There are many organizations around the world that are dedicated to helping hemophilia patients. Some of the well-known organizations are listed below.
The American Society of Hematology serves with the mission to further the understanding, diagnosis, treatment, and prevention of disorders affecting the blood, bone marrow, and the immunologic, hemostatic, and vascular system by promoting and supporting clinical and scientific hematology research through its innovative award programs, meetings, publications, and advocacy efforts.
Founded in 1948, National Hemophilia Foundation strives to support people with hemophilia through research, education, and advocacy with an aim to prevent additional problems these diseases may cause.
The Hemophilia Federation of America was founded in 1994 with a goal to take care of what the bleeding disorder community needed at that time. Its vision is to improve the care and quality of life for all hemophilia patients by eliminating the barriers to diagnosis, treatment, and cure.
The World Federation of Hemophilia is dedicated to improve and sustain care for people with inherited bleeding disorders around the world and bring the bleeding disorders community together in the name of Treatment for all.
Centers for Disease Control and Prevention works to improve the quality of life for people affected by the disorder and prevent the complications of hemophilia. They help to increase the awareness, education, and research on hemophilia.