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.
    Ash6f · 1 months ago
    Hi all I think this is ridiculous I know many people like my self don't get the severe element not because I would not qualify but because my full time carer recieves carers allowance so how do they categorise me under these rules 
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    Mrs B · 1 months ago
    Surprised to receive letter last week from the Health Assessments Advisory Service (HAAS), who replace ATOS in the region where UI live. They wanted to carry out a telephone assessment this Friday and it looks like they will basically be asking me about my various diagnoses, when the diagnosis was made, etc. all of which they should have substantial details about from my various ESA assessment forms/papers. I was initially put onto ESA in 2015, and since then after tribunals have been awarded the highest level of ESA. Rang them to say I want an advocate. I rang to ask for another date as my advocate could not make the date suggested, the woman I spoke to initially was OK and explained that I should get some dates when the advocate can't make it, and they will work around them. Not correct, it seems. Rang them again yesterday to explain I had not had dates yet from my advocate yet, and the man I spoke to was rude, obnoxious and overbearing. He told me I get three chances to be assessed; the second appointment will be sent to me since the first date has had to be cancelled.  He can't tell me what date it will be, and he actually told me that if I can't get an advocate for any of the dates then I'll just have to do it unsupported or lose my benefits. Callous? Probably deliberately so, and no no improvement on ATOS (my experience with them was horrific).  My advocate queries the award anyway; I am in receipt of the highest ESA I can get, and get the Severe Disability Premium, but the DWP letters still show I am in the WRAG group; yet meetings with the Job Centre (two meets in 4 years) ended with them saying I didn't need to look for work, do any journaling, or take any training courses. I tend to agree with the advocate, why are they even assessing me again? I'm currently being offered support for an eating disorder, I recently saw a psychiatrist as part of this process and his letter to my GP mentions my PTSD, my longstanding mental health issues, Autism etc. I am 18 months off state retirement age and can't believe they are still giving me grief. Now extremely worried and distressed and fear losing my ESA altogether. 
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    Andrew · 1 months ago
    Multiple physical issues - 3rd and 5th vertebrae swell in my neck, lower back pain, arthritis in the knees, trapped ulna nerve in my left arm being escalated to either injections or an operation

    Mental health issues - I have cyclothymia (its like bipolar but I bounce up and down daily), my next visit, they said they don't like labels because of the stigma...so they have changed cyclothymia to multiple personality issues with emotional traits. Now, how does that sound any better? It doesn't, in fact it makes it sound worse.

    More recently, I've been having memory issues and I've never had them before. My last bloods showed that I had bottomed out on Vit D (never had that before), Vit B12 (was having B12 injections every 3 months) and Folate(never had this either). 

    I have debilitating migraines and cluster headaches. I had to ask them to review my PIP because they didn't pass some information on. I'm still waiting on a decision won't know until the 26th March, I never mentioned the Vit D (got to be on it forever), Folate, and Vit B12 (probably going to be every 2 months instead of three, I told the gp months ago I didn't think the B12 was working and here we are, I knew it was wrong and I've been proven right. 

    I've qualifications in counselling and psychology and my tools I have, help me with interpreting my body better and as I've got older 
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      Annie · 1 months ago
      @Andrew Hi! I have a PhD in Psychology, and was working in academia when I got stuck with a dreadful psychiatrist (who proudly claimed she practiced psychiatry as a hobby as her husband was rich so she didn't have to work). Your experience with diagnosis, and qualifications in an allied field to psychiatry, are veeery familiar to me. I was diagnosed with bipolar disorder but found that my knowledge and education in Psychology (especially clinical) caused issues. I think the psychiatrists are not used to, and become suspicious, of patients who have our backgrounds and talk about emotions, cognition, and physical effects.

      I had a heated argument with my psychiatrist over my bro in law. He was in the hospital after acute psychotic episode associated with his schizophrenia. We both had her as our psychiatrist. Two appointments later I was discharged back to my GP. Three years later I found out, via a phone appointment with my occupational health dr, that she had changed my diagnosis at discharge. Despite never being diagnosed with depression in the 5 years I was with her (except for an episode of rapid cycling), and never being treated by a GP for it, she changed my diagnosis to "recurrent depressive disorder with emotional dysregulation". The latter was her getting a specific dig at me as this is, unfortunately, misinterpreted by others to mean I have a personality disorder and am difficult to deal with. I had wondered why my GP suddenly became very frosty towards me but having read my discharge letter I understand why. 

