The Fund supports networks of state health policy decision makers to help identify, inspire, and inform policy leaders.
A bipartisan group of state health policymakers from both the executive and legislative branches who are focused on improving population health.
Networks of state officials, advocates, and others aiming to invest in and transform primary care.
A program dedicated to advancing state-based efforts to make health care more affordable for residents, employers, and states.
The Milbank Memorial Fund supports two state leadership programs for legislative and executive branch state government officials committed to improving population health.
A leadership development program for early and mid-career state government officials who are committed to improving the health of all people in their communities.
A leadership program for senior state government officials who are committed to improving population health.
The Fund focuses on creating an affordable health care system built on strong primary care and partnerships that improve health outcomes for all.
Improving state leaders’ ability to enact and implement evidence-based health policies.
Advancing policies that create a more prevention- and primary care-oriented health system.
Improving population health through policies that contain health care cost growth.
Our state health policy resources offer relevant data analysis and best practices.
The Fund publishes reports, issues briefs, and case studies on state health policy issues.
Short takes on health policy issues from Milbank staff and guest authors.
Insights from Milbank President Debra Lubar on state health policymaking.
Reported articles and Q&As on timely health policy issues, as well as foundation updates.
Milbank Memorial Fund and Milbank Quarterly webinars featuring state health policymakers and researchers.
Updates and expert contact information for reporters.
The Milbank Memorial Fund is a private foundation that works to improve population health and health equity.
June 7, 2017
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In mid-April, the direct-to-consumer genetic testing firm 23andMe received US Food and Drug Administration (FDA) authorization to sell tests for 10 genetic health risk reports directly to consumers. As the New York Times reported on May 12, the tests pose potential programs for long-term care insurers who may not have access to results. While policymakers have been debating the appropriateness of these tests for more than a decade, little is known about past consumers’ views regarding the regulation of these products or whether personal experience with testing is related to these views. A new study in the June issue of The Milbank Quarterly by Sarah E. Gollust of the University of Minnesota School of Public Health and colleagues has found that a majority of consumers support expanded access to direct-to-consumer personal genomic testing (DTC-PGT) services and oppose additional government regulation, while those who have had a negative experience with the tests were less supportive of expanded availability without a medical professional.