23 Best Lupus Podcasts to Listen to (2026)

The Expert Series is an educational podcast series featuring empowering presentations from leading lupus experts with a focus on helping you live well with lupus. Presented by the Lupus Foundation of America, we touch on the daily issues that affect those with lupus: flares, health, medical care, exercise, managing doctor's appointments, diagnosis, and much more. more

Lupus LA enters the fastest growing media market with the new Your Story Our Fight® podcast which will give a voice to lupus patients while continuing Lupus LA's mission to raise lupus awareness worldwide. Hosted by the Chairman of Lupus LA and lupus patient himself, Adam Selkowitz, patients from all walks of life will share stories about their unique lupus journeys. With a focus on inspiration and hope, Lupus LA's podcast will provide support and optimism to a patient community looking for assurance that they are not alone. more

The Lupus Foundation of America, Greater Ohio Chapter welcomes you to My Lupus Living Room, a space where we get real about what it's like to live with lupus. Join our host, chapter President and CEO, Suzanne Tierney, for candid conversations about topics that so often get overlooked. You'll hear from our Ohio lupus community— including patients, caregivers, and medical experts— about the highs, lows, insights, and advice. Thanks for stopping by My Lupus Living Room. We hope you stay for a while. more

Welcome to the Calling in Sick, hosted by Alex Wildeson and produced by Just Media. On this podcast, Alex shares her unfiltered personal journey battling several autoimmune and chronic conditions including Polyarteritis Nodosa (PAN) Vasculitis, Mixed Connective Tissue Disease (MCTD) / Lupus, Endometriosis, and Complex Regional Pain Syndrome (CRPS). She also provides practical 'how-to' guides, explores hot topics, and welcomes other warriors, medical professionals, advocates and creators on the show to shed light on the latest healing modalities, promising treatments, and myth bust popular misconceptions and trendy health hacks. Tune in for some laughs, tears, and growth… but stay for the camaraderie and community. You can engage with Alex and the community through social media @callinginsickpod. We promise, you don't need a doctor's note for this one! more

The Lupus Living Podcast will inspire you to keep going through the challenges of living with lupus. Gwen Alexander, your host, was diagnosed with lupus after several emergency room visits and hospital stays. She has had to make many changes to her life since her diagnoses. She has been on a journey of making changes to her life that will help her still live a full life with lupus. Follow the podcast to learn how to navigate the flare ups of living with lupus. How to connect with Gwen:Email: ****@thegwenalexander.comWebsite: thegwenalexander.com/lupus-life-podcastFacebook: facebook.com/lupuslivingpodcastDisclaimer: The information in this podcast is for informational purposes only. The opinions of the guests are their own. The host of the podcast is not a medical professional. You should consult with your doctor or medical professional before you make any changes that may affect your health in any way. more

The Lupus Science & Medicine® podcast is your premier source for the latest insights and developments in lupus and related diseases. Each episode features in-depth interviews with authors and leading experts, covering the newest advances in lupus research and treatments. Lupus Science & Medicine® - lupus.bmj.com - is an esteemed international journal from the BMJ Group and the Lupus Foundation of America (LFA). The journal publishes basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. Subscribe now or listen on your favourite podcast platform to enhance your understanding of lupus. Podcast hosted by: Dr. Anna Wolska, The Lupus Foundation of America, USA more

Welcome to My Spoonie Sisters ! If you're wondering what a 'Spoonie' is, it's a term lovingly embraced by those living with chronic illnesses, based on the Spoon Theory. It's all about managing our limited energy (or 'spoons') while navigating life's challenges. Each week, join us to hear from your 'Spoonie Sisters' host, co-hosts, and our inspiring special guests as we share real-life stories, tips, and encouragement. Whether you're here to learn, connect, or feel less alone, you'll find a supportive space filled with understanding, laughter, and strength. Let's journey through chronic illness together! Tune in and join the sisterhood! All guests featured or mentioned in this podcast will be listed for your convenience. Don't forget to rate and subscribe to My Spoonie Sisters and follow @MySpoonieSisters on Instagram for updates on new episodes and more. If you have a story to share or want to be featured on My Spoonie Sisters, please email ****@gmail.com. We eagerly look forward to speaking and hearing from all our Spoonies! Disclaimer: While we are not doctors or healthcare Practitioners, we want to assure you that this podcast is a credible source of information. It's based on our guests' personal experiences and the strategies we've found effective for ourselves. However, everyone's body is unique, and what works for one person may not work for another. If you have any health-related questions, it's always best to consult your Primary Doctor or Rheumatologist. Remember, our goal at My Spoonie Sisters is to connect people and provide them with the support and tools they need to live better lives. more

Susan Hendrix is a lupus survivor who has achieved a great deal while dealing with this chronic illness. She will take you through her lows and highs, but most importantly she will bring further awareness to this chronic illness and allow others to know you can still live your life to the fullest. Susan Hendrix is educated in the field of Health and Science, at the age of 29 she became an entrepreneur and established her own Durable Medical Equipment Company along with a Medical Consulting Firm. Cover art photo by http://efeck.com('SM') more

Windy J Cumberbatch shares her journey living with Fibromyalgia, Lupus & Chronic Lyme Disease.After 11 years of being misdiagnosed, Windy finally got the diagnosis she sought.Join her along her journey of discovering healing, peace, joy and love in the midst of her illness.#invisibleillness#chronicpain#chronicillness#chronicillnessblog #migraine#anxiety#depression#fatigue#fibromyalgia#autoimmune#lupus#chroniclyme#pots#hypothyroidism#fibromyalgiawarrior#fibromyaalgiaawareness#chroniclife#chronicillnessawareness#windysjourney more

