We are actively monitoring the COVID-19 situation. Learn More. Please enjoy our Virtual Programs.
by Janet Fanaki It was December 2019 when I wrote my last article for this website. At the time, my […]
When a young person is diagnosed with a brain tumour, some common concerns often center around body image. When diagnosed […]
We all experience change, and as our community knows, nothing changes your view on life more than being diagnosed with a brain tumour. With this change comes feelings of grief.
Children are intelligent, observant and tend to know that something is going on in the adult world even when they […]
We’ve all faced tremendous challenges around access to programs and services since the start of the pandemic. Though our support […]
By Todd Goold – Support Services Specialist, Brain Tumour Foundation of Canada With the holidays right around the corner many […]
Every Canadian affected by a brain tumour has the right to have the information and support needed to fully participate […]
Through self-advocacy, those affected by brain tumours and their families can better understand their diagnosis, barriers to treatment, and rights […]
In late summer, Brain Tumour Foundation of Canada learned the story of Karen and her quest to cycle through the […]
Connect with children and their families affected by a brain tumour.
Find connections with others who have been affected by a brain tumour to promote and nurture wellbeing.
There are so many ways you can help make a difference in the lives of patients and families today.
Reach out for support, education and information and to learn about research.
This site uses cookies to improve user experience. Please select allow if you would like to allow the use of cookies.
