State Advocacy Team Summary - Michigan

The Michigan (MI) state advocacy team was led by chapter lead Zach Ryan, Government Relations and Communications Manager with the Hemophilia Foundation of Michigan; and HTC lead, Dave Rushlow, Program Administrator with the Northern Regional Bleeding Disorder Center at Munson Medical Center. The team was also supported by members Kaite Scott, Program Social Worker with the Hemophilia Foundation of Michigan; and Matt Delaney, Government Relations Manager with the National Bleeding Disorders Foundation.

Summary of Achievements


In their first year, the BD SUMHAC MI team successfully:

  1. Engaged with state officials from MI Department of Health and Human Services (DHHS), MI Department of Licensing and Regulatory Affairs (LARA), and the MI House of Representatives

  2. Identified a state champion

  3. Mapped the regulatory landscape of MH/SUD facilities with particular attention to policies related to:

    1. Self-administration of infusion and injection medications

    2. Staff assisted administration of infusion and injection medications

    3. External provider assisted administration of infusion and /injection medications

    4. Patient cherry-picking

  4. Drafted recommendations for state SUD regulations to increase clarity on access policies for the BD community and others with stable, well-managed, non-behavioral health medical conditions.

  5. The team’s accomplishments were also highlighted in a BD SUMHAC article that can be found here.

Regulatory Landscape Mapping

Sorted by landscape area. All regulatory Information is as of July 2024

SUD Facility Information

Self-infusions/ injections

Staff-assisted infusions/ injections

External provider-assisted infusions/injections

Medicaid SUD: Policies to prevent cherry-picking

MH Facility Information

Use of infusion and injection medication

Self-infusions/ injections

Staff assisted infusions/ injections

External provider assisted infusions/ injections

Next Steps for Advocacy

The MI team has determined the following goals for Phase 2:

  1. Submit recommendations to increase access for the BD community in the state SUD regulations.

  2. Draft and submit recommendations to increase access for the BD community in the state MH regulations.

  3. Create a step-by-step plan for the BD community in MI in the event of a denial to a MH/SUD facility.

  4. Seek opportunities to educate MH/SUD facilities on BDs and ways facilities can increase equitable access to care and treatment for the BD community.

More State Advocacy Resources

Tools for Advocacy