The Haemophilia Foundation of Nigeria (HFN) is a non-governmental organisation working under the World Federation of Hemophilia to bring treatment to persons living with bleeding disorders in Nigeria. HFN is committed to having a bleeding disorders community where there is Treatment for All.
This commitment is especially important during the COVID-19 crisis.

Our Vision and Mission

Our vision is to see that persons with bleeding disorders live a normal life.
The mission of HFN is to SUPPORT, EDUCATE and ADVOCATE for persons with bleeding disorders to have access to RIGHT and PROMPT treatment. In so doing, HFN aims to improve the level of expertise and treatment facilities in Nigeria to meet up with World Federation of Hemophilia standards.
We work to ensure every person including those living with hemophilia and von Willebrand disease (VWD), those with rare factor deficiencies, and women with bleeding disorders have access to world-class care and recognition of their condition.

Our corporate partners, donors, and volunteers all share this belief and we thank them for their past and ongoing contributions.