Welcome!
My name is Savannah...
...And I am the founder of Lupus Has No Face. Lupus Has No Face is a 501(c)(3) non-profit organization committed to creating a community of support for everyone impacted by lupus. We not only offer assistance to lupus patients, but we also aim to raise awareness and educate the public about this autoimmune disease. Our mission is to provide everyone with the necessary resources to cope with the emotional and mental impact of lupus, including self-care and health education. We believe that through creating a supportive community, we can encourage women to lead healthy, happy lives while living with lupus.
"Lupus has no face" is more than just our name, but our slogan too! It represents the fact that lupus affects people from all walks of life, and its symptoms can vary widely. But despite the challenges of living with lupus, our community remains strong and resilient. We are committed to supporting each other and spreading awareness about this chronic illness.
Lupus Has No Face
Book Courses & Supports Online!
Living Well With Lupus Series Session 1
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1 hr
40 US dollars
Living Well With Lupus Series Session 3
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1 hr
40 US dollars
Did you know that over 5 million people worldwide are affected by lupus? At Lupus Has No Face, we are committed to raising awareness and supporting those affected by this chronic autoimmune disease.
Lupus Has No Face
Upcoming Lupus Awareness Events
Previous Lupus Awareness Events
At Lupus Has No Face, we understand that lupus is a chronic and often misunderstood condition, which is why we are dedicated to providing resources and support to those who suffer from it. Our previous events have included educational classes, charity walks, social outings and parties, all of which aim to bring together people who have been affected by lupus, and offer them a sense of community and understanding. Our gallery contains a wealth of information on all of our events. Click the buttons below for pictures and videos to make it easy for you to see everything we have to offer.
