Long term unemployment: four people in their own words. And why the word “vulnerable” needs to go.

Below, I’ve posted four transcripts from interviews I’ve done with people who’ve been unemployed for several years. (Update 3 October – 5 interviews now as I’ve added another).

But a small rant first:

One of the reasons I’m posting these transcripts is that in the last week especially, we’ve not heard enough from people who’ve actually experienced long-term unemployment. We’ve heard from people who have a lot to say (and who are paid to say it) about people who are unemployed, but I feel that we could do with more from people who know the experience.

I also feel that we need to get away from some of the language that the media class uses to describe people who have these experiences. We definitely need to get away from words like “scrounger” and “workshy.” We definitely need that. But there are days (this is one) when I feel that we also need to get away from some of the crap that the so-called liberal media sprays around.

One thing I dislike, for example, is the use of words like “vulnerable” and “the poor” in reporting on people affected by austerity. (George Monbiot will even run to “the very poor” when he gets a tail wind).

I find the word “vulnerable” particularly tiring. I used it myself to begin with and then I got very tired of it. It’s patronising from that end. It sets people apart as victims – people whose life fortunes must always turn on the actions and philanthropy of the sort of well-appointed journos, etc, who like to use words like “vulnerable.” It sets people apart as Others and as objects for a bit of a sad read and middle-class pity. I’m over it. It’s become a kind of lazy media rhetoric. It doesn’t tell people’s whole stories. It certainly doesn’t tell the story of the political class that has robbed people of wages and services. And that is my point. There is nothing pathetic about the people whose stories I’ve posted below. They are simply people who, like most people, made the terminal mistake of not being born to immense privilege and of living in an era where that mistake can destroy you if you require a wage and public services.

Let’s not forget the common ground that most of us are on here. A requirement for decent housing and support services, and a shot at education, health and a reasonable retirement does not make people “vulnerable,” or “poor.” It makes people human. The mistake people have made is to present with these requirements at a time when the requirements of bankers, the Serco board, energy company chiefs, BBC executives demanding huge payoffs, overpaid media barons across the board and the likes of Chris Huhne are the priorities. That’s all austerity is. That’s our era. If you’re not born to privilege, the responsibility is all yours. If you are born to privilege, the responsibility is someone else’s. As I’ve said before: If you’re Nobody and fall into a hole, you’re left in it. If you’re Somebody and fall into a hole, David Cameron, or George Osborne, or Mark Thompson, or even Alan Rusbridger will help you up and even hand you a cheque when you’re out.

The moral of the stories below – make sure you’re born rich and/or get yourself in with the political and media classes so you can get your arse rescued if it hits the fan at some point. Otherwise – you can kiss that arse goodbye. Because the likes of Osborne will get around to you in the end and to all of us. No doubt about that in my mind at all.

To long-term unemployment, then:

John Evans, aged 60, Stroud:

“I was born in Yorkshire in Hull. I moved to Stroud when I was eight, because my dad had a job at the power station. I’ve been here ever since. I didn’t like school so I left. I got an apprenticeship making electric motors. They taught me everything I know about engineering. I wasn’t getting anywhere around here, so I went to British Aerospace in Preston. I was married, but my wife didn’t like it there, so I transferred. That was good, but the travelling was a lot and then they started putting me on nights which I didn’t like, so I moved into another job. I ended up staying in that job for 12 years.”

“I got made redundant and then got another job. They made flow metres – big tubes with magnets. I had my own department in the model shop. Somebody would come up with a design on a fag packet and you’d make it for them.

“But it was the model shop. Sometimes, we had so much work that we didn’t know what to do with it and sometimes it was a down period. You get made redundant. I got used to it. I got a glowing reference. I did a little bit of part time work, a bit of hacking, but nobody wants to know at my age. Then it gets really hard. You do part-time work and you get yelled at [by the jobcentre] for doing that.

“I went into the job centre once and I said – “I went for a job and I was told I was too old. He [the jobcentre worker] said – “well, that’s ageist. You can do them for that.” “I said – well, it’s not my place to do them. I said I won’t take it any further because being a smaller town word gets around.

