We are the UK’s only charity dedicated to lymphoma, the fifth most common cancer. We're here to help, however you are affected.
Latest information about COVID-19 and how it affects people with lymphoma. This information comes from authoritative sources, including the UK government, NICE and the NHS, and is updated to reflect the latest guidance.
As restrictions ease, you may find our free 'distance aware badge' useful. You can wear it to remind people to social distance when possible.
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You can count on us.
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Our team is specially trained to offer you a listening ear and the information you need about your lymphoma.
Our friendly support groups are held regularly around the country so you have the opportunity to meet other people affected by lymphoma and share experiences.
We can connect you to a buddy - specially trained volunteers who have a personal experience of lymphoma and can understand what you’re going through.
Lymphoma researchers at the NCRI would like to hear from you if you are a patient, carer or family member of someone diagnosed with follicular lymphoma at any stage, from active monitoring (watch and wait) to active treatment or follow-up.
12-year-old Harry walked one mile a day for 26 days to support our work
Very rare condition involving blood clots and unusual bleeding after vaccination with the AstraZeneca vaccine.
Imtiaz talks about his diagnosis of central nervous system (CNS) lymphoma.
Katie talks about people’s reaction to a Waldenström’s macroglobulinaemia diagnosis and shares her experience of a clinical trial.
All I want is for my son Jo to get well after his diagnosis of Hodgkin lymphoma.
25 years after treatment for diffuse large B-cell lymphoma, David talks about the importance of art and creativity.
Every 27 minutes someone is diagnosed with lymphoma. With your help we can provide the vital information and support they need to cope with their diagnosis, treatment and living with lymphoma.
