Three reasons why Labour's hands are red with the blood of the disabled and the sick.

Will Jeremy Corbyn apologise for the pogrom it unleashed while in power,  culminating in yesterday's announcement that nearly 90 people a month are dying after being declared fit for work ?

Corbyn has called for Iain Duncan Smith's resignation.Yet the Orwellian chain of events that led to yesterday's tragic announcement was devised and set in place by Labour.

Here are three reasons why Labour's hands are stained red:

1. It was Labour that introduced the Work Capability Assessment

Before the Coalition and the current Conservative government came to power seriously ill and disabled people , found fit for work under Labour were denied Employment Support Allowance (ESA) and then subsequently written off, just left to cope with greatly reduced benefits on Job Seekers Allowance and little support. (Source : Not Working . CAB Evidence on the WCA.)

That is because they had all been subjected to the notorious Work Capability Assessment (WCA) which took little account of variable symptoms, generalized pain, exhaustion or the underlying seriousness of a person’s condition.

Yet introducing ESA and the WCA in 2007, deemed fatally flawed , last year, by the Work and Pensions Select Committee, (W&P 2014),  Labour  described them as “A new, progressive vision .” (Hain P 2007)

2. It was Labour that introduced the biopsychosocial approach

Labour’s extraordinary counterintuitive reasoning , towards disability, had its roots, says Jonathan Rutherford in the American right’s philosophy that the poor are the cause of their own poverty because they fail to take advantage of the opportunities “available” to them..

It all began in 1994 when the Conservative Government brought in UNUM, the giant American Medical insurance Company, to advise them on welfare reform, a member of that group was Mansel Aylward, who in 1999, as Chief Medical Officer at the DWP, devised the new Personal Capability Assessment (PCA), contracted out to the American Corporation Atos Origin, who used a computer system, Logical Integrated Medical Assessment (LIMA), which neatly side steped any inconvenient medical opinion (syzygysue 2014), where the ” emphasis was no longer on entitlement, but on what a person is capable of doing.

The intellectual basis behind the PCA was UNUM’s “The Scientific and Conceptual Basis of Incapacity Benefits “ (SCBIB) by Gordon Waddell and Mansel Aylward followed by the 2006 report: Is work good for your health and well-being by Gordon Waddell and Kim Burton which are based upon the biopsychosocial model of illness, designed to “liberate” the disabled from the ” medical model” . According to the biopsychosocial model, under which untold tens of thousands of people, especially people with ME whose physical illness is almost completely denied and psychiatric treatment is the only treatment on offer , have suffered horrible abuse and even death.

The biopsychosocial model that Labour introduced was based upon the premise that ” Disease is the only objective, medically diagnosable pathology. Sickness is a temporary phenomenon. Illness is a behavior social phenomenon rather than a health problem. The solution is not to cure the sick, but a “fundamental transformation in the way society deals with sickness and disabilities.

The transformation is this : ” Sickness is a social and cultural phenomenon rather than a health problem. The solution is not to cure the sick, but to transform the culture of welfare. No one who is ill should have a straightforward right to receive benefit.”, this extreme agenda ” was adopted by the former banker that Labour brought in, David Freud , now Lord Freud .

Pushing the neoliberal agenda that Labour  pioneered to triumphant heights, ever since, the Coalition and the Conservatives have progressed some of the toughest, and most regressive social policies since the foundation of the welfare state. Building upon the “dependency-busting” foundation laid down by New Labour, never before has there been such a concerted onslaught on disabled/sick people, in terms of New Labour's distinction, entirely devoid of evidence, between the “deserving and undeserving poor”.(Roulstone )

Both the neoliberal politician and the private health insurance want to shrink the State, reduce public expenditure via privatisation and remove people from benefit entitlement . (Syzygysue 2011)

3. It was Labour that labeled the sick and disabled as “malingerers ”

It was a New Labour conference in November 2001 entitled Malingering and Illness Deception , together with their 2006 Green Paper: A New Deal for Welfare: empowering people to work – an independent assessment of the arguments for the proposed Incapacity Benefit reform that is responsible for the mind set that continues to this day : ‘malingering’ as being the motivation for claimants of disability benefits. (Stewart 2015)

In effect the DWP's agenda, ever since, has been motivated towards denying ‘illness’ and associated legitimate need, wherever possible. (Syzygysue 2011) This is despite the fact that all evidence supports the fact that, out of the entire DLA budget, less than 0.5% were bogus applications with 1.5% admin error. (Stewart M 2012)

As Laurie Pennie (2012) writes the consequent attack upon the disabled and sick has come from all fronts from “the financial to the moral – rewriting the social script in this country so that the needy are no longer full human beings with just as much right to a life as anyone else, but parasites, scroungers, burdens on the state, barely even human. “

Last Year a Conservative Welfare Minister suggested that disabled people should work for £2.00 an hour. (Morris 2014)

The consequences of the Coalition's policies have been terrible, with the disabled bearing the brunt of cuts. Benefits for disabled people and the poorest , this year, will have been cut by £18 billion, a cut of about 20%. (Duffy 2013)

In 2013 Amnesty International UK condemned this “regressive and lethal assault on our rights” (Left Foot Forward 2013).

