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The biggest barrier that disabled people face is a prejudiced government

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The very act of renaming incapacity benefit support for sick and disabled people “employment and support allowance” signaled the political intent to make that support precarious, with an aim of pushing people previously exempted from work on medical grounds from lifeline social security protection into work on political grounds, regardless of the consequences. The word “allowance” means the amount of something that is permitted, especially within a set of regulations or for a specified purpose. This language shift signaled the increasing contingency of support for disabled people.

It also reduced and transformed the sick role, making it increasingly transitory, redefining chronic, incurable conditions as somehow transient, and marking a shift from medical definitions of sickness and disability to psychopolitical redefinitions, which are ultimately aimed at pushing forward a small state neoliberalist agenda. Welfare provision is being steadily dismantled. 

However, changing the name and making the eligibility criteria for support much more stringent has not helped sick and disabled people into work. It has simply created circumstances of further disadvantage, hardship and distress for many people.

It hasn’t worked because many of those people affected by the nudge-styled rebranding of their lifeline support and draconian cuts to “incentivise” people to take up and cherish the Puritan work ethic, as the paternalistic Conservatives think we ought to, are simply too ill to work.

Of those that may be able to work, over time, their would-be employers have not engaged with legal requirements and provided adjustments in the workplace to support those disabled people seeking employment. The government have removed the Independent Living Fund, and reduced Access to Work support, Personal Independence Payment (PIP) is very difficult to access because of the stringent eligibility criteria, whilst the disability benefit Employment and Support Allowance was also redesigned to be increasingly difficult to qualify for.

But political word games, and intentions to attempt to shrink the categories of what is deemed “illness and disability” along with the ever-shrinking state, don’t cure illness and disability, and it’s offensive to witness a very wealthy first world so-called democratic government viciously hounding and shamefully coercing a group of people, negatively labeling them as a “burden on the taxpayer”, and forcing them to take any low paid, insecure work, without any support whatsoever, despite the fact their doctor and the state, via the work capability assessment, have deemed them already to be unfit for work, whilst at the same time leaving this group on an isolated, ever-shrinking island with ever-decreasing lifeline support.

Perhaps PIP ought to include invisible bootstraps in the aids and appliances categories.

This is juxtaposed with the recent gifted tax cuts for the wealthiest, indicating clearly that Conservatives perceive and construct social hierarchies with policies that extend inequality and discrimination. The axiom of our international human rights is that we each have equal worth. Conservative ideology is fundamentally  incompatable with the UK government’s Human Rights obligations and with Equality law. The chancellor clearly regards public funds for providing essential lifeline support for disabled people as expendable and better appropriated for adding to the disposable income for the wealthy.

Most people (over three-quarters ) who are disabled became so during their working life. There is an implicit political prejudice regarding disability, evident in policy-making, which is that it is an undesirable state and somehow preventable. There is another more explicitly stated prejudice, which relates to the oversimplistic false dichotomy of society. Citizens have been redefined as taxpayers or economic free-riders. However, not only have most disabled people worked and contributed tax and national insurance, people claiming social security also contribute significantly to the Treasury, because we pay VAT, council tax, bedroom tax and a variety of other stealth taxes.

The state confines its focus and responsibility mainly at re-connecting disabled people with the labor market, without any consideration of potential health and safety risks in the workplace, as a strategy of “support,” and justifies the draconian cuts to support as providing “incentives” for people to work, by constructing a narrative that rests on the bogus and socially divisive taxpayer/free-rider dichotomy:

 “You answer if a disabled person can’t work there is NO cut but if they can but won’t, why should taxpayers subsidise them & trolls go mad!”

 By “trolls” Michael Fabricant actually means disabled people and campaigners responding to his tweet.

What happens to those people that can’t work or cannot find an understanding employer, prepared to make reasonable adjustments in the workplace?

On becoming ill – it can happen to anyone

I am medically ill and my illness (lupus) affects my mobility, focus and general wellbeing. I am restricted in what I can do, and the symptoms and exacerbations are very unpredicable. However, it is economic, political and cultural forces which have created and continue to create my ongoing disability and social marginalisation, not my illness. Many of my problems are compounded because of an unadapted physical environment, a lack of resources and the attitudes of others, particularly the current government’s.

I don’t accept that health problems ought to be seen as the cause of the socioeconomic deprivation and exclusion that many of us are experiencing, because the real cause is entirely political. Policies, which exclude disabled people from their design and rationale, have extended and perpetuated institutional and cultural discrimination against disabled people.

My own illness arose partly because of a genetic predisposition, partly because of my gender and hormonal events which often trigger the illness, and probably a variety of other complex reasons, none of which specialists fully understand yet. Prior to becoming very ill, I led a very active and healthy life. I worked hard in a job I loved. My diet is and always has been balanced and healthy, I enjoyed outdoor activities such as climbing, abseiling, archery and walking. I was never inactive or overweight, and I am not stupid when it comes to health issues. Lupus isn’t a “lifestyle choice” and it didn’t arise because of something I did wrong.

All the same, I frequently get well-meaning but bad advice to try different diets, “natural” herbal remedies (people forget that they contain chemicals) – usually the immune- enhancing ones like echinacea, which my rheumatologist has already advised could be very dangerous – and the best one of all: “You should stop taking the heavy duty medication and ‘cleanse your system’.” That would be medication that I take to keep me alive because I tried and ran out of all the other options. I usually recommend a simple course of water melons for such “experts”, to be taken at four hourly intervals, rectally.

Like many other ill and disabled people, I have worked for most of my life. My work was rewarding, and the professional roles I took up have entailed developing inspirational ways to support and enable others, from voluntary work with Women’s Aid and Victim Support, to salaried youth and community work, social work, mental health work and delivering training. I worked whilst being ill for a number of years.

By 2010, I simply couldn’t work any more. My previous and mostly background joint, nerve and muscle pain suddenly became all consuming. My ankles, knees, wrists and fingers swelled. I caught a cold at work which turned to pneumonia on two occasions in 2009. I had apparently random finger abcesses, inexplicable kidney infections, and bruised every time I was touched. I had severe nerve pain in my face and optic nerves, which affects my vision. My hips and lower spine became stiff and painful, my shoulders became frozen. I had a painful rash across my face that looked like eczema, only it wasn’t. I was profoundly tired all of the time, and weighed less than eight stones. My GP ran some tests and everything came back lupus, with complications such as a severe autoimmune bleeding disorder, very low immunity to infection and neurological involvement.

Working put my safety, health and wellbeing at substantial risk. It also potentially exposed other people to risk, too, because of the impact of my illness on my judgments, reliability and consistency, eyesight, ability to supervise, mobility and so on. A tribunal agreed with this assessment in 2012.

It was a very painful recognition that I could no longer work, my decision to leave was very difficult, compounded by a sense of loss of self worth and meaning. I felt that my experience, developed skills, not to mention time and effort invested in studying for a highly vocational Master’s degree, were meaningless and unavailing. However, I was completely unprepared for the damaging impact of the political othering and socioeconomic outgrouping that followed from 2010.

And the poverty. I came to feel that I had been politically redefined as somehow “deviant” by 2012. A much needed transformation to add to the grieving process for the person I was before my body became a traitor. Cheers, Mr Cameron, for the milk of human blindness. The Sex Pistols got it a bit wrong back in the last days of counter-culture and agitprop: it’s not just anarchy that we need for the UK, it’s a modicum of empathy, too.

Doctors and rehabilitation professionals continually recommend medical treatments and practices even though they know that these will not necessarily improve my quality of life. Most of the treatments for autoimmune illnesses such as lupus are largely experimental: comprised of chemotherapies and immune suppressants that carry their own life-threatening risks, and being ill with lupus and other autoimmune illnesses presents a constant and difficult process of weighing up of such risks – life threats from the illness versus life threats and serious life-changing risks from the treatments. 

The dangers that arise when everyone thinks they are an expert on illness and disability

That didn’t stop a job advisor, during my time in the employment support allowance work-related activity, group telling me I should take the chemotherapy methotrexate because her friend with rheumatoid arthritis had some benefit from it. Methotrextate helps around 25% of people taking it, to various degrees, but it cannot cure the illness. Side-effects include sudden death, blindness, liver, kidney and heart failure, lung fibrosis, thrombocytopenia – a serious bleeding disorder which I already have – and death from an overwhelming infection, which I am already susceptible to, since my immune system is easily compromised and broken, amongst many other problems.

As it happens, I had already tried methotrexate for many months, administered by injection into my stomach. It didn’t work and the side-effects were truly diabolical, adding to my existing misery and multiplying symptoms. Another treatment, considered far less risky, called hydroxychloroquine, damaged my retina because I was prescribed too high a dosage, I’m now partially sighted.

However, the unqualified advice from a job coach overlooked that I have a different illness than her friend, and that methotrexate is a black box drug with life-threatening side-effects. Everyone seems to think they are a medical expert nowadays, and that’s the government’s doing, since they have been redefining illness and disability, making it a moral and public matter rather than a private, medical issue. Such political negative role-modelling has permitted a rise in expressions of social prejudice towards disabled people, which is why hate crime has risen significantly since 2010 and is now at the highest level since records began.  

