Show Notes
Hosts Lisa, Janine, and Janae discuss a recent April study showing a calorie-restricted, low-carb high-fat diet reduced body weight, leg volume, and pain in women with lipedema, then welcome guest Aurora McCausland. Aurora shares how she discovered lipedema after her sister’s complications, her diagnosis, a denied insurance claim that led her to speak with NBC, and the online responses she faced for being a stage-one patient. She describes her surgery experience, recovery tips (gentle daily movement, compression, and rest), and the relief she felt as leg fatigue decreased. The episode highlights validation for all stages of Lipedema, the power of social media to connect and inform, and resources for those seeking diagnosis or treatment. Follow Aurora on social media: @AuroraMcCausland.
More from Lipedema Stories Podcast
This episode explores a new study finding distinct systemic metabolic signatures in premenopausal women with lipedema despite similar BMI, and highlights what that means for diagnosis and treatment.Hosts Lisa and Janine talk with Patty about her lived experience, ADHD diagnosis and medication, her free anti-inflammatory guide and journal, practical lifestyle tips, and the importance of community while warning against misleading quick-fix claims.
This episode explores recent research on AI in lymphedema diagnosis and clinical charting, and how AI tools are already changing care. It features Dean, a supportive husband who shares his experience caring for his wife through lipedema surgeries, the challenges of recovery, and the emotional impact of regained confidence.They also celebrate lipedema receiving its own ICD-10 code and discuss what that change could mean for diagnosis, insurance, and future research. Practical tips for caregivers and the patient’s newfound freedom—like wearing swimsuits again—wrap up the conversation.
In this episode of Lipedema Stories, hosts Lisa and Janine talk with Kylie, a tactile rep and former wound nurse, about how lipoedema differs from lymphedema, the role of fibrosis in treatment outcomes, and why accurate documentation matters for insurance access.They discuss practical tools like at‑home pumps and compression, the emotional relief patients feel when validated, and how clinicians and reps can improve continuity of care, refitting, and patient education.
This episode opens with a research moment on meningeal lymphatics and their emerging role in brain health and neurodegenerative diseases, then dives into a personal Lipedema story.Guest Ariana Holiday shares her journey living with lipedema and Dercum's disease, her brain tumor experience, surgical treatments and recovery, the fight to get insurance coverage (including a successful Medicaid appeal), and how she uses music to heal and advocate for others.
In this episode the hosts open with a research moment on GLP-1 therapies (including tirzepatide) and their potential to reduce inflammation, fibrosis, and support weight loss in lipoedema patients. They discuss clinical implications, insurance challenges, and real-world experiences with these medications.Guest Beth shares her decades-long journey to diagnosis, her life-changing surgical experience, the role of post-op treatments (including tirzepatide), and her advocacy work with Lipedema Unfiltered—offering resources, community, and practical aftercare tips for others navigating lipoedema.