The Timms review has finally revealed its plans for a radical reform of personal independence payment (PIP) in which awards will be based on additional costs for items such as equipment, bedding and transport.  The proposals bear a remarkable similarity to those included in the infamous Conservative Green Paper published in 2024.

The Timms review September update, published last night, included details of the issues that will be put to the shaping recommendations workshops set to run from 15 September to 7 October.

Improving the current system

Some of the proposals relate to improving the current PIP system.  These include such things as:

  • Reducing unnecessary award reviews
  • Improving the PIP2 form  
  • Making DWP communications more respectful
  • Introducing an advocacy service to support PIP claims
  • Improving how PIP assesses fluctuating conditions

Some of the suggestions would be welcome improvements, but many are ill-defined and will be difficult to measure.

Radical reform

However, the changes to the current system appear to be designed simply to improve matters whilst a radically different method of deciding PIP awards is developed.

The recommendations for a reformed PIP award are that:

“the award will be non-means-tested

“cash will remain the foundation of the award

“some awards will also include services, and offer other non-cash support

“the award will contribute fairly to the extra costs that arise from disability and long-term health conditions and reflect fluctuating and cumulative impacts

“cost categories used to discuss the person’s circumstances, and therefore determine their award, could include equipment and aids; mobility and transport; clothing and bedding.

“people will be signposted to further relevant information and support”

What this appears to mean is that instead of the current points system, which assesses what difficulties claimants have with daily living activities and mobility, the proposed PIP system would look at what extra costs claimants have as a result of their condition.

It will be these “cost categories” that determine their award.

And whilst the recommendations make it clear that cash will remain the “foundation” of PIP awards, they do seem to suggest that for some conditions a proportion of the cash may be replaced by “services”, and “non-cash support”.

The cost of being prevented from accessing employment is not mentioned anywhere in the categories.

It seems likely that such a system would especially disadvantage claimants with mental health and neurodevelopmental conditions, where costs are harder to quantify.

Conservative proposals

The Timms review recommendations seem to have a great deal in common with the April 2024 Conservative consultation “Modernising support for independent living: the health and disability green paper”.

In that document, DWP secretary of state Mel Stride pointed out that in New Zealand people “provide estimates of their additional costs (eg.£50 per month for physiotherapy), which are then approved for an ongoing award”.  Meanwhile, in Denmark  “awards for extra costs are determined on a case-by-case basis and issued by local government”.

The 2024 Green Paper asked respondents to rank additional costs including:

  • equipment and aids
  • transport costs
  • energy and utility costs
  • food
  • clothing, footwear and bedding
  • personal assistance

The Timms recommendations suggest that cost categories used to determine awards could include:

  • equipment and aids
  • mobility and transport
  • clothing and bedding

The Conservative Green Paper also pointed out that various extra costs may already be being met by other provision and are thus duplicated, giving the example “people receiving the daily living component of PIP and who require aids such as walking sticks may have them supplied by the NHS.”

The Conservative document then went on to ask whether support for some people ought not to be cash but instead “improved access to healthcare (such as mental health provision or physiotherapy) or enhanced local authority support (such as care packages, respite or home adaptations).”

The Timms review recommendations are, at this point, much less open and detailed than the Conservative proposals were, but the similarity with the Conservative vision for a new PIP benefit are unmistakable.

Current PIP claimants

The Timms review remains utterly silent on whether current PIP claimants will be affected by the proposed changes.  But its terms of reference are very clear that “the Review will consider how recommendations might be applied to reassessments for people already claiming PIP to ensure it is fair and fit for both new and existing claimants”.

So, for the moment, we cannot rule out current claimants being subject to any new system.

What we can rule out, however, is any such changes being brought in quickly or without a great deal of new primary legislation.

So, for those readers who are troubled by these proposals, there will be many opportunities ahead to challenge them.  And here at Benefits and Work, we will do our best to support those who choose to do so.

You can read the full Timms Review: co-chair update, September 2026 here. 

