As the 2022 North American Cystic Fibrosis Conference begins, Vertex Save Us and Just Treatment have written to Vertex demanding urgent action to ensure global access to lifesaving cystic fibrosis treatment.
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NGOs warn that the cost of NHS medicines, 25% of which are supplied by India, could be affected if the UK forces India to change national laws related to intellectual property as a result of trade negotiations.
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The biggest Cystic Fibrosis (CF) related conference in the world takes place this week. We asked Rafaelle - a 22-year old CF patient from Brazil who cannot access lifesaving treatment - what message she wants to send to the conference.
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A report from our recent workshop ‘Capitalism is Making Us Sick: A Radical Response to the Youth Mental Health Crisis’ as part of The World Transformed 2022.
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Just Treatment’s new Senior Pharma Organiser Gayle reflects on the power of patient-led organising, and why we must use it to win global access to lifesaving cystic fibrosis medicine.
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With Rishi Sunak and Liz Truss battling it out to become the next Prime Minister, what - if anything - can we expect from the candidates when it comes to the NHS and patients’ right to health?
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At the end of Pride month, we reflect on the interconnection between the fight for health justice and human rights and the LGBTQ struggles that laid the foundation for the activism of today.
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Just Treatment patient leader Rajni reflects on the shameful role the UK government has played in blocking efforts to waive COVID monopolies at the World Trade Organization.
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Millions of patients - particularly children and young adults - are being put at risk by the crisis in mental health care. Here’s how some of our supporters have been affected by this critical issue.
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Over the past few weeks we’ve taken action alongside activists in many other countries to protest big pharma’s pandemic profiteering. Here’s what we’ve been up to…
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Campaigners unfurl banner outside GlaxoSmithKline Annual General Meeting demanding subsidiary ViiV Healthcare sell new injectable at a price comparable to generic oral prevention pills, and immediately commit to sharing technology with generic manufacturers.
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Just Treatment supporter Sakina Datoo reflects on the devastating loss of her father, who was unable to access a lifesaving COVID vaccine in Tanzania.
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London-based GP and mother of two Dr Rasha Mezher-Sikafi reflects on the passing of her grandmother, and how it shows what’s at stake in the fight for global vaccine access for all.
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Just Treatment supporter Melanie shares her experiences of living as a clinically vulnerable person through COVID, and why global vaccine access is so critical.
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Covid monopolies are a deadly barrier to saving lives and ending this pandemic - the deal announced yesterday won’t change that.
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A relief worker shares her experiences of dealing with vaccine disparity in refugee camps.
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A doctor shares his experience in dealing with a pandemic whilst grappling with vaccine inequity and shortages.
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NHS patient Willow reflects on her experiences as an extremely clinically vulnerable patient, and why ensuring global, equitable vaccine access is so vital.
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Over the past few weeks, Just Treatment supporters have been sending personal letters to crossbench members of the House of Lords, urging them to oppose the Health and Care Bill. Click to read more!
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On Thursday 13th January, MPs from a range of different parties debated the issue of global equitable vaccine access in Westminster Hall. Here’s what happened…
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