Dr China Mills shares her experiences of pulling together decades of evidence of deaths, protests and failures in the disability benefits system for a new timeline which holds the government to account

Philippa Day took her own life in 2019 after her disability benefits were stopped. Before she died, she told her sister that she knew the assessment system was going to kill her – “she felt that they were pressuring her to kill herself, she felt that she didn’t matter because she was disabled”.

In January 2021, the coroner at the inquest into Philippa’s death found that 28 separate “problems” with the administration of the personal independence payment (PIP) system had contributed to her death – concluding that these were not individual errors by DWP and its private sector contractor Capita and instead that these were systemic flaws.

Disabled people have been campaigning for over a decade about how welfare policies are killing them. As a researcher, who had been looking at the connections between welfare policy and suicide for a number of years, I knew there was so much evidence that connected the UK’s social security system to people’s deaths.

But it was well hidden – in the online equivalent of a building full of grey filing cabinets, in reports with no title and just a number, in responses to freedom of information requests.

In 2021, I asked John Pring, editor of Disability News Service and a disabled journalist, if he’d consider wading through the evidence together and finding a way to put it out into the world. He replied the same day and said yes.

Fast forward almost three years, and many emails later, Healing Justice London is launching the Deaths by Welfare timeline – a massive database of evidence showing how the disability benefits system creates life-threatening policies that lead to disabled people’s deaths.

From an initial draft based on Pring’s decade-long investigations and my own research into welfare reform and suicide, we created a draft timeline.

This was then shared with and added to by three disabled activists, Ellen Clifford, Dolly Sen and Rick Burgess, and welfare rights advisor Nick Dilworth, and then released for public consultation.

Where people’s deaths in the disability benefits system have been investigated, including by the DWP, they are often treated as private, individual cases. Bringing together all these documents into a timeline makes it possible to track patterns.

Patterns of harm that have led to people being left destitute, starving to death, and taking their own lives after encounters with the disability benefits system. These are patterns that remain hidden if we only examine individual ‘cases’. The timeline reveals other patterns too – damning evidence that the DWP, and its contractors, knew about these deaths and yet has repeatedly denied responsibility and refused to make systemic change.

Researchers like me often convince ourselves that we’re objective and removed from our investigations. But the experience of co-creating the timeline has been harrowing, heart-breaking and enraging. It’s the repetition that has worn me down and lodged in my heart – the number of times the government has been warned of harms, even from their own research, and the repetition of harms across so many people who have died.

Like many of us, I used to say that people’s deaths were the outcome of ‘flaws’ and ‘mistakes’ in the system – as though the system just needs tweaking to make it safer. But co-creating the Deaths by Welfare timeline made it frighteningly obvious that harm is much more deeply designed into the welfare system. It’s a feature, not a bug.

Yet the timeline isn’t one of despair – it is bursting with disabled people’s expertise, knowledge, activism, and creativity in resisting the violence of the welfare state. From protesting on the streets, holding up cardboard broken hearts bearing the names of just some of those who have died, to quieter resistance – relentless submission of FOIs and re-analysis of government data. It is threaded through with cross-disability and cross-movement solidarity, and solidarity between bereaved families and disabled people.

For example, in July 2021, when bereaved families write to the work and pensions secretary to demand a public inquiry into benefits-related deaths. And in 2012 and 2021, when Deaf, Disabled and Asylum seeking people came together, as part of the Disability Murals Project, to create a mural highlighting the barriers and state violence disabled asylum seekers face, including exclusion from the welfare system.

While justice means different things to different people, those campaigning for change know the problems lie in DWP systems, and many demand an independent inquiry into benefits-related deaths. Many see justice as coming from beyond the state – in demolishing the current system and creating life-affirming systems, with disabled people at the heart.

We created the Deaths by Welfare timeline as a tool for disability justice movement organising – a resource, a living document, that can move us towards accountability, transformation and justice.

To access the timeline visit www.deathsbywelfare.org

For our podcast episodes (all captioned and translated into BSL) please visit https://healingjusticeldn.org/deaths-by-welfare-project/

Dr China Millsis the Disability Justice Lead at Healing Justice Ldn. She manages the Deaths by Welfare Project, exploring how welfare policies harm people and what can be learned from the strategies of disabled people and bereaved families in fighting for justice.

  • Tammo-Korsai@kbin.social
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    1 year ago

    I love it when the DWP Aktion T4 question if I’m still autistic or not. Believe me, I wish I could stop being autistic and not have anxiety over very normal things and sudden changes. Even the initial application for PIP or DLA was a nightmare as an uncaring system was not convinced I was autistic despite all of the evidence provided by my GP. They very nearly ran me out of money when I got sanctioned without realising it, followed by a year of further paperwork battles as the DWP Aktion T4 continued to deliberately misinterpret everything.

    Then there’s a lot of anti-welfare crap swirling around the internet, so I sometimes feel guilty about claiming anything even though I know it’s legitimate. People are salivating at the idea of the DWP having enforcement powers, checking where you go on holiday (even though a flight can cost less than a train ticket) and other intrusive measures.

    Currently I’m at risk of losing my ESA since they decided to question my autism again and want to do a phone interview, which is exactly what I struggle with, so thank god there’s people who can support me with that call. Honestly, if I had to fight the DWP alone, I probably would have lost all of my benefits and offed myself by now. It’s tough enough even with my really good support network.

    • 520@kbin.social
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      1 year ago

      You know what the most ironic thing is? They do this under the guise of rooting out benefit cheats but if anything they just train people into being capable of benefit fraud. Because you have to think like a benefit fraud just to get what they publicly say you are due.

      • Tammo-Korsai@kbin.social
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        1 year ago

        Exactly. I sometimes grapple with an urge to slightly exaggerate my issues to make sure I get a fair assessment.

        • DessertStorms@kbin.socialOP
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          1 year ago

          A benefits adviser who was supporting me a while back gave me some really good pointers to consider when answering these forms:
          Can you do X safely and repeatedly?
          Can you do X on bad days?
          If the answer to either of those is no, the answer to the question is a no.
          I know it’s hard not to because I do it myself, but try not to feel the guilt they try to force on us. We are NOT the ones who are a drain on society, those who frame us as such are. We deserve to exist, and if to do that we need to claim benefits, then that’s that, and it’s nothing to feel guilty or ashamed of.

        • 520@kbin.social
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          1 year ago

          Honestly, just do it. Just recount your worst days. The DWP are looking for reasons to deny you, you don’t want to give them one by recounting a less-than-worse day.

          I’m autistic too, and that’s exactly what I did.

        • lolcatnip@reddthat.com
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          1 year ago

          As long as you can do it without an undue risk of getting caught, I see no reason not to. It sounds like you’ve already been gaslit into feeling guilty for asking for what’s owed to you, so I assume you’re actually downplaying your symptoms when you think you’re reporting them accurately.

      • VaultBoyNewVegas@lemmy.world
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        1 year ago

        That’s a good way of describing it. I’ve ibd and the nurse has told me to tell them how things are when it’s at its worst.

    • DessertStorms@kbin.socialOP
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      1 year ago

      Well said, and I’m sorry you’re having to go through this shit too, but I’m glad to hear you have support, I’m in the same boat - never would have managed it without that help.

      The link you shared reminded me of this I shared not long ago - https://www.benefitsandwork.co.uk/news/dwp-considers-powers-of-arrest,-seizure-and-collecting-information-on-where-claimants-spend-money

      It really is appalling and enraging the levels of privacy invasion and lets be honest- - humiliation we’re subjected to for the crime of being disabled, while those in power get away with literally robbing the entirety of society.