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.
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).Read more
0808 808 5555
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.
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.