Mar 232013
 

In the court case taken by five disabled people against the proposed closure of the Independent Living Fund (ILF) , and supported by a campaign led by DPAC and Inclusion London certain documents were used. These documents are mainly correspondence between civil servants at the Government’s Department for Works and Pensions (DWP) and the minister for disabled people: Esther McVey.

These documents were released and declassified after the court case because they had been mentioned in the case. This is a summary of those documents.

Early analysis of responses to the consultation on ILF Closure (undated)

This document gives a breakdown of responses and several points for McVey to take into account. First, the consultation asked:

Question 1Do you agree with the Government’s proposal that the care and support needs of current ILF users should be met within the mainstream care and support system, with funding devolved to local government in England and the devolved administrations in Scotland and Wales?[1] This would mean the closure of the ILF in 2015.

 

Question 2What are the key challenges that ILF users would face in moving from joint ILF/Local Authority to sole Local Authority funding of their care and support needs? How can any impacts be mitigated?

 

Question 3What impact would the closure of the ILF have on Local Authorities and the provision of care and support services more widely? How could any impacts be mitigated?

 As we see never were questions asked on extending the ILF or keeping it open. In fact question 1 is what is called a ‘leading question’

In the documents DWP tell McVey:

       ‘As we expected with the current challenges facing the care and support system, the majority of ILF users are opposed to closure of the fund, with many doing so on the basis that there could be no guarantee that their current level of funding would be protected in the future’

and….

           ‘A range of smaller national and local disability groups expressed similar concerns with our proposal. Some have been able to support the closures in principle but usually conditional on current user awards being protected as part of ring-fenced funding. The most vocal group has been the relatively new Disabled People against Cuts, DPAC. This group has taken a very strong critical position on a range of DWP policies’.

Yes we have and both Miller (our old mister for disabled people) and McVey refused to meet us and ILF users several times-in fact they didn’t even bother to respond to these requests!

We were very surprised to see this section advising McVey:

           ‘The consultation exercise has been immensely useful and we have been satisfied that we have listened to a collection of views that is representative of all those individuals or organisations that have an interest in or may be impacted by closure and devolution and have considered whether to modify the preferred position set out in the consultation in light of those views’ (emphasis added)

Amazing! Because if most said : keep it open, and if most said people would lose support or enter institutions, including responses from local authorities: what exactly did they listen to?

The documents recognize that ILF users will see a drop in support with some not being eligible for support at all

             ‘We do recognise that upon reassessment by LA’s most users are likely to see some reduction in the current funding levels, and there are a group of users with low care needs that may not be eligible for local authority support under current needs thresholds in most LA’s.’

The cost of closure will be £39 million! One document states that some of this has been achieved by the savings from closing ILF to new users in 2010. But closure cannot be publically defined as value for money-indeed!

        ‘The transfer costs mean that this proposal will cost rather than save money and therefore it cannot be defined as value for money. However the transfer costs are fully affordable’.

Not to ILF users they aren’t!

And wouldn’t £39 million, plus transfer cost be better put into ILF? Of course that’s not what they want to do, in spite of a consultation exercise where the majority appeared to say a resounding NO to closure.

Why did the DWP think it would Easy to Close the ILF?

One of the reasons given that the DWP found it so easy to close the ILF to new users in 2010 was the lack of any objections from the ‘big disability organisations’ which DWP call ‘Major Departmental Stakeholder Responses’ whatever that is.

In terms of the announcement of proposed closure in 2015 it was noted that none of these ‘stakeholders’ had requested a meeting with ministers from Westminster. Basically most had kept quiet, and hadn’t seen the closure of ILF as any big deal. Great support guys!

On this basis the DWP tell McVey in another document around the potential announcement of the closure in 2015

         ‘on the basis of attention shown so far, we do not think this will   receive  significant attention on its own…’

Guess they forgot about that vocal group DPAC and Deaf and Disabled Peoples’ Organisation: Inclusion London, because the closure of the ILF has now received significant attention in the UK and in Europe, at European Parliamentary level through MEPs and at UN level and we’ll make sure this continues.

