PIP investigation: ‘Lie after lie after lie’


Many more disabled people have come forward to describe how the healthcare professionals who assessed them for the government’s new disability benefit lied in the reports they compiled.

Their evidence further confirms the results of a two-month Disability News Service (DNS) investigation, which revealed last week how assessors working for the outsourcing companies Capita and Atos – most of them nurses – had repeatedly lied, ignored written evidence, and dishonestly reported the results of physical examinations.

Having read last week’s articles, more personal independence payment (PIP) claimants have come forward with their own evidence of dishonest assessors.

One PIP claimant, David*, who has impairments including ME, fibromyalgia and a heart condition, has described how his disability living allowance (DLA) award of the higher rates for both care and mobility was lost after his PIP assessment left him with zero points (a claimant needs eight for the PIP standard rate and 12 for the enhanced rate).

He remembers his assessor telling him when she arrived at his home and he asked if she knew anything about ME and fibromyalgia: “I’ve dealt with a couple of people with yuppy flu before.”

He said: “When I received the assessor’s report I thought it was for another person as it contained so many omissions, inaccuracies and conjecture. There was also several instances of fabrication.”

Information from his previous applications for incapacity benefit, DLA and employment and support allowance (ESA), and his successful appeal decisions for DLA and ESA at tribunal, had been omitted from her report.

David told DNS: “The report states I carried out tiptoe and ‘balancing on each foot’ tests and had no problems walking. I did not walk a step and did not carry out the tests described.

“The report states that I turned around in my chair and picked up a bottle of medicine from the surface behind me – the surface behind me was an oven hob and all my medication was on the table in front of the assessor.”

When he described how his medication had sent him to sleep in his back yard, the assessor claimed that he said instead: “I wonder [sic]round the fields outside my house,” while being able to open a ring-pull can was interpreted as “able to prepare a meal”.

He is appealing the decision, and is complaining about his assessor to the Nursing and Midwifery Council.

David said: “Since receiving the report, the consequences of dealing with the complaints procedure and making another tribunal appeal have been a noticeable deterioration in my health and have put a strain on both my wife’s and my own mental health (loss of peace of mind, anxiety, knocks to self-confidence and a feeling of being discriminated against because of the nature of my disability).”

Rachel*, a former mental health nurse, requested a copy of her assessment report after she was awarded zero points by DWP, following a PIP assessment by an Atos nurse in the Brighton assessment centre, when she had previously been claiming middle rate care and lower rate mobility under DLA.

She said: “In the report, I found details about a physical examination that was allegedly performed. It ran to one side of A4 paper.

“No examination ever happened; the report is a complete fabrication.”

She is now appealing, and is hoping to lodge a complaint about the nurse with the Nursing and Midwifery Council.

Julie*, who has both a physical and mental health condition, said she had been claiming the highest rate for both care and mobility under DLA, but as a result of a dishonest Atos assessment report by a nurse was granted only the standard rate of both daily living and mobility for PIP, and lost her Motability vehicle in January 2016.

After she requested a review of her case in November, she was assessed again – by another nurse – and again received a dishonest report.

The whole process, she said, had been “humiliating and degrading”.

In both reports, the nurse said Julie had refused a physical assessment, which she said was not true on either occasion, and was witnessed by a third party both times.

She said: “When it came to care, she ignored a lot of what was said, just picking out the fact I could shower but didn’t mention that my husband has to help me, the same with cooking and taking medication.  

“Even though my husband does all that and leaves me my lunch and phones me to remind me to take medication.”

Another claimant, Sandra*, said that the nurse who assessed her wrote in her report that she had no suicidal thoughts, even though Sandra had shown her copies of police incident reports written after her friends had expressed concerns for her safety.

The nurse also wrote that Sandra was in a “good mood and often smiling”, even though she had told her that her second dad had just died and she had spent a sleepless night crying.

The nurse wrote that Sandra can “manage medication/therapy unaided”, even though her flatmate helps her fill her tablets box and then hides the rest of the medication in his room to avoid her using it to overdose, as she has done previously.

Sandra had previously received the PIP enhanced rate for daily living, but as a result of the assessment report, received zero points and so lost her entitlement to £330 every four weeks.

She is now waiting for a tribunal to appeal that decision.

As a result of the problems this has caused, she has started to hear voices for the first time, and has been referred for urgent psychological treatment.

She cannot use public transport because of claustrophobia, and taxis are expensive, particularly because she has to travel to a neighbouring town for hospital appointments.

Michael* said that the stress of fighting his PIP case through a tribunal – and also having to take his ESA appeal to a tribunal – caused him to have a heart attack.

He said that both of the reports compiled by these assessors were “seriously dishonest, missing huge amounts of evidence I gave, some of which was extremely important to my case”.

