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Lupus Has No Face: Uniting and Empowering the Lupus CommunityLupus doesn’t have a single "look," but it does have a powerful community. Join host Savannah Burks on the Lupus Has...
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Lupus Has No Face: Uniting and Empowering the Lupus CommunityLupus doesn’t have a single "look," but it does have a powerful community. Join host Savannah Burks on the Lupus Has No Face Podcast, the audio home of our 501(c)(3) non-profit.
Living with a chronic illness is about more than just managing symptoms; it’s about navigating the emotional highs and lows that come with it. We invite patients, advocates, and mental health experts to the table to talk about self-care, health education, and the reality of life with an autoimmune disease.
If you’re looking for a community that understands the mental grit it takes to thrive with lupus, you’ve found your people.
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.
show less
Living with a chronic illness is about more than just managing symptoms; it’s about navigating the emotional highs and lows that come with it. We invite patients, advocates, and mental health experts to the table to talk about self-care, health education, and the reality of life with an autoimmune disease.
If you’re looking for a community that understands the mental grit it takes to thrive with lupus, you’ve found your people.
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.
Episodes & Posts
Episodes
Posts
Transcribed
8 APR 2026 · In this episode of Lupus Has No Face, hosts Tone and Savannah Burks are joined by Kanini McDaniel, author of Blinded by Pride. The conversation explores the intersection of emotional trauma and physical health, specifically how toxic relationships and stress can trigger lupus flare-ups. Kanini uses a "carnival and clown" metaphor to describe staying in toxic situations, while the hosts emphasize the life-saving importance of setting boundaries and advocating for oneself in relationships and healthcare. 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Explicit
Transcribed
2 APR 2026 · "Is Milwaukee ready for its biggest year yet?" 🏙️💉
In this powerhouse episode of Where I Come From MKE, host Antonio Luckett sits down with the people actually pulling the levers of change in our city. We go inside the Mayor's office with Cavalier Johnson to break down the "Year of Housing" initiative. We ask the tough questions about housing affordability, the demolition of Northridge, and his vision for making Milwaukee a global anchor. But growth isn't just about buildings; it’s about people. Savannah Burks, founder of Lupus Has No Face, joins us for a raw, unfiltered look at the Milwaukee healthcare system. She shares her personal journey with SLE and provides a survival guide for navigating medical gaslighting and demanding the care you deserve.
Inside this episode: 🏗️ The Mayor’s Roadmap: How 2026 will change the face of our neighborhoods. 🩺 Healthcare Truths: Why Savannah Burks says "staying down" for your health is a form of activism. ✊ Advocacy in Action: Practical steps for becoming a leader in your own life and community.
timestamps based on the key topics discussed: * **01:00** - Introduction and Icebreaker * **01:30** - Discussion on the 2026 City Budget and Sales Tax * **05:15** - Progress on Removing Lead Service Lines * **06:20** - Economic Growth and Job Creation in Milwaukee * **08:35** - Reconciling Fiscal Discipline with Community Spending * **10:45** - 2026: The Year of Housing in Milwaukee * **12:00** - Updating the City's Zoning Code * **13:00** - Affordable and Workforce Housing Initiatives * **15:00** - Navigating Neighborhood Concerns and Growth * **16:30** - Addressing Reckless Driving and Road Safety * **19:00** - Part 2: Health, Wellness, and Invisible Illnesses (Lupus) * **21:00** - The Role of the Milwaukee Health Department * **22:00** - Importance of Immunizations for Children * **23:00** - Early Diagnosis and Access to Care in Underserved Communities * **26:30** - Supporting Nonprofits and Grassroots Organizations * **28:00** - The Power of Community Partnerships * **30:00** - Strategy for Public Safety: Accountability and Prevention * **32:30** - Closing Message: Overcoming Adversity and Life Advice 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Transcribed
25 MAR 2026 · In this insightful episode of Lupus Has No Face, host Savannah Burks dives deep into the medical testing world with laboratory director and technical college owner, Ms. Charlene. They demystify the complexities of genetic testing, biomarkers, and the everyday realities of medical laboratories. Ms. Charlene provides a transparent, behind-the-scenes look at why lab results get delayed—ranging from mislabeled tubes to the vital importance of proper phlebotomy techniques. The conversation empowers patients to advocate for themselves, understand their "MyChart" portals, and recognize the critical importance of accuracy over speed when it comes to life-saving diagnoses. 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Explicit
Transcribed
18 MAR 2026 · What happens when a woman decides to stop hiding and starts unlocking her true potential? Today, we’re finding out.
