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A Statewide Approach to Collaboratively Improve Access to Medical Genetics Services in Wisconsin
Sara Zoran1, Jessica Scott Schwoerer2
1University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
A collaborative approach identified key medical genetics priorities in Wisconsin, including improved coordination, funding for newborn screening, and policy changes for genomic testing and counseling. This initiative advanced statewide collaboration and policy change for better genetic services access.
Area of Science:
- Medical Genetics
- Public Health Policy
Background:
- Lack of state-led initiatives for medical genetics in Wisconsin.
- Need for a collaborative approach to identify and address service gaps.
Purpose of the Study:
- To identify priority service-access needs in Wisconsin's medical genetics field.
- To establish strategies for addressing identified needs through stakeholder collaboration.
Main Methods:
- Utilized surveys and consensus-building tools.
- Engaged diverse stakeholders to drive the initiative.
Main Results:
- Identified four key priorities: improved coordination, increased Newborn Screening Program funding, Medicaid policy changes for genomic testing and genetic counseling reimbursement, and enhanced educational opportunities for providers.
- Established three active workgroups to advance these priorities.
- Achieved measurable progress including increased funding, policy advancements, and expanded education.
Conclusions:
- A stakeholder-driven process fostered engagement and collaboration within Wisconsin's medical genetics community.
- Workgroups facilitated progress in funding, policy, education, and advocacy.
- Sustained engagement is crucial for equitable access to genetic services statewide.
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