Just Treatment supporter Eileen shares reflections on emergency treatment, approach to diagnosis, and end of life care in the NHS based on what her late husband Mike experienced.
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After months of relentless campaigning, cystic fibrosis patients in Lithuania and Estonia will finally get access to lifesaving treatment!
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Our response to the major review into the state of the NHS led by Lord Darzi. The crisis is stark - now our NHS needs real solutions from Labour.
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Just Treatment supporter, Mike shares his story about the devastating loss of his daughter, Allyson, due to delays in emergency care.
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Just Treatment supporter Maggie shares her experience with delays in urgent care, and what it reveals about the dangerous path our NHS is on.
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Vertex have once again used their wealth to protect their monopoly profits, but our fight for global access goes on.
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With the new Health Secretary Wes Streeting pledging to increase reliance on the private sector, we break down why this is a bad idea for patients and the NHS.
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The Co-Chairs of our new Board of Directors say hello, give an update on Just Treatment’s operations and look ahead to an exciting future.
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Since Labour took government, there has been a lot reported about their plans for the NHS. Here’s what you need to know.
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Just Treatment supporter Ann shares her and her late husband’s NHS experiences, and what they tell us about the dangerous direction our NHS is going in.
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Just Treatment supporter Jane shares the horrors she has seen in a profit-driven US health system. Now, underfunding and privatisation threaten the NHS. We must protect and properly fund our public health service.
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Elizabeth Pfiester shares her NHS experience & highlights the urgent need for fully-funded and truly public NHS.
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Cystic fibrosis families at Breakthrough Prize awards ceremony, demanding global access to medicine.
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Dr. Greg Shay on the Desperate Need for Cystic Fibrosis Care in Gaza
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With the 2024 Budget, the government has once again starved our NHS of urgently needed investment. Here’s what you need to know…
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In a landmark legal case, South African cystic fibrosis patients are taking a giant drug company to court to fight for access to lifesaving treatment.
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This Children’s Mental Health Week, our Senior Organiser May reflects on their own experiences of navigating youth mental health services, and how the growing crisis demands both better provision and corporate accountability.
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Over the last two months we have confronted Vertex online and in person, and we’ve taken the fight for global access to the largest gathering of CF experts in the world! Read more here…
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Our new report with Connected By Data focuses on how people experience data when interacting with health services.
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