30 Years of Hope

Bringing Hope to Brain Tumour Patients in Canada for 30 Years

2012 marks Brain Tumour Foundation of Canada’s 30th year in operation. Since the early days of the organization, it has been our vision to find the cause of and cure for brain tumours while improving the quality of life for those affected. Today, it’s this purpose that continues to resonate and motivate thousands of volunteers, donors and supporters as we look to the future and a cure for this disease.

“This year is an important opportunity for the brain tumour community in Canada to pause and reflect on how far research and treatments have come since the three dedicated founders first began their effort to put a face and voice behind brain tumours,” says Executive Director, Susan Marshall. “It’s also a chance to look to the future, towards the exciting things to come for Brain Tumour Foundation of Canada.”

One significant effort this year will be to increase public awareness about brain tumours all across Canada. Brain tumours are more common than most people think: Every day in Canada, 27 people are diagnosed with a brain tumour and it is estimated that 55,000 Canadians currently live with the disease. Brain tumours don’t discriminate; they affect people of all ages and backgrounds. For individuals living with a brain tumour, and their families, this anniversary year is an opportunity to create awareness, raise support and share information about the devastating effects of this disease.

Steve Northey reflects on the organization's founding in 2007

Founded in 1982 in London, Ontario, Brain Tumour Foundation of Canada began after Steve Northey lost his eight-year-old daughter to a brain tumour. Together with Dr. Rolando Del Maestro, a neurosurgeon and researcher, and Pamela Del Maestro, a neuroscience nurse, the three worked to form an organization to improve the quality of life for those affected by a brain tumour.

Since that first meeting, Brain Tumour Foundation of Canada has evolved into the national leader of the effort to raise awareness and mobilize action on brain tumours. Since 1982, more than $3 million has been directed to fund vital research projects that contribute to progressing brain tumour treatment and care. Thousands of patients lean on the organization every year for information, education and support.

Come back to this area over the year to catch up on special stories and items that will honour and reflect on the 30 years of impact on the lives of brain tumour patients and their families - and how you can help propel the future with your donations. Just watch this section for all the details.


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Featured Story

Childhood Brain Tumour Signs & Symptoms

Earlier this year, you gave us your feedback in a survey on brain tumour signs and symptoms. One of the things we did with that survey was to compile a list of the most common signs & symptoms for children. Now, as part of Childhood Cancer Awareness Month, we are sharing compelling quotes from that survey and urging you to share them with this link to see the symptoms: www.braintumour.ca/symptoms. Thank you!

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Anthony's Story is Our Story

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Kate's Mum's Story

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Upcoming Events

  • 17/Oct/2018: Windsor Support Group: Meets at the United Way, Unit A1, 300 Giles Blvd. East... Learn more >
  • 17/Oct/2018: Calgary Support Group: Meets at Wellspring Calgary, 1404 Home Road NW, Calgary, Alberta, T3B 1G7... Learn more >
  • 17/Oct/2018: Niagara Region Support Group: Meets at Wellspring Niagara, 3250 Schmon Parkway, Thorold, ON, L2V 4Y6... Learn more >
  • 17/Oct/2018: Winnipeg Support Group: Sturgeon Creek United Church, 207 Thompson Drive, Winnipeg, MB... Learn more >
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