“I had my own house and I was married, but the nice lady decided that she wanted to go with someone else and so I had to sell the house. Then I heard that my landlord had some vacancies and I had to go and see him and give me a place. I live in a B&B. It’s not very good. I have a room. With a shared bathroom and toilet. It’s a room with a bed and a TV with a microwave which is my own. Eight people live in my house.

“I’m on jobseekers’ at the moment. I used to do Ring & Ride. It was voluntary, which I enjoyed – taking out people to places and appointments. I told the job centre that I was doing this and I got told off because on the three days that I did it – Wednesday, Thursday and Friday – I got told that I wasn’t actively seeking work and I couldn’t do it. You couldn’t make it up. I wasn’t not looking for work. It was just that I was doing that work. You can’t look for work 24-7 if you want to do something… I don’t know. I get worried because you hand in the [jobsearch] sheets and you don’t know whether they are going to stop your money or not. Then they just stop it. I just hope I get paid Friday.”

“They [the jobcentre] suggested that I went for a job as an engineer in Cheltenham. It started at six in the morning, but the first train wasn’t until seven and I would have got there at eight. So I said it was impossible to get there at that time in the morning. The answer was Move. But where do they think you’re going to find a place at our age with needing rent up front to get a place to live? The jobcentre said – “so you’re refusing? Well, we’ll have to sanction you.” But I mightn’t even get the job.”


Angela Barnes, in her 50s, Weymouth:

“I’ve been through just about every trauma in my life… I’ve been an alcoholic and raped and abused in all shapes and forms. I didn’t think I could go any lower. Human nature says there ain’t nothing lower…

“I was doing well. I had a home and I had a fiancé. I had a business. Life was good, relatively. Then I got scammed by some advertising companies, so my business started to suffer and I changed my priorities to concentrate on my partner who was also very disabled….not having the brain cells at the time to understand that if I concentrated on the business, I might have a bit more money to concentrate on him. Then, my housing benefit got mucked up. They stop and start the benefits on a whim – they do that.

“Then on the ninth of May [several years ago], I found myself out on the street and I’m like – hang on. I don’t quite understand where this has gone. My landlord decided that he wanted me out. He didn’t care if they (the housing benefit office) would pay [the rent] or if they’d backpay when they sorted it all out – [he just said] “I want you out. I want my rent.” I owed something like £1200 in rent, which was only about three or four months’ rent. He wasn’t having it. He would have got it all back – but this is what social landlords are frightened of, you know [not getting their rent], and then about 8 o’clock on the ninth of May in the evening, I suddenly found myself unexplainably out on the streets. My partner said – “Nah, that’s it,” [and he’s] gone. [So] what do I do? So after several suicide attempts, I just spent until December as a homeless person. It’s not good…

“I just spent my days wandering about. I remember one evening being sat on a bench in town and I had dark jeans on and I had white socks, because that’s all I had. When I was put on the streets, I had a couple of changes of clothes and underwear and that is all I had, plus the clothes I stood up in…I had dark jeans on and white socks and some lads come out of the nearby pub and just started cussing me. “Oh – love the socks. They’re real stylish” [she starts to cry] and I’m thinking – “why are you doing this? You don’t know me. I’ve been sat here quietly trying not to bawl my eyes out….and just getting abused.”

“I was as guilty as a young puppy. I would see a scruffy… I hate the word “tramp”. It’s an old fashioned word, but I’d see these dirty, homeless guys, drinking or whatever they were doing and I thought there was nothing that could make me go there. I think that was my first mistake, because the minute you say that you’re not going to end up there, you can be pretty sure you’re on the slide down….I think the Lord allowed me to be on the streets for as long as I was, because I had to learn how to be humble.

“[I don’t think people understand the lack of confidence]…now, [people without housing] come to me and say “We’re not getting our benefits. We need to phone the council to see if we can get on their [housing] list” and I say “okay, phone them up – you just pick the phone up and make a phone call.” [They will say] “Can you do it for me?” and that’s when I found out that [for a lot of people] it’s not just a case of picking up the phone and making a phone call.

