The Canadian Hemophilia Society (CHS) has a long-standing role in serving and supporting people in Canada living with inherited bleeding disorders. For decades, individuals, families, volunteers, health care professionals, and partners have come together through the CHS to support one another, share knowledge, and advocate for better care, safer treatments, and improved quality of life.
The 2026–2030 Strategic Plan reflects the voices, needs, and realities of the bleeding disorders community today. While progress has been made in care and treatment, many people still face challenges in being diagnosed, accessing care, and feeling understood or supported. This plan responds by placing inclusion and belonging at the centre of CHS’ work.