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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.
Upcoming Events-Walk to End Lupus 10/17/26
On Saturday, October 17th, the Faces of Lupus Organization will participate in this year's Walk to End Lupus, hosted by the Lupus Foundation of America. Please note that joining our team doesn't mean you're walking; it means you will show up to support the lupus community. There's no registration fee, but if you'd like to help us reach our goal, you can make a donation when you register.
https://support.lupus.org/site/TR/WTELN/General?pg=personal&px=3099647&fr_id=2279
About Faces of Lupus
Our Mission
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:
- Dignity and respect for the people we support
- Positive and encouraging attitude that motivates and empowers the participants
- Empathy and compassion that show understanding and care
- Commitment to quality care and support that meets the needs and preferences of the participants
Carla's Story
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 Goals, Approach, and Partnership
Our Goal
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.
Our Approach
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.
Our Partnerships
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.
Our Services/Programs
The Inner Butterfly Health & Wellness Program
Our Health & Wellness Program focuses on the social factors that influence mental health, particularly for those living with lupus. The journey of transformation starts with hope and involves deep reflection and preparation for change. By offering a platform to address mental, physical, and emotional aspects, the program empowers individuals to transform themselves from the inside out.
Support Group Meets 3rd Saturday of each month
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.
Luus Care Bridge Program Coming Soon
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.
Face of Lupus Merchandise
Support lupus warriors. Spread awareness. Wear the movement.
Gildan Unisex Heavy Cotton T-shirts $20/ea.
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
Help Our Cause
Your support and contributions will make a meaningful difference.
Click the donation link below.
Contact Us
Faces of Lupus Organization
317-797-1815 carla@facesoflupus.net Faces of Lupus Organization P.O. Box 26072 Indianapolis, IN. 46226
Hours
Today | By Appointment |
Our Partners
