Showing posts with label badd. Show all posts
Showing posts with label badd. Show all posts

Tuesday, 1 May 2012

Guest post: Disability benefits and the self-made mouth #badd2012

This is a guest post from @indigojo_uk that originally appeared here. It is reproduced here as part of Blogging Against Disablism Day 2012 as it's a write up about a disablist appearing on the radio decrying benefit claimants.


Last Saturday night, there was a debate on the Stephen Nolan show, a late-night phone-in on the BBC station Radio 5 Live, in which the former Apprentice contestant Katie Hopkins, who styles herself “the only candidate to say ‘no’ to Sir Alan” [Alan Sugar of Amstrad, who runs the TV series, The Apprentice], defended the government’s cuts to disability and housing benefits and Lisa “Lisybabe” Egan and one of the other callers tried to oppose her. Hopkins is clearly of the opinion that disability benefits are given out to an awful lot of people who aren’t really disabled or don’t deserve them, as shown by this tweet:



Her stance was that people need to rely on their own resources rather than the state as we live in “austere” times, a line that she trotted out again when Lisa reminded her that people had paid National Insurance and that the whole idea of an insurance scheme is that it pays out when things go wrong. As for housing benefit, she said she did not see why the state should pay for people to live in the south-east, without apparently realising that the majority of housing benefit recipients are actually in work. She also posted this rant about child benefits on her blog, claiming (without the slightest evidence, of course) that “for so many of our poorer families in this country the child does not benefit at all – but rather the overweight mother guzzling McDonalds with her large brown Primark bag bulging at her feet”. You can listen to the show here for the next week. (For non-British readers: a Primark bag does not signify affluence.)

The issue of housing benefit is not the main concern here, except to state that the majority of recipients are in fact in work, and much of it pays for the shortage of affordable housing stock, the political decision to sell off council houses, and the runaway house price inflation caused by the credit boom which ended in 2008. Disability benefits are a burden society has always had in one form or another, because there have always been people whose physical or mental condition, whether temporary or permanent, either does not allow them to work, or makes them a less attractive proposition to employers for one reason or another. There are two separate categories of disability benefit: the Disability Living Allowance, which covers the cost of being disabled (such as for care and mobility aids) and is paid regardless of whether the recipient is working — indeed, it may help them remain in work — and the former Incapacity Benefit, which supported people who were unable to work, whether due to illness or a complication of their disability. Many of those who currently receive DLA would previously have been institutionalised, a practice which ended because the public realised that there were rampant abuses, the care was often impersonal, taking no account of people’s needs and abilities, and there was little dignity or privacy in many of them, besides the fact that the vast majority of people do not need to be housed apart from their families and the community. They were paid for out of state expense as well, and the land they stood on is now in many cases prime real estate and the grand buildings have been demolished or converted into luxury flats, so a return to that is going to be extremely expensive as well as unsatisfactory for all concerned.

Hopkins introduced herself by saying that “as a taxpayer” it had become obvious to her that people could live where they choose, have as many children as they choose, and smoke if they choose and have the state pay for the consequences of that, and that benefits should be a privilege and that people should “look to themselves” rather than the state to provide for them. She also invited the others to come with her on “claimants’ day” to the benefit office to see people collecting their benefits in their pyjamas. (I was on Job Seekers’ Allowance for two years and I almost never saw people in the Job Centre in their pyjamas.) Lisa asked her if, in the event of her getting cancer or having an accident, she would try to use the national insurance contributions she had paid, and Hopkins replied no, that she had savings that would provide for her family in such circumstances, money she had made by “grafting” and getting up at 5:30am every morning to provide for her family. Further enquiries reveal that Hopkins has epilepsy, and if she expects everyone to rely on themselves rather than the state, she should explain whether she has used the NHS to provide either the medication or the care she needs such as consultations to decide which medications to take and so on, and hospitalisation in the event of a severe seizure. In any case, she is not the only one who gets up at that time or earlier, and the majority of us do not make a lot of money because our jobs do not pay us that much. Hopkins got lucky; she does not mention on her website that she invented anything or has actually run a business doing anything other than selling advice to other businesspeople and public speaking. She is, in other words, a professional mouth, someone with opinions who gets paid for them.

When Egan asked her if she really was so cruel as to insist that people with cancer not receive help from the state, she fell back on her claim that the benefit system was too generous. She claimed that the people she “accosts” in their pyjamas get “home allowance” of up to £400, job seekers’ allowance, disability allowance “although they’ve managed to walk very well to the job centre”, and that it makes it not worth your while to work part-time. In fact, having been on JSA, the last time I received it, it was about £65 per week, which is about a day and a half’s average pay and just enough to buy the bare essentials for a week with. The reason it is “not worth your while to work” is because the money is deducted from your allowance and the allowance is stopped if you have two days’ work that week, even if it is a one-off booking through an agency during a slump, so unless you get a permanent job or a prospect of a lot of casual work, accepting a work booking could well leave you worse off. This is simply a consequence of the version of means testing that is used for JSA, and it is one of a number of circumstances in which means testing is a proven disincentive to work.

Nobody really confronted Hopkins with why some benefits need to be paid, and disability benefits in particular. We either pay for people with disabilities to live at home, and for the necessary adaptations and home care arrangements, or we pay for them to live in a care facility, when the land is bought, and they’re built, and all the cooks, cleaners, nurses, managers and others are hired, at huge expense — there is no third option, unless you count leaving them to die or leaving them to beg on the streets. Some people with disabilities can work, and others can if they are provided with some assistance, or if people help them to find a niche they can cope with working in, or helps them through (or past) the interview process, and the benefits made to these people may be more than recouped in the taxes they pay because they are then able to work. Others cannot, either because they do not have the intellectual capacity, or because their physical limitations make it impractical, or because their health complications or mental health problems mean they will not be able to work reliably, or because prejudice or inconvenience means people will not hire them. Of course, some people with disabilities are very wealthy and can afford to pay for care themselves, and some can run their own business, but this is not the majority and the costs of being disabled or of having a long-term medical condition add considerably to the cost of living, which is why we have a health service and a welfare system.

