New show “Ask the Doctors” launches on EndoTV hosted by Diana Falzone
EndoFound and MyHealthTeams partner to bring community, conversation and content to the 1 in 10 women living with endometriosis
Foxx Discusses Her Endo Experience, Talking To Her Dad About Her Diagnosis and More on EndoTV: Let’s Talk Period
The Endometriosis Foundation of America invites the world to learn more about endometriosis by joining its International Patient Conference 2021, The Path Towards A Cure: Connecting Patients with Science. The conference is in partnership with…
Social distancing and lockdowns have left some girls and women without period supplies. Senator Sue Serino partners with EndoFound to distribute PeriodNow products in Poughkeepsie, NY, on January 28, 2021.
“Transplant” (NBC) Co-executive Producer Rachel Langar Discusses Her Struggle With Endometriosis On Premiere Episode
The Endometriosis Foundation of America (EndoFound) is excited to share that a historic amendment doubling federal research funding for endometriosis was approved this week by the U.S. Senate, allowing the National Institutes of Health to allocate…
New York, NY - October 7, 2020 – Journalist Diana Falzone & Actress Lexie Stevenson Launch Endometriosis Foundation of America 3-Day conference on October 16 The Endometriosis Foundation of America (EndoFound) announced today that…
Falzone sets sights on expanding endometriosis awareness on Capitol Hill and to state governments across the US.
When Barden found out she had endometriosis, she said she was grateful to get a diagnosis. "In my gut, I knew," she said. "I said, 'once we figure out the underlying cause, I will get pregnant.'"
by Lena Felton The condition affects 7 million women in the United States and 1 in 10 women worldwide Read More: thelily.com
PeriodNow was launched in May by the Endometriosis Foundation of America (EndoFound) as part of World Menstrual Hygiene Day. The short-term mission is to provide period supplies to women and girls in the city during the pandemic. The long-term…
When Barden found out she had endometriosis, she said she was grateful to get a diagnosis. "In my gut, I knew," she said. "I said, 'once we figure out the underlying cause, I will get pregnant.'"
The lack of obvious symptoms can cloud diagnosis, lead to fertility problems.
Padma Lakshmi was diagnosed with endometriosis in 2006, after experiencing symptoms for 23 years — and she’s been advocating for people with the condition ever since. About one in ten people born with a uterus have endometriosis,…
In a new report, the Society for Women's Health Research outlines reasons why women must fight to get a timely diagnosis and adequate care. By Beth Levine Although 10 percent of reproductive-age women live with endometriosis, a chronic disease…
By Beth Levine Living with endometriosis can be daunting, painful, and confusing. But there is no reason to give up hope. These resources can show you how to successfully navigate your symptoms and your care so that you can take back your life…
Painful sex and extreme period cramps can take a toll on your libido. Here’s how to get your mojo back. There’s no doubt that endometriosis can affect a woman’s quality of life — and that includes her libido. That’s…
If you have endometriosis, you might have a host of concerns ranging from how to quell the notoriously agonizing pain to how this condition may impact your fertility. Though estimates vary, some figures suggest that between 30 and 50 percent…
The Endometriosis Foundation of America (EndoFound) today announced the addition of Piraye Yurttas Beim, PhD, to its Executive Board of Directors.