      So, finally, one Dr with a fragile ego (she did much more than this across 5 years) can continue to have devastating effects on your life. I applied for ESA thinking I had bipolar disorder (which I actually do & have been hospitalized for it), and my GP won't have confirmed this. No wonder my appeal was rejected. It was during the application process for medical retirement that I discovered diagnosis had been changed), got turned down and the my GP retired. I tried to do right by my bro in law and the ripple effect caused by this doctor is still disrupting my life nearly 5 years later.
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    verydull · 1 months ago
    my concern is that this is in contrast to the forms where you have to state how your condition affects you on a day to day basis. By relying solely on specific conditions means the many people who have unrecognised conditions, or conditions that affect them severely but don't fit in the criteria lose out. It is weird to have such a contrast and have no general criteria of severity for rarer conditions, but this is not even disguised, this is just rationing. 
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      VanillaOrchidae · 1 months ago
      @verydull This reminds me of the little I've read about USA SSD: they have a list of conditions, and as long as you meet one of the thresholds, you get SSDI.
      It's in stark contrast to our PIP system, which is meant to be based upon functionality.
    • Thank you for your comment. Comments are moderated before being published.
      Fionn · 1 months ago
      @verydull This! It's very a worrying development that feels like the thin end of a wedge.
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    Jace · 1 months ago
    For a decade or more well since Incapacity benifit finished or those left remaining on it claimed pensions, the severe criteria has never been made clear cut. ESA had severe, support, Activity Group, certain income related amounts qualified people to claim SDA. But how many people that have condition that will never improve in the longer term and there is no known cure virtually everyone in the support group. But still there is a large amount that don't qualify as severe why because they don't claim another benefit or not entitled because have contribution related. Anyway as I've previously said' please tell me how you get to see your specialists today let alone get them to write a letter.  This new PIP criteria is purely to cull numbers and spending and erode top ups away until everyone has the same amount. They done the same from Incapacity to ESA in the longer term you will be poorer than if you remained on current payment. 
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    Elizabeth Vidler · 1 months ago
    I do have intractable epilepsy caused by a spontaneous genectic mutation which was not passed to me by my parents but which has not responded to any drug therapy and cannot be operated on, it is a fluctuating condition, but never really improves just changes 14 years ago I developed incontinence out of the blue which has never gone away.  But at approaching 52 I suspect I will not qualify for this, but am sick of the whole benefits system really not there to assist you just to make your life thorougly miserable all aided and abbeted by the msm.  Would give up on it if I could the govt is vile.
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    Pudding Bowl · 1 months ago
    I have got a statement from a specialist clinical psychologist from a regional specialist NHS clinic stating that I have been diagnosed: “Autism Spectrum Disorder (ASD) DSM-5 without an intellectual disability & without language delay/disorder.” I submitted that evidence at my last PIP review. I still only got a four year award though, as if someone like me is ever going to get any better, if you are born autistic, its never going to be cured.
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      Paul · 1 months ago
      @Pudding Bowl I would say if anything there’s a likely hood that a person with Autism Spectrum Disorder will degenerate as they age and have to deal with major life changing events.Also if the so called health care professionals who do PIP assessments are reading this,Disorder means that a person has difficulties with daily living 
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      VanillaOrchidae · 1 months ago
      @Pudding Bowl (joking here:) You sure if you don't just eat the right berries, and meditate in the DWP office you won't miraculously improve? (I am joking: know you are lifelong with this, and if anything may go through periods where you do have language issues or functional issues, if stress is too much)...... They did the same to one of my family members who had profound cerebral palsy without any communication skills -- he got full award, but time limited for only a few years..... The DWP system for claiming is so weirdly complex, and the results given are absurd: I'm sorry you went through this with the DWP.

