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This May so many of you asked for Brain Tumour Awareness Month to be changed from October to May and in doing so shared your experience with the health care system, talked about access to drugs, the need for increased funding for research and why we need to count every brain tumour.
From the need for equal access to treatments to the importance of counting every brain tumour, we must continue to tell government what needs to be done for the 55,000 Canadians living with a brain tumour.
If you want to be kept 'in the loop' and be one of the first to know about these kinds of opportunities in the future, sign up to be an advocate. We need you.
When you look back at Brain Tumour Foundation of Canada’s history, it’s clear that at the heart of the organization are the patients, survivors and loved ones who care for those diagnosed. It’s this amazing community of supporters – even amidst what is often a life-changing journey – who volunteer their time, host fundraising events and donate in memory of those they’ve lost to the disease.Learn more
Read why Katherine is now "filled with gratitude" despite a diagnosis of Anaplastic-Ependymoma, stage 3 brain cancer, at the age of...Learn more
When John Hatcher laces up his running shoes on Saturday, October 2, 2016 he joins over a dozen of his family members and friends for...Learn more