We are either deserving or non-deserving, abled or disabled, never just ill or physically disadvantaged. Our lives have somehow become public property, with all manner of unqualified people feeling entitled to intrude at an intimate level to tell us how to “manage” our illness better. Or to transform media tropes and political folk devils into forms of justification for abuse.

Job centre staff it seems will recommend anything, including unqualified advice about medical treatments, regardless of the risks that may be involved, to coerce people from what was once a social safety net and into any job, regardless of its appropriateness, quality, pay, security, and importantly, it’s potential impact on people’s health and safety.

Last October, I flagged up the extremely worrying government plans to place job coaches in GP practices, with provision made for job centre staff to “update” people’s medical files. The government hadn’t announced this  “intervention” in the lives of disabled people, nor had we been consulted or involved in its design. I found out about it quite by chance because I read Matthew Hancock’s recent conference speech: The Future of Public Services.

I researched a little further and found an article in Pulse which confirmed Hancock’s comments: GP practices to provide advice on job seeking in new pilot scheme.

The government plans to merge health and employment services, and are now attempting to redefine work as a clinical outcome. Unemployment has been stigmatised and politically redefined as a psychological disorder, and the government claims somewhat incoherently that the “cure” for unemployment due to illness and disability, and sickness absence from work, is work.

This is why I visit my doctor and not David Cameron or George Osborne when I need advice, support and treatment related to my medical (and not political) condition.

It’s a prejudiced government that has edited the script regarding sick roles – we no longer have medical sick notes, they have been replaced by political fit notes. The subtext is that we must participate in the world of mainstream work without any choices, without reasonable adaptations and without support. Without any acknowledgement of illness and disability, in fact. Or, we have to accept being redefined, our identity rewritten as “dependent”, “impaired” “unfit for work” as a trade-off for a degree of meagre support.

All of our previous achievements and contributions are forgotten. We once celebrated the achievements of disabled people, but now, we cannot, because disabled people are systematically repressed. We are politically defined as either fit for work (and thus not seen as “disabled”) or not. There are no other options for us, unless we happen to be very wealthy as well as ill.

Singing the body politic in our own voices

We don’t fit with neoliberal dogma and the Tory ideals of “individual responsibility”, competition, a “small state” and compulsory (low) paid employment to enhance profits for the elite’s old boys network. Any positive association with impairment, such as reasonable allowances made or degrees of freedom from the Tory notion of “social obligations” and “responsibilities,” is prohibited. We are faced with an overly simplistic, terribly reductive and dehumanising either/or choice.

We are deemed either fit for work, or too disabled to work, with no accommodation made for what we may be able to contribute in myriad ways to society, nor is our past accumulative experience and skill regarded as a valuable. The moment there is a hint we may have some kind of tenuous work-related capability, all support is withdrawn. However, once we are deemed unfit for work, we are denied full citizen’s status and economic inclusion.

This narrow political approach does nothing to enable and support people, nor does it reflect human diversity. It simply disables us further and denies us autonomy and the right to define ourselves. It’s an approach that actually punishes people for the abilities, experience and skills that they have, stifling human potential. The moment those abilities and skills are revealed at a work capability assessment, all support is withdrawn and those qualities remain unfulfilled. Instead of investing in personal development and extending opportunities, the government is simply cutting social security and public service costs at our expense. It’s not actually their money to cut.

We are expected to participate in an unaccommodating and increasingly competitive job market or suffer the dehumanising consequences and impoverishment of claiming social security long-term. And the people profiting from this are the competing, vulture capitalist private “service” providers.

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There is no support for creating circumstances where our skills may be transfered. There is no support to help anyone adapt their skills and experience to fit future employment. Access to higher education has been restricted because of the steep rise in cost, especially for mature and disabled students. There is nothing in place to ensure that employers recognise disabled people’s skills and experiences and make adaptations to accommodate people wanting to work, and no safety net at all to encourage personal development for disabled people, since all support is tied to rigid definitions of disability. You can either work or not.

Under the guise of lifting burdens on business, this government has imposed burdens on those with disabilities by removing the “reasonable adjustments” that make living our lives possible and allow us some dignity. The labor market is hostile and unaccommodating, providing business opportunities for making profit, but increasingly, the needs and rights of the workforce are being politically sidelined. This will invariably reduce opportunities for people to participate in the labor market because of its increasingly limiting terms and conditions.

This highlights the paramount importance of shifting the political focus to the pressing need to change a disabling culture and to actually listen to our lived experiences, including us in policy design from that of merely coercing us into fitting reductive Conservative definitions to accommodate and fit in with a neoliberal model of society.

We have smug, wealthy and healthy Conservatives redefining disablity, our identity is ascribed by others who have handed us a socially devalued status: we are being told who we are and how we must be.

Citizen’s “needs” are being aligned with politically defined neoliberal outcomes. Those most acutely aware of this are those politically assigned a lower status in the increasingly steep socioeconomic hierarchy. Stigma and othering is used politically to justify the hierarchy and the consequent crass inequalities, which are designed and mediated through policies, not citizens.

Stigma arises because of the perceptions of the oppressor, not those being oppressed. But perhaps it’s time that people who are “working hard” to contribute to the increasingly enclosed economy paused and observed what is going down, because disabled people are not the only ones being stigmatised and radically reduced by a particularly toxic combination of social conservatism and neoliberalism. Punitive and coercive welfare conditionality, including sanctioning, has recently been extended to those in low paid employment and part-time work, as tax credits and additional support vanish under the guise of “universal credit”. The bedroom tax is likely to be extended to the elderly. How does this in any way ensure that “work pays”?  All this will do is increase the precariousness of people’s situations and substantially increase their vulnerability.

The recognition and celebration of human potential, diversity and equal worth has been superceded by an all-pervasive Puritan “hard work” ethic. Our worth is being defined purely in terms of our economic contribution. We are measured out in pounds and pennies whilst making billions for a handful of other people. That is a value that comes exclusively from the dominant paradigm-shaping elite – the ones who actually profit from your hard work.

You don’t.

The government’s new “health and work” programme is actually workfare for sick and disabled people. Apparently, slave labor for big business is good for our “health” and has the added bonus of adding substantially to profits for friends of the Conservatives. It’s amazing how quickly the public have accepted the political semantic shifts, such as “work programme” – compulsory labor for no wage, which was originally about “exploitation” and has now been redefined as “work experience”. Apparently that is also “fair”, “inclusive”, “good” for our health and “makes work pay”.

Makes work pay for whom?

Disability can no longer be considered solely as a medical problem, affecting only a minority of the population. It must be seen for what it is: as a civil rights issue as central to mainstream political discourse. This government uses draconian policies to act UPON disabled people, it does not value our lived experiences nor does it listen and RESPOND to us. It’s a government that simply tells us how we must BE. That is profoundly undemocratic, it discriminates against us and excludes a social group on the basis of a protected characteristic.

There are and have been a lot of ways to define disability, it has variously has been defined through the eugenic model, a medical model, charity model, rights-based model, social model and a radical model. Now it’s time for a disabled people’s model, founded on our lived experiences and varied needs.

Understanding that oppressive situations have not arisen through any fault of our own, and that the oppression is real and has a basis in sociopolitical prejudice and discrimination provides us with the courage needed, and a more solid ground on which to fight for liberation. It always seems to be the case that fighting social injustice is left to the very people who have been excluded and systematically deprived of a political voice and power, it’s always down to us to make others listen. Yet it is invariably the case that when one social group is targeted for political prejudice and discriminatory policies, it affects everyone. Historically we have learned it quickly follows that other groups are singled out, too.

The universal character of human rights is founded on the inherent dignity of all human beings. It is therefore axiomatic that people with medical conditions that lead to disabilities, both mental and physical, have the same human rights as the rest of the human race.

The United Nations is currently investigating this government’s gross and systematic violations of the Convention on the Rights of Persons with Disabilities (CRPD), and a recent report from the House of Lords Select Committee on the Equality Act 2010 and Disability, investigating the Act’s impact on disabled people, has concluded that the Government is failing in its duty of care to disabled people, because it does not enforce the act.

Furthermore, the Select Committee concludes that the government’s red tape challenge is being used as a pretext for removing protections for disabled people. It’s a government that regards the rights and protections of disabled people as a mere bureaucratic inconvenience.

There’s a certain irony regarding the Conservative preoccupation with preserving social order: their rigid ideologically-driven policies create the very things they fear – dissent, insecurity, disorder and the raising of public awareness and recognition of a pressing need for social change and reform. It’s seems to be the case that Conservative governments prompt a growth of social challenges that encourage the flourishing of the very radicalism and revolutionary ideas that they fear and loathe.

That is what happens when people are oppressed.

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Picture courtesy of Robert Livingstone

 

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Welfare, Conditional Citizenship and the Neuroliberal State – Psychology Conference abstract and details

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Conference on Friday, October 7, 2016 from 9:30 AM to 4:30 PM at St Thomas Centre – Ardwick Green North, Manchester M12 6FZ, United Kingdom.

Psychologists and the benefits system

“Psychologists need to support people through the benefits system, whilst also working to affect necessary changes in the system. This event will explore some of the debates, challenges and skills necessary to take on these responsibilities.

