Anne was only able to access the treatment she needed after a public campaign brought the price down. Here she explains why she’s supporting the campaign for Plan B on Orkambi.
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We’re celebrating the news today that cystic fibrosis drugs Orkambi and Symkevi have been approved for use in Scotland. But what will this mean for the rest of the UK?
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Patient leader Fiona explains what a no deal Brexit could mean for patients - and why she’s calling for certainty.
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Patient leader Clare had to fight to access treatment. Now she’s supporting others facing similar battles.
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A US-UK free trade deal could spell disaster for our NHS. Diarmaid McDonald explains why in the Mirror.
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Negotiations with the drug company Vertex have reached stalemate. It’s time for plan B on Orkambi.
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Today we learnt the devastating news that cystic fibrosis drugs Orkambi and Symkevi have been deemed too expensive for NHS Scotland. It’s time for the government to take a stand and overturn Vertex’s monopoly.
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Emma Robertson argues that changes to medical trial consent processes could improve or even transform cancer research.
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Anna Bennett’s daughter has waited four years to access Orkambi. The newly founded CF Buyer’s Club offers hope - but Orkambi remains unaffordable for many.
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Patients and MPs demand the government acts now to bring down the price of cystic fibrosis drug Orkambi
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The amazing Clare has spent the last six months working with Just Treatment. Here are her thoughts on what she’s learned.
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Anna Bennett has a daughter with cystic fibrosis. She hopes MPs get answers to the questions she has about access to the medicine her child needs.
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In her second blog on our Plan B campaign Anna, the mother of a child who needs Orkambi, takes a look at Vertex’s behaviour around the world.
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Anna - mum to a three year old with cystic fibrosis - reflects on the whirlwind start to our campaign to win access to Orkambi.
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After a campaign engaging thousands Dunise won the fight for access to this breast cancer drug at a fair price for the NHS!
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One of the inspirational leaders who helped get Just Treatment get off the ground has very sadly passed away.
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We’re calling for government action to stop the greed of pharma company Vertex endangering the lives of cystic fibrosis patients like Luis.
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It’s time our governments challenge the pharmaceutical industry and put patients’ needs at the heart of our medical innovation model.
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Clare explains why our new report on pharma R&D matters to patients like her.
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We won an award for being brilliant!
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