UNCG & NCA&T Joint Ph.D. Program in Social Work

Lateasha
Grant-Lennon, LCSW

Doctoral student at the University of North Carolina Greensboro & North Carolina A&T State University and Case Manager for Piedmont Health Services & Sickle Cell Agency.

Portrait of Lateasha Grant-Lennon
About

An advocate, social worker, and researcher.

I am a second-year doctoral student in the UNCG & NCA&T Joint Ph.D. Program in Social Work at UNC Greensboro and North Carolina A&T State University. As a social worker, sickle cell disease advocate, and healthcare professional living with sickle cell disease, my research seeks to improve healthcare experiences and outcomes for individuals with sickle cell disease through culturally responsive, community-engaged research.

Accomplishments

Valerie Fund Scholar

2026–2027 Recipient

Vertex Foundation Scholar

2026–2027 Recipient

Dr. Charles F. Whiten Health Care Professional Award

Sickle Cell Association of New Jersey — 2022 Recipient

4.0 GPA

First-year doctoral coursework

Submission

Qualifying Portfolio Submission

Required Submission

How does healthcare-related stigma influence pain management and healthcare experiences among adults living with Sickle Cell Disease?

My full qualifying portfolio includes my research statement, literature gap, learning outcomes, theoretical framework, and references. Download the complete document here.

Download Portfolio
Research Interests

Where my work lives.

My research integrates qualitative, quantitative, participatory, and community-engaged research methods to understand and improve healthcare experiences for individuals living with sickle cell disease.

Sickle Cell Disease
Healthcare-Related Stigma
Health Equity
Pain Management
Mixed Methods Research
Health Advocacy
Social determinants of healthHealthcare utilizationPatient–provider relationshipsHealth disparities among Black adults

Current Research

My developing research agenda focuses on how healthcare related stigma influences pain management, healthcare decision making, and quality of life among adults living with sickle cell disease. Emerging directions include intimate relationships, social support, and interpersonal violence among adults with chronic illness.

Goals & Scholarship

Plans for Scholarly Activities.

Conference Presentations & Posters

Presenting emerging work on stigma, pain management, and lived experience in sickle cell care.

Manuscripts in Progress

Qualitative analyses of patient–provider communication and healthcare navigation.

Research Assistantships

Contributing to community-engaged studies centered on health equity for Black adults.

Research Methods Training

Advanced coursework in qualitative inquiry, thematic analysis, and mixed methods.

Education & Experience

Training and practice.

Education

  • Joint Ph.D. in Social Work

    UNC Greensboro & NC A&T State University

    In progress

  • Master of Social Work

    Rutgers, The State University of New Jersey

    Completed

  • Bachelor of Social Work

    Rutgers, The State University of New Jersey

    Completed

Professional Experience

  • Sickle Cell Case Manager & Transition Coordinator

  • Pediatric Sickle Cell Social Worker

  • Community Health Advocate

  • Program Development & Outreach

SCHOLARLY PAPERS

Coursework

A collection of representative coursework from my doctoral program. Click any title to download the paper.

Interview Guide and Implementation

SOWK/SWK 854 — Qualitative Methods in a Multicultural Context

Download PDF

Literature Review

SOWK/SWK 853-01 — Quantitative Methods in Social Work

Download PDF

Sickle Cell Healthcare Racial Stigma Scale (SCHRSS)

SOWK/SWK 853-01 — Quantitative Methods in Social Work

Download PDF
PERSONAL GOALS

Where my work is headed.

My long-term goal is to develop community-informed interventions that reduce healthcare stigma, improve patient–provider relationships, and promote equitable healthcare for individuals living with sickle cell disease. Through interdisciplinary research, I hope to influence clinical practice, health policy, and social work interventions that address structural barriers affecting historically underserved populations.

Contact

Let's connect.

Open to research collaborations, community partnerships, and academic conversations around equitable sickle cell care.

© 2026 Lateasha Grant-Lennon