The DWP has revealed more details of what now seems to be a shambolic system for assessing claimants for the Severe Disability Group. According to the latest DWP update, membership will be based on a confused, ad hoc collection of criteria. 

Depending on the claimant’s diagnosis, entry may be based on:

  • medically precise definitions that have no connection with the benefits system at all; or
  • on information that only the claimant or carer will know, but a specialist will still have to provide; or
  • the availability of specialist services where the claimant lives; or
  • even on no clear criteria at all.

There is also a lack of clarity on the overlap between the Severe Disability Group and the light-touch review system for PIP.

And some claimants are voicing the suspicion that the creation of separate group of severely disabled claimants could be aimed at reducing future payments for allegedly less severely disabled people.

What is the Severe Disability Group?

The purpose of the Severe Disability Group, according to the DWP, is to improve the assessment process for claimants who have conditions which are severely disabling, lifelong and with no realistic prospect of recovery.

Claimants who fit the criteria will not need to complete a detailed application form or go through a face-to-face assessment for PIP or the WCA.

There’s more details about the scheme here

But, in essence, claimants will need to show that they have a condition that will not improve, that it is managed or was diagnosed by a specialist, that they need help from another person with at least two daily living activities and that they would qualify for the support group or for at least one enhanced PIP component.

There are then different criteria for different conditions, which also need to be met.

Medically precise definitions

It has long been a basic principle of disability benefits that it is not the condition that matters, it is how it affects your everyday activities. 

Yet, for entry to the Severe Disability Group, it is very much the condition that counts.  In some cases, only those who meet specific medical assessment criteria will qualify.  For example (please note, the links are provided by Benefits and Work, not the DWP):

for autism you need to meet DSM 5 level 2 or 3;

for heart failure, New York Heart Association (NYHA) 3 or 4;

for multiple sclerosis you need to score more than 6 on the Expanded Disability Status Scale;

for  Parkinson’s Disease, you must score 21 to 30 on the UPDRS.

Very often, scores like this will not appear anywhere in NHS records, so new evidence will have to be provided by a specialist.

In addition, many claimants who do not meet these scores will still be in receipt of PIP at the enhanced levels for both components and have no possibility of their condition improving.  Yet they will not be eligible for the Severe Disability Group.

Only the claimant will know

For some conditions the criteria are not only less precisely defined, but they are also ones that a specialist will not be able to give first-hand give evidence on.

For epilepsy, you need to have “incapacitating seizures at least once per week despite optimal medical therapy”.  But probably the only person who can give detailed evidence on the frequency of seizures will be the claimant themselves or a carer, if they have one.  A consultant’s evidence will be hearsay at best.

The only criteria given for strokes is that the claimant “requires assistance from another person to mobilise, dress and feed themselves”.  But this is something that would probably be better judged by an occupational therapist than a specialist and, ultimately, only the claimant or their carer will have first-hand, daily knowledge about this.

Availability of services

For some conditions, access to the Severe Disability Group will depend on having services available in your area.

For example, for bipolar disorder or depression, you will need to show that you are “under the care of specialist psychiatric services” and have a “history of recurrent admissions or crisis team treatment”. If the NHS in your area is too overstretched to provide these services in your case, then you will be unlikely to qualify.

For OCD, you will need to show that you have failed to “respond to treatment by intensive specialist treatment services”.  This assumes that such services exist in your area and are available to you.

For ME/CFS, you will have to show that “all treatment options provided by specialist pain and fatigue services have been exhausted”.  Again, such services may not even exist where you live, may have a very long waiting list or may not be accessible to you because of the travel time involved.

No clear criteria at all

For people with multiple conditions – and that would include a huge proportion of claimants – the DWP explains that entry to the Severe Disability Group may be available:

multiple impairments, for example combinations of COPD, coronary artery disease, diabetes and obesity that would not meet the criteria as single conditions but may do so if present in combination.