“I do believe that if you want to learn about life, then spend an unknown indefinite time on the streets. All these stupid, idiotic studies that politicians do – you know, “I spent a week on job seekers’ allowance.” Anyone can tolerate a week if you know that it will end, but being out there and never knowing whether that this is your last day…

“I did have some issues with [getting my] benefits, but at the moment, I’m all right. They’ve taken me off incapacity benefit and got me onto ESA, but if that is going to be limited… [For other people] it’s just a nightmare. It seems that in Weymouth, benefits get stopped on a whim. My brother – his benefits get stopped just about every month. Then he gets into a place where he’s got to get crisis loans. Then if you’ve had about £1100 in crisis loans, you’re not entitled to any more. Then what do you live on?

“[Pawn-shop places]… [people] take something [there] that they’ve got, or that they’ve lifted and even then, it’s only five or ten quid that they’ve got. Then, they’ve got to buy [whatever they pawned] back at street value. My brother has done it several times and I’ve given him such a bollocking for it. I said – you don’t do that. If you’re stuck, talk to me. I’m on benefits and I haven’t got a lot to spare, but we’ll working something out…

“What really winds me up… is these stupid [Atos work capability assessment] medicals that people get sent to. You’ve got to go to them and prove you’re not well. My brother collapsed halfway through his medical. He couldn’t remember three words that were said to him at the beginning of the interview. His benefits got stopped, because he’s “fit for work.”

“[Dealing with social housing social landlords [and trying to find places for people on benefits who have nowhere to live] – it’s impossible. I’ve got three landlords that I can use [to help people into housing] and two I can use regularly. They’re at all various stages of good, bad and indifferent landlords. I do work really hard to vet the tenants – to make sure I’m putting the right tenant with the right landlord, but yeah, it’s hard. I need more landlords, I really do… I know the issues that they have – [they worry that because] people [social housing tenants] aren’t paying [rent] out of their own pockets, there is always a danger that they won’t look after the place properly and if they’ve got addictions or mental health problems that just increases the burden. Housing benefit is always [being] mucking about – you know, they pay three months in arrears and all that sort of stuff.”

Darren Bayliss, Cheltenham-Stroud:

“I’m trying to apply for employment and support allowance. I’m getting that for mental health issues and addiction drug dependency. I’m on antidepressants at the moment. My health is at risk. I’ve gone from ten stone one to eight and a half stone in four weeks, living on the streets. I lived in London on the streets for three years. At half six every morning, the cleaners at the back of the Savoy come down, and the council, and moved you on. The daycentre didn’t open until eight, so you just had to walk around.

“I’ve had my ESA suspended. I was using a care-of address and they’ve got me down at the social as actually living there. Me and my girlfriend were staying at this bloke’s house and the lady next door had grief with him… they contacted the social and they suspended my pay, saying that I’m paying in for my girlfriend, so I’ve had no money for the last eight weeks. I told them it was a care-of address.

“I live in the tent [at the moment]. There are two drinkers [in the same area] but they’re okay. You stay in numbers, you’re better in numbers. The tent’s dry, but the only problem is that it’s on a dry riverbed, so when the rain comes down, it’s all mud. It’s all mud. They won’t give us accommodation until we’ve been here for 12 months, because we’ve got no local connection. But after 12 months, we have. I walked from Cheltenham to here about three, four months ago. I walked 17 miles and I slept in a bus stop. I went to the Salvation from there and they gave me a lift to this place.

“I left Cheltenham because I wanted to get clean off the heroin. I’ve got a script. I have been clean for four weeks – stone cold turkey, but I done it. You thought that would have been the worst time to use, really. I’m getting on an emergency script next week. They’ve got me on these meetings – anger management, self-awareness, acupuncture. I get suicidal thoughts and things like that. Then, I’m going to rehab.

“Don’t get much hassle with [living in] the tent. There’s a bloke who comes down every morning and brings me a big flask of coffee. People have brought down a little camping stove, a little gas flask, and say “you need it more than me” and brought down pots and pans, but I do need to get off the streets. That’s a priority really. I stink of fire all the time [because of cooking outdoors]. I’m not usually like this. I’m only dirty because I’m sleeping on the streets and the fire.

“I was on heroin the first time round for about 12 years. Then I got clean. I was on methadone but I stopped that. That made me really ill. Then I got clean, but then I went on Suboxone. Then, I relapsed, because I went to a friend’s funeral who died of an overdose. When I came to Stroud, I had a raging habit, but since I’ve been here, I’ve been working with Turning Point.”


