#Endometriosis has an average diagnostic delay of up to 6.7 years in individuals. #SWHRtalksEndometriosis During the "Elevating Endometriosis" webinar learn more about closing these care gaps: ow.ly/7rNK50Qolkm Idhaliz Flores Jenneh Rishe BSN, RN PHSUniversity Johns Hopkins Medicine The Endometriosis Coalition

Happening next week! Join SWHR and Idhaliz Flores Jenneh Rishe BSN, RN PHSUniversity Johns Hopkins Medicine The Endometriosis Coalition for an #Endometriosis webinar about the persistent gaps in disease diagnosis and treatment: ow.ly/OwYk50Qol9q #SWHRtalksEndometriosis

Because there is no cure for #endometriosis, it is critical that individuals are empowered throughout their journey with this chronic disease. Tune in to SWHR's #SWHRtalksEndometriosis webinar: ow.ly/7TS950Qolau Idhaliz Flores Jenneh Rishe BSN, RN PHSUniversity Johns Hopkins Medicine The Endometriosis Coalition

Jenneh Rishe, BSN, RN Jenneh Rishe BSN, RN and founder of The Endometriosis Coalition Inc. The Endometriosis Coalition shares her #endometriosis story with us: Jenneh's symptoms first appeared at age 27. What started first as cyclical pain around her period soon became persistence and severe.

After years of countless doctor appointments, tests, and procedures, Jenneh received an #endometriosis diagnosis. Jenneh Rishe BSN, RN The Endometriosis Coalition It takes a full health care team of experts to diagnosis and treat endometriosis, Jenneh adds. #SWHRtalksEndometriosis

Be your own best advocate, says Jenneh. Jenneh Rishe BSN, RN The Endometriosis Coalition "We're told that our symptoms are normal, and they’re not. Excruciating pain is never normal. Excruciating pain that keeps you from functioning is never normal."

Jenneh Jenneh Rishe BSN, RN founded The Endometriosis Coalition Inc. The Endometriosis Coalition to create an advocacy and support space for individuals with #endometriosis. #SWHRtalksEndometriosis Learn more and get involved: theendo.co

A great opportunity to see Below the Belt for free alongside NYU medical students & faculty. You'll also have the opportunity to ask questions in a post-screening panel discussion with NYU's Division Director of Minimally Invasive Gynecological Surgery Dr. Ted Lee & Shannon Cohn.

Join us on 3/1 in NYC as we launch our official partnership with Little Words Project! Free to attend, but RSVP required here: littlewordsproject.com/pages/events

Happy #InternationalWomensDay to all of our amazing warriors 👏

From the patient perspective, what does Jenneh Rishe BSN, RN of The Endometriosis Coalition want to see investigated in regards to #endometriosis? Here more in this #SWHRtalksEndometriosis webinar clip! Watch the full conversation online this month: ow.ly/2Qhx50QE3na #EndometriosisAwarenessMonth

#Repost Meghan Maloof Berdellans 🖤 ⁣ “#1in10 women have Endometriosis. I am 1 in 10. Approximately 9 years ago, I first heard the word “#Endometriosis” and quite literally fainted (twice) in the doctor’s office. The word encapsulating the chronic illness that explained my 10+ years..."

I will proudly wear this bracelet in solidarity with my #endometriosis patients. END ENDO! Perfect sentiment. Thanks to the special patient and mother who were buying for themselves, and got me one too ❤️ #endendo #gynsurgeon The Endometriosis Coalition Little Words Project