But there is no explanation of how this would work in practice.  If you don’t meet the criteria for any single condition, what do you have to prove in order to meet the unexplained criteria for multiple impairments? 

And which health professional would be the one required to provide the evidence?

All of this remains unexplained.

Overlap with light-touch reviews

Oner of the questions that has yet to be answered is how the Severe Disability Group will overlap with the light-touch review system for PIP.

In July 2023 the DWP began sending out the PIP AR2 light-touch review form to claimants who have:

  • very stable needs which are unlikely to change over time
  • high level needs which will either stay the same or get worse
  • a planned award review date due on or at State Pension age

The AR2 form is very much shorter, is unlikely to result in a face-to-face assessment and has to be completed only once every ten years.

On the face of it, this seems to be similar to the Severe Disability Group, at least for PIP claimants.  And it has the advantage that it does not require any medical evidence in order to qualify.

But what isn’t clear is whether the Severe Disability Group will replace the light-touch system, run parallel with it or whether a claimant could be subject to both systems.

Lower payments for non-severe claimants?

Government voices have been issuing warnings about the cost of disability and incapacity benefits for some time. They claim that far too many people are being placed in the support group and that the cost of PIP is spiralling out of control.

This has led some claimants to suspect that the Severe Disability Group is the first step towards cutting the cost of these benefits in the future.

The theory is that, if you divide disabled claimants in to severe and non-severe groups, you can argue that claimants who are not severely disabled should not be entitled to as high a rate of support as those who are.

This is exactly what was done with the WCA, when new claimants in the limited capability for work category were deprived of the additional amount that had previously been awarded.  For new claims now, only those with limited capability for work-related activity get an additional amount.

It is very unlikely that any government would try to reduce current PIP claimants’ awards, because of the unquestionably enormous backlash.

But an altered payments system for new PIP claimants in the future is not hard to imagine and would cause much less controversy, though we should stress that the DWP have made no suggestion that this is their intention.

Specific condition criteria

Below, we’ve listed some of the more detailed criteria that the DWP have now published for different conditions.  There’s more on this DWP page.

We’d really like to hear from claimants with experience of any of these conditions as to whether you think the criteria are reasonable and whether you think you would qualify.  Please use the comments section to let us know.

Please note, the links are provided by Benefits and \Work, not the DWP.

Arthritis

Late or poorly controlled inflammatory arthritis

Autism

Autism spectrum disorders - meet the DSM 5 level 2 or level 3 criteria - requiring substantial or very substantial support (annex 2)

Bipolar disorder/depression

Long term severe depression or bipolar disorder failing to significantly respond to treatment, under the care of specialist psychiatric services, indicators of unstable mood and worsening functioning requiring ongoing high levels of care or supervision including history of recurrent admissions or crisis team treatment, decreasing intervals between episodes of relapse or rapid cycling

COPD

Severe chronic respiratory condition (e.g. chronic obstructive pulmonary disease (COPD), fibrotic interstitial lung disease, diffuse pleural thickening) with grade 5 MRC breathlessness (too breathless to leave the house or breathless when dressing or undressing)

Epilepsy

Intractable epilepsy with associated cognitive impairment and incapacitating seizures at least once per week despite optimal medical therapy

Heart failure

Heart failure with reduced ejection fraction on maximal possible tolerated medical therapy and cardiac resynchronisation therapy if indicated, with ongoing limiting symptoms, New York Heart Association (NYHA) 3 or 4 and not a candidate for cardiac transplant

IBD

Treatment resistant inflammatory bowel disease

OCD

Longstanding obsessive-compulsive disorder (OCD), failing to respond to treatment by intensive specialist treatment services, with severe ongoing symptoms resulting in significant difficulties with ADLs

ME/CFS

Syndromes characterised by chronic pain and fatigue where symptoms are longstanding, affect multiple activities of daily living (ADLs) and confirmation that all treatment options provided by specialist pain and fatigue services have been exhausted

