For everyone with a bleeding disorder in the UK.
The Haemophilia Society is the only UK-wide charity for everyone affected by a genetic and acquired bleeding disorder. We support our community through our information, events and advocacy services.
One in 2,000 men, women and children in the UK have a diagnosed bleeding disorder. As many as a third of bleeding disorder diagnoses have no known family history and can be the result of a random gene mutation. This means a diagnosis can come completely out of the blue.
Every diagnosis deserves our support and compassion, backed by our knowledge and specialist information. We’re proud to be here for everyone with a bleeding disorder.
We align with the following UN Sustainable Development Goals: