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Updates

DWP Staff Caught in £2M Benefit Fraud Scandal Amid Harmful Disability Rhetoric

July 23, 2025
A Man in Black Sweater Holding Letter Board with Fraud Text

For months now, disabled people across the UK have been subjected to an increasingly hostile narrative driven by the DWP. One built on stigma, stereotypes, and a complete disregard for lived experience. We’ve seen damaging rhetoric from public figures and …

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Categories Updates

Challenging Harmful and Out-of-Date DWP Training on M.E./C.F.S.

July 21, 2025

A serious issue that has recently come to our attention, which poses a direct threat to the wellbeing of the M.E./C.F.S. community. Through a series of Freedom of Information requests, we have obtained the training materials used by the Department for …

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Categories Updates

Universal Credit Bill: Key Concerns to Be Raised in House of Lords Debate

July 20, 2025
Men and women in formal clothing are sat in a Chamber.

On Tuesday 22nd July, Members of the House of Lords will debate the Universal Credit Bill (previously the Personal Independence Payment and Universal Credit Bill), a piece of legislation that has generated significant concern across the chronically ill and disabled …

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Categories Politics, Updates

The Case for Change: Recognising M.E. in PIP Assessment Policy

July 4, 2025
People with Binders in Close Up

Stripy Lightbulb CIC has today published (and sent to policy leads in the DWP) a new policy briefing that highlights a pressing issue in disability benefits assessment: the failure to properly recognise the long-term, disabling nature of Myalgic Encephalomyelitis (M.E.) …

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Categories Politics, Updates

Statement from Stripy Lightbulb CIC on the Welfare Reform Bill Debate and Vote

July 2, 2025July 2, 2025
Fragments of Broken Glass on a Black Surface

Stripy Lightbulb CIC is appalled by the events surrounding yesterday’s Welfare Reform Bill debate and vote. After nine months of robust, evidence-led advocacy in collaboration with the M.E. community and wider disabled community, we watched in dismay as Clause 5 …

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Categories Updates

OPEN LETTER – Before You Vote: Why Members of Parliament Must Grasp the Realities of the Benefit System

June 1, 2025
View of the Houses of Parliament in London, in the foreground is a river.

To all Members of Parliament, As you prepare to cast votes on crucial reforms to the UK’s benefit system in the coming month, we write to you with urgency and concern. These are not simply bureaucratic adjustments; they are life-altering …

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Categories Updates

M.E./C.F.S. and the Fight for Fair Benefits: Why the DBC’s Work is More Vital Than Ever.

May 23, 2025
Black Text on White and Black Wall. Text reads 'fight for it'

As Stripy lightbulb CIC, a proud member of the Disability Benefits Consortium (DBC), we know first-hand the profound challenges faced by individuals living with Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome (M.E./C.F.S.). The fluctuating, often invisible nature of M.E./C.F.S. symptoms – from …

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Categories Updates

Ignoring M.E./C.F.S.: A Cost the UK Can’t Afford

May 23, 2025
A grey price tag on a white background. On the tag are the letters ME/CFS written in blue.

On January 20th, 2025, a critical letter was posted Special Delivery to the office of Rt Hon Rachel Reeves MP, the Chancellor of the Exchequer, with a copy also sent to the Secretary of State for Health and Social Care. …

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Categories Updates

The Forgotten Voices: Trapped Between Illness and ‘The System’

April 21, 2025April 21, 2025
Person holds hands against glass window pane.

The clamour for person-centred disability reform rightly echoes across our society at the moment with the UK Labour Government proposing yet more harsh changes to the welfare system. We see campaigns highlighting the potential additional struggles for those at risk …

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Categories Politics, Updates

The Shocking Toll of Neglect: How the DALY Score Exposes ME/CFS Research Underfunding

April 14, 2025

Image/table above is from this research study Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a debilitating chronic neurological disease affecting an estimated 1.25 million people in the UK. Characterised by post-exertional malaise (a worsening of symptoms after even minimal activity), unrefreshing …

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Categories Issues, Social Issue, Updates
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Recent Posts

  • Hampshire/IoW – Help Us Represent M.E./C.F.S. Within Urgent Care
  • When Language Distracts From Biology: Why M.E./C.F.S. is Not “Acquired Neurodivergence”
  • Help to Shape the Future of Health and Social Care in Hampshire: Your Lived Experience Matters
  • Miscategorisation of M.E./C.F.S. in Ministry of Justice Datasets
  • M.E./C.F.S. in the Workplace: Essential Guidance for HR and Occupational Health Teams.

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