Part 1 Catching Up w/ Lipedema Foundation's Kasi Grosvenor: Surgery, Mast Cell, GLP-1
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This week we’re catching up with our friend Kasi Grosvenor, project manager for the Lipedema Foundation. It’s been a year since we last talked, and wow… so much has happened! Kasi shares more on her lipedema removal surgeries, living with mast cell disease, and talks about her journey with GLP-1. It’s real, it’s encouraging, and it’s only part 1! Next week we talk about what it's like parenting teenage daughters with lipedema. Big thanks to our amazing sponsors—Lipoelastic, Marena Compression, and AIROS Medical—for always standing beside women with lipedema. ✨ Lipoelastic Shop medical-grade compression at www.lipoelasticshop.com Follow on Instagram: @lipoelastic_usa Use code LIPPYMAMAS for 10% off in the UK or US ✨ AIROS Medical Discover pneumatic compression therapy at www.airosmedical.com/lipedemamamas ✨ Marena Explore high-quality compression garments at www.marena.com Use code LIPEDEMAMAMAS20 at checkout. 💡 New to the Lipedema Community? Start your journey with confidence at www.lipedemacourses.com — your go-to resource for conservative lipedema management. ✨ Connect With Us: Follow Shawn on Instagram: @the_lipedema_mama Follow Ashley on Instagram: @the_lippy_lady 💖 Loving the Podcast? Please take a moment to leave a 5-star rating and review—it helps us reach more women who need support, guidance, and hope.
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