Sickle Cell Disease Association of Canada/ Association d'anémie falciforme du Canada

The Sickle Cell Disease Association of Canada provides support, education, and advocacy for people living with sickle cell disease and their families across Canada. The organization raises awareness about this genetic blood disorder, which disproportionately affects Black communities, and works to improve access to quality care and treatment options. Based in Toronto, the association offers resources, peer support, and educational programs to help individuals navigate their diagnosis and manage their health. The charity also engages in policy advocacy to address healthcare gaps and reduce stigma surrounding the condition. Through community outreach and partnerships with healthcare providers, the association strives to improve outcomes and quality of life for those affected by sickle cell disease in Canada.