      DLA was actually so much easier, as it was so open for how disability impacts someone. Pip is weirdly more complex/complicated..... At a time when the government stated they were trying to "simplify" benefits. Ugh.
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      Goose · 1 months ago
      @Pudding Bowl I have this too (nhs diagnosed later in life)along with severe anxiety/dep and have Fibromyalgia as well and I only get 4 years at a time. Due again 25. 
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    Cheekyfeet · 1 months ago
    SDG is just another name for the Support Group with harsher criteria, will there still be any work conditionality for the claimant commitment at JCP for this group of people if they get into the SDG? 
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    Carole · 2 months ago
    All this is so confusing and worrying. My son has acquired brain injury through illness that many people have never heard of.  He doesn't need to see a consultant because they can't mend his brain. He has daily carers for a number of reasons all to do with his brain injury . He is assessed by social workers who organise the care which he has to partly pay for out of his  benefits. He looks and sounds OK but but has many problems
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    Gis · 2 months ago
    By "Arthritis - Late or poorly controlled inflammatory arthritis" are they completely excluding osteoarthritis?
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      LL007 · 1 months ago
      @Fionn psoriatic arthritis is inflammatory arthritis and belongs to the polyarthritis group?

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      Gaynor Horton · 1 months ago
      @Fionn Or OA right down the spine with osteophytes (increasing as you age) and affecting nerves/causing spinal cord compression.  Maybe the DWP rule makers would like to try living with it!
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      Fionn · 1 months ago
      @Gis I'm not sure. Osteoarthritis isn't usually categorised as inflammatory - it means arthritis caused by the immune system going wrong, such as rheumatoid, psoriatic, lupus arthritis, etc. (I have both the osteo and inflammatory types, and asked the consultant to explain the difference.)

      That *wouldn't* mean disability caused by osteoarthritis would be excluded – obviously it can be just as severe – only that it might not always fall under these rules. But DWP makes it up as they go along anyway, so who knows!
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      Liz · 1 months ago
      @den1mon yes as osteoarthritis is a joint degenerative condition whereas rheumatoid arthritis is the inflammatory arthritis.🥲.
    • Thank you for your comment. Comments are moderated before being published.
      den1mon · 2 months ago
      @Gis Of course not.
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    Mb · 2 months ago
    I have been mentally ill due to childhood trauma, officially since 1990, the first time I saw a psychiatrist. However subsenquent bad experiences have led me to refuse to be consigned to the mainstream services so although I have been receiving weekly psychotherapy for over 20 years I do not have a psychiatric diagnosis. I have always been able claim without one as I have still have medical evidence of symptoms. I am now in my 50s and am unlikely ever to improve. But I will never submit to the control of psychiatrists, ever. So I will have to remain on the DWP hell wheel forever then...
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    den1mon · 2 months ago
    Yes I would qualify.
    I don't know what all the fuss is about.
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    The Dog Mother · 2 months ago
    As I said before.. it sounds like nonsense from the get go. 
    The utter confusion they churn out in panic at trying to reduce numbers claiming is pathetic,And I'm pretty certain nothing is ever set up to help us.
    It's about time the dwp staff rebelled and said enough is enough. They can't possibly keep up with all these proposed changes,one after another, how are we meant to.Its mind bending. 
    • Thank you for your comment. Comments are moderated before being published.
      Helen · 1 months ago
      @MrFibro Really! Anyone can apply for the job,
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      Neil · 1 months ago
      @MrFibro Have you seen the latest news on work coaches? They’re going sick and resigning en masse due to the pressure of the job. Obs the job description and responsibilities is as opaque as the rules for claimants but with unofficial targets for numbers sanctioed
    • Thank you for your comment. Comments are moderated before being published.
      MrFibro · 1 months ago
      @The Dog Mother The dog mother,

      The DWP staff may look at it this way, it creates more work for them.  Equals keep them in a cushy well pensioned job.
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    Katie · 2 months ago
    Given that the NICE guidelines for ME/CFS were updated to state that there are no treatment options, it seems that the DWP need to update their files on that one. How can we try something that doesn’t exist? 
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      JC · 1 months ago
      @Julia Agree.
      Although I'm wondering if they consider CBT and 'Fatigue Physio' (the newly branded GET) as treatment.
      Most of us with ME who've been to a specialist fatigue clinic of a hospital have been signed off once those are complete and are under no treatment at all, not even 5 year check ups.
    • Thank you for your comment. Comments are moderated before being published.
      Rob · 1 months ago
      @Julia what frightens me is that there are still clinics and doctors around offering snake oil CBT and GET. The DWP might require a sufferer to undergo a treatment that is actively harmful. At the very least, the guidelines should state "in accordance with NICE guidelines".
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      Jan R · 1 months ago
      @Katie I was wondering the same Katie, I was recently diagnosed and it says on my letter that there are no treatment options and that the 'pathway' of support will be self managed pacing. I'm waiting to hear from the dwp about my lcwwra application, the whole thing is so messy and difficult to navigate 
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      Julia · 1 months ago
      @Katie Agree!  ME for 36 years.  Ideas for treatment long since exhausted!

