We are the UK’s only charity dedicated to lymphoma, the fifth most common cancer. We're here to help, however you are affected.
You can count on us.
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.
Connect to other people affected by lymphoma any time through our online discussion forums and ask those important questions from those who have been there.
The Lymphoma Coalition Europe (LCE) is looking for people to be members of a new Lymphoma CAB - if you want to influence research and help create a louder voice for the lymphoma community register your interest today.
The NHS Long Term Plan has been published and whilst lymphoma is not specifically mentioned, we're glad to see the more personalised, co-ordinated approach to cancer care. We hope the government supports the commitments with the resources and staffing needed.
Have your say on bendamustine with rituximab for relapsed low-grade non-Hodgkin lymphoma.
In this video, Laura talks about her experience of her 5 year old son having lymphoma.
25 years ago Andrew (right) donated his bone marrow to his brother Stephen (left) who needed a transplant to treat his T-cell non-Hodgkin lymphoma
Hayley talks about her experience of Hodgkin lymphoma, adapting to a new life and finally accepting that it is OK to be angry about what happened.
Carl talks about his diagnosis of CLL, four years on active monitoring and treatment on a clinical trial
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.