Dan K (Weymouth, in his late 40s. Name changed):

“I lost my job and I couldn’t afford to pay my rent… and [like] that Norman Tebbit said, I got on my bike and went looking for work but ultimately there was…well yeah, there ain’t no jobs out there.”

“That’s the economy. The government is in charge of the economy and it does what it does. We had the computer boom and there was plenty of cheap money going… I was sleeping rough. That is my background – I know IT and there is military experience in that background. In my lifetime, I’ve seen all the different technology. My uncle used to work on Concorde.”

“Council houses – they let people buy houses and then they sold them off without replacing them. [That’s the problem]. You can’t base an economy on just a few houses and shops. We used to build ships and things.

“I just put in for a job the other day [Dan must apply for jobs to keep collecting jobseekers’ allowance]. It’s for a job in IT.

“You can’t imagine it [my situation], can you – like, everything you have got now is gone. You’ve got no money. You’ve got to go through the system and trying to get more – it’s really hard. I had a meeting yesterday at the job club and as soon as you change anything, your housing benefit is gone…so I went round to the council, because they put me off ESA and put me back onto jobseekers’ [Dan was not sure what I meant when I told him that people on Employment Support Allowance were being reassessed and are put on JSA if found fit for work]. I went three weeks without any money. I went to the council and three bloody forms I had to fill in. I said – Excuse me: how many trees [are you killing]? I can’t wait for you to wipe out the rainforest, because I won’t have to worry about breathing any more…

“[In the end], the British Legion helped me out and got me in a room into a house. [Before that] I was helped out by a few guys – they put me in a tent for a few months. But before then, it was out in the streets wherever I could put me head down and then you have the police coming along saying “You can’t sleep there.” I actually went round to the council one morning – I was so done in because I was sleeping on the pier and it was chucking it down with rain, gale force winds and I had only had 30 minutes’ sleep because of the fucking generators going on the bastard ferry, I walked into the council and told them why don’t you take me to the hospital and give me a lethal injection.”

“Spain is at [an] 22% unemployment rate [now] and we’re going to hit 11% in the next ten years… then, your bosses are saying you have to get your job done so that they can have a bloody good life – the wealthy, this is how I see it. The government who don’t give a shit about the people, just their friends. They’ve given massive tax breaks and they’ll never spend it if they live for another 100 lifetimes. Yeah, you got people at the other end who can’t even afford to put their heating on and buy some food, that to me is… I don’t know what they call it. They’ve got to be the biggest bastards ever on the planet. They’re not kings – they don’t look after their people.”

Amen to that.


Stephen W, 54, Newcastle. Has a long term schizoprehnia diagnoses. I attended his Atos ESA assessment last year. He was found fit for work and told to apply for JSA, but then was put into the ESA support group on appeal. He has been on JSA before and there is nothing to say he won’t be put there again after further assessments. He says that his symptoms – depression, and auditory and visual hallucinations – are getting worse and cuts to services mean that he is struggling to find counselling and the regular support he needs to function. He talks a lot about isolation and is especially concerned about finding and keeping a job without regular professional support. Perhaps needless to say, he’s done best with study and work in his life at the times when he had good counselling and mental health support.

“About 30 years ago, I was diagnosed as schizophrenic. I couldn’t talk to people, including my own parents, about things that were worrying me, particularly socially, and at the first school I went to, I was told that I was a waste of space and I got bullied. In the end, my parents ended up calling in the emergency doctor and then they called in a friend of theirs who is a doctor. He advised them to get a psychiatrist he knew.

“I was given massive injections and the next thing I knew, I was on my way to the hospital. That was just before my first attempt at college and final year exams and that was stress anyway. I was in there for one and a half weeks and came back to do the last exam, but I didn’t do that, because it [the schizophrenia] started to kick in again as the effects of the medication wore off.

“Things have got better in some ways since then, but they’re not brilliant. I do have suicidal thoughts and I get really depressed, but I usually manage to talk myself out of it. Also, I made a promise to a psychiatrist as well when I was in hospital that I wouldn’t do anything stupid, but I find it very hard. I tell people that I’m a member of society, but I feel on the fringes of it, as if I’m an outlaw and not in the mainstream.

