There are growing signs of a DWP push to claim that conditions like ADHD, autism, anxiety and depression are less likely to lead to significant additional costs and, therefore, should be treated differently by the benefits system. In order to challenge this argument, we’d like to hear about the extra costs you face if you live with one of these conditions, or care for someone who does.

Cost-free conditions

Jean-André Prager is a member of the Timms review steering group.  He is also the co-author of a new report for a right-wing think tank calling for up to 70% fewer child DLA awards for mental health, learning difficulties and neurodevelopmental conditions.  This would apply both to new and existing claimants when their award is reviewed.

Prager argues that needs such as tube feeding, oxygen or substantial mobility assistance have readily identifiable costs.  But he claims that “where the principal additional need takes the form of prompting, behavioural management, supervision or motivation, the burden may fall primarily in the form of parental time, vigilance and complexity rather than direct expenditure.”

In other words, mental health, learning difficulties and neurodevelopmental conditions take parental time but are relatively cost free conditions.

Secretary of state, Pat McFadden told MPs in June of this year that he had raised the issue of neurodevelopmental conditions with the Timms review steering group, who are tasked with redesigning PIP: 

“In particular, there has been an increase in conditions like anxiety and depression, neurodiverse conditions and so on. Is this benefit fit for purpose in the way that it is designed, in dealing with that variety of conditions? That is a very interesting question for the reviewers. When I went to speak to them a few months ago in one of their sessions, that is the question I put to them to consider.”

McFadden doesn’t directly call for cash awards to be replaced, but the implication is clearly there.

And in July this year, Timms was asked by Tory MP Joe Robertson whether he accepted that “a system of cash payments to some people with conditions such as attention deficit hyperactivity disorder, where half the claimants are aged between 16 to 24, is not what they need most?”

Timms responded that “The steering group is clear that the provision of cash to meet the additional costs of disability is vital. We will not be moving away from the importance of that, but I think there is a question about whether the process can also point people towards help that may be valuable to them in addition to, or in some cases perhaps instead of, a cash payment.”

The possibility that some people could get help instead of a cash payment for conditions like ADHD is, therefore, one that the Timms review is considering.

DLA for children

Benefits and Work believes that autism, ADHD and mental health conditions result in substantial additional costs when caring for children. These may include:

Transport:  children may need accompanying on journeys when other children of the same age travel independently.

Clothing: frequent replacement because it gets lost or damaged, clothing that meets sensory needs.

Learning and activities:  additional learning support and specialist play schemes.

Sensory aids and adaptations: noise-cancelling headphones, ear protection, suitable lighting or blackout blinds; specialist software.

Food:  cost of wasted food, compulsive eating or the need to eat particular foods.

Household items:  cost of replacement because of breakages or rough handling.

Home education:  the cost of materials, tutors if available and travel associated with home education because your child was bullied or insufficiently supported at school.

Healthcare:  because the assessments or treatment your child needs are not available on the NHS or the wait is impossibly long, you have to pay for them.

Lost income: time off work to provide additional care, including when a child is excluded from school.  DLA is not an income replacement benefit, but this is a major cost for many parents.

PIP for adults

In relation to adults and PIP, some of the costs of these conditions may include:

Transport:  taxis because of difficulty navigating journeys on foot or using public transport. 

Shopping:  the cost of deliveries because you are unable to visit supermarkets or shops.

Food:  ready-prepared meals because difficulty initiating and completing tasks or executive-function issues prevent cooking.

Sensory aids and equipment: as above.

Private assessments and therapies:  especially private sector mental health support, because it may not be available on the NHS.

Utilities:  more heating and electricity because your condition means you seldom leave home. 

Managing money:  problems with managing money lead to late-payment charges and additional borrowing costs.

Help at home:  because of fatigue or difficulty initiating and completing tasks you may have to pay for help around the home - including cleaning and gardening - in order to keep it safe and habitable.

Tell us your experience

We’d like to put together some evidence to challenge the cost-free conditions argument.  So - as a first step - we’d like to hear from readers who live with ADHD, autism, depression or anxiety or who care for someone else, including a child, who does.

What are the extra costs involved?  Can you estimate how much extra you spend on different activities?  Please include things you need but cannot afford, because having no money to spend does not mean having no additional costs.

If you can, give rough weekly, monthly or one-off amounts.