Neither DPAC nor Inclusion London has the millions for campaigning that the big disability charities have, nor dedicated media, press and campaign teams. But we do have passion, and we do care about what happens to us all as disabled people, and we care what happens to independent living. ILF users taking the case and supporting the case have appeared on TV, on radio and in newspapers to get the message across that ILF is important and this will continue too.

Any journalists that want to know more or run stories can contact: mail@dpac.uk.net

So what did these so called ‘stakeholders’ say in response to the consultation? According to the DWP, there was not enough resistance at all.

In the early analysis document those who the DWP define as key stakeholders are broken down and their responses analysed. Below is what DWP said of their ‘Major Departmental Stakeholder Responses’ in the exact words of the DWP to McVey

 Carers UK-Weakly Disagree

-User packages would be reduced placing extra demand on unpaid care

Disability Rights UK-Concerned

-Lack of choice and flexibility under Local Authorities (Las)

-User packages will be reduced

-Poor perception and past support of Las

-Difficult for ILF users to transition easily

 Disability Wales- Strongly Disagree

-users packages would be reduced which could make it impossible to support ILF users in a family environment

-since the 2010 closure of the fund to applicants disabled people have had to start entering residential care.

-believes the government is targeting the disabled for cuts

-LAs could not cope with the additional workload

-Lack of choice, flexibility and dignity for ILF users under LAs

-Do not believe transitional protection will be offered

 Inclusion Scotland-Strongly Disagree

-The proposal would create a postcode lottery of support

-User packages would be reduced

-LA support is budget led rather than needs led

-ILF expertise would be lost

-Lack of choice and flexibility under LAs

 MENCAP-Pragmatic Agreement

-If reforms go ahead they should be about finding a better system, not cutting costs

-Funding should be allocated to LAs as a separate ring fenced funding stream based on current ILF regional spending patterns in which current users enjoy time-limited protection

-need for Government to provide advice and information to all parties

 MS Society- Concerned Agreement

-Consolidation of funding streams would simplify the care system

-The proposal should not be enacted until the impact of current welfare reform is understood

-Lack of choice, flexibility and dignity for ILF users under LAs needs to be addressed

-LAs need as far as possible, to replicate the personalised expertise of ILF

-Representative groups need to be closely involved in the transition design

 RNIB-Weak Concern

-Concerned that closure might lead to a breach of article 19 on UN Convention of the Rights of Persons with Disabilities

-Representative groups must be closely involved in transition design

-Current levels of support must be maintained

 SCOPE-Concerned Weak Agreement

 -Consolidation of funding streams would simplify the care system

-The proposal should not be enacted during current funding constraints

-The mainstream care and support system needs more experience and commitment to independent living to be able to undertake the responsibilities of the ILF

 Spinal Injuries Association-Disagree

 -Funding is likely to disappear into wider LA budgets on transfer

-ILF is more efficient than LAs

 

‘Rights not Charity’ seems very apt as the major charities for disabled people appeared to agree with the closure, after all more institutionalisation of disabled people might benefit them mightn’t it?  Disability Rights UK (DRUK) a so called user-led organisation incorporating, but clearly forgetting the principles of National Centre for Independent Living, did not offer more than ‘concern’.  The Spinal Injuries Association ‘disagreed’ but what this needed was for all to come out and say ‘Strongly Disagree’ as Disability Wales and Inclusion Scotland did.

 Remember that when the charities ask you for money, remember that when those groups that didn’t come out fully against the closure of the ILF say they are on the side of disabled people or are working for disabled people: we believe they can no longer justify either of those statements.

 The DWP told McVey that ‘stakeholders’ (SCOPE, DRUK etc)

‘..have traditionally found it hard to defend the ILF model of funding care..’

‘none of the largest national disability organisations requested ministerial meetings and many did not submit responses to the consultation. While we have had an increasing number of letters from MPs on users’ behalf, the proposal to close the fund has received almost no attention in the mainstream media’ (correspondence to McVey 7th November 2012)

We will work through more of the documents looking at issues on transition, and the DWP’s media strategy which is unsurprisingly at odds with any issues raised by disabled people-you know the stuff Closure of ILF will give ‘choice and control’ , ‘committed to supporting disabled people’ blah, blah, blah.

