Atos/WCA documentary's

Did anyone see the dispatches or panorama documentaries last week?

Very interesting to see Atos & DWP lies exposed, its a shame that most people won't care and allow Chris "Mengele" Grayling to get away with it.

  • Goatworshiper said:

    My point being if you had all of that evidence when applying for IB you might have got on it? I completely accept that it absurd not to accept Crohns disease as being unfit to work.

    That's just it - I wasn't unfit for work!

    I also wasn't fit to be on JSA though.

    And that was the whole problem with the old system - it was too black or white - you were either 'fit to actively seek work' or you were 'incapable of work' - I didn't fit into either of those boxes.

    I'd say I was also not unfit for work when I applied for ESA, although the additional stress of being on JSA in the intervening time had made me much closer to not being fit for work.

    However, after appeal, I was awarded ESA and, rightly, placed in the Work Related activity group.

    It was only after that that I had my diagnosis of AS, so I think it had little bearing on either claims failure and success.

    In fact the main difference the AS diagnosis has made has been for my eligibility for DLA.

    I also applied for DLA after I first applied for ESA, and iirc, after I had won the appeal - and was turned down.

    However I was sent ESA and DLA forms shortly after my AS diagnosis (because it was 6 months after the appeal), and this time was awarded lowest rate on both components of DLA.

    It may have helped with ESA, granted, as I've not needed to appeal since the diagnosis.

  • Hope said:

    Yep, he was the man. A homophobe  too.

    So he's just missing a bit of Anti-Semitism and Racism Undecided

  • Yep, he was the man. A homophobe  too.

  • Scorpion0x17 said:

    I know in another thread you mentioned that you have AS and Crohns. But you were rejected for Crohns alone, did you ever submit a claim under the old system which included both lots of circumstances?

    No, I was only diagnosed with AS about 2 years ago - not only after ESA was introduced, but also after I successfully appealed the initial rejection of my ESA claim (which was based on Crohn's alone - I didn't get a diagnosis of AS until after the appeal in fact).

    When I tried claiming IB I didn't even get as far as an assessment, and it was clear, or at seemed clear to me at the time, that appealing that decision would have been utterly pointless.

    I can see how someone who succefully claimed IB pre-ESA might see the new system as worse, however ESA seems a much better system than IB, if, like me, you had been stuck on the other side of the 'fit-for-work' fence, getting more and more depressed because the system simply refused to acknowledge your need for support, whilst simultaneously putting you under more and more pressure (despite it being known that Crohn's is made worse by stress) to meet their demands.

    [/quote]

    My point being if you had all of that evidence when applying for IB you might have got on it? I completely accept that it absurd not to accept Crohns disease as being unfit to work.

    Join the chase...I think Atos won the contract because the alternative was G4$. So sorry to here about your struggles. Unfortunately it seems as though this is way the goverment and specifically Chris "Mengele" Grayling wants to play it.

    On a side note, Isnt Chris "Mengele" Grayling the fella who said B&B owners should have the right not to allow homosexuals to have a room? 

  • Thought I'd just add my experiences here.

