For over 2 decades, the “Hemophilia Foundation Pakistan [HFP]” has provided national leadership to improve and sustain care for people with inherited bleeding disorders, including hemophilia, von Willebrand disease, rare factor deficiencies, and inherited platelet disorders.
We save and improve lives of our community by:
Empowering patients in order to make them community activists;
Advocating for adequate supply of safe treatment products; and
Educating people with bleeding disorders to help them live healthier, longer and more productive lives.
Through our network of committed volunteers and associated stakeholders, the HFP acts as a catalyst to bring about needed change. To this effect, the HFP operates through its Chapters to work with motivated health care providers, patients, their families and members of the community to foster quality health care for people with bleeding disorders.
The Hemophilia Foundation Pakistan [HFP], a national not-for-profit organization, was established in 1995. It is a national network of patients with Hemophilia and has official recognition from the World Federation of Hemophilia [WFH] as National Member Organization [NMO].