The big difference here is that it is clear from the documents  that the DWP are perfectly aware that ILF users will lose funding and that their needs won’t be adequately met through the local authority system.

Cuts versus Reform

Finally, the DWP were keen to try and put the message out that the closure of the ILF was not about ‘cuts’ but about ‘reform’ –what’s the difference? They do appear to believe that if they say reform we all think this is a good thing, rather than identifying that everything that comes under the heading of reform is actually another cut.

The documents cannot be clearer: this is a cut

A cut to the dignity, life chances and lives of disabled people-not just those who are currently supported to lead independent lives through ILF , but also those who would have qualified before closure to new applicants in 2010 and all who could benefit from the ILF system in the future

Support ILF users now; support a better future-say no to the closure of the ILF!

 

 

 

 

 

 



[1] Funding for ILF users in Northern Ireland is currently the responsibility of the Northern Ireland Department for Social Development, not the Department for Work and Pensions.

Mar 112013
 

DPAC Logo 3 amendment 1 (Small)  enil logo

11 March 2013 – On 7 March, the Conference of Presidents[1] agreed to place an oral question on the impact of austerity on the living conditions of disabled people on the agenda of the European Parliament.

The question debated and adopted by the Employment and Social Affairs Committee last month, is based on a proposal by the European Network on Independent Living (ENIL) and cooperating European organisations. ENIL welcomes the debate, scheduled to take place in the plenary meeting on 12 March, but notes with regret that the Conference of Presidents missed this opportunity to vote on a Resolution on the same issue. We see this as a clear sign of the lack of understanding by MEPs for the precarious situation of disabled EU citizens brought on by the cuts in public spending.

 The European Network on Independent Living (ENIL) launched the Proposal for a Parliament Resolution in September 2009, when a range of cuts to services and benefits for disabled people was first announced in many Member States. Today, disabled people are feeling the effects of these cuts. Their support to live independently, in the community, is being reduced or taken away and the threat of institutionalisation, or re-institutionalisation, is a reality for many.[2]

 An increasing number of voices in Europe and internationally, including DPAC, are pointing to the disproportionate effect of the financial crisis on disabled people, and warning about the long-term consequences for the entire society. ENIL and DPAC have been working with a number of European and national organisations[3] over the past 18 months, as well as with some MEPs, in order to ensure an adequate response of the European Parliament and the European Commission to austerity measures imposed by the Member States.

 The oral question to the European Commission, which will be debated on Tues 12th March, is an opportunity to get the worsening situation of disabled people in the EU on the political agenda. It is the first step towards a Resolution of the European Parliament, which can ensure that the Member States take concrete steps to reconsider and reverse the measures which are negatively affecting the rights of disabled people. ENIL and DPAC believe that a Parliament Resolution will send a strong signal to the Member States, and will continue campaigning for its adoption in the coming months.

 To support ENIL’s Resolution on the effect of cuts in public spending, please write to your MEP today! Together, we can make MEPs from all political groups aware of the impact of austerity measures on the lives of people they are representing and ask them to take immediate action.  Thank you for your support!

 To follow the debate in the European Parliament on 12 March, please use this link, select ‘Live’ and ‘Current debate’, and then click on the desired language. An estimated starting time will be shown on the website at 16:00 GMT, with the debate likely to take place in the evening.

 Background information

 Text of the oral question 

 Subject: The impact of austerity on the living conditions of people with disabilities  
In the European Union, evidence shows that persons with disabilities, including people with intellectual disabilities, are to a disproportionate degree affected by cuts in public spending and by a resulting loss of support measures – such as personal assistance and direct payments – that are essential if they are to live independently in the community

.1. Austerity policies will lead to an increase in the number of people living in long-term institutional care in many Member States, and to the further social exclusion of persons with disabilities. What steps does the Commission intend to take to remedy and reverse this trend?

