The Haemophilia Society is working for people with haemophilia, von Willebrand's or a related bleeding disorder and their families to secure the best possible care, treatment and support.

The Society was established in 1950 and is the national charity in the UK of and for people with haemophilia, von Willebrand's and related bleeding disorders. We have over 4000 members and supporter as well as a network of 16 local groups throughout the UK. We provide information, advice and support services and we advocate and campaign to secure the best possible care and treatment.
We also provide services for people with haemophilia affected by HIV and hepatitis C.The Haemophilia Society has a strict confidentiality policy and is committed to equal opportunities. We also have a policy on complaints and a leaflet can be provided on request.

Have a look at 'Young Bloods' our new website for children and young people.  Or click here to take part in a study on attitudes to treatment.

New book about Lord Morris - Alf Morris: people's parliamentarian - is now available.