You can leave a comment below or contact us to tell us more.  We may publish extracts from your email responses anonymously, so please leave out identifying details and only include information you are comfortable having published.

 

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  • Thank you for your comment. Comments are moderated before being published.
    · 20 days ago
    Question first, is fibromyalgia and menopause related issues also being considered in these 'cost free' conditions? 

    As to the one's mentioned, I already have significant costs due to budgeting issues eg going overdrawn due to impulse spending, lack of organisation (with adhd the clues in the title) then lack of motivation and shame to sort things out myself, utter lack of any support let alone appropriate support...pip wouldn't touch the cost of private help that would allow me to function optimally let alone scrape by. The burnout and ptsd and chronic pain mean everything takes many times longer and my unsuitable housing association flat is an additional health risk that has led to additional problems due to living above 2 SMI tenants whom have many loud parties and screaming sessions and dubious visitors. Pip makes it possible to survive but definitely not thrive 
    • Thank you for your comment. Comments are moderated before being published.
      · 15 days ago
      @Anon My son is 25 and autistic.  Most of his PIP go into personal assistant costs to escort him to his training and daycare locations, health appointments etc - he uses public transport so he does not use any of his money on taxis but he has been deemed unable to travel on his own.  Also, please can anyone explain to me how "more direct parental intervention" is not a cost?  Are they seriously telling us that if carers end up limiting their working hours or - as in my case - are too tired to carry on working and caring and decide to leave work altogether, there are no costs involved?  I hate to break it to them, but yes there definitely is!  So much for encouraging people to get the "fulfilment that work provides" apparently.  These people (academics I presume?) have no understanding of the real lives of disabled people and just come up with total loads of word-salads that say more about their own biased and sheltered lives.
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    My depression and anxiety often leave me unable to cook, shop, or collect medication. 
    Online grocery shopping, takeaways and a carer all cost money.
    Panic attacks mean I often need taxis instead of walking, and the nightmares mean more washing because of the sweats they bring on, whereas vomiting due to anxiety means bedsheets, clothing and the carpets/rugs have to be cleaned often or replaced.
    My suicide attempts mean trips to hospital, which is a £40 taxi tide home due to the lack of public transport. 

  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    I consider my autism to cost me on the basis that my social difficulties mean I find it very hard to get a job and even harder to stay in work. I've never lasted more than a few weeks in work despite successfully finishing university! The difference was education was willing to support me while work never did. 

    It's especially hard to quantify a cost to struggling to adjust to change and routines but its definitely a real and quite limiting cost. Basically the costs for me mainly come from going without in a world that is not that accessible to me in the first place.

    I would also be seriously isolated without the disabled bus pass and disabled railcard.

    Utilities and managing money are probably what applies to me most on the list, burnout means I have periods where I'm at home most of the time, barely going out once a week! I'm also a night owl so there's costs with bills there too. While the sense of money can fall out the window with my special interests which has caused debt in the past.

    Personally I don't see why it's the government's business if I use my PIP (or UC+LCWRA) on things I enjoy doing, like taking the train to a national park or the seaside or a historic old town or museum to walk around somewhere that helps me cope with the world as it is! Going somewhere I like when I'm burnt out or distressed by the world is far more effective than any mental health service I've ever used.
    • Thank you for your comment. Comments are moderated before being published.
      · 19 days ago
      @rookie Good analogy there. 

      What they conveniently forget is not everything has direct or obvious costs nor is it easy to give an actual number but the cost is there, limiting the costs to money is far too limited.

      Also because my PIP review had someone completely unqualified look at me, I'm at the mandatory reconsideration stage yet again! Amazing they can acknowledge my social difficulties and yet apparently this neatly doesn't impact on everything else day to day according to them! I got LCWRA because of the impact of my functional difficulties. The department literally can't even add 2+2 together.
    • Thank you for your comment. Comments are moderated before being published.
      · 20 days ago
      @asmith25 You have a personal and independent way of managing your conditions, so you need a personal independence payment.

