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.
If you are clinically extremely vulnerable or over 70, you live in England, and you haven't yet been offered an appointment to have your coronavirus vaccine, you can now book directly online or by calling 119 (7am-11pm).
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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.
Dorothy Reed challenged medical opinion of the day to give Hodgkin lymphoma a clear diagnostic marker.
Some people have mixed feelings about the gradual easing of lockdown restrictions and the end of shielding in the UK. Find out how you can reduce your risk when society begins to open up again.
NICE is not recommending mogamulizumab for the treatment of relapsed or refractory mycosis fungoides or Sézary syndrome.
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.