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  • Thank you for your comment. Comments are moderated before being published.
    · 5 days ago
    Mental health Trust are already saying my DLA (yes, not PIP - hopefully will be if successful on transfer...) should pay for my mental health social care agency costs that exceed council-assessed Direct Payment. (Is S117 aftercare which they are trying to get rid of.) So will have little money to pay for other costs such as items listed by Timm's review, which I currently pay for from DLA. If Timm's review does cut mental health cash instead to item costs will not be able to afford excess social care costs. Have asked for Care Act Assessment and have been told local council is / will soon be in special measures so, as before, when needs assessed as required, will likely be told again council can't be afford. Gets very confusing when councils and central government are pulling in different directions.
  • Thank you for your comment. Comments are moderated before being published.
    · 5 days ago
    Well wheelchairs are expensive l needed one £2,000 was one another more so l had to struggle. If you are on pip if they included my taxi only costs to go out it's £5 per trip just to Drs or £12 to hospital it mounts up. 
  • Thank you for your comment. Comments are moderated before being published.
    · 7 days ago
    Surely the results of your survey could be emailed directly to various relevant Government individuals? Don't rely on the remote possibility that a B&W member happens to be a workshop participant and might have an opportunity to present your findings in some way, during a very carefully managed session. It's not gonna happen!

    You have the information. Please make use of it. Email Timms, the Committee and even Andy Burnham himself. Publish the information and ask members to email it to their MP. We have the power to bombard the Government with this.
  • Thank you for your comment. Comments are moderated before being published.
    · 7 days ago
    This appears to be largely focused on physical disability. People with a brain injury which impacts their general ability to deal with 'life', but few physical limitations may well lose out. 
  • Thank you for your comment. Comments are moderated before being published.
    · 7 days ago
    Leaving aside the effects on us individually, if the Government moves to a system of vouchers and specified services that’s actually going to increase costs due to the bureaucracy involved. So the only way to reduce the benefits bill, as is their claimed intent, is to cut benefits even harder to pay for the added bureaucracy. It’s utterly deranged.
  • Thank you for your comment. Comments are moderated before being published.
    · 7 days ago
    My son uses all his PIP to pay for a support worker. Would that be an allowable expense under the Timms proposals?
    • Thank you for your comment. Comments are moderated before being published.
      · 5 days ago
      @B C Yes i do the same as your son i hate social care and services as i have multiple conditions including parond disorder and I have a private career i pay myself 
      She used to also care for my son who's disabled however hes now 18 and hes also paying to get a private male career who's not changed and we can just have that 1 person i still make mine wait outside the gp room as I don't trust anyone fully 
      Probably sounds silly but I don't want to disclose my whole life and I am struggling with this as I have pip appeal hearing soon and i have been suicidal and waiting since jan 25 ongoing incorrectly awarded for 10 years 
      They then wounder why you have issues with service provider and trust noone
      Hope your son is doing well if you are able to social care are able to provide assessment and they have care options but my experience is just so wrong I don't like anyone official 
  • Thank you for your comment. Comments are moderated before being published.
    · 7 days ago
    my disabled relative is still on DLA indefinite award for care and mobility. His local council already take all his DLA care component towards his care costs, thereby leaving him with his mobility component to cover all his other extra costs etc.
  • Thank you for your comment. Comments are moderated before being published.
    · 7 days ago
    I agree with Wynn our needs are individual and change regular. Times thinks we are all the same were not so stop categorizing us. Leave us to use the money to enable us to live as a life as everyone else
  • Thank you for your comment. Comments are moderated before being published.
    · 8 days ago
    I have said this before and I will repeat it again - the problem with the system is not the people who need it but those who operate it and the system itself.
    I never claimed anything always worked and paid my own way and never begrudged anyone who needed assistance. I have always stated that I would far rather my tax money went to those in need then the over inflated monies given to those who hold power. They talk about the need to give "value" to the tax payer - so they can explain how paying an average of £20 per day to a disabled person is not value to the tax payer but paying £300 per day to a member of the house of Lords is?? The list of the expenses, subsidies and external income that politicians claim and take on top of the wage they are given is endless. Yet they want, without irony, to penalise those who are the most vulnerable - it is beyond disgusting. They have no clue how difficult life is for those who have this need. Even when I contacted my local MP Chris Ward, when these cuts were first being announced by Labour the response was incredulous - again the talk of "value" for the tax payer and that disabled people and I quote "have no dignity if they are not in work"
    Well now due to cancer I am one of those people who need help. I have never been through a more demoralising and humiliating experience in my life. You are treated as a cheat and liar from the very beginning. Being judged by someone who has no medical knowledge and zero understanding of your condition, who is only interested in which "boxes" they can tick. Every assessment is a control to prove you are lying or attempting to defraud, the questions asked during an assessment are disgraceful - exactly why does an assessor need to know if I can wipe my own a**?? and why does an assessor "observing" me holding a medicine bottle prove I must be faking my own condition when there is medical evidence from specialist hospitals and reports from specialist consultants who have worked in the field for decades explaining exactly what is wrong with me? how do these keyboard monkeys even begin to justify thier "opinion" against stacks of verified medical evidence?
    Whatever these politicians come up with you can guarantee it will not benefit or make life any easier for the most vulnerable - look at the changes to the mobility scheme already people are having to give up thier cars and independence and Reform UK want to scrap it altogether?? God forbid they should close the tax loopholes and sweetheart deals for all thier rich mates and tax them properly no lets crucify the minority group we think are the least able to fight back - there are not strong enough words to express my anger at the whole system and those who run it.
    The whole system needs to be torn down and started again, only this time with real people with real life experience running the show, not these greedy grasping career politicians.

