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THE ENDO CO with Jenne Rishe

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Interview with Endo Coalition's Jenneh Rishe
We’re all familiar with March being Women’s History Month, but did you know it is also Endometriosis awareness month? If you didn’t, don’t worry you certainly are not alone. In fact, despite the statistics that say 1 in 10 women in the US are living with endometriosis, many are suffering in silence. There are a number of reasons for this, ranging from lack of awareness, to misdiagnosis, and lack of funding for research toward endometriosis, all of which contribute to a widespread problem that deserves more education and amplification.

So this is our theme for the month, and I am super excited for our interviews in this periodical. It will actually be a two-part episode, and in this first part, I will be speaking with Jenneh Rishe, the founder and executive director of an advocacy organization called The Endometriosis Coalition.

Jenneh has been a Registered Nurse for over a decade, working in internal medicine, trauma, kidney transplant, oncology, and leukemia/bone marrow transplant. It took over 4 years, but Jenneh's medical background gave her the knowledge and skills to navigate how to finally get good care after she was diagnosed with endometriosis. With her love for healthcare, education, and teaching, she felt inspired to use her abilities to help other women understand the disease better. She is also the author of Part of You, Not All of You: Shared Wisdom and Guided Journaling for Life With Chronic Illness. Jenneh is originally from New Jersey, and lives in Los Angeles. When asked why she felt so passionately about starting the The Endometriosis Coalition, she says "endometriosis is criminally under researched and horribly misunderstood, and I want to be a part of changing that, sooner rather than later."

So let’s get into the discussion!

SHOW NOTES:

Support the Show.

If you haven’t already, subscribe to our monthly newsletter where you will get each episode of the pod straight to your inbox. Learn more at reprofilm.org or at @reprofilm The rePROFilm Podcast is executive produced by mamafilm. Looking forward to bringing you our next conversation!

  continue reading

36 episodes

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Manage episode 322775660 series 3305728
Content provided by rePROFilm. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by rePROFilm or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Interview with Endo Coalition's Jenneh Rishe
We’re all familiar with March being Women’s History Month, but did you know it is also Endometriosis awareness month? If you didn’t, don’t worry you certainly are not alone. In fact, despite the statistics that say 1 in 10 women in the US are living with endometriosis, many are suffering in silence. There are a number of reasons for this, ranging from lack of awareness, to misdiagnosis, and lack of funding for research toward endometriosis, all of which contribute to a widespread problem that deserves more education and amplification.

So this is our theme for the month, and I am super excited for our interviews in this periodical. It will actually be a two-part episode, and in this first part, I will be speaking with Jenneh Rishe, the founder and executive director of an advocacy organization called The Endometriosis Coalition.

Jenneh has been a Registered Nurse for over a decade, working in internal medicine, trauma, kidney transplant, oncology, and leukemia/bone marrow transplant. It took over 4 years, but Jenneh's medical background gave her the knowledge and skills to navigate how to finally get good care after she was diagnosed with endometriosis. With her love for healthcare, education, and teaching, she felt inspired to use her abilities to help other women understand the disease better. She is also the author of Part of You, Not All of You: Shared Wisdom and Guided Journaling for Life With Chronic Illness. Jenneh is originally from New Jersey, and lives in Los Angeles. When asked why she felt so passionately about starting the The Endometriosis Coalition, she says "endometriosis is criminally under researched and horribly misunderstood, and I want to be a part of changing that, sooner rather than later."

So let’s get into the discussion!

SHOW NOTES:

Support the Show.

If you haven’t already, subscribe to our monthly newsletter where you will get each episode of the pod straight to your inbox. Learn more at reprofilm.org or at @reprofilm The rePROFilm Podcast is executive produced by mamafilm. Looking forward to bringing you our next conversation!

  continue reading

36 episodes

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