He had been assessed for PIP by an Atos physiotherapist, who failed to mention the “multiple pulmonary embolisms on my lungs which though I had suffered with from my first heart attack two years previously had only just been diagnosed”.

He also claimed that Michael experienced only “mild pain”, when he had been told about his “neck and back injuries, a broken right kneecap, arthritis of the knees and angina, to name just a few of my problems”.

As a result of the assessment, he was awarded no PIP payments at all, and it took him 18 months to reach tribunal, where he was finally awarded enhanced mobility and standard daily living.

Another PIP claimant, Michelle*, said she was “devastated” when she received a copy of the “fictional” report compiled by the Atos nurse who assessed her.

She plans to lodge a complaint with the nursing regulator, the Nursing and Midwifery Council.

The report mentions the results of a hip rotation test, and a test to see if she could put a hand behind her back, neither of which she said she was asked to do.

The nurse also said that she “can raise arm within normal range”, something she cannot and did not do.

The report, she said, repeatedly states that she has “no significant restrictions in upper limbs and hands”, even though she has “severe cervical spondylosis and a deformed posture. My head is tilted and twisted. Obvious to anyone who looks at me.”

The nurse also claimed that she took the top off a sports drinking bottle with “adequate dexterity”, when that was done by her son, and that she “passed prescription across the desk”, again something that was done by her son.

Michelle had previously been receiving an indefinite award for the highest rates of both care and mobility under DLA for more than nine years.

Following her assessment, that was reduced to the standard rates of PIP for mobility and daily living.

She said: “This means I will lose [my]Motability car and won’t be able to get to hospital appointments, doctors or visit family.

“Devastated that a member of medical profession could set out to deliberately discredit my application and defame my character.”

Nicola* was assessed at home by a mental health nurse working for Capita. Even though the assessment was recorded, with the knowledge of both the assessor and Capita, she said he still “lied throughout the report”.

Among the lies, he wrote that she saw friends every day and spoke to them daily on the phone, visited her GP in a taxi, and did not know what one of her inhalers was for, all of which was disproved by the recording, she said, while he also ignored her depression and emphysema.

She said: “The whole system is corrupt and not fit for purpose. The DWP are fully aware of the lies that are told in the reports [but]they give their full support to Capita [and]Atos.”

Christopher Brogan told DNS this week how he accompanied his partner, Mandy Cooper, to her PIP assessment in Birmingham last November.

A Capita nurse assessor wrote that Mandy can visit a local shop on her own, even though she was not asked if she could do that, and cannot walk that far.

The assessor said she had climbed a couple of steps at the assessment centre, even though there had been no steps in the building for her to climb and she had entered the building via a ramp.

As a result of the report, Mandy’s higher rate mobility and care under DLA was changed to standard rate daily living and no mobility under PIP.

They are taking her case to a tribunal.

Barrie Davies told DNS this week that the Atos physiotherapist who assessed him in Wigan a few weeks ago told “lie after lie after lie” in his report.

He failed to mention in the report that when the assessor asked Davies if he could touch his toes, he replied: “No, because I have broken my back.”

Scans show two breaks in his spine, which is also “bulging, twisted and collapsing. I gave that evidence to him and it didn’t appear in his report.”

As a result of the assessment, he had to hand back his Motability car this week, 17 years after a previous dishonest assessment report by a doctor led to him having his Motability car removed.

He had previously been claiming the higher rate mobility and middle rate care component of DLA, but as a result of the latest assessment report, that was changed to the standard rate of PIP for both daily living and mobility.

Davies said: “He said I can walk down steps without crutches and that is a lie.

“I can’t move my neck at all. He said I have got good movement in it.

“He said rotation of my back was perfect and my specialist said I can’t move it at all.”

He is appealing against the decision, with support from the online welfare advice group Fightback4Justice.

One claimant, who commented on last week’s story on the DNS website, described how his assessment report had proved to be “not just a pack of lies but contained 19 spelling mistakes, three sentences that were complete gibberish and at least two contradictory statements”.

He said: “Among the lies, the report claims I’m taking a type of medication that I can’t swallow, one of the notes claims I’m doing all my own housework when it was made clear I had to employ someone to do this while another says I can use public transport, which I also made very clear was not the case.”

He now plans to report his assessor to his local police force for alleged fraud by misrepresentation.

Capita asked to see anonymous summaries of the latest cases this week, but then – after its media team had read them – refused to add to last week’s statement, in which it said it expected “all assessors to behave in a way that meets both our high professional standards and those of their professions”.

Atos again refused to comment.

A DWP spokeswoman said: “We expect the highest standards from the contractors who carry out PIP assessments.

