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Touching People's Lives Living with Lupus.
Call Faces of Lupus today. Find comfort and strength in our community of individuals living with Lupus.
See The Tickets and Sponsorships Section to Purchase Tickets For Our Events.
Call Faces of Lupus today. Find comfort and strength in our community of individuals living with Lupus.
Faces of Lupus Organization exists to transform lived experience into advocacy, education, and compassionate support for every person and family affected by lupus. Founded by Carla Day, a 38‑year lupus warrior, our mission is to ensure that no individual or caregiver walks this journey alone.
We are deeply committed to supporting famili
Faces of Lupus Organization exists to transform lived experience into advocacy, education, and compassionate support for every person and family affected by lupus. Founded by Carla Day, a 38‑year lupus warrior, our mission is to ensure that no individual or caregiver walks this journey alone.
We are deeply committed to supporting families—including children impacted by lupus—by assisting with medical needs, addressing food insecurity, and offering accessible resources that promote stability and well-being. Through wellness programs and community-centered initiatives, we honor each person’s story and empower them to navigate lupus with dignity, strength, and hope.
Guided by truth, resilience, and purpose, we work to advance understanding, expand access to care, and build a supportive community where every lupus warrior and their family feelThe seen, heard, supported, and valued.
Our Vision:
Faces of Lupus envisions a world where every lupus warrior is seen, supported, and empowered to live a full and thriving life. We strive for a future where early diagnosis, equitable care, and compassionate understanding are the norm—not the exception. Guided by lived experience and a commitment to health equity, we work toward a community where no one faces lupus in silence, where stories are honored, and where hope, access, and advocacy transform lives.
Our Values:

My name is Carla Day, and I am the Founder of Faces of Lupus Organization and a 38‑year lupus warrior. I was diagnosed with lupus at a young age, and for nearly four decades, I have lived through the realities of this disease—the flares, the uncertainty, the resilience, and the strength it takes to keep going.
Living with lupus has shape
My name is Carla Day, and I am the Founder of Faces of Lupus Organization and a 38‑year lupus warrior. I was diagnosed with lupus at a young age, and for nearly four decades, I have lived through the realities of this disease—the flares, the uncertainty, the resilience, and the strength it takes to keep going.
Living with lupus has shaped who I am, but it has never limited who I can become. My journey taught me the importance of advocacy, education, and compassion—especially for those who often feel unseen, unheard, or misunderstood. It is that lived experience that inspired me to create Faces of Lupus: a community rooted in support, truth, and hope.
Through Faces of Lupus, my mission is to ensure that no lupus warrior or caregiver walks this journey alone. We work to provide education, wellness programs, patient resources, and awareness initiatives that meet people where they are and honor their stories. I believe that lived experience is powerful, that community is healing, and that care should never be delayed or denied.
Every step of my work is guided by one truth: lupus may be part of my story, but purpose is what defines it. I am committed to turning pain into purpose and using my voice to uplift others—because understanding, access, and compassion save lives.
“Lupus changed my life, but it did not define my limits. I choose purpose, advocacy, and hope—because no one should face lupus alone.”

Our goal at Faces of Lupus Organization is to create a world where everyone can access the support services they need to thrive. We believe that everyone deserves to live a healthy and fulfilling life, and we are committed to working towards this goal every day.

At Faces of Lupus Organization, we take a holistic approach to community support. We believe that in order to truly support individuals and families, we must address all aspects of their lives, including physical health, mental health, and social support.

We work closely with a variety of community partners to ensure that we are meeting the needs of everyone in our community. Our partnerships include local schools, healthcare providers, and other community organizations.

Transforming from the Inside Out
The Inner Butterfly Wellness Program is a Health & Wellness initiative designed to address the social, mental, physical, and emotional factors that can influence overall well-being, with a particular focus on individuals living with lupus.
The journey of transformation begi
Transforming from the Inside Out
The Inner Butterfly Wellness Program is a Health & Wellness initiative designed to address the social, mental, physical, and emotional factors that can influence overall well-being, with a particular focus on individuals living with lupus.
The journey of transformation begins with hope and creates space for self-reflection, personal growth, healing, and preparation for meaningful change. Through a holistic approach, the program provides participants with tools, support, education, and encouragement to strengthen their overall wellness and discover their capacity for transformation.
The Inner Butterfly Wellness Program empowers participants to embrace their journey from the inside out—building self-awareness, developing healthy coping strategies, nurturing resilience, strengthening connections, and creating a stronger foundation for lifelong wellness.
The program is offered annually from February through September, providing participants with an ongoing opportunity to learn, grow, connect, heal, and transform throughout their wellness journey.
Inner Butterfly Wellness Program
Transforming from the Inside Out
Because true transformation begins within.

Creating change starts with you. Vital resources for lupus support are just a click away. A supportive community of connections is available to enhance your journey with lupus. Join us today. Click the link below to register.

The Lupus Care Bridge Program is designed to address one of the most pressing challenges for individuals living with lupus: inconsistent access to coordinated care, patient support services, and disease‑management resources. More details coming soon.
Stronger Together. Healthier Together. Hopeful Together.
The Faces of Lupus Organization, in partnership with the Inner Butterfly Wellness Program, invites you to join our empowering community walk — a movement of strength, awareness, and hope.
Together, we lift each other, share hope, and make a difference in the lives of those affected by lupus.
Every Monday and Thursday, 6:00 PM – 7:00 PM
Where: Broad Ripple Community Center
1500 Broad Ripple Avenue, Indianapolis, IN 46220

We’re gearing up for another unforgettable year, and the excitement is already building. Our 2027 signature event is on the horizon — and trust us, you won’t want to miss what’s coming.
Faces of Lupus is preparing a powerful, community‑driven experience filled with inspiration, connection, and purpose. New features, new partners, and new opportunities to elevate lupus awareness are all in the works.
Stay tuned right here on our website as details roll out. Big announcements are coming — and we want YOU to be part of the movement.

This T‑shirt is available in black with white lettering. You’ll be able to select your preferred style at checkout.
All Proceeds Directly Benefit Our Support Programs and Services

Your support and contributions will make a meaningful difference.
Click the donation link below.
317-797-1815 carla@facesoflupus.net Faces of Lupus Organization P.O. Box 26072 Indianapolis, IN. 46226
Today | By Appointment |

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Faces of Lupus Organization
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