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Ep59: Interview: Extra Pelvic Endometriosis (Part 1) with Wendy Bingham DPT, Founder of ExtraPelvic Not Rare

Ep59: Interview: Extra Pelvic Endometriosis (Part 1) with Wendy Bingham DPT, Founder of ExtraPelvic Not Rare

FromIn Sixteen Years of Endometriosis


Ep59: Interview: Extra Pelvic Endometriosis (Part 1) with Wendy Bingham DPT, Founder of ExtraPelvic Not Rare

FromIn Sixteen Years of Endometriosis

ratings:
Length:
85 minutes
Released:
Mar 18, 2021
Format:
Podcast episode

Description

As a part of Endometriosis Awareness Month, we speak with Wendy Bingham DPT, the founder of the non-profit called 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 why the definition of endometriosis desperately needs an overhaul and the proposed definitions from the scientific community for it. Likewise, we speak about the problems with the current definition of extrapelvic endo. We discuss the ICD (International Classification of Diseases) codes and why these negatively affect our ability to truly know the statistics of extrapelvic endo. Finally, we talk about various theories to the origin of endo, and why it’s vital that the medical community understand that extrapelvic disease is much more common than they believe. 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:
Mar 18, 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.