The day will include presentations from public health, sociology, people with lived experience, clinical psychologists, the Child Poverty Action Group (CPAG) and other professionals. There will also be workshops focussed on skill development, with particular attention on report writing, navigating the benefits system and DWP safeguarding procedures.

This will be a challenging, supportive, thought-provoking day.” Event organiser, Dr Stephen Weatherhead.

Contact: s.weatherhead@lancaster.ac.uk 

Please see here for further details.

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Abstract for my presentation

The consolidation of neoliberalism with Conservative moral authoritarianism has resulted in welfare policy design with a reductive and punitive behaviour change agenda. This decontextualises citizens and personalises responsibility for circumstances of socioeconomic hardship.

The emergent psychopolitical form of governance, founded on expressions of an established hierarchy of power and influence, has some profound implications for traditional notions of welfare, democracy, cognitive autonomy, citizen agency, equality and human rights. Not only does this behaviourist mode of administration fundamentally change the relationship between state and citizen, it extends inequality, prejudice, stigma and outgrouping, with damaging consequences for sociopolitical inclusion, self-perception and selfhood.

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Call for evidence – Future of Jobcentre Plus inquiry launched

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The Work and Pensions Committee has launched an inquiry into the future of Jobcentre Plus (JCP), the public employment service arm of the Department for Work and Pensions (DWP).

Changes affecting Jobcentre Plus services

A number of important changes will affect the services offered by JCP over the next few years, including:

  • The full implementation of Universal Credit (UC), which, particularly once a fully-functioning digital service is developed, will be a largely online process and have implications for digital inclusion
  • More frequent interviews at the Jobcentre for unemployed claimants in the early stages of benefit claims
  • Delayed referral of long-term unemployed claimants to externally-contracted employment services (welfare-to-work) providers, meaning that JCP will support people who remain out of work for two years
  • The development of a support offer for UC claimants who are in work but on very low incomes
  • Plans for greater co-location of JCP offices with other local services such as council benefit teams and physical and mental health services, including IAPT services
  • Plans for JCP to offer advice, particularly on traineeships and apprenticeships, to 12 to 18 year old school pupils
  • The process of devolution of employment services to combined local authorities and the devolved governments

Call for written submissions

The Committee invites written submissions addressing one or more of the following areas:

  • The likely effects of the planned changes on claimants, including on the quality of services offered to them and the implications in relation to digital inclusion
  • The potential implications for JCP, including in relation to:
    • Resourcing of JCP
    • Jobcentre “footfall” and the configuration of JCP offices
    • The development of suitable performance measures
  • JCP’s capability to provide new, tailored services for particular groups of people, including people with mental health problems
  • Opportunities afforded by coordination with other local services, including the NHS and schools
  • The extent to which reforms will require cultural change within JCP, and the DWP’s capability successfully to foster this change
  • The opportunities and challenges for JCP presented by greater devolution of employment services to regional and national governments

Send a written submission through the Future of Jobcentre Plus inquiry page.

The deadline for written submissions is Friday 22 April 2016.

Committee comments

Heidi Allen MP, Committee Member, said:

“In the brave new world of Universal Credit, the Jobcentre will become so much more than the place where people simply ‘sign on.’ I am in absolutely no doubt that UC marks the beginning of a new age in which the individual and the state are partners in the future potential of the individual, but the Jobcentre and its staff will need to undergo significant transformation. We must ensure Jobcentre Plus has the capacity and capability to change with the times, and deliver quality services which are sensitive to the increasingly varied needs of the individuals it serves.”

 Craig Williams MP, Committee Member, said:

“As much as different people have different needs, so do different places. The DWP has run a pretty centralised network of Jobcentre Plus offices, for perhaps too long. We will want to consider carefully the potential opportunities for greater decentralisation of employment-related services to combined authorities and the devolved governments.”

Further information

Some initial thoughts and concerns regarding the JCP’s capability to provide new, tailored services for particular groups of people, including people with mental health problems

The government’s Work and Health programme involves a plan to integrate health and employment services, aligning the outcome frameworks of health services, Improving Access To Psychological Therapies (IAPT), Jobcentre Plus and the Work Programme. 

There are concerns that the government have already come close to redefining unemployment as a psychological disorder, and now they aim to redefine work as a clinical outcome.

The Work and Health programme in particular is aimed at finding ways of: “preventing people from falling out of the jobs market and going onto Employment and Support Allowance (ESA).”

“These include GPs prescribing a work coach, and a health and work passport to collate employment and health information. These emerged from research with people on ESA, and are now being tested with local teams of Jobcentres, GPs and employers.”  Source: Matthew Hancock’s conference speech: The Future of Public Services.

Whilst for some clients, improving employment prospects may be realistic and what they want, for many others this is not the case and such an intrusive state intervention may be profoundly anxiety-provoking and potentially psychologically damaging. People sometimes become too ill to work. GP surgeries are not the place to subject people to what may be perceived, essentially, as a blunt state behaviour modification programme, designed to coerce people to work regardless of their current capacity of doing so.

People placed in both Employment Support Allowance groups (work related activity group and support group) have been deemed unable to work by both their own qualified doctors and by the state via the work capability assessment. It may well be the case that some people feel able to and want to work in the future, and ask for support to find suitable employment, but it extremely unethical to coerce people to work that are too ill to do so.

That is why an absolute assurance of the voluntary element of client engagement is of paramount importance, it has to be a central underpinning principle of the work and health programme. Furthermore, it has to be assured that any proposed treatment may proceed only on the basis of (and provision for) informed consent from the client.

The principle of consent is an important part of medical ethics and international human rights law. Consent is required by law from a patient regardless of the intervention.

Generally, for consent to be valid it must be informed consent. For this to be the case it must be:

  • Given voluntarily (with no coercion or deceit)
  • Given by an individual who has capacity
  • Given by an individual who has been fully informed about the issue.

GPs have raised their own concerns about sharing patient data with the Department for Work and Pensions – and quite properly so. Pulse reports that the Department for Work and Pensions (DWP) plans to extract information from GP records, including the number of Med3s or so-called “fit notes” issued by each practice and the number of patients recorded as “unfit” or “maybe fit” for work, in an intrusive move described by GP leaders as amounting to “state snooping.”

There are also very serious concerns regarding the plans to permit medically unqualified job coaches to access and “update” patients medical records. That must not happen. Citizen’s complex health conditions and healthcare should never be subject to state editing and nor should these be conflated with political aims. That is potentially very dangerous and has nothing to do with the health and wellbeing of patients. A person’s employment status has no bearing on objective professional and specialist accounts of a person’s illness, diagnosis, medical tests and treatments. Work does not cure illness.

Patients have the right to explicitly refuse their consent to data sharing. The Data Protection Act 1998 covers personal information including health records. Further provision under Article 8 of the Human Rights Act 1998 establishes a right to respect for private and family life. This underscores the duty to protect the privacy of individuals and preserve the confidentiality of their health records. This right must remain intact. There is also additional guidance from the British Medical Association (BMA) here – GPs as Data controllers guidance. (PDF)

The government’s expressed aim is to prompt public services to “speak with one voice.” This proposed multi-agency approach is potentially very reductive, rather than being about formulating expansive, coherent, comprehensive and importantly, responsive provision. There is a danger that such a cross-agency approach will simply involve the co-opting of service providers and professionals as state enforcers, conflating complex citizen needs with simply getting people to work.

Public services “speaking with one voice” will make accessing support conditional, and potentially further isolate already marginalised social groups. It may damage trust between people needing support and professionals who are meant to deliver essential public services, not government slogans and potenially damaging messages. Places that have traditionally provided safe havens for people on low incomes, such as community centres, will no longer be places where people may feel they can escape the pressures and distresses of their circumstances and be relatively and unconditionally secure.

Human beings are subjects, not objects of policy, and the worrying trend towards the government instructing citizens how to be, under the guise of libertarian paternalism, is profoundly antidemocratic, non-dialogic and intrusive – it curtails citizen’s autonomy and basic freedoms and is incongruent with the democratic role of government in formulating policies that meet citizen’s needs. Instead, citizens are being coerced into meeting government aims and policy outcomes.

The move to “join up all public services to ‘get local people back to work'”, including housing and foodbanks may also be used as additional opportunity to extend welfare conditionality, including sanctions, to people who were previously exempted because of their circumstances.

Not only would this raise some serious ethical problems regarding the enforcing of a limited but mandatory state “treatment” on people who cannot work because they are ill, based on a political prejudice that work is somehow “good” for them, it would also limit access to other services that ordinarily provide a broader scope of support with a wider range of aims and outcomes that are more in line with a holistic approach to complex client needs, health and wellbeing.

It would potentially undermine people’s right to health care and support by making provision conditional to finding a job.

In linking receipt of welfare with health services, other public provision providers and access to “therapy,” with the single intended outcome explicitly expressed as employment, the government runs the risk of conflating citizen’s widely varied needs with diktats, and isolating people from traditionally non-partisan networks of relatively unconditional support, such as the health service, social services, community services and mental health services.

