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
- Employment Opportunities
- Camp Old Beagle
April 17, 2015
Bavarian Inn Lodge, Frankenmuth, MI
Please Join Us for SpringFest 2015, April 17-19, 2015. Val Byas, CEO of the National Hemophilia Foundation will be joining us in person with a special presentation! Online Registration is NOW Open and continues through April 6, 2015. For more information, please contact the HFM Office at 734.544.0015. View Event Details »
Lansing Day 2015
May 6, 2015
State Capitol in Lansing
Please join us on Wednesday, February 16th for the first of two Lansing Days. Contact Ann LeWalk at 734-544-0015 or email@example.com for more information. View calendar »
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 Who Qualifies?Any person who has a bleeding disorder or who is a symptomatic carrier Who:¨ Is not currently covered by any dental insurance¨ Unable to afford the coverage your employer offers¨ Is underinsured | 01.23.2015
Thank you to 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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