      The government's offer of costs is an imposition of a limited set of aids and therapies they consider appropriate. It's the equivalent of making the food bank the only option, just with less compassion.
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    Buying a lot of expensive supplements to deal with all sorts of co occurring ailments (gut problems, deficiencies, sleep, etc…)
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    Yes, all that and not being able to return ordered stuff that’s wrong or incompatible/not needed anymore due to not being able to go out/drop off, not able to open door to collector (social/communication issues)/ in time…
    Always had to buy multiples in shoes/clothes which often got forgotten or essentially rejected, also worries about change/money for public transport so disability bus card was such a relief!
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    Thank you, Benefits and Work, for challenging this. Please add FASD (Fetal Alcohol Spectrum Disorder) to the conditions under threat. FASD affects an estimated 2–4% of people. It is often misdiagnosed as, or overlaps with, ADHD, autism or attachment issues, so many people with FASD are already among these claimants.

    FASD is not "cost-free." It is a full-body diagnosis with more than 400 conditions that can occur alongside it, affecting hearing, vision, the heart, kidneys, bones and mental health. That means more appointments, more treatment, more equipment and more travel, on top of the daily support with memory, planning and safety.

    National FASD's Cost of Inaction on FASD report estimates that FASD costs UK society around £9.2 billion a year, and around £160 billion over 30 years. The lifetime cost of one case is about £359,800 when it is diagnosed and £431,800 when it is not. Around 92% of that £9.2 billion falls on people who have never been diagnosed. That money is spent late, in crisis, across the NHS, schools, social care, justice and housing.

    Families pay too: lost earnings, reduced working hours and out-of-pocket costs for healthcare, education and managing behaviour. Many of these families are adoptive and kinship carers. Supervision and prompting are not free just because a parent provides them.

    Cutting cash support won't save money. Diagnosis and the right support will: the report finds every £1 invested returns £3.56.

    In the words of the UK FASD Manifesto, written with more than 60 people with FASD: "Just because you can't see our disability doesn't mean we don't have one."
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @The National Organisation for So well said FASD organisation. I have known in my life, one teenager and at least one adult with FASD. The teenager was adopted and I don't know how their life turned out as I moved away. The adult also adopted, a dear friend is sadly no longer with us having succumbed to alcohol addiction himself, a tragedy. And having cost the NHS a lot on the way.
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @The National Organisation for Exactly! Only because you’re a parent it shouldn’t be ‘free’! Could only ever work 50% while school age and now can’t do any because it’s EXHAUSTING! All that work for FREE…?Living on minimum…
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    We are going to have to make a collective effort not to allow dwp to use the fact that we use pip for subsistence spending (rather than extra costs associated with disability) as an excuse to cut pip.

    However justified, the spending (cost of living: food, transport, energy, rent crises), pip is not officially awarded for living costs common to everyone.

    Our reasons for claiming and spending pip have to be seen to be related specifically to costs incurred because of sickness or disablement, so, for example, we need a special diet so our food costs more; we need to take taxis because we cannot use public transport; our energy and water bills are high because of medical conditions; our housing is more expensive because we needed adapted accommodation , or because no social housing is available for us or because we pay the bedroom tax because we are not able to withstand the upheaval of moving somewher cheaper.

    If we say we just need pip to help with the cost of living, without relating costs to disability/sickness,
    we are playing into the hands of those who see pip claimants as receiving financial advantage, especially over standard benefit claimants, because everyone's costs have risen.
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @JBob1234 The real problem is that few of our MPs seem to understand the effects of either disability or poverty, never mind a combination of both.
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @keepingitreal While PIP is a in and out of work benefit. The difference between out of work standard benefit claimants and disabled benefit claimants is ability to work.

      Out of work benefits for those work capable our designed to be punitive, only be suitable for short-term subsistence with no quality of life, so people will not opt for a life on benefits and will take any job to improve their circumstances.

      Out of work benefits for those not work capable due to disability are supposed to be suitable for long-term survival with some quality of life. So people unable to work are not living in material deprivation and unable to afford anything to make their lives more enjoyable.

      The problem is benefits have been cut again and again over the years so they are no longer fit for purpose. Making people reliant on PIP to survive. Labour have already massively cut UC LCWRA for new claimants, and now looks likely to try and cut PIP, and then plans to make UC health dependent on receiving PIP daily living, and possibly only for those age 25+. People will simply not have enough money to survive or will be merely subsisting in severe material deprivation. Cutting PIP is simply not acceptable unless accompanied by increasing UC health, and reducing UC health eligibility is simply not acceptable if people are due to disability effectively unable to work or have no likely prospect of getting a job due to employer discrimination.
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    Why do we have to keep justifying ourselves? Why do we have to breakdown our additional costs when other groups don’t? 