All policies are expressed political intentions regarding how our society is organised and governed. They have calculated social and economic aims and consequences. In democratic societies, citizen’s accounts of the impacts of policies ought to matter.

The government have not got a reassuring track record regarding the assessment of people’s illnesses, disability and capability for work, it has to be said. When serious concerns have been raised with ministers regarding the negative and often distressing experiences of sick and disabled people because of government policies, such concerns have been met with denial and a refusal to investigate or indeed, to engage any further.

I should like to know when those citizens who will be directly affected by the proposed policies, especially the work and health programme, were consulted? Have service users had any say at all in the design and aims of these proposed interventions?

It’s worth remembering that governments in first-world liberal democracies are for creating policies that actually meet public needs, rather than imposing totalitarian levels of control, manipulating and micromanaging citizens to meet government needs and political outcomes.

 

The Government’s brutal cuts to disability support isn’t ‘increasing spending’, Chancellor, but handing out tax cuts to the rich is

Chancellor George Osborne

 

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Source: Hansard

Context

Many of us recognised in 2012, when the welfare “reforms” and other cuts to public services that support the poorest citizens were forced through parliament despite considerable opposition, using only the “financial privilege” of the Commons as a justification, that the Conservatives are on an ideological crusade, which flies in the face of public needs, democracy and sound economics, to shrink the welfare state and privatise our essential services.

In a wealth transfer from the poorest to the very rich, we have witnessed the profits of public services being privatised, but the losses have been socialised – entailing a process of economic enclosure for the wealthiest, whilst the burden of losses have been placed on the poorest social groups and our most vulnerable citizens – largely those who are ill, disabled and elderly. The Conservative’s justification narratives regarding their draconian policies, targeting the poorest social groups, have led to media scapegoating, social outgrouping, persistent political denial of the aims and consequences of policies and reflect a wider process of political disenfranchisement of the poorest citizens, especially sick and disabled people.

That the cuts are ideologically driven, and have nothing whatsoever to do with economic necessity, was demonstrated only too well by the National Audit Office (NAO) report earlier this year. The NAO scrutinises public spending for Parliament and is independent of government. The report indicates how public services are being appropriated for purely private benefit.

The audit report in January concluded that the Department for Work and Pension’s spending on contracts for disability benefit assessments is expected to double in 2016/17 compared with 2014/15. The government’s flagship welfare-cut scheme will be actually spending more money on the assessments conducted by private companies than it is saving in reductions to the benefits bill.

From the report:

£1.6 billion
Estimated cost of contracted-out health and disability assessments over three years, 2015 to 2018

£0.4 billion
Latest expected reduction in annual disability benefit spending.

This summary reflects staggering economic incompetence, a flagrant, politically motivated waste of tax payers money and even worse, the higher spending has not created a competent or ethical assessment framework, nor is it improving the lives of sick and disabled people. Some people are dying after being wrongly assessed as “fit for work” and having their lifeline benefits brutally withdrawn. Maximus is certainly not helping the government to serve even the most basic needs of sick and disabled people.

However, Maximus is serving the private needs of a “small state” doctrinaire neoliberal government, and making lots of private profit whilst it does so. The Conservatives are systematically dismantling the UK’s social security system, not because there is an empirically justifiable reason or economic need to do so, but because the government has purely ideological, anticollectivist, antidemocratic, profoundly uncivilising prescriptions and longstanding prejudices.

Last week I wrote about the £30 a week Employmen Support Allowance (ESA) work related activity group (WRAG) cuts, which the Government have forced through the legislative process, despite meeting with widespread opposition, the government claim that it is their financial privilege to do so. Yesterday I wrote about the brutal cuts that are planned for Personal Independence Payments (PIP) for sick and disabled people, which are aimed at saving money by reducing eligibility for the support. The cut, it is estimated, will affect at least 640,000 disabled people by 2020, who may lose up to £150 a week. This is money that provides essential support for people who need help to prepare food, use the toilet or dress themselves, amongst other things, and to maintain a degree of dignity and independence.

The cuts to ESA and Personal Independent Payments (PIP) take place in the context of a Tory manifesto that included a pledge not to cut disability benefits. In fact in March last year, the Prime Minister signalled that the Conservatives will protect disabled claimants from welfare cuts in the next parliament (this one). Cameron said the Conservatives would not “undermine” PIP, which was introduced under the Coalition to save money by “targeting those most in need.” Now it seems those most in need are not the ones originally defined as such.

At the time he told BBC Breakfast: “We’ve replaced one benefit – Disability Living Allowance – with a new benefit – Personal Independence Payment – it’s working well, it is also going to lead to some savings over time and we haven’t created that benefit in order to undermine it. We want to enhance it and safeguard it.”

Semantic thrifts: being Conservative with the truth

Only a Conservative minister would claim that taking money from sick and disabled people is somehow “fair,” or about “helping”, “supporting” or insultingly, “incentivising” sick and disabled people who have already been deemed unfit for work by their doctors and the state via the work capability assessment to work.

The Tories all too frequently employ such semantic shifts and euphemism – linguistic strategies – as an integral part of a wider range of techniques of neutralisation that are used, for example, to provide linguistic relief from conscience and to suspend moral constraint – to silence both “inner protest” and public objections – to the political violation of social and moral norms; to justify acts that cause harm to others whilst also denying there is any subsequent harm being inflicted; to deny the target’s and casualties’ accounts and experiences of political acts of harm, and to neutralise remorse felt by themselves or other witnesses.

Media discourse has often preempted the Conservative austerity cuts, resulting in the identification, stereotyping and scapegoating of the groups in advance of the targeted, discriminatory policies. Media discourse is being used as a vehicle for the government to push their ideological agenda forward without meeting legitimate criticism, public scrutiny and without due regard for essential democratic processes and safeguards.

The five neutralisation techniques identified by Gresham Sykes and David Matza are: denial of responsibility, denial of injury, denial of victims, appeal to higher loyalties, and condemnation of condemners.

The really critical part of Sykes and Matza’s argument is that rationalisations precede immoral, cruel or controversial acts and are a key factor in making deviant behaviour possible (amongst delinquents, the mafia or Conservative ministers). As such, the rationalisations betray intent.

The cuts of £120 a month to the disability benefit Employment Support Allowance  are also claimed to be “fair.” and “supportive.” Though I have yet to hear a coherent and rational  explanation of how this can possibly be the case. Ministers claimed that people subjected to the ESA Work Related Activity Group cuts could claim PIP if they required support with extra living costs, but now we are told that PIP is to be cut, too.

Osborne’s techniques of neutralisation: calling a cut “increased spending”

The chancellor has defended his decision to use the cuts in disability benefits to fund tax breaks for the wealthy. On the Andrew Marr show yesterday, he was questioned about his decision to cut PIP, currently made to over 640,000 disabled people in a bid to save at least £1.2 billion. Many severely disabled people are facing a cut of up to £150 a week under the new reduced eligibility assessment criteria.

Controversially, the cuts to disability benefits will fund tax cuts for the most affluent – the top 7% of earners. The Chancellor is set to raise the threshold at which people start paying 40p tax, in a move that will probably see  many wealthier people pulled out of the higher rate of income tax, in the coming budget. Mr Osborne says he wants to “accelerate progress” towards the Conservative’s manifesto pledge of raising the threshold for the 40p rate to £50,000 in 2020, it is understood. The average annual income in the UK is around £27,000. 

Andrew Marr said: You’re taking money out of the pockets of some of the most vulnerable people in this country, disabled people. These are the people who can least afford the sacrifice, the people with the weakest shoulders.

And you’re changing the rules to hit them. Is that really your priority?”

Osborne ludicrously claimed that the Conservative government was “increasing spending on disabled people”, he said: “Controlling welfare bills is part of what you need to do if you’re a secure country confronting the problems in the world.”

But as Marr pointed out, the cuts to ESA and PIP show an intended substantial reduction on government spending to essential support for disabled people.

From January 2017, the cut to PIP is likely to hit sick and disabled people who face fundamental barriers to health and essential basic care. The cut, it is estimated, will affect at least 640,000 disabled people by 2020.

Andrew Marr went on to say: “At the same time as you’re raising thresholds to help middle-class tax payers, it’s going to seem a very callous set of priorities.”

However, Mr Osborne maintained that the brutal and uncivilised cuts were “necessary to improve the economic conditions in the UK”. He said: “Yes, times are tough. The fiscal situation is a difficult one. All Western countries are not productive enough.”

You can see the interview here:


Austerity and premature mortality

Since 2011, a year after the government began their austerity programme, mortality rates have increased rapidly. Advisers to Public Health England (PHE) have warned that the 4-year trend may be the worst since World War II.

Data from the Office of National Statistics shows a 5.4% (27,000) increase in deaths in the past year alone, prompting calls for an urgent investigation. The year-on-year rise, to a total of 528,340 deaths, is the highest since 1968.

PHE said the elderly were bearing the worst of Tory austerity cuts, with women suffering disproportionately, though this is partly because they live longer, however, it is also due to a growing crisis in the NHS and cuts to social care. Professor Danny Dorling, from Oxford University, an advisor to PHE on older age life expectancy, said:

“When we look at 2015, we are not just looking at one bad year. We have seen excessive mortality – especially among women – since 2012.”

