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Whew… this one’s close to my heart. In today’s bonus episode, I’m sharing the raw, behind-the-scenes truth of what it really looks like to live with lupus — especially the things most people don’t see. This isn’t about complaining… it’s about naming the invisible.The fatigue. The body changes. The …
The Future of Lupus Treatment with Dr. Megan Clowse: What You Need to Know Now In this special Lupus Awareness Month episode, I’m sitting down with Dr. Megan Clowse—one of the leading rheumatologists in the lupus space and a fierce advocate for women’s health. We’re talking real talk about what it …
In this episode, I’m joined by Gabby, lupus warrior and founder of The L Life, a nonprofit dedicated to empowering women living with lupus. Gabby opens up about her diagnosis in 2012 during college, the mental and physical toll it took, and how her faith helped her shift from fear to purpose. We ta…
💜 Episode Summary Hey sis. Today’s bonus episode is personal. I’m sharing the truth about what it really felt like after I was diagnosed with lupus—and how I slowly started reclaiming my power, one choice at a time. I talk about what it’s like to live in survival mode, to wake up in pain, and still…
Ansvarsfraskrivelse: Podkasten og kunstværket, det finnes indlejret på denne siden, er fra Shedrica Shante | Chronically Planned Podcast, som tilhører dens eier og ikke er tilknyttet eller godkjent av Listen Notes, Inc.