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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.
About Faces of Lupus
Our Mission
Faces of Lupus Organization exists to transform lived experience into advocacy, education, and compassionate support for every person 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 committed to providing accessible resources, wel
Faces of Lupus Organization exists to transform lived experience into advocacy, education, and compassionate support for every person 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 committed to providing accessible resources, wellness programs, and community‑centered initiatives that honor each person’s story and empower them to navigate lupus with dignity 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 feels seen, heard, 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.
Event Ticket Purchase & Sponsorship Opportunities
Faces of Lupus Organization Skating Party April 16, 2026
Get ready to lace up your skates and roll into a night of fun, music, and community impact! This isn’t just a party — it’s a vibrant celebration to raise awareness and support for lupus warriors everywhere.
What’s Happening
- DJ K‑LOVE Spinning the Tunes
Keeping the energy high and the vibes strong all night long. - Photo Booth
Snap unforgettable moments with friends and family — props, backdrops, and instant memories included! - Unlimited Cheese Pizza & Soda
Fuel up with everyone’s favorite combo — no limits, just good eats. - Gift Bags for Every Guest
Packed with surprises, lupus awareness swag, and treats to take home. - 💜 Faces of Lupus Awareness Station
Learn, connect, and support — with stories, resources, and ways to get involved.
Why It Matters
Every ticket, every spin, every slice of pizza helps raise funds for the Faces of Lupus Organization — supporting outreach, education, and advocacy for those living with lupus.
"Our Unsung Lupus Warriors Gala" Awards Ceremony May 30, 2026
On May 30, 2026, we will host “Unsung Lupus Warriors Gala,” an event that honors individuals battling lupus who demonstrate resilience, courage, and unwavering determination to overcome the unpredictable challenges of living with the disease. The Black-Tie Award Ceremony event will include a delicious plated meal, music, dancing, and much more. This event will serve as a powerful platform to encourage, empower, and celebrate their remarkable achievements.
Contact us for sponsorship details
317-797-1815
Proceeds Benefit the PATH (Patients Access to Healthcare) Program
Lupus Mystery Mash October 10, 2026
On October 10, 2026, we will host “Lupus Mystery Mash,” a Halloween Party. Hosting a Halloween-themed fundraising event is a fantastic way to celebrate the spooky season while raising money for a good cause. Lupus is a mysterious and challenging disease, making it the perfect time to "spook the socks off" lupus awareness. Join us for a classic Halloween party and help raise funds for lupus patients who face the unpredictable nature of this condition.
Contact us for sponsorship details
317-797-1815
Tickets Available Soon
Face of Lupus Merchandise
Engraved/Personalization
Faces of Lupus engraved merchandise would be a great addition to your daily task either by taking notes or journaling your thoughts. Every Face has a Story, let Faces of Lupus be a part of your story. Use the link to purchase. Must include contact information (name, address, phone number, and email) and the option selection in the notes section to complete your order. Missing information may cause a delay in your order.
Notebook/Journal w/Pen Set
$30
Our leather notebook/journal with matching pen comes in two colors, purple & gray.
Engraved Option 1: Faces of Lupus
Engraved Option 2: Supporter of Faces of Lupus
Personalization-$10 extra per set
Our proud Marketing Partner, PSR Designs Personalization, exclusively handcrafts our notebooks
Men & Women Care Kits
$25/ea
Men's Care Kits include a beard brush, face soap, trimming scissors, and beard oil.
Women's Care Kits-Body Scrub, Whipped Body Butter, Gold Spoon for Body Scrub, and Lofa
Our kits are exclusively handcrafted by our proud Spa & Wellness Partner, Wellera Spa & Wellness.
Gift Sets
$15
Our gift sets make the perfect gift and a great way to show support for your favorite lupus warriors.
Gift set option:
Option 1: Support Is the Key Bamboo Key ring, Bamboo Pen, Bamboo or Clear Acrylic Bookmark
Option 2: Qty 2 Bookmark, Support is The Key Bamboo Key ring
Option 3: Support is the Key Bamboo Key ring, Qty 2 Bamboo Pen
Our proud Marketing Partner, PSR Designs Personalization, exclusively handcrafts our gift sets.
Home | Personalized Gifts by PSR Designs
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
