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
    My daughter falls into ME/CFS category.she has been told by two specialists  that they can’t do any more for her. She spent 10 years in the care of an immunologist, and at least 10 years in the care of an ENT consultant. Both consultants concluded that they can’t do anything further to treat her. Her conditions have deteriorated, and she suffers chronic pain and fatigue. It would be such a relief if she didn't have the added stress of having to complete a PIP form, when she has explained so often that there is no chance of any improvement in her condition.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Regarding Parkinson's, I was placed in the Protected Group for UC after winning a tribunal (with a lot of help from B&W documentation!).

    What the Benefits Agency needs to understand is that there is huge variation between Parkinson's patients, in both the set of symptoms we experience and the sequence in which they develop.

    I certainly would not qualify under this latest set of criteria, despite the devastating impact that the condition has on all aspects of my life. 

    It is horrifying to think that these criteria may be rigidly applied to people who are suffering from a progressive, debilitating and currently incurable condition, causing untold hardship and suffering.
    And all to support the Government's destructive fetish for tax cuts.

  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    It's taken me since 1985 to get DLA (Now PIP) allowed for more than 2 years at a time; had numerous appeals, 7 tribunals - all won and now have high rate PIP, both daily living and mobility indefinitely . However I don't have one condition they have listed. I have 5 different problems affecting my   a spine; spondylitis, scoliosis, Degenerative Disc disease , Maigne synrome and spondilo-lysthesis plus Fibromyalgia.  Also peripheral neuropathy, subacromial impingement sydrome in both shoulders; bladder and bowel adhesions; a heart attack and stents; extra systolic arrhythmia and now osteoarthritis  and chronic pain. All of them will get worse and there is no specific treatment for any of them so I have no consultant in charge of anything and most of those who diagnosed them, have, over 30 years retired or died. It's only if something suddenly gets a lot worse that I get a new referral  to a new consultant whop says "Can't do anything " and discharges me. My pain consultant retired and the new one says there's no more he can do even though my opiates no longer work. I've tried everything available except CBD. The last time I applied for PIP I had 11 extra pages of information and two full A4 pages  of consultants I'd seen over the years; not one of them still working.  Apart from my GP who is there they could contact about my condition? Not one of those conditions appears on the DWP  list. My life is completely ruled by these conditions. I can't stand for more than 3 minutes and can no longer use my wheelchair because of damage to my shoulders. I only leave the house for medical appointments because it's simply too painful.
    Despite them finally allowing PIP indefinitely , would I be automatically put on the list?
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    The small amount I read (in local newspaper) about Stage 4 cancer, suggests the DWP are being overly strict with regards Stage 4 Cancer patients. Particularly that Stage 4 cancer be split into two groups: those who can be put into remission from metastases (via treatment or surgery); and for whom remission will be impossible (eg the cancer is in the vertebrae, impossible to safely treat; or is in brain/nerves)..... The DWP doesn't seem to distinguish between these two groups.... Plus both groups are subjected to a weirdly strict criteria not used in oncology here..... I'm under a hospice & palliative care, but the criteria seem to be so strict they may not include me: which seems absurd. I am now terminal, whilst in my 40s, with several conditions stacked -- albeit I'm not "end of life within 12 months" terminal..... Yet I wouldn't qualify for this new group either..... 

    The "severe disability group", and DWP attitude in entirety, seems to be really harsh for stage 4 cancer patients??!!

    I don't understand.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Regarding Autism. The DSM categories seem only to refer to being a child. I am an Autistic Adult. Behaviours in adults can look very different. I have no health nor social care worker who could provide evidence on a renewed year to year basis. I am Autistic. It doesn’t go away! It is the same from diagnosis. Like having one less or one more limb. Co-morbidities are likely to include Mental ill health too (as a result of living into adulthood in a society not accommodating for Autistic adults). Many Autistic people also have physical co-morbidities like IBS (bowel), HSD (hypermobility Spectrum disorders) and/or EDS. Some Autistic people have trouble accessing appropriate care which results in severity of MH and PH symptoms of long term illness or conditions and problems with documentation due to the very process of doing so making the Autistic person very much more ill.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I currently qualify as LCWRA due to various conditions, including Autism (Asperger's) and CFS/ME. According to this, I need to meet the DSM 5 level 2 or level 3 criteria, which were not mentioned in the assessment report done for my diagnosis in 2018. As I get no support for this, it would be difficult to get any documentation to say what support I need. Regarding my CFS/ME, it says that it needs confirmation that all treatment options provided by specialist pain and fatigue services have been exhausted. I have previously been referred to a CFS/ME service, which has now discharged me three times as there is nothing more they can do to help me, and I believe I have also been discharged from the pain clinic. I have never even heard of a fatigue service in our area, so how I could have exhausted their treatment options, I have no idea. 

