Brain Tumour Foundation of Canada is made up of a dedicated team of staff, volunteers and health care professionals, all working together for the same goal: End brain tumours. Our head office is located in London, Ontario. We are unique in that we work to serve the needs of Canadians affected by both malignant <em>and</em> non-malignant brain tumours.

Hope and support are at the core of everything we do – whether it’s funding new and exciting research into brain tumour treatments, or bringing patients, survivors, and families closer together at our Brain Tumour Walk events and support groups.

By providing support, education, information and research funding, Brain Tumour Foundation of Canada has been making a difference in the lives of the over 55,000 Canadians currently living with a brain tumour and thousands more before them.

<strong>Since 1985, more than $9.4 million in direct funding to research has been raised.</strong>

Cystic Fibrosis Canada is a national charitable not-for-profit corporation established in 1960, and is one of the world’s top three charitable organisations committed to finding a cure for cystic fibrosis (CF). Cystic Fibrosis is a fatal genetic disease impacting over 4,200 Canadians. People with Cystic Fibrosis must adhere to a strict infection control policies which means they cannot connect to others with the disease indoors. Despite this social isolation, we are working hard to continue to sustain our incredible, unique community!