Minister defends decision to abolish ‘different era’ DPTAC

A transport minister has described the government’s accessible transport advice body as “a creature from another era”, as he tried to justify the decision to abolish it.

Liberal Democrat Norman Baker was speaking as two members of the Disabled Persons Transport Advisory Committee (DPTAC) were in north London to help him launch government reform of the blue badge parking scheme.

Four months ago, the government announced that DPTAC would be abolished, as part of its so-called “bonfire of the quangos”.

Baker accepted that DPTAC had played an important role in advising on the reforms, and he said: “We also listen very carefully to DPTAC.”

But when asked by Disability News Service why the government was scrapping the advisory body, he said: “They were created in a time when legislation did not mainstream disability issues. They are a creature from a different era.”

He said the government would “still have access to the expertise” but would “just arrange it in a different way”.

Dai Powell, chair of DPTAC, replied: “I am a creature from a different era and hopefully for the future as well.”

He said the government had worked “very closely” with DPTAC on its blue badge reforms.

When asked whether he was happy that the government was abolishing DPTAC, he said: “It is important for us that the views of disabled people are heard at the highest level.”

Helen Dolphin, a DPTAC member and director of policy and campaigns for the charity Mobilise, who was also at the launch, added: “We also have to recognise that although there have been improvements it is still very, very difficult for disabled people to get around.

“There has been progress but it is still a very inaccessible transport system for disabled people.”

She said later: “I sincerely hope there will be a successor body.”

News provided by John Pring at www.disabilitynewsservice.com

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Blue badge reforms are ‘huge step forward’

The government has announced major reforms of the blue badge parking scheme for disabled people – the first on such a scale since its launch 40 years ago.

Councils will be forced to use more independent mobility assessments – instead of asking GPs to assess applicants – of those who do not qualify automatically for a badge.

How this will work has not yet been finalised, with new guidance for councils expected in May or June.

Included in the reforms is a long-awaited plan for a national database of the 2.5 million badge-holders, which should make it easier for councils to enforce the scheme. The database could include badges issued in Wales and Scotland.

Councils will be given “tough” new enforcement powers, including the right to cancel badges that have been lost, stolen, have expired or been withdrawn due to misuse, and on-the-spot powers to confiscate such badges.

The government also plans to contract a company to design, print and supply all blue badges across England – with a new electronic badge that will be harder to forge and alter – although councils will still process applications.

The maximum fee a council can charge will rise from £2 to £10, the first increase in nearly 30 years.

It will also be possible to renew badges online through the government’s directgov website.

The government says faster renewals and less abuse could save £20 million a year.

The National Fraud Authority’s latest estimate is that blue badge fraud costs the UK about £46 million a year.

Norman Baker, the Liberal Democrat transport minister, said at the launch of the new plans in Camden, north London, that they would ensure the badge was “fit for purpose” and that “people who need blue badges can get them and use them”.

He also promised to write to supermarkets to encourage them to tackle abuse of accessible parking bays in their own carparks.

Dai Powell, chair of the Disabled Persons Transport Advisory Committee (DPTAC), said the plans were “a huge step forward” but it was vital that they delivered “integrity” to the scheme.

Helen Dolphin, a DPTAC member and director of policy and campaigns at the charity Mobilise, said: “I am pleased that at last we have some reforms that are hopefully going to make a difference to the tremendous abuse the scheme is still suffering from.”

She said too many local authorities were issuing badges to people who do not need them.

Eligibility for the badge will also be extended to more disabled children aged between two and three, with automatic entitlement given to disabled service personnel and veterans with high support needs.

Many of the changes announced will be introduced within a year.

News provided by John Pring at www.disabilitynewsservice.com

Report’s author criticises government over weak response

The author of a report on services for people with “profound intellectual and multiple disabilities” has criticised the coalition government for its weak response to his recommendations.

Professor Jim Mansell said the government had failed to describe how it would address the problems he described in his report, which covers areas including housing, personalisation, self-advocacy and assistive technology.

And he criticised the government for simply repeating steps it was already taking, while saying it was for local social care and health agencies to resolve the other issues.

He said: “Since the report was commissioned on the basis that government recognised that existing arrangements were not doing enough for adults with profound intellectual and multiple disabilities, I find it difficult to believe that the specific attention needed will now be forthcoming.”

Mansell said that new policies introduced by the coalition government – including removing the mobility component of disability living allowance from most people in residential care and closing the Independent Living Fund to new members – “betray lack of understanding of the issues involved” and were “undermining the spread of good practice”.

