Do they realise what this does to people? — Scope | Disability forum
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Do they realise what this does to people?

axwy62
axwy62 Community member Posts: 142 Pioneering
I've (luckily) been left alone since 2014 but this morning received an ESA50 form for reassessment. It's taken nearly a week to get to me and in the 3 and a bit weeks remaining for me to get it back to them I have a family reunion weekend, my eldest son's wedding and a two week holiday booked - we get back 2 days after the return date.

My immediate response was unprintable and since then I've just felt sick all day and can still barely type for shaking. The first assessment was a complete nightmare, took 6 weeks short of 2 years to complete, involved 12 cancelled appointments and landed me in hospital twice. I simply cannot go through that again and don't want to even fill in their stupid form. I'm probably only being reassessed at all because the stupid doctor who assessed me expected me to make a miraculous recovery from an incurable and irreversible conditon and a genetic condition which will only deteriorate. 

I know myself well enough to know this is going to keep me awake at night and lead to obsessive investigation of every possible outcome until it's over. If I could get hold of anyone even remotely involved in this inhumane system right now ....
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Comments

  • janice_in_wonderland
    janice_in_wonderland Community member Posts: 265 Pioneering
    @axwy62 Very sorry to hear how this is affecting you and many others inc myself 

    I don’t know what to say but I sincerely hope you feel better soon

    Yes I agree it’s quite an ordeal for anyone to go through 
  • debsidoo
    debsidoo Community member Posts: 325 Pioneering
    Hi @axwy62
    If you don’t think you can get your response back to them in time you could try and ask for an extension.I have a friend who got a two week extension as she was waiting for results to get back from hospital.
    You could telephone them and ask if they would allow you extra time explaining you are unable to complete on time they may allow you a grace period.Good luck.
         Debsidoo.x
  • poppy123456
    poppy123456 Community member Posts: 53,330 Disability Gamechanger
    There's no extensions for returning the ESA50 form and it has to be returned by the date stated in the letter otherwise your benefits will stop. The only exception to this rule is if you're claiming ESA for mental health, otherwise it has to be returned. The ESA50 form is sent directly from the health assessment providers and not DWP. 
    I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.
    If i see a question that i know the answer to i will try my best to help.
  • Lynette1066
    Lynette1066 Community member Posts: 47 Connected
    I had my first, ESA medical 6 weeks ago, since claim made 5 years ago. I went through total hell. But personally it has been worse since the medical. Waiting for that phone call. I am in WRAG group, 12 month review. Then I expect to be found fit for work. So have to get on with it.
    I can give you this advice. When you have been for the medical. Go online to DWP, and request under freedom of information act. All your information from a specific date, and including the medical assessment report. I am pleased I did get mine. As this enables me, to point out a few things in the jobcentre tomorrow.
    It will not be a good day, but have to get on with it. I know this government does not understand what these do to a persons mental health. For myself it is DWP sanctions as well, and not being able to get through the interview at the jobcentre.
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    I have no problem at all with the assessment, it's a necessary evil and I have very little doubt about the outcome - being in a powered wheelchair alone should put me in the support group, but I also meet at least one other support group criteria.

    What is bothering me is that both of the assessments I've had before have been an absolute nightmare to arrange - 12 cancelled appointments in just under 2 years for the first, a home visit because none of their centres around here are wheelchair accessible, and after all that they took 10 minutes to decide I should be in the support group and left. The assessment was recorded, I have a copy of the report and the recording, and even in 10 minutes there are muliple discrepancies between what was said and what was recorded - none of them in my favour despite the outcome.

    The second one only involved 2 cancelled appointments - the first over 2 hours away in a non-accessible building with no parking, the second a home visit for which they just didn't turn up. I was so stressed by the no show, having had several sleepless nights worrying about it and having been hanging around doing nothing for the 4 hour time slot they gave me, that I ended up in hospital the next day with a serious flare up. I also have a copy of that report and again, it's total trash, according to that I can walk between 10 and 50 metres whereas in fact I can walk a few steps at best, and there's no mention of a wheelchair at all - perhaps the nurse didn't notice it. Again, the 'errors' didn't affect the outcome, but I do object to people writing lies about me.