“Yes, I do hallucinate [especially at night]…I see things like giant squid and things like that…I think I’m being eaten alive…. the drugs, the Sulpiride I take, it’s got quite bad side effects in that my limbs shake every night when I go to bed and keep me up half the night anyway.

“It has basically gone on since I was 18, if not before. I’ve coped reasonably well, but there are limits to things I can do and to the desire to do them and the motivation as well. I mean, when I get tired and run down, that’s when things can kick off again.

“When I first got out of hospital, when I was 18, I was given a job by my dad, so that he could look after me day to day and see how I was doing. Since then, I have either worked part time, or gone into full time education, or basically been on training schemes, or been on the welfare state. The labelling [as someone with schizophrenia], I think stigmatises and discriminates against you in the minds of employers.

“I’m in my 50s anyway and that’s another thing against me…and what it has meant is huge great holes in my CV which have been covered by little bits of volunteering. I can’t do really physical stuff. I don’t drive because of the medication and both prescriptions say don’t drive or use machinery or use alcohol if at all drowsy. Also, the schizophrenia means that I’ve got thought disturbance, image disturbance, particularly at night.

“I’ve been on this medication since 1998. I got recommended to go to university – the university, thank god, picked me up through student services and gave me counselling every week and gave me help to write essays. Otherwise, I wouldn’t have got my degree. But I’ve rarely seen psychiatrists since 2004 and when I was at K_, the most concerned they seemed to have been was about whether I was going to use a chainsaw or not. After that, it seemed to be a succession of different psychiatrists every time who seemed to just want to go back into the past – what medication you’re on and so on.

“The community mental health team is overwhelmed…I’m not as ill as others, I acknowledge that, but I do think that I need some help and I get very little. I’ve had to fight for what I’ve got so far, even when I’ve had a relapse and the police have been called and things like that.

“Here, you have got to go through your GP to get a meeting with a psychiatrist…I was originally referred to the cognitive behavioural therapy team. They didn’t want to know, because I had a diagnosis with schizophrenia, so they sent me back to the GP. They sent me to the community mental health team and they originally didn’t want to know and I went back to the GP again and on the second time of asking, they took me seriously. It’s taken eight months of being messed around and of getting worse and worse and feeling more anxious…

“Originally, I was on income support with an incapacity element – this was years ago, so my memory is slightly faulty. This will be my third Atos assessment. I know people who have had four or more over four years – one a year basically and tribunals as well and still been asked back..

“I got a work capability assessment under New Labour back in 2008 and I treated it like a job interview, because I didn’t know what to expect. There was nothing in [my town back then] to advise me and the job centre would have just been a joke. I didn’t know about the disability forum, which was just starting out on this thing. The whole system has become more onerous since the coalition got in and I’ve been yo-yoing between jobseekers’ and employment support allowance. If there’s someone who has asked me to do something, someone in authority, I usually try and do that thing even if I know it is going to hurt me or make me stiff. I usually try and do my best. And that’s what they are counting on – people not knowing the system.

“I would like to see someone to talk to on a regular basis, just for motivation and reassurance. And to be able to have enough a personal budget to employ someone like a gardener and a cleaner because I’m conscious of the fact that the neighbours have done most of the garden and I find mowing the lawn very hard – not just physically, but mentally – getting round to it and doing it. Also, just someone to pop in on a fairly regular basis, just once or twice a month, just to see how I was doing.

“I’d also like a psychiatrist just sort of in the background in case things get worse, but I find that making appointments with the doctor just horrendously difficult. You can’t always get an appointment straight away and frequently, I need one pretty quickly.

“I’ve got a two bedrooom house, but it’s it’s in need of a clean. You know, I’m not very good at remembering to do things like the dishes and clothes washing on a regular basis.

“Having the ESA/JSA is very important. I still get help which is organised by my family, but that’s to pay the bills. It’s never been good since the new government come in and made the conditions harder and harder. You’ve got to jump through more hoops to justify yourself and you’re looked upon as a scrounger and people ask why you’re not working. They just don’t seem to have any idea what it’s like.