    I have had 3 previous assessments. 2 needed to be appealed. 1 said there was literally NOTHING wrong with me. The first assessment I asked for "reconsideration" (I was told this was the first stage of appeal anyway, and that I would still get basic payments). After 4 months it was decided, but I wasn't paid at all during that time. I did get a rebate, but the point is they don't know their own system. During the first assessment, I was asked for names and addresses of all my specialists - I was being treated for depression only at this time, but gave them GP, consultant psychiatrist, consultant psychologist and CPN. Having turned me down, I found out they hadn't contacted ANY of those people to ask about my health.
    After that horrible experience, I took my CPN to my second assessment. She had to take time out of her working day to come with me as I was far too anxious to drive, and am too anxious in general to use public transport. This assessment was successful.
    Third assessment - CPN also with me. Cried for over half the interview. Didn't look the assessor in the eye once. Leg was shaking throughout. Was told my behaviour was normal?? Refused again, had to appeal. Took another 4 months, but at least got basic pay this time, as we went straight to appeal, and got a rebate for the difference.
    It's worth saying at this point that over the time these interviews took place, I was placed in the "work related activity group" - the group designed to get people back to work with help. I got 1 letter right at the beginning saying I would get a personal advisor to talk to and to help me. I never heard any more. Didn't get a personal advisor. Was never contacted about what help I'd need to work. Was never contacted in any way about what work I could do or anything at all.
    After 2nd appeal successful, I inexplicably got a letter saying I had been moved from work related activity to "support group" - the group where they don't expect you to work again. I fully expect to work again, just not right now. No explanation given for why it was changed.
    Due to the indescribable level of stress caused by previous experiences, I was advised to ask for a home visit this time instead of going to the strange place with strange people which works me up. After 4 months (see a theme here) of waiting, finally got told when my appointment would be. Had said in the form we couldn't do tues or thurs in general because I needed my mum with me and she worked those days. Appt organised for a tuesday. Rang up to change this and was told it would count as a cancellation and any more would stop my benefits. My mum (who was speaking for me as I hate phones) calmly said she didn't think it should count as a cancellation as we'd already said we couldn't do those days for legit reasons. Operator called my mum arsey. My mother has never in her life been arsey, and certainly wasn't this time as I was listening to the conversation.

    Had my home visit 2 weeks ago. Freaking out every time the phone goes in case it's them stopping my benefits which - on the balance of probabilities - they will be. This is the first one since my diagnosis though, so you never know. 

    All in all, I'm not at all surprised that people have killed themselves over these assessments. I would have hoped the government had enough humanity to realise that any system that makes people kill themselves is not appropriate. But clearly not - they've just awarded new contracts to Atos :(

  • The only good thing about ESA is there being a group for people who might be able to work in the future. However, it's unrealistic. If you're permantely disabled and can't work now, how can you work in a year or so?

  • Goatworshiper said:

    I know in another thread you mentioned that you have AS and Crohns. But you were rejected for Crohns alone, did you ever submit a claim under the old system which included both lots of circumstances?

    No, I was only diagnosed with AS about 2 years ago - not only after ESA was introduced, but also after I successfully appealed the initial rejection of my ESA claim (which was based on Crohn's alone - I didn't get a diagnosis of AS until after the appeal in fact).

    When I tried claiming IB I didn't even get as far as an assessment, and it was clear, or at seemed clear to me at the time, that appealing that decision would have been utterly pointless.

    I can see how someone who succefully claimed IB pre-ESA might see the new system as worse, however ESA seems a much better system than IB, if, like me, you had been stuck on the other side of the 'fit-for-work' fence, getting more and more depressed because the system simply refused to acknowledge your need for support, whilst simultaneously putting you under more and more pressure (despite it being known that Crohn's is made worse by stress) to meet their demands.

  • I know in another thread you mentioned that you have AS and Crohns. But you were rejected for Crohns alone, did you ever submit a claim under the old system which included both lots of circumstances?

    I completely agree about JSA, it's barely fit for a person with nothing going on let alone problems and sometimes of a hidden nature. However I can remember in 2003 they Job Center staff threating me directly that I could lose my benifit if I refused to go canoe'ing. I was argueing that I felt unsafe in water with people I didn't know (who to be honest were very rough as they were in other "new deal" groups with me).

  • Goatworshiper said:

    my take on the situation

    Yes it is. But it is merely a perception. Just as mine is too. Is right that I should be attacked just becuase my perception of the situation is different to yours?

    [/quote]

    I wasn't aware that anyone attacked you in this thread? I have attacked the government, Atos(ers) and ideology of the system.[/quote]

    It may not have been intended as an attack, but some of the posts have certainly come across, to me, that way.

    Goatworshiper said:
    Do you honestly view the new system as being better than the old?

    Yes. Under the old system I was deemed 'fit to work' and therefore forced to claim JSA, and endure a system that was not even designed to cater for my needs.

    Under ESA they at least recognise that whilst I wish to work, I need support in achieveing that goal, and I am no subjected to the oppressive regime of the JobCenter.

    Goatworshiper said:
    The idea may be appealling, but in my view and experience it's just propaganda that keeps disabled rights campaigners and tax payers quiet.

    That is not my experience.

