I am joining thousands of people across the country for the Walk to End Lupus Now®.
In October of 2022 I was diagnosed with Lupus, specifically SLE (systemic lupus erythematosus). If receiving a chronic autoimmune disease diagnosis wasn’t tough enough, the physical pain over this past year has been unlike anything I have ever experienced. I have good days and bad days but my journey is not over. While we celebrate the big and small victories in the battle against Lupus, help us raise money to find a cure! Our team, Flare Fighters will be walking on October 7th and would greatly appreciate your support!
You can make a difference by donating to help me reach my personal fundraising goal and support the Foundation's efforts to improve the quality of life for all people affected by lupus! A contribution of any amount can make a huge impact.
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.
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!