In 1953, a small group of hemophiliacs, their families and physicians in Montreal founded the Canadian Hemophilia Society. Their dream at the time was to improve the quality of life and find a cure for hemophilia. The close collaboration among patients, health care providers and researchers was unique then… and remains so today. Through their tireless efforts, the CHS quickly developed from a small, Montreal-based support group to a national volunteer organization. Ontario created the first provincial chapter in 1957, followed by Quebec in 1959. By 1969, chapters existed in each province. Today, the Canadian Hemophilia Society is governed by a group of experienced and dedicated volunteers from across the country. They are actively involved in the development of programs and services to meet the needs of all people with inherited bleeding disorders.