Hopkins clearly does not know much about what she is talking about here, only that she doesn’t want to pay to finance anyone else’s lifestyle. She promotes herself as some sort of “self-made”, self-employed person who “tells it like it is” as a social commentator and public speaker (reinforcing her “tough” image by boasting that she went to the Sandhurst military officers’ academy), but on this evidence that seems to consist of making bigoted and ill-informed comments that might go down well with all the well-paid drunks at a corporate party but do not add much to this discussion. There is a lot of talk about scroungers in pyjamas claiming benefits that were enough to live on comfortably without working, yet no solution has been given as to how to get the idlers off benefits without impoverishing people who are in real need and are unable to work; the government did not come up with one and neither has she. Yet again, British talk radio allows a serious and important debate to descend into a slanging match by giving undue prominence to an opinionated but uninformed guest — at the expense of the licence fee payer!

Image source: The Sun.

Tuesday, 3 May 2011

#badd2011 Round-up post

Here's a collection of this year's Blogging Against Disablism Day posts that are about benefits or care funding in the UK.

Lets start with the 3 posts we hosted here on WtB. Firstly Goldfish - who organises and hosts BADD every year - posted a vlog about "people like me" (and with excellent outtakes including a fascination with ears). Then David wrote about integrity, honesty, objectivity and impartiality. The final WtB post for the day was mine on the subject of vulnerability and how the government keeps talking about how they want to protect the "most vulnerable" while actually creating vulnerability.

WtB writers also wrote about WtB-relevant issues on our own blogs. Kaliya used the characters and plotlines from the Harry Potter books as a metaphor for the political position in Britain today. David wrote about how politicians and newspapers picking on disabled benefits claimants has become socially acceptable. My personal post was mostly a self-indulgent whinge about how I can't get a girlfriend, but I do address how the benefits system, especially the plans for ESA, makes being with me an even less attractive prospect.

Crimson Crip looked at a similar issue to David, how disablism is starting at the top with politicians and media and filtering down through our society. Kethry used recent headlines about benefit claimants to assess the media's demonisation of disabled people.

Gaina looked at how non-disabled people are the ones making decisions about us, for example non-disabled people devised the WCA, and suggests we should be excluding non-disableds from the decision-making process.

Finally psychosis & soyabeans looked at the problems with ESA and their own fears about being reassessed.

There are hundreds of BADD posts this year, which is an excellent thing. But it does mean that I can't get around to reading all of them. If you have read, or if you wrote, a BADD post about benefits and care funding in the UK (or maybe even in another country, it might be interesting to compare systems) please do post the link in the comments section.

Sunday, 1 May 2011

#badd2011 Vulnerability

The government keep banging on about how benefit reforms will still see the "most vulnerable" supported.

But what do they mean by "vulnerable"? Innately I don't think of myself as vulnerable, I'm confident and articulate enough to stand up for myself (metaphorically at least). Despite my brittle bones I've stepped into the middle of a physical fight to break it up on many an occasion because I felt the benefits of doing so outweighed any "vulnerability" on my part. (And for the record it's never resulted in me getting punched. Something about people not wanting to hit a speccy disabled girl.)

But this government, with their cuts and their propaganda, are making me vulnerable.

Is this disablism though? Abso-bleeding-lutely when so many of the cuts and so much of the hate is aimed at us.

I'm vulnerable because I'm facing a future with no income because the DWP keep deciding ill people are allegedly "fit for work". If I end up losing everything how can I go on living? Other disabled people have already killed themselves because they lost their income. I'm not suicidal at the moment, I have no reason to be. But I'm vulnerable to finding myself suicidal in the near future because of the government.

Lets imagine I do get to keep my income replacement benefit (currently IB, soon to be ESA) and housing benefit. I'm still at risk of losing my Disability Living Allowance. DLA is a benefit paid to cover some of the extra costs of being disabled. Without my DLA I won't be able to shop to get food in. I currently have a Motability car, which I will lose if I'm one of the 1 in 5 DLA claimants who'll lose their money. I know some people who don't/can't drive who use their DLA to pay for online supermarket deliveries, without my DLA that'll be out of my price range. So I'm vulnerable to, you know, starvation thanks to the government's disablist cuts.

Then there's care funding. At the moment I don't get direct payments. I've toyed with the idea of applying but because there's so much paperwork involved it's less work to just struggle with domestic tasks myself and then guzzle painkillers in a House-esque fashion afterwards. As I smash up more joints that balance will change and I'll eventually pass the tipping point where the paperwork will become the easier of the two options. I used to live in one of the few local authorities in the country that provided care packages for people assessed as having less than "substantial" needs. Not any more. It's one of the things that got cut in my local council's budget this year. So if I sustain an injury (likely what with having brittle bones) I'm vulnerable to getting completely stuck and being unable to manage simple things like cooking because the council won't give me any assistance.

Thanks to the propaganda we see daily in papers like the Daily Mail and Express - encouraged by the government with their "scrounger" rhetoric and DWP press releases filled with half truths - I'm now more vulnerable to hate crime and being falsely accused of benefit fraud.

These brutal, unnecessary, unfair and disablist cuts are creating a raft of vulnerable people like me. People who are only vulnerable because of this government's actions.

If they truly cared about protecting us they wouldn't have put us in this position in the first place.