Figures show that the number of deaths had been falling steadily until 2011, a year after the government began their austerity programme, when deaths rates began to increase rapidly.

Professor Dorling cited Tory austerity as the biggest cause:

“I suspect the largest factor here is cuts to social services – to meals on wheels, to visits to the elderly.”

Empirical research published two years ago demonstrated the high a cost the country paid in terms of health and wellbeing for the Thatcher administration’s economic and social policies. The study, which looked at material from existing research and data from the Office for National Statistics, illustrates that Thatcherism resulted in the unnecessary and unjust premature deaths of British citizens, together with a substantial and continuing burden of suffering and a widespread degradation of wellbeing. Co-author and researcher Professor Clare Bambra from the Wolfson Research Institute of Health and Wellbeing said that deaths from violence and suicide all increased substantially during the Thatcher era in comparison with other countries. Regional inequalities in life expectancy between north and south were also exacerbated, as were health inequalities between the richest and poorest in British society.

Professor Bambra also says that the welfare cuts implemented by Thatcher’s governments led to a rise in poverty rates from 6.7% in 1975 to 12% by 1985; poverty is well known to be one of the major causes of ill health and mortality. Income inequality also increased in the Thatcher period, as the richest 0.01% of society had 28 times the mean national average income in 1978 but 70 times the average by 1990. Other research (The Spirit Level) indicates that income inequality is internationally associated with higher mortality and morbidity.

Welfare reform minister, Lord Freud, refused to monitor the number of people who take their own lives as a result of the £120-a-month cut planned for those people in the work related activity group (WRAG), claiming employment and support allowance from April 2017. Concerns were raised in the House of Lords last week, when Baroness Meacher, amongst others, warned that for the most vulnerable, the cut was “terrifying” and bound to lead to increased debt.

Condemning the truly callous and terrible actions of the Treasury, she urged ministers to monitor the number of suicides in the year after the change comes in, adding: “I am certain there will be people who cannot face the debt and the loss of their home, who will take their lives.”

Many people have died as a consequence of the welfare “reforms.”

Not only have the government failed to carry out an impact assessment regarding the cuts, Lord Freud said that the impact, potential increase in deaths and suicides won’t be monitored, apart from “privately” because individual details can’t be shared and because that isn’t a “useful approach”.

He went on to say “We have recently produced a large analysis on this, which I will send to the noble Baroness. That analysis makes it absolutely clear that you cannot make these causal links between the likelihood of dying – however you die – and the fact that someone is claiming benefit.”

Actually, a political refusal to investigate an established correlation between the welfare “reforms” and an increase in the mortality statistics of those hit the hardest by the cuts – sick and disabled people – is not the same thing as there being no causal link. Often, correlation implies causality and therefore such established links require further investigation. It is not possible to disprove a causal link without further investigation.

Whilst the government continue to deny there is a causal link between their welfare policies, austerity measures and an increase in premature deaths and suicides, they cannot deny there is a clear correlation establised, which warrants further research and political accountability.

Then they came for the ESA Support Group …

Despite the fact that this government face a UN inquiry into grave and systematic abuses of the human rights of disabled people, the blatant attacks on a social group with legally protected characteristics continues and the Conservatives continue to target disabled people for a disproportionately large and unfair burden of austerity cuts.

A government advisor, who is a specialist in labour economics and econometrics, has proposed scrapping all ESA sickness and disability benefits. Matthew Oakley, a senior researcher at the Social Market Foundation, recently published a report entitled Closing the gap: creating a framework for tackling the disability employment gap in the UK, in which he proposes abolishing the ESA Support Group. To meet extra living costs because of disability, Oakley says that existing spending on PIP and the Support Group element of ESA should be brought together to finance a new extra costs benefit. Eligibility for this benefit should be determined on the basis of need, with an assessment replacing the WCA and PIP assessment. The Conservative definition of “the basis of need” seems to be an ever-shrinking category.

Oakely also suggests considering a “role that a form of privately run social insurance could play in both increasing benefit generosity and improving the support that individuals get to manage their conditions and move back to work.”

I’m sure the private company Unum would jump at the opportunity. Steeped in controversy, with a wake of scandals that entailed the company denying people their disabilty insurance, in 2004, Unum entered into a regulatory settlement agreement (RSA) with insurance regulators in over 40 US states. The settlement related to Unum’s handling of disability claims and required the company “to make significant changes in corporate governance, implement revisions to claim procedures and provide for a full re-examination of both reassessed claims and disability insurance claim decisions.

The company is the top disability insurer in both the United States and United Kingdom. By coincidence, the  company has been involved with the UK’s controversial Welfare Reform Bill, advising the government on how to cut spending, particularly on disability support. What could possibly go right?

It’s difficult to see how someone with a serious, chronic and often progressive illness, (which most people in the ESA Support Group have) can actually “manage” their illness and “move back into work.” The use of the extremely misinformed, patronising and very misleading term manage implies that very ill people actually have some kind of choice in the matter. For people with Parkinson’s disease, rheumatoid arthritis, lupus and multiple sclerosis, cancer and kidney failure, for example, mind over matter doesn’t fix those problems, positive thinking and sheer will power cannot cure these illnesses sadly. Nor does benefit conditionality and being coerced into work by callously insensitive and medically ignorant assessors, advisors and ministers.

The Reform think tank has also recently proposed scrapping what is left of the disability benefit support system, in their report Working welfare: a radically new approach to sickness and disability benefits and has called for the government to set a single rate for all out of work benefits and reform the way sick and disabled people are assessed. 

Reform says the government should cut the weekly support paid to 1.3 million sick and disabled people in the ESA Support Group from £131 to £73. This is the same amount that Jobseeker’s Allowance claimants receive. However, those people placed in the Support Group after assessement have been deemed by the state as unlikely to be able to work again. It would therefore be very difficult to justify this proposed cut.

Yet the authors of the report doggedly insist that having a higher rate of weekly benefit for extremely sick and disabled people encourages them “to stay on sickness benefits rather than move into work.”

The report recommended savings which result from removing the disability-related additions to the standard allowance should be reinvested in support services and extra costs benefits – PIP. However, as outlined, the government have ensured that eligibility for that support is rapidly contracting, with the ever-shrinking political and economic re-interpretation of medically defined sickness and disability categories and a significant reduction in what the government deem to be a legitimate exemption from being “incentivised” into hard work.

The current United Nations investigation into the systematic and gross violations of the rights of disabled people in the UK because of the Conservative welfare “reforms” is a clear indication that there is no longer any political commitment to supporting disabled people in this country, with the Independent Living Fund being scrapped by this government, ESA for the work related activiy group (WRAG) cut back, PIP is becoming increasingly very difficult to access, and now there are threats to the ESA Support Group. The Conservative’s actions have led to breaches in the CONVENTION on the RIGHTS of PERSONS with DISABILITIES – CRPD articles 4, 8, 9, 12, 13, 14, 15, 17, and especially 19, 20, 27 and 29 (at the very least.) There are also probable violations of articles 22, 23, 25, 30, 31.

The investigation began before the latest round of cuts to ESA and PIP were announced.

 

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Reverse the ESA disability benefit cut: sign the petition

Extend the PIP consultation & stop cuts to supporting terminally ill & disabled: sign the petition

 

Related

A tale of two suicides and a very undemocratic, inconsistent government

Paternalistic Libertarianism and Freud’s comments in context

Let’s keep the job centre out of GP surgeries and the DWP out of our confidential medical records

Conservative governments are bad for your health

Research finds strong correlation between Work Capability Assessment and suicide

Benefits Assessor: How Long Are You Likely To Have Parkinson’s?

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Labour Party To Refer Groundless Iain Duncan Smith Claim To Statistics Watchdog Again

Steve Bell cartoon


Iain Duncan Smith is telling fibs again. Work and pensions secretary claims that 75% of jobseekers think that benefit sanctions have helped them “focus and get on.”

The following is reported by Rowena Mason and Patrick Butler, for theguardian.com on Saturday 12th March 2016:

Labour is to challenge Iain Duncan Smith’s claim that 75% of jobseekers think benefit sanctions have helped them “focus and get on” by lodging a complaint with the official statistics watchdog.

Owen Smith, the shadow work and pensions secretary, said he would write to Duncan Smith challenging him to back up the “groundless” figure and refer the matter to the UK Statistics Authority for investigation.

The work and pensions secretary made the claim in an interview with the Camden New Journal, in which he suggested many claimants were grateful for the consequences of benefit sanctions.

“Seventy-five per cent of all those who have been sanctioned say it helped them focus and get on. Even the people in the jobcentres think it’s the right thing to do … sanctions are the reason why we now have the highest employment levels ever in the UK, and more women in work,” Duncan Smith said.

“What we say is: ‘We’ll give you all the support but at the end of the day we expect you to do something for it: go back to work, take the job, take the interviews.’ And it works, talk to any of the advisers in the jobcentres.”

While out campaigning for the Tory London mayoral candidate, Zac Goldsmith, Duncan Smith also dismissed protests about the controversial sanctions regime as “a classic buzz from the left” and claimed “these people are never going to vote for us – you have to understand, these people hate us”.