“At my second Atos appointment, I didn’t go with anyone. That was a mistake. I’ve learned now. I got help to prepare all the documents and that sort of thing with the disability forum here and I was told what to take. I have done [the same] this time as well, but the first one I did, I had no idea what to expect and no idea about anything – no idea about medical evidence. I thought you took a note of what your GP said, but they seemed to ignore that, so that’s why I’ve made a point this time of getting back to the community mental health team and secondary services because I think they might pay a bit more attention to them than to a GP.

“The way I feel varies. Some days I just can’t be bothered to get out of bed – I just feel so low. Sometimes, that goes and I physically can’t get out of bed. Even the GP reckoned years ago that I couldn’t handle stress very well, so he was very surprised when I went to university. I always got a bit of extra time, because they were very good – they acknowledged that I had difficulties and they worked around them. I just wish employers would, because I reckon that I’ll be found fit for work again. It’s got to be limited – it’s got to be limited travel, no more than 20 hours a week and less than an hour a day travel, but beggars can’t be choosers, I’m afraid.

“I think I’ll need a bit of advice after [his next work capability assessment], to see what I’m going to do – whether I’m going to appeal. I certainly will if I get no points at all. I need 15. If they say there’s nothing wrong with you, I will appeal, but if they say there is – you have got this health issue but we can work around it, I’ll probably go to the disability employment advisor again. I’ll have to go through jobseekers’ again. Otherwise, I will appeal for my employment support allowance if they say there is nothing wrong with me.

“I just think that the whole welfare state and people who depend on it are being attacked wrongly and the elite bankers are getting away with it – fraudulent things, but getting a mere slap across the wrists and I think it’s totally wrong, it’s immoral. Neither New labour or the Tories are going to rapidly change this. There’s one law for the rich and one law for the poor and I just happen to be in the second bracket.

“I would hate to think where I’d be in six months’ time without support. I think I would be back in hospital at the very least, if not on my deathbed. It’s been a constant struggle anyway, with what limited support I get and I’m trying to get more, but if I didn’t have what I’ve got I think it’d be even worse and I think I’d be on far more medication.

“The help I’ve got at the moment – well, I come here [to a voluntary support organisation for people with mental health problems] as often as I can. I go and see my GP when I think I need to, but that’s difficult, trying to get an appointment. I want to be able to almost on a switch of a button talk to someone, but you’ve got to plan it and even then, there are lots of other people with other problems trying to access their GP as well. I think I need a visit from a carer, or a social worker, a couple of times a month just to see how I’m getting on, but with these cuts I don’t think I’ll get that. And as I say, a fairly regular meeting with a psychiatrist, or a self help group.

“The report I got back said that I am a very passive individual. I thought – oh what else? Then it went through the descriptors and it was like – none of this applies sort of thing and that’s the reason that I appealed. I eventually got to the tribunal and during that wait, I was getting worse.”

9 thoughts on “Long term unemployment: four people in their own words. And why the word “vulnerable” needs to go.

  1. That was a good read, Kate. A bit difficult to follow in parts, but definitely, definitely important to get the voices of those actually affected out there. And I agree with you regarding the word “vulnerability”.

    Makes me want to do go into social research again but the academic stuff wasn’t going anywhere, didn’t seem to be actually achieving anything.

    How do you get into the position of conducting the interviews, so that you can put the voices of people affected out there?


    • It’s a combination of things. I saved up money for a few years so that I could afford to get around to different parts of the country and meet people from all over. Then I also contact people who run different services and ask if I can come and visit and talk to people – Soulfood in Weymouth and the Marah Trust in Stroud for these articles. Often I’ll also approach people I meet here and there and we start to talk. The best part is sitting down and talking to people for ages. I really like that. Some of the guys I spoke to in Stroud were sitting having a few drinks in the churchyard where an anti-cuts meeting was taking place so we hung out there for a while and chatted. Things like that really. I do really like talking with people for hours. It’s my favourite thing.