2. It is of paramount importance for people with disabilities that austerity measures do not affect primary and daytime care, which, on the contrary, should be expanded further. At the same time, the provision of home care should be enhanced. What concrete steps does the Commission plan to take to encourage the organisation of these community-based services?

3. The EU’s commitments to prevent discrimination when it comes to access to employment and occupation, and to promote the social inclusion of persons with disabilities, are not being met. There is still poor awareness of the enormous potential for improving the integration of disabled people into the labour market, which would also contribute to the employment target set in the framework of EU 2020. What recommendations or good practices can guide the Member States in their efforts to promote the participation of people with disabilities in the society, and in the labour market, and to promote a more sustainable society?

4. Parliament’s resolution of 25 October 2011 on mobility and inclusion of people with disabilities(1) and the European Disability Strategy 2010-2020 stress the need for further action in several areas. What steps does the Commission intend to take to implement the European Disability Strategy 2010-2020 and to ensure that the EU fulfils its obligations under the UN Convention on the Rights of Persons with Disabilities?

 

(1) Text adopted P7_TA(2011)0453.

 Click on the links below to:

 Find your MEP

Download Template letter from link below 

http://www.dpac.uk.net/wp-content/uploads/2013/03/MEP-template-letter.doc

ENIL

-       Information about ENIL’s Campaign against the Cuts

-       Action Toolkit

-       Study of the European Foundation Centre on the impact of austerity measures on people with disabilities

-       Contact: mail@dpac.uk.net

 



[1] The Conference of Presidents consists of the President of Parliament and the chairmen of the political groups (who may arrange to be represented by a member of their group)

[2] For more information, please see Hauben, H. et al. (2012) Assessing the impact of European governments’ austerity plans on the rights of people with disabilities – European report. European Foundation Centre. Available at: http://www.enil.eu/wp-content/uploads/2012/12/Austerity-European-Report_FINAL.pdf

[3] AGE Platform Europe, Autism Europe, European Anti-Poverty Network (EAPN), European Association of Service Providers for Persons with Disabilities (EASPD), European Disability Forum (EDF), Inclusion Europe, European Network of Users and Survivors of Psychiatry, Mental Health Europe (MHE), European Foundation Centre (EFC), Disabled People Against the Cuts (DPAC), UK and Onafhankelijk Leven, Belgium

Sep 262012
 

We often don’t get a chance to let people know what we do other then our street protests and direct actions so we thought you might all be interested in what we’re all going to be doing over the next few weeks. Of course as well as this we have surveys to analyse and information to put together to submit to various UN bodies. Plus we have our normal campaigns to run especially those on WCA and ILF funding which seem to be going well.

All- attending Inclusion London conference on Rethinking Disability Equality Policy in a Hostile Climate.

October 7th- protest at the Tory party conference,Birmingham

October 20th – TUC march,London.

Roger – Recently spoke at Walthamstow anti-cuts mobilising meeting, also speaking inPortsmouth, at GMB Equality conference, and inLiverpool at a NW anti-cuts conference.

Ellen – Speaking inOxford, Tower Hamlets and at Unite the Resistance conference. Doing workshop at Climate Justice Collective event and manning a stall at the Anarchists Bookfare. PCS meeting.

Linda- Derby speaking at ALLFIE conference, PCS meeting and PCS-led Equality conference in Liverpool doing a joint workshop with Laurence Clark. Workshop with Faryal from Transport for All for Inclusion London leadership course.

Debbie- speaking at Disability Wales AGM, ENIL meeting inAntwerpand another ENIL meeting about austerity cuts.

Andy- Cuts Café workshop, Meeting in Luton, PCS meeting and full day networking event with activists in London.

We also have Mike speaking for us at a Unite the Resistance meeting inSheffield.

There may well be more that I’ve forgotten.

 

 Posted by at 12:28
Dec 142011
 

In March 2011 I wrote about the ways media portrayed disabled people at a time of punitive cuts to disabled peoples’ social and financial supports.