    I am luckier than most in that I'm not going to starve if they stop my benefit (at least not until Hubby has to retire next year) so I can imagine how much worse it must be for people who rely on that money as their only income, I think it really would finish me off.
  • SHEBA
    SHEBA Community member Posts: 13 Connected
    I have been for 3 assessments ,the first,I was told ,that I would not be bothered again ,and they apologised for bothering me.Then the second ,I got through.The third ,I was refused,went through the Mandatory appeal,got that denied,despite being worse,having recently lost my mum,my pet dog ,being hassled by housing ,and my family disowning me!I went to a wonderful organisation,Disability Solutions,who helped me through the next stage ,a tribunal,and were priceless,supporting me at the event ,and with advice,support,and attended the tribunal with me.This was after 15 months without ESA,despite my circumstances getting worse,and losing any support from any services,I would like to thank them from the bottom of my heart,for their help,no one else came forward,I don't now how I got through it,but I have ,and am stoical in getting myself up to a better level,/mood.
  • Government_needs_reform
    Government_needs_reform Community member Posts: 859 Pioneering
    I feel for each and everyone of us having to keep proving ones self everytime.

    Ive also had my fair share of this **** from the DWP and am in the process of waiting my ESA reassessment, paperwork all sent back in June and awaiting either Paper Based or assessment at a centre. The mind boggles I've decided I will neve go to any assessment ever agian thus they will stop my money, I've now got to the point also I just can't and will not dance or have my life controlled by them the DWP any longer. Enough is enough.

    They Know full well the DWP that I am buggered. So I have made my decision if it all goes wrong I will live on the street at least I will be free of them. 

    Yes for me it's been hard for me to take this direction to go homeless I really cannot do this anymore, I have a safe place to camp and hopefully live off the land and get some food, but I will finally be rid of the DWP to me it will be priceless.

    I have over the last few months been preparing my supplies to keep me going for a few years to live DWP free.

    How dare some A hole that can judge how I don't cope within a 10 minute interview and dictate my destiny, where my medical record speaks for itself, personally I'm just awaiting my fate one way or another.

    I just like many of us just can't cope with this year in year out any further.

    When I know my fate I will be posting the result of my future whether I will have a home or be homeless.

    God bless one and all....



    ⬇️
    I created one of the campaign election videos for Labour, and Jeremy Corbyn,
    This is a new version of Emeli Sande, Hope "You Are Not Alone
    I highlighted everything that's wrong with this country from benefits, NHS, UC etc, but now we have to put up with the hate now that is the Tories. 

    You can see the video here.
    https://m.youtube.com/watch?v=P5o8hRHh9IY


  • SHEBA
    SHEBA Community member Posts: 13 Connected
    I hear you its fundamentally wrong ,for ANYONE to decide your worth,or how much MISERY,you have to endure ,based on numbers ,not a human beings life ,already majorly limited by societies small minded ,media conditioned bigotry.In one hour ,your entire existence is decided ,what right ,does anyone,let alone government lackies have to do this to anyone.?I sincerely hope you get the just result ,that you should get.The fact that with degenerative illnesses,you STILL,have to be questioned ,is senseless,£200 million spent on this by the Tories,to remove the rights of those most vulnerable,while they do nothing ,to billionaires who dodge £120+ billion per yr  in unpaid taxes,and the royals ,DOUBLE their "benefits"...millions.Obscene ,that's what it is.
  • debsidoo
    debsidoo Community member Posts: 325 Pioneering
    Hi again as poppy said.
    There's no extensions for returning the ESA50 form and it has to be returned by the date stated in the letter otherwise your benefits will stop. The only exception to this rule is if you're claiming ESA for mental health, otherwise it has to be returned. The ESA50 form is sent directly from the health assessment providers and not DWP.  
    My apologies for this.I thought the rules were the same as for pip.Sorry Poppy.
                Debsidoo.x
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    I basically have 4 free days left to complete this form, it's so far taken me two days just to update the various lists of conditions, medications and consultants etc.
    I wasn't planning to take my laptop on holiday with me, but I will have to if I'm still filling in the form, and it's all such a waste of time anyway because the default positon for Maximus, ATOS, Capita and DWP seems to be that everyone is exagerating at best. I could probably write it in Hobbit and they wouldn't notice because I'm sure no one actually reads what's written, at least not until 5 minutes before the assessment. I wish I had the nerve to try it!
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    Does anyone know if there is DWP guidance on when home visits should be offered?
    I know Maximus are the worst for refusing to do home visits without making you jump through more hoops, including paying for yet another GP letter, after which they say that if you can go to your GP to get a letter, you can go to an assessment centre.
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    In limbo. Managed to finish completing the form before we left home and got a minion to post it (with proof, I don't trust any of these companies not to lose it) so now the wait begins.
    I'm hoping for a decision letter from DWP but expecting an appointment to attend yet another inaccessible assessment centre, probably 40 miles away and with no parking.
  • poppy123456
    poppy123456 Community member Posts: 53,330 Disability Gamechanger
    First appointments are computer generated so it usually gives out the first available appointment. You can of course cancel 1 appointment if it's not convenient, if you are called for another assessment. Good luck.
    I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.
    If i see a question that i know the answer to i will try my best to help.
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    First appointments are computer generated so it usually gives out the first available appointment. You can of course cancel 1 appointment if it's not convenient, if you are called for another assessment. Good luck.
    Which begs the question why bother to ask what special arrangements might be needed on the form? Like most people, I assumed that if I'm asked if, for example, I need a wheelchair accessible assessment centre then this will be taken into account before an appointment is booked. Even the Independent Case Examiner (wrongly) believes that information provided on PIP and ESA forms regarding the assessment is taken into account prior to an appointment being offered, so if anyone can provide proof that this isn't the case I'd love to see it and pass it on to them as this was the only reason they didn't fully uphold my complaint about the fiasco that was my last assessment.

