Nandi's Smile Foundation

Nandi's Smile Foundation Through awareness, advocacy, and action, we are committed to changing the narrative around Lupus and making a lasting impact in the lives of those it touches.

Nandi’s Smile Foundation, is a nonprofit organization founded in memory of Jasmine Nandi-Marie Gordon (1992-2014), who was a ‘Lupus Warrior.’ The goal is bring awareness to Lupus and provide scholarships to those going into Music or STEM fields. Our mission is to educate the public and those affected by lupus, advocate for greater awareness and improved care, and support individuals and families

with the resources and community they need to thrive. We envision a world where Lupus is not only better understood by the public and medical community, but where those affected feel seen, supported, and never alone. Empowering Lives, Advancing Lupus Awareness

Scholarships Fund: Since 2019, the foundation has awarded two annual $500 scholarships to local high school students pursuing studies in music and STEM fields — areas Jasmine was passionate about. Lupus Research & Advocacy: In partnership with the Alliance for Lupus Research (lupusresearch.org), the foundation helps fund research efforts to not only discover a cure, but to improve the quality of life for those currently living with Lupus. Since 2015, we’ve participated in the Walk to End Lupus Now, hosted by the Lupus Foundation of America, raising funds for research, education, and support services. In 2018 and 2019, we hosted the annual Purple Praise Party — a powerful evening of praise, worship, and Lupus awareness that united the community in faith, hope, and support. Looking Ahead: The future of Nandi’s Smile Foundation includes expanding our scholarship program and increasing our capacity to support families impacted by Lupus and other critical illnesses. Our goal is to meet real needs and offer hope, one smile at a time.

05/02/2026

Flight of the Butterflies

Spreading Lupus Awareness One Butterfly at a time

Let this butterfly flutter all over cyberspace!

Day 2 Lupus Fact

Lupus is not contagious. It cannot be passed from one person to another. It cannot be transmitted sexually. There is no need to avoid being near someone who has lupus. The cause or causes of lupus are not known with certainty. Hormones, genes and environment are said to play a role.

This is your Butterfly of Hope Fact for today.

We need awareness! We need a cure!

Encourage everyone you know to let it FLY!

04/03/2026

Not all lupus flares start with something obvious.
Sometimes it’s subtle…
a shift in energy,
a strange ache,
a feeling you can’t explain.
Your body gives warning signs—
we just aren’t always taught to recognize them.
💜 You’re not imagining it.
💜 You’re not overreacting.
👇 What’s YOUR first sign a flare is starting?

💜Lupus and Me

11/05/2025

Please support our Annual Scholarship Fund this Thanksgiving season!

We're so grateful for your generosity during this season of gratitude and sharing. Your fundraising efforts help us award two $500 scholarships each year to deserving students, giving them the opportunity to pursue their educational dreams.

Whether someone donates $5 or $500, every contribution brings us closer to changing lives through education. Thank you for being part of the Nandi's Smile Foundation community and for making a meaningful difference this holiday season! 🙏💜🎗️

Send a message to learn more

💜 WE'RE SHIFTING FOCUS💜After much reflection, we're transforming this page into a Legacy & Updates Hub for Nand...
08/02/2025

💜 WE'RE SHIFTING FOCUS💜

After much reflection, we're transforming this page into a Legacy & Updates Hub for Nandi's Smile Foundation.

What This Means:
✨ We'll post less frequently—sharing quarterly updates and celebrating big moments like:
• Scholarship announcements & recipient spotlights
• Lupus Awareness Month (May)
• Jasmine's birthday celebrations
• Major foundation milestones

Visit our website for resources and ways to get involved:
👉 **https://nandissmilefoundation.org**

Thank you for understanding as we evolve to serve our mission more effectively. Nandi's legacy of spreading smiles and supporting others continues—just with a more focused approach.

Keep smiling, keep fighting, keep making a difference. 💜

07/31/2025

The Positive Side of Adversity: Sometimes our greatest challenges become our greatest teachers. Jasmine's lupus journey has brought unexpected gifts: a deeper relationship with her mother, profound life lessons about not taking anything for granted, and the wisdom to recognize genuine love and support. She's learned that the people who truly care will be there "no matter what." While she sometimes feels the heat is too much to bear, she knows she'll "persevere and come out glistening." Her story reminds us that even in our darkest moments, we can find light, growth, and purpose. ✨

07/30/2025

📖 Midweek Mindset: “You don’t have to be strong every day. Just keep showing up.” 💜

🤝 Happy Friendship Day! To the friends who stand by us during flares, fatigue, and fear — THANK YOU 💜
07/30/2025

🤝 Happy Friendship Day! To the friends who stand by us during flares, fatigue, and fear — THANK YOU 💜

07/29/2025

Finding Strength in Struggle: "I'm a diamond in the rough." Despite the daily challenges, monthly chemotherapy sessions, and moments when the pain feels overwhelming, Jasmine refuses to give up. She's learned not to take life for granted and has grown closer to her mom, who accompanies her to those long hospital days. Even when life gets "hectic, frustrating," and brings her to tears, she holds onto her faith and the belief that she's going through this journey for a reason. Her mother often says she would have given up long ago facing the same challenges—but Jasmine knows she's stronger than she realizes. 💎

07/28/2025

🌞 Shine Anyway: Even on cloudy days, you’re radiant. Keep showing up 💜

07/27/2025

🛀 Reclaim Your Peace: Set your boundaries. Say no without guilt. Rest without shame 💜

07/26/2025

🖍️ Creative Coping: Art, poetry, music — what helps you cope on tough days? Share below 👇

07/25/2025

Daily Life with Lupus: Living with lupus means adapting, not giving up. Jasmine takes 12 medications daily and deals with side effects like short-term memory loss that require her to write everything down. She experiences "lupus fog"—moments of unfocusedness that can last about a minute—and arthritis pain that makes everyday tasks challenging. Planning her week became essential to avoid overwhelming herself. She even has to explain her condition to new teachers and sometimes record conversations to help with memory. These aren't excuses—they're adaptations that allow her to keep living fully. 📝

Address

Louisville, KY

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