is no formal Advisory Group. The assessment criteria for Personal Independence Payment were developed in close collaboration with the Assessment Development Group. Although members sometimes submitted written comments on proposals, advice was generally given verbally and captured in meeting minutes. There is therefore no formal report from the Group, nor is there a requirement to publish their advice, although we have published details of the development process in the explanatory notes which have accompanied the first and second drafts of the assessment criteria. The explanatory notes can be found at http://www.dwp.gov.uk/policy/disability/personal-independence-payment/the-assessment-criteria/

I hope this reply is helpful to the Committee.

Esther McVey MP
Parliamentary Under Secretary of State and Minister for Disabled People

 

Picture by Robert Livingstone

Pictures courtesy of Rob Livingstone 

I ought to update this in light of recent events. Campaigners won an important victory regarding an essential regulation being excluded from the PIP legislation, namely, the “reliably, repeatedly and safely” adjustment, that is an essential mechanism in ensuring that “fluctuating” conditions are fairly considered and assessed.

However, many disabled activists were shocked and angry when Esther McVey, the Conservative minister for disabled people, suddenly announced the unexpected changes in December. The alterations to the regulations that will decide who is eligible for the new personal independence payment (PIP) – which will gradually replace working-age disability living allowance from this April – saw the key walking distance criteria reduced from 50 to 20 metres.

There has been absolutely NO Consultation on this whatsoever. That in itself warrants a legal challenge. The alteration of the distance criteria has been challenged by the Labour  Party, too. Anne McGuire, Labour’s shadow minister for disabled people, said disabled people had “been alarmed at the hurdle they will now face before being awarded the enhanced mobility rate”.

She said: “Most of those who have looked at these descriptors would say that a 20-metre qualifying distance simply does not provide a practical level of mobility.”

She said about 200 disabled people in every parliamentary constituency were likely to lose their Motability vehicle with a 20-metre qualifying distance.

And she pointed out that one of the Department for Transport’s own publications, Inclusive Mobility, recommends that “seating should be provided on pedestrian routes at intervals of no more than 50 metres, and that parking spaces for blue badge holders should preferably be provided within 50 metres of the facilities they serve”.

Another issue that concerns me is that McVey as good as admitted there are built in targets to reduce/remove eligibility for PIP. How could she know in advance of assessments, otherwise, that “330,000 of claimants are expected to either lose their benefit altogether or see their payments reduced”, as she informed the House of Commons?

http://www.guardian.co.uk/society/2013/apr/08/disabled-claimants-legal-action-mobility-tests