    Also, you can cancel as many appointments as you need to so long as you have good reason - whilst Maximus will make a fuss, DWP know better than to try to enforce something which has no legal validity whatsoever particularly when ATOS/Maximus cancel appointments willy nilly with no regard to how long you've been kept waiting to be seen.
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    Still waiting.
    The optimistic me thinks the paperwork will be returned to DWP with a recommendation that I continue in the Support group and no further assessment will be required.
    The pessimistic me thinks that it will once again take 2 years and multiple cancelled appointments before someone finally actually turns up to assess me but doesn't notice the wheelchair or the pages of medical evidence or decides I'm making it all up and that we've paid for all these aids because I'm lazy and so decides I'm fit for work, after which I'll have months and months of waiting for the outcome of mandatory reconsiderations and tribunals before eventually getting the right decision.
    I can't quite bring myself to contact them and ask how long it might be before I hear something.
  • poppy123456
    poppy123456 Community member Posts: 53,330 Disability Gamechanger
    The Support Group descriptors are here and you need to satisfy at least one of them to remain in the group. https://www.benefitsandwork.co.uk/employment-and-support-allowance/esa-glossary/1353-support-group-descriptors
    There's also reg 35 which is explained here.

    ESA is about the work you can do rather than the work you can't do and this is what they assess you on.

    I can't imagine ringing the health assessment providers will help you much because backlogs are in all areas so there's no timescales.

    Hopefully it won't be too long before you hear something. Good luck.



    I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.
    If i see a question that i know the answer to i will try my best to help.
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    So as expected, no one even looked at any of the information on my form before sticking me in the assessment queue to go to an assessment centre. When I queried it I got the stock 'you need a letter from your GP ....', which was of course included with the form. I am now told I might have to wait 6-9 months for a home assessment.
    I am not putting up with this again, it's an entirely pointless exercise anyway and why should I be penalised for being too disabled to be admitted to their assessment centres? As well as the cost of the letter from my GP, the stress from having a sword that could cut off my income hanging over my neck for months on end is intolerable. The last ESA assessment took near enough 2 years to complete and put my mental health recovery back 5 years, the PIP assessment put me in hospital.
    I'm already collecting the evidence I need for an Equality Act claim, and I will be reporting any identifiable HCPs to the relevant governing bodies. Enough.
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    To justify asking me to go to an assessment centre, Maximus have picked out just one comment from the masses of medical evidence I sent in. The comment was preceded by confirmation that I've been wheelchair bound since 2012 and that following further surgery in early 2016 there is nothing more the specialist can do for me, but that I should 'be as active as possible despite the wheelchair'. 
    Maximus wrote 'your specialist has recommended that you be more mobile'. As justification for making me go to an assessment centre which won't let wheelchair users in, I find that somewhat lacking. I am also trying not to be seriously offended - is it me, or are they actually suggesting that if I tried harder I could manage without the wheelchair? I can't work out what else they could possibly mean.
  • Sam_Alumni
    Sam_Alumni Scope alumni Posts: 7,671 Disability Gamechanger
    Oh I am sorry to hear this @axwy62 :( It is so tough and I understand how unfair it all feels.

    When you say " an assessment centre which won't let wheelchair users in" do you mean that it is now wheelchair accessible?
    Scope
    Senior online community officer
  • axwy62
    axwy62 Community member Posts: 142 Pioneering
    All the assessment centres in my area are above the ground floor. DWP rules are that if you can't get down the stairs unaided, you cannnot go above the ground floor in their buildings, therefore accessible or not, lift or not, they simply won't let me in.

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