Owen Smith said: “Iain Duncan Smith’s claim that 75% of people who had been sanctioned say it ‘helped them focus and get on’ is groundless and shows he is out of touch with the real impacts of policies introduced by his department.

In reality, widespread concerns have been raised about this government’s use of sanctions, including from their own advisers, which is why the cross-party work and pensions select committee called for a full independent review into the system.

However, Iain Duncan Smith is reluctant to accept such scrutiny. Labour is calling for far greater transparency and honesty in this debate, so we can ensure greater numbers of people are actually helped into work, while being treated fairly.

That is why I will be writing to the secretary of state to inform him that we will refer his use of data to the Statistics Authority and calling for the long overdue independent review into sanctions to begin.”

Duncan Smith is believed to have been referring to DWP research that found 72% of jobseeker’s allowance (JSA) claimants said awareness of sanctions made them “more likely to follow the rules.”

However, that paper also said: “There was no evidence from the survey that knowledge of JSA conditions led to actual movement into work. Respondents who said they were more likely to look for work because of their knowledge of JSA conditions were no more likely than other respondents to have moved into work when they left JSA.”

After the interview, the Department for Work and Pensions released a statement saying: “Decisions on sanctions aren’t taken lightly but are an important part of our benefits system – they are only ever used as a last resort and the number of sanctions continues to fall.”

It is not the first time the UK statistics watchdog has been asked to adjudicate on the DWP’s approach to the sanctions regime.

Last year, it asked the DWP to ensure its statements on jobseeker sanctions are “objective and impartial” following a series of complaints by experts.

At the time, the authority’s chair, Sir Andrew Dilnot, wrote to the DWP’s top statistician asking the department to publish far more data and give the public a clearer understanding of how it is imposing sanctions on jobseekers.

Sanctions are used by civil servants to penalise jobseekers when they are alleged to have broken benefit rules, with punishments becoming increasingly severe over the last parliament.

The government has faced repeated calls from Labour to rethink the system, but is resisting pressure for an independent inquiry.

The Commons work and pensions committee last year urged the government to hold a wide-ranging independent review of the regime to address widespread concerns that it is unfair, excessively punitive, and does little to help people get into work.

© Guardian News & Media Limited 2010.

Related

A List of Official Rebukes For Tory Lies

Department of Work and Pensions officials admit to using fake claimant’s comments to justify benefit sanctions

The Department of Whopping Porkies is rebuked as claimants suddenly develop mysterious superpowers after being sanctioned

A letter of complaint to Andrew Dilnot regarding Coalition lies about employment statistics

Audit finds whereabouts and circumstances of 1.5 million people leaving welfare records each year “a mystery”

Essentialising marginalised groups and using stigmatising personality constructs to justify dismantling social security is not “science”, it’s psychopolitics

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“It’s fear of the political-correctness brigade that has stopped my colleagues going public — quite sensibly, as it turns out. But I felt I owed it to the taxpayers who are funding the welfare state to publish these data.” Adam Perkins.

Tax payers who “fund the welfare state” are not a discrete class of citizens: most of them come to rely on it as a safety net to ensure they can meet their basic needs at some time in their life. Those currently claiming  social security benefits, who are not all of the same people who did last year or the year before, still contribute to one of the largest sources of revenue for the Treasury – VAT and other stealth taxes, such as council tax. In fact almost all benefits are paid back as taxes. The biggest beneficiaries of welfare are those employed to administrate it, especially the growing number of private sector “providers”.

Adam Perkins wrote a book that attempts to link neurobiology with psychiatry, personality and behavioural epigenetics, Lamarkian evolution, economics, politics and social policy. Having made an impulsive inferential leap across a number of chasmic logical gaps from neurobiology and evolution into the realms of social policy and political science, seemingly unfazed by disciplinary tensions between the natural and social sciences, particularly the considerable scope for paradigmatic incommensurability, he then made a highly politicised complaint that people are criticising his work on the grounds of his highly biased libertarian paternalist framework, his highly partisan New Right social Conservatism and neoliberal antiwelfarist discourse. 

The problem of discrete disciplinary discursive practices and idiomatic semantics, each presenting the problem of complex internal rules of interpretation, was seemingly sidestepped by Perkins, who transported himself with apparent ease simply on leaps of semantic faith to doggedly pursue and reach his neoliberal destination. He is certainly very fluent in the language of New Right Conservatism, it has to be said. I’m certain he must be very good friends with Charles Murray, of the Bell Curve fame during the Thatcher and Reagan era..

Many from across the political spectrum have objected to Perkins’s book because of the strong whiff of eugenics and social Darwinism that has hit the fan, along with the stench of the long-rotten corpse of Nazism. The atrocities associated with essentialising social groups – attributing “natural”, essential characteristics to members of specific culturally defined groups (based on gender, age, ethnic, “racial”, socioeconomic status, for example) – were thought to be long buried under the brutal and horrifying lessons of history, and quite properly considered taboo.

When societies essentialise others, it is assumed that individual differences can be explained by “inherent”, biological, “natural” characteristics shared by members of a group. Essentialising results in thinking, speaking and acting in ways that promote stereotypical and inaccurate interpretations of individual differences. It invariably involves political discourse that decontextualises structural inequality, using narrative that “relocates” it, coercing the responsibility, internalisation and containment of social problems within some individuals and groups. This always involves processes of projection, stigmatising, outgrouping and scapegoating.

Essentialist thinking is anchored in binary conceptual schema – simplistic and dualistic (two-categories: either this – or that) modes of thought. Both classic and contemporary social theorists have identified and challenged essentialist and dualistic ways of thinking about the social world. Essentialising as a process targets and stigmatises minority groups who historically do not have equal access to power in the cultural production and validation of “knowledge”.

In Perkins’s previous co-authored work – Personality and occupational markers of ‘solid citizenship’ are associated with having fewer children, which is a study of associations between personality and reproductive fitness, he claims that such associations may reveal the adaptive significance of human behavioural traits. He says: “What we dub ‘solid-citizenship’ personality characteristics such as self-control, diligence and responsibility may repay study from an evolutionary perspective as they protect against negative life-outcomes.” 

“Perkins et al. tend to regard risk as a synonym of probability and so equate evolutionary fitness with moral hazard.Hubert Huzzah.

Low conscientiousness, criminality, low educational attainment, low occupational status, extraversion, neuroticism, catholicism, a lack of diligence, responsibility, self control and other assigned personality characteristics are then linked with contraception use, and conflated with low socioeconomic status and negative life-outcomes that are curiously isolated from a wider socioeconomic context.

Again, the very idea that citizenship is defined by certain perceived personal qualities associated with conformity and Conservative values indicates Perkins’s tendency to politicise concepts of human “nature”, and conflate them with New Right narratives, reflected in his interests, choice of research topics and demonstrated in the framing of his conclusions. This reflects a wider current tendency towards the political medicalisation of social problems, which shifts public attention from the sociopolitical and economic context of inequality, poverty and social injustice to politically inculpated, marginalised outgroups.

I have written a lengthy critique of Adam Perkin’s controversial book called “The Welfare Trait.” Whilst I have criticised the work because of its quite blatant partisan ideological, political and economic inception and framing, I have also raised other important issues regarding problematic underpinning assumptions, which include commiting a fallacy of inventing fictitious proximal causes for behaviour, such as “perverse incentives,” problems with constructs of personality and difficulties measuring behaviour traits.

Much of the current understanding of personality from a neurobiological perspective places an emphasis on the biochemistry of the behavioural systems of reward, motivation, and punishment. But those are largely extrinsic factors, located, for example, in political and socioeconomic environments, external to the individual, who responds to their context. This theoretical stance is therefore both limited in terms of depth and explanatory coherence and limiting in terms of generating understanding – the study lacks comprehensiveness and methodological rigour – there is very little consideration of confounding variables, for example, which hinders further potential investigation and discovery. It also reflects in part a re-platforming of an over-simplistic Pavlovian behaviourism. Definition and theory of the biological basis of personality is not universally accepted. There are many conflicting theories of personality in the fields of psychology, psychiatry, philosophy, and neuroscience.

Perkins implies that welfare somehow creates personality disorders and “undesirable” traits. However, such pathologies are defined by experiences and behaviours that differ from societal norms and expectations.

Personality disorder (and mental illness) categories are culturally and historically relative. Diagnostic criteria and categories are always open to sociopolitical and economic definition, highly subjective judgments, and are particularly prone to political abuse.

As I’ve pointed out elsewhere, personality traits are notoriously difficult to measure reliably, and it is often far easier to agree on the behaviours that typify a disorder than on the reasons why they occur. As it is, there is debate as to whether or not personality disorders are an objective disorder, a clinical disease, or simply expressions of human distress and ways of coping. At the very least, there are implications regarding diagnoses that raise important questions about context, which include political and social issues such as inequality, poverty, class struggle, oppression, abuse, stigma, scapegoating and other structural impositions.

An over-reliance on a fixed set of behavioural indicators, some have argued, undermines validity, leaving personality disorder categories prone to “construct drift,” as the diagnostic criteria simply don’t provide adequate coverage of the construct they were designed to measure. There are no physical tests that can be carried out to diagnose someone with a personality disorder – there is no single, reliable diagnostic tool such as a blood test, brain scan or genetic test. Diagnosis depends on subjective judgment rather than objective measurement.