  2. Spot on Kate many years ago I went to the Eden project it showed ways in which the world lives you know what if it was followed nobody be hungry sadly real life ain’t this bringing my kids up like most family on a budget I would every year take my kids up to London usually to look in self ridges window at the Christmas displays lights etc then have burger whatever this was the treat always we had penny pot coppers put in pots used to collect through the year made my kids learn talk not aaaa shame just like general conversation same as you talk to any we all s..t f..t and cry and where I live on the seafront there is a man I think he happy to live as he does and gets help past 7 years always talk he is a very interesting man another guy I worked with years ago he was a kp in a hotel where I worked omg other staff other staff so unkind one time I saw him coming out of staff accommodation suited and booted very smart waved said hello next day at work on coffee break he was talking and explained day before he was off to publishers and I said good for you to which he said haven’t always been a kp Brigitte and he explained he had a high powered job in the city and at 42 his parents died he said he totally cracked and ended up on the streets so no ifs and butts could happen to any as I have learnt and pleeeeeese not the vulnerable word it’s the system as I have learnt that has brought me to saying I don’t want to live and as asked I now expect answers because for sure I ain’t ever walking this road again

  3. First, I’d like to say thank you Kate (hope you don’t mind me calling you that) and to the other comments above, hope things work out for you. I am 61 in a few weeks, should be on my state pension now – at least then, I needn’t worry too much financially. I failed my 11 plus (only maths I was told – my worse subject. However, I did gain 8 CSE’s (failed maths again), got paid work in an office, did evening class and day release for commerce, typing, shorthand and English. I had to leave them though for various reasons. Got a better job in insurance, got made redundant from there, but, luckily got a further job – jobs were easy to get in 1969. Was doing well for 5 years, got married but left when I was 8 months pregnant. Brought up my children (husband worked) and my youngest child died aged 23 months. I was 6 and a half months pregnant then. Unfortunately, my marriage broke down 6 years later, eventually met someone else and was in the role of “housewife”. I didn’t need to work, or rather, go out to work but didn’t get any benefits (didn’t know anything about them) as my new partner had a good job as an engineer. When, my youngest daughter was 15, I went back to work but, due to lack of confidence, only took low paid work. I ended up working as a care assistant, then – as I had a car – looked after the vulnerable in the community. I worked 62 hours a week, every Christmas, bank holidays etc. However, my partner couldn’t cope with my working long hours and he started drinking heavily and became very abusive, physically and mentally. I had to leave and spent some time at a refuge and then, lived in a private flat. At first, it was ok, but then, my ex-partner died and, as we hadn’t been married, found I had no rights to his property, assets and his will was invalid, couldn’t claim any of his private pension or widow’s pension. After a year, I had no savings left and had to sell my car, give up work through ill health. So, I went on benefit but still had to pay shortfall towards rent etc. I became very ill then and spent time in hospital. I eventually got council accommodation but still have only second hand furnishings. I got a part time job but was told by benifit agency, I couldn’t keep it as I would lose all benefit. This became the pattern of my life. I looked for work but couldn’t get full time work, no matter how hard I tried. I went to college part time, did little City & Guild courses, all to help my CV. My illness is getting worse and my GP is arranging for me to go for Cognitive therapy. Atos refused my doctor’s letter explaining I was in no situation for work, even though I was in a very bad way when I was there. They said I was well and I have just been told by the tribunal the same thing. I am appealing again as I really couldn’t live with all the sanctions being imposed by the government. I am almost housebound and don’t see much of my family. I am now on no benefit as BA are telling me different things, one is that I have to go on JSA and yet another, that I can go back on ESA. I took legal advice at the CAB who told me as long as I send in a new medical certificate and am applying to the second tier of the tribunal. How can I get a full time job at my age? I am now suffering real physical symptoms and can’t cope with all of this.

  4. Its really important that real peoples experiences get heard. All too often people make assumptions just because the’ve been luck and fortunate, but it doesn’t take much going wrong in your life for you to end up at the bottom of the heap. I agree about the word “vulnerability” “poor” “scrounger” and “workshy.”
    I also would like to get rid of the new Tory term “something for nothing culture”. This is because with many people it isn’t something for nothing, The’ve worked and paid their NI and taxes, they are recieving contribution benefit (part of the agreement of working and paying your taxes and stamp) that may be topped up slightly if they are a couple or got children into income based( or means tested) benefits that they are entitled to the safety net of benefits when you fall on hard times, so its not something for nothing its something for the money you’ve already given to the governement.

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