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
August 30, 2015
Detroit Zoo, Royal Oak
Walk • Volunteer • Sponsor • Donate$20 fee includes a family friendly walk, tee-shirt, delicious food, fun activities, entertainment and the opportunity to come together as a strong community supporting those with bleeding disorders.Southeast MichiganSunday, August 30, 2015Detroit ZooRoyal Oak, MI7:45am Registration opens8:45am Walk beginscontact WalkEast@hfmich.org“This is one of the most special days of the year for our family. We walk with our friends and show them the good side of having hemophilia.”~ Aunt of a child with hemophilia 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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