    This looks like the DWP expects us to jump through NHS hoops that don't exist. The current hoop jumping is hard enough, but when they're expecting us to access services that don't exist, how can we prove we've tried everything they can do for us? 
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @LoopyLou Similarly, I was diagnosed in 2022, in my late 50s, after years of seeking a diagnosis after being advised to do so by other Mental Health professionals. While I did receive a DSM 5  notification document after my assessments, there was no mention of a further breakdown into 'levels'. I also received no further support or input beyond that diagnosis (even though the document itself indicated I needed it).

      As usual, this is all just another example of the DWP goalpost-shifting within a dubiously-legal framework in order to cut costs.
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @LoopyLou @Loopy Lou I am a bit similar I had Asperger’s diagnosis 13 years ago done by nhs psychologist and my report never mentioned Dsm-5 either way back then Asperger’s was seen as level one but nowadays is all under same umbrella as autism spectrum disorder I think the Dwp criteria says must have level 2 or 3 but I think that is how much support you need I don’t get any nhs care my mum calls round and does  all for me so I don’t know?confused myself😳
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I am Autistic and in my report there are two DSM criterions. One relating to social communication impairment which is Level 1 and then restricted, repetitive behaviours is Level 2 on the DSM. I would assume because a part of my Autism diagnosis is met at Level 2 I would then in theory be applicable for the SDG? Any advice? Thank you.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I've had to go to 3 tribunals,won all, and now awaiting  to continue getting PIP, despite things getting worse ? I've got arthritis,bad back, sleep apnea, arterial fribulation,, depression,bad back, hernia in groin, high blood pressure etc etc can remember all ! Why all hassle, can't fake most of my problems? 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    They don't consider emotionally unstable Borderline personality disorder then... Try living with it! Assessors are not trained to even recognise the half of it, let alone see it face to face... I give up sick of constant turmoil of fear and panic that they take pip from me. I'm 64 and it just goes on an on... I wish I didn't have to claim , I lost my severe disability allowance as I went on universal credit,,, i don't know why even. Soz for rant. Just in tears over it all. 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    How would affect people in Scotland as most will transfer to APD this year ?

  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have Bipolar Disorder yet will not qualify as there is no community mental health service for severe mental illness where I live, due to austerity cuts and also my Trust is in special measures. I was discharged 3 years ago along with everyone else with severe mental illness. There are also never any inpatient beds or any decent, urgent crisis support. This new DWP scheme is just ridiculous and just more stress for us all. It’s not our fault there are no secondary services anymore but we’re the ones who will have to suffer! 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    If I knew then what I now know I'd rather have shot myself than deal with DWP, GPs once not in employment & Adult  social Services than go to work for DWP with it having the audacity to consider itself an equal opportunity employer with values.   
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @Elizabeth Vidler Worked for the DWP, left after 7 months due to the negative view of clients - it isn't customer focussed at all. Don't know many GP who'd need to work for the DWP or could take the discriminatory practices. The DWP has no humanity in it, for example if one of my clients was late due to a bus delay and soaking wet - I'd want to give them a cup of tea and an area to dry off in not sanction them for a few bob in salary. The DWP is a regulatory body with sticks and carrots & using the sticks too much on those on the social margins. Some fall into the benefit "trap" - it is at trap cos claimants are vilified for being unwell by being termed " scroungers" & not well enough to work to get away from the social distain, media demonising of PIP claimants. 
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @DRH I must admit I worked but had to give up due to uncontrolled seizures and associated incontinence, but to be frank I was sadly disappointed by the treatment dished out by the DWP and had I realised what a demorisling humilating experience it would turn out to be I would have struggled on and stayed in my job which I had been for 20 years, anything would be better than going through these reviews and being denegraded by msm and others as a lazy scrounger.  
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago

