In this episode of the Lipoedema podcast, hosts Shell and Tiana speak with Sharon Frantz, a board member of Lipoedema Australia, about her journey with lipoedema, the challenges of diagnosis, and the importance of self-care and community support. They discuss the impact of medical misogyny, the significance of research in understanding lipoedema, and the emotional toll of living with a chronic condition. Sharon shares her insights on managing lipoedema through nutrition and compression, as well as her academic pursuits in researching the psychological impact of the diagnosis.
Chapters
00:00 Introduction to Lipoedema and Personal Journeys
02:45 Understanding Lipoedema: Diagnosis and Acceptance
05:08 Body Changes: Pregnancy, Perimenopause, and Self-Perception
07:41 Managing Lipoedema: Strategies and Lifestyle Choices
10:13 The Role of Research and Advocacy in Lipoedema Awareness
16:11 Pursuing a PhD: Personal Motivation and Research Focus
21:03 The Impact of Delayed Diagnosis and Medical Misogyny
25:10 Self-Care and Community Support for Lipoedema
29:52 Conclusion: Hope and Future Directions for Lipoedema Awareness
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Tiana
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