    • Thank you for your comment. Comments are moderated before being published.
      · 4 days ago
      @Tracey Hi have you looked into direct payments? Just a thought as I do it this way. The council give funded hours I hire self employed PAs and then they assess you for a contribution mine is about £250 a month but I get 22 hours care a week. I do it all myself i choose the PAs and I call the bank to pay them after checking invoices. Works well for me x
    • Thank you for your comment. Comments are moderated before being published.
      · 5 days ago
      @mave666 This is really well said 

      They are making disabled people like me be housebound for 10 years because I am not able to afford to pay for the career to help me as im on standard care only £290 a month 
      With severe depression and anxiety and parond disorder since 1988 and bipolar and emotional unstable personality disorders and severe incontinence issues with fibermalga and menopausal and severe back pain and curved spinal injury in constant pain i believe that people are laughing at me and I will get angry with them and I have offended people because I can say things that I didn't mean I just got so much distress of the breathing issues with the mental health issues and the constant pain and needing to go tolilet and the fact that the nhs only want to provide full baby nappies and I am only 50 its not exceptable so more expensive because I have to pay over £20 a week just to get incontinence pads 
      No family or friends in the area moved with 2 disabled children due to domestic violence dwp even use the fact that I am appointed person to fill in the forms against me 
      Thanks for your reasonable look at the fact that sometimes people really need the help means alot 
    • Thank you for your comment. Comments are moderated before being published.
      · 5 days ago
      @mave666 Thankyou your post says it all it is disgusting how we are treated l have 3 separate nerve damage issues all neurological. They don't show on the outside. The pain however is very real. Nerves must firing all the time. When l stand now l wobble like am drunk due to the brain tumour they cannot remove.  I don't think people who are not medical consultants should be allowed assess our needs. Everyone is different in them. The GPs cannot help it's like they try to guess so l have to say what drugs help what doesn't.  Needing a wheelchair is complicated.  Needing rails and equipment to pull myself up in my bed. All costs l had borrow money pay for things. 
    • Thank you for your comment. Comments are moderated before being published.
      · 7 days ago
      @mave666 This very eloquently captures how I feel too. I'm so angry, the cruelty and the corruption are undeniable.
  • Thank you for your comment. Comments are moderated before being published.
    · 11 days ago
    I’m the same as Nicky A life going well up until a brain tumour changed my life and families I’m struggling to work 20 hours a week half the amount I used to . If I didn’t get pip I would probably loss my house luckily I have a cheap mortgage my part time pays that and what’s left goes towards bills pip pays my food bill for the month. Professor Tim’s come and live in my world and everybody else’s for a month they make your mind up before shafting us
     
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      · 5 days ago
      @Matt p I know exactly how my tumour changed my life so totally all my right side is affected. I am deaf now have no peripheral vision. I cannot walk in a straight line. All of it changes how we live l was a social worker. Now l cannot work. I had give up my karate and my history reenactment.  I miss my life.
  • Thank you for your comment. Comments are moderated before being published.
    · 11 days ago
    Without wishing to repeat what has already been said, the bottom line is that the "independence" factor of PIP will be removed.  People will be unable to independently choose what is best for their needs.

