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.
The Hemophilia Foundation of Michigan offers numerous programs to support people living with bleeding and clotting disorders:
- Camping Programs
- Teen Retreat
- Holiday Party
- Bleeder and a Buddy
- Lansing Overnight Lock-in
- Camp Staff Opportunities
- Camp Old Beagle
HFM Highlighted Events
May 17, 2016
Capital Area, Lansing
Please join HFM as we travel to the state capital to advocate for our community! This will be a two-day event, free of charge! Please help us speak up for our community. We need your voice! View Event Details »
May 19, 2016
Grand Rapids Art Museum 101 Monroe Center St NW Grand Rapids, MI 49503
Please join us for this first-time evening event to raise funds for HFM’s camping programs. Guests will enjoy a strolling dinner, silent auction, beautiful music and hear amazing stories of inspiration and hope, all while surrounded by magnificient works of art. View Event Details »
Support HFM with your tax-deductible donation.
Today, fewer than 30% of bleeding disorders patients are registered for the Patient Notification System (PNS). The PNS is a fast, free, and confidential service that notifies registered patients, caregivers, and providers within the first 24 hours of a recall or withdrawal of their factor therapy or associated ancillary products. Take Action. Learn more about PNS and register today! | 02.10.2015
Lansing Day Wednesday, May 6, 2015 Please join us to educate legislators about bleeding disorders. - THIS EVENT IS FREE OF CHARGE - | 02.5.2015
Free or Low Cost Dental Program for any person who has a bleeding disorder or who is a symptomatic carrier. Click for more details. | 01.23.2015
Thank you to the National Hemophilia Foundation for making a list of Patient Assistance Programs available to our community! | 12.8.2014
The Hemophilia Foundation of Michigan supports families who are new to the hemophilia community. Parents have many opportunities throughout the year to meet with other parents and learn more of the basics of raising a child with hemophilia. Programs not only educate new families, but also help them connect to other people and resources in the community. HFM supplies an informative packet filled with programs and events happening state-wide.
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