We seek to raise awareness and education of Lupus globally by speaking with medical professionals, physicians, researchers and patients to better understand the lupus journey, diagnosis and treatments. For more information about Lupus and Lupus Ontario, please visit Lupus Ontario at www.lupusontario.org, or follow us on Instagram, Twitter, Facebook or YouTube. We'd love to hear from you! If you have topic suggestions for the podcast, reach out to us at ****@lupusontario.org. more

Hi! Welcome to the Lively Living With Lupus podcast. I'm Lydia Romero Johnson, RN & holistic health coach. I teach women with lupus how to regain their energy, thrive without pain, and create the life of their dreams.My intention here is to help you realize that while you have lupus, you also have many tools, strategies, and resources available to live YOUR happiest and healthiest life. I've struggled with lupus, and now I thrive. I want to create a ripple effect of women using natural solutions to thrive with their diagnosis. Join the conversation! Love always, Lydia more

Life of a differently-abled Lesbian Woman of color living with Lupus/Sjgournes and other autoimmune illnesses. In my podcast we will talk all things from. Lupus Lesbian spilling the tea on ♥️💨relationships while being disabled.💋 Dr's appointments Navigating the medical world You will hear how I use my tool box of ideas to navigate staying connected to this earth.. staying happy..finding love in me and others. So please come along it's going to be a great ride....Love you guys...thank you in advance.💋💋💋 more

Lupus In Color podcast to educate, inspire, encourage and empower lupus warriors.

This podcast is for those who know someone with an autoimmune disease or chronic illness, and for the warriors newly embarking on this journey. This space is about harnessing our power to fight and triumph over these battles. It's about having a strong will, a resilient mindset, and the support of loved ones. We are committed to empowering, educating, and connecting individuals facing daily challenges due to chronic illnesses. We'll delve into the nuances of living with conditions like lupus and offer practical advice, all while nurturing a supportive community. more

✨Just chronic illness things✨Welcome to Happily Healed w/ Tenille, a safe space for everyone and anyone navigating life with Lupus or chronic illness. Over here, we celebrate resilience and strength, sharing laughter and heartwarming stories with people who live extraordinary lives in the face of health adversities. Together, we find joy in the journey, break through the hard stuff, and embrace the fact that a diagnosis is just the beginning of an incredibly powerful, hope-filled story. Join us as we uplift, inspire, and remind each other that healing, in many forms, is possible! more

The Lupus Academy has been providing accredited education in SLE for healthcare professionals since 2012 and in this monthly podcast Raquel Faria, an Internal Medicine Consultant at the Centro Hospitalar in Porto, will talk with experts from the Lupus Academy Steering Committee about SLE highlights of congresses, we will discuss difficult cases and we have an annual episode where we review all the exciting things that have been happening in lupus that year. more

I share hope, perspective, and honest reflections for anyone who needs a moment to breathe, feel seen, and smile.Living with chronic illnesses (Lupus and Thrombotic Thrombocytopenic Purpura), I open up about life, the thoughts we don't always say out loud, and what it means to keep going through it all.A space for deep conversations, real experiences, and reminders that even in the hardest moments, there is still life to be lived.Ig and TT: @JuanabananaorgBlog: juanabanana.orgContent is for informational and entertainment purposes only and should not replace professional advice more

Hello! We are Kat and Mel, We are sisters who have been diagnosed with Lupus, SLE. We encourage you to come listen to our podcast, where we share real-life experiences living with chronic illness, our struggles, our accomplishments, and our overall lives . Our goals are to offer support, raise awareness, and inspire others living with chronic illness. You are not alone. I f you're interested in that kinda thing or you're just digging our vibe, stay and listen for a while . more

Listen to Medscape InDiscussion: Systemic Lupus Erythematosus, a podcast series where thought leaders and clinical experts share their diverse insights and practical ideas for optimizing patient care. Relevant disclosures can be found with the episode show notes on Medscape https://www.medscape.com/viewarticle/1002123. The topics and discussions are planned, produced, and reviewed independently of advertisers. This podcast is intended only for US healthcare professionals. more

Welcome to the Lupus Forum. The Lupus Forum is an educational website developed under the auspices of the University of Leeds and is dedicated to the dissemination of the latest developments in the field of lupus. It provides continuing medical education to clinicians around the globe to facilitate greater understanding of lupus, its treatments, and clinical practice. more

Lupus Has No Face: Uniting and Empowering the Lupus Community Lupus 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 . more

The Lupus in Community Podcast is a supportive space for people living with lupus, caregivers, advocates, and anyone walking alongside the lupus community. Through honest conversations, real-life stories, and simple health education, we explore what it truly means to navigate lupus day by day.Each episode covers topics like flares, symptoms, mental health, wellness, relationships, faith, advocacy, navigating healthcare, and caring for the whole person — mind, body, and spirit. You'll hear from people living with lupus, caregivers, health professionals, and community voices sharing practical insight, encouragement, and hope.This podcast exists to help you feel seen, supported, informed, and stronger — because no one should navigate lupus alone. more

The Light, Lupus and I is a podcast about Jesus Christ the 'Light', lupus diagnosis and encounters with family and friends 'lupus' and me your host Salathiel DeLoach 'I'. This podcast was birthed from realization that God has given me a light out of one of the darkest spaces of my life. He allowed and is still yet allowing me to shine my light as I travel on this journey as someone who has been diagnosed with Lupus. This podcast is used to share my story, encourage others on their journey, chat with a few guest, and an ask and answer platform if you the listeners so desire. Speaking Life! more