And he said the government’s suggestion that families could ensure their needs were met through local campaigning was “not credible” as they were “already often fully stretched trying to get the help they need” and “often fear that if they agitate for better services their disabled relative will be punished by lack of services they need”.

Mansell’s Raising Our Sights report was commissioned, and published, by the Labour government, but the coalition government has now published its response.

The PMLD [profound and multiple learning disabilities] Network and the charity Mencap said the government’s response was “extremely disappointing”, and they accused it of “not taking responsibility to ensure the needs of people with PMLD are met”.

Paul Burstow, the care services minister, said the government “fully support” the report and have “taken on board its central message that prejudice, discrimination and low expectations are major obstacles that all people with learning disabilities face”.

He said achieving the “best outcomes” for people who need support “requires a more personalised service and we will ensure that progress continues in this area so that more people benefit”.

But a Department of Health spokeswoman declined to comment on Mansell’s criticisms of the government’s response.

There are about 16,000 people with profound intellectual and multiple disabilities in England, who all have great difficulty communicating, limited understanding, and high support needs.

News provided by John Pring at www.disabilitynewsservice.com

Government ‘failed to consider equality in school building cuts’

Inclusive education campaigners have welcomed a court’s ruling that the government failed to take account of the impact on disabled pupils and other minority groups when it scrapped a string of school building projects.

Education secretary Michael Gove has been told he did not consult widely enough over his plans to scrap the projects, and failed to pay enough attention to equalities issues in reaching his decision.

It is the second time in a month that a judge has told a public body to rethink plans to reduce spending because of a failure to carry out a proper assessment of how the cuts would affect disabled people and other minority groups.

It follows a court ruling on the decision by London Councils to slash spending on a London-wide grants programme.

Simone Aspis, policy and campaigns coordinator for the Alliance for Inclusive Education (ALLFIE), said Gove’s decision had meant there was no opportunity “for spanking new buildings that are accessible to disabled learners”.

She said ALLFIE hoped the ruling would provide an opportunity for local disabled people’s organisations and family groups promoting inclusive education to “lobby hard” with both their local authorities and the secretary of state to allow the projects to go ahead.

Aspis said the court’s ruling was another boost to the fight against spending cuts and showed that “you cannot just go ahead with policies without doing a proper equality impact assessment on what the implications will mean for disabled people”.

Although the judge, Mr Justice Holman, did not order Gove to reinstate funding for any of the projects, he did tell him to reconsider his decisions.

But the judge said that the final decision on the projects rested with Gove, and that he “may save all, some, a few, or none” of them, while “no one should gain false hope from this decision”.

The judicial review was brought by Luton, Waltham Forest, Nottingham, Newham, Kent and Sandwell councils, following Gove’s decision in July 2010 to cancel projects under Labour’s Building Schools for the Future scheme in their areas.

The aim of the scheme, introduced in 2004, was to rebuild or refurbish every secondary school in England over the following 15 to 20 years.

A Department for Education spokesperson said: “We are delighted that the judge did not call into question the decision to end the wasteful and bureaucratic Building Schools for the Future programme.”

News provided by John Pring at www.disabilitynewsservice.com

Inquiry aims to expose impact of cuts on independent living

An inquiry by MPs and peers will investigate how the coalition government’s regime of spending cuts is affecting disabled people’s right to independent living.

The decision by the joint committee on human rights – whose members include the disabled peer Baroness [Jane] Campbell – to hold the inquiry on independent living has been welcomed by a string of leading disabled activists.

The committee has issued a public call for evidence, with a deadline of 29 April.

The inquiry will particularly focus on the impact of the cuts announced in the comprehensive spending review and emergency budget, and how they have affected disabled people’s right to independent living, which is guaranteed under the UN Convention on the Rights of Persons with Disabilities.

Dr Hywel Francis, chair of the committee, said he was “keen to hear evidence from disabled people about how effectively this right is upheld in practice, how policy could be improved, and the possible impact of the comprehensive spending review”.

Sue Bott, director of the National Centre for Independent Living (NCIL), said the inquiry was “very welcome, very timely” and that NCIL would be encouraging its members to submit evidence.

She said: “We are increasingly seeing that disabled people are facing cutbacks, particularly to packages of care, which really calls into question independent living and being able to participate in society on the basis of equality.”

Anne Novis, a leading disabled activist, said the cuts were “undermining independent living policies, people’s rights to be safe, to have a quality of life, to be able to get up in the morning and get out”.

She said: “I do believe it is an important process and I want to encourage people to give evidence, but I am not convinced that this current government will take any notice of this inquiry’s findings.”

