Today we’re speaking with USC Brain Health’s new Community Outreach Coordinator Katrina Shealy.

Shealy, who served as a South Carolina State Senator for 12 years and as a licensed insurance agent for 40, is a powerhouse advocate for people with Alzheimer’s disease and other dementias. We are pleased to have her join the USC Brain Health team.

 What sparked your interest in service?

When I reflect on my life’s journey, it’s humbling to think about how far I’ve come—from stocking shelves in my father’s grocery store to serving as a South Carolina State Senator. This path wasn’t one I could have predicted, but it’s been one of purpose, persistence and a relentless commitment to service.

Growing up in a small town, my father’s grocery store was more than just a place of business, it was a community hub. My father ran the store with integrity and a belief in treating every customer with respect, no matter their background. Watching him, I learned that hard work wasn’t just about putting in hours; it was about building relationships and solving problems for people who counted on you.

Later, my father transitioned to the insurance business, and I followed in his footsteps, earning my insurance license at just 18 years old. For more than 40 years, I worked in the industry, eventually specializing in forestry insurance—a field not many women had ventured into. It was a steep learning curve, requiring technical expertise and the ability to navigate a male-dominated space. But I thrived on the challenge, developing a reputation as a problem solver and advocate for my clients.

That period of my life taught me two crucial lessons: that determination could break down barriers, and that meaningful work always involves serving others.

How did you get involved in politics?

Although my insurance career was fulfilling, I couldn’t ignore the gaps I saw in our systems. My clients often faced challenges beyond my ability to help as an agent, whether it was navigating regulations, accessing resources or addressing systemic inequities. I began volunteering, believing I could make a difference by supporting candidates who shared my values.

But over time, I realized I could do more. After leading campaigns and working behind the scenes, I decided to run for office myself. Winning a seat in the South Carolina State Senate was a turning point—not just for me, but for representation for the state.

As the only woman in the Senate at the time, I felt a deep responsibility to bring attention to issues often overlooked in policymaking. I advocated for human-centered legislation: improving education, protecting children from abuse, supporting veterans, addressing elder care and ensuring underserved communities had a voice in the chamber.

Legislative work quickly became my passion. Though the position was officially part-time, it required my full-time commitment, which I gladly gave. Every bill I sponsored, every debate I participated in, and every constituent I helped reminded me of the power of public service to create meaningful change.

How did you become an advocate for people with Alzheimer’s disease?

Life threw me a curveball when my husband was diagnosed with Alzheimer’s disease. His family history made the diagnosis less surprising but no less devastating. Overnight, I became not just a wife but a caregiver, navigating a healthcare system that often seemed more focused on bureaucracy than on providing support.

“For me, this work is about more than just building better systems. It’s about creating a world where no one feels alone in facing these challenges.”

I immersed myself in learning about cognitive health and quickly saw the gaps in resources, education and support available to families. I’ve worked closely with doctors and researchers, advocated for funding and tackled the stigma surrounding Alzheimer’s head-on. While there are days when the obstacles seem overwhelming—like a lack of resources in rural areas or the persistent shame people feel about seeking help—I refuse to give up. For me, this work is about more than just building better systems. It’s about creating a world where no one feels alone in facing these challenges.

I became deeply involved with the Alzheimer’s Association and other advocacy organizations. I worked tirelessly to raise awareness, push for better resources and educate others about the disease. One of my proudest moments was receiving an award from Leeza Gibbons for my work in Alzheimer’s advocacy—a recognition that underscored how far I had come in using my voice to make a difference.

Why did you join the USC Brain Health team?

One of the areas I’ve focused on is addressing brain health disparities in rural communities, which is exactly what USC Brain Health does. I’ve seen firsthand how stigma and a lack of resources prevent people from seeking the care they need. Specialists aren’t coming to rural areas unless we build the facilities to attract them, so I’ve embraced the mindset of “if you build it, they will come.” My vision is to help create a world-class Brain Health Network and Brain Health Center that will serve as beacons of hope for people across the state, offering the care and support they deserve.

I also know that this isn’t just about infrastructure; it’s about building trust and changing perceptions. People in these communities need to see brain health as a priority, and I’m committed in my new position to fostering that cultural shift. I want everyone to feel empowered to seek help without fear of judgment or financial burden.

The impact of this work goes beyond what I can see today. By advocating for world-class Brain Health facilities, expanding outreach to rural areas and tackling stigma, I hope to create a foundation that will benefit countless individuals and families. I dream of finding the “first person” who will be cured of Alzheimer’s. That hope fuels my determination, reminding me that this work isn’t just about addressing today’s needs, it’s about changing lives for generations to come.

What’s it like to have your drive and sense of purpose?

This mission is deeply personal for me. Every day, I see my husband’s pride in the work I’m doing, and it motivates me to keep going. Navigating his Alzheimer’s journey has been heartbreaking, but it’s also strengthened my resolve to honor him by making a difference. His experience is a constant reminder of the humanity at the heart of this work.

My life’s work—whether as a caregiver, a mentor, or an advocate—reflects my belief that compassion and determination can change the world. As I step into my role as Community Outreach Coordinator, I’m ready to bring my energy, experience and unwavering dedication to this fight. I’m not just raising awareness; I’m building a movement, and I’m determined to leave a legacy of hope, resilience and transformation.