“We do not accept it to be the case that there is dishonesty amongst them.

“As we said, we are committed to making sure the PIP assessment process works fairly and effectively, which is why we welcome independent reviews such as the ones led by Paul Gray, the second of which is expected in April 2017.

“Anyone not happy with their benefit decision can ask for it to be looked at again, and then appeal to an independent tribunal.

“There is also a comprehensive complaints procedure in place for claimants who are not happy with the service they have received from providers.”

*Not their real names

  • User Ratings (26 Votes)
  • Cheryl Slater

    I too have had lies in my assessment report, medical evidence ignored, a mandatory reconsideration refused, gp letter phsyciatrist evaluation and a full explanation of my daily struggles and lots of emphasis on reliability and repetition all totally ignored because I am able to drive a car. I am unable however, to take my case to appeal as I do not have the fight left in me to explain to complete strangers the complexities of my health conditions and how they affect me every day.

  • Daniel Easson

    Not Just DWP at it..The appeal system done by the appeal court is just as bad..!!

    Had an appeal hearing to make my industrial injury benefit for a
    Reconstructed ankle, with chronic pain to be made permenent.
    They refuse my appeal and reduced my award by 15% on the grounds of unrelated health issues, no mention of any other health issues in the medical report or shown in the refusal document..only mention on that doc refereed to my ankle being normal.

    Doctor seemed to take an instant dislike to me on the day, possibly because turned up wearing my walking boot, which I need for short distance walking outside and that I was well dressed and shaved, wearing a shirt and tie.

    She was very agressi in her questions and the whole thing was more like an interigation.

    Her medical exam took 2 mins and she said the ankle looks in good condition and colour and can be moved without pain….Firstly..I have a very weak ankle and had fallen 2 days earlier and my foot and ankle were badly brushed and painful..during exam I asked her to be careful as I was in some pain..she asked me to be quiet as she was not allowed to speak to me during the medical..what!!!!…she put in her report both feet and colour were normal..she asked me to lift my left leg up..ok no problem…asked me to lift my right leg, the one with the injury..I had to hold my leg up due to pain..her report said I had lifted both legs without any problems.

    I have since found out recently that the doctor via a freedom of information request..work for DWP as medical assessor at various centers in Glasgow, but she is also working for the tribunal services as a medical member of the appeal panel. She was mentioned in a legal action in which she was accused for professional bias when a man was taken of pip..he appealed and again was denied his award..his lawyer took his case to the house of Lords and won on appeal.

    Bother DWP and The Tribunal Service were told is was both unfair for the DWP medical advisor who rejects a claim to be the same person deciding on an appeal for the same claiment.

    I also found out the doctor only did medical exams and had not worked as a NHS doctor since 1998 , she worked 4 days for DWP and 1 day for The Tribunal Service.

    How can this go on….?…?

  • Trevor Playford

    I had the same experience in my assessment by atos, I’ve have mental health issues and fibromyalgia, I am accompanied everywhere I go. The report detailed that I spoke with confidence and cracked jokes, when actually it was my brother who spoke. The report detailed a physical examination in which she claimed she examined my ankles, knees, hips, back, shoulders, elbows, wrists and dexterity, no such examination was carried out. She also claimed I was able to get on and off the examination bed without any struggle, she also claimed to witness me bending down to sign out, when my brother is the one who signed us out. I threatened legal action for forging legal documents. I went to tribunal and was awarded the standard rate living and mobility. This process was ongoing for just under a year, which had massive impact on my health and well being. I am now starting the process over again as my claim is coming to an end and been told I had to reapply, rather than just having a reassessment for an ongoing claim. I have filled in the forms again and included all relevant documents, just waiting to hear, I’m desperately hoping I do not have to go through what I did before, it was so much to deal with after my overdose, don’t think I would survive it again

  • Ian Byers

    I have had the same treatment, I have fibromyalgia, ME, Generalised Anxiety Disorder and depression. I got 6 points and there was lies and fabrication from the assessment. The accessor didn’t follow government guide lines and fabricated information. I then took it to court. The appeal was a sham there was a Dr who was a professor said I looked ok when i walked in the room. My illnesses he said was not really understood and little to say it even exists.. I was told out right by welfare rights because I drive a manual car I would not get it awarded any help. It was brought up in the appeal as they expected. It’s a total disgrace the whole system is degrading, discriminatory and do not care about human rights. It’s just about stopping any support and benefits for anyone who had illness and disability. There is no recognition of mental health issues in the forms and assessment. Anyone who thinks putting a pen in a top pocket quantifies being able to hold down a full time job is an isaine idiot of all proportion and should not be associated with health care. Why are these people running the country and acting like a nazi dictatorship in a holocaust. They want to kill people off clearly to save money. It’s all it comes down to. What gets me is people who have no health problems do not understand or relate to this until they are in the same boat.

