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Our Values

Compassion

We lead with empathy and dignity in every interaction

Equity

We serve all patients with fairness and understanding

Community

We believe in the power of collective care and connection

Access

We break down barriers to essential care and education

Advocacy

We speak up for those who deserve to be heard

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Lend a Hand.
Leave an  Impact.

Volunteers are the heart of our mission — and we can’t do it without you. Give your time. Share your heart. Be part of something bigger. Every hour you give supports families impacted by sickle cell disease.

Father and Daughter

50 Years of Standing Strong With Sickle Cell Warriors

Half a century of care, advocacy and community. For over 50 years, we’ve stood beside sickle cell warriors and their families — providing care, raising awareness and building stronger communities across South Carolina.

COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS.  ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS.  ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY. COMPASSION. EQUITY. COMMUNITY. ACCESS. ADVOCACY.

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Our Mission

To improve the quality of healthcare and the quality of life for individuals and families impacted by sickle cell disease through education, direct support and compassionate community partnerships.

Three Generations

Our Vision

A world where every person living with sickle cell has access to informed care, meaningful support and equitable resources — regardless of background, income or location.

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A Legacy of
Service Since 1974

The L.D. Barksdale Sickle Cell Foundation was founded by Louvenia Delores Barksdale in 1974 with a simple but powerful mission: to stand in the gap for those affected by sickle cell disease. What began as a grassroots response to unmet needs has grown into a trusted source of support for more than 20,000 individuals and families across South Carolina.

A former English teacher and community advocate, Ms. Barksdale brought both compassion and conviction to this work. She began her teaching career at Carver High School in 1938, later earning degrees from Allen University and Columbia University. Her passion for education and public health led her to serve on numerous local and national boards — from the National Council for Sickle Cell Disease to the Spartanburg County Foster Care Review Board.

She was also a founding voice in statewide efforts to expand newborn screening and testing for sickle cell anemia and served as the foundation’s first Executive Director. In 1982, the organization was officially named in her honor.

For five decades, her legacy has lived on through our programs, partnerships and continued commitment to making sure those living with sickle cell are not only seen, but supported every step of the way.

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Our Reach

We proudly serve 15 counties in the Upstate and Midlands of South Carolina through free screenings, educational programs, outreach events and direct patient support.

Individuals served since our founding

+20,000

Counties supported across two regions

15

Screenings & referrals conducted

1k+

Annual community events hosted

12

Our LDBF Team

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Rhonda Young

Executive Director

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Tamara Davis

Community Outreach Coordinator

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Joyce Brewton

Registered Nurse

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Harriett Cleveland

Office Manager

Our Board of Directors

The Board of Directors provides strategic oversight, financial stewardship and organizational accountability for L.D. Barksdale Foundation. This group of dedicated leaders ensures our mission is fulfilled with integrity, guiding long-term decisions, approving key initiatives and supporting sustainable growth.

Sherrie A. Ballenger,
Chair

Spartanburg Regional

Wescina Thompson,
Co-Chair

Prisma Health

Deirdre Corbit,
Board Member

South Carolina Community Member

Tamara D. Davis,
​Board Member

Silver Hill Memorial

Wandra J. McElrath,
Board Member

Silver Hill Memorial

Patsi J. Lann,
Board Member

Belk Corporate

Sherilyn Lee,
Board Member

South Carolina Community Member

Sean Dogan,
Chair

Chair

Lillian Brock Flemming,
Co-Chair

South Carolina Community Member

Peggy B. Baxter,
Community Advisory Member

South Carolina Community Member

Jabecca Banks,
Community Advisory Member

South Carolina Community Member

Ruby Coleman,
Community Advisory Member

South Carolina Community Member

Miranda Lilley,
Community Advisory Member

South Carolina Community Member

Ruth Richburg,
Community Advisory Member

South Carolina Community Member

Jenny Weidenbenner,
Community Advisory Member

South Carolina Community Member

Our Community
Advisory Board

The Community Advisory Board serves as a bridge between the foundation and the communities we serve. Composed of local advocates, patients, caregivers and health professionals, this board offers valuable insight, feedback and lived experience to help shape our programs, outreach efforts and partnerships from the ground up.

Together, We’re Building a Stronger Support System for the Sickle Cell Community

Whether you want to meet the people behind the mission, offer your time or make a gift — there’s a place for you here.

KNOW YOUR GENES.

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