I am joining thousands of people across the country for the Walk to End Lupus Now®. I hope that you will join me either by lacing up your sneakers or by donating to my fundraising page.
I hope to see you Saturday October 7th, 2023 in NYC to walk with Team Sara in raising awareness for Lupus.
My mom was diagnosed with Lupus when i was in grade school. I’ve watched her fight almost my whole life. She never gives up not even for a second. She is one of the strongest people I know.
I believe Lupus should be as well know as other diseases. It is harmful and eats away at the body. Please join me and other lupus warriors on spreading awareness on Lupus.
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 generous contribution of $5 or $50 can make a definite impact. Every single dollar counts.
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 and/or joints to the heart and/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!