    ASD is a disability and to have to justify the lifetime of cost is discriminatory. 

    Why is this site legitimatising discrimination by gathering evidence for the government. 


    • Thank you for your comment. Comments are moderated before being published.
      · 20 days ago
      @Old Mother
      "Why is this site legitimatising discrimination by gathering evidence for the government"

      Oh dear.. you have completely misunderstood the brief. 
      Go read it again. 

      Do keep up to speed with the proposals we know of, and why we need to speak / shout up.
  • Thank you for your comment. Comments are moderated before being published.
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    The Resolution Foundation think tank report Hard truths Rethinking Personal Independence Payment is out today. It recommends removing PIP from 12% of existing claimants, and a further 4% of existing claimants also losing cash payments but getting support in kind. On the justification that they have no additional costs of disability. And while acknowledging this would cause mass poverty, dismissing that as not an issue for PIP, PIP is for the additional costs of disability, it is an issue for UC. But, as it also goes on about how much money it would save, they are not advocating that UC would have to be increased to alleviate the poverty they know would be caused by removing PIP.
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    Inclusion London want disabled people to start reporting to them:


    Perhaps Benefits and Work may wish to post a news article on this?
  • Thank you for your comment. Comments are moderated before being published.
    · 21 days ago
    We’re still disabled even if they’re not physical or obvious 
    Our costs might just look different but still necessary to live, survive, keep distracted. Type of foods, rent, bills, special interests, leisure, activities, therapy, support worker, transport.
    This idea that PIP is only for physically disabled people is the wrong way to look at this. If someone’s condition including mental health or neurodivergence affects their daily life to the point they need PIP then they are entitled to it. The independence payment means we can spend money on things we need to help us. Sometimes for me that’s distractions, safe foods, splints for chronic joint pain
    This is also where the voucher idea falls apart because you cannot tell what someone needs 
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @Catherine @Catherine "the voucher idea falls apart because you cannot tell what someone needs"

      and they couldn't give vouchers for all those needs, it would be unworkable to get provider participation for everything That's the whole point of pip - it allows autonomy, independence, not being tied down or having your spending restricted. We're limited enough as it is.
  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    As an adult who lives alone with ASD, depression, anxiety disorders, OCD, some of my costs are:

    Therapy: £70 / week ongoing, for a lower level therapist than what I need. £120 for my more complex needs but can't afford this. NHS stated they cannot provide the flexibility in therapy which I require to engage.

    Home help / support worker: £25 per hour - can't afford what I really need.

    Cleaner (I do what can but I struggle to maintain reasonable hygienic standards): £20 per hour.

    Transport: Can't travel alone or use public transport. Would cost £30 to visit my parents once in taxi fees alone. Lack of friends and contacts due to my conditions.

    Food: £30 - £40 extra per week. Can't eat or drink normally, so groceries that I can eat cost substantially more. Food gets spoiled when I get distracted and forget to close the fridge/freezer which is often.

    Restricted clothing: My clothing choices are restricted and I often need to source the same items, which cost extra. Can't just shop around.

    Basic gardening: £250 per year

    There are too different instances of added costs to list, but many are also things people wouldn't realise or consider if they have no idea what it is like to live with certain struggles. Normal things cost extra.

    I would not survive without PIP.  I would not be able to meet the minimum standards of being able to keep my tenancy, or basic health. I would fall into crisis and it would cost my local authority much more in the end.


  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    They seem to forget that in the case of ASD - there are likely to be co morbidities. For example OCD, severe anxiety, PTSD etc. 

    Auto immune issues can also be more common with the severe de habilitating effects on everyday life. These can leave one incapable of maintaining a home or catering unaided. 

    All of the above are disabling and make leading a ‘normal’ life difficult. 




  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    I am approaching 40, diagnosed Autistic, have visual impairment and am medically complex with several progressive chronic illnesses.

    I have a care package paid for through Direct Payments. Because my rent is so expensive (£415 p/m more than the Housing costs element of my UC) I don't have to contribute anything towards the cost of my care package.

    The 4-weekly cost of my care package is £2829. That is over £2000 per 4 weeks more than my full PIP.