In this deeply personal and uplifting episode of Lupus Has No Face, host Savannah Burks sits down with the phenomenal Felicia Rodriguez to explore the transformative power of visibility. Felicia opens up about the heart behind "Felicia Unlocked" magazine—a platform dedicated to pulling back the curtain on the lives of resilient women and giving them the stage they deserve
Together, they dive into why "empowerment" isn't just a buzzword, but a necessity for survival and success. From the importance of sharing our authentic stories to the magic that happens when women intentionally lift one another up, this conversation is a masterclass in sisterhood and the strength found in being truly seen.
If this conversation moved you, please subscribe, leave a 5-star review, and share this episode with a woman in your life who needs to hear that her voice matters. 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Explicit
Transcribed
11 MAR 2026 · Motherhood doesn’t come with a manual, and when you are navigating it as a teenager, the script is incredibly hard to write. But what happens when you refuse to let society’s statistics define you, and instead turn early adversity into the foundation for an entire community?
Welcome to a very special Women’s HERstory Month episode. Host Savannah Burks is honored to sit down with the deeply inspiring Kela King, the visionary Founder of Mommies Make It Better (MMIB).
In this raw and uplifting conversation, Kela pulls back the curtain on her deeply personal journey of navigating life as a teen mother. She shares how she transformed her most challenging moments,the fear, the isolation, and the pain, into a powerful, driven purpose. Together, Savannah and Kela explore the heartfelt mission behind MMIB and dive into the powerful details of Kela's very first program, More Than: Life Begins.
This episode is a beautiful testament to resilience, the power of community, and the undeniable strength of women supporting women. Whether you are a young mother looking for guidance, or simply someone who needs a reminder that your struggles can birth your greatest triumphs, this conversation is for you. 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Explicit
Transcribed
4 MAR 2026 · Living with Lupus is often described as a physical battle, but the emotional and mental toll is just as significant. In this powerful episode of Lupus Has No Face, hosts Savannah Burks and Dia sit down with globally recognized Mental Wellness Expert, Dr. Lia Knox, to pull back the curtain on the "invisible" side of chronic illness.
Managing symptoms is only half the battle; protecting your peace is the other. Dr. Knox brings her extensive expertise as a Licensed Professional Counselor with a Doctorate in Counseling Psychology from Auburn University to discuss the intersection of mental wellness and physical diagnosis. As the Founder/CEO of Knox Behavioral Health Solutions and Co-Founder of Black Space Inc., she has dedicated her life to providing free therapeutic spaces and breaking the stigma around mental health in underserved communities.
A true community icon and recipient of the Vel Phillips Trailblazer Award and the Milwaukee Business Journal Woman of Influence Award, Dr. Knox dives deep into Cultural Competency. She specifically addresses how those in the Black community navigating Lupus can bridge the gap between their medical journey and their mental well-being.
Tune in as we discuss navigating the emotional highs and lows of a "flaring" mind, the importance of advocacy, and why your mental health is a priority, not an afterthought. 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Transcribed
26 FEB 2026 · In this incredibly episode of the Lupus Has No Face, Savannah and Tone switch gears to celebrate a major personal triumph. Savannah is taking on a brand-new title: Actress.
We’re giving you a backstage pass to her acting debut. Together, we'll unpack the raw emotion of landing the part, the mental grind of mastering the lines, and how she pushed past imposter syndrome to face the cameras for the very first time.
From the shock of the casting call to the adrenaline rush of wrapping the trailer, this conversation is a masterclass in leaving your comfort zone. It’s a powerful reminder that an invisible illness doesn't rewrite your dreams; sometimes, it simply prepares you for a bigger role. 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Explicit
Transcribed
18 FEB 2026 · When the director yells "cut," the real work of loving someone with a chronic illness begins. But how do you keep showing up for your co-star when the sequel is just as unpredictable as the first act?
Welcome back to Part 2 of our deeply moving series, "On Camera, On Purpose: Supporting Someone with Lupus in Real Life." In this episode of the Lupus Has No Face Podcast, host Savannah Burks sits down with special guest Dasani to continue the profound conversation about what it truly means to be a steadfast partner to a Lupus warrior.
Building on the cinematic themes of our last episode, Savannah and Dasani dive deeper into the emotional endurance required behind the scenes. They explore how to read the unspoken cues when the "Lead Actor" is too exhausted to speak, the importance of maintaining your own energy as a supportive "Co-Star," and how to find joy and laughter even when the script throws you a curveball. This episode is a beautiful, candid look at the resilience of love, the power of active empathy, and the everyday heroics of simply being there when the cameras stop rolling.