MS

Advanced multiple sclerosis scoring more than 6 on the Expanded Disability Status Scale (EDSS)

Multiple physical conditions

Multiple impairments, for example combinations of COPD, coronary artery disease, diabetes and obesity that would not meet the criteria as single conditions but may do so if present in combination

Parkinson’s disease

Advanced Parkinson’s disease with bilateral symptoms of tremor, rigidity and bradykinesia and impairment of balance, a Unified Parkinson’s Disease Rating Scale (UPDRS) score of 21 to 30 and requiring assistance from another person with most activities of daily living

Schizophrenia

Longstanding schizophrenia, failing to significantly respond to all treatment or rehabilitative options, under the care of specialist psychiatric or support services, significant continuing symptoms and poor self-care requiring ongoing high levels of care and or supervision

Stroke

Stroke, for example where the person requires assistance from another person to mobilise, dress and feed themselves

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  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have clinicial depression and tried to take my own life a few years ago,we think this is because  I have had multipul operations on my back and that has left me with various issues, ie incontinence, mobility is poor, pain so times extreme pain. I have had two consultants and two GP's write letters stating I will never improve this is concidered perminant.( THOSE WORDS,  I had DLA awarded indeffinatly and I still had to to through all the pip degrading assessments when i changed from DLA to PIP .  I have already told my son should I have to jump through hoops with my claim again, I will end my life, but im not due due a review for about 18 months,  after I tried to take my own life they told me next time would be a light touch but I  dont believe them.  I am 58 years old so I am getting old anyway. I wonder if they realise that some of us have carers that would be out  of work if we lost any of our benifits. I have three part time carers
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    There’s only one reason for them to move their own goal posts, to deprive and defund. When you are dependent on home help for your independence and they constantly threaten to remove essential funding you fear for your health & safety.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    The whole thinking on autism is evolving and the fact that the DSM5 mentions 'a child must have persistent deficits in each of three areas of social communication and interaction' is alarming. What about adults? Women present very differently. You have to meet the criteria anyway for a diagnosis of autism. I actually got help from Winvisble (for women with invisible disablities) and they were incredibly helpful and wrote a letter of support for my ESA. One of the things was that people who have a lifelong condition shouldn't keep having to do repeated assessments (this was for ESA but could also be argued for PIP). Autism is a lifelong condition and you need to demonstrate this in assessment. The worry more is for people who self-diagnosis which is perfectly legit in the autism community.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have ME and fibro (19 years) yet each PIP renewal in the past they tried to reduce me from standard care (realistically need enhanced but the crash from appealing before and what I later found to be wrong information from them about take what you had before and you won't have to go to trial made me not fight for enhanced care) enhanced mobility to just standard mobility. 3 months of fighting and I got it back. This time I'm awaiting a response as my situation has changed and now have to do more on my own but still waiting for OT assessment that might back up my PIP papers. I was under CFS/ME (their labelling & based in psychotrauma department so not biomedical) and Pain Management at Bart's and both discharged me - the first saying I'm doing pacing and as pain is main issue they'll leave it to Pain Management, and the latter saying I've sorted as much as I can and GP can increase levels of meds if need be but come back if anything changes. There are now no ME services in E London apparently. Not sure if that constitutes confirmation that all treatment options provided by specialist pain and fatigue services have been exhausted but I did try loads of drugs, acupuncture, lignocaine infusion and being discharged from physio because the effort of actually getting there set me back for weeks without actually doing exercise.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    “For ME/CFS, you will have to show that “all treatment options provided by specialist pain and fatigue services have been exhausted”.”
    Well, given that the NICE Guidelines make it clear there is no treatment for ME/CFS…
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Inflammatory Arthritis excludes Osteo Arthritis which is degenerative and affects many people.
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @Mumar Especially when it is in the spine, with osteophytes right down, affecting nerves and causing spinal cord compression/degenerative cervical myelopathy etc and increasing pressure as you age.  The spinal operations are considered a success if they manage to stem progression creating more room for the nerves which may not even recover from bruising, nothing is guaranteed, it can halt progression but most likely not last, it can make it considerably worse (risk of paralysis)it can weaken the spine above and/or below it, it may appear to give an improvement but rare ever lasts.  OA can become much of a gamble. I'm guessing you too have it somewhere, as do I in many joints.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have autism but they never said what level it was. I’m also on a waiting list for adhd  I’m heading to aged 55. I have OA and a knee issue. I wear specs for a squint . And I get a skin condition. The arthritis is in my back elbows and the knee is wear and tear. I have 3 degenerative discs which give if I try to sit for too long or repeatedly reach bend and lift and ae painful and . I have anxiety, depression and ptsd and socially I don’t fit anywhere. My last pip form was posted. Late January end of January. I get side effects off meds. I also have GERD and IBS. Most of these things are autism co morbidities of autism. I was diagnosed when I was 51-52. My last pip form was called a reward review form. Most of it was the same but they didn’t have my autism and possible adhd until this pip form. Will I get pip. Idk but social services are trying to help me with things. I got pip he last assessment. I wasn’t supposed to be assessed til around July to September but they did it 6 months early. I hadn’t realised the last award I got three years  not two. But then they did it earlier. 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Interesting that DWP doesn’t include ME/CFS under “Neurological Conditions”, when the World Health Organisation classifies it as a Neurological Condition. Perhaps DWP needs to do its homework on this, as ME/CFS has a new set of NICE guidelines (Oct 22) which very clearly sets out the nature and progressive stages of the illness, and that by its very nature is only diagnosed when all other causes have been ruled out, and no further treatment is available nor any improvement is likely. We are, by definition, incurable. 
    So anyone with a diagnosis of ME/CFS who hits or has hit the ‘enhanced’ level of DL or M should be immediately spared any further scrutiny by DWP. Believe me, if any of us miraculously get better, we won’t be keeping it a secret!
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Also, people with Severe ME/CFS will not even be able to attend clinics or treatments, firstly they/we are too ill, and secondly the clinics that do exist almost always refuse to see those who are Severe. We are too ill - all the care disappears back to the GP we can't get to, and the carers we can't afford. 