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    MrFibro · 2 months ago
    As this news headline states..... SHAMBOLIC!!!

    This government and the DWP combined don't know the difference from their elbows or their arises.

    It's as though they choose to keep changing the goal posts in order to cause more confusion, distress, despair, anxiety, and depression to the claimants.

    If they want to save money, then there's loads of ways to achieve, not pick on disabled sick claimants.  They say they want to help the vulnerable in our society, ermm yeah right!

    • Thank you for your comment. Comments are moderated before being published.
      MrFibro · 1 months ago
      @Catriona catriona,

      Thanks for your reply.  I have multiple illnesses, and still its been a nightmare trying to convince the dwp assessors that I am disabled, and will never be able to work again.  To answer your question I am a bit doubtful, even though Fibromyalgia is now classed as a real illness which is debilitating in its own right. (this was debated quite a while back by MP's in parliament) (date i don't remember now but it can be googled.)

      But many others disbelieve this and will push to make sure or harder that's it's remains an illness, which basically is in the persons/ claimants head.

      Which as you know is far from the truth.

      I wish you & all other subscriber here good luck for the future.
    • Thank you for your comment. Comments are moderated before being published.
      Catriona · 1 months ago
      @MrFibro Mrfibro i take it you have fibromyalgia as I do. Do u think we will qualify fornthe sdg group? 
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    James · 2 months ago
    I said before I only have level 1 autism so I won’t qualify i don’t care anyway I will be middle 50s if they do bring all this in what will probably happen is the non severe illness will have to go in for interviews with a work coach the Dwp are just making it harder and harder to get left alone now 
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    keepingitreal · 2 months ago
    Surprised much?
    • Thank you for your comment. Comments are moderated before being published.
      Sara · 1 months ago
      @keepingitreal I went to the consultation and this was discussed. Sorry to get Political but this is. They need the money to provide Tax cuts. Those people in these groups are defenceless. Many are only just existing. My daughter is on enhanced Living and mobility because she has a condition that will never change. There is frankly no need to review her in a rational sense. I have all the evidence. They scratch around in the hope that they will find(very vulnerable) people who are supported and do not have the skills to fight back and get all the correct paperwork to qualify for something that they are legally entitled to. I have been helping someone with severe Autism who had PIP from a child. It lasted as his parents threw him out- they could not cope and he spent 10 years homeless!!, so in 2019 he re-applied. He failed as he had know idea what he was dealing with and no support this is when we began to support him. I supported him at a Tribunal from this reapplication, which was a terrible experience and actually unbelievable? I had already joined this wonderful group to seek advice and I made a new application for him as suggested on this forum and we achieved PIP basic level for living. ( thank you everyone here) Last March he had a review (3 years)  and we filled in all the forms with the help of a wonderful lady from the CAB ( by this time we had found evidence and his original DLA paperwork) and this January, he was finally given  Enhanced Living which he should have received in the first place! We literally could not believe it ???? After being at the consulation for the proposed changes  in London  I am under no illusion that disabled people's money  will be used to fund vanity projects. Not one person in that room including a Jobs coach really understands long term severe disability. They were all young and carefree. There was a man who came to try to explain to them his life situation himself. My heart bled for him. The most scary person was the lady from the ministry in Whitehall who just wanted to stay on the Agenda - ie not listen. So we have a battle ahead I am afraid 
      My daughter is being reviewed now and as her condition will not change I have asked for a 10 year + review but I am not hopeful. This process grinds in the pain of Mental disability, is in no way healing or supportive and we desperately need a change of emphasis by the powers that be. The actual savings are tiny in comparison to the overall spend of the Treasury on these things in this system. It a war on our most vulnerable citizens.  Sorry for the Politics. 
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