Perkins also conflates descriptive statements with prescriptive ones. Moral conclusions can’t be drawn from non-moral premises. In other words, just because someone claims to have knowledge of how the world is or how groups of people are (descriptive statements), this doesn’t automatically prove or demonstrate that he or she knows how the world ought to be (prescriptive statements).

There is a considerable logical gap between the claim that welfare is somehow “creating” some new kind of personality disorder, called “the employment-resistant personality”,  and advocating the withdrawal of support calculated to meet only the basic physiological needs of individuals – social security benefits only cover the costs of food, fuel and shelter.

Perkins does nothing to consider, isolate and explore confounding variables regarding the behaviours and responses of people needing social security support. He claims our current level of support is too high. However empirical evidence clearly indicates it is set far too low to meet people’s physiological needs fully.

Poverty affects people’s mental health as well as their physical health. There is a weight of empirical evidence confirming that food deprivation and income insecurity are profoundly psychologically harmful as well as physiologically damaging. (See the Minnesota semistarvation experiment, for example.) Describing people’s anger, despondency and distress at their circumstances as “antisocial” is profoundly oppressive. The draconian policies that contribute to creating those circumstances are antisocial, not the people impacted by those policies.

Climbing Allport’s Ladder of Prejudice

Since writing my own response to The Welfare Trait I have encountered a surprisingly high number of people in the UK who believe that anyone who can’t work should be left with no money at all to meet their basic survival needs. To clarify, that means they think that not everyone should have a fundamental right to life. My work was labelled “hysterical dogma” by one commentator on the Adam Smith Institute website. I have been very struck by how normalised social Darwinism and related perspectives have become over the last few years, again. And how people that disagree with those views are defined, increasingly as the other. Along with the growing number of other politically defined others. It’s a symptom of an increasingly authoritarian climate.

I was called a “politically correct bleeding heart leftard” by a eugenics advocate on the Telegraph comments section, and was truly baffled that someone could see social conscience, a sense of justice, basic, ordinary qualities of caring, empathy and compassion as somehow pathological qualities. It’s also remarkable that a group of people who claim that sanctions, which entail the removal of people’s means of meeting basic survival needs is “helping” or “supporting” people into work, somehow “fair” and about “making work pay” feel they can lecture anyone else on appropriate language choices, techniques of neutralisation, modes of linguistic behaviourism and censorship.

I have always felt strongly that we have a democratic duty to protect marginalised groups and look out for the cultural underdog –  it’s the oppressed that are denied a voice, their rights, autonomy and identity, not the oppressors. Underdogs are generally seen as casualties of injustice or persecution. They are also most often predicted to be losers in a struggle.

Of course not all underdogs remain underdogs. J.K. Rowling, a lone mother claiming social security, who wrote seven of the best-selling books of all time, created a vulnerable, lovable underdog character, Harry Potter – an oppressed but passionate orphan with character, modesty, integrity and all the best of human qualities. He grew up in a cupboard, wearing oversized hand-me-down clothes and doing accidental bursts of magic to get by. He came to face and fight the forces of evil that had oppressed and terrorised two generations of wizards and witches, and non-magical folk alike.

Jo Rowling had a very difficult seven-year period that left her coping with the death of her mother, who had multiple sclerosis, severe depression, the birth of her first child, divorce from her first husband and relative poverty until she finished the first novel in the series.

What is remarkable about Rowling isn’t her “rags to riches” success, though that is undoubtedly a commendable achievement: it’s the social, moral, and political inspiration she has given to so many, young and old alike, that really stands out, and her considerable philanthropy.

Rowling said: “I wanted Harry to leave our world and find exactly the same problems in the wizarding world. So you have the intent to impose a hierarchy, you have bigotry, and this notion of purity, which is this great fallacy, but it crops up all over the world. People like to think themselves superior and that if they can pride themselves in nothing else they can pride themselves on perceived purity.

Defining a group’s superiority and purity always means defining others as “inferior.”

But is it not normal to care about such issues? Surely that is how we relate to others, our inclination to bond originating from relationships within our families and with significant others, extending to wider communities, and to society as a whole? Yet this way of seeing the world is being pathologised by a growing number of people who see the world only in terms of hierarchies of status and human worth: a raw, “red in tooth and claw” competitive individualism, and always, it seems, for what they can get, how much they can profit and how much they can take from others, rather than what they can give to society.

The general public over the past 5 years have been generally treated by a government of elitist, antidemocratic, cognitive and class supremicists as a political means to an end. Meanwhile people raising genuine concerns about corruption, greed, the stigmatisation of minorities and the growing human rights abuses of marginalised social groups, authoritarianism and so on are ostracised, treated with scorn, ridicule and contempt, and turned into the growing number of Conservative folk devil constructs.

Names such as “extremists”, “raving trot” “loony leftie” “leftard” are bandied around so much now that those using the labels have lost sight of the fact that these are offensive and rude. The really worrying thing is my views are hardly extreme or remotely  radical  – I’m no “commie.” Most people on the political Left are just regular people wanting regular fairness, social justice, equal rights for all, an end to cruel and unnecessary cuts which target only the poorest, and an end to such crass socioeconomic policies that result in massive inequality and poverty. How did being so normal become so non-mainstreamed?

How can it possibly be that to care for the wellbeing of others in our society, and the kind of world our children will inherit from us is somehow wrong, that values of cooperation, mutual aid and compassion are not the norm, that taking a clear ethical position is something to be ashamed of or a reason to be mocked?

The Conservatives have a moralising, rather than a moral political position, and have you noticed that Tory moralising only ever applies to the poorest people and invariably generates public prejudice, discriminatory policies and fosters social divisions?

Political Correctness

It’s a sure sign that the Right have no arguments and critical reasoning to support their fundamental ideological position, that whenever their partisan narratives are challenged by our own narrative, then we are met with blatant attempts to close down debate by a barrage of nasty, resentful, immature name-calling and outrage that is thrown at anyone and everyone that challenges the cultural, epistemological and right-wing ontological status quo and neoliberal doxa.

Some people use the “freedom of speech” plea to justify their prejudice. They say they have a right to express their thoughts. However, speech is an intentional ACT. Hate speech is intended to do harm – it’s used purposefully to intimidate and exclude marginalised, disempowered and vulnerable groups. Hate speech does not “democratise” speech, it tends to monopolise it. Nor is it based on reason, critical thinking or open to debate. Bigotry is a crass parody of opinion and free speech. Furthermore, bigots are conformists – they tend not to have independent thought. Prejudice thrives on Groupthink.

Being inequitable, petty, resentful, vindictive and prejudiced isn’t “being truthful” or “telling it like it is” – a claim which is an increasingly common tactic for the Right – it’s just being inequitable, petty, resentful and prejudiced. And some things are not worth saying. We do have an equal right to express an opinion, but not all opinions are of equal worth. Free speech carries with it some responsibilities.

And the right-wing do frequently dally with hate speech. Hate speech generally is any speech that attacks a person or group on the basis of their race, religion, gender, disability, or sexual orientation. In law, hate speech is any speech, gesture or conduct, writing, or display which is forbidden because it may incite violence or prejudicial action against or by a protected individual or group, or because it disparages or intimidates a protected individual or group. Critics have argued that the term “hate speech” is a contemporary example of Newspeak, used to silence critics of social policies that have been poorly implemented in order to appear politically correct.

However, “political correctness” was adopted by US  New Right Conservatives as a pejorative term for all manner of attempts to promote civil rights, multiculturalism and identity politics, particularly, attempts to introduce new terms that sought to leave behind discriminatory baggage attached to older ones, and conversely, to try to make older ones taboo.

Importantly, political correctness arose originally from attempts at making language more culturally inclusive. Critics of political correctness show a curious blindness when it comes to examples of “Conservative correctness.” Most often, the case is entirely ignored, or censorship of the Left is justified as a positive virtue. Perhaps the key argument supporting this form of linguistic and conceptual inclusion is that we still need it, unfortunately. We have a right-wing Logocracy, creating pseudo-reality by prejudicial and discimatory narrative and words. We are witnessing that narrative being embedded in extremely oppressive policies and in their justification.

The negative impacts of hate speech cannot be mitigated by the responses of third-party observers, as hate speech aims at two goals. Firstly, it is an attempt to tell bigots that they are not alone. It validates and reinforces prejudice.

The second purpose of hate speech is to intimidate a targeted minority, leading them to question whether their dignity and social status is secure. In many cases, such intimidation is successful. Furthermore, hate speech is a gateway to harassment and violence. (See Allport’s scale of prejudice, which shows clearly how the Nazis used “freedom of speech” to incite hatred and then to incite genocide.) As Allport’s scale indicates, hate speech and incitement to genocide start from often subtle expressions of prejudice, which advance culturally by almost inscrutable degrees.

The dignity, worth and equality of every individual is the axiom of international human rights. International law condemns statements which deny the equality of all human beings. Article 20(2) of the ICCPR requires states to prohibit hate speech. Hate speech is prohibited by international and national laws, not because it is offensive, but rather, because it amounts to the intentional degradation and repression of groups that have been historically oppressed.

