Lymphoma Canada is wholly Canadian. All of our resources are derived from Canadian statistics and feature only Canadian specific information. All of our materials are reviewed and approved by our Scientific Advisory Board comprised of Canadian researchers and clinicians. All members of our Board of Directors reside in Canada and Lymphoma Canada funds only Canadian researchers.
Empower patients and the lymphoma community through education, support, advocacy, and research.
Life unlimited by lymphoma.
Lymphoma affects many people, from patients, family and caregivers, to medical professionals and researchers. Lymphoma Canada connects and empowers this community. Together we are promoting early detection, finding new and better treatments, helping patients access those treatments, learning lymphoma’s causes, and finding a cure.
Lymphoma Canada provides, at no cost and in both official languages: electronic and print materials on the Hodgkin lymphoma, non-Hodgkin lymphoma and CLL, peer and caregiver support groups, educational forums and advocacy on behalf of patients. Lymphoma Canada also funds Canadian research.
We are Canada’s only national organization focused entirely on lymphoma.
A registered charity, we are led by a volunteer board of directors drawn from the Canadian lymphoma community. Our board includes lymphoma patients and medical and research professionals. A small, dedicated staff brings expertise in program implementation, communications, fundraising, and administration. We are guided by expert members of a Scientific Advisory Board. Lymphoma patients across the country help organize, and participate in, education events, support groups, online webinars, and fundraising events.
Lymphoma Canada operates in both official languages, with staffed offices in Ontario and Quebec and a volunteer presence across the country.