I created this post because my wife Sarah was diagnosed with Lupus and Rheumatoid Arthritis just over 11 years ago. Over the years she never had any issues or flare ups until about 2 year ago. During that time she was experiencing chronic pain and several other symptoms. In Jan 2021 she was diagnosed with Lupus Nephritis (kidney disease). After talking with doctors and getting educated about the disease we are more knowledgeable about what we need to do moving forward. We are now dialed in to fight and help others wherever we can and share her story.

Our Goal is the raise $500 by Sept 20th, 2022 all donations go to the Lupus Foundation! With all your help and support we can make that happen. Anyone that donates will receive a Lupus Wristband. We will be participating in the 2022 Walk to End Lupus Now in Los Angeles on Sept 24th 2022. 

Team Shirts for avail purchase DM me! 

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!