The most effective way to diffuse prejudice is an early preventative approach via dialogue: positive parenting, education and debate. Our schools, media and public figures have a vital part to play in positive role-modelling, like parents, in challenging bigotry, encouraging social solidarity, respect for diversity and in helping to promote understanding and empathy with others.

Hate speech categories are NOT about “disagreement” or “offence.” Hate speech doesn’t invite debate. It’s about using speech to intentionally oppress others. It escalates when permitted, into harassment and violence. We learned this from history, and formulated human rights as a consequence. In this context, political correctness is about inclusive free speech, with rationality, critical thinking, democratic civility and a degree of mutual respect chucked in.

I’m proud to be a part of an ethical, rational, reasonable, decent and civilised Left-wing.

And politically correct?

Damn right I am.

free speech - microphone

Freedom of speech isn’t about shouting the loudest, trying to intimidate, silence and disempower others or having the last word.

 —

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Job vacancies fall as fears over potential Brexit brings uncertainty to the labour market

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New figures published yesterday reveal a 7.3% drop in the number of advertised job vacancies in the UK since the start of the year, as experts warn fears that the UK may leave the European Union are fueling job market uncertainty.

One of the biggest uncertainties surrounding “Brexit” is the fact that such an exit has never been done before, so no one really knows what the exact fallout will be. This is in addition to major concerns that the impact of a Brexit would be profound and irreversible, and would lead to a significantly diminished international role for the UK.

There has been a marked drop in advertised vacancies since the start of the year, and warnings that discussions about the UK leaving the European Union is fuelling job market uncertainty. 

“Hiring habits are changing, it’s a sign of potential instability and employers are retaining their best workers for longer,” says Doug Monro, co-founder of Adzuna.

According to Adzunda’s latest Job Market Report, jobseekers are facing fewer options in 2016, as falling vacancies and rising competition impact upon work prospects. This contradicts the Department for Work and Pensions statement that:

“Official figures show that job vacancies are at an all-time high, with a record 31.4 million people in work and the unemployment rate now at a 10-year low.”

The Job Market report summarises that:

  • ‘New year, new job’ phenomenon fails to take off, as employer hiring drops off amid bosses’ successful long term focus on retaining and upskilling existing employees
  • January sees number of advertised vacancies fall 7.3% to 1,079,711, declining for the second consecutive month as jobseekers find themselves with fewer choices
  • Competition for jobs hots up, rising to 0.61 applicants per vacancy from 0.54 in December, as Northern cities Sunderland and Hull see toughest competition
  • Manufacturing, Finance, Energy, Media and Retail sectors see cuts in January, resulting in thousands of job losses across the UK’s core industries
  • Advertised salaries, meanwhile, show a glimmer of hope, rising 0.8% month-on-month to reach £33,593 in January, with Northern Ireland and Wales leading the recovery
  • French the top foreign language for new hires in the UK jobs market despite Brexit fears, with 8,401 current vacancies looking for French linguistic skills.

Monro comments: “January’s jobs market has failed to take flight. The normal rhythm of hiring hasn’t happened – vacancy levels are down and job competition is getting tougher. Fewer options for those looking for new jobs is putting pressure on career plans. Hiring habits are changing in a sign of potential instability and employers are retaining their best workers for longer.”

He goes on to say:

 “A potential Brexit brings new unknowns into the jobs market. Politicians are at risk of fuelling uncertainty fears – and only increasing doubts. By doing so they’re risking a weaker jobs market. It’s a dangerous game to play – thousands of employers and employees are already on edge. This lack of consensus is causing understandable concern for many companies. Business expansions and hiring sprees are being put on hold as a result. EU languages are still in high demand throughout the UK and whichever road the referendum takes us down, this is sure to remain so.”

“Languages have always been vital to the international ambitions of companies. But now they’re becoming even more lucrative to have as a jobseeker. A French speaker, or German speaker in a company can make all the difference and open up new business channels and deals. In the interconnected world, learning a second language is a fantastic way to differentiate yourself from other applicants and claim a higher salary. It’s hard work to learn a foreign tongue, but employers are willing to pay more for it – so it’s a skill worth pursuing. For industries such as IT, which is growing its international reach, and for healthcare, which is dealing with more diverse patients than ever, having another language may soon become a necessity.”

January saw a total of 1,079,711 job vacancies advertised in the UK, down 7.3% from 1,164,502 in December – in the largest monthly drop since 2012. Advertised job vacancies have now fallen 13.7% since November, when 165,000 more jobs were on the market (1,244,772). A long-term focus on upskilling existing employees and prioritising retention means companies can now sidestep the search for fresh talent, filling positions in-house rather than looking elsewhere.

Widespread job losses across a range of UK sectors mean several industry key players are no longer in a position to take on new hires. Energy giant BP cut 7,000 jobs earlier this month, alongside the loss of over 2,500 manufacturing roles by Tata and Bombardier. Lloyds and Virgin Media similarly saw large job losses of 1,755 and 900 employees respectively. The Retail and Manufacturing sectors have seen large vacancy falls in the wake of job losses in January. Current vacancies in the Manufacturing sector stand at 14,022 – down 9% from 15,466 roles last month. Similarly, the Retail sector saw vacant positions fall 13% to 32,143, from 36,881 in December.

Jobseekers with language skills are managing to buck the downward vacancy trend however, as demand for multilingual workers has risen.

There are currently over 35,000 job vacancies for applicants with linguistic skills and with an average advertised salary of £36,026 for bilingual positions across the UK.

French is the most popular language with employers, with 8,401 available positions currently asking for proficiency. This is closely followed by German (7,820 vacancies), Spanish (4,267) and Italian (3,856).

There is a rare consensus amongst UK economists: they overwhelmingly believe that leaving the EU is bad for the country’s economic prospects. In the Financial Times’s annual poll of more than 100 leading thinkers, not one thought a vote for Brexit would enhance UK growth in 2016.

A recent Government report has also warned that it could take more than 10 years to set up new trade details and negotiate Brexit, and car manufacturing, farming, financial services and the lives of millions of Britons would be impacted negatively. Bosses at more than a third of the UK’s biggest businesses have also signed a letter supporting the campaign to remain in the European Union. Chairmen and chief executives at 36 FTSE 100 companies – including BT, Marks & Spencer, Kingfisher and Vodafone – warned a Brexit would “deter investment and threaten jobs.” The 36 are among the names of 200 business leaders, representing 1.2 million employees, to put their names to the letter.

The heads of six British companies owned by German car giant BMW, including  Mini and Rolls-Royce have told British workers that exit from the European Union could drive up costs and have an impact on its workforce. A letter was sent to 8,000 Rolls-Royce employees, including workers in Goodwood, West Sussex, and Oxford. A report produced this week warned that the car industry would be badly hit by Brexit.

It outlines how more than half of MINIs and most of the British-made engines and components are exported to the EU. Also, it described how Brexit would hit hard the way Rolls Royce brings in cars and spare parts from the continent.

“Tariff barriers would mean higher costs and higher prices and we cannot assume that the UK would be granted free trade with Europe from outside the EU.

“Our employment base could also be affected, with skilled men and women from most EU countries included in the 30 nationalities currently represented at the home of Rolls-Royce here at Goodwood,” the letter said.

Nearly 1,000 projects at 78 UK universities and research centres are dependent on funds from the European Research Council (ERC). The UK has more ERC-funded projects than any other country, accounting for 22% of all ERC-funded projects – more than 25 recipient countries put together. The collaborations that have made the UK such an important player are dependent on the free movement of scientists into the UK. About 15% of academic staff at UK institutions are non-UK EU nationals, a figure that rises to 20% among elite universities.

You can read the full Job Market Report here

Welcome to the Labour Party’s excellent Economic Advisory Committee of experts

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Labour Press released this in September 2015:

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WordPress theme error: for Fs sake

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I usually use the Syntax theme for my site, because its fonts are easy to read and the simplicity of the theme tends to emphasise the content of articles rather than the style. However, yesterday a curious fault developed, and letter Fs were removed from texts – it was any F followed by the letter I or L. So words like “financial”, “benefit” and deficit” were F less.

I tried changing the font first of all, but that didn’t make any difference to the problem.

I was forced to change the site theme, which remedied the error. However some of my articles have now got seemingly random font irregularities and some paragraph spacing problems. Some of the text has what looks like superscript whimsically inserted here and there. I do apologise if you come across any articles that have been re-translated into a facetious font-styled slapstick comedy show with randomly allocated, frivolously large gaps chucked in.

If there are any affected articles that you want to share, let me know and I will address the errors as quickly as possible. Meanwhile, it’s just a case of plodding through each one I find and putting it right manually, editing and updating.

As well as affecting Syntax, it seems the newer Ecto theme has also been blighted by the same “un F ing” error.

WordPress are reporting that: “A glitch with liguatures (like fl and fi) was introduced in the Merriweather font a few days ago.”

These things are sent to try us. Though for what, I don’t know.

Still at least I’m back to being fully furnished with Fs and can get on with being my usual brand of


on my F inclusive site