A Commons debate this month was told that universal credit sanctions are “back with a vengeance”, as the number of claimants hit has risen by two and a half times.

In the benefits sanctions debate on 13 December, MPs learned that in the last quarter, the number of UC sanctions was 250% higher than in the three months before the pandemic. 

This is a massive increase even allowing for the increased number of UC claimants.  It amounts to 2.5% of claimants being sanctioned each month compared to 1.4% before the pandemic.

The number of UC claimants who were serving a sanction in August was 115,274, after a peak of 117,999 in July. That is more than three times the pre-pandemic peak of 36,771 in October 2019.

In June 2022, £34 million was taken from claimants by way of sanctions, in July £34.9 million and in August, over £36 million.

Clearly sanctions are saving the DWP a significant amount of cash.

According to Labour MP Beth Winter “The latest sanctions were worth, on average, £262 a month. That is nearly a third of the average UC payment. This is a full-frontal attack on universal credit recipients that must end.”

As SNP MP Chris Stephens said, “Sanctions appear to be back with a vengeance”.

Answering for the government,  minister for employment, Guy Opperman repeatedly ducked the question why the number of sanctions had increased so rapidly unless the DWP had changed its policy on applying them.

All Opperman would say was that:

“The hon. Gentleman asked specifically about the rise in the number of sanctions. Some 98.2% of sanctions are for missing a meeting with a work coach.”

However, Opperman offered no explanation as to why twice as many claimants were now apparently choosing to miss appointments.

MPs raised the issue that claimants could be sanctioned for refusing to take a zero hours contract even if they already had a secure job, but for fewer hours.

Other claimants have been sanctioned because an appointment was created by a job coach on their journal at a time when the claimant had no data on their phone and no money to buy any.  By the time they could get afford additional data and saw the appointment, they had already missed it and been sanctioned.

SNP MP for Glasgow North East Anne McLaughlin said she is telling her constituents “If you have your benefits sanctioned, do not take it lying down. Contact me and I will fight this for you, because this is wrong and nobody should have to live on less than the minimum income”

Another SNP MP, Chris Stephens said that:

 “There are concerns that jobcentres have been told by senior managers and Ministers to “up their game” when it comes to sanctions . . .  There is inter-office competition, whereby different offices’ statistics are compared, pushing for higher sanction and deferral rates . . . There are also real effects on disabled claimants who are thrown into a group of those most likely to get a sanction, and the relative rate of sanctions for claimants with disabilities—all of that really needs to be explored further.”

You can read the full record of the debate on the Hansard site.

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    ? · 4 days ago
    The comments below are months old and cannot relate to the news item above.
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    Chris Nasher Nash · 3 months ago
    Hi I have recieved pip since 2017 
    I recently had a telephone assessment by a stand in nurse which was 2 and a half hours after my appointed time so she could read my notes.
    I am reasonably happy for my award however saying that 
    I do believe the nurse did not listen or write what I told her on our conversation.
    I had sent evidence from an expert consultation to say I had left hemisphere brain damage but they say because of how I talked to the assessor she said I don’t show any signs of depression or mental illness.
    I never had that part of pip awarded they say because I don’t go for therapy or attend any classes I don’t have any depression or mental illnesses.
    The experts examined me prior to a court hearing.
    That was 5 years after my accident and they stated clearly that my condition would not alter at this late stage.
    Even my gp wrote to them to say the industrial injuries benefit tribunal acknowledged that I have a brain injury so why does the DWP Pip not acknowledge it.
    He told them just because I don’t go on about my depression does not mean I don’t have it !!
    She also in my descriptors ignored that I don’t use certain 
    AIDS to assist me like perching stool and double handled cups and utensils to eat and drink from, Or that I only shower less frequently than I probably should do.
    I know this because I ask for a copy of her recorded notes as well as DWP returning all the medical evidence also extra evidence sent in  since the phone assessment.
    I was going to ask for a mandatory reconsideration,
    But reading that a lot of persons came of worse decided not to follow it through.
    I am 66 and the nurse reccomended I be given a 2 year award and then be reassessed, however pip gave me a 10 year award.
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    LB · 5 months ago
    An update on my claim. I was awarded zero points on the care element of the pip form and enhanced rate for mobility. The decision on the ruling is so Indifferent, dismissing my epilepsy as ‘manageable’, even when I stated the difficulties I have as a result of seizures. They ignored any mention of my Type 2 Respiratory Failure and glaucoma issues. Three consultants, an Epilepsy clinic, a lung function clinic, has been overruled by a disability assessor who did the assessment.

    I wish I was surprised, but I am not. The DWP seem determined to punish claimants or put them off appealing. I’m going to appeal. There’s no other option. 
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    GS/MM · 5 months ago
    Hi 
    My partner had to claim PIP for thr first time 4 years ago, she suffers from drug resistant epilepsy, in that here siezures are not controlled and she gets no warning of onset. She went through the initial review, zero points, then the mandatory reconsideration which netted higher mobility at 12 points, but still nothing for the care element, the award was only for 18months at this stage.
    She then appealed and it took just over a year to get to the tribunal, then in front of the judge and two other health professionals She had to explain her condition, how it affects her life and the dangers.

    The DWP conceeded that the case should have been reviewed as their opening statement and offered medium rate care and higher mobility, the judge reviewed the evidence spoke to my partner along with other members of the panel and awarded high rate care and mobility for five years.

    The DWP tried scare tactics when she went for the mandatory reconsideration saying she could loose everything, however when we did finally get to the tribunal the judge told her what had already been awarded was not in question, just the length of the award and if she was entitled to anything more.

