For many years, I've been deeply involved with the Walk to End Lupus Now DE event, serving on the walk committee. Since 2008, I've navigated life with Lupus & Sjogren's, alongside several family members and friends who also battle lupus. This journey has given me firsthand insight into the daily challenges faced by Lupus Warriors, fueling my passion for raising funds and awareness.
I'm honored to stand among thousands across the nation in the Walk to End Lupus Now®. I invite you to join me virtually, walking with Team Purplegeckos, or by supporting my fundraising efforts. Your contribution, no matter the size, is invaluable in reaching my personal goal and advancing the Foundation's mission to enhance the lives of those affected by lupus. If your employer offers a Matching Gift Program, consider leveraging it to double your impact—it's a small effort with significant results.
The unwavering support of family and friends is my anchor through the challenges of living with Lupus. Their encouragement, understanding, and assistance have been a lifeline, turning what could be an overwhelming journey into one marked by resilience and hope. Together, with love and solidarity, we demonstrate that thriving is possible despite a lupus diagnosis.
With heartfelt gratitude,
Lisa
Did you know?
Lupus is a mysterious and misunderstood autoimmune disease. It strikes without warning, affects each person differently, and has no known causes or cure.
Lupus symptoms can be severe and highly unpredictable and can damage any organ or tissue, from the skin or joints to the heart or kidneys.
While lupus can strike anyone at any time, 90% of people living with lupus are women. Women of color are at especially high risk.
Lupus is hard to diagnose, but the Lupus Foundation of America is working to make life easier and more comfortable for the estimated 1.5 million people living with lupus in the United States. Together, we can solve the cruel mystery of lupus. Thank you for your generosity!