    If ESA had not come in when it did, I would probably be at best homeless, at worst dead.

    So, yeah, to me, that makes the new system better.

    Goatworshiper said:
    .....And the new workfare scheme reminds me of the old extra tenner schemes (ET) but without the tenner.

    The ESA schemes are not manditory, and one will not have one's benefit cut, or completely withdrawn, if one didn't attend.

    That is, and was, the case when on JSA.

  • Scorpion0x17 said:

    my take on the situation

    Yes it is. But it is merely a perception. Just as mine is too. Is right that I should be attacked just becuase my perception of the situation is different to yours?

    [/quote]

    I wasn't aware that anyone attacked you in this thread? I have attacked the government, Atos(ers) and ideology of the system.

    Do you honestly view the new system as being better than the old?

    The idea may be appealling, but in my view and experience it's just propaganda that keeps disabled rights campaigners and tax payers quiet.

    .....And the new workfare scheme reminds me of the old extra tenner schemes (ET) but without the tenner.

  • The idea of ESA is to get as many people off benefits as possible. They simply don't care any more. The descriptors have nothing to do with work in the slightest. There is nothing about actually getting up at a reasonable time, getting dressed, etc. and being able to get out of the door and get to work safely.

  • Goatworshiper said:
    my take on the situation

    Yes it is. But it is merely a perception. Just as mine is too. Is right that I should be attacked just becuase my perception of the situation is different to yours?

  • some one said:

    Again I will try to explain, I never made any direct comparison between jews, gas chambers and this issue, It was not my analogy,

    No, but you decided to borrow it to back up your argument.

    some one said:

    When it comes to atos “interviews”, I maintain its the majority but not necessarily not “all”

    Well, neither of us can, or do, know whether it is the majority, some, or a few.

    And, if you were indeed not meaning to tar all assessors with the same brush, which it certainly appeared you were doing, then I appologise for reading that in what you said.

    some one said:

    I don't know just how many times I need to repeat this simple idea for you to get it, but I'll try again

    Theres no need to be rude over it[/quote]

    I was merely stating a fact. I was not intending to be rude.

    some one said:
    far too many people are being treated unfairly for no reason , I hope we can at least agree on that and leave it there

    Yes, I can agree with you on that.

  • Scorpion0x17 said:

    It's like saying "I have a red apple, and I've only ever seen red apples, therefore all apples must be red".

    You simply can not take one, a hundred, or even a thousand, examples of a lack of compassion and simply extrapolate that out to all cases.

    But there is a whole world of difference between some jerk being a jerk in a WCA, and someone carting off jews, gays, and the disabled to be gassed, during WWII.

    When we're being carted of to the gas chambers, then I'll agree with you.

    It is also an offense to those that did die at the hands the nazi machine during the holocaust.

    Now, I'm sure you know that neither of us has access to the information, or the resources, to actually conduct such research in the proper manner, so suggesting such a thing is really quite pointless.

    Labelling all WCA assessors as discompassionate is as bad as labelling all benefits claiments as scroungers.

    Again I will try to explain, I never made any direct comparison between jews, gas chambers and this issue, It was not my analogy,

    I have never mentioned either of those words until now in response to you, I already explained my comparison, if I didn’t make it clear I am sorry about that, but I am trying to explain something via computer here and you know for us neurotypicals its not always that easy to do Laughing

    My comparison was on the issue of compassion and the justification of them ‘doing their job’ not anything else, and as the comparison was not mine to begin with i dont feel i "offended" anyone, it was there, i saw it, if that is an offense i cant do much about that

    I have had several of these “interviews” over the last few years, with different “interviewers” and I had many long before they changed, I have been on long term disability for many years, so I kinda know a wee bit about when and what changed about the system, and the people interviewing

    And so Im not taking “one” example, but it doesn’t really matter, you have your views on it, and you can only go based on your experience

    To be honest, I had to research that to appeal my own claim, its easy, type in atos/complaints/interview you get thousands of them, all saying the same things, or visit your local mp, who will no doubt have been inundated, as ours had said he was, with atos “interview” complaints

    This isn’t a “one off or a few” we all wish it was, this has been happening all over Britain

    I have to point out, probably a bit pedantically, that I have never said “all” about atos, I said all in general, about the system and “all” of these issues, I apologise if I didn’t make that clear it was in reference you having said this “I mean when the politicians say one thing, the DWP another, and Atos yet another, who are you meant to believe?