    Hers and my advice is don't give up,

    She is currently going through the process for yhr second time, hopefully this will be easier, however armed with the experience from the first claim she should be better prepared.



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    Alison · 5 months ago
    I was extremely depressed and suffered from anxiety amongst other things. I never went out the house and had to move in to my parents home along with my daughter. 
    I was with my Dad waiting to go in for the assessment and he made me laugh. 
    Even though I was really struggling in the interview & became quite distressed when I had to talk about how I felt and what help I needed. 
    When I received my award letter I didn’t have enough points for either mobility or living. 
    It stated I wasn’t really depressed as she didn’t believe me as she had been watching me with my Dad laughing before I went in the start the interview!!! It was a nervous laugh as I had never had to claim anything before. 
    Needless to say it was overturned on Mandatory Consideration after a rather forthright letter from my GP. 
    I got the higher rate award in both mobility & care. 
    I couldn’t believe they were sat observing me before I went in the room. It made my claim form & interview a joke. It was like she was talking about someone else. 
  • Thank you for your comment. Comments are moderated before being published.
    LB · 5 months ago
    I have had one success PIP claim, after a mandatory review and I am waiting for a decision on my latest claim. It’s been almost twelve months (early December 2022) since I returned the form, Capita ‘lost’ my first telephone interview and I had to do a second one over a month later. I didn’t know, but you can request a cd copy of your telephone interview by your assessor, instead of a download link. My ‘link’ failed three times with Capita blaming their system. Hard copy is better and it works. It takes up to twenty one days to arrive but you will receive it.

    On both forms, I have used Gov. UK’s website for the ruling by the Upper Tribunal Administration Appeals Chamber  to support my claim on seizures without warning and the interpretation of ‘safety’ for the purpose of supervision. 

    Full title: RJ, GMcL and CS vs Secretary of State for Work and Pensions vs RJ (PIP) : [2017] UKUT 105 (AAC); [2017] AACR 32

    It’s long, but well worth reading, especially when you have infrequent seizures as I do. Having a risk assessor for a husband who was able to claim that the nurse who dismissed my epilepsy as a reason for pip had no basis in which to argue that she knew better than a fully qualified health and safety professional helped. 

    One thing that was raised in my first claim interview was who managed my epilepsy care. She mentioned an epilepsy clinic as one of the options. I had never heard of them. Unfortunately, I discovered mine when I had six cluster seizures in one night and was admitted to my local hospital. I did have an epileptic consultant and he had set up an epileptic clinic in his department at the hospital.
    The clinic took over my epileptic care. I speak or message the epilepsy nurses whenever I have an issue and they call after speaking to the consultant. I have a yearly discussion with a doctor and review all my medications through them. Waiting for so long for a decision on my latest claim has caused me to increase my prescription and this was arranged by the epileptic nurses who contacted my gp directly. Having a hospital manage my care seemed to make more impact in my last interview than just using the local doctor. The clinic also wrote a letter to support my claim and to outline the type of epileptic seizures I have and the damage I have sustained as a result of them. 

    I’m not sure if it helps as the DWP like to avoid external cases, but did anyone read the Health and Safety case against Morrisons? They had been warned that one of their employees who has infrequent seizures should not have his locker upstairs. They ignored the warning. He suffered a seizure and fell down the stairs and died. It resulted in over a million pounds fine. No matter what they say, infrequent seizures result in serious consequences for those who ignore or say they aren’t relevant for PIP claims. The courts of appeals and Health and Safety think otherwise.

    One thing that I did have after my first claim was denied and appealed against was photographs after a seizure. I hit a radiator and as my doctor said; the bruising was very impressive. I hope you don’t need this kind of evidence, but take photos if you have a seizure to record any bruises or injuries you may have sustained. I’d even recommend taking pictures of a room if you damaged anything. I threw coffee over a chair and wall one time and hit a leather chair on my last seizure. 
    I do have other issues, along with epilepsy, that are on my claim, but I repeatedly mentioned in my interview that I needed to be supervised to carry out tasks. I am lucky that all my issues are managed by hospital consultants as it appears that they hold more ‘weight’ in deciding whether I should receive PIP or not. I won’t know if it’s true until my decision comes through. I still expect to be refused PIP, but I will appeal. 




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    Dawn · 5 months ago
    I have recently applied and received standard rate for PIP, I suffer both major and minor epilepsy. I made the point that many things are unsafe for me to do without supervision especially when the minor attacks occur. This can be 4 days a week and last from an hour to all day. The return letter said because I hadn't had a major fit for 6 years made my epilepsy not a problem huh! I wish they had to live with it. I've gone 10 years without a fit then had 3 in one month. While talking to the interviewer she only wanted to know how I am on a good day, she kept joking about different things and that was all held against me so beware they do try to trap you
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    Paula · 5 months ago
    Took a four year fight for pip. I have uncontrolled epilepsy, peripheral nerve damage, osteoarthritis, liver disease, mental heath issues following a nervous breakdown, and asthma plus  few other things. I was told epilepsy was not a disability.  Four years, had to keep reapplying after failed tribunals.  I get high rate mobility and standard daily care now. I had the help fron the citizens advice throughout this. Back pay was just over £2000 no backpay for previous years of fighting . I've lost all my confidence I used to work in hospitality now I barely go out. Never stop fighting for what you are entitled to. Before I took so ill I was a full time unpaid carer for my mother who had terminal lung cancer, and a carer for my special needs son. 
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    Angela · 5 months ago
    My husband receives pip for epilepsy and gets high mobility but unfortunately nothing for care, he is waiting at the moment for a decision on his review, he has been waiting since 5th May 23 for them to deal with it, we are hoping that he is awarded some care component, if you have epilepsy it's worth making a claim