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Home
About Melissa
Research
Bounded Justice
Biocultural Citizenship
Antiracist Health Research
Sickle Cell and Global Health
Scholarship
Around the Web
Teaching
Gallery
Archived Blog
Contact
Around the Web
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Articles
Events
Podcasts and Interviews
Public Engagement: Top Michigan Minds of the Year
December 31, 2022
A Look at Anti-Racism and Community-based Participatory Research Principles
December 19, 2022
Race, Racism, and Data Practices in Public Health
October 21, 2022
VIDEO Bounded Justice: Navigating the Limits of Equity
October 6, 2022
Understanding Sickle Cell Disease and the Concept of Bounded Justice
September 15, 2022
Covid-19 Vaccine and the Right to Public Health
July 26, 2022
Until Structural Inequalities are Addressed, Policies Promising Health Equity or Reparations will Continue to be Limited
July 15, 2022
Imaging Innovative Digital Health Futures
April 7, 2022
Health Inequities and Employment
April 1, 2022
Study Shows how Bias can Creep into Medical Databanks that drive Precision Health and Clinical AI
December 6, 2021
Bounded Justice: A Critical Appraisal of DEI
November 12, 2021
We Need to Ground Truth Assumptions about Gene Therapy
October 22, 2021
Interview: Sickle Cell Disease Treatment
October 22, 2021
Disparities in Bleeding Disorders
October 20, 2021
BNC News Appearance: Sickle Cell Disease Treatment and Awareness
September 28, 2021
Digging Deep to Find Community-Based Health Justice
September 24, 2021
OVPR, NCID Award Eight Grants to Advance Anti-racism Research, Scholarship
September 22, 2021
U.S. Life Expectancy Decreased by an ‘Alarming’ Amount During Pandemic
June 23, 2021
Leading with HEART: Working toward Health Equity with Anti-Racist Teaching
April 29, 2021
As Michigan COVID Vaccine Rates Ebb, Pop-up Clinics and Casino Cash Appear
April 21, 2021
Black and Latino Communities are Being Left Behind in the Vaccine Rollout
February 24, 2021
The Black-white life expectancy gap grew in 2020 — but it can be reversed
February 24, 2021
The Impact of Race on Data
February 16, 2021
COVID “Long Haulers” Ask, “What am I Gaining to Say that I’m Still Sick?”
January 5, 2021
A Black Woman Getting the First U.S. Coronavirus Vaccine Sparked Celebrations — and Suspicion
December 16, 2020
Obamacare Repeal would be Particularly Devastating for Communities of Color
November 23, 2020
Detroit Health Department: Life through a Pandemic
October 14, 2020
Column: Public Health and Systemic Racism are on the Ballot in Prosecutor Elections
July 28, 2020
How COVID-19 has highlighted racism as a health risk
June 11, 2020
Sickle Cell Disease As a Lens for Health Policy and Equity
May 7, 2020
Racial Disparities in the Time of COVID-19
May 4, 2020
What’s Behind the Racial Disparity in COVID-19 Cases
May 2, 2020
COVID-19 Pandemic Highlights, Exacerbates Health Inequities in Marginalized Communities
April 8, 2020
Detroit is a COVID-19 Hotspot. What the Data Do, and Don’t Tell Us
March 26, 2020
Closing in On a Cure
September 1, 2019
Why We Wander Episode 14: Travel and Chronic Illness with Melissa Creary
June 21, 2019
Alumni Reflections | Emory Laney Graduate School
August 1, 2017
The Place of Afro-Brazilian Women in the World Cup
June 17, 2014
Advancing Care and Awareness of Sickle Cell Disease
December 27, 2011
Advancing Care and Awareness of Sickle Cell Disease
December 27, 2011
Federal Faces: Melissa S. Creary
December 26, 2011
Researcher on Ethical Tensions of Sickle Cell Disease Selected as “Ebony Magazine’s Annual Power 100”
December 8, 2011
Fortaleza Symposium promotes meetings between researchers and patients
October 24, 2011
American Researcher Knows Brazilian Sickle Cell Disease Care Programs
August 12, 2011
A Century of Sickle Cell
September 16, 2010
Sickle Cell Patients Grow Up, But Face New Challenges
August 1, 2010
