Skip to main content

Help Chelsea raise money

For participating in 2021 Virtual Banff Jasper Relay

Why We Relay

Thank you for helping me fundraise for the Brain Tumour Foundation of Canada! They have been an incredible resource for me and my family as my father has undergone treatment for and continues to live with a brain tumour. With continued research advances and a great support system there is so much to be hopeful for!

About the Brain Tumour Foundation of Canada:

We are a dedicated team of volunteers, patients, survivors, family members, health care professionals and staff, determined to make the journey with a brain tumour one full of hope and support. We work collaboratively to serve the needs of those Canadians affected by all types of brain tumours.

Brain tumours are unpredictable and complex. We’re here to help anyone affected by any type of brain tumour. Support from donors, corporations and community foundations means the estimated 55,000 Canadians living with a brain tumour can find hope. Hope through research. Hope through patient and survivor support. Hope for a cure.

Description

Thank you for helping to raise money for the Brain Tumour Foundation of Canada! The Banff Jasper Relay is on a mission to #endbraintumours.

The Brain Tumour Foundation of Canada is a national, not-for-profit organization dedicated to reaching every person in Canada affected by a brain tumour with support, education and information, and to funding brain tumour research.  Every year, we help thousands of Canadians affected by brain tumours find emotional support and comfort while gaining a better understanding and knowledge of their disease. Brain tumours are unpredictable and complex. The disease does not discriminate and affects people of all ages and backgrounds. A brain tumour can impact vision, hearing, memory, balance and mobility. And the effects are physical, emotional, financial, and last a lifetime. Lifting this burden for anyone affected is the goal of Brain Tumour Foundation of Canada. With 55,000 Canadians living with the disease, families across the country depend on this unique organization to address patients’ quality of life needs while also funding the research necessary to find the ever-elusive cure.