Advancing Care and Hope for the Sickle Cell Community
At L.D. Barksdale Sickle Cell Foundation, we understand that living with sickle cell disease affects every part of life — physically, emotionally and financially.
That’s why our services are designed to offer support, education and relief at every stage of the journey. We walk alongside patients and families in the Upstate and Midlands of South Carolina, helping them navigate care, access critical resources and find a sense of community.
Proudly Serving South Carolina Across 15 Counties
We provide direct services and community-centered care across two regions in South Carolina.
Upstate
Abbeville, Anderson, Cherokee, Greenville, Greenwood, Laurens, McCormick, Oconee, Pickens, Spartanburg and Union
Midlands
Chester, Edgefield, Saluda and York
Sickle Cell Trait Testing and Counseling
Knowing your sickle cell status is a key step in protecting your health and your family’s future. We provide free DPH-certified trait testing, along with professional counseling to help individuals understand their results and explore options for care or prevention.
Whether you're planning a family, seeking clarity or supporting a loved one, our testing and education services empower you with knowledge — no cost, no stigma, just support.
Financial Assistance
We understand that the cost of managing a chronic illness can quickly become a burden. For families facing financial challenges, we offer limited assistance to help cover essential expenses like medications, transportation or utility bills.
This program is about providing relief in moments that matter most. If you're struggling to make ends meet while managing care, we’re here to help you breathe a little easier.
Support Group Meetings
Sometimes the best healing happens when you’re not alone. Our support groups are a space for connection, conversation and shared experience — open to individuals living with sickle cell and their families.
Each session includes a free meal and relevant topics that matter to our community, from health education to emotional wellness. It’s not just support — it’s solidarity.
Patient Events
We believe in joy, even in the face of hardship. Throughout the year, we host special events that give patients and their families a chance to unwind, celebrate and simply enjoy time together.
Whether it’s a community picnic, holiday gathering or fun day out, these moments are designed to restore hope and strengthen the bonds that carry our community forward.
Psychosocial Assessments and Referrals
Living with or caring for someone with sickle cell disease can be emotionally overwhelming. That’s why we offer psychosocial assessments and connect patients with compassionate mental health professionals who understand the unique challenges they face.
We believe emotional wellness is just as vital as physical health. Our goal is to ensure every individual feels seen, supported and equipped to navigate life with strength and resilience.
Impacted Over 1,000 Lives Since Inception
Behind every number is a name, a family a story. Our impact reflects decades of trust-building, community care and support for those living with or affected by sickle cell disease. What began as a local mission has grown into a trusted source of hope, resources and advocacy — a reflection of what’s possible when care is compassionate and rooted in community.
Individuals diagnosed with Sickle Cell Disease who reside within the L.D. Barksdale Sickle Cell Foundation’s service area are eligible for services. Specific programs, such as utility assistance, may have additional documentation requirements including a valid photo ID and a disconnect notice.
Yes — the Foundation offers limited financial assistance for utility bills to eligible clients with Sickle Cell Disease. Clients may receive up to $100.00 per calendar year, based on available funding and provided they meet all criteria. Assistance is given on a first come, first served basis and requires proof of need, including denial letters from other community support agencies.
A formal referral is not required to access support services; however, clients must provide necessary documentation depending on the type of assistance requested. For utility assistance, this includes a valid ID, a utility bill in the client's name, a disconnect notice and proof that other local support options have been exhausted.
NCFM Sickle Cell Support Group
A self-paced, interactive platform designed to empower patients, caregivers and families with a deeper understanding of sickle cell disease. Learn about symptoms, treatment options and day-to-day management through videos, quizzes and educational tools you can access anytime.
Understanding SCD
This comprehensive guide helps parents and caregivers navigate the unique challenges of supporting a child with sickle cell disease. Inside, you’ll find tips on managing pain, promoting healthy routines, communicating with your care team and creating a support system at home and school.
Living With Sickle Cell Disease
Published by the National Heart, Lung, and Blood Institute, this guide offers practical advice on staying healthy, preventing complications and planning for long-term wellness with sickle cell disease. A helpful resource for both newly diagnosed individuals and long-term patients.
SCD Diagnosis & Treatment
Trusted by healthcare professionals, this resource outlines how sickle cell anemia is diagnosed and treated. From medications to blood transfusions and pain management strategies, this article is a solid starting point for understanding medical care options.
Where to Find Care Near You
Need to schedule an appointment, test or clinic visit? Here are trusted locations in the Upstate and Midlands:
Stay Informed With National Organizations
If You’re in Crisis or Need Urgent Help
If you’re experiencing a medical emergency, dial 911 or go to the nearest emergency room.
For local assistance with utilities, prescriptions or crisis needs, please call our 24-hour assistance line for help at 864-582-9420.