    If my PIP were to be taken away and "replaced" with "services" i.e the costs of my care package that is provided by staff who have been specially trained in my medical conditions, that would a) cost the government a lot more than my PIP does at present, and b) leave me with effectively nothing to live on for food, energy/water costs, transport etc, as the LCWRA element of my UC would have to go towards the rent shortfall for my adapted home.
  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    The idea that professional help is widely available for these conditions is pie in the sky, and anyway, it would be much more expensive to provide than the cost of DLA or PIP because professionals expect to be paid higher fees for their input than family members who are entitled to Carers' Allowance if they're lucky - currently £86.45 per week for upwards of 35 hours' worth of caring duties. I'm not ungrateful for this - as a family, we've been very glad of the help from DLA, PIP and Carers' Allowance over the years since my son was diagnosed with autism - but I wonder how many professionals would want to work for that amount? Since these conditions are lifelong, the help would need to be ongoing too, but I suspect the government is thinking of a one-off session with a psychiatrist who would offer advice on how to cope, when what is really needed is ongoing, reliable support with the practicalities of day-to-day life. Surely this is why a previous government initiated DLA and Carers’ Allowance in the first place - so that any help provided on a daily basis would not need to be given by professionals who would expect to be paid far more for their input?
    • Thank you for your comment. Comments are moderated before being published.
      · 22 days ago
      @Wendy Woo Professionals wouldn't even be allowed to work for that money, unless they had a private income. The benefits system enforces minimum hours and income thresholds. Carer's allowance doesn't even buy you 7 hours at the national living wage.

      Another example of the low value given to those who cannot work. Only earners count.
  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    What really ire's me about this is that they fail to grasp that there are plenty of us out there with disabilities that simply can't do full-time work, but do try part-time when we can. We might never have the full income of a non-disabled person through no fault of our own, so even if the condition doesn't come with a one-to-one direct cost we are penalised.

    Where is the dignity in that? The respect for human life? I'd be better off claiming to be unfit for work even though I can (and currently are).
  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    I'll be honest. I don't know if this coment is welcome here but it's how it is for me and others I know with these conditions. I'm 33 with ASD and unable to work. I receive both PIP and UC.

    I think for a lot of people the "extra costs" premise for PIP is just window dressing. The reality is that UC, even with the health element, is simply not enough to live off of especially if you don't have anyone else like family or a partner. If you want any sort of dignity or more than just literally scraping by then you need the additional money from PIP. This is even more true now for new claimants who receive and even lower amount of money from UC, even if completely unable to work or even prepare for work.

    I don't really have additional costs. I actually probably have less costs because I can take the time to prepare meals and I'm happy eating the same staple foods. I dont use busses or taxis because that puts me in uncomfortable proximity to people, and ordering food and having to deal with a delivery person is more stressful to me than putting my headphones on and walking to the shops and using the self-checkout. Are the headphones an extra cost? Maybe, but I mostly just wear them because they're a useful "don't interact with me" signal.

    I don't go to therapy since my condition doesn't improve with therapy and I am otherwise okay if left to myself. I don't want help from anyone because I value my space and privacy. I suppose spending time at home means I incur some extra costs related to heating and electricity, but this is certainly offset by lack of costs I would otherwise incur by having to work - commuting, additional food from increased energy expenditure, etc. 

    But if I want to be able to afford the food and heat my home and maybe have a little money to make my life not entirely miserable then I need the income from PIP to do it. The Government know this, and are actively choosing to attack from this angle because they know they can argue the extra costs are less than currently framed and seek to argue it's currently being "misused" because people are spending it to keep warm and feed themselves.

    For what it's worth this is considered a pretty "open secret" amongst disabled people. I think most of us are just using a large chunk of that money to pay toward bills and food and similar costs. To fix or replace something when it breaks. And yes, to occasionally experience a little joy and dignity in our lives where we are able.
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @JBob1234 @JBob1234

      "it should be about quality of life, enabling people to live independently and with dignity, and able to take part in society"

      That's it - disabled people should not be socially excluded. It's not all about wheelchairs and wet rooms. It's about facilitating family gatherings, travel, cultural events, where there are so many extra considerations.
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @Old Mother @Old Mother So not true, maybe not speaking for everyone, nor claiming to be, but not only speaking for themselves.
    • Thank you for your comment. Comments are moderated before being published.
      · 21 days ago
      @Avie @Avie Totally agree. By bringing concrete costs into the equation the government might insist that your and others' lives did not involve 'extra costs'.

