Diagnosed with Hodgkin lymphoma at 24, and during a pandemic, Cassie talks about finding the treatment tough, and the challenge of losing her hair.
COVID-19 and lymphoma, including vaccine information
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.Read more
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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.
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.
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