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!
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