Have you ever looked in the mirror and felt like you no longer recognize yourself? 💜 After years of living with #lupus, Phara has experienced how skin changes can impact confidence.

Join us on 10/14 to discuss skin health, confidence, and more: buff.ly/bwLYbOO

Living with #lupus can change the way you care for your skin. 💜 For Alyssa, navigating skin sensitivities and sun protection have shown her that skin care is about more than appearance.

Join us on 10/14 to learn how to protect your skin and confidence: buff.ly/bwLYbOO

👟 #WalktoEndLupusNow is going strong! ➡️ Swipe to see highlights from across the country, where walkers showed up for the #lupus community this October.

There's still time to join us. Find a walk near you and register today: buff.ly/VoNd2Lt

“To know her was to love her.” 💜 After losing her mom, Rachel carried her legacy into Inspira. Her memory inspired its butterfly logo and commitment to give back as a Purple for Purpose partner.

Read their story: buff.ly/DuBpsQI

Join us next week as our dynamic panel of speakers discusses practical strategies for protecting your skin from UV exposure, navigating cosmetic procedures safely, and choosing the right products.

Register today ⬇️
buff.ly/GnR5Pl0

🆕 A new episode of The Expert Series is live! Dr. Feldman shares ways people with #lupus can manage their care when regular access to a rheumatologist is limited, from preparing for appointments to navigating medications and telehealth.

🎧 Listen now: buff.ly/mczDi0V

Este #MesDeLaHerenciaHispana, estamos destacando Be Fierce. Take Control.™, un programa que educa a mujeres jóvenes afroamericanas y latinas con mayor riesgo de #lupus. Mira cómo las guerreras del lupus comparten cómo están tomando control de su salud.

Más información: buff.ly/y31oOfY

This #HispanicHeritageMonth, we’re highlighting Be Fierce. Take Control.™, a program that educates young African American and Latina women at higher risk for #lupus.

Watch lupus warriors share how they’re taking control of their health.

Learn more: buff.ly/y31oOfY

Nearly 2,000 lupus warriors, families, friends and supporters filled NYC with purple for #WalktoEndLupusNow! 💜

Lupus warriors and LFA CEO Louise Vetter spoke with PIX11 about the impact of lupus, the power of community and lupus research.

Watch now: buff.ly/fPqSayt

💜 Meet Alejandra, diagnosed with #lupus at 16. Originally from Guatemala, she found connection through the LFA community. Through her photos, she's sharing an honest look at life with lupus, from hospital stays to everyday moments.

➡️ Share your journey: buff.ly/RLzbMre

💜 Conoce a Alejandra, diagnosticada con #lupus a los 16. Originalmente de Guatemala, encontró conexión a través de la comunidad de LFA. A través de sus fotos, comparte una mirada honesta de la vida con lupus.

➡️ Comparte tu experiencia: buff.ly/RLzbMre

Adicet Bio reported early results from a Phase 1 study for prula-cel, an investigational CAR-T therapy being studied in people with #lupus, including lupus nephritis. Read more here: buff.ly/kCW0RBF

Access to trusted #lupus education matters, and language should not be a barrier. 💜 This #HispanicHeritageMonth, explore Spanish-language resources and tools designed to help you better understand and manage lupus.

👉 Explore the blog: buff.ly/EuCNxcu

El acceso a información confiable sobre el lupus es fundamental, y el idioma no debería ser una barrera. 💜 Este Mes de la Herencia Hispana, explora recursos y herramientas en español diseñados para ayudarte a comprender y controlar mejor el lupus.

👉 Explora el blog: buff.ly/EuCNxcu

A new study found more than 80% of adults with #lupus reported using dietary supplements, and nearly 1 in 3 had a potential supplement-medication interaction. Findings highlight the importance of discussing supplement use with providers. Read more: buff.ly/jcl4rJY

✨ lupus charity last milestone update ⭐
I decided on the Upcoming Sakuraco snack box 🎁 We'll be trying snacks on stream on twitch or discord, whichever works in the time it arrives!

Thank you for patience and the support given during fundraising! You can always donate to lupus.org @lupus.org

We’re 2️⃣ weeks away from our October 14 Lupus & You webinar: Embracing Skin Care!

Join us for this free event to hear tips on protecting your skin from UV exposure, navigating cosmetic procedures safely, and choosing the right products.

Register today: buff.ly/GnR5Pl0

💜 Meet Mi'yana, diagnosed with lupus at 15. Through the LFA, she's expanded her knowledge and found she's not alone. From hospital visits to everyday moments in between, Mi'yana is showing what her life with lupus looks like.

➡️ Share your photos today: buff.ly/RLzbMre

⏰ Today is the last day of our budget year. Your support helped 7,000+ people access #lupus webinars, brought 2,700 together at Empowerment Conferences, connected 3,000+ people with support, and much more!

Help continue this support in the year ahead: buff.ly/CmTncwA

Deadline extended! 🏃 Applications to join our inaugural Race to End Lupus team at the 2027 TCS Dobule London Marathon are now open through October 19.

Make your miles matter for people impacted by #lupus. Apply today: buff.ly/4JsUvBx
#LondonMarathon