    Furthermore there are so many costs faced by disabled people which do not fall into simple categories.  For example, we recently had a damp problem and had to get it repaired as my husband has, amongst other things, respiratory issues.  Damp can exacerbate it.  It resulted in further work - plastering and decorating....where would that cost be attributed to? This was obviously not a disabled aid, but was a necessity for his health.

    Every person has individual needs and a one stop fits all simply won't work.

    I would also question the costs of implementing a new system and the ongoing additional cost of administering it.
  • Thank you for your comment. Comments are moderated before being published.
    · 12 days ago
    The government have no idea what they are doing & they don't care, as financially each member has more than enough money they have no understanding how difficult it can be! 
    I worked full time & never claimed anything I used to earn £28,000 as a deputy manager working with learning disabilities.
    I then had a brain tumour & now I have num 3 growing I cannot work now not my choice.
    I now live on a small amount of money which pays for my bills,wellbeing, equipment & gadgets.
    I also use PIP once a mth to socialise with friends & need a taxi there & back making me feel totally inadequate with only a little indendance left.
    It's not a huge amount of money & I can't afford healthy food or much forcing me to go to my local food bank for support so I get anxious & fed up when the government wants to change everything,who are they helping themselves or us??
  • Thank you for your comment. Comments are moderated before being published.
    · 12 days ago
    PIP should be about people, not simply about putting a price on disability.

    I am deeply concerned about any system in which a disabled person's award could increasingly be determined by predefined categories of additional costs rather than by their individual circumstances, needs and the barriers they face.

    Two people can have the same diagnosis but completely different needs. Disability-related costs can also fluctuate from week to week and may not always come with a receipt or fit neatly into categories such as equipment, transport, clothing or bedding. The Timms Review's own evidence recognises that disability-related costs can be continuous, variable and interconnected.
    Most importantly, disabled people should retain choice and control over how their PIP is used. People themselves are often best placed to understand what will enable them to live independently and participate in society. Turning support into prescribed services, vouchers or restricted forms of assistance risks undermining that independence, even if cash remains part of the system.
    I also believe we need to separate two issues that are increasingly being blurred together: PIP and social care.

    PIP should provide disabled people with flexible financial support to meet the additional costs and consequences of disability. Social care should be a properly funded public service, available according to assessed need rather than being used as a substitute for PIP.

    Instead of making disabled people's financial support carry the burden of inadequate services, governments should invest in accessible housing, social care, transport, mental health services, community services, equipment and other essential support. These should be developed as universal public services and rights, so that disabled people are not effectively forced to use their PIP to compensate for failures elsewhere.

    The principle should be simple: support should follow the person, not force the person to fit the support. Disabled people deserve choice, dignity, independence and control over their own lives.
  • Thank you for your comment. Comments are moderated before being published.
    · 12 days ago
    I Agree with what Karen Rix and TJD have to say that vouchers and sevices are not the way to go as this takes away our support networks of friends and relatives who help us when we need it and it takes away our humanity and right to live our lives are we want to.
    How would they like to be in our shoes?? and have all thier choices taken away and their living dependent on vouchers and services that are not fit for purpose and are over whelmed with to many people trying to access help they need. 
    The Tims report is a sham and the people who are running it are sharlatons. 
  • Thank you for your comment. Comments are moderated before being published.
    · 12 days ago
    As a human being being brought up in the medical environment having been born with Stills Disease and low spine l4 l5 issue the doctors instilled in me from the very early age to strive to do as much as i can for myself independantly as i can without using equipment if possible and to help mental health and wellbeing as i became an adult. This means it was medical guidance that i try NOT to depend on equipment and with the paid cash gives me independence to choose as i need my own choices to help myself and not depend on vouchers [ which by definition restrict choice and cause obsticales on what we can and cannot choose for ourselves] Because then the choice they offer within their schemes is restricted again.
    When this happens to them [ God forbid they never need to disabled and need support] then they will truely understand the point of view from a disabled persons need to navigate life on their tried and trusted ways that work for us in making our own choices as any other human being can do with cash at point of need. This is a basic human right to live as every other human being does in daily life. We never choose to be disabled, when will the powers that consistanly try to restrict our lives really understand? We disabled need to be a part of society live as everyone else and not treated like we cannot choose for ourselves what makes us live our very best life because vouchers and equipment that THEY choose for us will NEVER be that definition.
  • Thank you for your comment. Comments are moderated before being published.
    · 12 days ago
    Replacing cash benefits with state chosen equipment or vouchers destroys our final piece of independence that a disabled person has. Equipment cannot pay for petrol when a friend ,family or neighbour goes to get you your shopping and a voucher cannot compensate a friend, neighbour, or family member who loses wages to take you to take you to a doctors, hospital 'physiotherapy appointments. Removing cash doesn't just reduce choices it breaks the informal networks of family ,friends and neighbours we rely on, forcing us into complete isolation because we can no longer contribute our fair share. When help is needed. 
    • Thank you for your comment. Comments are moderated before being published.
      · 7 days ago
      @Louise Exactly! Or paying for ingredients if a friend offers to cook for you. The costs of being disabled are random and a voucher based system would ruin lives
  • Thank you for your comment. Comments are moderated before being published.
    · 12 days ago
    I have been declined twice yet I know others with long covid who have this. My replies have never mentioned the fluctuations and variability of the condition. Costs may be useful as we buy unlicensed drugs recommended by a Consultant. 
  • Thank you for your comment. Comments are moderated before being published.
    · 13 days ago
    NO CASH CUTS, NO SERVICE TRAPS!
    NO VOUCHERS, NO LIES, INDEPENDENCE SURVIVES!

