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The Bardo Foundation joins Cancer52
Cancer52’s newest member, The Bardo Foundation is an international childhood cancer charity founded in memory of Bernardo “Bardo” Eggesbø.


Leiomyosarcoma Research UK joins Cancer52
Leiomyosarcoma Research UK has joined Cancer52.


Rare Cancers Act 2026
The Rare Cancers Act 2026 will prioritise long overlooked aspects of research, and has the potential to transform outcomes for those affected by rare and less common cancers.


MOVE Against Cancer joins Cancer52
MOVE Against Cancer has joined Cancer52! Their mission is to support and empower everyone impacted by cancer to be more active because movement matters. They deliver evidence-based support through 5k Your Way community groups, tailored online programmes and accessible resources, improving wellbeing and supporting health outcomes during and after treatment.


Cancer52’s newest member is Lymphoma Out Loud
Cancer52 is pleased to welcome Lymphoma Out Loud as our newest member! Lymphoma Out Loud is a UK charity educating and raising awareness of lymphoma, one of the most common cancers in young people. They are a young charity with a rebel spirit, on a mission to disrupt lymphoma by educating, empowering, and amplifying patient voices through bold campaigns, education and lived experience. Find out more on their website - lymphomaoutloud.org


The Big Cancer52 Conversation, June 2025
Cancer52 hosted The Big Cancer52 Conversation in Canary Wharf, London on 24th June 2025. This was the sixth Big Cancer52 Conversation,...


Get A-Head Charitable Trust joins Cancer52
Cancer52 is delighted to welcome The Get A-Head Charitable Trust as our newest member!
Cancer52 has responded to the Call for Evidence for the National Cancer Plan for England
Cancer52 has submitted a response to the call for evidence to shape the National Cancer Plan for England


Big Cancer52 Conversation, March 2025
Cancer52 held the Big Cancer52 Conversation on 26th March in Manchester.


Improving Diagnosis Report
Cancer52 is proud to launch their report ‘Improving diagnosis: Patient and clinician perspectives on increasing early diagnosis in rare and
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