Among the cuts the committee will examine are the decision to remove the mobility component of disability living allowance from most people in residential care, restrictions on council social care budgets, and the decision to close the Independent Living Fund (ILF) to new members.

Anne Pridmore, chair of Being the Boss, a user-led organisation which supports disabled people who employ personal assistants, said she believed independent living for disabled people had “gone back 20 years” because of the government’s cuts.

She is convinced ILF will close completely in 2015. When this happens, she will lose half her support funding.

She said: “I am going to do everything I possibly can in the next four years because after that I am going to be in an old people’s home.”

News provided by John Pring at www.disabilitynewsservice.com

MPs hear first-hand evidence of DLA fears

An influential committee of MPs has heard direct evidence from disabled people about their fears over the government’s disability benefit reforms.

Dame Anne Begg, the Labour MP who chairs the Commons work and pensions committee, had asked disabled people to take part in the experimental session so she and her colleagues could hear the “real voices of the people that are affected” by the reforms.

One of those invited, Kate Gordon, told the committee about her fears over disability living allowance (DLA) reforms, and said DLA had “totally supported me to get into work”, while being able to obtain a car under the Motability scheme had “totally transformed my life”.

She raised the fear that wheelchair-users like herself who were able to wheel a certain distance would not be found eligible to receive the personal independence payment (PIP), which is set to replace DLA.

Caroline Richardson, another wheelchair-user, added: “Immediately you develop those skills you’re no longer disabled – that’s the inference of [the DLA consultation] document.”

She said the consultation document was “inaccurate” and that she could “go through it line by line” and “tear it apart”.

Dr Sharon McConville, who has a mental health condition and receives DLA, said she would probably be assessed as having “lower needs” under the government’s reforms and so would lose her DLA funding.

If that happened, she said, she could “quite rapidly fall into the category of the greatest need”.

Jayne Leak, who has autism, told the MPs she was “very concerned” that she was “one of those people that is going to be marginalised and fall out under the PIP”, and would develop mental health problems as a result.

But the Conservative MP Oliver Heald said that neither the development of new independent living aids nor the Disability Discrimination Act had stopped the “remorseless rise in the number of people claiming and the amount of money being spent” on DLA.

The second half of the session was devoted to concerns around the work capability assessment (WCA) – the controversial eligibility test for out-of-work disability benefits.

Among the concerns, MPs heard about the failure of Atos Healthcare, the company that carries out the assessments, to make reasonable adjustments for disabled people taking the test.

Afterwards, Dame Anne said the committee would visit Burnley next month where she hoped to arrange a “town hall meeting” to hear from disabled people who have been involved in the pilot scheme to use the WCA to test the “fitness for work” of incapacity benefit claimants.

News provided by John Pring at www.disabilitynewsservice.com

Maynard pledges to hold bosses to account on access

Leisure, public transport, tourism and university bosses are to be brought in front of a new group of MPs and “held to account” for their failure to make services accessible to young disabled people.

Paul Maynard, chair of the new all party parliamentary group (APPG) for young disabled people, made the pledge at the group’s launch in Westminster this week.

Maynard, the disabled Conservative MP for Blackpool North and Cleveleys, said the group would highlight those areas “where service provision simply is not good enough” for young disabled people.

He said: “What we want to make sure happens is that all those service providers get summoned here… are made to stand in front of us as MPs and are held to account for what they are doing and what they are not doing.”

Maynard said he wanted to ensure that at every one of the group’s agms “we can point to successes where we have changed the culture of service provision in this country”.

He said he particularly wanted to challenge problems faced by young disabled people with complex needs as they make the transition from childhood to adulthood.

The APPG – which will be vice-chaired by Labour’s shadow equalities minister Fiona Mactaggart – has been set up with the support of Trailblazers, a campaigning group of more than 300 young disabled people run by the Muscular Dystrophy Campaign.

Members of Trailblazers were at the launch to talk about the investigations they have carried out since 2008 into the inequalities they face in public transport, employment, higher education, tourism and leisure facilities.

Oxford University student Zoe Hallam said that many young disabled people “get the impression that they are turned away because of their disability because employers think of us as risks or inconveniences”.

She added: “If we are capable of doing the job, and we are capable of doing the job, there should not really be any barriers.”

Social worker Hannah-Lou Blackall told MPs at the launch that young disabled people need “boundless determination, problem-solving skills and a robust sense of humour” just to plan a holiday.

News provided by John Pring at www.disabilitynewsservice.com