  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    There is no treatment for ME/CFS. Do they not know that?   They have completely missed the point that it's Post Exertional Malaise that creates the disability, not the fatigue. There are three now banned treatments which either do harm or make no difference. (GET and Lightning Process are rightly banned by NICE and CBT can traumatise the patient if it's pretending to be curative, or it simply has no effect). What happens if the local ME clinic is attempting to offer the now banned GET, will claimants be forced to attend and participate and suffer harm from a treatment banned internationally as well as by NICE? The whole thing doesn't add up. ADLs need to be a measure, but they haven't grasped the nature of the disease and that there is no treatment. 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    The condition that is never covered by DWP criteria properly is lymphoedema I find, and of course that's what I suffer from. Agreed, for me I do obviously have a specialist diagnosis and ongoing care, but a specialist can't comment on how it affects my daily living challenges! I am in fact housebound with carers 4 times a day, so, yes, my carers/care agency would be the best option to provide information, but that won't happen!
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Oh, and I notice that the arthritis is for inflammatory type and not osteoarthritis (i.e., the one your Dr doesn't care about). 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Spot the irony in the ME/CFS section about all treatment options being 'exhausted'. Long covid belongs there too. I guess it's 'too new' for the government to accept it's a long term condition, even though in some it is following the same trajectory as ME.

    The criteria do seem to vary wildly across conditions, though the gov. do state that these are examples, so it might not be (intended, in theory) to be as definitive as it could seem at first reading.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    The bipolar, and schizophrenia, criteria skirt around the significant cognitive impairment that can occur, either due to the illness or medication or both, and that it tends to only ever get worse, not better. Cognitive impairment is poorly recognised by psychiatrists, they don't look into it, measure it, or enquire about it at each appt. The psychiatrist I had shouted "of course you've got cognitive impairment! Stop talking about it!". She never once mentioned it in reports to my occupational health Dr even though my employer was looking to pay to have an occupational functioning test conducted on me.

