Our podcast is dedicated to a diverse audience that includes individuals diagnosed with Lupus seeking information and support, as well as their friends and family who strive to understand the condition better. We also cater to healthcare professionals looking for insights into patient experiences, members of support groups focused on chronic illnesses, advocates raising awareness about autoimmune diseases, and mental health professionals assisting patients with the emotional impacts of chronic conditions.  Lupus Has No Face is more than just a podcast; it is also a 501(c)(3) non-profit organization committed to fostering a supportive community for those impacted by Lupus. Our mission encompasses not only assisting lupus patients but also raising public awareness and providing crucial education regarding this autoimmune disease. We aim to equip individuals with the resources necessary to cope with the emotional and mental aspects of Lupus, emphasizing self-care and health education. Through community building, we aspire to empower individuals, especially women, to lead fulfilling lives while managing their condition.