Lupus Has No Face: Uniting and Empowering the Lupus Community
Welcome to the Lupus Has No Face Podcast, hosted by Savannah Burks! We're more than just a podcast; we're also a 501(c)(3) non-profit organization committed to building a supportive community for everyone affected by Lupus.
This is your space, whether you're living with a Lupus diagnosis and seeking support, a friend or family member trying to understand the condition better, or a healthcare professional looking for patient insights. We also welcome chronic illness support groups, autoimmune disease advocates, and mental health professionals who help patients navigate the emotional impacts of chronic conditions.
Our mission is clear: we don't just help Lupus patients; we also raise public awareness and provide vital education about this autoimmune disease. We're here to give you the tools you need to cope with the emotional and mental challenges of Lupus, emphasizing self-care and health education. Through powerful stories and building a strong community, we aim to empower individuals, especially women, to live fulfilling lives while managing their condition.
Join us as we put a face to Lupus, one story at a time. To keep up with all our latest content, subscribe to the podcast. If you've enjoyed this episode, please leave a review.
All content for Lupus has No face Podcast is the property of Savannah Burks | Lupus Advocate & Host and is served directly from their servers
with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
Lupus Has No Face: Uniting and Empowering the Lupus Community
Welcome to the Lupus Has No Face Podcast, hosted by Savannah Burks! We're more than just a podcast; we're also a 501(c)(3) non-profit organization committed to building a supportive community for everyone affected by Lupus.
This is your space, whether you're living with a Lupus diagnosis and seeking support, a friend or family member trying to understand the condition better, or a healthcare professional looking for patient insights. We also welcome chronic illness support groups, autoimmune disease advocates, and mental health professionals who help patients navigate the emotional impacts of chronic conditions.
Our mission is clear: we don't just help Lupus patients; we also raise public awareness and provide vital education about this autoimmune disease. We're here to give you the tools you need to cope with the emotional and mental challenges of Lupus, emphasizing self-care and health education. Through powerful stories and building a strong community, we aim to empower individuals, especially women, to live fulfilling lives while managing their condition.
Join us as we put a face to Lupus, one story at a time. To keep up with all our latest content, subscribe to the podcast. If you've enjoyed this episode, please leave a review.
In this engaging episode, Savannah Burks dives into the world of nonprofits—what they are, how to identify genuine organizations, and their vital role in supporting the lupus community. Joined by her sister, Dr. Verola, they share expert insights, practical tips for due diligence, and lessons learned from experience to help listeners navigate and support reputable lupus nonprofits. Whether you're a supporter, potential donor, or someone interested in starting an organization, this episode offers valuable guidance on building trust, ensuring transparency, and making a meaningful impact. Tune in for an honest, informative discussion aimed at strengthening the philanthropic efforts within the lupus community. Don't miss it!
Thank you for tuning in to "Lupus Has No Face," a podcast dedicated to sharing real stories and insights on living with Lupus and other invisible illnesses. Join your host, Savannah Burks, as she explores the struggles and triumphs of individuals navigating their health journeys, all while juggling life's many challenges. Don't miss an episode! Subscribe, listen, and share on all major podcast platforms. For more content and updates, follow us on social media and join the conversation.
Lupus has No face Podcast
Lupus Has No Face: Uniting and Empowering the Lupus Community
Welcome to the Lupus Has No Face Podcast, hosted by Savannah Burks! We're more than just a podcast; we're also a 501(c)(3) non-profit organization committed to building a supportive community for everyone affected by Lupus.
This is your space, whether you're living with a Lupus diagnosis and seeking support, a friend or family member trying to understand the condition better, or a healthcare professional looking for patient insights. We also welcome chronic illness support groups, autoimmune disease advocates, and mental health professionals who help patients navigate the emotional impacts of chronic conditions.
Our mission is clear: we don't just help Lupus patients; we also raise public awareness and provide vital education about this autoimmune disease. We're here to give you the tools you need to cope with the emotional and mental challenges of Lupus, emphasizing self-care and health education. Through powerful stories and building a strong community, we aim to empower individuals, especially women, to live fulfilling lives while managing their condition.
Join us as we put a face to Lupus, one story at a time. To keep up with all our latest content, subscribe to the podcast. If you've enjoyed this episode, please leave a review.