    The cognitive impairment is brutal and it gets in the way of everything and no Dr is interested. I even failed that 3 question memory test the GPs use but got "well, you have bipolar so what do you expect"
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    The entry for ME/CFS would be hilarious if it weren't so terrifyingly wrong.

    1)  ME/CFS is not primarily fatigue, despite the belittling name "chronic fatigue syndrome" made up by psychologists for the benefit of US insurance companies. Much of the physical disability is caused by rapid muscle fatiguability and post-exertional worsening, not fatigue.

    2) The NHS refuses to prescribe painkillers to many people with chronic illness, and pain clinics are almost as difficult to access. Not everyone with ME/CFS even has disabling pain – for some people, severe cognitive impairment has a much bigger impact.

    3) The National Institute for Clinical Excellence (NICE) has issued guidelines saying there are no treatment options for ME/CFS. 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have Anklosing Spondylitis. My neck has fused and I have severe posture problems and kyphosis.  I can't move my neck at all. I would be stunned if I didn't qualify for the severe disability group or whatever it is called 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Hi I have bipolar, bpd, fibromyalgia and I’m on the autism pathway .  But severe disability eligibility say I need to have been hospitalised , to qualify.  I’m limited to life at home , there is no hospital space for MH.  Should I still apply? I’ve now moved  into a UC area and it’s been a nightmare with benefits already . 
    • Thank you for your comment. Comments are moderated before being published.
      · 7 months ago
      @Nicola I am dreading the forced switch from legacy benefits onto UC, so I really feel for you. UC is an absolute joke. But as for your question - I would apply for anything and everything you believe you are entitled to, despite the stress and fear the application process (and reviews for that matter) induce. I am convinced that DWP purposely makes it all as scary as possible to put as many people off as they can. It is often the case that the people most in need of the support of disability benefits are not in receipt of any of them, because they are too unwell to face subjecting themselves to the application process, or are unable to complete the application forms, or return them in time. A lot of people worry that the money that they already get might be decreased, and don't want to rock the boat by applying for additional support. Often people are turned down and either can't face appealing or don't realise that they can/should - when the statistics show that they overturn a huge percentage of their negative decisions on appeal.
      If we do not push for what we are legally and morally entitled to, we are helping DWP to keep us down. Don't give up - keep fighting, for all our sakes! You are as worthy and deserving as any other disabled claimant.
      Good luck to everyone on here
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have been claiming PIP for disability for over 6 years now. I have metal plates in my ankle making walking difficult, arthritis in BOTH hips and two slipped discs in the back. I have been waitimg for over two years to see a specialist for my back. My last appointment was in Decmeber 2023 but the NHS cancelled it. The next one is september 2024!

    I am also awaiting consultation regarding hip replacement.

    Do I think I'll pass the test? NO! The DWP don't care about striking Doctors or waiting lists, they just seem to think that if you can cope without the treatment (waiting) then you don't need it!
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have severe heart failure,dialated cardiomyopathy and left bundle branch block.  I have a pacemaker and defibrillator fitted and have top doses of medication. I am  still graded a ls 3 on the NY scale but because I may qualify for a heart transplant I do not qualify. How is this  fair? Surely  I should qualify  but it be withdrawn if I have a heart transplant.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I was moved from DLA to PIP IN 2017. I have quite severe erosive arthritis & have had 4 joint replacements and more to come. I was in the higher group for both living & getting around. I was reassessed & put into standard for both forms . I took it to appeal & they refused to budge. I met the chap from the DWP when I was leaving the building & he said to me that if I couldn’t drive I would have got full benefit. But because I can still get around by driving I lost it. I was very upset because I lost my motability car. 

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