….a range of false accusations against disabled people and those with long term health conditions are visible in the media. Rather than offering support to disabled people, certain sections of the media prefer to label disabled people as unsustainable, unproductive or immoral members of their communities. The major accusation, however, is that disabled people are not disabled at all, but profiting from fraudulent benefit claims

Eight months on there is a clear escalation of the negative portrayal of disabled people in the UK media. These attacks are no longer confined to screaming newspaper headlines in the Daily Mail and Daily Express declaring that the majority of people on disability benefits are frauds, but a whole host of television programs setting out the Saints and Sinners, even programs with usually good credentials such as Panorama have jumped on to the band wagon of who’s responsible for ‘Broken Britain’. Since March 2011 negative and unbalanced reporting has become worse.

Social and Economic facts versus ideological messages

At the same time unemployment has increased to the highest rates ever recorded for youth and women, and the highest since 1992. On average vacancies have decreased from an average of 2/1 (2005) vacancy rate to a 6/1 (2011) with six people chasing one job according to the Office of National Statistics (ONS). Figures on averages hide local variations which are often much higher.

Yet, still unemployment or any need for state support is consistently identified as a personal failing regardless of personal circumstances or societal limitations: it’s this ideological message, rather than economic and statistical facts that gathers pace and shouts out loud and clear from some sectors of the media, with disabled people most often identified as the group needing to leave welfare and get jobs because they are ‘faking it’.

How the Newspapers are reporting Disability

A recent report commissioned by the organisation Inclusion London and carried out by the Strathclyde Disability Research Group and Glasgow Media Studies group at the University of Glasgow: Bad News for Disabled People: How the Newspapers are reporting Disability, found significant changes in media reporting of disabled people which show a clearly defined increase in stories and views identifying disabled people as ‘undeserving’.

The report identified changes in reporting through comparative content analysis of tabloid newspapers in 2005/6 and 2010/11and through focus groups. The researchers found that incidents of negative language regarding disabled people in print media had more than doubled over the time period, while what they termed ‘sympathetic’ stories had more or less disappeared in the tabloid press. Terms such as ‘burden’, ‘scrounger’, and ‘cheat’ were used repeatedly in 2011with a rapidly decreasing use of articles on disability discrimination. In addition stories outlining the political and economic context were rare. When the focus groups were asked to describe a typical disability story in the newspapers: disability benefit fraud was the top theme.

 The media examined were the Mirror, the Sun, the Daily Mail, the Daily Express, and for balance the Guardian. The researchers also carried out a number of focus groups asking what each group thought the level of disability benefit fraud was, there were variations from rates of 50% to 70% of perceived disability fraud from focus groups.

The reality in terms of incapacity benefit it is just 0.03% according to the ONS the report states. The Department of Work and Pensions own figures on Disability Living Allowance are 0.05% both stats also include administrative errors within their figures. The media strategy appears to be working when focus groups state perceived incidents of fraud of up to 70% which is more in line with Daily Mail and Daily Express headlines, than any statistical realities.

The report’s timely commission by Inclusion London, a London wide Deaf and Disabled Peoples’ organisation provides more evidence for further campaigns and for those who doubted that the print media in particular were objective. In addition, there have been several examples of stories usefully backed by a quote or two from Iain Duncan Smith MP welfare and pensions’ secretary. The most stunning in the Sun newspaper in 2011 when he happily implied that disabled people were responsible for the UK deficit, the most recent quoting him as ‘enraged’ and ‘shocked’ based a story that carried false figures regarding mobility cars. He wasn’t shocked by the inaccuracies but by the figures which weren’t checked before publication, but false figures are par for the course, as are false accusations.

The Cuts, Media and ‘real life’ Implications

Sheffield Hallam University have also produced a report outlining the impact of the cuts in incapacity benefit, claiming that almost half of those now receiving incapacity benefits will lose them, not because of fraud, but because of a tightening of the qualifying criteria for the replacement of lower income benefit Employment Support Allowance. The report by the Centre for Regional Economic and Social Research at Sheffield Hallam University, estimates that the reforms will cut the number of disabled people on out-of-work disability benefits by nearly one million in just three years. Add to this other reforms set to take away any support from disabled people and those already carried out removing over 9 billion pounds worth of support and we see a very different story from one of fraud. We see a story of ‘cuts’ to a group that the UK public had consistently agreed to be deserving of support in national surveys such as the British Attitudes Survey.

