The Kenya Haemophilia Association (KHA) was established in Nairobi in 1979. In 1992, it was recognized as a National Member Organisation (NMO) by the World Federation of Hemophilia (WFH). With this status, it is the official Kenyan patient organisation in charge of representing the rights of all patients living with Haemophilia and allied bleeding disorders in Kenya.
To achieve the highest standard of care for people living with Haemophilia and other bleeding disorders in Kenya.
To work together with other stakeholders for the social good and greater benefit of all people living with Haemophilia and other bleeding disorders in Kenya.
To provide clinical support, management and care for people living with haemophilia and other bleeding disorders in Kenya;
To lobby the government, agencies and institutions concerned to provide a conducive environment for the holistic management of haemophilia and other bleeding disorders in Kenya;
To create awareness to the general public on haemophilia and other bleeding disorders
To engage in resource mobilisation activities that will facilitate the activities of the Association;
To promote research and education through dissemination of information on haemophilia and other bleeding disorders
To train and build the capacity of caregivers involved in the management of haemophilia and other bleeding disorders.