Previous DWP mortality figures showed that 10, 600 people died in eleven months in 2011.(Pring 2015). The figures, released yesterday show 2,650 former claimants of sickness-related benefits died within six weeks of being declared “fit for work” between December 2011 and February 2014.

My wife, who has Very Severe ME, has been chronically sick and disabled for over two decades. Last time we spoke to a Labour Party member, back in 1995, he informed us that 90% of the sick and disabled are scroungers.

The carnage continues.

Greg Crowhurst

References :

Duffy S (2013) A fair society? How the cuts target disabled people

Morris N (2014) Lord Freud: Tory welfare minister apologises after saying disabled people are 'not worth’ the minimum wage

Penny L ( 2012) Laurie Penny on the coalition’s war on the disabled and destitute

Pring J (2015) DWP told to publish ESA deaths report, after two-year delay

Roulstone A Coalition Disability Policy-A Consolidation of Neo-Liberalism or Benign Pragmatism?


Stewart M (2015)The influence of private insurance on UK welfare reforms

syzygysue (2011) Welfare reform and the US insurance giant Unum.
W&P 2014: ESA needs fundamental redesign, says MPs: July 2014
DWP Work & Pensions Select Committee 23rd July 2014: News release

syzygysue(2014) Welfare Reform and ME/CFS


  1. Thank you so much Mary !! What I haven't conveyed is how this process of denial and the labeling of the sick and disabled as "malingerers" cut its teeth on people with ME : where a whole disease has been written off. If only the process was widely understood nobody could take the psychiatric lobby seriously.

  2. Peter Lilley, a cabinet minister in the Thatcher Government started this disgraceful UK public policy ball rolling and then Blair and Brown's "New Labour" government from 1997 well and truly ran with that ball. Greg Crowhurst's 'Three reasons why Labour's hands are red with the blood of the disabled and the sick' is a timely reminder of the complicity of New Labour in the long-running saga of ME patient abuse in our country via official UK policy. A useful overview of such policy is available at:
    Anglia ME Action

  3. Thanks for spelling out the "truth" so comprehensively Greg. A family member, also severely affected by ME in past years has refused to even process any state benefit entitlements because of a refusal to engage with the humiliation, degradation, idiocy, repeated cock ups by Job Centre Plus, DWP, ATOS, maladministration, misdirection throughout, the intragegency of call centre staff reading from the set "scripts", having the phone put done on them mid sentence, the blatancy of their lies over mistakes, the failure to even follow their own manuals and policy documents many of which they are unaware of or in denial of, the failure to carry out Harrington Review recommendations, the failure to comply with the laws on Advocacy arrangments; the above all point to failure of Human Rights...... But don't bother with invoking the Human Rights Act as it has been highjacked by criminals and other exploitative individuals who cite such nonsense as development land refusal to build as a breach of their " quiet enjoyment " of their land and making lots of money despite potential harm to the environment!
    The law in this country is no better and an advocate friend has just lots his first benefit tribunal case in 3 years, a sign of where things are going with the judiciary.
    My friends daughter aged 35 with ME and fibromyalgia will be cremated in York this Friday. She had years of battle with health and benefits. She had consequent complications which proved fatal Friday before last. She had spent her last summer helping to raise funds for MERUK.......whilst undergoing intense chemotherapy.
    She had been fobbed off with "It's only your ME....". Rest in peace Josie.

    I have been forced to take forward a judicial challenge myself on environmental and planning I too am at the mercy of the law. Wish me luck! Rant over benefit!

    1. So good to hear from you Barbara ! What a brilliant, biting, poignant account of the lies, misdirection, maladministration that is the "welfare" system. The neglect of people, especially with ME, is off the scale. As you know Linda, my wife, has lived a tormented, agonising existence with no proper medical help or input,for more than tow decades now. It is an unspeakable tragedy to hear about your friend's daughter , someone so young with such commitment.Good to hear you are still campaigning Barbara. Good luck.
      Much love xxx


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