Grab your headphones and join us for this beautiful continuation! 🎧 If you or someone you love is navigating the unpredictable world of autoimmune diseases, this episode is your reminder that you don't have to play this role alone. Tune in now, hit that Subscribe button, and share this with the real-life co-stars in your world! 💜 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Explicit
Transcribed
12 FEB 2026 · Life with Lupus isn't a rehearsed screenplay; it’s an improv performance where the genre can switch from romance to medical drama in a single heartbeat. When the script flips from "Dinner Date" to "Bed Rest," who is the co-star holding the scene together?
In this cinematic and deeply moving episode of the Lupus Has No Face Podcast, host Savannah Burks is joined by special guest Aaron Fourston to explore the vital role of the "Co-Star" in the life of a Lupus warrior. Together, they discuss the art of "Improvisational Acting", learning to pivot without blame when a flare-up demands a sudden script change.
Aaron breaks down the subtle, often invisible work of a supportive partner, from reading the subtext of the "I'm Fine" Monologue to mastering "Shadow Work"—literally blocking the sun to protect the Lead Actor. The conversation dives into the practicalities of "Stunt Coordination," where offering an arm for stability or pre-opening a water bottle becomes an act of love, and "Saving the Scene" socially when Lupus Fog clouds the mind.
Whether it’s managing the "Press" questions or handling the "Post-Performance Crash" behind the scenes, this episode reveals how a true partner protects the Co-star's dignity, maintains chemistry through physical changes, and uses humor to break character when the drama gets too heavy.
Guest Info:
Instagram: mr_4ston / AOEDEaf
Facebook: Aaron Fourston
X (Twitter): mr_4ston
YouTube: mr_4ston
TikTok: mr_4s 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Transcribed
5 FEB 2026 · In this powerful episode, host Savannah Bert sits down with Director Teddy Worten and Assistant Director Bre Harris to discuss "Lights, Camera, Action: How Directors Support Individuals with Autoimmune Diseases." Using the framework of a film production, they explore the necessity of a supportive work environment for those living with invisible illnesses like lupus. Learn about the emotional toll of "masking" pain, the strategies for preventing burnout, the power of clear communication, and the importance of surrounding yourself with a strong, aligned team. This is a must-watch for creators, directors, actors, and anyone managing a chronic condition.
🎬 CHAPTERS 🎬
00:01:22 - Welcome to the Episode & Guest Introductions
00:03:23 - Defining the Director’s Role in Illness Support
00:07:35 - The Pressure to Perform & Recognizing Burnout
00:19:24 - How to Combat Guilt and Take Necessary Rest
00:25:51 - Dealing with Unsolicited Advice & Team Advocacy
00:46:12 - Lupus, Partnership, Love, and Stability
00:53:31 - Self-Care for Directors & Mental Health Talk
00:59:16 - Closing Truths: Finding Your Safe Set 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. Tune in to be inspired, empowered, and reminded that your story matters. ✨
Resource Links
- Official Website: http://www.lupushasnoface.com
- Savannah Burks Brand: www.SavannahBurks.com
- @LHNF on Social<
Lupus Has No Face: Uniting and Empowering the Lupus CommunityLupus doesn’t have a single "look," but it does have a powerful community. Join host Savannah Burks on the Lupus Has...
show more
Lupus Has No Face: Uniting and Empowering the Lupus CommunityLupus doesn’t have a single "look," but it does have a powerful community. Join host Savannah Burks on the Lupus Has No Face Podcast, the audio home of our 501(c)(3) non-profit.
Living with a chronic illness is about more than just managing symptoms; it’s about navigating the emotional highs and lows that come with it. We invite patients, advocates, and mental health experts to the table to talk about self-care, health education, and the reality of life with an autoimmune disease.
If you’re looking for a community that understands the mental grit it takes to thrive with lupus, you’ve found your people.
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.
show less
Living with a chronic illness is about more than just managing symptoms; it’s about navigating the emotional highs and lows that come with it. We invite patients, advocates, and mental health experts to the table to talk about self-care, health education, and the reality of life with an autoimmune disease.
If you’re looking for a community that understands the mental grit it takes to thrive with lupus, you’ve found your people.
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.
Information
| Author | TDR Network |
| Organization | TDR Podcasting Network |
| Categories | Health & Fitness , Non-Profit , Self-Improvement |
| Website | www.LUPUSHASNOFACE.com |
| lhnfpodcast@gmail.com |
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