    • donna rawlinson

      the whole lot of mine what they put on it was lies i sat other day and nearly changed every single word that they put on mine and am now sending it back to them with a letter so it goes to court even have 2 hospital doctors doing letters to send to them had to have my epilepsy medication put up even highier because off this

  • donna rawlinson

    i had my p.i.p turned down twice in a space on 3 months telling me im fit yet i have epilepsy , mitrocondrial disease .arthritas in both knees and high blood pressure yet they tell me cause i can touch the womens finger and done my handbag up that wasnt even done up due to being broke ive been on disability living allowance since i was 16 im now 34 next month had my car taken off me week before christmas cant even take the kids to school anymore cause my knee keeps giving way on me even after they had letters from all my doctors at gps and hospitals

    • pamela thanson

      Not ignoring anyone, just not enough pep left, for those few days, exhaustion is one of my problems;but hey pip says I’m fine. i am so sorry, I know how hard it is, I asked my MP questions to ask those concerned why so many people up and down the country – with different assessors, in different areas speak of the same regimen of lies. Citizens advice B is collecting information about this. Surely there must be by now enough persons injured and lied about – to bring a ‘class act’ multiple action against them. I will share my questions to parliament and her replies if and when I get them xx I understand inside out is making a programme on the subject. x

      • donna rawlinson

        well im now going to take it to court as well and see what happens u can use mine if u want to

  • pamela thanson

    my assessment for pip, which I’m too old to receive I’m over 64, was at odds with all other assessments I received Concerning: my treatment from consultants, having adaptions, wet room, stairs lift, level thresh hold access, being fitted for splints for knees, wrists, and my wheels. And the High rate DLA awarded for life. I have a inherited genetic syndrome,(marfan’s) which cannot suddenly disappear and is degenerating down, affects my skeleton, all connective tissue, heart, lungs, eyes, ligaments, veins etc, I suffer from joint dislocations,high blood pressure, in danger of aortic dissection, and am exhausted and in pain all the time. my skeletal frame is obvious to sight twisted and bent. My DLA has been taken away, I couldn’t believe the lies told in what I can only describe as a “i have decided- fictional rant”. My consultant will not write a supporting letter,…. says they pip have enough proof, He will write a detailed report if they ask for it……pip wont. Neither did they inquire of my cardiologist, rheumatologist, or gp, they pip said, by law they didn’t have to; they can just decide, so there am I stuck, Mobility withdrawn, left a prisoner in my home,,, I cannot get to a bus stop, nor the train station (which has no disabled access anyway) Surely this cannot be legal, my understanding of the disability discrimination bill – is money cannot be a factor in withdrawal of aid. Its all about money isnt it.

    • JP Pete

      Sorry to hear this but please note that no benefits are for life as all benefits are now open to further review.

      • pamela thanson

        ok that’s how it is now, but when it’s you – who have been led to believe, know you have, and are assessed as having a life long disability which needs assistance to function and live; have that assistance suddenly removed, what then? I cannot go out to work, age, exhaustion, pain, is a daily factor. Also knowing government is clearing 800 people a week out of their cars ( and I’m one of them) doesn’t help. It makes the manner of the action all the more shameful, the lies, are also unnecessary and shameful in nature, if this government action is good, above board – why are so many reporting lies? If it’s a fine course of action why so many country wide are reporting, off colour, lying statements As is the dismissal of 800 people a week;and those are only the ones we know about in cars. Who is counting the additional “other’s” who have assistance withdrawn who didn’t have cars? Being left with debt, is not acceptable. Being still tied into a monthly payments – which I have to pay whether I have a car or not, is unacceptable,and I know I am not alone in this.

  • JP Pete

    I wonder if it would be best for claimants to first mention and make clear the fact that they would be unable to undergo a physical examination at assessment when filling out the benefit application form.
    This way they would have a future point of reference if/when it come to a Mandatory reconsideration and also more likely than not when having to then attend a tribunal hearing.
    Couple this with making sure you inform everyone concerned as to why you would be unable to comply with a request.
    Make sure at the end of the assessment that the assessor has noted the reasons given and not simply noted it as a refusal.
    Everyone needs to request a copy of the assessors report this can be done a few days after the assessment.
    If a MR (Mandatory reconsideration) is then sought be informed that you do not have to wait on the arrival of the assessment report before submitting the MR (just write a couple of lines outlining briefly you reasons why you are requesting an MR also importantly make sure you inform the DWP that you are awaiting the arrival of the report and to not make a decision until you have received/read the report as further evidence may be forth coming.) Always belt and braces write and phone and keep copies of all request/letters/communications.