South African Haemophilia Foundation
Established in 1970, the SAHF advocates for South Africans living with haemophilia, von Willebrand disease and other rare bleeding disorders.
The South African Haemophilia Foundation (SAHF) was established in 1970 to advocate for the needs of people living with bleeding disorders in South Africa. For more than five decades it has worked to improve access to treatment, provide education and support for patients and their families, and strengthen collaboration between healthcare professionals, treatment centres and the wider bleeding disorders community.
The Foundation supports people living with haemophilia, von Willebrand disease and rare bleeding disorders through education, advocacy and community programmes. Its vision is a world in which people with bleeding disorders receive optimal care and have the opportunity to live full and active lives.
A bleeding disorder is critical information in a trauma emergency. An engraved emblem communicates it in the seconds that matter.
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