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The Hemophilia Foundation of Michigan strives to improve the quality of life for all people affected by hemophilia, von Willebrand’s disease, other coagulation disorders and related complications, including HIV/AIDS and hepatitis.
The Hemophilia Foundation of Michigan provides educational, social and supportive services to the bleeding disorders community. We host several retreats, programs and conferences throughout the year as well as fundraising events. Our camping programs provide a unique opportunity for those aged 6-16+ to participate in camp activities and to become independent teens and adults by learning to self-infuse or other methods to control their bleeding disorder.
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