Professor Fothergill author of the report on Incapacity Benefit changes said

The large numbers that will pushed off incapacity benefits over the next two to three years are entirely the result of changes in the benefit rules” and added that this ..’would impoverish vast numbers of households and cause untold distress to countless more. The incapacity numbers need to be brought down, but this is not the way’

He is also clear that this is not about fraud, but about ‘changes in the benefit rules’ see Jolly . He adds: “Incapacity claimants often face multiple obstacles to working again and their concentration in the weakest local economies and most disadvantaged communities means they usually have little chance of finding work.”

Yet, it is the benefit fraud stories that abound despite the 0.03% figure; people believe the figure is much higher. A rise in disability hate crime has been linked to the media strategy on the demonising of disabled people. One example was reported on 4th December, one day after the International Day of People with Disabilities. It tells of Peter Greener’s constant barrage of abuse from his neighbour.

Sometimes, it was eggs thrown at his house, stones thrown at his windows or paint thrown at his fence; more often, it was words hurled in his face: spastic, cripple, scum, scrounger. These assaults went on for months, leaving the former Nissan car-sprayer in floods of tears, feeling suicidal and on antidepressants. He was scared to leave his home in Hebburn in South Tyneside and blamed himself for the upset it caused his wife and two children. “It made our lives hell,” he said.

Like many people with conditions such as multiple sclerosis, Greener’s regressive condition fluctuates. One day, it affects his memory, the next his speech. Sometimes, he uses a wheelchair; at other times, he can haul himself around on crutches. But this only led to more abuse, with angry shouts he was faking his disabilities and exaggerating his problems to get benefits

This is just one story; but the climate of fear is clearly working, there are disabled people who are frightened to leave their homes because of verbal and physical abuse, and accusations of being scroungers and frauds. There are those who refuse to claim their entitlement to support in spite of previously paying years of national insurance when they were in work, because they do not want to be labelled as benefit cheats. In total 16 million pounds worth of entitlements goes unclaimed. There are also those denied entitlement to support through the tougher regimes for claiming any benefit such as the replacement for incapacity benefit through the work capability assessment, carried out by the private company Atos who are being paid 100 million pounds per year by the government. The sums do not add up, but the strategy seems to:

A further report carried out by BT showed that a third of those questioned demonstrated increasingly negative attitudes towards disabled people. Reasons cited for this ranged from disabled people being seen as a burden on society (38%), ill feeling around the perceived extra support given to disabled people (28%), and the personal worries and sensitivities which rise to the fore during a recession (79%).

European Media Strategies

The media attacks on disabled people are not just happening in the UK. In Holland up to 90% is being cut from support for disabled people, similar media demonization is taking place in the popular press identifying perceived ‘undeserving’ cases. In Sweden cuts are being made to assistance to support disabled people with tougher qualifying criteria being put in place, they too have a focus on those who defraud the system highlighting such stories while record numbers of people loose entitlement to support.

The figures for fraud are just 0.05% in Holland. Yet, the magazine Vrij Nederland, a major quality magazine in Holland reproduces outrageous comments from the Secretary of State, responsible for the drastic 90% cuts:

The State Secretary of Health, Marlies van Zanten Veldhuijzen finds it unacceptable that some thirty percent of people with a personal budget (PGB) wrongly receive it. She said in an interview this week: “It can have you on the internet looking for the name of a disease, and then think: look, I can get 2000 Euros per month. With PGB we need to sort the wheat from the chaff.

 She states that 30% receive a budget without having the right to receive it, as if it is a fact. Yet, here is no existing evidence or research confirming or even indicating this. Before receiving a PGB, as in most countries, a strict assessment is carried out. However, here we have a government minister saying that individuals can simply choose a disease at random by searching the internet to gain these funds.

