The sick way Britain treats her sick and disabled

This is an article by Liberal blogger George Potter. It concerns the way in which sick and disabled people are treated in the UK. He asked for the article to be cross posted and I am pleased to oblige.

One of the ways that you judge a country is how it treats its poor, its old, its young and its sick. The UK fails dismally on all of these measures, with the poor getting poorer, the old dumped in underfunded private homes to rot away until they die, the young being deprived of a useful education and of suitable jobs, and the sick treated as if they are lying, cheating fraudsters stealing public funds, ironically by a group of lying cheating fraudsters who have been stealing public funds.

I'm reminded of a speech made by His Royal Highness the Duke of Rothsay, in which he said that he had always considered it to be a great privilege to be born British. Clearly he had never had to go through an Atos interview.

Tris

The main form of support which sick and disabled people receive, is called the Employment Support Allowance (ESA) which is the successor to the old Incapacity Benefit (IB). This is to help with their living costs, which tend to be much higher than those of able bodied people - the cost of petrol for regular hospital trips can quickly add up, for example.

The current system of determining eligibility for support originates with Labour who created a system based on the (incorrect) assumption that the many of those receiving IB were perfectly healthy due to Thatcher moving people onto it during the 80s in order to massage the unemployment figures.

But, while it is true that the number of people receiving IB had remained mostly static at around 3 million for twenty years, the people on it have changed. It is years since able bodied people were deliberately moved onto IB and most of them had died by the time the system was overhauled. The reason the number of claimants had remained static was because both medicine and diagnoses had improved so that people who would have died or gone undiagnosed in the past were now on the system when they hadn’t been before.

Yet this one, utterly flawed assumption, was used as the basis of the last government’s treatment of those on IB. Under the auspices of Labour’s James Purnell, a system was created whereby those seeking to claim IB had to go through an assessment process run by the private French IT company Atos.

The assessment process developed works on the basis of an interview. In this interview, claimants are asked a series of questions by interviewers reading off a points-based, tick-box system on their screen. The system offers a selection of possible answers and the interviewer has to choose the one which best fits the claimants answer. The problem is that the people who designed the assessment did not have medical knowledge of all the conditions possible, nor does the test even begin to take into account the time variant nature of many conditions.

People with time variant conditions, such as disability campaigner Sue Marsh, can’t, on her worst days, get out of bed, can't walk at all, can't eat, vomits every twenty minutes and has to shove needles into herself every 2-4 hours to control the pain and nausea. Yet, on a good day, she might actually be well enough to do most of the things an able bodied person can. But the test only concerns itself with the ability of claimants to complete basic physical tasks on the day - if Sue were assessed on one of her rare good days then she’d be deemed as needing no support whatsoever despite the fact that most days she’s in near constant pain and lacks the strength to even go on a short walk by herself. The system utterly fails people like Sue, who has recently received an assessment decision letter telling her she is perfectly healthy. And it’s not just Sue, I know of a man in a wheelchair who was classed as being as capable of moving about as an able bodied person and of a man with terminal cancer who was told he was fit to work then died three months later.

This horrendous flaw is compounded by the fact the assessment does not at any point consider the medical history of claimants. A claimant can have been diagnosed by the best medical minds on the planet and none of that would matter as no medical evidence is taken into account during the assessment process.

The new coalition government has recently replaced IB with ESA and all those on IB are now being migrated to ESA with the assumption that some of them will fail to qualify and that the welfare bill will be reduced. The DWP is already encouraging that expectation by the recent, and utterly false claim, that 75% of all those being assessed for ESA are fit to work - a figure which the Office for National Statistics has described as “misleading”.

The assessment system for ESA is identical, in all major aspects, to the assessment system for IB. Because of the flaws in the old system, appeal tribunals were set up for those dissatisfied with the decisions made by Atos. On average, 40% of decisions appealed are overturned at tribunal and this rises to 70% when those appealing are given aid and advice from the Citizen’s Advice Bureau - an organisation which is stringently critical of the flawed way in which the system operates. The cost of the appeal system has been increasing rapidly as more and more people successfully appeal incorrect decisions.

This increased cost is on top of the £100 million cost of the Atos contract - a contract which does not include any fines for the extra cost to the taxpayer when Atos get a decision wrong. But the estimated cost of fraud with regards to ESA is £25 million. So, in addition to human cost on the sick and disabled of these flaws, the system doesn’t even save money. In fact, the only cases of fraud identified so far have been discovered by special investigation teams. This is because deliberate fraudsters know how to play the system while the genuine sick and disabled do not.

On top of that, those found eligible for ESA only receive it for a maximum of 12 months if they have made a national insurance payment in the past three years - so if someone has held a job before becoming sick or disabled then they can only have support for a year. After that, the assumption is that they will have recovered and should be able to work and support themselves.

The only way they can become eligible for support again is if they end up in a situation with total assets worth less than £7,500. Only once they have entered destitution does the system consider helping them again.

And as for those put in the Work Related Activity Group (WRAG), who are put in a half way house between being fit as a fiddle and eligible for ESA, they receive partial ESA - but only subject to strict conditions that they meet exactly the same kind of requirements as able bodied unemployed people. They are expected to attend several interviews a week and meet other, similar conditions, or face stiff financial sanctions. But these are not healthy unemployed people, these are people with severe medical conditions and disabilities who need support to help them find and apply for the kind of work they are capable of doing. They need a helping hand but are made to jump through hoops or face strict punishments instead.

I wish I were making all of this up, but I’m not. The system which is supposed to support our sick and disabled really is like this. The most vulnerable people in our society really are dependent on a system as flawed and uncaring as this. A Liberal Youth sponsored motion which deals with this very issue will be debated at Lib Dem Autumn Conference on Saturday the 17th of September and I urge any Lib Dems reading this to lobby their reps to attend the debate and to back both the motion and the amendment.

George Potter