Hemophilia Foundation of Michigan

Non-Profit - Ypsilanti, MI, US

Hemophilia Foundation of Michigan Employees
Anthony Stevens

Educational Services Manager / Associate Camp Director

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Susan Lerch

Executive Director & Great Lakes Regional Director

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Janelle Gunn

Special Events Manager, West Michigan

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Lisa Clothier

Outreach and Community Education Manager

Contact Lisa Clothier

Sarah Procario

Advocacy & Communications Manager

Contact Sarah Procario

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Hemophilia Foundation of Michigan Details

Beginning in 1956, the Hemophilia Foundation of Michigan strives to improve the quality of life for all people affected by hemophilia, von Willebrand disease, other coagulation disorders, and related complications, including HIV/AIDS and hepatitis. HFM provides a variety of programs and services to support the Michigan bleeding disorders community, including summer camping program. In 1969, HFM began the first summer camp in the nation for children with bleeding disorders. Today, HFM provides over 6 weeks of camping programs for children and adults affected by bleeding disorders. HFM also serves as the Regional Core Center for all federally funded hemophilia treatment centers (HTCs) in Michigan, Ohio, and Indiana. HFM secures and administers federal funding from Health Resources and Service Administration and the Center for Disease Control and Prevention (through American Thrombosis & Hemostasis Network) to support both comprehensive care and prevention programs at HTCs.

Hemophilia Foundation of Michigan logo, Hemophilia Foundation of Michigan contact details
Website: hfmich.org
Employees: 20 - 49
HQ: 734 544-0015
Location: Ypsilanti, MI, US
Revenue: 20 - 50 Million
hemophilia bleeding disorders von Willebrands Disease Advocacy education International Hemophilia Adoption Community Connections Non-Profit Nonprofit Organization Management
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