Ep. 80 ~ Lipoedema warrior Sharon Frantz

Ep. 80 ~ Lipoedema warrior Sharon Frantz

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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Hosts on Instagram

Shelley ⁠https://www.instagram.com/all_things_lipoedema⁠

Tiana

⁠https://www.instagram.com/me_and_my_lipoedema⁠

The Lipoedema Podcast

Instagram

⁠https://www.instagram.com/the_lipoedema_podcast/⁠

Facebook

⁠https://www.facebook.com/thelipoedemapodcast⁠

YouTube

⁠https://www.youtube.com/@thelipoedemapodcast⁠

Spotify

⁠https://open.spotify.com/show/⁠thelipoedemapodcast

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Avsnitt(149)

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