    For ME/CFS I see:
    -‘confirmation that all treatment options provided by specialist pain and fatigue services have been exhausted’.
    This assumes that that patient has been referred, been through the long wait and tried all the options offered? My questions would be:
    1. What happens to the ones that have no referral?
    2. What happens to the many unable to attend hospital appointments because of their illness, or who can only attend sporadically?
    3. What happens to those who have had a referral, are on the waiting list (assuming along with all the long Covid patients still waiting) or perhaps slowly working their way through a list of ‘treatments?’
    4. What happens to those who are prescribed exercise based treatments (these are no longer approved by NICE as the are proven to make more than fifty percent worse but are still in use at numerous services)?
    5. Is there any point in going to all the difficulty of trying to get a consultants’ letter or a supportive statement from the doctor if these hoops have not already been jumped though? Surely this statement would be used as a strict ‘qualifying criteria’.
    6. What happens to the patients who cannot provide evidence of attendance at pain and fatigue services for any reason at all.
    Will these patients be they refused or taken out of support group and put on whatever is the equivalent of WRaG? 
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @ALI Please stay here ALI, we like your company even if DWP don't. Their problem, not yours. So very sorry for the loss of your son. Our daughter with CFS & FM also makes any appointments in the afternoon. Shopping is online. She refused pain clinic as it was in a city outskirts 25 miles away, impossible to get there by public transport for the full days they wanted. I hope it makes you a teeny bit cheered just to know how you are not alone.
    • Thank you for your comment. Comments are moderated before being published.
      · 8 months ago
      @Mandy S amongst others I also have CFS  and fibromyalgia... after seeking help from rheumatologist and gp... I was eventually offered to go to a pain clinic... I refused purely on the facts that I'd never be able to keep appointments  as my tiredness  is off the scale... I sleep most days away... any effort I do like shopping knocks me out for at least a day !!   I now have other issues like bronchiectasis  (a lung  condition and newly diagnosed with asthma)  but my fatigue  is really bad ... I have to make any appointments for late afternoon to build my self up to get there !   so I'm guessing I'd be turned down as I DIDNT go to pain clinics  ...  I lost my 44 Yr old son suddenly last year... I live alone and  rarely leave my house... its so depressing and hearing this just makes me feel like throwing in the towel now 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    My epilepsy doesn’t happen every week but I can have up to six in a week but then that takes more than a week to recover or may be hospitalised. Does this mean that I wouldn’t qualify? During my years with this condition I have tried to get jobs and even offered to work for nothing in charity shops etc but to no avail as they cannot rely on me or they aren’t insured medically to take me on. Most of the people I know would not have a regular pattern to their epilepsy. 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have Parkinson’s which was diagnosed almost 17years ago. Initially, but  some time after diagnosis, I applied for DLA and was awarded standard care and higher mobility which meant I was able to access the motobility scheme. Then when I was transferred to PiP I initially lost both but on a MR was awarded both the standard rate. I found the whole experience of PiP the most degrading experience of my life trying to explain how a degenerative neurological condition impacts on my life by trying to fit into a box of their making to be honest the mobility component in its current format will never enable me to meet the higher rate and yet I am unable to access family, social activity without access to a vehicle. While this new system seemed a bit more promising for me personally who on earth is going to complete this extremely detailed scoring system. Having read it I cannot see my consultant or PD nurse having the time and I only see either of them once a year, I don’t see my GP for my Parkinson’s as they always consider the PD nurse as the expert. The back log is tremendous now how on earth will this be any better.
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I receive the higher rate mobility component of PIP and phoned them to find out if my multitude of medical problems some of which are serious entitled me to claim anything ? I was told that I would have to undergo a reassessment and the outcome might be that I lose my " Mobility " Without my car I would be stuck ! so what was said had the desired effect and scared me off ! since I finished work and was thrown onto the benefits system it has been horrendous !  
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I find the idea that all “medical avenues have been exhausted” is open to interpretation and ambiguity. I have had severe back pain for 20years no treatment offered, scoliosis and osteoarthritis only diagnosed 6 years ago, a surgeon looked at my spine and found no surgical options only last year. I have waited 5 years for the nhs to get to me for medial branch blocks which may or may not be effective and if they are then my next option would be nerve ablation. Who decides when medical avenues were exhausted? 20 years ago I was told there was nothing they could do, the opinion has changed constantly and any time I pay for a private physician there are many more avenues to try! The same with my Hashimoto’s disease, nhs have offered me zero medical avenues but privately I have found I could be medicated or could have surgery but those aren’t avenues available to me currently. For fibromyalgia I’m under pain management and my treatment options change constantly. All of my illness and disease can be changeable and some days I am bed ridden, some days I use a wheelchair and some days I walk my kids miles. I don’t see how any of these criteria would apply to autoimmune diseases. 
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have progressive MS .. As usual the amount of information coming out of DWP is non existent …The system seems to be in crisis from top to bottom .. and yes I have a joint bank account with my wife and she is my carer …!!!!
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    Many people have a portfolio of illnesses and disability Each on there own may not qualify them But in combination they would How would that work ? 
    As someone  who has been on a list to see a specialist from the gastroenterology for over 10 months How is all this extra work for this going to get done ? 
    Many peoples heath issues do not fit nicely into a  tick box I fear many will be penalised because of this
  • Thank you for your comment. Comments are moderated before being published.
    · 8 months ago
    I have CFS, Chronic migraine and Fibromyalgia to name a few, I should qualify but will I ? The million £ question.  The usual S**t show from DWP new ideas not thought out

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