I was diagnosed with SLE in 2012 and I was 6 months pregnant. I was so scared, mainly because I had absolutely no knowledge of Lupus. In reality the only time I have heard of Lupus, was from watching the TV show House (they blamed everything they couldn't figure out on Lupus). The doctors were certain that I would carry to term and that my body would start shutting down. Well I showed them, I gave birth to a completely healthy baby.  Through the years I've learned so much about my own diagnosis and I've also try to help spread awareness and knowledge to as many people as I can. 

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 like me affected by lupus! A generous contribution of anything really can make a definite impact. What’s more, if your employer offers a Matching Gift Program to employees, you may be able to double your contribution with just a little bit of paperwork. Trust me, it’s worth the effort! 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 or joints to the heart or kidneys.

While lupus can strike anyone at any time, 90% of people living with lupus are women. 

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!