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.
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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.
The Fashion of Awareness: A Call for Unity - Cancer Awareness Fashion Show
Lupus has No face Podcast
1 hour 2 minutes
1 month ago
The Fashion of Awareness: A Call for Unity - Cancer Awareness Fashion Show
Join Savannah Burks for an emotional and uplifting conversation with Nichole Muex of Common Threads. Nichole shares the deeply personal story of losing her mother to pancreatic cancer a decade ago, a loss that fueled her drive to create change. She reveals why she's dedicated to highlighting the universal impact of cancer, emphasizing that "there isn’t a single person who has NOT been touched by cancer in some form or fashion." Don't just listen—ACT! Join Nichole Muex in the fight to prove that CANCER DOES NOT DISCRIMINATE. Get your tickets now for the Common Threads for Cancer Awareness Fashion Show on Sunday, November 9th, at The Clybourn in Milwaukee. Visit Nichole Muex's Common Threads pages to buy tickets, volunteer your time, or explore sponsorship opportunities. Your support uplifts voices, honors legacies, and helps make a difference, one thread at a time. Go buy a ticket and support the cause!
Event Name Commons Threads for Cancer Awareness Fashion Show Presented By Nichole Muex (Common Threads) Date Sunday, November 9, 2025 Time 4:00 PM – 8:00 PM CST Location The Clybourn Address 2202 West Clybourn Street, Milwaukee, WI 53233
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.