      However you have engineered living to the bare bones, on which you should be congratulated, but why should you have to do that or be penalised for it when it's no fault of your own that you cannot make the extra to lead a fuller life?

      Maybe if the right sort of therapy were available it might help you to be less isolated and find joy in the company of friends. You should have the choice, anyway.

      You say if you 'want to be able to afford the food and heat my home and maybe have a little money to make my life not entirely miserable then I need the income from PIP to do it', and you, and all of us, should have that.

      If people incur quantifiable extra costs they could be awarded as extra, but we do not want to see existing awards cut (they were designed to meet the extra costs of disability, but now definitely do not). 
    • Thank you for your comment. Comments are moderated before being published.
      · 22 days ago
      @Avie I agree that's the case for us (at the moment, although this will change as my husband's condition deteriorates) and I can imagine it will be the case for my recently diagnosed autistic daughter. We do need the money to pay for 'general living' to a minimum standard, as I can't work full time due to my caring responsibilities, my husband can't work at all, and UC with the health element isn't enough. It's not the case for every autistic person i'm sure, but you're not wrong to point out it is true for some. Nothing to be ashamed of, that we need that money to just get by. 
    • Thank you for your comment. Comments are moderated before being published.
      · 22 days ago
      @Avie The Timms review is well aware many people need PIP to pay towards their living costs due to other benefits being inadequate to live on. Especially long-term and with any quality of life. And that without PIP many would end up barely subsisting in severe material deprivation. Yet in the interim report they dismissed it as PIP cannot be for everything for everyone, PIP is for the additional costs of disability. Easy for them to say when none of them appear to be poor and reliant on benefits to survive. And at the same time they go on about keeping PIP as a non means tested, tax free, cash benefit, refocused on the most severely disabled, who they define as people like them. So they will be fine, they might even get more money.

      I think the whole premise from the very starting point of PIP being for the extra costs of disability should be challenged. And it should be about quality of life, enabling people to live independently and with dignity, and able to take part in society. Not subsisting in severe material deprivation. The same goes for LCWRA. It is shocking Labour reduced it by over 50% for new claimants despite knowing large numbers of already existing LCWRA claimants are living in poverty, and heating and food insecurity, and material deprivation. Politicians and the media are despicable, and the scapegoating, demonisation and inciting of public hate frightening.
  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    Recovery in the bin did a survey on this a couple of years back https://recoveryinthebin.org/2025/02/27/it-costs-more-to-be-disabled-whatever-the-government-says/
  • Thank you for your comment. Comments are moderated before being published.
    · 22 days ago
    It is not just ADHD, autism, depression, anxiety that are potentially under threat. It is all health conditions where people need supervision to keep them safe, encouragement, prompting or assistance. Things that can be done by a parent or a carer could be used as justification for the ill or disabled person not needing as much or any cash for additional costs from DLA or PIP. As if a carer is needed they are paid for via carer's allowance and UC not DLA or PIP.

    And it is not just the above justification that could be used to reduce eligibility. Those who need to use disability aids or take additional time to do tasks could also be targeted. If the cash benefit is based on ongoing additional costs of disability. Disability aids could be viewed as one off costs not ongoing, and taking extra time could be viewed as incurring no cost. This could be how they possibly target some of those with muscular skeletal health conditions.

    Then there are all those who currently get LCWRA but not PIP. Especially those who get LCWRA due to likely risk of substantial detrimental effect to health if required to work or undertake work related activities. What happens to them if as planned the work capability assessment is abolished in 2028, and PIP daily living is used to give eligibility to UC health. There has been no indication from the Timms PIP review as to if PIP eligibility will be extended to them. And if it is if the substantial risk eligibility criteria would be the same or higher than it is under the WCA.
    • Thank you for your comment. Comments are moderated before being published.
      · 22 days ago
      @JBob1234 Excuse me Sir I have circulated an email to prominent various people to try and stand up for the rights of disabled people like myself who has autism to MPs. ,journalists and DPOs . Lets be honest McFadden has no moral or social conscience in targeting the poor, sick and vulnerable.The Benefits and Work Team deserve commendations in standing up for rights of all disabled people. A true voice of reason My sincere thanks to all at the Benefits and Work Team for their support.
    • Thank you for your comment. Comments are moderated before being published.
      · 22 days ago
      @JBob1234 Exactly, the entire social security system is under threat, for everyone!
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