    Any suggestion whatsoever, that services or care services should replace cash support with vouchers is a step backwards in society.

    Local authority care services in most areas still promote the principle that care is about choice. However, where I live that is NOT so, and it results in needs not only not being met, but an influx or unreliable service provision and people having to rely on their PIP money to meet their disability needs.

    Once a person loses the ability to make their own choices and exercise their own control, the risk of abuse increases. Independence cannot survive if autonomy is removed. 

    I GENUINELY DO KNOW THIS BECAUSE I HAVE EXPERIENCED WHAT HAPPENS WHEN SAFEGUARDING FAILS, ABUSE OOCUR, AD A DISABLED PERSON IS LEFT TRAPPED WITHIN A SYSTEM THAT IS SUPPOSED TO PROTECT THEM.

    WHEN CHOICE IS REMOVED AND AUTONOMY DIES . ABUSE SURVIVES. 
  • Thank you for your comment. Comments are moderated before being published.
    · 14 days ago
    I fully understand the need to cut back on all benefits but if you asked me as a disabled person that worked until I was dismissed due to being disabled from a job I took due to being able to sit down and not do anything I could not manage, the firm decided it was going to change it’s policy and everyone including the disabled workers were expected to be able to do everything I ended up being treated like I wasn’t important and dismissed I, I did succeed in taking them to tribunal. but my point is even if disabled people who even in severe pain and never take a day off due to having multiple medical conditions can be treated as if they don’t matter what chance will any of us have if out benefits are taken away or reduced that just means the little independence and dignity that is left them after dwp is finished with them is just taken away by people who know nothing about genuine disabled people 
  • Thank you for your comment. Comments are moderated before being published.
    · 14 days ago
    I think there is a fundamental question here about why the DWP is considering incorporating services, equipment or other non-cash support into PIP awards at all
    I completely support disabled people having access to a much wider range of practical support, equipment and services than many of us can currently obtain. But surely improving that provision is primarily a matter for health and social care. It should be available alongside PIP, not potentially become part of the way a PIP award is determined or delivered
    PIP serves a different purpose. It gives disabled people flexible financial support towards the additional and often unpredictable consequences of disability allowing us to decide what enables our own independence. Those needs cannot always be reduced to a list of equipment services or easily evidenced costs
    Disability also does not exist in neat compartments. A physical disability can interact with mental-health difficulties caring responsibilities, family life transport and the ability to work. A service or piece of equipment may meet one need while doing absolutely nothing about the other additional costs that person faces.
    If disabled people are not receiving adequate mobility equipment, social care or other support, then surely the answer is to improve those services rather than use PIP to compensate for deficiencies elsewhere - particularly if doing so risks reducing disabled people's control over their own award
    The clue really is in the name: Personal Independence Payment. If the aim is genuinely to increase disabled people's choice, dignity and independence, then additional services should be additional They should not come at the expense of the flexible financial support that allows each disabled person to decide what independence means in their own life
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