    When it comes to atos “interviews”, I maintain its the majority but not necessarily not “all”


    Scorpion0x17 said:

    I don't know just how many times I need to repeat this simple idea for you to get it, but I'll try again

    Theres no need to be rude over it

    But, if they are hired and told what to do, it seems to be logical that they will ,as a majority ,do it, as we both agree its their job to do it, they will be fired if they don’t, and thats even if its not the way they normally are

    So whether its “all” literally or not, is far too many, and far too many people are being treated unfairly for no reason , I hope we can at least agree on that and leave it there

    Smile

  • You are too unwell to work at this point in time, therefore we will leave you alone for you to have sufficient respite. If you feel you are capable of work, you can end you claim and start employment. Whilst on this benifit you can go to college, university or attend a course that will help your health and you chances of sustainable employment. However should you not acheive due to your health you can fall back on to you Incapacity benifit. You will have a medical by a panel of fully qualified GP's to ensure you are not making a false claim ocasionally.

    or

    We need to reduce the national debt and taxpayers hate the concept of something for nothing (if they're not in on it). So were redesigning the system so your entitled to less. We will make WCA manditory, we will asses your positive strength's and manipulate your limited quality of life to our ends. We will offer you support (code name harrass you and make you feel guilty) back in to employment. The employment we offer will be trivial, usually temporary and farly meaningless but you should be gratefull that anyone wants you at all. Once your in employment we will make it extremely difficult for you to reclaim benifits if it doesnt work out. If you want to do a course to help you get sustainable employment well thats your problem, other people do it themselves, being disabled isnt a privledge. When you are assesed will cause you maximum anxiety, treat you like the turd you are and remember with ESA were "In this Together". 

    Now there been a massive rise in people being referred to IMHS in my area since ESA and WCA was introduced. Granted there is a recesion too, however my GF's MH worker claims there case load has more than tripple since the introduction of the new systems. People who have physical disabilities are having more attempts at ending it all, people with chronic health complaints are suffer anxiety and depression due to failing a clealy flawed test according to the people in IMHS I come into contact with.

    That's my take on the situation. But remember "Were in this together".

  • I dunno, maybe it's just me, but I find "We recognise that you want to work, but require, and can offer you, support, even if it is somewhat limited, in achieving that" (ESA) far better than "You have been deemed never fit to work ever again, please go and sit quitely on the rubbish heap of life" (IB).

  • I was given one of these assessments ages ago. I thought the assessment itself was very poor, the main thing I can remember is a series of simple mental arithmetic questions. I was surprised when they decided in my favour without need for appeal.

    Likewise, my mother was recently being moved from Income Support due to incapacity, over to ESA. It's fair to say she had come the wrong side of these assessments previously and needed to appeal. However, there didn't seem to be an issue this time around. I guess it could have been because of the previous appeal etc. However, my partner's Dad recently had such an assessment and wasn't successful.

    To be completely fair, I would say I and my mother are actually capable of work to some extent. The problem, as always, being whether someone would actually employ me. Fortunately I am starting a job soon, after getting a lucky break through doing a work experience placement - I still have not, and probably never will, get a job off the back of an interview. I think it would do a world of good for my mother to be doing something with her life, and to have a purpose. However, again, the problem is whether anyone would employ her - and I doubt they would. So forcing her to go on the job market probably wouldn't be a good thing, as it would cause more harm than good. The way the system works, with two groups as a not expected to work, and expected to work, if you're in the not expected to work group, then clearly you're written off. There should definitely be some sort of help available to those who want it and are in the not expected to work group.

    In some ways, the *** were more humane than the WCAs. At least when you're rounded up, gassed and dead, you don't have to live with the mental anguish and torture inflicted by the system. (I know that's a gross over-simplification, and will be an unpopular view - but you got to admit it has *some* validity, if you ever see the anguish these things put people through.)

