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Ep74: Interview: Thoracic Endometriosis with Wendy Bingham of ExtraPelvic Not Rare

Ep74: Interview: Thoracic Endometriosis with Wendy Bingham of ExtraPelvic Not Rare

FromIn Sixteen Years of Endometriosis


Ep74: Interview: Thoracic Endometriosis with Wendy Bingham of ExtraPelvic Not Rare

FromIn Sixteen Years of Endometriosis

ratings:
Length:
49 minutes
Released:
Oct 14, 2021
Format:
Podcast episode

Description

We are back with Wendy Bingham DPT, founder of the non-profit ExtraPelvic Not Rare, which is dedicated to starting conversation about extrapelvic endometriosis, while providing correct, up-to-date information about the signs and symptoms, diagnostics, and appropriate treatment referrals. In this episode, we speak about thoracic endometriosis: what it is, the symptoms, the treatment, how it’s diagnosed and more. Wendy also tells us her vision for the future of endo treatment. WENDY'S WEBSITE: extrapelvicnotrare.org WENDY'S INSTAGRAM: @extrapelvicnotrare WENDY'S FB GROUP: ExtraPelvic Not Rare Endo Support and Education Group LIKE OUR SHOW? Please rate it or leave a review! CONNECT WITH US! INSTAGRAM: @in16yearsofendo WEBSITE AND RESOURCES: insixteenyears.com
Released:
Oct 14, 2021
Format:
Podcast episode

Titles in the series (100)

Laugh, cry, and shout with us as we talk all things endometriosis. We’re 2 witty best friends that pride ourselves on sharing accurate, well-researched information. We delve into all those embarrassing did-that-really-just-happen?! endo stories, talk vulnerably about our personal growth, and share disease facts with a side of humor. We hope our podcast will support and empower you. —Important note on inclusive language: We hadn’t yet been educated about inclusive language when we began our podcast; but after learning, we used this language midway through the show and going forward.