The Hemophilia Foundation of Michigan is a nonprofit organization dedicated to improving the quality of life for individuals and families affected by hemophilia, von Willebrand disease, and other bleeding disorders through education, advocacy, support services, and community programs.
Healthcare access, insurance coverage protections, funding for bleeding disorder treatment programs, patient assistance services, public health policy, and protections for individuals with pre-existing conditions
Charitable donations, foundation grants, corporate sponsorships, fundraising events, and limited government and industry grants
National Bleeding Disorders Foundation, Hemophilia Treatment Centers in Michigan, and national bleeding disorder advocacy coalitions
Non-profit organization