  • While the goverment continues to demonise a specific group I will 1000% persist with Nazi analogy's.

    The template is similar, however the final result isnt as extreme. The final solution to the disabilty problem. Systematic degredation as a result of governmental command. 

    It starts by creating hatred within the populous towards a group, it make's a said group live in fear. Look at the collective responsibility and the way that the condoms are using it now "were in this together". mmm Im sure collective responsibility was a favourite in the kingdom of bavaria before becoming particulary popular along the Polish/Ukrainian borders and the hotspot in the south of Poland. Im not being histerical and labeling everyone who disagrees with my philosophy a Nazi, I'm pointing out that the methodology of the system is remarkably similar. I don't even brand every racist a Nazi.

    Why was there not this level of kickback with the older system? Because It was fairer, I knew people who failed medicals on the old system but they didn't feel so aggrieved. People did not feel it was results driven. People thought the assesors were compasionate. People may have disagreed with results, but now we have a system that is dispised by those who it is supposedly there to help. The system was flawed but working, lets create a new system with more flaws that doesnt work, what a splendid idea.

    One thing I can say is none of the current UK political party's have the efficiency of the Germans.

    PS my GF had a positive outcome in the respect she wasn't messed about, but the methods used were not particulat benificial to her health. Infact detrimental as she started to question her role and validity in society. Under the previous system she did not experience this as she had faith in the system. I don't think anyone at all is against the concept of a medical.

  • some one said:
    fair enough, you have your views and expriences i have mine, all i know is the majority of experiences i hear about, via people i know or stories from ducumentaries , have been negative, its good you had a positive one, but sadly its rare for most of us

    Well, yes. That is the nature of these things. People who have a good experience don't complain because, well, there's nothing to complain about!

    So you do only ever hear about the bad experiences. However it is a logical fallacy to go from "I only hear about bad experiences" to "all interviewers must lack compassion because all I ever hear about is a lack of compassion".

    It's like saying "I have a red apple, and I've only ever seen red apples, therefore all apples must be red".

    Which is patently untrue.

    You simply can not take one, a hundred, or even a thousand, examples of a lack of compassion and simply extrapolate that out to all cases.

    some one said:
    as for the analogy, i merely suggested we go with it, it was not my analogy, i didn't create i just went with it

    if you have a problem with that analogy talk to the person who brought it up, i merely suggested 2 things,

    its about comparison to having compassion and no or little compassiosn for the "interviewee"

    , and the fact that 'doing their job' is never an excuse to treat people badly

    No it's not, and I'm not saying it is.

    But there is a whole world of difference between some jerk being a jerk in a WCA, and someone carting off jews, gays, and the disabled to be gassed, during WWII.

    some one said:
    as we are on a form on autism, an issue which faces lots of discrimination because of the issues related to it, id woould have thought it was relevant

    When we're being carted of to the gas chambers, then I'll agree with you.

    some one said:
    if its your view that it is "belittling and lowering" to compare

    No, I said it belittles oneself to use such a comparison.

    It is also an offense to those that did die at the hands the nazi machine during the holocaust.

    some one said:

    all i ask is you research just how many people are afected by atos "interviews" and ask them directly why they were affected

    And I ask you to research just how many people have had a positive outcome from the WCA assessments, and ask them how it was for them.

    Now, I'm sure you know that neither of us has access to the information, or the resources, to actually conduct such research in the proper manner, so suggesting such a thing is really quite pointless.

    some one said:

    we have had a system for a long time, but it wasnt always this way, something changed and who they began to hire changed, and why they hired them

    I agree the system changed, however I don't believe that the people doing the assessments now are significantly different to the people that did the assessments previously. Again, it is the system that is at fault here. Not the people.

    Labelling all WCA assessors as discompassionate is as bad as labelling all benefits claiments as scroungers.

    I don't know just how many times I need to repeat this simple idea for you to get it, but I'll try again: Just because one or two people within a larger group conform to a certain stereotype that does not mean that all of them do!

    If we are to have any legitimacy in our fight against denegration by a system that tries to label us in such a manner, then we must raise ourselves, our standards, and our opinions, above those of the enemy we face.