As a volunteer group founded in 1956, the Hemophilia Foundation of Michigan (HFM) strives to improve the quality of life for all people affected by hemophilia, von Willebrand’s disease, other coagulation disorders and related complications, including HIV/AIDS and hepatitis. Over time, the organization has evolved into a nonprofit foundation providing services in Michigan, Ohio, and Indiana. HFM collaborates with 19 hemophilia treatment centers in those states, and oversees several federal care and prevention programs.
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