Stories used by media to usher in cuts to disability support appear to converge into strategies by particular populist media to create a media panic around the extra perceived support given to disabled people for the extra costs of disability. This is proving effective , especially when there are examples of ‘undeserving’ cases being presented to shift the traditional view of disabled people as ‘tragic victims of circumstance’ –the  claim of ‘tragic victims’ has always been rejected by many in the disabled peoples’ movement –maybe this will change as the 21st century welfare reform policies and the media strategies in the UK and Europe reinvent millions of disabled people as the tragic victims of the circumstance of recession and easy targets for savings from the state budget.

The political use of media to promote demonization of disabled people is aiding the work of governments’ intent on cutting the support and the human rights of disabled people.  There are rising cases of verbal abuse against disabled people such as that endured by Peter Greener and rising cases of suicide amongst disabled people with one couple entering a suicide pact after surviving for a year by walking 10 miles to receive food parcels which they made last all week.

The Challenges

Ann McGuire Westminster Shadow minister for work and pensions wrote recently:

Disabled people say they are fed up with being labelled as scroungers in the media – and are beginning to point the finger in the direction of the Government. Yesterday at Work and Pensions questions I asked the Minister for Disabled People to assure the House, and disabled people up and down the country, that Ministers are not behind the stories knocking disabled people that seem to be emerging with alarming regularity…

 McGuire called on the minister for disabled people to quell the insidious media attacks, a challenge that was also made directly to Miller at a recent disability conference in London: McGuire said:

The Minister for Disabled People has a responsibility as the champion of disabled people inside government to challenge some of the more outrageous and outlandish comments by some of her senior colleagues and others associated with her government…And I call on her to do so.

UN Convention on the Rights of Persons with Disabilities

Article 8(2c) of the Convention on the Rights of Persons with Disabilities states:

‘Encouraging all organs of the media to portray persons with disabilities in a manner consistent with the purpose of the present Convention’.

This would include any change in reporting over time: it seems that there has been a change in reporting which is clearly not in line with the convention’s principles of promoting, protecting and ensuring the full and equal enjoyment of all human rights and fundamental freedoms nor with promoting respect for disabled peoples’ inherent dignity. In fact the opposite seems to be occurring.

UK Responses

Inclusion London, the pan Deaf and Disabled Peoples’ organisation that commissioned the Glasgow University research into the media have led a response on the Leveson Inquiry. The response: titled ‘Open Season on Disabled People?’ supported by Disabled People against Cuts and others states:

  • The Government must issue a clear and public rebuttal every time the media release inaccurate information citing Government / Department of Work and Pensions (DWP) statistics.
  • That the Government commit to full transparency in their dealings with the press including  keeping a publically available record of all communications between Government officials, Ministers, their aides and special advisors and the media.
  • That there needs to be an independent review of how the Department of Work and Pensions (DWP) releases and provides commentary on its statistics to assess how fair and balanced this data is presented and communicated.
  • That the Equality and Human Rights Commission (EHRC) must carry out further research on the impact of media coverage on disabled people and the implications this has for disability hate crime, disabled people’s protection under The Equalities Act and the UN Convention on the rights of disabled people.

We call on the Leveson inquiry, Press Complaints Commission, and OFCOM to:

  • Carry out an independent investigation into the media reporting of disabled people. This investigation needs to include the impact this coverage is having on disabled people and the implications this biased and inaccurate reporting has for the culture, practices, ethics and standards of the press. It must also examine the opportunities disabled people should have for effective redress.

 Debbie Jolly

Debbie Jolly is on twitter: @redjolly1

___________________________________________________________________________

An edited version of this paper is published on British Politics and Policy London School of Economics,  entitled: ‘As the government moves to cut the number of disabled people on benefits, the media is increasingly portraying them as ‘undeserving fraudsters’.http://blogs.lse.ac.uk/politicsandpolicy/2011/12/14/disabled-people-media-attacks/

 Acknowledgements: I would like to acknowledge the assistance and kind support of Jamie Bolling Executive Director of the European Network for Independent Living (ENIL) and Peter Lambreghts of ENIL and the Expertise Centre Independent Living

Please see and support: www.enil.eu  and http://www-en.independentliving.be/

 



 

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