The PCS union has warned of “staffing chaos” at the DWP, with work coach roles being particularly affected as the government seeks to hire thousands of new staff, having just made hundreds of workers redundant.

According to the PCS the DWP needs around 5,900 staff to carry out a Targeted Case Review of incorrect UC claims.   

However, this means not only mass recruitment, but also moving large numbers of current DWP staff into new roles to carry out the review.

This is at a time when the DWP have only recently made 800 staff redundant.

As a result of the staffing chaos, additional ‘support measures’ are being put in place in Jobcentres to manage the workload of work coaches.

This includes reducing the frequency of work coach contact with some claimants from fortnightly to monthly and shortening some meetings from 50 minutes to 30 minutes.

The PCS argues that:

“The difficulty that DWP is having in recruiting is apparent from the raft of panic measures that have been introduced to mitigate against it . . . It is clear that working for DWP is an unattractive proposition. The DWP really needs to improve on poor pay and terms and conditions to ensure the most vulnerable in society receive the kind of service they deserve.”

To make matters even worse, at the Conservative party conference the Chancellor announced an end to civil service expansion with an immediate cap on the civil service headcount, with a view to reducing it to pre-pandemic levels

As the PCS put it:

PCS members have been reporting for years that chronic under-staffing and backlogs of work have led to toxic working environments, with stress levels going through the roof and pressure ramping up as more is expected for less. Yesterday's announcement by the chancellor will only add to the concerns of our members.”

With the DWP failing to manage its current workload, the idea that tens of thousands of additional claimants can be removed from the LCWRA group and given effective support to help them into work is clearly nonsense.

It suggests that the sole purpose of making the WCA much harsher is simply to save money by reducing the amount of benefit claimants receive, with not the slightest interest in what happens to them as a result.

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  • Thank you for your comment. Comments are moderated before being published.
    Anon · 6 months ago
    I'm a Senior Healthcare Support Worker working in the Scottish NHS. I caught Covid at work back in April 2020, which developed into Long Covid. I've somehow managed to keep working, despite various hospital admissions and major collapses. I've previously helped one of my sons claim PIP for an ASD and co-morbid conditions, which was an extremely unpleasant business over many years. As a result, I didn't bother applying for PIP, now replaced by Scottish Adult Disability Payment, as I didn't feel like being put through the mill while unwell myself.
    However, my Occupational Therapist persuaded me to apply for Scottish Adult Disability, saying that the system is a lot better and the staff don't appear incentivised to block applications. I made a couple of phone calls, wrote up an application as the Social Security Scotland staff recommended, and had my application approved in less than two months. It was astonishingly straightforward and non-judgmental compared with years of dealing with the DWP and its subcontractors. 

    I was awarded the standard rate, which has been a big help as I've had to go private for support with Long Covid, paying for private GP, private LC/MC/CFS specialist doctor  and (soon) private neurophysiotherapy. Unfortunately my health board (and employer!) decided to go for a GP-led approach to LC and my rural surgery does not appear to accept my condition is genuine - despite diagnoses from various consultants. The payment also helps with the cost of incontinence products as the neurological impact of my LC presentation has given me severe bowel issues on top of chronic fatigue, chronic pain, cardiac issues, hearing and sight issues, numbness, cardiac issues and more. 

    The Scottish approach to Adult Disability applications, in my experiences, is a million times better than the DWP's approach.
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    Heather Mcbirnie · 6 months ago
    I was diagnosed with Long Covid while in hospital as went into a coma with it. I was in the hospital for a full month and when I came home my house had to get certain amendments made for me. It took me 18mths to get PIP and the process was a disgrace. I had medical people helping me and thus made no difference to my claim in the end my daughter had to go to an outside aid organisation that helps us where we stay. I also have had 2 strokes and other serious illnesses so it shows that they are out to put you off as much as possible and I will tell anyone to appeal and get as much help as you can.
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    Vee · 7 months ago
    I'm 26 and got long covid a year and a half ago. I made a PIP claim last summer and was awarded higher mobility and standard daily living. I made sure to explain that I feel too tired to walk anywhere most of the time (key phrase is 'less than half the time'), and when I do walk I can only do very short distances and very slowly.
    They didn't seem as interested in hearing about my difficulties with daily living tasks. There are no points for things like not being able to do the dishes or wash your clothes or clean your house sadly.
    I think a key factor in my good outcome was having letters from the long covid clinic I am under. I had written in detail about my limitations and they and my GP had then signed it.
    What I wish I had known: make sure you save your online form at the end because otherwise you won't be able to see what you wrote
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    Star · 7 months ago
    I’m a Mental Health Professional who contracted Covid at work (NHS) - previously fit, healthy and young!

    I’m not severely disabled by one infection. I can not walk and now rely on wheelchair or crutch most days, although majority of the time I’m couch / bedbound.

    I now suffer with a condition called MCAS mast cell activation syndrome- meaning I am now allergic to EVERYTHING! - I’ve have been forced to eat only 9 foods | water only since my infection last March 2022.
    I’ve lost substantial amounts of weight - weighing similar to a child.

    I can no longer use toothpaste, body care | hair products or anything that involves chemicals, scents or other!
    - I have allergic reactions to them all. Even natural products such as coconut oil.

    Furthermore, I can no longer go out in the sun - because I’m now allergic to UV rays.

    I can no longer tolerate any supplement, medications- which puts me at risk of getting unwell and suffering more. However, if I take these medications etc - I can go into anaphylactic states, just like when I try to eat foods and all the rest.

    I also react to the environment including VOCs such as toxins released from new carpets and other furniture types. 

    I have around 7 permanent conditions that I have been diagnosed with, inc ME/CFS, POTS, Fibro , MCAS, Sun Allergy, Food intolerances and still under investigation for others.

    My experience with claiming PIP was fortunately successful, however very stressful. I had to get help to complete the forms and provide additional evidence and personal statements from people who help care for me and other documentation from all of my specialists I am currently seeing. 

    I fear the day, I have to reapply. I claim ESA too - which I find more difficult to navigate.

    I am no longer able to function independently and can no longer continue to work in the capacity I did. I am in the process of potentially losing my career, as I have been on sick leave since I caught Covid last year.

    It has destroyed my whole life!