The Endometriosis Coalition works to raise awareness, promote reliable education and increase research funding for endometriosis • 501(c)(3)
Philadelphia, PA
Joined May 2017
- Tweets342
- Following64
- Followers827
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The Endometriosis Coalition retweeted
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 @theendoco @littlewordsproj
The Endometriosis Coalition retweeted
#Repost @megconnolly_ 🖤
“#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..."
The Endometriosis Coalition retweeted
From the patient perspective, what does @JayRishe of @theendoco 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
The Endometriosis Coalition retweeted
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.
The Endometriosis Coalition retweeted
Jenneh Rishe, BSN, RN @JayRishe and founder of The Endometriosis Coalition Inc. @theendoco 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.
The Endometriosis Coalition retweeted
After years of countless doctor appointments, tests, and procedures, Jenneh received an #endometriosis diagnosis. @JayRishe @theendoco
It takes a full health care team of experts to diagnosis and treat endometriosis, Jenneh adds. #SWHRtalksEndometriosis
The Endometriosis Coalition retweeted
Be your own best advocate, says Jenneh. @JayRishe @theendoco
"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."
The Endometriosis Coalition retweeted
Jenneh @JayRishe founded The Endometriosis Coalition Inc. @theendoco to create an advocacy and support space for individuals with #endometriosis.
#SWHRtalksEndometriosis
Learn more and get involved: theendo.co/
The Endometriosis Coalition retweeted
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
@zilahdi @JayRishe @PonceHealthSU @HopkinsMedicine @theendoco
The Endometriosis Coalition retweeted
Happening next week! Join SWHR and @zilahdi @JayRishe @PonceHealthSU @HopkinsMedicine @theendoco for an #Endometriosis webinar about the persistent gaps in disease diagnosis and treatment: ow.ly/OwYk50Qol9q #SWHRtalksEndometriosis
The Endometriosis Coalition retweeted
#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 @zilahdi @JayRishe @PonceHealthSU @HopkinsMedicine @theendoco
The Endometriosis Coalition retweeted
I've always believed in the power of research to save lives and ensure Americans get the care they need.
Starting today, the first-ever White House Initiative on Women’s Health Research will work towards that goal, changing how we approach and fund women’s health research.
ALT President Biden is pictured seated following signing a Presidential Memorandum establishing the White House Initiative on Women's Health Research in the Oval Office of the White House. Among others, Dr. Victor Dzau, Dr. Carolyn Mazure, Shalanda Young, Secretary Xavier Becerra, and the First Lady attend.
The Endometriosis Coalition retweeted
This new White House Initiative on Women’s Health Research will help change that by identifying bold solutions to uncover the answers that every woman and her family deserves.
The Endometriosis Coalition retweeted
Every woman I know has a story about leaving her doctor’s office with more questions than answers. Not because our doctors are withholding information, but because there’s not enough research yet on how to treat common women’s health conditions.
In 2023, that is unacceptable.
The Endometriosis Coalition retweeted
Today, Joe is announcing the first-ever White House Initiative on Women’s Health Research.
I’m excited to help lead this effort, alongside the Gender Policy Council. Together, we have a clear goal: to fundamentally change how we approach and fund women’s health research.
The Endometriosis Coalition retweeted
Head over to our Instagram for a chance to win our #giveaway with @JayRishe, Founder of The Endometriosis Coalition (@theendoco) and author of 'Part of You, Not All of You' buff.ly/3yWrwX9
The Endometriosis Coalition retweeted
A new documentary, “Below the Belt,” is shining a light on endometriosis, which affects one in nine women and is often left undiagnosed. @RhiannonAlly has more.
The Endometriosis Coalition retweeted
It affects around 200m people globally yet as a new Hilary Clinton-produced #documentary shows, #endometriosis is still a misunderstood and under-researched condition.
Read our new @guardian article here:
theguardian.com/tv-and-radio…
#premiere #pbs
The Endometriosis Coalition retweeted
Endometriosis affects millions of women and girls. But we don't talk about it. I'm proud to have been an executive producer of "Below the Belt," a documentary airing on PBS on June 21 that breaks the silence. Don't miss this moving, informative, and infuriating film. pbs.org/show/below-belt-last…
The Endometriosis Coalition retweeted
Thank you so much to @TamronHallShow for having us on to talk about #endometriosis 🧡
Airs this MONDAY, MAY 1 on ABC nationwide in the US! 📺
#endo #chronicillness #endometriosisawareness
@JayRishe
@tamronhall
