The Hemophilia Foundation of Michigan (HFM) strives to improve the quality of life for all people affected by hemophilia, von Willebrand disease, other coagulation disorders, and related complications.
HFM was founded in 1956 as an all-volunteer chapter of the National Hemophilia Foundation, and in 1969, started the first-ever summer camp for children with bleeding disorders, now called Camp Bold Eagle. Our camp mission, which carries over to all our youth programming, is to educate and empower children, teens, and young adults with bleeding disorders to live a life of freedom and independence.
In addition to traditional camp activities, we pride ourselves on offering a can-do experience at camp. Adult leaders, often impacted by bleeding disorders themselves, together with compassionate medical care providers, come together to provide safe, yet challenging experiences for our campers. By learning how to manager their disorders, campers are able to take “Eagle Steps” toward possibilities rather than limitations.
HFM’s camping programs have now grown to seven weeks of camp each summer in order to provide the magic of camp to more than 200 children and adults with bleeding disorders.
MEET THE HFM STAFF
Susan Fenters Lerch
Executive Director // email@example.com
Camp Director/Youth Services Manager // firstname.lastname@example.org
Educational Services Manager/ Associate Camp Director // email@example.com
Anthony is the Educational Services Manager/Associate Camp Director at HFM.
MD Medical Director
RN Health Center Director
The following HTCs partner with HFM in providing health care to our campers