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The Kelly Society was named for the special little girl who inspired the creation of Brain Tumour Foundation of Canada in 1982. The Northey family remembers their child in a very special way through the Kelly Northey Legacy Fund which provides endowments to fund information, education and support programs, particularly for young patients with brain tumours.Members of the Kelly Society are generous individuals who lead by example, making significant contributions to Brain Tumour Foundation of Canada over a period of three years. The Kelly Society was created to thank these leaders. Membership is exclusive to individuals who commit to making a minimum gift of $500 per year for three years.

Membership in the Kelly Society recognizes your leadership role at Brain Tumour Foundation of Canada, and the important role you play in making a difference for brain tumour patients and their families.
Susan Relecom
srelecom@braintumour.ca
1-800-265-5106 or 519-642-7755, ext. 227
Members of our special Kelly Society and friends took a trip to visit Dr. James Rutka and the Arthur and Sonia Labatt Brain Tumour Research Center in Toronto.
Read the story and see photos from the tour >
It was August of 1985 when Shelley Fitak first began to learn about brain tumours. It was then that her first husband, Bob Thierman, was diagnosed with a brain tumour. At the time, little was known about brain tumours. In addition, there was very little support or information available across Canada ...
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