Imtiaz talks about his diagnosis of central nervous system (CNS) lymphoma.
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.
With restrictions being lifted and shielding for the clinically extremely vulnerable coming to an end, you may feel a mixture of emotions. This video looks at approaches you may find helpful if you are feeling worried at this time.
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.