The Mission of the Thalassemia Foundation of Canada
is to support and fund thalassemia scientific research, treatment, patient services, public awareness and education. Established in 1982, originally began as a small support group for parents and patients. Over the years, the Thalassemia Foundation of Canada has grown to national organization with the support of dedicated volunteers and donors. 
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Recent Updates
Bill 255
Thalassemia Foundation of Canada is delighted that #Bill 255, has passed 2nd reading at the Ontario Legislation on March 2nd. The Thalassemia Community is extremely appreciative for the support of MPP Rudy Cuzzetto and MPP Andrea Khanjin for co-sponsoring the bill. Please read the press release. If passed, Bill 255
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Our Fundraising Page Is Now LIVE!
Dear Friends and Supporters, We hope you are all keeping well and safe during these unprecedented times. Due to the ongoing COVID-19 pandemic, we had to postpone our annual Gala event this year. In lieu of this initiative, we have launched an online fundraising campaign. All of us at the Thalassemiaread more
What's Happening
News
- 2017 Newsletter
The latest Thal-a-vision 2017 newsletter is now available.read more
Events & Fundraisers
- Our Fundraising Page Is Now LIVE!
Dear Friends and Supporters, We hope you are all keeping well and safe during these unprecedented times.read more