Advocacy

August 14, 2025

Advocacy Webinar: Disclosing Your Diagnosis

Join us for an Advocacy webinar to discuss disclosing your diagnosis. REGISTRATION COMING SOON Speaker: information to come. HFM will treat attendees to dinner during this educational program.  Order carryout or delivery and send a photo of your itemized receipt to Laura at lolson@hfmich.org. You will be reimbursed for your meal (up to $30 per family). […]

August 14, 2025

Advocacy Webinar: Disclosing Your Diagnosis
Read More »

Advocacy Updates: Patient Advocate Spotlight

Michigan Advocacy Update   Patient Advocate Spotlight Throughout the year, HFM and the Michigan All Copays Count Coalition have been working to raise awareness of the issue of copay accumulators and increase public pressure for legislative action. We are proud to share that one of HFM’s advocates, Ken Martin published a piece at the beginning of

Advocacy Updates: Patient Advocate Spotlight Read More »

State of the State: General Elections

Elected officials have a direct impact on the lives of Michiganders with bleeding disorders. Join us as we discuss the general election results and how the changes may impact Michiganders and our policy priorities in 2025. REGISTER Speaker: information to come. HFM will treat attendees to dinner during this educational program.  Order carryout or delivery

State of the State: General Elections Read More »

Advocacy Updates: Michigan and Ohio

Michigan Advocacy Update   Lansing Days  On Tuesday, March 21 and Wednesday, March 22, 2023, twenty-nine Michigan bleeding disorders advocates joined the Hemophilia Foundation of Michigan (HFM) for our legislative advocacy event, Lansing Days. Special thank you to our HTC representatives for joining us: Dave Rushlow, Kathi Sheldon, and Alice Cakebread! Together, our group of bleeding

Advocacy Updates: Michigan and Ohio Read More »

Skip to content