Whether you are newly diagnosed with lupus or you have been navigating the disease for years, the Lupus Foundation of America has the resources you need, created and curated with trusted experts and community members. Check it out >>> | Lupus Foundation of America

509 reactions · 204 shares | Has lupus touched your life or family? Do you have questions about this cruel & complex disease? We have resources for you! This Lupus Awareness Month, we can all help #MakeLupusVisible. Learn more today. | Lupus Foundation of America | Facebook

March is #AutoimmuneAwarenessMonth. Let's shed light on lupus, an autoimmune disease affecting millions worldwide. Common symptoms include extreme fatigue, joint pain, skin rashes, fever and more. Help us spread awareness this month by watching and sharing our brief video. | Lupus Foundation of America

1.9K views · 55 reactions | One of the ways we contribute to lupus research is by funding research projects of scientists who are just getting started so we can continue to grow the field of lupus researchers. Watch this video to learn how this grant helps encourage these scientists to stay and grow in the lupus research field. | Lupus Foundation of America | Facebook

13K views · 139 reactions | The Lupus Research Alliance has invested...

From the onset of symptoms, it takes an average of six years to get an accurate lupus diagnosis. We’ll be with you every step of the way. Visit the National Resource Center on Lupus for more information about symptoms and treatment options. | Lupus Foundation of America

“But you don’t look sick.” If you’ve heard this before, you’re not alone. Watch as Lupus Fiasco calls out things people shouldn’t say to people with #lupus. 💬 Comment a purple heart 💜 if you’ve heard one of these before. | Lupus Foundation of America